Quality Coordinator
Thermo Fisher Scientific · Horsham, United Kingdom · Global
Quality Improvement
–
Not yet analysed
Demand60
Career growth55
Healthcare fit55
Remote potential20
5-year outlook
Quality/compliance roles in large pharma and lab services tend to offer stable, moderate progression from coordinator into specialist or QA management tracks. Exact pay depends heavily on location, business unit, and whether the role sits in manufacturing, lab services, or clinical research, so no figure should be assumed without the full posting.
Clinical license
Not required
Applicant reach
unclear
Seniority
entry
Employment type
–
Date found
2026-10-02
Intelligence details
Flexible work details
- Eligible countries
- United Kingdom
Eligibility, licensing, and location restrictions can change. Always confirm details on the source posting before applying.
Why this is worth applying to
Worth a look if you want a low-barrier entry point into pharma/lab quality and are comfortable with documentation-heavy, process-driven work. Because the description is missing, verify the business unit, shift pattern, onsite expectations, and whether any clinical research exposure exists before investing time.
Who should apply
Clinicians and healthcare graduates (nurses, pharmacists, allied health, IMGs) seeking a first non-clinical move into pharma or lab quality; detail-oriented clinicians with audit, documentation, or protocol-compliance exposure; anyone targeting Thermo Fisher/PPD as a long-term employer.
CV angle
Reframe real clinical experience as quality-system experience: chart audit and documentation accuracy, adherence to protocols and SOPs, incident/deviation reporting, infection-control or medication-safety compliance, and root-cause thinking from morbidity reviews. Emphasise regulatory-adjacent habits (GDP, data integrity, traceability) and any exposure to accreditation inspections (JCI, NABH, CQC, GMP-adjacent audits) without overstating scope.
Skills to highlight
- Documentation accuracy and record review
- SOP and protocol adherence
- Incident/deviation reporting and CAPA familiarity
- Audit and inspection preparation support
- Root cause analysis and corrective action follow-through
- Data integrity and confidentiality (GDP/GCP awareness)
- Cross-functional coordination with labs, pharmacy, or clinical teams
- Attention to detail under high-volume deadlines
Role summary
A Quality Coordinator at Thermo Fisher Scientific typically supports quality systems in a pharma, laboratory, or clinical research environment — maintaining documentation, tracking deviations and CAPAs, supporting audits and inspections, and helping ensure processes meet internal and regulatory standards. The posting text was empty, so the exact business unit and duties are unconfirmed.
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