receiving and verifying sanitation activities. Identification of quality concerns and finding corrective action remedies is a large function of the job requirements. Ideal candidates will have previous supervisory or leadership experience with the ability to be detail oriented and accurately identify problems and corrections as necessary.
This is NOT an entry level position for training. A minimum of three years of recent continuous employment is required. 12 Hour Shift position, working nights. Other examples of the QC work performed are: Various tests for incoming ingredients, including sieve, NIR, moisture, and mycotoxin, salmonella and other bacterial tests. Other duties as assigned
such as: Routinely check operator paperwork for accuracy and completeness, check label, bags and seals. Also perform additional duties and functions as assigned by Quality Control Manager/Diamond Management.
Must be able to lift 50 pounds of product routinely Must be able to climb ladders and can't not be afraid of heights. This position is NOT funded for relocation and is open for immediate hiring. At Diamond Pet Foods, we believe in family. At Diamond Pet Foods, we believe in family. We pay 100% of Medical Insurance premiums, company paid Life Insurance, AD & D, and Long Term Disability Insurance (after 30 days) for you, your eligible spouse, and your dependents. Dental, Vision, additional
voluntary life and AD & D insurance, plus Short Term Disability coverage are also available at group discounts.
Some of our other benefits include six paid Holidays, Paid Time Off days (vacation), and a 401K retirement plan (upon meeting employment requirements and plan provisions). Diamond Pet Foods provides for equal employment opportunities (EEO) to all employees and applicants for employment without regard to race, color, religion, gender, interactionual orientation, gender identity or expression, national origin, age, disability, genetic information, marital status, amnesty, or status as a covered veteran in accordance with applicable federal, state and local laws.
Diamond Pet Food Processors of South Carolina complies with applicable state and local laws governing non-discrimination in employment in every location in which the company has facilities. We'd be proud to have you join our family. Diamond Pet Food Processors of South Carolina 100 Wood Trail Drive Gaston, SC 29053 No phone calls please. Job Type: Full-time Salary: From $23.75 per hour Benefits: 401(k) 401(k) matching Dental insurance Employee discount Health insurance Life insurance Paid time off Referral program Tuition reimbursement Vision insurance Schedule: 12 hour shift Supplemental pay types: Bonus pay Work Location: One location
Atlantic Ocean, to stealth bombers, to landing on the moon. We look for people who have bold new ideas, courage and a pioneering spirit to join forces to invent the future, and have fun along the way. Our culture thrives on intellectual curiosity, cognitive diversity and bringing your whole self to work - and we have an insatiable drive to do what others think is impossible.
Our employees are not only part of history, they're making history. At Northrop Grumman, our employees have incredible opportunities to work on revolutionary systems that impact people's lives around the world today, and for generations to come. Embark on a career putting innovative, reliable, and agile products and
ideas into orbit, and beyond. Northrop Grumman has opportunities waiting for you that play a vital role in human space exploration, national defense, and scientific discovery, supporting multiple programs across the universe.
With us, you'll discover a culture of curiosity and collaboration that will have you Defining Possible from the day you start. Our space systems connect and protect millions of people on earth every day, now and for the future. Explore your future and launch your career today. Northrop Grumman Space Systems is currently seeking a Tool Quality Engineer to provide support for our Tool Quality Teams in Clearfield, Utah and Iuka, Mississippi. Successful candidate for
this position will reside in Clearfield, UT. This position may be filled as either a Quality Engineer (level 2) or a Principal Quality Engineer (level 3).
Role description Duties and Responsibilities: Successful candidate will be responsible for performing Tool Quality Engineer functions to help assure the quality of tooling and to ensure the tooling meets the company's quality standards and support the efficiency and effectiveness of tools use in production. Job responsibilities will include: Evaluate tool designs for compliance to industry dimension and tolerancing standards. Evaluate design to determine manufacturability of tool design to produce an acceptable, functional tool.
Create and provide accurate Tool Inspection Records to various organizations to tools meet engineering requirements. Concur with tooling review board dispositions for tooling non-conformances. Coordinate, identify tooling non-conformance history, and communicate trends. Provide and support tooling nonconformance analysis and associated processes. Review Supplier data package for accuracy completeness. Maintain accurate tool history data packets. Effectively interact with Tool engineering, Tool Quality Inspection, Operations, Materials and Process experts, Quality engineering and Process engineering, and Design engineering.
Day-to-day, side-by-side participation with operations, engineering, and inspection personnel to ensure high quality tooling and product associated for critical hardware support. Inspect tool configuration for drawing compliance, including fit, form and function. Support tooling suppliers as needed during tool fabrication and inspection. Support continuous improvement. Support Operations and Process Engineering in the use of tooling Competencies for Success: Strong interpersonal skills with ability to interface with an organization at all levels.
Excellent problem-solving skills Able to deal effectively with stress and conflict. High energy, results oriented, self-reliant, team player. Ability to multitask and prioritize. Excellent organizational and multi-tasking skills Strong attention to detail Demonstrated work ethic. Basic Qualifications for a Tool Quality Engineer (level 2): 2 Years with Bachelors in Science; 0 Years with Masters, in science or a STEM discipline experience in manufacturing or quality assurance Knowledge of ISO 9001 and AS9100 Application of Geometric Dimensioning and Tolerancing (ANSI/AMSE Y14.5) Dimensional Inspection Techniques Ability to interpret Engineering Drawings Experience using product verification instruments including Laser tracker is a plus.
Experience and familiarity with machine shop and weld shop practices is a plus. Organization skills to maintain accurate history records. Must be able to obtain a Do D Secret Clearance. Knowledge in reviewing and understanding customer certifications, specifications, contracts and purchasing requirements. Physical demands include standing or moving about the plant more than half the time. Some travel to suppliers required and supplier on-site backssment experience a plus.
Basic Qualifications for a Tool Quality Engineer (level 3): 5 Years with Bachelors in Science; 3 Years with Masters; 0 Years with Ph D, in science or a STEM discipline experience in manufacturing or quality assurance Knowledge of ISO 9001 and AS9100 Application of Geometric Dimensioning and Tolerancing (ANSI/AMSE Y14.5) Dimensional Inspection Techniques Ability to interpret Engineering Drawings Experience using product verification instruments including Laser tracker is a plus. Experience and familiarity with machine shop and weld shop practices is a plus. Organization skills to maintain accurate history records.
Must be able to obtain a Do D Secret Clearance. Knowledge in reviewing and understanding customer certifications, specifications, contracts and purchasing requirements. Physical demands include standing or moving about the plant more than half the time. Some travel to suppliers required and supplier on-site backssment experience a plus. Preferred Qualifications: Geometric Dimensioning & Tolerancing knowledge Blueprint reading Machine Shop experience / knowledge Welding experience / knowledge Tool inspection experience / knowledge Active Do D Secret Clearance Salary Range: $68,500 - $102,700 Salary Range 2: $84,200 - $126,400The above salary range represents a general guideline; however, Northrop Grumman considers a number of factors when determining base salary offers such as the scope and responsibilities of the position and the candidate's experience, education, skills and current market conditions.
Employees may be eligible for a discretionary bonus in addition to base pay. Annual bonuses are designed to reward individual contributions as well as allow employees to share in company results. Employees in Vice President or Director positions may be eligible for Long Term Incentives.
In addition, Northrop Grumman provides a variety of benefits including health insurance coverage, life and disability insurance, savings plan, Company paid holidays and paid time off (PTO) for vacation and/or personal business. Northrop Grumman is committed to hiring and retaining a diverse workforce. We are proud to be an Equal Opportunity/Affirmative Action Employer, making decisions without regard to race, color, religion, creed, interaction, interactionual orientation, gender identity, marital status, national origin, age, veteran status, disability, or any other protected class.
For our complete EEO/AA and Pay Transparency statement, please visit http: ///EEO. U. S. Citizenship is required for most positions. PDN-9ae9da71-247d-4e52-bbbd-fced358ffeaf
procedures, support training of the operators and inspectors on inspection and gaging techniques and the use of procedures. Assists in the control of material certification documents. Monitor quality records and buck-on graphs from in-house or sub-contract process.
Monitor work order packets for accuracy and acceptability. Support and maintain documented processes for ordering, receipt and control of gages and related documents. Supervise other QA personnel as required. Generate or revise QA documents such as procedures, work instructions and specifications as needed; and train affected personnel on such documents. Interface with subcontractors on clarification of quality requirements.
Use knowledge of product and inspection/testing requirements to collect data and perform evaluation when customer issues arise. Utilize 8D problem solving to address customer claims.
Implement and maintain program of root cause analysis and corrective action of non-conformance to reduce variation of key process indicators, mitigate rework, reduce cost and improve quality. Collect appropriate data and use advanced problem-solving techniques such as process capability, SPC, FMEA and Design of Experiments to isolate and reduce sources of variation and to resolve production and quality issues. Review customer specifications/requirements to evaluate capability and develop quality plans
as needed. Perform internal and supplier/subcontractors process and management system audits as scheduled or needed.
Support project activities and product industrialization by working with operations, operations technology, research and development, product engineering, industrial performance, planning/scheduling, and external suppliers/organizations. Promote effective communication vertically and horizontally within the organization. Must follow all company policies, practices and regulations to include Quality and Safety. Any other duties as assigned. REQUIREMENTS Strong quality engineering background in manufacturing environment. Experience in machining operations is desired.
Proficient in wide range of problem-solving tools and methods, including Six Sigma Methodology and advanced statistics. Has extensive, in-depth knowledge of quality requirements and systems. Experience with ISO9001 and API quality/product standards is required. OCTG and connections knowledge is highly desired. The individual must be proficient in Microsoft Office Suite including Excel, and Power Point as well as statistical analysis software, such as Minitab. Highly motivated, willingness to dig into situations and work with all functions of the business.
The ability to work in diverse groups to achieve a common goal is critical to the success of this position. Ability to effectively communicate with all levels of the organization. Capable of working independently in a self-directed environment Excellent written and verbal communication skills EDUCATION, TRAINING, AND CERTIFICATIONS: BS in quality engineering or in another engineering discipline with quality experience such as Mechanical or Industrial Engineer is required. MBA preferred. Lead auditor training is required (ISO 9001, API Q1) Six Sigma black belt or green belt certification or training preferred.
ASQ - Certified Quality Engineer (CQE) preferred. CRITICAL COMPETENCIES & CAPABILITIES: The position will require demonstrated leadership skills and the ability to concisely communicate objectives and results to reach targeted goals. Strong understanding of quality assurance/process control principles as well as manufacturing quality control methods (inspection and gaging).
Location: South Bay Salary $90-110k/yr. (depending on experience) Summary: The Quality Engineer position will ensure product and process producibility is optimized through: Reduced Costs, Improved Quality, Effective Corrective Action, Reduced Cycle Times, and Process Capability.
Essential Functions: Develops solutions to a wide range of technical problems related to the product being manufactured Develops, monitors and analyzes product/process trend data and or tooling/manufacturing & inspection techniques to optimize performance, minimize product, and process variability, and associated production costs Provides support for the MRR system, including submitting non-conforming parts to
the customer and working with other departments to develop root cause and corrective action plans necessary to reduce: Scrap, Rework, and Repair Costs Evaluates initial/existing programs for conformance to customer contractual requirements Coordinates / Monitors results necessary to validate improvements Coordinates with respective customers, vendors, and subcontractors on technical issues Develops product quality plans and inspection methodologies; makes modifications to existing procedures, production processes, and inspection techniques Qualifications: 2-3 years' experience in aerospace Experience in aircraft manufacturing - Metal forming and CNC Machining a must Experience in Blueprint reading
and geometric dimensioning and tolerances (GD&T) BS or BA required Pando Logic.
Keywords: Quality Control / Quality Assurance Engineer, Location: Gardena, CA - 90247 , PL: 572868048 Associated topics: aero, aerospace engineer, air craft, aircraft maintenance, astronautical, avionic, f 35, missle, pilot, space craft
Florida markets, Preferred Materials provides municipalities, developers, architects, engineers, contractors, builders and suppliers a wide variety of construction materials and products. Our employees make Preferred Materials a great place to work. We promote a strong safety culture, where employees take responsibility for their own safety.
This position is for our Ocala West Location in Ocala, FL. Preferred Materials, Inc. is seeking a Quality Control Technician. Experience testing concrete is preferred, but willing to train. Candidates should be in possession of ACI Field Testing Grade I certification. Responsibilities include testing plastic and hardened concrete, and the raw materials
used to produce concrete. Candidates should have experience testing gradation, specific gravity, and absorption of fine and coarse aggregates per ASTM specifications.
Key Responsibilities (Essential Duties and Functions) Ensure Health & Safety standards are met by complying with legislation, company policies and promoting a safe work environment Must be able to communicate details of concrete mix adherence to specifications with a Sr QC Technician or a QC Manager in order to determine course of action for mix design adjustments in the field. Must be able to communicate concrete mix design issues to a Sr QC Technician or QC Manager from the field in order to determine if loads should be
accepted or rejected. Collect samples from concrete or aggregate plants.
Perform field tests, trail batches, densities of materials and other properties. Processes samples using a variety of testing equipment and procedures. Preforms Research and development on new materials to be used. Records data and enters information into computer systems. Must be able to obtain and maintain the following ACI certifications in a timely manner: ACI Field Testing Technician Certification Level 1. ACI Concrete Laboratory Testing Technician Level 1. ACI Aggregate Testing Technician Level 1. Concrete Strength Testing Technician. FDOT Batch Plant Operator Ability to clearly and efficiently communicate with plant staff and area management when needed.
Must be willing to work nights and weekends when necessary. Perform general clean-up and maintenance duties as assigned. Must be able to maintain acceptable attendance in a flexible work schedule. Properly follow & promote all company policies and OSHA regulations for safe working procedures and environment. Must maintain at all times a strict adherence to safety requirements and procedures. Must be available to travel and work at multiple construction sites within your geographic region. May perform other duties including but not limited to operating equipment.
Must possess a professional attitude while interacting with peers, contractors and general public. Education/Experience: High School diploma or GED, some advanced education preferred but not required. Chemistry background/experience Good penmanship, record keeping, and basic computer skills. Strong Knowledge of Excel needed. Ability to understand, communicate and follow verbal and written instruction. Ability to read, write and do basic mathematical calculations in English and Metric Ability to communicate effectively over the company radio. Clean driving record.
1 year of related construction industry experience preferred, but not required. Qualifications To perform this job successfully, an individual must be able to perform each essential duty according to Preferred Materials guidelines and standards. Work Requirements Must pass pre-employment physical, drug screen, criminal background check and driving record review. Must be willing to work flexible schedule including: nights, weekends and holidays when necessary. Must be legally authorized to work in The United States. Must demonstrate a strong commitment to safety. Regular and timely attendance is required.
Ability to use basic power tools. Ability to lift up to 40 pounds What CRH Offers You Highly competitive base pay Comprehensive medical, dental and disability benefits programs Group retirement savings program Health and wellness programs A diverse and inclusive culture that values opportunity for growth, development, and internal promotion About CRH CRH has a long and proud heritage. We are a collection of hundreds of family businesses, regional companies and large enterprises that together form the CRH family. CRH operates in a decentralized, diversified structure that allows you to work in a small company environment while having the career opportunities of large international organization.
If you’re up for a rewarding challenge, we invite you to take the first step and apply today! Once you click apply now, you will be brought to our official employment application. Please complete your online profile and it will be sent to the hiring manager. Our system allows you to view and track your status 24 hours a day. Thank you for your interest! Preferred Materials, Inc. a CRH Company, is an Affirmative Action and Equal Opportunity Employer. EOE/Vet/Disability--If you want to know more, please click on this link.
kick off meeting, as well as weekly project meeting. Participate in to tech transfer activity. Represent quality department during client meetings. Work with trifunctional department to ensure project related activity is completed on time. This role supports internal and external audits which may include interaction with Health Authorities and clients.
Essential Functions and Responsibilities Below is the summary of the role responsibilities. This is not necessarily an exhaustive list of all responsibilities, duties, skills, efforts, requirements or working conditions associated with the role. While this is intended to be an accurate reflection of the current job, management reserves
the right to revise the job or to require that other or different tasks be performed as assigned with or without notice. Attends project kick-off meetings to understand the scope of the project.
Creates, updates, reviews and/or approves project related documents such SOPs, Batch release templates, label templates, batch records, change controls, etc. according to client requirements and project scope. Participates in tech transfer activity to ensure adherence to company quality system standards. Proactively identifies risk and prepares mitigation strategies associated with project and client work. Represents QA Client Services during scheduled meetings with client and cross functional
department. Ensures all necessary quality documents are closed prior to batch released; responsible for batch released on timely manner according to schedule.
Participates in client meetings and monitor quality activities of internal team members as they relate to contract deliverables. Draft initial Quality agreement and complete necessary revisions based on client and company requirements. Promptly and effectively communicates any successes, challenges, and/or constraints internally and externally with clients as appropriate. Provides quality data to Project Manager for the purpose of creating KPI metrics. Builds rapport with clients and troubleshoots issues of concern with internal team in order to provide the highest quality services which meet the needs and requirements of our clients.
Updates and maintains accurate information for each client on project-related documentation repository (i. e. Share Point). Communicates internally within QA team to provide key updates on project status, timelines, and deliverables. Formulates and prioritizes appropriate responses to client requests or concerns. Trains Quality Associates on client specific processes to ensure records are complete, accurate and submitted by agreed deadline. Supports, participates and follows up appropriately to internal, regulatory agency and client audit requests on a timely basis.
Identifies and supports continuous improvement opportunities working cross departmentally or cross functionally n order to enhance operations. Other duties may be assigned Qualifications Bachelor's Degree in Life Sciences Minimum 5 years experience in QA in a life sciences company with a strong focus in the manufacturing and/or testing of biologics preferred. Experience in authoring, reviewing, and /or approving c GMP/c GTP related documents (Investigation report, CAPA report, SOPs etc. ) required.
Understanding of quality system applications, including the use of electronic applications for training, deviations, CAPA management, etc. Familiar with FDA, ISO, and other regulatory agency guidelines. Understanding of Good Manufacturing Practices (GMP), Good Documentation Practices (GDP) and Good Laboratory Practices (GLP) required. Working knowledge and technical understanding of aseptic manufacture of biologics preferred. Experience in both clinical and commercial manufacturing is preferred. Experience participating health authority inspections and/or client audits preferred. Experience in organizing teams for effective and timely completion of projects.
Competencies/Candidate Profile Customer Focus: Is dedicated to meeting the expectations and requirements of internal and external customers; gets first-hand customer information and uses it for improvements in products and services; acts with customers in mind; establishes and maintains effective relationships with customers and gains their trust and respect. Process Management: Good at figuring out the processes necessary to get things done; knows how to organize people and activities; understands how to separate and combine tasks into efficient work flow; knows what to measure and how to measure it; can see opportunities for synergy and integration where others can't; can simplify complex processes; gets more out of fewer resources.
Decision Quality: Makes good decisions based upon a mixture of analysis, wisdom, experience, and judgment; most of his/her solutions and suggestions turn out to be correct and accurate when judged over time; sought out by others for advice and solutions. Negotiating: Can negotiate skillfully in tough situations with both internal and external groups; can settle differences with minimum noise; can win concessions without damaging relationships; can be both direct and forceful as well as diplomatic; gains trust quickly of other parties to the negotiations; has a good sense of timing.
Composure: Is cool under pressure; does not become defensive or irritated when times are tough; is considered mature; can be counted on to hold things together during tough times; can handle stress; is not knocked off balance by the unexpected; doesnt show frustration when resisted or blocked; is a settling influence in a crisis. Learning on the Fly: Learns quickly when facing new problems; a relentless and versatile learner; open to change; analyzes both successes and failures for clues to improvement; experiments and will try anything to find solutions; enjoys the challenge of unfamiliar tasks; quickly grasps the essence and the underlying structure of anything.
tools. To apply, please send email to with reference to IT Quality Analyst II in the subject line. Salary range: $76,686 - $80,000 Benefits: ∙ PTO∙ Medical, dental, vision plans, employee assistance program, as well as life insurance and LTD plans; ∙ Supplemental life insurance∙ Voluntary accident and critical illness insurance, respectively∙ Flexible Spending Account available∙ 401k plan
and in support of biodefense programs. The Early Research and Development Group (ERDG) and the Advanced Research and Development Group (ARDG) at Mapp Biomedical are responsible for the execution of high-quality Research and Development activities to ensure the achievement of a robust portfolio through CMC, Nonclinical, Regulatory, Project Management, and Clinical activities consistent with Mapp's product development objectives.
The Director of Quality Assurance - Gx P Analytical is an individual contributor who is a strategic thinking employee functioning as a key member of the Quality Assurance team who also partners with the CMC, Nonclinical, and Clinical development functions to ensure
data integrity and phase-appropriate compliance. Additionally, the Director of Quality Assurance - Gx P Analytical partners with Principal Investigators and the program teams to deliver on Mapp's portfolio.
Basic Qualifications BS/BA Degree in a related Science; MS Degree in related Science preferred 10+ Years of a combination of development experience in regulated medical roles, preferably within a Biologics/m Ab Product Development environment A significant amount of this time in a position that led or supported analytical and quality control operations for Drug Substance and Drug Product development and manufacturing Experience in a QA-Gx P role or a role that interacted with Quality
Assurance A solid background in analytical technologies and troubleshooting for large molecule products (preferably monoclonal antibodies) Strong background and in-depth knowledge in analytical chemistry across a wide range of technologies Demonstrated proficiency in method qualification, validation, stability programs and specifications setting and comprehensive understanding and significant experience in executing phase-appropriate qualification/validation strategies Excellent knowledge of c GMPs or equivalent regulations, e.
g. ICH, and the ability to interpret and relate Quality standards for implementation and review Experience in working with external parties (CDMOs, Contract Labs) Possesses the knowledge to act as a SME on any QA-Gx P data integrity issues Knowledge of drug development regulations such as the GCPs, GMPs and GLPs Willingness to travel required (up to 25% domestic and international) Previous technical CMC experience with large molecule (preferably monoclonal antibody) Drug Substance and/or Drug Product development/commercialization Previous experience with auditing biological and parenteral manufacturing facilities, laboratories that perform regulated activities, and/or clinical sites Experience overseeing Gx Ps (as a Sponsor) at third-party locations in a small or mid-sized Biotechnology company Preferred Qualifications MS Degree in related Science preferred Experience across all phases of biologic drug development (Clinical phases 1 thru 4 of drug development) preferred Experience in a technical or QA role for the oversight or execution of monoclonal antibody Drug Substance and Drug Product manufacture Experience working virtual preferred Mapp offers a competitive compensation and benefits package in addition to this exciting and challenging job.
Mapp's anticipated pay scale for this position is $130,000 to $250,000 plus any applicable bonuses.
The final salary offered to a successful candidate will be dependent on several factors that may include but are not limited to the candidate's level of education, and type and length of experience within the job and/or within the industry. Medical, dental, and vision insurance benefits are available to eligible employees and their families. Mapp also provides basic life insurance, short and long term disability, and a 401K plan that includes Company contributions to eligible employees. Full-time employees will be provided 7 days of sick time, 14 paid holidays, and will also accrue 18 days of vacation throughout the calendar year.
If your job responsibilities allow, you may choose to work remotely. Willingness to Travel (Domestic Travel = Approximately Once per month + International Travel = Approximately Twice per year) will be required for this position. Mapp wants you to join their team and invites you to apply by submitting your information through mappbio. /jobs/. This job will remain open for twenty (20) days after being posted on Mapp's Job Openings website page (see link). No Solicitors, agents or placement agencies please. Mapp utilizes E-Verify.
Mapp is an Equal Opportunity/Affirmative Action/Disability/Veterans Employer - Qualified applicants will receive consideration for employment without regard to race, color, religion, interaction, interactionual orientation, gender identity, national origin, disability, protected Veteran status, or any other characteristic protected by applicable federal, state, or local law. Job Posted by Applicant Pro
as part of a managed team Detailed knowledge of web application and network based P en testing security tools. MINIMUM REQUIRED QUALIFICATIONS: Must have a Secret Clearance with the ability to get TS/SCI. In addition to specific security clearance requirements all FEMA SOC employees are required to obtain an Entry on Duty (EOD) clearance to support this program.
4 years in Pen Testing and Vulnerability backssment 4-6 years of professional experience in incident detection and response, malware analysis, or cyber forensics. Experience with any three of the seven tools listed below: Kali Linux Metaspoilt Burp suite Cobalt Strike Tenable Nessus Web Inspect Scuba App detective Must have one
of the following Certifications: GPEN, GWAPT, GISF, GXPN, OSCP, OSCE, OSWP, OSEE, CISSP, CEH Preferred Qualifications: Prior System Administrator experience a plus.
Previous IT experience is preferred, specifically 7 years of professional experience in a Computer Science discipline is ideal. Education & Experience: Bachelors Degree and 8 – 12 years of prior relevant experience in order to operate within the scope contemplated by the level. Experience in lieu of degree Pay Range: Pay Range $101,400.00 - $183,300.00 The Leidos pay range for this job level is a general guideline only and not a guarantee of compensation or salary. Additional factors considered in extending an offer include
(but are not limited to) responsibilities of the job, education, experience, knowledge, skills, and abilities, as well as internal equity, alignment with market data, applicable bargaining agreement (if any), or other law.
Original Posting Date: 12/11/2023 While subject to change based on business needs, Leidos reasonably anticipates that this job requisition will remain open for at least 3 days with an anticipated close date of no earlier than 3 days after the original posting date as listed above. For more details: jobs-search. org/penetration-tester_bluemont-c449230/penetration-tester-security-clearance-required-bluemont_i1969457989
and procedures to ensure work processes, products, or services satisfy expectations and quality standards. backsses quality assurance programs of other Department of Defense (Do D) services and analyzes commercial maintenance practices to establish a comprehensive Quality Program (QP) for the AASF.
Develops quality backssment plans to evaluate and improve quality of maintenance production and work processes. backssments include reviews of management and organization; quality systems; personnel qualifications and training; supply procedures; facilities; tools and test equipment; maintenance documentation; operations and training requirements, and equipment failures. Develops local regulations
and/or operating instructions for implementation of the quality assurance and reliability program and ensures compliance with procedures. Prepares quality assurance operating instructions, local forms, checklists, and other material.
Serves as quality assurance authority in the AASF. Provides the Logistics Management Officer/Supervisory Maintenance Test Pilot and maintenance supervisors with definitive technical information and advice on maintenance procedures and techniques. Resolves technical problems in support of the quality assurance program. Maintains the AASF master library. Ensures that appropriate directives and operating instructions are current and complete. Reviews incoming
publications to determine their applicability. Provides technical guidance and expertise in interpretation of technical manuals (TM), and acts as the authoritative reference on quality methods, techniques, and procedures.
Monitors the AASF publication improvement system to include the recommended changes to publications and blank forms (DA Form 2028) and material deficiency, and Quality Deficiency Reports (QDR). Manages the Safety-of-Flight (SOF) and Aviation Safety Action Message (ASAM) programs to ensure effective and timely accomplishment. Reviews incoming SOF/ASAM for applicability to AASF supported equipment. Monitors compliance actions and prepares and forwards compliance reports.
Monitors aircraft acceptance/transfer inspections, aircraft configurations, and component timechange requirements. Periodically reviews aircraft historical records and logbooks for accuracy and condition. Monitors the Army Oil Analysis Program (AOAP). Manages the weight and balance program. Performs inventories of and calibration of electronic weighing apparatus; monitors aircraft weighing operations; verifies instrument readings, resolves weight and balance problems, and certifies weight and balance computations. Performs command directed quality inspections and special inspections for all aspects of aircraft and associated equipment.
Records discrepancies, provides definitive corrective recommendations, and reviews adequacy of corrective action taken. Performs inspections of maintenance shops for safety and condition of equipment. Monitors calibration of shop and test equipment. Certifies and maintains files of personnel authorized to perform quality inspections. Performs management and compliance reviews over a wide range of functions within the AASF. Prepares recommendations on the resolution of deficiencies affecting production or maintenance quality.
Reviews and validates all locally developed maintenance procedures before adoption within the AASF. Investigates equipment failure trends on airframes, components and systems. Makes recommendations regarding equipment performance engineering design changes. Incumbent is required to wear appropriate protective clothing or gear and observe all safety precautions when accomplishing inspections. Conducts formal training of quality assurance and quality compliance principles, procedures, techniques, and skills. Provides initial training for the certification of status symbol clearing authority.
Provides refresher training for the maintenance of AASF quality standards. Reviews, evaluates and audits quality compliance inspections performed by production units. Provides on-the-spot assistance regarding the inspection process. Recommends corrective actions or changes in inspection methods and work procedures. Assists production supervisors and personnel in implementing changes. Evaluates completed reports for adequacy of actions taken by work center supervisors. Serves as the primary point of contact (POC) to, and provides liaison services between, the AASF and external organizations regarding QA matters.
Attends conferences, briefings, and meetings on quality assurance matters. Serves as the Contracting Officer Representative (COR) for a life cycle contractor support aircraft maintenance contract. Requirements Conditions of Employment NATIONAL GUARD MEMBERSHIP IS REQUIRED. If you are not sure you are eligible for military membership, please contact a National Guard recruiter prior to applying for this position. This is an excepted service position that requires membership in a compatible military assignment in the employing state's National Guard, required prior to the effective date of placement.
Selectee will be required to wear the military uniform. Acceptance of an excepted service position constitutes concurrence with these requirements as a condition of employment. Applicants who are not currently a member of the National Guard must be eligible for immediate membership and employment in the National Guard in the military grade listed in this announcement. Males born after 31 December 1959 must be registered for Selective Service. Federal employment suitability as determined by a background investigation. May be required to successfully complete a probationary period.
Participation in direct deposit is mandatory. This position is covered by the Domestic Violence Misdemeanor Amendment (30 Sep 96) of the Gun Control Act (Lautenberg Amendment) of 196 8. An individual convicted of a qualifying crime of domestic violence may not perform the duties of this position. Ability to establish effective professional working relationships with coworkers and customers, contributing to a cooperative working environment and successful accomplishment of the mission. Irregular and/or overtime (compensatory) hours may be required to support operational requirements or contingencies or may be required to work hours outside of the normal duty day.
The duties and responsibilities of your job may significantly impact the environment. You are responsible to maintain awareness of your environmental responsibilities as dictated by legal and regulatory requirements, your organization, and its changing mission. Qualifications Military Grades: E4-E8 GENERAL EXPERIENCE : Experience, education, or training involving planning, developing, or administering quality assurance programs (i. e. supporting the development, acquisition, production, use, maintenance, storage, and supply of products concerned with the systematic prevention of defects and non-conformances, the identification of unsatisfactory trends and conditions, and the correction of factors which may contribute to defective items).
Experience using computer and automation systems. SPECIALIZED EXPERIENCE : Must have at least 24 months experience, education, or training, involving principles, techniques and accepted practices of quality assurance work (i. e. the application of statistical sampling techniques sufficient to perform assignments or preparation of technical reports on quality levels to identify specific problems).
Experience in the application and theory of specialization using applicable publications. Experience in the preparation of technical reports on quality levels to identify specific problem areas and to recommend corrective action. Comprehensive knowledge of assigned aircraft, component systems, and support equipment to include aircraft specifications and standards. Incumbent utilizes aircraft mechanical skill and knowledge in applying quality assurance to the evaluation and resolution of complex operating and quality issues. -- Thorough knowledge of the principles, concepts, and methodology of quality assurance functional programs and skills in applying this knowledge to the planning and execution of aircraft maintenance production and processes.
-- Knowledge of aircraft inspection methods, techniques and practices to detect conditions, which may compromise quality and the ability to use precision measuring equipment, gauges and instrumentation for testing and special inspections as required. -- Skill in applying statistical analysis, sampling methods, and techniques to determine compliance with the established standards and the ability to interpret and apply contract and engineering specifications, regulations, policy statements and other guideline material to the maintenance functions of the AASF.
-- Knowledge of operating practices and procedures related to the maintenance of aircraft, systems and components. Skill to verify, by work document review, material and procedure checks and onsite surveillance, that essential quality requirements have been met. -- Ability to conduct technical reviews, analyze findings and develop recommendations for corrections or improvements in the quality assurance program. Ability to prepare technical reports on quality levels, to identify specific problem areas and to recommend corrective action.
How You Will Be Evaluated You will be evaluated for this job based on how well you meet the qualifications above. Once the announcement has closed, your resume and supporting documentation will be used to determine if you meet the qualifications listed on this announcement. If you are minimally qualified, your resume and supporting documentation will be compared to your responses on the backssment questionnaire to determine your level of experience. If you rate yourself higher than is supported by your application package, your responses may be adjusted and/or you may be excluded from consideration for this position.
If you are found to be among the top qualified candidates, you will be referred to the selecting official for employment consideration. Your qualifications will be evaluated on the following competencies (Quality Assurance and Technical Competence): Required Documents To apply for this position, you must submit a complete Application Package which includes: 1. Your resume: Your resume may be submitted in any format and must support the specialized experience described in this announcement.
If your resume includes a photograph, other PII (Personally Identifiable information) or other inappropriate material or content, it will not be used to make eligibility and qualification determinations and you may not be considered for this vacancy. For qualifications determinations your resume must contain hours worked per week and the dates of employment (i. e. Hours per week and month/year to month/year or month/year to present ex. 03/2020-06/2022 or 03/2020-Present). If your resume does not contain this information, your application may be marked as incomplete, and you may not receive consideration for this position.
For additional information see:2. Other supporting documents (as applicable): Certifications DD-214 or NGB 22 SF-50 Official Transcripts If you are NOT a current member of the Oklahoma National Guard, you must submit documentation showing your current/ previous military affiliation (DD 214, NGB 22, copy of an award/order, statement of service) etc. with your application to receive consideration for this position. Failure on your part to submit the requested documents will prevent further consideration for this position. If you have any questions concerning this requirement, contact our office at (405) 228-xyz X.
If you are relying on your education to meet qualification requirements: Education must be accredited by an accrediting institution recognized by the U. S. Department of Education in order for it to be credited towards qualifications. Therefore, provide only the attendance and/or degrees from. Failure to provide all of the required information as stated in this vacancy announcement may result in an ineligible rating or may affect the overall rating. PDN-9ae7f01c-87ed-4751-b743-22959c6f2ddc
manufacturing and services, enabling the digital-rail-and-transit ecosystems. Wabtec is focused on performance that drives progress, creating transportation solutions that move and improve the world. Wabtec has approximately 27,000 employees in facilities throughout the world.
Visit the company's new website at: http: //. It's not just about your career. or your job title.it's about who you are and the impact you are going to make on the world. Do you want to go into uncharted waters.do things that haven't been done to make yours and someone else's life better? Wabtec has been doing that for decades and we will continue to do so! Through our people, leadership development, services, technology
and scale, Wabtec delivers better outcomes for global customers by speaking the language of industry. Summary: The mission of the Quality Engineer is to ensure that products manufactured in the shop are capable and will meet specified quality standards.
Understanding of manufacturing processes for analysis of non-conforming parts to identify root causes and address appropriate corrective actions. Keep communication with customers internal and external customers to track solution of non-conformities and implement effective corrective actions that will prevent recurrence in the future. Duties and Responsibilities: Drive culture of quality and process discipline. Analyze non-conformity issues
and provide a disposition of parts, follow up in the quality system until completion of disposition.
Lead containment activities to minimize customer impact. Perform root cause analysis and corrective action to prevent recurrence in production line. Lead activities to ensure execution to quality metrics within assigned area. Establish and execute quality plan for compliance with international quality standards (ISO-9001, AAR, IRIS, etc. ) Establish quality control plans to drive proactive quality improvements in area of responsibility. Work on project(s) to improve process control, reduce defects, scrap and rework in the shop. Monitor and report quality KPIs lead propose and lead action plans to improve product or process quality.
Minimum Qualifications Bachelor's degree from an accredited university, from Mechanical, Electrical, Industrial Engineering, or similar career. Experience in Quality Assurance or similar roles. Experience with corrective action activities (5-Why, 8D, Etc. ) Fluent English with oral and written communication skills. Able to work in a cross-functional matrix environment. Experience at least 4 years in related areas. Blue print reading Understanding of Gauging concepts and measurement techniques Competencies, Knowledge, Skills and Abilities: Experience or good knowledge of Manufacturing assembly processes.
Experience or good knowledge of Microsoft Office (Excel, Power Point, Word, etc). Knowledge of Lean Six Sigma or Quality tools. Green belt or black belt certification preferred. Certified Internal Auditor. Ability to coordinate several projects/tasks simultaneously. Effective problem identification and solution skills. Authority: [ Defined decision-making level. The Plant GM is the main authority at site level. To be able to give authority, any employee in the organization shall first receive it from their manager or upper level, up to the General Manager.
] Authority to update, approve, and release product quality documentation. Authority to disposition any material on the floor. All WPT employees have the authority to stop the process they are performing, should the process become unsafe or the outputs nonconforming. Physical Demands: (The physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.
) Employee is required to stand for up to 4 hours per day. Employee is regularly required to lift and/or move up to 25 pounds, and occasionally lift and/or move 50 pounds. Requires daily face-to-face interaction with employees on production line. Work Environment: (The work environment characteristics described here are representative of those an employee encounters while performing the essential functions of this job. ) Office and manufacturing environments. May involve exposure to cold and hot temperatures, humidity, dust, vapors, fumes, vibration, and other loud noises from the plant.
The work environment characteristics described here are representative of those an employee encounters while performing the essential functions of this job. Is occasionally exposed to fumes or airborne particles, toxic or caustic chemicals, and loud noise. Relocation assistance lump sum available for qualified candidates. Wabtec Corporation is committed to taking on the world's toughest challenges. In order to fulfill that commitment we rely on a culture of leadership, diversity and inclusiveness. We aim to employ the world's brightest minds to help us create a limitless source of ideas and opportunities.
We believe in hiring talented people of varied backgrounds, experiences and styles.people like you! Wabtec Corporation is committed to equal employment opportunity regardless of race, color, ancestry, religion, interaction, national origin, interactionual orientation, age, citizenship, marital status, disability, gender identity or expression, or protected Veteran status. If you have a disability or special need that requires accommodation, please let us know. PDN-9ae7c187-a3d7-46f0-b33b-b4d750899648
at the point of occurrence and supporting operations with corrective & preventive actions. Working with supplier quality engineers to identify continual improvement opportunities with key suppliers. Reviewing customer ITP (inspection test plans) against routings and confirm routing steps as needed.
Supporting daily production activity with incoming, in-process, and final inspection. Inspecting parts to drawings with measuring equipment and CMM (Coordinate Measuring Machine). Working closely with product engineering, supplier quality, sourcing, and operations to disposition nonconformities. Fuel your passion To be successful in this role you will: Have a diploma in mechanical or relevant
technical education or a GED with 3-5 years' of relevant experience. Have 3+ years' experience working in quality inspection. Have experience with control, safety, and safety relief valves or similar mechanical products.
Have SAP-ERP Quality Control experience. Have experience and must be able to demonstrate operating CMM. Work in a way that works for you We recognize that everyone is different and that the way in which people want to work and deliver at their best is different for everyone too. In this role, we can offer the following flexible working patterns: Working flexible hours - flexing the times when you work in the day to help you fit everything in and work when you are the
most productive Working with us Our people are at the heart of what we do at Baker Hughes.
We know we are better when all of our people are developed, engaged and able to bring their whole authentic selves to work. We invest in the health and well-being of our workforce, train and reward talent and develop leaders at all levels to bring out the best in each other. Working for you Our inventions have revolutionized energy for over a century. But to keep going forward tomorrow, we know we have to push the boundaries today. We prioritize rewarding those who embrace change with a package that reflects how much we value their input. Join us, and you can expect: Contemporary work-life balance policies and wellbeing activities Comprehensive private medical care options Safety net of life insurance and disability programs Tailored financial programs Additional elected or voluntary benefits About Us: We are an energy technology company that provides solutions to energy and industrial customers worldwide.
Built on a century of experience and conducting business in over 120 countries, our innovative technologies and services are taking energy forward - making it safer, cleaner and more efficient for people and the planet. Join Us: Are you seeking an opportunity to make a real difference in a company that values innovation and progress?
Join us and become part of a team of people who will challenge and inspire you! Let's come together and take energy forward. Baker Hughes Company is an Equal Opportunity Employer. Employment decisions are made without regard to race, color, religion, national or ethnic origin, interaction, interactionual orientation, gender identity or expression, age, disability, protected veteran status or other characteristics protected by law. PDN-9ae7efba-da-7c03abd508d5
of our billions of Med Tech products per year-to look at the impossible and find transformative solutions that turn dreams into possibilities. We believe that the human element, across our global teams, is what allows us to continually evolve. Join us and discover an environment in which you'll be supported to learn, grow and become your best self.
Become a maker of possible with us. The Senior Supplier Quality Engineer is responsible to define and implement the supplier management activities required to approve suppliers and maintain their approved status throughout the product lifecycle. This is achieved by ensuring the conformance of the supplier to applicable quality specifications
of components, products, materials, or services delivered to BD, in compliance with BD supplier management policies and procedures, as well as applicable standards and regulations.
Responsibilities Support identification of prospective suppliers. Define the optimum supplier approval strategy, and create supplier approval plans. Facilitate, manage, and track supplier progress toward Approved status, supporting both new product development launches and sustaining engineering changes. Conduct supplier quality audits backssments as necessary including for-cause audits, and complete follow-up and closure of any non-conformances. Author, negotiate, and finalize both Quality and Technical Agreements
with suppliers. Review and approve supplier FMEAs, SPC strategies, MSA documentation, control plans and inspection methods as required by the Supplier Approval Plan.
Provide Supplier Quality Assurance support to all existing suppliers and assigned projects (including suppliers for new product development). Collect and archive all relevant Supplier documentation and required statements. Support Supplier Quality performance monitoring. Create Supplier Quality Roadmap. Manage changes initiated by suppliers while coordinating with the appropriate project teams. Lead problem solving activities with assigned Suppliers related to escalated customer complaints or manufacturing deviations.
Knowledge and Skills : Auditing experience. Understanding of industry standards and regulations such as ISO 9001, ISO 13485, 21CFR820, ISO 14971, MDSAP, EU MDD/MDR. Excellent written and oral communication skills. Working knowledge of problem-solving techniques such as PDCA, 8D investigation, etc. Ability to handle multiple tasks/projects simultaneously with limited supervision. Ability to work with diverse, multi-national, cross-functional teams. Working knowledge of statistics. Minimum Requirement: BS degree in Engineering, Science, or other related discipline At least 5 years of medical device, biologic, medical, or diagnostic industry experience (or equivalent).
Minimum 3 years in a quality organization dealing with suppliers, customers or Operation-Quality. For certain roles at BD, employment is contingent upon the Company's receipt of sufficient proof that you are fully vaccinated against COVID-19. In some locations, testing for COVID-19 may be available and/or required. Consistent with BD's Workplace Accommodations Policy, requests for accommodation will be considered pursuant to applicable law. Why Join Us? A career at BD means being part of a team that values your opinions and contributions and that encourages you to bring your authentic self to work.
It's also a place where we help each other be great, we do what's right, we hold each other accountable, and learn and improve every day. To find purpose in the possibilities, we need people who can see the bigger picture, who understand the human story that underpins everything we do. We encourage people with the creativity and aim to help us reinvent the future of health. At BD, you'll discover a culture in which you can learn, grow, and thrive. And find satisfaction in doing your part to make the world a better place.
To learn more about BD visit /careers Becton, partinson and Company is an Equal Opportunity/Affirmative Action Employer. We do not unlawfully discriminate on the basis of race, color, religion, age, interaction, creed, national origin, ancestry, citizenship status, marital or domestic or civil union status, familial status, affectional or interactionual orientation, gender identity or expression, genetics, disability, military eligibility or veteran status, or any other protected status. PDN Primary Work Location USA NJ - Franklin Lakes Additional Locations Work Shift NA (United States of America) Apply Save Job Responsibilities Job Description Summary Job Description We are the makers of possible BD is one of the largest global medical technology companies in the world.
Advancing the world of health is our Purpose, and it's no small feat. It takes the imagination and passion of all of us-from design and engineering to the manufacturing and marketing of our billions of Med Tech products per year-to look at the impossible and find transformative solutions that turn dreams into possibilities. We believe that the human element, across our global teams, is what allows us to continually evolve.
Join us and discover an environment in which you'll be supported to learn, grow and become your best self. Become a maker of possible with us. The Senior Supplier Quality Engineer is responsible to define and implement the supplier management activities required to approve suppliers and maintain their approved status throughout the product lifecycle. This is achieved by ensuring the conformance of the supplier to applicable quality specifications of components, products, materials, or services delivered to BD, in compliance with BD supplier management policies and procedures, as well as applicable standards and regulations.
Responsibilities Support identification of prospective suppliers. Define the optimum supplier approval strategy, and create supplier approval plans. Facilitate, manage, and track supplier progress toward Approved status, supporting both new product development launches and sustaining engineering changes. Conduct supplier quality audits backssments as necessary including for-cause audits, and complete follow-up and closure of any non-conformances. Author, negotiate, and finalize both Quality and Technical Agreements with suppliers.
Review and approve supplier FMEAs, SPC strategies, MSA documentation, control plans and inspection methods as required by the Supplier Approval Plan. Provide Supplier Quality Assurance support to all existing suppliers and assigned projects (including suppliers for new product development). Collect and archive all relevant Supplier documentation and required statements. Support Supplier Quality performance monitoring. Create Supplier Quality Roadmap. Manage changes initiated by suppliers while coordinating with the appropriate project teams. Lead problem solving activities with assigned Suppliers related to escalated customer complaints or manufacturing deviations.
Knowledge and Skills : Auditing experience. Understanding of industry standards and regulations such as ISO 9001, ISO 13485, 21CFR820, ISO 14971, MDSAP, EU MDD/MDR. Excellent written and oral communication skills. Working knowledge of problem-solving techniques such as PDCA, 8D investigation, etc. Ability to handle multiple tasks/projects simultaneously with limited supervision. Ability to work with diverse, multi-national, cross-functional teams. Working knowledge of statistics. Minimum Requirement: BS degree in Engineering, Science, or other related discipline At least 5 years of medical device, biologic, medical, or diagnostic industry experience (or equivalent).
Minimum 3 years in a quality organization dealing with suppliers, customers or Operation-Quality. For certain roles at BD, employment is contingent upon the Company's receipt of sufficient proof that you are fully vaccinated against COVID-19. In some locations, testing for COVID-19 may be available and/or required. Consistent with BD's Workplace Accommodations Policy, requests for accommodation will be considered pursuant to applicable law.
Why Join Us? A career at BD means being part of a team that values your opinions and contributions and that encourages you to bring your authentic self to work. It's also a place where we help each other be great, we do what's right, we hold each other accountable, and learn and improve every day. To find purpose in the possibilities, we need people who can see the bigger picture, who understand the human story that underpins everything we do. We encourage people with the creativity and aim to help us reinvent the future of health. At BD, you'll discover a culture in which you can learn, grow, and thrive.
And find satisfaction in doing your part to make the world a better place. To learn more about BD visit /careers Becton, partinson and Company is an Equal Opportunity/Affirmative Action Employer. We do not unlawfully discriminate on the basis of race, color, religion, age, interaction, creed, national origin, ancestry, citizenship status, marital or domestic or civil union status, familial status, affectional or interactionual orientation, gender identity or expression, genetics, disability, military eligibility or veteran status, or any other protected status. PDN Primary Work Location USA NJ - Franklin Lakes Additional Locations Work Shift NA (United States of America) Apply Save Job PDN-9ae7db20-2dba-4c1c-b8ba-a18d92fecad3
