Scientist III - Analytical Chemist (Cleaning Verification) - FSP
About The Position
Parexel is hiring a Scientist III - Analytical Chemist to work as a full-time Parexel FSP employee on a long-term assignment onsite at a client location in Rahway, New Jersey. The role supports cleaning verification, cleaning validation, and related analytical work for GMP manufacturing areas. It includes chromatographic analysis, data interpretation and reporting, preparation of GMP documentation, and adherence to safe laboratory practices and GMP requirements. Parexel FSP includes the CMC Operations group, which provides pharmaceutical and biopharmaceutical companies with technical professionals to support the development and delivery of new therapies. This position offers full benefits, sick time, a 401(k), paid holidays, and paid time off.
Requirements
- Bachelor's degree in chemistry or a closely related field and at least 3–5 years of hands-on research experience, or a master's degree in analytical chemistry or a closely related field and at least 1–2 years of hands-on research experience.
- Hands-on experience with chromatographic analysis using various LC techniques.
- General knowledge of separation science.
- Strong computer, scientific, and organizational skills.
- Excellent oral and written communication skills and attention to detail.
- Ability to organize, multitask, and manage multiple projects.
- Ability to work independently and as part of a team.
- Good understanding of GMP compliance requirements and ALCOA documentation principles.
Nice To Haves
- Hands-on experience with chromatographic analysis using GC.
- Experience with Empower chromatographic software and analysis of drug formulations.
- Hands-on experience with method development and validation.
- Experience with cleaning validation or verification.
- Skill in method and instrument troubleshooting, specifically for LC and GC methods and systems.
- Experience with KF moisture analysis.
Responsibilities
- Support cleaning verification and cleaning verification swab analysis for GMP manufacturing areas.
- Support cleaning validation and cleaning verification analysis for GMP manufacturing areas.
- Perform or support In-Process Control (IPC) testing / process control testing.
- Interpret and process data, and prepare reports.
- Prepare GMP documentation, including cleaning verification protocols and reports.
- Follow safe laboratory practices and maintain the work area in a clean, orderly, and safe manner.
- Apply a general understanding of analytical method development and method validation.
Benefits
- Full benefits
- Sick time
- 401(k)
- Paid holidays
- Paid time off
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What This Job Offers
Job Type
Full-time
Career Level
Mid Level
