QA Officer

Consult; Buxton; On-site; GBP 30,000 - 50,000; Full time

Job summary

An established industry player is seeking a dedicated QA Officer to join a dynamic team in a contract testing laboratory. This role offers an exciting opportunity to ensure quality and compliance in a fast-paced environment, adhering to ISO 17025 and GMP standards. The successful candidate will be responsible for managing documentation, conducting audits, and liaising with regulatory bodies. If you're detail-oriented and passionate about quality assurance, this position is perfect for you. Join a supportive team where your contributions will make a real impact in the healthcare and related industries.

Benefits

Statutory Sick Pay

Pension Scheme with Employer Contribution

Qualifications

• Experience in a QA role within a laboratory or regulated environment.
• Knowledge of ISO 17025 or GMP standards.

Responsibilities

• Ensure compliance with ISO 17025 and GMP standards.
• Review and amend documentation such as SOPs.
• Conduct internal audits and manage external audits.

Skills

Attention to Detail

Quality Assurance

ISO 17025 Knowledge

GMP Compliance

Communication Skills

Education

Degree in Science or Related Field

Job description

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Business Manager - Scientific at Consult.Expert Scientific Recruiter, People Manager, Masters Graduate in Drug Chemistry and former Analytical…

QA Officer

Near Buxton (Fully Onsite)

My client is a contract testing laboratory supporting the healthcare and related industries. We are looking for a highly motivated and detail-oriented QA Officer to join a small and friendly team based in Tideswell, UK. This is an exciting opportunity to work in a fast-paced environment, ensuring the quality and compliance of laboratory work in line with ISO 17025 and GMP standards.

Key Responsibilities:

• Ensure compliance with company policies and procedures, including Health and Safety, ISO 17025, and GMP.
• Review, write, and amend documentation such as SOPs.
• Manage controlled documentation and maintain its circulation and availability.
• Audit GMP data, including reviewing raw data prior to releasing GMP CoA or CoP.
• Coordinate quality issues, investigations, and CAPA.
• Assist with OOS, NC, NTF, CMP, RA, and CAPA investigations.
• Participate in the change control process to ensure changes maintain GMP compliance.
• Track, trend, and gather data for meetings as per procedures.
• Conduct staff training on quality matters when required.
• Liaise with customers or regulatory representatives.
• Host and manage external audits by customers or regulatory bodies.
• Respond to external audit report findings and plan corrective actions.
• Release and obtain necessary documentation in a controlled manner.
• Plan and conduct internal audits.
• Maintain the archives.

The Ideal Candidate:

• Strong attention to detail and commitment to compliance with industry standards.
• Experience in a QA role within a laboratory or regulated environment.
• Knowledge of ISO 17025 or GMP, and controlled documentation.
• Strong communication skills and the ability to liaise with internal and external stakeholders.
• Ability to work independently and manage multiple priorities.

Other Information:

• Please note - private transport is essential to access the site unless you live in the immediate area
• Full-time role, 37.5 hours per week (some overtime may be required).
• Statutory Sick Pay.
• Auto-enrolment into a pension scheme with a 6% employer contribution after probation.

If you're interested in the above role then please click apply or get in touch to discuss further.

Consult will endeavour to contact candidates within 14 days of application. However, if you do not hear back after 2 weeks then please assume on this occasion, unfortunately, you have not been successful.

Seniority level

• Seniority level

  Associate

Employment type

• Employment type

  Full-time

Job function

• Job function

  Science and Quality Assurance

• Industries

  Pharmaceutical Manufacturing and Chemical Manufacturing

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