and scientific aspects of development and validation of new assays including Gx P studies May have direct reports and work as a group leader As a team leader, oversee the project timelines and put the best efforts to increase productivity. May represents the company in the scientific conferences or participates in the sales meetings Work with management and QA to maintain and improve quality systems Provide leadership and training to assigned research staff Provide high-quality documentation of all lab-related activities, including, for example, assay batch record, sample inventory, etc.
Perform a QC function to review data and reports to ensure the accuracy of all laboratory-related
processes. Maintain regular communication with the study director and other project staff and become a point of contact to the client. Job Qualifications and Requirements: A minimum of a Bachelor's in a scientific field with 5+ years or an advanced degree (MS/Ph.
D. ) with at least 3 years of relevant experience. Experience with assay development and validation is required. Experience with ELISA, Western Blot, Luminex, and cell-based assays is critical. Strong experience with GLP and c GMP is required. Ability to quickly acquire new skills and craft creative solutions. Must be detail-oriented with the ability to multi-task and work as part of a team to complete projects with strong communication
skills. Relocation may be available. This Associate Scientist position earns a competitive salary , depending on experience.
We also offer a full suite of benefits to choose from, including medical, dental, vision, a health reimbursement account funded by the employer, a healthcare & dependent flexible spending account (FSA), a 401(k) plan, 100%-employer-paid voluntary life/AD&D insurance, and profit-sharing. If this sounds like the right opportunity in medical research and cell & gene therapy for you, apply today! Pharmaron Lab Services cares about our work community and offers a variety of benefits allowing employees the opportunity to customize a comprehensive benefits package that meets their personal needs.
Pharmaron Lab Services is proud to be an Equal Employment Opportunity and Affirmative Action employer.
by following policies, processes, and acting in a safe manner at all times. Segregate chemicals by hazard class, packing compatible materials in appropriate containers and preparing for transportation, completing necessary paperwork per job, conducting various facility inspections as required.
Collects hazardous and non-hazardous materials from various onsite locations and transports via push cart or company van to waste collection areas. Characterize materials. Follows proper placarding and load segregation requirements when loading hazardous materials. Develop good client relations by effectively communicating with customers. Directs Field Technicians/Drivers assisting with waste collection.
Maintain a log of waste stored in the waste area. Advise when supplies are to be ordered. Maintain good housekeeping in storage areas. Heritage believes that each employee makes a significant contribution to our success.
That contribution should not be limited by the assigned responsibilities. Therefore, this position description is designed to outline primary duties, qualifications and job scope, but not limit the incumbent nor the company to just the work identified. It is our expectation that each employee will offer his/her services wherever and whenever necessary to ensure the success of our endeavors. Education: High school diploma or its equivalent required. Four year college degree
(Science major preferred) or 2+ years Lab packing or environmental experience preferred.
Experience: Prior lab packing or environmental waste experience preferred. Knowledge and Abilities: This is a safety sensitive position. The ability to work in a constant state of alertness and in a safe manner is an essential function. Introductory knowledge of high hazard materials management backssment and cylinder handling. Good knowledge and understanding of all federal, state, and local laws and regulations pertaining to the Environmental Services Industry. Excellent interpersonal skills necessary to effectively communicate with internal and external contacts.
Regular and predictable attendance is an essential function of this job. Requirements: Due to potential exposure to atmospheres/waste/materials this position requires that you must be able to be clean shaven at all times to don a respirator for your protection. Must have a valid driver's license. Ability to pass Motor Vehicle Record search to company standards. A post offer drug screen will be required. EEO including disability/veteran
where you belong and can be the best version of yourself. If you're passionate about achieving goals, trying new things and making an impact every day, we want to hear from you! POSITION SUMMARY: We're looking for a Sr. Scientist (R&D Technical Services) experienced in the Food & Beverage industry to lead our R&D technicians, and support a diverse set of teams across the Enterprise through product technical services and R&D systems management.
This position is key to the operation of the R&D team and has significant impact on the maintenance of our portfolio of shelf stable and refrigerated juices, sparkling beverages and fruit-based spreads. WHAT YOU'LL DO: Serve as the R&D lead for
the qualification and approval of new sources for existing ingredients Provide technical support and address inquiries on existing specifications, ingredients or products from Procurement, Quality, Manufacturing or Sales Serve as the R&D lead for the management of our Product Lifecycle Management (PLM) Specification System Update existing or generate new specifications within the scope of the role (formula, finished product, ingredients, and analytical test methods) Troubleshoot and work within the R&D functions of the PLM system, provide support & training to the broader R&D team Lead projects aimed at optimizing and leveraging the R&D functions of the PLM system (streamlining, incorporation
of new businesses or processes) General oversight of the product development analytical lab and instruments Manage and coach the R&D technicians, ensuring performance, engagement and career development opportunities Manage the technicians resource calendar to ensure the appropriate support across all R&D May be asked to perform other tasks or handle other responsibilities, as needed WHO YOU ARE: An ideal candidate: Enjoys challenges and problem solving; is technically deep and curious Is detail oriented and fast learner Exhibits good written and oral communication, along with strong collaboration skills Has familiarity and ability to work within a database environment and to follow digital links to other systems Has familiarity with basic analytical instruments such as refractometers, titrators, and spectrophotometers Able to self-manage projects including excellent organizational and time management skills Is hands on, resourceful and decisive; seeks practical approaches with a bias for action to quickly solve problems SKILLS AND EXPERIENCE: REQUIRED Bachelor's Degree in Food Science, Chemistry, or closely related fields.
Master's preferred. Candidates should have at least 5-7 years of experience in a product Technical Service, R&D or Quality role in the Food & Beverage industry, with a focus on juice or beverages preferred Ability to work cross-functionally with collaboration experience including Procurement, Quality, and Manufacturing, among others Technical knowledge of ingredients, products and manufacturing processes of beverages or foods Problem-solving skills and experience dealing with ambiguity Able to manage multiple projects and complete work in a timely manner Proficient in Microsoft Office Must be able to travel based on project requirements (about 10%) PREFERRED Familiarity working with PLM systems Experience managing personnel Product Development experience for Food and Beverages WHAT YOU'LL ENJOY: Organization with a bold, clear purpose.
Authentic culture that supports working together to deliver results. Workplace where teams care about each other and your voice is heard. Core and voluntary benefits so you can choose the right recipe for you. 40 hours paid volunteering time off for all non-union exmployees Generous 401(k) plan with annual company match. Flexible schedules so you can balance your work life priorities. Learning and development opportunities with coaching. Safe and clean working environment.
Welch's believes that our differences make the difference, and we take pride in being an Equal Opportunity Employer Disability/Vets. Job Posted by Applicant Pro
quality focused QC Chemist with analytical or quality control laboratory experience in a Manufacturing environment. REPORTS TO: Laboratory Supervisor or Stability Coordinator EDUCATION/EXPERIENCE: Bachelors degree in chemistry or related field. Minimum of one-year experience in analytical or quality control laboratory preferred.
Passing of company required tests. WAGE CATEGORY: Non-Exempt DUTIES: Under direction from the Laboratory Supervisor, performs quality control analysis on any or all of the following samples: incoming raw materials in-process samples finished/filled products process validation/evaluation stability testing customer complaint Routine, repetitive checking and testing
of production product, including visual and sample inspections of parts used, weights, and measures. Inspect production (compounding & filling) equipment for various Q.
C. aspects. Maintain proper documentation for filling quality control as required Assists in experiments relative to the discovery and development of new products. Makes pilot batches of experimental products. Create processing batch sheets from work orders including: Allocation sheet -log W. O. into allocation book. Batch sheets -determine proper number of batches per mixing devise, check scratch program for batch size, check ingredient amounts and order of addition. QC sheet -insure QC requirements are in order. Method
of MFG -print out appropriate Method of manufacturing. Create packaging batch records (PBR's), check artwork, crimp code, log sheets, & shipping requirements.
Prepare artwork ingredient list. Complete Certificate of Analysis for customer orders. Send letters and samples to outside contract laboratories. Create Bulk labeling stickers. General electronic and hard copy file maintenance. Housekeeping with respect to records control. Maintain and update as needed the NS database and MSDS log. Maintain cleanliness and appearance of department. Assist in the disposal of hazardous (laboratory) waste Assist in laboratory instrument qualification and/or calibration Act as subject matter expert for laboratory instrumentation or analytical techniques Maintain proper liaison with all departments to contribute to the team philosophy.
Responsible for following all safety regulations and complying with S. O. P. 's, DEP, EPA, OSHA, FDA, and c GMP's while performing duties. Other assigned tasks as necessary assigned by Management. Follow all Environmental and OSHA requirements. Attend in-house training sessions. Sheffield medicals is an Equal Employment Opportunity employer. We provide equal opportunity to employees and applicants for employment without regard to race, creed, color, religion, interaction, age, national origin, physical or mental disability, interactionual orientation, marital or familial status, genetic information, protected veteran status, or other basis protected by law.
' ' Work Remotely No Job Type: Full-time Pay: From $18.00 per hour Benefits: 401(k) 401(k) matching Dental Insurance Employee assistance program Flexible spending account Health insurance Health savings account Life insurance Paid time off Referral program Vision insurance Schedule: 8-hour shift Monday to Friday Work Location: One location
with applications across the textile, flooring, chemical and healthcare businesses, the company harnesses a shared sense of integrity and excellence to positively impact the world for generations. Discover more about Milliken’s curious minds and inspired solutions at and on Facebook , Instagram , Linked In and Twitter.
POSITION TITLE Research and Development Chemist, Fine Chemical Products POSITION OVERVIEW The individual will be challenged to safely lead efforts to design, develop, optimize, and implement new chemical processes. The individual will be located at the R&D facility in Gainesville, FL. JOB RESPONSIBILITIES Lead teams that develop and design/optimize safe and reliable processes
to manufacture target molecules. Lead projects that support business efforts that move chemical processes from the lab, pilot, and into the production facility.
Specific tasks will involve evaluating safety and regulatory requirements, assisting in writing plant operational instructions, coordinating efforts with plant engineers and operators, assist developing and designing proper equipment, leading safety reviews of the process and supporting the operational staff during initial plant runs of the process. On all projects, apply sound knowledge of scientific principles, practices, advanced techniques, and modification and/or extension of theories and practices to assigned projects. Where
possible, utilize internal and external scientific, technological databases to extend personal knowledge and provide a basis for future work.
Interpret data and be able to make meaningful decisions and designs for chemical processes. Provide leadership for improving the safety. Beyond familiarity with and compliance with applicable regulations, internal procedures and attendance in safety meetings. This requires leadership in updating procedures and demonstrated constant attention to preventing and resolving safety problems. Drive the continual improvement of housekeeping and safety in the lab, plant, and lab community. Work to understand the customer’s quality needs and integrate these needs into process design.
Effectively communicate (both written and verbal) within R&D and with other departments both at the site and within the larger corporate structure. Regularly maintain laboratory notebook. Keep project portfolio and plans up to date, follow stage-gate process. Keep supervisor apprised of progress, or lack thereof, on a regular basis. The individual will work with highly diverse teams and must be able to professionally work and communicate in this type of setting. The individual will need to be willing to learn and be able to use this acquired knowledge to improve the organization.
QUALIFICATIONS – REQUIRED Bachelor’s degree in chemistry or chemical engineering Strong communication skills with all levels within an organization and problem solving skills Strong problem solving and project management skills Ability to travel up to 15% of time QUALIFICATIONS - PREFERRED Ph D. or equivalent in Chemistry or Chemical Engineering 4 years + experience in an industrial setting Experience in developing processes for materials into the semi-conductor industry Experience in scale up of processes for the silicon industry Experience in developing continuous/flow processes Milliken is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to actual or perceived race, color, creed, religion, interaction or gender (including pregnancy, childbirth or related medical condition, including but not limited to lactation), interactionual orientation, gender identity or gender expression (including transgender status), ancestry, national origin, citizenship, age physical or mental disability, genetic information, marital status, veteran or military status or any other characteristic protected by applicable law.
skills will play an important role in the work we perform. In return, we’ll help you build a career that you can feel passionate about. Job Summary SALARY: The salary for this position is $70,000. Please note that salaries vary within the range based on factors including, but not limited to, experience, skills, education, certifications, and location.
The Immunology and Immunochemistry disciplines support large molecule drug development using ligand binding assays (LBA), such as enzyme-linked immunosorbent assay (ELISA), to measure large molecules and their immune responses. The main types of assays include Pharmacokinetic (PK) assays to measure drug and Immunogenicity assay to measure
anti-drug antibodies (ADA) and neutralizing antibodies (NAb). Other assay types also performed are branched DNA (b DNA) and cell-based assays. An array of platforms are used to support these assays that include spectrophotometer, Meso Scale Discovery (MSD), Luminex and Gyrolab.
Utilizing these platforms/assays, the teams are responsible for the method development, validation and routine sample analysis in both the regulated and non-regulated space of non-clinical and clinical studies. Essential Functions (The fundamental Competencies/Skills & Responsibilities of the role (products and services provided/results accomplished) include, but are not limited to, those listed: · Efficiently
perform and document all procedures, materials and results in compliance with applicable regulatory standards as applicable (protocols, methods, SOPs, etc.
) · Actively communicate and collaborate across operational areas in order to adhere to timelines and produce quality data · Assist with the completion of laboratory investigations, assay troubleshooting, quality observations, and problem solving of technical and/or regulatory issues with oversight · Effectively develop and validate quantitative/qualitative methods/procedures with limited complexity/scope in one operational area with oversight · Perform data analysis in appropriate software for at least one analytical platform with oversight · Operate laboratory instruments including their respective software applications with oversight · Develop critical thinking, troubleshooting and time management skills aligned with needs of operational areas · Demonstrate effective communication skills through informal discussions with peers, supervisor, and team · Develop ability to recognize method and/or data issues and communicate them to management to minimize study impact with oversight · Prepare summary of method development data with oversight · Write both study and non-study deviations with oversight · Performs all other related duties as assigned Job Qualifications Qualifications (Knowledge, Experience, Skills and Abilities required to accomplish the essential functions) include but are not limited to: · Bachelor’s degree (BA/BS) with 3-5 years of relevant working experience.
Master’s degree (MS) with no previous work experience · An equivalent combination of education and experience may be accepted as a satisfactory substitute for the specific education and experience listed above · Ability to communicate verbally and in writing at all levels inside and outside the organization · Basic familiarity with Microsoft Office Suite · Computer skills, commensurate with Essential Functions, including the ability to learn a validated system · Ability to work extended hours beyond normal work schedule to include, but not limited to evenings, weekends, extended shifts, and/or extra shifts; sometimes on short notice · Ability to work under specific time constraints About Safety backssment Charles River is committed to helping our partners expedite their preclinical drug development with exceptional safety backssment services, state-of-the-art facilities and expert regulatory guidance.
From individual specialty toxicology and IND enabling studies to tailored packages and total laboratory support, our deeply experienced team can design and execute programs that anticipate challenges and avoid roadblocks for a smooth, efficient journey to market. Each year approximately 300 investigational new drug (IND) programs are conducted in our Safety backssment facilities. About Charles River Charles River is an early-stage contract research organization (CRO). We have built upon our foundation of laboratory animal medicine and science to develop a diverse portfolio of discovery and safety backssment services, both Good Laboratory Practice (GLP) and non-GLP, to support clients from target identification through preclinical development.
Charles River also provides a suite of products and services to support our clients’ clinical laboratory testing needs and manufacturing activities. Utilizing this broad portfolio of products and services enables our clients to create a more flexible drug development model, which reduces their costs, enhances their productivity and effectiveness to increase speed to market. With over 20,000 employees within 110 facilities in over 20 countries around the globe, we are strategically positioned to coordinate worldwide resources and apply multidisciplinary perspectives in resolving our client’s unique challenges.
Our client base includes global medical companies, biotechnology companies, government agencies and hospitals and academic institutions around the world. At Charles River, we are passionate about our role in improving the quality of people’s lives. Our mission, our excellent science and our strong sense of purpose guide us in all that we do, and we approach each day with the knowledge that our work helps to improve the health and well-being of many across the globe.
We have proudly supported the development of 86% of the drugs approved by the FDA in 2021. Equal Employment Opportunity Charles River Laboratories is an Equal Opportunity Employer - all qualified applicants will receive consideration for employment without regard to race, color, religion, interaction, interactionual orientation, gender identity, national origin, veteran or disability status. If you are interested in applying to Charles River Laboratories and need special assistance or an accommodation due to a disability to complete any forms or to otherwise participate in the resume submission process, please contact a member of our Human Resources team by sending an e-mail message to xyz X@.
This contact is for accommodation requests for individuals with disabilities only and cannot be used to inquire about the status of applications. For more information, please visit.
Assay Lab in Lake County, IL for a highly motivated and skilled Associate Scientist II/Scientist I or Scientist II in vitro biochemist/enzymologist that will make substantial contributions to the progression of oncology drug discovery programs in a highly collaborative environment.
The successful candidate will be a member of the Oncology Discovery Research area focused on delivering high quality drug development candidates for promising novel therapeutic targets. Major responsibilities will include novel biochemical/cellular assay development and performing biochemical/cellular assays to enable and support multiple biology and chemistry project teams. Other responsibilities will include
compound preparation and handling, automation protocol development, assay troubleshooting, mechanistic analyses of enzyme reaction mechanisms and modes of inhibition, data analysis/interpretation, and data reporting.
An important responsibility will be to investigate, identify, develop, and optimize new methods/ techniques to generate reliable and reproducible data in a timely manner. The candidate will be expected to rapidly learn the daily operation of the lab, readily adapt to changing needs and priorities, semi-independently plan and execute projects, and develop appropriate problem-solving skills. Excellent teamwork, communication skills and adherence to good laboratory conduct,
documentation practices and safety guidelines are essential.
Associate Scientist II - Bachelor's Degree, or equivalent education, with typically 3 or more years' experience or Master's Degree or equivalent education Scientist I - Bachelor's Degree or equivalent education with typically 5 years of experience, or Master's Degree or equivalent education with typically two years of experience. Scientist II - BS or equivalent education with typically 7 or more years of experience or MS or equivalent education with typically 5 or more years of experience. Familiarity with high-throughput assay capabilities and automation such as liquid handlers & plate readers.
Ability to interpret, document & communicate information and experimental outcomes effectively and transparently. Ability to plan and conduct experiments and prepare reports with minimal supervision. Prior wet lab bench work experience and familiarity with general biology lab procedures. Experience with mammalian cell culture employing aseptic technique. Experience with in vitro cell proliferation assays. Ability to perform routine tasks in a timeline driven and goal-oriented team environment. Abb Vie is committed to operating with integrity, driving innovation, transforming lives, serving our community, and embracing diversity and inclusion.
It is Abb Vie's policy to employ qualified persons of the greatest ability without discrimination against any employee or applicant for employment because of race, color, religion, national origin, age, interaction (including pregnancy), physical or mental disability, medical condition, genetic information, gender identity or expression, interactionual orientation, marital status, status as a protected veteran, or any other legally protected group status.
key to our becoming one of the world's leading biotechnology companies, reaching over 10 million patients worldwide. Come do your best work alongside other innovative, driven professionals in this meaningful role. Sr. Scientist, Oncology Biomarker Discovery Live What you will do Let's do this.
Let's change the world. The Amgen Oncology Research is seeking a highly motivated scientist dedicated to biomarker discovery in the areas of cancer immunology. The focus of this role is on the discovery of biomarkers to support the progression of therapeutic candidates from discovery to early clinical development. Ours is a highly matrixed environment that drives scientific and technical innovation
collaboratively. In this vital role you will interact closely with other members of the Inflammation & Oncology group, as well as with other functions including the Clinical Biomarker & Diagnostics Team, Translational Medicine, Human Genetics and Computational Biology.
Develop deep disease area expertise for key indications Investigate disease biology and heterogeneity using human genetics, single cell transcriptomics, proteomics, cellular assays and/or disease animal models Discover and prioritize disease stratification and target engagement biomarker candidates for multiple pipeline projects Generate and transition key pharmacodynamic and patient stratification biomarker discovery data
to support clinical biomarker assay development Work together with the Clinical Biomarker Lead to support translational biomarker activities for therapeutic assets, including presenting at investigator meetings and advisor boards, and participating in investigator-sponsored studies Publish and present at national/international conferences Win What we expect of you We are all different, yet we all use our unique contributions to serve patients.
The dynamic professional we seek is a scientist with these qualifications. Basic Qualifications: Doctorate degree and 3 years of scientific experience ORMaster's degree and 6 years of scientific experience ORBachelor's degree and 8 years of scientific experience Preferred Qualifications: Ph D or MD, with postdoctoral trainings and research experience in the field of immunology, cancer biology, cancer immunology, or molecular biology Demonstrated track record of independent critical thinking and scientific achievement in research, exemplified by a strong publication record and/or significant contributions to a therapeutic development or biomarker discovery program Technical expertise in one or more of the following areas: Multi-color flow cytometry, complex cell-based functional assays, genetic manipulation of cell lines and/or primary cells, cell signaling/biochemistry, in vivo mouse models of disease, and bioinformatics Strong verbal and written communication skills.
Ability to collaborate and troubleshoot to solve problems Experience with implementing multiple technology platforms Experience working in teams and consistently delivering results Thrive What you can expect of us As we work to develop treatments that take care of others, we also work to care for our teammates' professional and personal growth and well-being. Amgen offers a Total Rewards Plan comprising health and welfare plans for staff and eligible dependents, financial plans with opportunities to save towards retirement or other goals, work/life balance, and career development opportunities including: Comprehensive employee benefits package, including a Retirement and Savings Plan with generous company contributions, group medical, dental and vision coverage, life and disability insurance, and flexible spending accounts.
A discretionary annual bonus program, or for field sales representatives, a sales-based incentive plan Stock-based long-term incentives Award-winning time-off plans and bi-annual company-wide shutdowns Flexible work models, including remote work arrangements, where possible Apply now for a career that defies imagination Objects in your future are closer than they appear.
Join us. careers. Amgen is an Equal Opportunity employer and will consider you without regard to your race, color, religion, interaction, interactionual orientation, gender identity, national origin, protected veteran status, or disability status. We will ensure that individuals with disabilities are provided reasonable accommodation to participate in the job application or interview process, to perform essential job functions, and to receive other benefits and privileges of employment.
Please contact us to request accommodation. Amgen will consider for employment qualified applicants with criminal histories in a manner consistent with the San Francisco Fair Chance Ordinance. Salary Range 158,148.00 USD - 173,481.00 USD
flow and reproducibility) Modeling, Inference, and Prediction: (Data modeling and backssment, domain-specific considerations). Responsibilities may include: Devise strategies for extracting meaning and value from large datasets Make and communicate principled conclusions from data using elements of mathematics, statistics, computer science, and applications Analytic modeling, statistical analysis and programming Develop and implement qualitative and quantitative methods for characterizing, exploring, and backssing large datasets in various states of organization, cleanliness, and structure that account for the unique features and limitations inherent in customer data holdings.
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practical mission needs and analytic questions related to large datasets into technical requirements and assist with drawing conclusions from data analysis Communicate complex technical information to non-technical audiences Recommend technical solutions by maintaining awareness of the constantly-shifting customer collection, processing, storage and analytic capabilities and limitations Qualifications Basic Qualifications: An Associate's degree with 10 years of relevant experience OR a Bachelor's Degree with 12 years of relevant experience Degree in Math, Applied Math, Statistics, Applied Statistics, MAchine Language, Data Science, Operations Research, or Computer Science.
A degree in
a related field (e. g. Computer Info Sys, Engineering, in the physical/hard sciences, or other science disciplines with a substantial computational component (typically 5 or more courses in advanced mathematics and/or CS (e.
g. algorithms, programming, data structures, data mining, AI). Other degrees may be considered if accompanied by a Certificate in Data Scientist. Relevant experience is considered: Designing/implementing Machine Language (ML) Data Science (DS) advanced analytical algorithms data mining, advanced statistical analysis (e. g. statistical foundations of ML, statistical approaches to missing data, time series), advanced mathematical foundations ( e.
g. numerical methods, graph theory) AI, workflow and reproducibility, data management and curation, data modeling and backssment (e. g. model selection, evaluation, and sensitivity analysis) Experience with programming languages (such as Python or C) Experience as a Data Scientist (DS) or Software Engineer (SWE) Active TS SCI security clearance with a current polygraph is required Peraton offers enhanced benefits to employees working on this critical National Security program, which include heavily subsidized employee benefits coverage for you and your dependents, 25 days of PTO accrued annually up to a generous PTO cap and participation in an attractive bonus plan.
#MPOJobs #AJCM Peraton Overview Peraton drives missions of consequence spanning the globe and extending to the farthest reaches of the galaxy. As the world's leading mission capability integrator and transformative enterprise IT provider, we deliver trusted and highly differentiated national security solutions and technologies that keep people safe and secure. Peraton serves as a valued partner to essential government agencies across the intelligence, space, cyber, defense, civilian, health, and state and local markets.
Every day, our employees do the can't be done, solving the most daunting challenges facing our customers. Target Salary Range $146,000 - $234,000. This represents the typical salary range for this position based on experience and other factors. EEO An Equal Opportunity Employer including Disability/Veteran. All For more details: jobs-search. org/technology_fort-meade-c433937/data-scientist-senior-security-clearance-required-fort-meade_i1971321954
acquiring, processing, and refining large and/or complex data sets utilizing computer programming where necessary. Successful candidates will need to be highly analytical and comfortable with applying critical thinking and problem-solving skills to effectively interpret data.
They will also collaborate with engineering and product development teams to propose solutions to challenges and present information using data visualization techniques. Basis Path is a rapidly growing woman and veteran-owned small business that is looking to hire talented candidates to meet our expanding contractual needs. We offer signing bonuses, relocation assistance, expense reimbursement, 100% paid for health
insurance, aggressive compensation, excellent benefits, growth opportunities, profit sharing, relevant training, and plenty of PTO. Our company prides itself on putting our employees first and we want you to be part of our team!
For more details: jobs-search. org/data-scientist_virginia-r782088/data-scientist-security-clearance-required-united-states_i1971659162
for our customers, our people, and our community. Our Mission, Vision, and Values guide the way we do business. If this sounds like the kind of environment where you can thrive, keep reading! Leidos Intelligence Group uses a wide range of capabilities in Digital Modernization, Mission Software Systems, and enabling technologies like Artificial Intelligence and Machine Learning to support our customers’ mission to defend against evolving threats around the world.
Our team’s focus is ensuring our intelligence customers have the right tools, technologies, and tactics to keep pace with an ever-evolving security landscape and succeed in their pursuit to protect people and critical assets.
Your greatest work is ahead! The Intelligence Group at Leidos has multiple openings for Data Scientists to support our customer. You will analyze actual and predictable interacting operational activities of give target sets and client requests to obtain a quantitative, rational basis for decision making through the application of logic and scientific or economic disciplines and techniques.
This position is contingent upon contract award. What you’ll be doing: Analyze actual and predictable interacting operational activities of given target sets and client requests to obtain a quantitative, rational basis for decision making through the application of logic and scientific or economic disciplines
and techniques. Devise modeling and measuring techniques; utilize mathematics, statistical methods, engineering methods, operational mathematics techniques (linear programming, game theory, probability theory, symbolic language, etc.
), and other principles and laws of scientific and economic disciplines. Identify and evaluate standardized methods, models and algorithms to address intelligence problems of limited scale as directed. Provide documentation for methods and algorithms use in data science solutions to the client and address outstanding items. Must have demonstrated good oral and written communication skills. What does Leidos need from me? Top Secret/SCI (TS/SCI) security clearance required.
Bachelor’s and/or Masters degree and at least 5 years of relevant GEOINT analysis experience. Strong knowledge of programming languages (e. g. Python, Java Script, SQL, Pig, or R), Elasticsearch, spatial analysis tools and concepts, data mining methods, database structures, and analytic information extraction and visualization. Ability to identify, retrieve, manipulate, relate and/or exploit multiple structured and unstructured data sets from various sources, including building or generating new data sets as appropriate. Ability to interpret and evaluate the results of data science community’s methods models and/or algorithms, understanding the meaning, limitations and scope of the results, and translate them into insightful output for data science and/or mission and identifying other applications for use.
Ability to initiate the efficient implementation of methods, tools, and algorithms using a comprehensive range of technologies. Ability to lead work unit proactively addressing and responding to the most difficult data science-related challenges in a timely manner while effectively balancing competing priorities. Demonstrated strong writing and briefing skills to educate managers, senior internal officers and the IC.
Proficiency in MS Office suite. Strong time management skills. Comfortable working independently. Favorable if you have: Prior military service or familiarity. Demonstrated ability to work in a very dynamic and demanding work environment. Demonstrated ability to brief staff officers to affect decisions. Demonstrated ability to work cooperatively as a team member and provide guidance to customer analysts to build effective customer relationships. 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/technology_maryland-r782062/senior-data-scientist-security-clearance-required-suitland-silver-hill_i1971446255
and resources needed to realize unreasonable results. The Role FL97 is seeking an experienced, creative, and talented Senior Scientist or Principal Scientist, Cellular Biology to join our team. You will be part of an agile, cross-functional team responsible for building the mammalian cell culture, cell engineering, and cell-based assay capabilities of our autonomous discovery campaigns.
Together with biologists, machine learning scientists, software developers, and automation engineers, you will work toward building and automating cell-based workflowsacross a variety of valuable applications. All scientists must be willing to learn and use basic Python and/or R programming. The ideal
candidate brings primary expertise in mammalian cell biology, culture, and genetic engineering, with a proven track record of building high quality in vivo assay platforms.
Industry experience in cell therapy, i PSCs, and/or regenerative medicine is a plus. Candidates should have experience and interest in: Cutting edge cell-based assays and automation Mammalian gene editing technology (KO, targeted KI) Nonviral payload delivery using electroporation, Piggy BAC, or other relevant systems Radically new working styles and scientific approaches Learning to code experimental protocols and data analysis workflows in Python In this role, you would: Work in a small, diverse, project-based team
Flexibly react to new information within an agile framework Build novel, robust, working prototypes of engineered biological products Collaborate with machine learning, software, and automation experts Provide hands-on training to Research Associates and computational colleagues Actively shape and plan new projects at regular intervals Working at FL97, you would have access to advanced technology in the areas of: AI experimental design and simulation Automated liquid handling and cell culture Fully digital lab workflows About Flagship Flagship Pioneering is a biotechnology company that invents and builds platform companies, each with the potential for multiple products that transform human health or sustainability.
Since its launch in 2000, Flagship has originated and fostered more than 100 scientific ventures, resulting in more than $90 billion in aggregate value. Many of the companies Flagship has founded have addressed humanity's most urgent challenges: vaccinating billions of people against COVID-19, curing intractable diseases, improving human health, preempting illness, and feeding the world by improving the resiliency and sustainability of agriculture. Flagship has been recognized twice on FORTUNE's " Change the World" list, an annual ranking of companies that have made a positive social and environmental impact through activities that are part of their core business strategies, and has been twice named to Fast Company's annual list of the World's Most Innovative Companies.
Learn more about Flagship at . Flagship Pioneering and our ecosystem companies are committed to equal employment opportunity regardless of race, color, ancestry, religion, interaction, national origin, interactionual orientation, age, citizenship, marital status, disability, gender identity or Veteran status. At Flagship, we recognize there is no perfect candidate.
If you have some of the experience listed above but not all, please apply anyway. Experience comes in many forms, skills are transferable, and passion goes a long way. We are dedicated to building diverse and inclusive teams and look forward to learning more about your unique background. Recruitment & Staffing Agencies : Flagship Pioneering and its affiliated Flagship Lab companies (collectively, " FSP" ) do not accept unsolicited resumes from any source other than candidates. The submission of unsolicited resumes by recruitment or staffing agencies to FSP or its employees is strictly prohibited unless contacted directly by Flagship Pioneering's internal Talent Acquisition team.
Any resume submitted by an agency in the absence of a signed agreement will automatically become the property of FSP, and FSP will not owe any referral or other fees with respect thereto.
communities through philanthropy and volunteerism. We give our best effort to our work, and we put people first. We're looking for people who are determined to make life better for people around the world. Akouos is building a leading gene therapy company focused on hearing disorders.
We are a precision genetic medicine company dedicated to developing gene therapies with the potential to restore, improve, and preserve high-acuity physiologic hearing for individuals living with disabling hearing loss worldwide. Restoring, improving, and preserving high-acuity hearing is an area of high unmet need in medicine: 466 million people worldwide have disabling hearing loss, and there are no FDA-approved
therapies to address its underlying causes. Akouos was founded in 2016 by leaders in the fields of neurotology, genetics, inner ear drug delivery, and AAV gene therapy.
Listening is in our DNA. We believe the only way to achieve our ambitious goals is to engage as one team, listen to each other, and trust in ourselves and our science. The Target Discovery and Genetic Technology and Innovation teams are seeking a motivated and committed scientist, with deep experience in molecular biology, to contribute to the evaluation and development of AAV vectors for the treatment of genetic and acquired forms of hearing loss. A successful candidate will work independently and perform benchwork that
supports discovery efforts and contributes to IND-enabling studies.
The scope of work includes the design, execution, and analysis of in vitro and ex vivo experiments using novel AAV vectors, with an emphasis on Next-Generation Sequencing (NGS) studies, and the implementation of organizational methods to support everyday lab operations. The successful candidate will be self-motivated and creative, with a desire to succeed in a highly collaborative and fast-paced environment. Job Responsibilities: Execute in vitro and ex vivo nonclinical experiments for the development of genetic medicines for the inner ear, including the following: Design and conduct in vitro , ex vivo , and in vivo single-nuclei RNA-seq experiments including sample processing, implementing 10X Genomics workflows, library generation and Illumina sequencing.
Design, conduct, and analyze in vitro transfection and transduction experiments using clonal cell lines and/or primary cell lines and performing such readouts as cell-based assays, luminescence readouts, epifluorescent microscopy, flow cytometry, q PCR, and/or western blot. Maintain accurate and timely documentation of activities through meticulous lab notebook practices and contributions to reports. Analyze, interpret, and present data for experiments, with the ability to clearly communicate results in written and oral formats for team feedback.
Organize key lab operations including leading and executing coordinated orders of specialized materials and instruments, and generation and maintenance of databases for samples and reagents. Basic Qualifications: Bachelor's Degree and/or Master's Degree in cellular biology, molecular biology, virology, medicine, or related field with 7+ years of relevant laboratory work experience; biotech or medical industry experience preferred but not required. Additional Skills/Preferences: Extensive experience in sample processing and execution of NGS studies for bulk and single-cell RNA-Seq, including sample preparation, 10X Genomics platform, library preparation, and sequencing.
Experience with RNA analyses (q PCR) and protein analyses (western blot). Experience with mouse handling, mouse tissue harvest, and tissue handling. Demonstrated ability to function as a member of an interdisciplinary team and contribute within a highly collaborative and fast-paced environment. Exceptionally organized and detail oriented. Excellent computer skills and Microsoft Products proficiency (Outlook, Excel, Word, Power Point, etc.
) to support database tracking of key lab operations, including samples, and protocols. Eli Lilly and Company, Lilly USA, LLC and our wholly owned subsidiaries (collectively " Lilly" ) are committed to help individuals with disabilities to participate in the workforce and ensure equal opportunity to compete for jobs. If you require an accommodation to submit a resume for positions at Lilly, please email Lilly Human Resources ( xyz X@lists. ) for further assistance. Please note This email address is intended for use only to request an accommodation as part of the application process.
Any other correspondence will not receive a response. Lilly is an EEO/Affirmative Action Employer and does not discriminate on the basis of age, race, color, religion, gender, interactionual orientation, gender identity, gender expression, national origin, protected veteran status, disability or any other legally protected status. Our employee resource groups (ERGs) offer strong support networks for their members and help our company develop talented individuals for future leadership roles. Our current groups include: Africa, Middle East, Central Asia Network, African American Network, Chinese Culture Network, Early Career Professionals, Japanese International Leadership Network (JILN), Lilly India Network, Organization of Latinos at Lilly, PRIDE (LGBTQ + Allies), Veterans Leadership Network, Women's Network, Working and Living with Disabilities.
Learn more about all of our groups. #We Are Lilly
transforms the lives of patients, and the careers of those who do it. You'll get the chance to grow and thrive through opportunities uncommon in scale and scope, alongside high-achieving teams rich in diversity. Take your career farther than you thought possible.
Bristol Myers Squibb recognizes the importance of balance and flexibility in our work environment. We offer a wide variety of competitive benefits, services and programs that provide our employees with the resources to pursue their goals, both at work and in their personal lives. Read more: careers. /working-with-us. Working with Us: Challenging. Meaningful. Life-changing. Those aren't words that are usually associated with a
job. But working at Bristol Myers Squibb is anything but usual. Here, uniquely interesting work happens every day, in every department. From optimizing a production line to the latest breakthroughs in cell therapy, this is work that transforms the lives of patients, and the careers of those who do it.
You'll get the chance to grow and thrive through opportunities uncommon in scale and scope, alongside high-achieving teams rich in diversity. Take your career farther than you thought possible. Bristol-Myers Squibb is a global biomedical company whose mission is to discover, develop and deliver innovative medicines that help patients prevail over serious diseases. We are passionate about
making an impact on the lives of patients through research. This open position offers the opportunity to join a vibrant and collaborative research community striving to find new disease targets and develop innovative therapies.
We seek a highly motivated, passionate, and collaborative drug hunter with demonstrated experience in oncology discovery biology and preclinical drug development to join BMS in Cambridge, MA. The ideal candidate will have a deep understanding of cancer cell signaling, small molecule drug development, in vivo pharmacology, and translational sciences. Proven ability in therapeutically exploiting synthetic lethal or undruggable vulnerabilities is preferable.
The qualified candidate will lead several drug discovery efforts and work closely with global cross-functional teams, including Target-ID, chemistry, in vivo pharmacology, toxicology, DMPK, and translational biology, to advance novel ideas from concept to the clinic. S/he will supervise a team of associates and biology leads to support their project responsibilities and contribute to team objectives, including but not limited to investigating drug mechanisms of action, assay development, pharmacodynamics readouts, and exploring therapeutic hypotheses. Excellent oral and written communication skills are required, with the ability to thrive in a fast-paced matrix environment.
The successful candidate will have the presentation skills to influence and inform scientific decisions at senior management, cross-functional, or external meetings. They will also have opportunities to develop and foster external partnerships or academic collaborations to advance internal programs, as appropriate. BMS is committed to people development and fosters a learning environment to build scientific and leadership skills. In addition to leading scientific projects, the candidate will also be able to participate in and lead site initiatives and influence broader portfolio, strategic, and business development decisions.
Basic Qualifications: Bachelor's Degree 10+ years of academic and / or industry experience Or Master's Degree 8+ years of academic and / or industry experience Or Ph. D. or equivalent advanced degree in the Life Sciences 6+ years of academic and / or industry experience 2+ years of leadership experience Preferred Qualifications: A Ph. D. degree with a minimum of 8 years of relevant industry experience in preclinical drug discovery and cancer biology. Industry experience will be prioritized over academia.
In-depth knowledge of cancer cell signaling, small molecule drug development, in vivo pharmacology, and translational biology Demonstrated ability to lead a cross-functional drug discovery team and advance preclinical drug discovery from target validation to clinical candidate Strong leadership skills, excellent interpersonal, oral, and written communication skills Demonstrated ability to supervise and support the development of a high-performing team of associates and/or facilitate career progression Demonstrated ability to effectively influence stakeholders and cross-functional leadership in a dynamic, fast-paced matrixed organization Ability to effectively and seamlessly multitask and prioritize across multiple portfolio assets, with complex strategies and accelerated development timelines Demonstrated ability to advise and participate in business development due-diligence evaluations If you come across a role that intrigues you but doesn't perfectly line up with your resume, we encourage you to apply anyway.
You could be one step away from work that will transform your life and career. Uniquely Interesting Work, Life-changing Careers With a single vision as inspiring as " Transforming patients' lives through science™ " every BMS employee plays an integral role in work that goes far beyond ordinary.
Each of us is empowered to apply our individual talents and unique perspectives in an inclusive culture, promoting diversity in clinical trials, while our shared values of passion, innovation, urgency, accountability, inclusion and integrity bring out the highest potential of each of our colleagues. On-site Protocol Physical presence at the BMS worksite or physical presence in the field is a necessary job function of this role, which the Company deems critical to collaboration, innovation, productivity, employee well-being and engagement, and it enhances the Company culture.
BMS is dedicated to ensuring that people with disabilities can excel through a transparent recruitment process, reasonable workplace accommodations/adjustments and ongoing support in their roles. Applicants can request a reasonable workplace accommodation/adjustment prior to accepting a job offer. If you require reasonable accommodations/adjustments in completing this application, or in any part of the recruitment process, direct your inquiries to xyz X@.
Visit careers. /eeo-accessibility to access our complete Equal Employment Opportunity statement. BMS cares about your well-being and the well-being of our staff, customers, patients, and communities. As a result, the Company strongly recommends that all employees be fully vaccinated for Covid-19 and keep up to date with Covid-19 boosters. BMS will consider for employment qualified applicants with arrest and conviction records, pursuant to applicable laws in your area. Any data processed in connection with role applications will be treated in accordance with applicable data privacy policies and regulations.
