Senior Quality Assurance Specialist

Job Title:QA Specialist – GMP

Location:Hybrid in Slough

Industry:Pharmaceuticals / Biotech / Life Sciences

About the Role:

We are seeking a detail-oriented and proactiveQA Specialistwith a strong foundation inGood Manufacturing Practice (GMP)to join our Quality Assurance team. In this pivotal role, you will support the ongoing development and maintenance of robust quality systems, ensuring compliance with internal procedures and regulatory requirements.

Key Responsibilities:

• Manage and maintain GMP documentation systems, ensuring timely and accurate record keeping.
• Support the implementation and continuous improvement of global quality systems and processes.
• Participate in validation and qualification activities for systems and equipment as needed.
• Coordinate enrolment and monitoring of GMP-related training programs across relevant departments.
• Act as a primary point of contact for day-to-day quality system queries, offering guidance and resolution.
• Monitor the timely closure of internal quality records (e.g., deviations, CAPAs, change controls).
• Collaborate closely with global QA teams and stakeholders to ensure aligned execution of quality initiatives.
• Assist in preparation for internal and external audits and inspections.
• Foster and promote a strong quality culture across the organization.
• Carry out additional quality-related tasks and projects as assigned by management.

Requirements:

• Bachelor’s degree in Life Sciences, Pharmacy, or related field.
• 2+ years’ experience in a GMP-regulated environment, ideally in Quality Assurance.
• Solid understanding of GMP principles and relevant regulatory expectations.
• Strong organizational and communication skills.
• Ability to work both independently and collaboratively in a fast-paced environment.
• Experience with quality systems and documentation platforms is a plus.