CrawlJobs Logo
Baxter Logo Baxter · IT - Software Development

Research Associate I, R&D Complex Product Development

India, Ahmedabad Employment contract · Job Posted June 14, 2026
Apply Position
Job Link Share

Job Description

This is where new knowledge is discovered. Baxter’s Research and Development teams work cross functionally to innovate, develop and introduce creative solutions for patients needs globally. From Scientists to Engineers, your work creates the products that save and sustain lives. This is where your work makes a difference. At Baxter, we believe every person—regardless of who they are or where they are from—deserves a chance to live a healthy life. It was our founding belief in 1931 and continues to be our guiding principle. We are redefining healthcare delivery to make a greater impact today, tomorrow, and beyond. Our Baxter colleagues are united by our Mission to Save and Sustain Lives. Together, our community is driven by a culture of courage, trust, and collaboration. Every individual is empowered to take ownership and make a meaningful impact. We strive for efficient and effective operations, and we hold each other accountable for delivering exceptional results. Here, you will find more than just a job—you will find purpose and pride.

Job Responsibility

  • To perform advanced characterization of complex injectable drugs, including iron formulations, proteins & peptides, oligonucleotides, carbohydrates & other biomolecular APIs and various impurities in lyophilized, liquid, emulsions & other formulations for regulatory submission following GLP norms
  • To manage outsourced studies at CROs, academic institutes & other external facilities, from study design, execution, analysis and report preparation. Traveling to external facilities, as and when required, is a mandatory requirement for this position
  • To demonstrate subject matter expertise and help overcome technical challenges in product development, by liaising with formulation and other cross-functional teams as a Subject Matter Expertise (SME)
  • To understand the project with guidance of Sub-department Manager and follow their instructions
  • To provide necessary assistance for various procurement activities, review quotations, engage suppliers to procure required goods & services in a timebound manner
  • To complete the planned work in the stipulated time frame, inform the Sub-department Manager if any deviation or issues are observed
  • To keep track of each activity related to product analysis and development activities
  • To carry out all the testing and data recording according to the approved SOPs/ ALCOA++ principle and current pharmacopoeia. Data recording in ELN and sign off must be completed on time
  • To verify the shelf life of the chemical or reagent before performing analysis of the material or product
  • To follow Good Documentation Practices & Good Laboratory Practices, maintain lab notebooks & other records appropriately
  • To investigate if any deviation / abnormalities are observed and report to Sub-department Manager
  • To check the trend of results before reporting the results
  • To keep the status of daily work and report to Sub-department Manager on daily basis
  • To undertake operation, calibration, preventive and breakdown mainte the instruments as per approved standard operating procedure. To report on the conclusion of preventive maintenance and breakdown maintenance to Sub-department Manager
  • To list all resources required for the study and keep track of routine requirements and ensure timely procurement of the same, verify the materials received for analysis from supplier as per given requirement
  • To complete training as per the quality matrix targets
  • To prepare and update the SOPs. To prepare method development and verification report
  • To perform the work as allocated by Sub-department Manager
  • To liaise with customers, staff and suppliers
  • To write / fill the record in legible writing
  • To keep the documentation online with analysis
  • To compile required data for Management Information System and provide to Sub-department Manager
  • In the absence of Officer, Sub-department Manager will ensure his roles and responsibilities
  • To communicate about any failure or abnormal notification or non-compliance in results to Sub- department Manager and help resolve them in a timely manner
  • To communicate project related issues to Sub-department Manager and follow the action plan
  • To keep status of daily work and report to Sub-department Manager on daily basis

Requirements

  • Masters (Pharmacy, or equivalent discipline) with 6 to 10 years of experience, or, PhD (biophysics, biochemistry or equivalent discipline) with 0 to 5 years of experience in SEC-UV-MALS and related methods encompassing liquid chromatography, light scattering, diffraction and light obscuration
  • Competency in the acquisition, processing and data analysis by SEC-UV-MALS and light scattering/diffraction/obscuration techniques for analysis of peptides and iron colloidal products for regulatory submissions is mandatory
  • Expertise in computational chemistry, molecular modeling and statistical methods are beneficial attributes
  • Basic understanding of working principles of biophysical & spectroscopic methods, like CD, FTIR, UV, EPR, Mossbauer, and fluorescence spectroscopy, particle XRD, microscopy methods (AFM & EM) & related orthogonal methods to assess structural properties of proteins and iron colloids
  • Proficiency in literature search through publication and patent databases, repositories (e.g. Pubmed), scientific webinars by regulatory agencies, etc, to remain updated on advanced characterization methods and recent scientific developments
  • Knowledge of pharmacopoeia, ICH Guidelines and means to implement them for product development
  • Experience in the operation, calibration and preventive maintenance of NMR and other instruments to ensure continued usage
  • Trouble shooting of various problems obtain during the product development
  • Knowledge of good laboratory practices and good documentation practices
  • Communication skills
  • Presentation skills
  • Analytical skills
  • Lateral coordination
  • Positive Attitude
  • Policy compliance
  • Documentation Skills

What we offer

  • Support for Parents
  • Continuing Education/ Professional Development
  • Employee Heath & Well-Being Benefits
  • Paid Time Off
  • 2 Days a Year to Volunteer
Baxter - All Job Offers

Looking for more opportunities?

Search for other job offers that match your skills and interests.

Suggested Tags: Frontend Developer Secretary Talent Manager Salesforce Administrator Data Analyst
Similar Jobs for

Research Associate I, R&D Complex Product Development

8 matching positions

Research Associate I, R&D Complex Product Development

This is where new knowledge is discovered. Baxter's Research and Development tea...
Location
Location
India , Ahmedabad
Salary
Salary:
Not provided
https://www.baxter.com/ Logo
Baxter
Expiration Date
Until further notice
Flip Icon
Requirements
Requirements
  • Masters (Pharmacy, or equivalent discipline) with 6 to 10 years of experience, or, PhD (biophysics, biochemistry or equivalent discipline) with 0 to 5 years of experience in SEC-UV-MALS and related methods encompassing liquid chromatography, light scattering, diffraction and light obscuration
  • Competency in the acquisition, processing and data analysis by SEC-UV-MALS and light scattering/diffraction/obscuration techniques for analysis of peptides and iron colloidal products for regulatory submissions is mandatory
  • Expertise in computational chemistry, molecular modeling and statistical methods are beneficial attributes
  • Basic understanding of working principles of biophysical & spectroscopic methods, like CD, FTIR, UV, EPR, Mossbauer, and fluorescence spectroscopy, particle XRD, microscopy methods (AFM & EM) & related orthogonal methods to assess structural properties of proteins and iron colloids
  • Proficiency in literature search through publication and patent databases, repositories (e.g. Pubmed), scientific webinars by regulatory agencies, etc, to remain updated on advanced characterization methods and recent scientific developments
  • Knowledge of pharmacopoeia, ICH Guidelines and means to implement them for product development
  • Experience in the operation, calibration and preventive maintenance of NMR and other instruments to ensure continued usage
  • Trouble shooting of various problems obtain during the product development
  • Knowledge of good laboratory practices and good documentation practices
  • Communication skills
Job Responsibility
Job Responsibility
  • Perform advanced characterization of complex injectable drugs, including iron formulations, proteins & peptides, oligonucleotides, carbohydrates & other biomolecular APIs and various impurities for regulatory submission following GLP norms
  • Manage outsourced studies at CROs, academic institutes & other external facilities, from study design, execution, analysis and report preparation
  • Travel to external facilities
  • Demonstrate subject matter expertise and help overcome technical challenges in product development, by liaising with formulation and other cross-functional teams
  • Understand the project with guidance of Sub-department Manager and follow their instructions
  • Provide necessary assistance for various procurement activities, review quotations, engage suppliers to procure required goods & services
  • Complete the planned work in the stipulated time frame
  • Keep track of each activity related to product analysis and development activities
  • Carry out all the testing and data recording according to the approved SOPs/ ALCOA++ principle and current pharmacopoeia
  • Verify the shelf life of the chemical or reagent before performing analysis
What we offer
What we offer
  • Support for Parents
  • Continuing Education/ Professional Development
  • Employee Heath & Well-Being Benefits
  • Paid Time Off
  • 2 Days a Year to Volunteer
Read More
Arrow Right

Research Associate I, R&D Complex Product Development

This is where your work makes a difference. At Baxter, we believe every person—r...
Location
Location
India , Ahmedabad
Salary
Salary:
Not provided
https://www.baxter.com/ Logo
Baxter
Expiration Date
Until further notice
Flip Icon
Requirements
Requirements
  • Masters (Pharmacy, or equivalent discipline) with 6 to 10 years of experience
  • PhD (biophysics, biochemistry or equivalent discipline) with 0 to 5 years of experience
  • Competency in the acquisition, processing and data analysis by SEC-UV-MALS and light scattering/diffraction/obscuration techniques for analysis of peptides and iron colloidal products for regulatory submissions is mandatory
  • Basic understanding of working principles of biophysical & spectroscopic methods
  • Knowledge of pharmacopoeia, ICH Guidelines
  • Experience in the operation, calibration and preventive maintenance of NMR and other instruments
  • Knowledge of good laboratory practices and good documentation practices
  • Communication skills
  • Presentation skills
  • Analytical skills
Job Responsibility
Job Responsibility
  • To perform advanced characterization of complex injectable drugs
  • To manage outsourced studies at CROs, academic institutes & other external facilities
  • To demonstrate subject matter expertise and help overcome technical challenges in product development
  • To provide necessary assistance for various procurement activities
  • To complete the planned work in the stipulated time frame
  • To keep track of each activity related to product analysis and development activities
  • To carry out all the testing and data recording according to the approved SOPs/ ALCOA++ principle
  • To verify the shelf life of the chemical or reagent before performing analysis
  • To follow Good Documentation Practices & Good Laboratory Practices
  • To investigate if any deviation / abnormalities are observed
What we offer
What we offer
  • Support for Parents
  • Continuing Education/ Professional Development
  • Employee Heath & Well-Being Benefits
  • Paid Time Off
  • 2 Days a Year to Volunteer
Read More
Arrow Right

Research Associate I, R&D Complex Product Development

This is where new knowledge is discovered. Baxter's Research and Development tea...
Location
Location
India , Ahmedabad
Salary
Salary:
Not provided
https://www.baxter.com/ Logo
Baxter
Expiration Date
Until further notice
Flip Icon
Requirements
Requirements
  • Masters (Pharmacy, or equivalent discipline) with 6 to 10 years of experience, or, PhD (biophysics, biochemistry or equivalent discipline) with 0 to 5 years of experience in SEC-UV-MALS and related methods encompassing liquid chromatography, light scattering, diffraction and light obscuration
  • Competency in the acquisition, processing and data analysis by SEC-UV-MALS and light scattering/diffraction/obscuration techniques for analysis of peptides and iron colloidal products for regulatory submissions is mandatory
  • Expertise in computational chemistry, molecular modeling and statistical methods are beneficial attributes
  • Basic understanding of working principles of biophysical & spectroscopic methods, like CD, FTIR, UV, EPR, Mossbauer, and fluorescence spectroscopy, particle XRD, microscopy methods (AFM & EM) & related orthogonal methods to assess structural properties of proteins and iron colloids
  • Proficiency in literature search through publication and patent databases, repositories (e.g. Pubmed), scientific webinars by regulatory agencies, etc, to remain updated on advanced characterization methods and recent scientific developments
  • Knowledge of pharmacopoeia, ICH Guidelines and means to implement them for product development
  • Experience in the operation, calibration and preventive maintenance of NMR and other instruments to ensure continued usage
  • Trouble shooting of various problems obtain during the product development
  • Knowledge of good laboratory practices and good documentation practices
  • Communication skills
Job Responsibility
Job Responsibility
  • To perform advanced characterization of complex injectable drugs, including iron formulations, proteins & peptides, oligonucleotides, carbohydrates & other biomolecular APIs and various impurities in lyophilized, liquid, emulsions & other formulations for regulatory submission following GLP norms
  • To manage outsourced studies at CROs, academic institutes & other external facilities, from study design, execution, analysis and report preparation
  • To demonstrate subject matter expertise and help overcome technical challenges in product development, by liaising with formulation and other cross-functional teams as a Subject Matter Expertise (SME)
  • To understand the project with guidance of Sub-department Manager and follow their instructions
  • To provide necessary assistance for various procurement activities, review quotations, engage suppliers to procure required goods & services in a timebound manner
  • To complete the planned work in the stipulated time frame, inform the Sub-department Manager if any deviation or issues are observed
  • To keep track of each activity related to product analysis and development activities
  • To carry out all the testing and data recording according to the approved SOPs/ ALCOA++ principle and current pharmacopoeia
  • To verify the shelf life of the chemical or reagent before performing analysis of the material or product
  • To follow Good Documentation Practices & Good Laboratory Practices, maintain lab notebooks & other records appropriately
What we offer
What we offer
  • Support for Parents
  • Continuing Education/ Professional Development
  • Employee Heath & Well-Being Benefits
  • Paid Time Off
  • 2 Days a Year to Volunteer
  • Fulltime
Read More
Arrow Right

Research Associate I - R&D, Complex Product Development

This is where new knowledge is discovered. Baxter's Research and Development tea...
Location
Location
India , Ahmedabad
Salary
Salary:
Not provided
https://www.baxter.com/ Logo
Baxter
Expiration Date
Until further notice
Flip Icon
Requirements
Requirements
  • Master in Pharmacy or equivalent discipline with 6 to 10 years of experience
  • PhD in biophysics, biochemistry or equivalent discipline with 0 to 5 years of experience with spectroscopic and biophysical methods, including CD, FTIR, fluorescence spectroscopy
  • Competency in the acquisition, processing and data analysis by CD, FTIR, and fluorescence spectroscopy for analysis of proteins and peptides for regulatory submissions
  • Basic understanding of working principles of liquid chromatographic methods, dynamic light scattering, AF4-MALS, SV-AUC, & related orthogonal methods to assess protein higher order structures
  • Proficiency in literature search through publication and patent databases, repositories (e.g. Pubmed), scientific webinars by regulatory agencies
  • Knowledge of pharmacopoeia, ICH Guidelines and means to implement them for product development
  • Experience in the operation, calibration and preventive maintenance of NMR and other instruments
  • Trouble shooting of various problems obtain during the product development
  • Knowledge of good laboratory practices and good documentation practices
  • Communication skills
Job Responsibility
Job Responsibility
  • To perform advanced characterization of complex injectable drugs, including proteins & peptides, oligonucleotides, iron formulations, carbohydrates & other biomolecular APIs and various impurities in lyophilized, liquid, emulsions & other formulations for regulatory submission following GLP norms
  • To manage outsourced studies at CROs, academic institutes & other external facilities, from study design, execution, analysis and report preparation
  • To demonstrate subject matter expertise and help overcome technical challenges in product development, by liaising with formulation and other cross-functional teams as a Subject Matter Expertise (SME)
  • To understand the project with guidance of Sub-department Manager and follow their instructions
  • To provide necessary assistance for various procurement activities, review quotations, engage suppliers to procure required goods & services in a timebound manner
  • To complete the planned work in the stipulated time frame, inform the Sub-department Manager if any deviation or issues are observed
  • To keep track of each activity related to product analysis and development activities
  • To carry out all the testing and data recording according to the approved SOPs/ ALCOA++ principle and current pharmacopoeia
  • To verify the shelf life of the chemical or reagent before performing analysis of the material or product
  • To follow Good Documentation Practices & Good Laboratory Practices, maintain lab notebooks & other records appropriately
What we offer
What we offer
  • Support for Parents
  • Continuing Education/ Professional Development
  • Employee Heath & Well-Being Benefits
  • Paid Time Off
  • 2 Days a Year to Volunteer
  • Fulltime
Read More
Arrow Right

Research Associate I - R&D, Complex Product Development

This is where new knowledge is discovered. Baxter's Research and Development tea...
Location
Location
India , Ahmedabad
Salary
Salary:
Not provided
https://www.baxter.com/ Logo
Baxter
Expiration Date
Until further notice
Flip Icon
Requirements
Requirements
  • Masters (Pharmacy, or equivalent discipline) with 6 to 10 years of experience, or, PhD (biophysics, biochemistry or equivalent discipline) with 0 to 5 years of experience with spectroscopic and biophysical methods, including CD, FTIR, fluorescence spectroscopy
  • Competency in the acquisition, processing and data analysis by CD, FTIR, and fluorescence spectroscopy for analysis of proteins and peptides for regulatory submissions is mandatory
  • Expertise in computational chemistry, molecular modeling and statistical methods are beneficial attributes
  • Basic understanding of working principles of liquid chromatographic methods, dynamic light scattering, AF4-MALS, SV-AUC, & related orthogonal methods to assess protein higher order structures
  • Proficiency in literature search through publication and patent databases, repositories (e.g. Pubmed), scientific webinars by regulatory agencies, etc, to remain updated on advanced characterization methods and recent scientific developments
  • Knowledge of pharmacopoeia, ICH Guidelines and means to implement them for product development
  • Experience in the operation, calibration and preventive maintenance of NMR and other instruments to ensure continued usage
  • Trouble shooting of various problems obtain during the product development
  • Knowledge of good laboratory practices and good documentation practices
  • Communication skills
Job Responsibility
Job Responsibility
  • To perform advanced characterization of complex injectable drugs, including proteins & peptides, oligonucleotides, iron formulations, carbohydrates & other biomolecular APIs and various impurities in lyophilized, liquid, emulsions & other formulations for regulatory submission following GLP norms
  • To manage outsourced studies at CROs, academic institutes & other external facilities, from study design, execution, analysis and report preparation
  • Traveling to external facilities, as and when required, is a mandatory requirement for this position
  • To demonstrate subject matter expertise and help overcome technical challenges in product development, by liaising with formulation and other cross-functional teams as a Subject Matter Expertise (SME)
  • To understand the project with guidance of Sub-department Manager and follow their instructions
  • To provide necessary assistance for various procurement activities, review quotations, engage suppliers to procure required goods & services in a timebound manner
  • To complete the planned work in the stipulated time frame, inform the Sub-department Manager if any deviation or issues are observed
  • To keep track of each activity related to product analysis and development activities
  • To carry out all the testing and data recording according to the approved SOPs/ ALCOA++ principle and current pharmacopoeia
  • Data recording in ELN and sign off must be completed on time
What we offer
What we offer
  • Support for Parents
  • Continuing Education/ Professional Development
  • Employee Heath & Well-Being Benefits
  • Paid Time Off
  • 2 Days a Year to Volunteer
  • Fulltime
Read More
Arrow Right

Research Associate I - R&D, Complex Product Development

This is where new knowledge is discovered. Baxter's Research and Development tea...
Location
Location
India , Ahmedabad
Salary
Salary:
Not provided
https://www.baxter.com/ Logo
Baxter
Expiration Date
Until further notice
Flip Icon
Requirements
Requirements
  • Masters (Pharmacy, or equivalent discipline) with 6 to 10 years of experience, or, PhD (biophysics, biochemistry or equivalent discipline) with 0 to 5 years of experience with spectroscopic and biophysical methods, including CD, FTIR, fluorescence spectroscopy
  • Competency in the acquisition, processing and data analysis by CD, FTIR, and fluorescence spectroscopy for analysis of proteins and peptides for regulatory submissions is mandatory
  • Expertise in computational chemistry, molecular modeling and statistical methods are beneficial attributes
  • Basic understanding of working principles of liquid chromatographic methods, dynamic light scattering, AF4-MALS, SV-AUC, & related orthogonal methods to assess protein higher order structures
  • Proficiency in literature search through publication and patent databases, repositories (e.g. Pubmed), scientific webinars by regulatory agencies, etc, to remain updated on advanced characterization methods and recent scientific developments
  • Knowledge of pharmacopoeia, ICH Guidelines and means to implement them for product development
  • Experience in the operation, calibration and preventive maintenance of NMR and other instruments to ensure continued usage
  • Trouble shooting of various problems obtain during the product development
  • Knowledge of good laboratory practices and good documentation practices
  • Communication skills
Job Responsibility
Job Responsibility
  • To perform advanced characterization of complex injectable drugs, including proteins & peptides, oligonucleotides, iron formulations, carbohydrates & other biomolecular APIs and various impurities in lyophilized, liquid, emulsions & other formulations for regulatory submission following GLP norms
  • To manage outsourced studies at CROs, academic institutes & other external facilities, from study design, execution, analysis and report preparation
  • To demonstrate subject matter expertise and help overcome technical challenges in product development, by liaising with formulation and other cross-functional teams as a Subject Matter Expertise (SME)
  • To understand the project with guidance of Sub-department Manager and follow their instructions
  • To provide necessary assistance for various procurement activities, review quotations, engage suppliers to procure required goods & services in a timebound manner
  • To complete the planned work in the stipulated time frame, inform the Sub-department Manager if any deviation or issues are observed
  • To keep track of each activity related to product analysis and development activities
  • To carry out all the testing and data recording according to the approved SOPs/ ALCOA++ principle and current pharmacopoeia
  • To verify the shelf life of the chemical or reagent before performing analysis of the material or product
  • To follow Good Documentation Practices & Good Laboratory Practices, maintain lab notebooks & other records appropriately
What we offer
What we offer
  • Support for Parents
  • Continuing Education/ Professional Development
  • Employee Heath & Well-Being Benefits
  • Paid Time Off
  • 2 Days a Year to Volunteer
  • Fulltime
Read More
Arrow Right

Associate Director, R&D Product Development, Wellbeing Collective

The Americas & EU Technical Leader, Wellbeing International R&D is responsible f...
Location
Location
United States , Trumbull
Salary
Salary:
146200.00 - 219400.00 USD / Year
unilever.com Logo
Unilever
Expiration Date
Until further notice
Flip Icon
Requirements
Requirements
  • Strong R&D TPL experience (senior-level)
  • Deep expertise in gummy formulation
  • Based in China with Mandarin fluency to speak to the manufacturers in China
  • Experience working on TPL projects beyond China, ideally with a regional or global lens
  • Bachelor's degree required in science or engineering
  • BS with 12+ years, Masters with 10+ years, or PhD with 7+ years’ experience in formulation development or technology development of which at least 3 years as Technical Project Lead
  • Excellent understanding of Product development Principles – formulation development for consumer-friendly ingestible dosage forms such as Powders, Gummies/capsules, material understanding, product scale up, product costing, ingredient sources and GMP
  • Experience working with cross functional teams across geographies
  • Ability to lead more complex portfolio of innovation/quality & Value Improvement Project (VIP) projects including multiple brands/regions/technologies
  • Technical leadership by exhibiting and fostering initiative, motivation, judgment, flexibility, and breadth
Job Responsibility
Job Responsibility
  • Drive best-in-class product development to support growth ambitions of the Wellbeing Collective international business
  • Lead innovation and new market entry across Canada, Latin America, the UK, and Europe for WBC brands
  • Own end-to-end technical delivery for innovation and market expansion
  • Partner closely with cross-functional teams (Marketing, Supply Chain, Procurement, SERs, Nutrition Science, Quality, and Regulatory) to deliver projects on time and in compliance
  • Build and deliver a robust innovation pipeline in partnership with the global marketing team
  • Drive cost savings and strategic business continuity initiatives
  • Lead and develop a team of formulators and process engineers
  • Lead end-to-end product development and commercialization
  • Design cost-effective, sensorially superior, and scalable formulations
  • Own technical delivery on project teams
What we offer
What we offer
  • Health insurance (including prescription drug, dental, and vision coverage)
  • Retirement savings benefits
  • Life insurance and disability benefits
  • Parental leave
  • Sick leave
  • Paid vacation and holidays
  • Access to numerous voluntary benefits
  • Bonus eligible
  • Long-Term Incentive (LTI) eligible
  • Fulltime
Read More
Arrow Right
New

Senior/Principal R&D Systems Engineer - Component and Material Evaluation

We are seeking an R&D Systems Engineer for the Component and Material Evaluation...
Location
Location
United States , Albuquerque
Salary
Salary:
117500.00 - 235700.00 USD / Year
sandia.gov Logo
Sandia National Laboratories
Expiration Date
Until further notice
Flip Icon
Requirements
Requirements
  • A bachelor's degree in a relevant discipline and five (5) years of directly relevant experience, or an equivalent combination of directly relevant education and engineering or scientific experience that demonstrates the knowledge, skills, and ability to perform independent research and development
  • Ability to obtain and maintain a DOE Q Clearance and Sigma 15 access, which will require random polygraphs
Job Responsibility
Job Responsibility
  • Plan and manage the execution of engineering programs for Sandia's customers and sponsors
  • Serve as the primary representative to customers and partners for ND modernization programs, negotiating, managing, and delivering all component evaluation scope for several technology families
  • Establish strong relationships with key influencers and collaborate with cross-functional teams, including systems and component engineering teams, our Science and Technology (S&T) community, independent technical assessment partners, and production agencies
  • Identify defects and aging trends, understand performance margins, and make predictive assessments of weapon components and their materials through comprehensive component evaluation activities
  • Chair Stockpile Finding Investigations (SFIs) as a System Evaluation Engineer (SEE) to determine the root cause of anomalies discovered during component evaluations, assess their impact on the safety, security, and reliability of the stockpile, and guide discussions to ensure thorough understanding and resolution of issues
  • Engage in lifecycle management of evaluated components, focusing on key phases such as design, testing, and production
  • Identify and manage risks associated with component evaluations, employing strategies for risk assessment and mitigation
  • Document findings and recommendations, preparing reports that communicate complex technical information clearly and effectively to stakeholders
What we offer
What we offer
  • Challenging work with amazing impact that contributes to security, peace, and freedom worldwide
  • Extraordinary co-workers
  • Some of the best tools, equipment, and research facilities in the world
  • Career advancement and enrichment opportunities
  • Flexible work arrangements for many positions include 9/80 (work 80 hours every two weeks, with every other Friday off) and 4/10 (work 4 ten-hour days each week) compressed workweeks, part-time work, and telecommuting (a mix of onsite work and working from home)
  • Generous vacation, strong medical and other benefits, competitive 401k, learning opportunities, relocation assistance and amenities aimed at creating a solid work/life balance
  • Fulltime
Read More
Arrow Right