Senior Technical Transfer Manager
Neuraxpharm, Spain
Job Description
Neuraxpharm is a leading European specialty pharmaceutical company focused on the treatment of central nervous system disorders (CNS). We have a direct presence in 19 countries and plan further geographic expansion as part of our strategy to strengthen our position as a European leader in CNS treatments.
With its focus on CNS, Neuraxpharm develops and commercializes established brands, value added medicines, generics, Consumer Healthcare products, medical cannabis and beyond-the-pill-solutions and is continuously striving to offer a wide range of effective, high quality and affordable CNS treatment options in Europe.
Present with our products in more than 50 countries, Neuraxpharm also manufactures pharmaceutical forms and active pharmaceutical ingredients in our own manufacturing sites in Spain. With more than 900 professionals, Neuraxpharm has a unique understanding of the CNS market built over 35 years.
Neuraxpharm is searching for a vacancy: Senior Technical Transfer Manager
Job Purpose
Team leader of transfer team and project management of finish product production transfer to new contract manufacturers and product optimization for supply chain and cost improvement.
Major Accountabilities:
- Responsibility for project management of transfer projects with corporate or external contract manufacturers
- Strong communication with contract manufacturers and internal interdisciplinary team of all departments, especially quality assurance, quality control, marketing, regulatory affairs, and supply chain
- Time and cost planing and control. Incl. negotiation of offer and contracts.
- Evaluation and risk estimation of product optimizations (formulation and manufacturing process)
- Proof and approval of GMP-relevant documents
- Team leader incl. supervision and training of transfer team members
Requirements
- Experience in Pharmaceutical industry
- Understanding of GMP rules, Quality Assurance requirements, product formulation and manufacturing processes and regulatory affairs requirements
- Project management skills
- Bachelor’s degree in science, pharma, chemical engneering or education in technology at production site or similar background
- Fluent English and German would be a plus
Benefits
- Individual Professional development in a leading European pharmaceutical company with an ambitious international growth strategy.
- Economic conditions will be according to the experience and skills provided.
- A motivated and committed environment based on a diverse and inclusive culture.
- A specialized team focused on our core activity: Improving our patients’ lives.