What are the responsibilities and job description for the Quality Assurance Specialist position at Mix Talent?
Quality Assurance Specialist I – Biotech/Pharma (Batch Record Review)
Milford, MA
Mix Talent has partnered with a growing biotech organization to hire a Quality Assurance Specialist I. This role offers a contract-to-hire pathway with conversion at 6 months, including benefits.
Pay Rate: $24–$28/hour (must be comfortable within this range)
Schedule: Full-time, 1st shift, onsite in Milford, MA
Important: This is a quality assurance role in biotech/pharma (NOT IT/computer QA, NOT regulatory); batch record review experience is required.
About The Role
The QA Specialist I will be responsible for raw material documentation, batch record review, and product release activities to ensure compliance with GMP, ISO, and customer requirements. This role is ideal for someone with 1–3 years of QA experience in biotech or life sciences who is eager to grow within a collaborative quality team.
Key Responsibilities
Job Identifier: #8133
Milford, MA
Mix Talent has partnered with a growing biotech organization to hire a Quality Assurance Specialist I. This role offers a contract-to-hire pathway with conversion at 6 months, including benefits.
Pay Rate: $24–$28/hour (must be comfortable within this range)
Schedule: Full-time, 1st shift, onsite in Milford, MA
Important: This is a quality assurance role in biotech/pharma (NOT IT/computer QA, NOT regulatory); batch record review experience is required.
About The Role
The QA Specialist I will be responsible for raw material documentation, batch record review, and product release activities to ensure compliance with GMP, ISO, and customer requirements. This role is ideal for someone with 1–3 years of QA experience in biotech or life sciences who is eager to grow within a collaborative quality team.
Key Responsibilities
- Review batch records and related documentation for accuracy and compliance with GDP.
- Release or reject raw materials, intermediates, packaging, and labeling materials.
- Maintain vendor files and collect CoAs/SDS from suppliers.
- Communicate with vendors to obtain required documentation.
- Generate CoAs, BSE/TSE statements, and other customer-requested quality documents.
- Assist in maintaining eQMS, QMS records, and controlled documents.
- Support vendor qualification and quality system updates as needed.
- Partner with cross-functional teams to ensure products meet quality standards.
- Associate’s or Bachelor’s degree in a scientific discipline.
- 1–3 years of QA experience within life sciences or biotech.
- Direct batch record review experience required.
- Familiarity with GMP and ISO 13485.
- Strong written/verbal communication and attention to detail.
- Proficiency in Microsoft Office; prior experience with eQMS or similar systems is a plus.
- Ability to work independently and collaboratively in a fast-paced environment.
Job Identifier: #8133
Salary : $24 - $28