For my client – a leading pharmaceutical company with a strong commitment to innovation and sustainable medicine manufacturing – I am looking for an FDF Manager to play a key role in developing new processes for Finished Dosage Forms (FDF).
Job Description Reporting to the Laboratory Head, the FDF Manager will:
Lead new product formulation and process development in collaboration with CDMOs by setting the strategic direction across all project phases.
Be accountable for delivering against the business case mandate across the entire project scope.
Coordinate cross-functional teams, manage deliverables, and report status through governance structures.
Evaluate process quality and safety to ensure readiness for scale-up.
Oversee technology transfer to manufacturing sites, collaborating with Tech Ops to ensure successful implementation.
Lead collaborations with partners and CROs, bringing deep expertise in applied technologies.
Ensure compliance with GMP and Safety regulations across all activities.
Stay updated on internal and external industry developments, benchmarking technologies against competitors through literature and IP searches.
Key Responsibilities
Achieve project milestones in line with project plans.
Monitor and integrate data science methodologies to enhance process development.
Foster a strong SHE (Safety, Health, and Environment) culture.
Develop and optimize processes for Finished Dosage Forms (FDF).
Demonstrate leadership in managing teams and cross-functional collaborations.
Apply strong project management skills to ensure project success.
Key Requirements
At least 10 years of experience in Pharmaceutical Technology, preferably in generics.
Master’s degree (MSc) in Technology, Pharmacy, Biochemistry, or a related field. An advanced degree is preferred.
Extensive experience in pharmaceutical development from test to pilot or full-scale production.
Strong knowledge of Quality and SHE (Safety, Health, and Environment) policies.
Proven leadership and project management skills.
Experience collaborating with international third parties (CDMOs, CROs, and partners).
Successful track record in bringing generics to market.
Practicalities
Location: Barcelona, Spain
Duration: Permanent Position
Start Date: ASAP
Sound interesting? Send your CV to Khanyi Mabena at k.mabena@panda-int.com or contact her at +31 2020 44502.