Current jobs related to Associate Scientist, Stability Studies Support AZ28968 - New Haven - ADPI

  • Associate Scientist

    3 weeks ago

    New Haven, Connecticut, United States Nesco Resource Full time

    Job Title: Associate ScientistWe are seeking an Associate Scientist to join our Injectable Drug Product Development group at Nesco Resource. As an Associate Scientist, you will be responsible for conducting experimental work on various aspects of drug product characterization, including formulation development, in-use compatibility studies, and process...

  • Associate Scientist: Drug Product Development

    3 weeks ago

    New Haven, United States Proclinical Staffing Full time

    Associate Scientist: Drug Product Development - Contract - New Haven, CTProclinical is seeking an Associate Scientist for Drug Product Development. In this role, you will design and execute development studies for clinical drug candidates and commercial products, focusing on characterizing protein drug stability using industry-standard methodologies. You...

  • Associate Scientist: Drug Product Development

    3 weeks ago

    New Haven, United States Proclinical Staffing Full time

    Associate Scientist: Drug Product Development - Contract - New Haven, CTProclinical is seeking an Associate Scientist for Drug Product Development. In this role, you will design and execute development studies for clinical drug candidates and commercial products, focusing on characterizing protein drug stability using industry-standard methodologies. You...

  • Associate Scientist: Protein Characterization

    1 month ago

    New Haven, United States Proclinical Staffing Full time

    Associate Scientist: Protein Characterization - Contract - New Haven, CTProclinical is seeking a dedicated and innovative Biochemical Development Specialist. This is a contract position located in New Haven, CT.Primary Responsibilities:The successful candidate will be responsible for designing and executing development studies for clinical drug candidates...

  • Associate Scientist: Protein Characterization

    1 month ago

    New Haven, United States Proclinical Staffing Full time

    Associate Scientist: Protein Characterization - Contract - New Haven, CTProclinical is seeking a dedicated and innovative Biochemical Development Specialist. This is a contract position located in New Haven, CT.Primary Responsibilities:The successful candidate will be responsible for designing and executing development studies for clinical drug candidates...

  • Senior Scientist Stability

    3 weeks ago

    New Brunswick, New Jersey, United States Bristol-Myers Squibb Full time

    Job SummaryBristol-Myers Squibb is seeking a highly skilled and experienced Principal Scientist Stability to join our team. As a key member of our stability team, you will be responsible for the stability product strategy and oversight of product stability programs for commercial small molecules Drug Substances and Drug Products.Key ResponsibilitiesDevelop...

  • Principal Scientist Stability Expert

    1 month ago

    New Brunswick, New Jersey, United States Bristol-Myers Squibb Full time

    Transforming Patients' Lives through ScienceBristol Myers Squibb is a leading pharmaceutical company dedicated to transforming patients' lives through science. We are seeking a highly skilled Principal Scientist Stability to join our team.About the RoleThe Principal Scientist Stability will be responsible for leading the stability program for commercial...

  • Associate Scientist

    3 weeks ago

    New Haven, United States Integrated Resources, Inc Full time

    Job DescriptionJob DescriptionJob Title: Associate ScientistLocation: New Haven, CTDuration: 12+ months Pay range: $22.75/hour. on W2Job description:The position is required to join Injectable Drug Product Development group of Client Rare Disease Pharmaceuticals’ Pharmaceutical Development and Clinical Supply (PDCS) department. The job entails experimental...

  • Associate Research Scientist in Genetics

    3 weeks ago

    New Haven, Connecticut, United States The University of Texas MD Anderson Cancer Center Full time

    Job Title: Associate Research Scientist in GeneticsJob Summary:We are seeking a highly motivated and experienced Associate Research Scientist in Genetics to join our team at Yale University. The successful candidate will be responsible for leading projects involving gene editing in muscle disease genes in patient cells and relevant mouse...

  • Associate Scientist

    3 weeks ago

    New Haven, United States Nesco Resource Full time

    Location: New Haven, CT 4-5 Days OnsiteThis is what you will do:The position is required to join Injectable Drug Product Development group of Alexion-AstraZeneca Rare Disease Pharmaceuticals' Pharmaceutical Development and Clinical Supply (PDCS) departmentThe job entails experimental work on various aspects of drug product characterization, including...

  • Associate Scientist

    1 week ago

    New Haven, United States eTeam Full time

    This is what you will do:The position is required to join Injectable Drug Product Development group of Client-Client Rare Disease Pharmaceuticals’ Pharmaceutical Development and Clinical Supply (PDCS) department.The job entails experimental work on various aspects of drug product characterization, including formulation development, in use compatibility...

  • Associate Scientist

    3 weeks ago

    New Haven, United States eTeam Full time

    This is what you will do:The position is required to join Injectable Drug Product Development group of Client-Client Rare Disease Pharmaceuticals’ Pharmaceutical Development and Clinical Supply (PDCS) department.The job entails experimental work on various aspects of drug product characterization, including formulation development, in use compatibility...

  • Associate Scientist

    3 weeks ago

    New Haven, United States eTeam Full time

    This is what you will do:The position is required to join Injectable Drug Product Development group of Client-Client Rare Disease Pharmaceuticals’ Pharmaceutical Development and Clinical Supply (PDCS) department.The job entails experimental work on various aspects of drug product characterization, including formulation development, in use compatibility...

  • Protein Characterization Specialist

    1 month ago

    New Haven, Connecticut, United States Proclinical Staffing Full time

    Job Title: Associate Scientist: Protein CharacterizationWe are seeking a highly skilled and motivated Associate Scientist to join our team at Proclinical Staffing. As a key member of our development team, you will be responsible for designing and executing development studies for clinical drug candidates and commercial products.Key Responsibilities:Design...

  • Protein Characterization Specialist

    4 weeks ago

    New Haven, Connecticut, United States Proclinical Staffing Full time

    Job Title: Associate Scientist: Protein CharacterizationWe are seeking a highly skilled Associate Scientist to join our team at Proclinical Staffing. As a key member of our biochemical development team, you will be responsible for designing and executing development studies for clinical drug candidates and commercial products.Key Responsibilities:Design and...

  • Associate Research Scientist

    3 weeks ago

    New York, New York, United States Pearson Full time

    Job Title: Associate Research ScientistThe Associate Research Scientist position is a key role within the Pearson Psychometric and Research Services group, which is part of the US School Assessment group and larger Assessment and Qualifications team. As a member of this team, you will provide psychometric support to state and national customers, develop...

  • Scientist, Study Director

    7 days ago

    New Port Richey, Florida, United States Altasciences Full time

    About the RoleThe Scientist, Study Director will have a passion for preclinical research. This individual will represent the single point of control for assigned studies and will be responsible for the interpretation, analysis, documentation, and reporting of study results for GLP and non-GLP studies.The Study Director will be responsible for the technical...

  • Scientist

    2 months ago

    New Haven, United States Integrated Resources, Inc ( IRI ) Full time

    This is what you will do: The position is required to join Injectable Drug Product Development group of company pharmaceuticals’ Analytical and Pharmaceutical Development department. This position is required to conduct studies to enable Drug Product characterization activities, including combination products at high protein concentration, as well as...

  • Research Scientist II

    5 months ago

    New Orleans, United States InsideHigherEd Full time

    Research Scientist IITNPRC - PathologyLocation: Covington, LASummaryThe Research Scientist's primary responsibility is to conduct research on HIV-associated atherosclerosis projects and to utilize the universal cell ablation model for the study of cellular functionality in the pathogenesis of human diseases, such as multiple sclerosis; he/she will keep a lab...

  • Clinical Trial Associate

    7 days ago

    New Brunswick, New Jersey, United States Allen Spolden Full time

    Job SummaryThe Clinical Trial Associate - Study Support will play a key role in supporting the operational strategy and execution of clinical studies at Allen Spolden. This position will work closely with the Clinical Operations Manager, study teams, and Clinical Research Organizations (CROs) to ensure the successful execution of clinical trials.Key...

Associate Scientist, Stability Studies Support AZ28968

2 months ago

New Haven, United States ADPI Full time

Associate Scientist, Stability Studies Support AZ28968

12 Month Contract

New Haven, CT - onsite 5x per week



Scope of Work: Candidate will support stability studies for new drying technologies for drug substance. Stability studies will include impact to drug product formulations with dried DS. Additional work may be assigned to support formulation development efforts for existing programs. This work includes lab work, data generation, analysis and interpretation, as well as data discussion in meetings and report generation.



This is what you will do:

The position is required to join Injectable Drug Product Development group of pharmaceuticals’ Analytical and Pharmaceutical Development department. This position is required to conduct studies to enable Drug Product characterization activities, including combination products at high protein concentration, as well as commercial products. The job entails experimental work on various aspects of Drug Product characterization, including formulation development, safety risk assessment of excipients as well as process reagents, extractables and leachables, in use compatibility studies for intravenous and subcutaneous administration, process development to support drug product manufacturing support, particulates testing. The ability to work with minimal supervision as well as part of the team is essential. The position entails execution of the studies and data processing and compiling to generate and support development reports as well as other required documentation. Understanding of assay development, biotherapeutics development is a plus. Understanding of the basic principles of protein chemistry and/or drug product process is required. Experience with electronic record keeping software, like ELN, EndNote, e-logbooks; maintenance of laboratory instrumentation (organizing PMs, data backup, SW upgrade, etc.) and familiarity with design and maintenance of databases will be a plus.



You will need to have:

  • BS in Chemistry, Biochemistry, Biophysics, Chemical engineering, or relevant field with 2+ years of experience or MS degree with 1+ years of relevant experience is required. Solid background in protein chemistry, chemistry, biochemistry, or equivalent is highly preferred.
  • Position requires scientific and practical knowledge of protein chemistry or drug product process
  • Previous experience in biotherapeutics development as well as understanding of the biotechnology products life cycle and factors impacting protein molecule stability is a plus
  • Hands-on experience with instrumentation, used in protein pharmaceutical and analytical development as well as characterization and knowledge of cGMP and quality guidelines is a plus
  • Ability to take initiative in problem solving and finding solutions to scientific challenges with minimal supervision is preferred
  • Shows ability to take instructions and execute experiments and other activities with minimal supervision is required
  • The individual must be able to work in a collaborative setting and has ability to adhere to timelines with minimal supervision is essential
  • Excellent interpersonal skills are required, as is the strong ability to communicate effectively