QC Analytical Chemist III (HPLC / GC)

job summary:
Advance your pharmaceutical career with a Top-Tier Global Biopharma Leader in Pearl River, NY. This on-site, 6-month contract role (Monday–Friday day shift) offers high-impact analytical work in a paperless, state-of-the-art QC laboratory supporting life-saving oncology drug substances and commercial products.

location: Pearl River, NY
job type: 6 month contract
pay: $43.26 per hour
work hours: Monday through Friday, 9:00AM - 5:00PM (flexibility in the scheduling for 8a-4p)  
education: Bachelor's or Master's degree

 

responsibilities:

• Perform routine and complex analytical release and stability testing on raw materials, in-process samples, drug substances, and finished oncology products.

• Operate, maintain, and troubleshoot key analytical instrumentation, including HPLC, GC, UV-Vis, CGE, and TOC analyzers.

• Accurately document analytical results, perform peer data review, and manage workflows within a paperless LIMS environment.

• Maintain strict adherence to cGMP regulations, site SOPs, OSHA requirements, and chemical hygiene standards for high-potency compounds.

• Support audit readiness and participate in internal/external regulatory inspections through compliant laboratory documentation.

qualifications:

required:

• Bachelor’s or Master’s degree in Chemistry, Biochemistry, Pharmaceutical Sciences, or related scientific discipline.

• Minimum 5 years of QC laboratory experience within a GMP-regulated pharmaceutical or biopharmaceutical environment.

• Proven hands-on proficiency with analytical techniques, specifically HPLC, GC, and wet chemistry.

• Strong knowledge of cGMP documentation standards, regulatory guidelines, and electronic laboratory data systems (LIMS).

• Ability to work comfortably in a controlled laboratory requiring personal protective equipment (PPE) and respiratory protection.

preferred:

• 5–7 years of pharmaceutical QC experience using Empower chromatography data software.

• Prior experience conducting peer reviews of laboratory documentation and SOPs in an audit-ready setting.

skills:  HPLC, GC, UV-Vis Spectroscopy, CGE, LIMS, Empower, cGMP, Stability Testing, Release Testing, Wet Chemistry, Peer Review, Data Integrity, Oncology Testing, TOC Analyzer

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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 View email address on 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: medical, prescription, dental, vision, AD&D, and life insurance offerings, short-term disability, and a 401K plan (all benefits are based on eligibility).


This posting is open for thirty (30) days.