Quality Control Analyst

Avecia Pharma; Milford, Northern (MA, KY); On-site; USD 62,000 - 76,000; Full time

Job summary

Avecia Pharma in Milford, MA seeks a QC Analyst I to perform routine testing and analysis of raw materials, in‑process samples, and finished products in a GMP setting.

The role involves laboratory and manufacturing space work following procedures and instructions.

Qualifications

• BS in chemistry, biology or related discipline or equivalent combination of education and experience.
• 0-2 years of experience in a laboratory environment.
• Familiarity with analytical testing equipment and methodology.

Responsibilities

• Test and analyze samples
• Conduct environmental monitoring in the clean space
• Review data for compliance with specifications and GMP regulations
• Plan and schedule work assigned to them
• Writes/revises QC documents within their scope of expertise
• Performs experiments with guidance

Skills

Laboratory experience

GMP understanding

Education

BS in chemistry or biology or related discipline

Tools

Analytical testing equipment

Job description

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The QC Analyst I is responsible for conducting routing analysis of raw materials, in-process samples, and finished products in a strict GMP setting. The position involves working in the QC laboratory and in the manufacturing space on assigned tasks following written procedures and verbal instructions.

Key Responsibilities:

• Test and analyze samples
• Conduct environmental monitoring in the clean space
• Review data for compliance with specifications and GMP regulations
• Plan and schedule work assigned to them
• Writes/revises QC documents within their scope of expertise
• Performs experiments with guidance

Required Skills/Abilities:

• BS in chemistry, biology or related discipline or equivalent combination of education and experience
• 0-2 years of experience in a laboratory environment
• Familiarity with analytical testing equipment and methodology

The annualized salary for this role is $62,300 - $76,300.