FDF (Finished Dosage Forms) Manager

FDF Manager

For my client - a leading pharmaceutical company in Barcelona, Spain, 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, you wioll 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 or contact her at .