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 +31 2020 44502 .