Industrial Pharmacist - Good Manufacturing Practices
Role Overview
Full-time, on-site Technical Manager / Industrial Pharmacist role in Dubai Healthcare City, UAE.
Oversee GMP-compliant manufacturing and cleanroom operations for breast milk preservation and powder production.
Serve as a technical liaison with the Emirates Drug Establishment (EDE).
Key Skills for This Role
Full Job Posting
Role overview
Full-time, on-site Technical Manager / Industrial Pharmacist role in Dubai Healthcare City, UAE.
Oversee GMP-compliant manufacturing and cleanroom operations for breast milk preservation and powder production.
Serve as a technical liaison with the Emirates Drug Establishment (EDE).
About the facility
Mom’s Pure Milk R&D FZ LLC is a breast milk preservation and freeze-drying research facility.
Each customer’s milk is processed individually and returned only to that customer; batches are never mixed.
Orders follow handling, packaging, quality assurance, and optional nutritional testing protocols.
Responsibilities
- Supervise and document production according to approved SOPs and GMP.
- Maintain strict segregation and end-to-end traceability of every customer batch.
- Review batch records, deviations, and technical documentation; support CAPA and change control.
- Oversee environmental monitoring, hygiene, cleaning, and sanitation controls.
- Participate in batch review and release under the approved Quality Management System.
- Support audits, regulatory inspections, and process validation.
- Train and assess production staff on GMP requirements.
- Review and improve SOPs and support R&D projects.
Required qualifications
- Bachelor’s degree in Pharmacy.
- UAE pharmacist license, or eligibility to obtain it before regulatory appointment.
- At least 3 years of experience in pharmaceutical manufacturing, GMP production, QA/QC, or cleanroom operations.
- Practical GMP knowledge of batch documentation, deviation investigation, CAPA, change control, and batch release.
- Ability to supervise and train technical staff.
- Comfort participating in regulatory assessments, inspections, and technical interviews.
- Strong written and spoken English.
- Appointment as Technical Manager depends on applicable licensing and qualification requirements and acceptance by relevant UAE regulatory authorities, including EDE where applicable.
Preferred experience
- Experience with EDE/MOHAP or GMP inspections is preferred.
- Experience in non-sterile pharmaceutical manufacturing, ISO-classified cleanrooms, biological products, environmental monitoring, or equipment qualification is preferred.
Application notes
- Applications should include a CV listing GMP/manufacturing employers, roles, and dates, plus a short cover letter stating UAE licensing status and GMP experience.
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