Quality Control Analyst II (2nd Shift)

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

Job summary

A leading pharmaceutical manufacturing company is seeking a Quality Control Analyst II for their second shift. This role involves conducting routine analyses of raw materials and finished products, ensuring compliance with cGMP guidelines, and providing training to other analysts. Candidates should have a BS in chemistry or biology and 2-5 years of 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 a wide variety of routine testing.
• Review data for compliance against specifications and GMP regulations.
• Generate stability reports and assist in developing experimental procedures.

Skills

Analytical testing

HPLC

Karl Fischer

Spectrophotometry (UV/VIS)

LCMS

Education

BS in chemistry

BS in biology

Related discipline

Job description

Join to apply for the Quality Control Analyst II (2nd Shift) role at Nitto Avecia.

About This Opportunity
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.

• 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 SOPs, testing procedures, and material specifications.
• Provide training and guidance to other analysts.

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 SOPs, 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.

Seniority level

• Mid-Senior level

Employment type

• Full-time

Job function

• Quality Assurance

Industries

• Pharmaceutical Manufacturing