quality control technical transfer analyst 3 Position Available In Rockingham, New Hampshire

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life, physical, and social science occupations
quality control technical transfer analyst 3
quality control technical transfer analyst 3.
portsmouth, new hampshire
posted december 10, 2024 job details summary $28.05 – $33 per hour
contract
associate degree
category
life, physical, and social science occupations
reference
49585
job summary:
Join a Leading Biologics & Cell/Gene Therapy Company! Seeking candidates with experience in biologics Quality Control, particularly analytical and molecular assays supporting product release, stability, and method transfer to join a top-tier, biologics and cell & gene therapy company in a dynamic, fast-paced environment! The Quality Control Technical Transfer Analyst 3 will act as a team member of the Quality Control department to support production by contributing to the completion of the technical transfer activities. Also participate in quality testing for customer in-process, final product testing and stability studies when needed.

location:

Portsmouth, New Hampshire
job type: Contract
salary: $28.05 – 33.00 per hour
work hours: 8 to 4
education: Associate responsibilities: Running test samples for In-Process, Lot Release and Stability studies.
Testing to include: Capillary Electrophoresis – SDS (CE-SDS), ELISA, UV-Vis, qPCR, etc.
Running test samples for (but not limited to) investigations, transfers and validations.
Reviewing assays
Writing – Quality Records (Deviations, CAPA, Change Control) and Test Methods
Projects – such as method transfers, new instruments, method qualifications
Use of Microsoft Suites (Word, Excel, PowerPoint)
Use of Laboratory computer systems
Potential previous use of GMP Quality Systems such as: TrackWise, LIMS qualifications:

Required:

Associate’s Degree (AS) Biology, Microbiology, Biochemistry, Cell Biology, Molecular Biology, or Related Science Fields
In-process testing, method development, and transfer across various stages of drug development (early to late)
Experience with biologics analytical methods such as qPCR, ELISA, SDS-PAGE, and HPLC
Experience supporting method transfer, development, or validation in a GMP environment
Strong ability to interpret data both alone and with guidance.

Preferred:

Exposure to or willingness to learn specialized methods like A280, CE-SDS, icIEF, SoloVPE
Familiarity coordinating with CDMOs and contributing to tech transfer documentation
Familiarity with viral vectors (AAV) or gene therapy products
#LI-DB1 skills: Molecular Biology, Quality control, Cell Biology, PCR, CAPA, Assay Method, Biology, Chromatography, Immunoassays, Microbiology, GMP (Good Manufacturing Practice),

RT-PCR Equal Opportunity Employer:

Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status. At Randstad, we welcome people of all abilities and want to ensure that our hiring and interview process meets the needs of all applicants. If you require a reasonable accommodation to make your application or interview experience a great one, please contact HRsupport@randstadusa.com. Pay offered to a successful candidate will be based on several factors including the candidate’s education, work experience, work location, specific job duties, certifications, etc. In addition, Randstad offers a comprehensive benefits package, including health, an incentive and recognition program, and 401K contribution (all benefits are based on eligibility). This posting is open for thirty (30) days.