QA Officer

QA Officer

Posted Today by TieTalent

Negotiable
Undetermined
Undetermined
Derby, England, United Kingdom

Summary: The role of Temporary QA Officer involves supporting the management of Quality Management System (QMS) activities for a duration of 3-6 months. The position requires experienced QA professionals to execute routine tasks, maintain quality records, and ensure compliance with GMP and regulatory standards. Candidates should possess a strong background in QA within the pharmaceutical or biotech industries. This is a temporary opportunity aimed at making a significant impact in quality assurance.

Key Responsibilities:

  • Support and execute routine QMS tasks and compliance actions
  • Assist in maintaining quality records and documentation
  • Participate in audits and CAPA processes
  • Collaborate with cross-functional teams to ensure GMP and regulatory compliance

Key Skills:

  • Previous experience in a QA role within the pharmaceutical, biotech, or related industry
  • Strong understanding of QMS processes and documentation
  • Detail-oriented with good communication and organisational skills
  • Able to work independently and as part of a team

Salary (Rate): undetermined

City: Derby

Country: United Kingdom

Working Arrangements: undetermined

IR35 Status: undetermined

Seniority Level: undetermined

Industry: Other

Detailed Description From Employer:

Job Opportunity: Temporary QA Officers (3-6 Months)

Location: Derby

Job Type: Temporary (3-6 Months)

Salary: Competitive - To Be Confirmed

Are you an experienced Quality Assurance Officer, Senior QA Officer, or QA Specialist looking for a short-term opportunity to make an impact? We are currently seeking motivated QA professionals to join our team on a temporary 3-6 month contract, supporting the day-to-day management of Quality Management System (QMS) activities.

Key Responsibilities

  • Support and execute routine QMS tasks and compliance actions
  • Assist in maintaining quality records and documentation
  • Participate in audits and CAPA processes
  • Collaborate with cross-functional teams to ensure GMP and regulatory compliance

Ideal Candidate

  • Previous experience in a QA role within the pharmaceutical, biotech, or related industry
  • Strong understanding of QMS processes and documentation
  • Detail-oriented with good communication and organisational skills
  • Able to work independently and as part of a team

Interested? Apply now or send your CV and availability to: Simon Fowler at NGAGE Smart4Sciences on (phone number removed) or Join us in ensuring quality and compliance at the highest standards