Head Solids (m/f/d)

  • Responsible for providing leadership for the site PU organization including Manufacturing and Packaging
  • Accountable for efficient and effective manufacturing of Product related to Quality, Cost, Schedule, Resources
  • Continuous improvement of the area of responsibility
  • Supervise and follow approved pharmaceutical regulations (e.g. AMG, cGMP, AMWHV, BtMG, etc.) in the area of responsibility
  • Act according to regulation as "Leiter Herstellung nach AMWHV"
  • Supervision of Maintenance, Rooms and Equipment incl. qualification and validation status
  • Ensure relevant training of operators
  • Take over employer obligation according to german legislation §12UVV in the area of responsibility related to work- and healthsafety as well as accident prevention (e.g ArbSchG, UVEG-SGB, GUV, BGB, ASiG, etc.)
  • Signature and Procurement Responsibilities according to approved internal guidelines
  • Responsible for creation and approval of batch records, manufacturing records and SOPs
  • Ensure collaboration with OPEX for product / process improvements (harmonized agenda & priorities).
  • Degree in Pharmacy, Pharmaceutical Technology, Chemistry or equivalent scientific degree
  • Fluent in German and English in mandatory, both written and spoken
  • A minimum of 10 years of experience in Pharmaceutical (i.e. Production / QA) with high experience in cGMP
  • Proficient in Manufacturing of Pharmaceuticals and Expert role on the shopfloor
  • Proven process understanding (Pharma, GMP, Regulatory aspects)

» Job description

STADA Arzneimittel AG
61118 Bad Vilbel