Quality Assurance Supervisor

Barrington James; United States; Remote; USD 105,000 - 155,000; Full time

Job summary

A leading recruitment firm is seeking a QA Supervisor to develop and maintain quality management systems and ensure compliance in a collaborative biotech environment. The ideal candidate holds a Bachelor’s degree in a scientific field and has over 4 years of relevant experience. This full-time position offers remote work options, preferably within Central or Eastern Time Zones.

Qualifications

• 4+ years’ experience in pharmaceutical, CRO, or Biotech.
• Experience in sterile manufactured products is preferred.
• Interest in Regulatory Affairs is a plus.

Responsibilities

• Develop/improve, implement, and maintain the quality management system.
• Oversee evaluation and management of suppliers.
• Work with Clinical Operations on quality risk management strategies.
• Collaborate with other departments to ensure consistent quality.

Skills

Quality management system development

Supplier evaluation and management

Clinical quality risk management

Collaboration with cross-functional teams

Education

Bachelor’s degree in a scientific field

Job description

Base pay range

$105,000.00/yr - $155,000.00/yr

Direct message the job poster from Barrington James

Working at Barrington James as a Recruitment Consultant

QA Supervisor | Full Time | Remote (ideally Central or Eastern Time Zones)

Innovative company whose aim is to brighten the future for those fighting cancer

Agile, tenacious, collaborative biotechnology start-up with a relentless focus on advancing real- time cancer imaging.

Responsibilities

• Develop/improve, implement, and maintain the quality management system (QMS) to comply with FDA, and regulatory
• Oversee the evaluation and management of suppliers to ensure the quality of products or services provided by GxP suppliers.
• Work with Clinical Operations to develop and implement clinical quality risk management strategies ensuring compliance with Good Clinical Practices (GCP).
• Collaborate with other departments, such as CMC, Clinical, Research and Development, and Regulatory Affairs, to ensure consistent quality across all aspects of the product lifecycle.

Qualifications & Skills

• Bachelor’s degree in a scientific field (e.g. Biochemistry / Biology / Chemistry).
• 4+ years’ experience in pharmaceutical / CRO / Biotech
• Experience in sterile manufactured products preferred
• Exposure to Regulatory Affairs or an interest in learning the Regulatory Affairs role is a plus.

Seniority level

• Mid-Senior level

Employment type

• Full-time

Job function

• Science

Industries

• Research Services

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