around the globe. We have 12,000 employees worldwide, with over 3,000 in Customer-facing sales and service roles. Founded as Innovative Medical Technologies in Ohio in 1985, the company was renamed STERIS in 1987. Many of the businesses that have been acquired and integrated into STERIS have much longer operating histories, notably the American Sterilizer Company founded in 1894.
The STERIS Vision is inspired by our Customers' efforts to create a healthier and safer world, and guided by our legacy of leadership and innovation; we strive to be a Great Company. To STERIS, this means we will make a difference by providing world-class product and service solutions for our Customers, safe
and rewarding work for our People, and superior returns for our Shareholders. Position Summary Provides technical leadership in large projects supporting testing, fixtures development & building/testing prototypes.
Influences lab activities and acts as the technical expert in infection prevention product lines, primary lab safety contact and maintenance. Duties Execute tests and collect data using test equipment that measures temperature, electricity, light, flow, pressure, strain, force, distance, time, noise, weight etc. Assists in analyzing equipment failures and factory work stoppage problems. Design, Develop, Build, qualify test fixtures when needed. Maintain facility in a safe,
clean, and orderly manner always in compliance with OSHA VPP standards.
Fabricates, repairs, improves designs and constructs mechanical and electromechanical equipment. Maintains detailed and up to date test data in laboratory notebook and active test logs. Support Customer escalations, when needed. Support manufacturing ramp up, and design transfer during product development Assists engineers in determining test methods and test design Assumes complex project assignment responsibility Ability to operate, set up and program Data Acquisition Systems and associated software Supports highly visible business critical escalations from Customers / Operations when needed Required Experience1.
Two-year Associate Degree or equivalent, apprenticeship or comparable specialized study in mechanical and/or electrical engineering, beyond high school level.2. 10+ years experience in electrical/mechanical and mechanical assemblies3. Demonstrated technical leadership presence4. Travel to Customers and operations sites, including up to 20% internationally Skills1. Skilled in the set-up and operation of electrical and mechanical test equipment and measuring tools necessary. Must be able to use drill press, band saw, metal working tools role modeling excellent machine shop practices.2.
Able to operate test equipment that measures temperature, electricity, light, flow, pressure, strain, force, distance, time, noise and weight.3. Works from prints, sketches, written and verbal instructions and is capable of interpreting specifications.4. Demonstrated proficiency in reading and reviewing for accuracy wiring/electrical schematics, plumbing schematics and engineering drawings. 5. Design, assembly and troubleshooting of complex plumbing assemblies and systems necessary.6. Demonstrated ability to work effectively as an integral part of a team and independently as necessary.7.
Skilled in planning, organizing, and controlling assigned activities and group activities8. Proficient in computer use and applications and familiarity with Data Acquisition systems 9. Self-motivated10. Excellent communication skills11. Excellent problem-solving skills
of Quality Systems Compilation, Review & Management of overall Product Quality Reviews system. Act as site coordinator for change controls & management of change control system. Management of Deviation system. Management of Market complaint investigation system.
Act as QA focal point for OOS/OOT management. Management of Training system. Oversight on Pest Control system. To perform Nitrosamine backssment & review. Management of ICHQ3D requirements. Site coordinator for Implementation of Sanofi Global Standards (STDs) and Global Operating Procedures (GOPs) Act as focal point for Suppliers' management. Act as focal point for Subcontractors/ Service Providers management. Act as focal point
for Third Party audit handling. Management of overall Validation systems (Process, cleaning, transport & computerized system) Management of CAPA System. Quality Management Systems Coordinating for conducting self-inspection as per planner and associated self-inspection activities.
Review and Approval of Gx P documents, batch manufacturing record and batch packing record in electronic-document system. Implementation of quality documents, management, and control of documents, such as SOPs, Master Documents etc. Coordination of c GMP training activity including training of the people & review of training module. Initiation, implementation, and closure of change controls. Initiation of deviation
and support in deviation investigation. Support in Market Complaint investigation.
Implementation of assigned CAPAs and support in closure. Implementation of assigned Efficiency Reviews (ERs). Act as PPO (Primary Process Owner) for QMI (Quality Maturity Index) as assigned. Batch release & response to queries from QP. Management of Data integrity aspects. Participation and support in SMS initiatives. Support for HSE activities. Handling of Site Master File (SMF). Calibration document review of Engineering/QC/PMTD. User access management & review Analytical method creation Audit trail review Document archival/retrieval management. Validation & Qualifications Quality focal point for all validations [Process, cleaning, transport & computerized system] and qualification activities.
Quality focal point for temperature/ relative humidity mapping activities. Quality focal point for study related to hold time of products, cleaned/uncleaned equipment hold time, campaign length. Quality focal point for utilities & purified water system. Management of Site Qualification & Validation Master Plan In-Process Quality Assurance [IPQA] Review & Approval of Master Batch Records & executed Batch Records Review and Approval of logbooks. Line clearance in Production.
To perform In-process checks in Production. Sampling of products during routine production and validation. Quality oversight on shopfloor. HSE Adherence to all health safety & environmental aspects as required by company policies and procedures. Ensure that the implementation of HSE systems, safe working conditions and maintain a culture of continuous improvement. Conducting daily training in the +QDCI meeting address any unsafe condition. Take suggestion from associates to improve the work conditions with great safety and zero risk. Periodic review of the implemented procedures and evaluation of the same.
Train people on safety and their job to ensure zero LTI and IWLT at workplace. Languages : English, Hindi, Konkani, Marathi Qualification : B. Pharm/M. Pharm Experience -3-5 years experience Pursue progress, discover extraordinary Better is out there. Better medications, better outcomes, better science. But progress doesn't happen without people - people from different backgrounds, in different locations, doing different roles, all united by one thing: a desire to make miracles happen. So, let's be those people. At Sanofi, we provide equal opportunities to all regardless of race, colour, ancestry, religion, interaction, national origin, interactionual orientation, age, citizenship, marital status, disability, or gender identity.
Watch our ALL IN video and check out our Diversity Equity and Inclusion actions at ! At Sanofi diversity and inclusion is foundational to how we operate and embedded in our Core Values. We recognize to truly tap into the richness diversity brings we must lead with inclusion and have a workplace where those differences can thrive and be leveraged to empower the lives of our colleagues, patients and customers. We respect and celebrate the diversity of our people, their backgrounds and experiences and provide equal opportunity for all.
Job title : Executive QA Our Team: Implement Quality Assurance activities at Goa, Pharma adhering to global quality documents and HSE guidelines with optimum utilization of resources to ensure consistent good quality of products to meet with customers' requirements, living Group's Values and Code of Ethics. Main responsibilities: Management of Quality Systems Compilation, Review & Management of overall Product Quality Reviews system. Act as site coordinator for change controls & management of change control system.
Management of Deviation system. Management of Market complaint investigation system. Act as QA focal point for OOS/OOT management. Management of Training system. Oversight on Pest Control system. To perform Nitrosamine backssment & review. Management of ICHQ3D requirements. Site coordinator for Implementation of Sanofi Global Standards (STDs) and Global Operating Procedures (GOPs) Act as focal point for Suppliers' management. Act as focal point for Subcontractors/ Service Providers management. Act as focal point for Third Party audit handling. Management of overall Validation systems (Process, cleaning, transport & computerized system) Management of CAPA System.
Quality Management Systems Coordinating for conducting self-inspection as per planner and associated self-inspection activities. Review and Approval of Gx P documents, batch manufacturing record and batch packing record in electronic-document system. Implementation of quality documents, management, and control of documents, such as SOPs, Master Documents etc. Coordination of c GMP training activity including training of the people & review of training module. Initiation, implementation, and closure of change controls.
Initiation of deviation and support in deviation investigation. Support in Market Complaint investigation. Implementation of assigned CAPAs and support in closure. Implementation of assigned Efficiency Reviews (ERs). Act as PPO (Primary Process Owner) for QMI (Quality Maturity Index) as assigned. Batch release & response to queries from QP. Management of Data integrity aspects. Participation and support in SMS initiatives. Support for HSE activities. Handling of Site Master File (SMF). Calibration document review of Engineering/QC/PMTD. User access management & review Analytical method creation Audit trail review Document archival/retrieval management.
Validation & Qualifications Quality focal point for all validations [Process, cleaning, transport & computerized system] and qualification activities. Quality focal point for temperature/ relative humidity mapping activities. Quality focal point for study related to hold time of products, cleaned/uncleaned equipment hold time, campaign length. Quality focal point for utilities & purified water system. Management of Site Qualification & Validation Master Plan In-Process Quality Assurance [IPQA] Review & Approval of Master Batch Records & executed Batch Records Review and Approval of logbooks.
Line clearance in Production. To perform In-process checks in Production. Sampling of products during routine production and validation. Quality oversight on shopfloor. HSE Adherence to all health safety & environmental aspects as required by company policies and procedures. Ensure that the implementation of HSE systems, safe working conditions and maintain a culture of continuous improvement. Conducting daily training in the +QDCI meeting address any unsafe condition. Take suggestion from associates to improve the work conditions with great safety and zero risk.
Periodic review of the implemented procedures and evaluation of the same. Train people on safety and their job to ensure zero LTI and IWLT at workplace. Languages : English, Hindi, Konkani, Marathi Qualification : B. Pharm/M. Pharm Experience -3-5 years experience Pursue progress, discover extraordinary Better is out there. Better medications, better outcomes, better science. But progress doesn't happen without people - people from different backgrounds, in different locations, doing different roles, all united by one thing: a desire to make miracles happen.
So, let's be those people. At Sanofi, we provide equal opportunities to all regardless of race, colour, ancestry, religion, interaction, national origin, interactionual orientation, age, citizenship, marital status, disability, or gender identity. Watch our ALL IN video and check out our Diversity Equity and Inclusion actions at ! At Sanofi diversity and inclusion is foundational to how we operate and embedded in our Core Values. We recognize to truly tap into the richness diversity brings we must lead with inclusion and have a workplace where those differences can thrive and be leveraged to empower the lives of our colleagues, patients and customers.
We respect and celebrate the diversity of our people, their backgrounds and experiences and provide equal opportunity for all. PDN-99f26e84-bfd9-43ba-8ad2-b8269109f73f
by a 12% shift differential. We offer competitive salary and may include a sign on bonus! Job Functions / Responsibilities Conduct tests on heavy duty diesel engines using a dynamometer cell and test automation software Follow technical instructions and work closely with engineering staff to assure engines are performing as requested during testing Prepare engines for dynamometer cell testing, including replacing components and installing measurement instrumentation Maintain, troubleshoot, and repair test engines Troubleshoot, maintain, and repair engine test cell equipment Support maximum test cell utilization and downtime reduction Maintain detailed electronic records and project documentation
Maintain the highest level of work area safety, cleanliness, and organization Keep abreast of new engine and testing technologies, recommend and implement continuous improvements Perform duties safely and efficiently with minimal supervision Respond to shifting time and project demands Qualifications Minimum 3 years’ experience working in the diesel, heavy duty truck or automotive industry Proficiency in troubleshooting complex mechanical and electronic engine systems Must demonstrate independent creativity based on technical theory to solve challenges for which routine solutions are not available High attention to detail, organization, and thoroughness Excellent mechanical aptitude Strong computer
skills – Microsoft Office and data acquisition software proficiency desired Strong verbal and written communication skills Must be able to work independently as well as in a team environment to achieve common goals Education Two-year degree in diesel/automotive technology or equivalent degree Division Information The PACCAR Technical Center provides engineering excellence to the truck, engine, and winch divisions of PACCAR Inc.
through innovative product development and testing. The Technical Center is located in the Skagit Valley about 65 miles north of Seattle, Washington. PACCAR Benefits As a U. S. PACCAR employee, you have a full range of benefit options including: 401k with up to a 5% company match Fully funded pension plan that provides monthly benefits after retirement Comprehensive paid time off – minimum of 10 paid vacation days (additional days are provided with additional seniority/years of service), 12 paid holidays, and sick time Tuition reimbursement for continued education Medical, dental, and vision plans for you and your family Flexible spending accounts (FSA) and health savings account (HSA) Paid short-and long-term disability programs Life and accidental death and dismemberment insurance EAP services including wellness plans, estate planning, financial counseling and more Additional Job Board Information PACCAR is an Equal Opportunity Employer/Protected Veteran/Disability and E-Verify Employer.
At PACCAR, we value talent and promote growth and development. We carefully consider numerous compensation factors including your education, training, or experience. The salary range for the Diesel Engine Test Technician is $55,400 - $83,100 annually. Additionally, this role is eligible for the full range of benefit options listed above.
