QC Chemistry Supervisor

By | October 18, 2025

QC Chemistry Supervisor

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Job ID: 9852669

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Skillam, NJ, US

Scientific

Bachelors Degree

Full Time, Temporary

$40.00-$55.00/hour

Experienced (Non-Manager)

On-site

Biotechnology/Pharmaceuticals

First Shift (Day)

Skillam, NJ, US

$40.00-$55.00/hour

Experienced (Non-Manager)

Full Time, Temporary

Biotechnology/Pharmaceuticals

On-site

Scientific

Bachelors Degree

First Shift (Day)

Apply Now Applied

Job details

Job Title: QC Chemistry Supervisor- Contract to Hire- Princeton NJ
The QC Chemistry Supervisor will lead all Quality Control Chemistry laboratory operations to support GMP manufacturing, testing, and release of raw materials, intermediates, and finished products in compliance with FDA, EU, and international regulatory standards.
Key Responsibilities:

  • Lead and manage the setup and operationalization of a new QC Chemistry laboratory. Conduct or supervise bench-level testing as needed.

  • Oversee daily QC Chemistry lab operations, ensuring timely and accurate testing for in-process materials, drug substance (DS), drug product (DP), and stability samples. Maintain compliance with FDA, EU and cGMP requirements.

  • Oversee the development and implementation of SOPs, test methods, specifications, and related documentation.

  • Lead and manage investigations related to OOS results, deviations, laboratory errors, and instrument malfunctions; implement effective CAPAs.

  • Manage and coordinate method transfers and method validation/verification activities, including strategy development and protocol/report approvals.

Required Qualifications:

  • Bachelor’s or advanced degree in Chemistry, Biochemistry, Pharmaceutical

  • Minimum 5–7 years of relevant industry experience in a cGMP-regulated pharmaceutical or biotechnology environment.

  • At least 2 years of leadership or supervisory experience in a QC laboratory setting.

  • Strong working knowledge of analytical techniques including HPLC, UHPLC, size exclusion chromatography, capillary electrophoresis, cIEF, peptide and oligo mapping, etc. Familiarity with USP, EP, and ICH guidelines.

  • Experience with analytical method validation, method transfers, and instrument qualification (IQ/OQ/PQ). Proficiency with laboratory documentation systems and software (e.g., LIMS, Empower, chromatography data systems).

  • In-depth understanding of cGMP/GLP principles and regulatory expectations

  • High attention to detail with a commitment to data integrity and quality.

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