Hays is a global leader in professional recruitment, connecting top talent with leading companies across Europe and worldwide. We specialize in placing professionals in both permanent and contract roles across diverse industries.
Role-Batch Record Reviewer – Pharmaceutical Location:
On‑Site in Latina(ITALY) Employment Type:
Freelancing ️
Language:
Italian & English
⚠️
Note: Candidate must be based in Italy – No sponsorship available
About the Opportunity A leading pharmaceutical organization is seeking a
Batch Record Reviewer
to support its dynamic and highly outsourced
sterile manufacturing
environment. This role suits professionals who enjoy close collaboration with production teams and are committed to
GMP compliance, accuracy, and operational excellence. Your work will directly contribute to
product quality and patient safety, making this a high‑impact position.
Key Responsibilities Review
Batch Records
for accuracy, completeness, and
GMP compliance. Collaborate daily with
Production,
Quality Assurance, and cross‑functional teams. Support
internal and external audits
with required documentation. Identify, report, and help manage
deviations and non‑conformities. Contribute to
process improvements
and documentation optimization.
Requirements E xperience in BRR, QA, or similar roles in
sterile/aseptic manufacturing. Strong knowledge of
GMP regulations
and pharma production processes. Understanding of
sterile/aseptic operations
(preferred). Excellent teamwork and communication skills. 100% on‑site availability in Latina
(local profiles preferred). Freelancers/consultants welcome.
Why This Role Stands Out High‑impact role within a major pharmaceutical environment. Close collaboration with production teams for hands‑on involvement. Freelance‑friendly, offering flexibility with full‑time on‑site engagement.
Ready to take your Pharmaceutical career to the next level? Apply now or tag someone who fits this role!