Pharmaceutical Production Specialist

Vor 6 Tagen

BitterfeldWolfen, Sachsen-Anhalt, Deutschland GULP – experts united Vollzeit

GULP – experts united is seeking a dedicated and experienced Pharmaceutical Production Specialist to join our team at our Bitterfeld-Wolfen site.

In this role, you will contribute to the production of high-quality liquid and semi-solid bulk preparations within a GMP environment. Your responsibilities will encompass a wide range of tasks, from operating production equipment to ensuring meticulous documentation and adherence to quality standards.

Your Responsibilities
  • Produce liquid and semi-solid bulk preparations in accordance with established manufacturing documents, including working under clean room conditions.
  • Manage material flow, cleaning, and sterilization of production equipment according to GMP and SOP guidelines.
  • Maintain accurate documentation in manufacturing protocols, machine logs, and shift records.
  • Implement in-process controls (IPC) to ensure product quality throughout the manufacturing process.
  • Document material movements effectively within the merchandise management system.
  • Operate and maintain measuring and testing equipment for quality assurance.
  • Contribute to the creation and revision of pharmaceutical production documents.
  • Set up, operate, monitor, maintain, and clean all production facilities, equipment, and rooms used in manufacturing.
  • Collaborate on production projects, including those focused on quality, GMP, and LEAN methodologies.
  • Assist with the calibration and maintenance of production equipment.
  • Support validation measures and contribute to galenic development projects.
Your Profile
  • Completed technical training as a pharmaceutical technician or several years of relevant professional experience in the pharmaceutical industry or comparable field.
  • Proven experience working within the pharmaceutical industry, demonstrating a strong understanding of GMP principles and quality awareness.
  • Extensive knowledge of GMP-compliant documentation practices.
  • Excellent written and spoken German language skills.
  • Flexibility to work in a 3-shift rotation.
  • A meticulous and conscientious approach to your work.

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