Quality Specialist

Planet Pharma; Slough; Hybrid; GBP 32,000 - 42,000; Full time

Benefits offered by this job

Hybrid work (3 days onsite)

Job summary

Planet Pharma is seeking a Quality Specialist to join a leading global life sciences organisation in Berkshire on a 12-month contract. The role focuses on GMP/GDP quality activities, deviations, CAPAs and change controls within a highly regulated environment.

The candidate will review quality documentation, assist with investigations, and support audits and regulatory inspections. Strong communication and proactive quality mindset are essential.

Qualifications

• Experience in a pharmaceutical, biotech or life sciences quality environment.
• Strong understanding of GMP and GDP requirements.
• Experience with CAPAs, deviations, investigations and quality systems.
• Excellent communication and stakeholder management skills.
• Proactive and hands-on approach to quality compliance.

Responsibilities

• Support GMP and GDP quality activities.
• Manage deviations, CAPAs and change controls.
• Assist with product complaint investigations.
• Review and maintain quality documentation and SOPs.
• Support audits and regulatory inspections.
• Collaborate with internal stakeholders to maintain compliance standards.

Skills

GMP/GDP knowledge

CAPAs

Deviations

Investigations

Quality systems

SOPs

Communication

Stakeholder management

Job description

Quality Specialist | GMP & GDP | 12-Month Contract | Berkshire Area

We're supporting a leading global life sciences organisation in the search for a Quality Specialist to join their Quality team on a 12-month contract.

This is an excellent opportunity for an early-career to mid-level Quality professional looking to develop their experience within a highly regulated pharmaceutical environment.

Key Responsibilities:

• Support GMP and GDP quality activities
• Manage deviations, CAPAs and change controls
• Assist with product complaint investigations
• Review and maintain quality documentation and SOPs
• Support audits and regulatory inspections
• Partner with internal stakeholders to maintain compliance standards

What We're Looking For:

• Experience within a pharmaceutical, biotech or life sciences quality environment
• Strong understanding of GMP and GDP requirements
• Experience with CAPAs, deviations, investigations and quality systems
• Excellent communication and stakeholder management skills
• A proactive and hands-on approach to quality compliance

Additional Information:

• 12-month contract
• Hybrid working (3 days onsite)
• Collaborative, research-focused environment
• Fast interview process with immediate consideration available