Quality Control Analyst II (2nd Shift)

Avecia Pharma; Milford (MA); On-site; USD 60,000 - 80,000; Full time

Job summary

A leading company in the pharmaceutical industry is seeking a QC Analyst II for their second shift. This role involves conducting a variety of analyses in compliance with cGMP guidelines, training other analysts, and contributing to the development of experimental procedures. Candidates should have a BS degree and relevant experience in a GMP environment.

Qualifications

• 2-5 years’ experience as a QC analyst/chemist in a GMP environment.
• Experience with analytical testing equipment and methodology.

Responsibilities

• Conduct routine and non-routine analyses of materials.
• Generate stability reports and assist in developing procedures.
• Provide training and guidance to other analysts.

Skills

Analytical testing

Problem-solving

Attention to detail

Education

BS in chemistry, biology, or related discipline

Tools

HPLC

Karl Fischer

Spectrophotometry (UV/VIS)

LCMS

Job description

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The QC Analyst II is responsible for conducting routine and non-routine analyses of raw materials, in-process materials and finished products in accordance with cGMP guidelines. The appropriately trained individual may provide training and guidance to other QC Analysts. The individual troubleshoots problems associated with methods and instruments resolving them where possible or seeking guidance/authorization where required. This is a second shift role.

Key Responsibilities:

• Conduct a wide variety of routine testing.
• Test and analyze samples in a timely manner in support of project plans in accordance with cGMP guidelines.
• Review data for compliance against specifications and GMP regulations.
• Generate stability reports, and assist in the development of experimental procedures and protocols
• Assist with developing/revising documentation such as SOP, testing procedures and material specifications.
• Provide training and guidance to other analysts.

Required Skills/Abilities:

• BS in chemistry, biology, or related discipline
• 2-5 years’ experience as a QC analyst/chemist in a GMP environment
• Experience and familiarity with analytical testing equipment and methodology including HPLC, Karl Fischer, Spectrophotometry (UV/VIS), and LCMS