QA Shop Floor Specialist (Pirbright, United Kingdom, Surrey)
About this opportunity
THE POSITION
The QA Shop Floor Specialist plays a pivotal role in providing real-time Quality Assurance support within operational manufacturing environments. This position ensures compliance with EU GMP, biosafety, HSE requirements, and internal Boehringer Ingelheim standards. The role requires strong independent judgment, the ability to manage multiple priorities, and a proactive approach to identifying, assessing, and resolving quality events that may impact products and processes. Through coaching and collaboration, this role also drives continuous improvement and promotes a strong and sustainable quality culture across the site.
This is a fully site-based position in Pirbright, offered on a fixed-term contract until 31 December 2027.
TASKS & RESPONSIBILITIES
• Provide real-time QA support on the shop floor, ensuring compliance with GMP, data integrity, and internal standards
• Review and approve batch records and manufacturing documentation in line with right-first-time principles
• Support and lead investigations (deviations, discrepancies, OOX, complaints), including QA assessment and final approval
• Perform risk-based evaluations and ensure compliant handling of materials (e.g. quarantine, disposition)
• Review and approve CAPAs and change controls, ensuring quality, compliance, and effectiveness
• Support validation, qualification, and maintenance activities across manufacturing systems and processes
• Monitor QMS activities (deviations, CAPAs, change controls), ensuring timely closure and KPI adherence
• Identify trends and drive continuous improvement initiatives in collaboration with operational teams
• Ensure audit and inspection readiness, and actively participate in internal audits and regulatory inspections
• Support quality risk management activities and promote a strong quality culture across the site
REQUIREMENTS
Education
• Bachelor’s degree in a scientific or technical discipline
• Relevant Quality experience within a life sciences or related regulated industry
Skills & Experience
• Strong knowledge of EU GMP, Quality Assurance, and Quality Systems
• Experience in batch record review and documentation approval
• Hands-on experience with deviations, investigations, CAPA, and change control processes
• Understanding of validation, qualification, and regulated manufacturing processes (e.g. aseptic processing, QC testing, sterilisation)
• Experience with electronic quality systems (e.g. TrackWise, e-DMS or similar)
• Ability to apply regulatory and compliance requirements to complex situations
• Strong root cause analysis, risk assessment, and problem-solving skills
• Ability to make independent, sound decisions in a fast-paced environment
• Excellent organizational and prioritisation skills
• Strong communication skills (written and verbal) and ability to engage stakeholders at all levels
• Ability to coach and train operational teams
• High attention to detail and customer-focused mindset
WHY THIS IS A GREAT PLACE TO WORK
Boehringer Ingelheim is recognised as a Top Employer in the UK, reflecting our commitment to exceptional workplace standards, career development and a purpose-driven culture. Our employees contribute to meaningful work, creating long-term value for people, animals and the environment.
Learn more about why BI is a great place to work:
https://www.boehringer-ingelheim.co.uk/careers/uk-careers/why-great-place-work
Candidates may be asked to undergo a Basic Disclosure and Barring Service (DBS) Security check. Any offer of employment will be subject to satisfactory DBS certificate.
]]>
Job details
How this role compares
Computed from every other active Quality role in our database, not just this employer's listings.
We currently track 644 comparable Quality roles across 85 biopharma companies.
Salary context
110 of 644 peers report a salary range (USD, annualized)
Peers share this role's job function. This posting doesn't list a seniority level, so peers aren't narrowed by seniority either -- the range below may span more levels than usual.
Where these roles are based
Top locations among the 644 comparable roles
+ 39 more countries
Seniority mix
309 of 644 peers have a known seniority level
Therapeutic area mix
0 of 644 peers have a known therapeutic area; the rest are genuinely unlabeled, not hidden
No peers with a known therapeutic area yet.
Similar opportunities
The closest matches from our peer group, ranked by how similar they are, not how well you'd qualify for them -- treat this as market context, not a guaranteed shortlist; a weak match is labeled as one below.
How we calculate "similar"
No black box, no LLM guesswork: a deterministic score built from four normalized attributes. Here's this role's own peer group at different match levels, so you can see the mechanism, not just the result.
Every comparison starts from the same 100-point budget: 25 for working in the same function, 40 for the same therapeutic area, 20 for the same or adjacent seniority, 15 for the same country. A dimension we can't confirm on both sides contributes nothing, never a guess, never a free pass.
0 points, never a partial guess. A role we know almost nothing about beyond its function bottoms out at 25%; it never inflates to 100% just because there's little to compare against. Seniority uses a defined ladder (Associate → Manager → Associate Director → Senior → Principal → Director → Senior Director → Executive/VP) so "Director" and "Senior Director" count as adjacent, but "Director" and "Executive/VP" do not.