QA Officer - Biotechnology

Russell Taylor Group; Alderley Edge; On-site; GBP 28,000 - 33,000; Full time

Job summary

A biotechnology company based in Alderley Edge is looking for a QA Officer to oversee various quality assurance responsibilities. The role requires a degree in a relevant scientific discipline, good knowledge of GMP, and strong IT and interpersonal skills. The position offers a salary range of £28,000 to £33,000 per annum along with benefits including private medical, share options scheme, and a company pension.

Benefits

25 days holiday + Bank Holidays

Private medical

Share option scheme

Company pension

On site parking

Qualifications

• Experience in CAPA, Deviations, OOS, OOT, and internal auditing preferred.
• Customer complaints handling would be advantageous.

Responsibilities

• Generate or review SOPs and other documents.
• Provide support to customers and answer queries.
• Coordinate and resolve immediate customer complaints.

Skills

Good knowledge of GMP

Strong IT skills

Good interpersonal skills

Strong verbal/written report writing

Education

Degree in a relevant scientific discipline

Job description

Overview

Vacancy: QA Officer - Biotechnology
Location: Alderley Edge, Cheshire (onsite)
Type: Permanent
Salary: £28000 - £33000 per annum
Benefits: 25 days holiday + Bank Holidays, private medical, share option scheme, company pension, on site parking

Start Date: 2025-09-12

REF: J91985325
Contact: Tom Hammond
Email: [e-mail]

Responsibilities

• Generation or review of SOPs and other documents (where applicable)
• Provide support to customers, answer queries and assist with product investigations
• Coordinate and resolve immediate/urgent customer complaints, ensuring prompt responses and resolutions
• Participate in the internal audit programme to ensure GMP compliance of all site activities
• Utilise scientific resources to improve the quality of products and services
• Maintain personal training records in an auditable state
• Maintain the quality documentation system
• Participate in quality improvement initiatives
• Support in the process of maintaining and archiving documentation
• Support and execute external audits where applicable
• Support management when hosting regulatory audits
• Work on executing and maintaining the QMS, including but not limited to: Risk Assessments, Change Controls, CAPAs, Deviations, Complaints, Recalls, OOS/OOT

The Person / Qualifications

• Degree in a relevant scientific discipline
• Good knowledge of GMP
• Experience in CAPA, Deviations, OOS, OOT, internal auditing (preferred); customer complaints handling would be advantageous
• Strong IT skills (Microsoft applications)
• Good interpersonal skills and strong written/verbal report writing skills

Salary and Benefits

Salary: £25000-£32000 (dependant on experience) (note: this aligns with role details provided)

Benefits: 25 days holiday + bank holidays, private medical, share options scheme, company pension

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