Stability Lab Scientist — GMP & Sample Management

Parexel

Pennsylvania

On-site

USD 65,000 - 90,000

Full time

24 hours ago
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Benefits offered by this job

Full benefits
Sick time
401K
Paid holidays
Paid time off

Job summary

Parexel is seeking a Scientist 2 or 3 to support stability sample management for late-stage pharmaceutical development. The role is a full-time, on-site assignment at a client location in West Point, PA, with comprehensive benefits and PTO. The ideal candidate will support stability studies, sample handling, documentation, and regulatory compliance within a GMP environment.

The position requires B.S. with 1–2 years (Scientist 2) or B.S./M.S.

Qualifications

  • B.S. with 1–2 years of experience for Scientist 2; M.S. with 0–1 years
  • B.S. with 3–5 years of experience for Scientist 3; M.S. with 1–2 years
  • Hands-on experience in a pharmaceutical cGMP environment supporting stability sample management and stability chamber operations
  • Experience with LIMS and electronic laboratory notebook

Responsibilities

  • Lift, carry, and place filled sample bins, shipping containers, and cold-chain coolers
  • Coordinate setup of new stability studies
  • Perform routine sample pulls from stability chambers
  • Prepare and label samples for stability studies
  • Prepare samples for shipments to testing laboratories and process samples for destruction
  • Second scientist review of analytical data and GMP documents
  • Notify management of non-conforming events
  • Complete applicable GMP training
  • Ensure compliance with cGMP and internal policies
  • Maintain sample chain of custody records
  • Maintain up-to-date cGMP training and knowledge of USP, Ph.Eur, ICH

Skills

cGMP experience
Stability sampling
LIMS
Documentation
Cross-functional support
MS Office
Communication
Problem solving

Education

B.S. in related field
M.S. in related field

Tools

LIMS
ELN
Stability chambers
MS Office

Job description

Parexel is seeking a Scientist 2 or 3 to support stability sample management for late-stage pharmaceutical development. The role is a full-time, on-site assignment at a client location in West Point, PA, with comprehensive benefits and PTO. The ideal candidate will support stability studies, sample handling, documentation, and regulatory compliance within a GMP environment.

The position requires B.S. with 1–2 years (Scientist 2) or B.S./M.S.

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