Quality Control Chemist

Kelly Science, Engineering, Technology & Telecom; Raritan (NJ); On-site; USD 80,000 - 180,000; Full time

Job summary

A leading company in the pharmaceutical sector is seeking a QC Scientist in Raritan, NJ. The successful candidate will handle routine testing of finished products and raw materials, emphasizing solid dosage forms. This full-time position requires a strong background in pharmaceutical testing and proficiency with various lab instruments. Competitive salary and benefits, including medical, vision, and a 401(k) plan, are offered.

Benefits

Medical insurance

Vision insurance

401(k)

Pension plan

Disability insurance

Qualifications

• Hands-on experience in QC analysis of pharmaceuticals.
• Experience with chromatography software preferred.
• Strong understanding of testing methods and adherence to regulations.

Responsibilities

• Conduct routine analysis of finished products and raw materials.
• Utilize laboratory instruments for testing and compliance.
• Document results and adhere to standard operating procedures.

Skills

Pharmaceutical testing methods

Chromatography experience

Data review processes

Adhering to SOPs

Education

4-8 years of laboratory experience

Degree in relevant field (not explicitly mentioned)

Tools

HPLC

UPLC

GC

Karl Fischer

FTIR

pH meters

Empower 3 software

Job description

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Direct message the job poster from Kelly Science, Engineering, Technology & Telecom

Scientific Recruiter @ Kelly Science | Staffing, Biotech, Pharma, Clinical

The QC Scientist will be responsible for routine testing and analysis of finished products (tablets, capsules, sub-gels) and raw materials, utilizing a variety of laboratory instruments and techniques. The ideal candidate will have a strong background in pharmaceutical testing and a proven track record working with oral solid dosage forms.

Key Responsibilities:

• Routine Testing and Analysis: Conduct routine analysis of finished products and raw materials, including weight, chemistry tests for raw materials, and stability sample testing
• Instrument Proficiency: HPLC, UPLC, GC, Karl Fischer, FTIR, visualization testers, and pH meters. Experience with chromatography software (e.g., Empower 3) is highly preferred.

Education and Experience:

• 4-8 years of hands-on experience in a laboratory setting, with a focus on oral solid dosage forms (tablets, capsules, sub-gels) and raw materials.
• Experience with laboratory instrumentation such as HPLC, UPLC, GC, Karl Fischer, FTIR, and pH meters. Prior experience with Empower 3 software or similar chromatography software is a significant advantage.

Skills and Knowledge:

• Strong understanding of pharmaceutical testing methods, including assay, identity testing, content uniformity, and impurity analysis.
• Knowledge of data review processes, trending, and documentation of test results.
• Ability to adhere to SOPs, USP monographs, and GMP regulations.

Seniority level

• Seniority level

  Mid-Senior level

Employment type

• Employment type

  Full-time

Job function

• Job function

  Science and Research

• Industries

  Pharmaceutical Manufacturing, Biotechnology Research, and Chemical Manufacturing

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Inferred from the description for this job

Medical insurance

Vision insurance

401(k)

Pension plan

Disability insurance

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