Senior Scientific Associate Clinical Manufacturing (897256-ED)

6 days left

Canton of Basel-Stadt (CH)
02 Feb 2021
04 Mar 2021
Full Time
Contract Type
Experience Level
Experienced (non-manager)

Senior Scientific Associate Clinical Manufacturing (897256-ED)


Our client, an innovative and dynamic bio-pharmaceutical company headquartered in Switzerland, covering multiple therapeutic areas, committed into delivering products on the market over the next 5 years, is looking for a Senior Scientific Associate for a permanent contract based in Basel area.

The ideal candidate should have more than 5 years of previous experience in the pharmaceutical industry within formulation development and GMP manufacture environment. Also full proficiency, scientific understanding of microbiology and technical knowledge in liquid filling and aseptic practices are strongly recommended.

Main Responsibilities:

As a Senior scientific associate in a new clinical manufacturing unit, you will support in-house development and manufacturing of sterile liquids and semi-solids dosage forms and participate in activities supporting the production up to phase III.

Your main tasks will consist in :

  • Review of relevant documentation (SOPs,WIS, validation documents) link to the new facility and the new products
  • Formulation and manufacturing process development of liquid forms under aseptic conditions / Planning and execution of experiments and IPC tests
  • Manufacture of batches and documentation of the manufacturing process according to cGMP for clinical trials and beginning of commercial
  • Technical development documentation, incl. the first assessment of the results; support drafting of master batch records, archiving
  • Operation / cleaning of rooms and equipment according to SOPs
  • Contributing to manufacturing and cleaning procedures, reports and instructions and / or SOP's and to the evaluation of new manufacturing or lab equipment
  • Support of inspections by internal or external authorities





Qualifications and Experience:

  • Relevant working/residency permit or Swiss/EU-Citizenship required.
  • Bachelor's degree in pharmacy / chemistry with minimum 5 years of industrial experience or Education as a laboratory technician, with more than 7 years of experience in pharmaceutical formulation development combined with cGMP manufacture. Knowledge in microbiology is an advantage.
  • Profound technical knowledge in liquid filling (syringes and vials) and aseptic practices as well as basic knowledge in visual inspection
  • Knowledge in process equipment such as autoclave, filter integrity, filling machine
  • Solid experience in optimizing existing processes and contributing to new process development
  • Fluent English both written and spoken
  • Ability to work with multi-disciplinary team including external suppliers and scientists
  • Readiness to work in cGMP environment in grade A and B

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