Pharmacist (m/f/d) (Pharmazeut/in)

Welcome to Abbvie! As part of an international company with approx. 50,000 employees worldwide and around 3,000 employees in Germany, you have the opportunity to work closely with us to master the health challenges of tomorrow. Do you have a passion for improving healthcare across the globe? Do you want to use your expertise to improve the quality of life for patients? In a challenging work environment that offers you the opportunity to expand and develop your own skills? Then you've come to the right place!

Prove your know-how and become part of our team at the Ludwigshafen location as

Head of Manufacturing of Clinical Investigational Medicinal Products Parenterals (all genders) In this responsible leadership role, you will take on the deputy management of the manufacturing of clinical investigational medicinal products for parenteral administration. You will bear the operational responsibility for the GMP-compliant manufacturing and visual inspection of parenteral bulk goods (vials and syringes) for clinical trials. If you bring expertise in aseptic manufacturing, enjoy team leadership, and want to work in an international, scientifically oriented environment, we look forward to your application.

Specifically, this means:

• Exercising the function as deputy head of manufacturing in accordance with AMG, AMWHV, EU-GMP guidelines, as well as other relevant laws and regulations including AbbVie specifications
• Planning, implementation, monitoring, and evaluation of the manufacturing of clinical investigational medicinal products for parenteral administration
• Review and approval of manufacturing documents
• Review and approval of deviation reports, validation, and qualification documents
• Processing of deviations, root cause analysis, as well as determining corrective and/or preventive actions (CAPA)
• Responsible for pharmaceutical quality management within the area of responsibility
• Responsible for aseptic process simulations and contamination control
• Active participation in the preparation and execution of regulatory inspections and audits
• Collaboration in investment planning and commissioning of new equipment
• Member of multidisciplinary project teams for the development of medicinal products and manufacturing processes
• Leadership, further development, and assessment of subordinate employees

How you make the difference:

• Successfully completed studies in pharmacy with licensure as a pharmacist or a comparable scientific study
• At least 5 years of experience in the field of aseptic manufacturing, pharmaceutical development, or in another GMP-regulated environment
• At least 2 years of experience as a manager
• Sound knowledge of regulatory requirements and their influence on workflows and documentation requirements (national and international drug law, EU-GMP guidelines)
• Business English in spoken and written form
• Good IT skills
• Structured way of working with high initiative and willingness to take on responsibility
• High flexibility and willingness to adapt to changing requirements in development projects
• Excellent oral and written communication skills
• Strong team and cooperation skills, even in international and multidisciplinary teams

• with a diverse work environment where you can make a difference
• with an open corporate culture
• with attractive compensation
• with intensive onboarding including a mentor*
• with flexible working models for a healthy work-life balance
• with occupational health management with comprehensive health and exercise programs
• with company social benefits
• with diverse career opportunities in an international organization
• with high-profile, attractive development opportunities
• with a strong, international netw... </body>