Lead Technician GMP Operations DSP // Johnson & Johnson in Bern

veröffentlicht
Kontakt
Stephan Zoebeli, Randstad JnJ Bern
Jobtyp
Temporär
jetzt bewerben

job details

veröffentlicht
Ort
Bern
Sektor
Life Sciences
Jobtyp
Temporär
Referenznummer
127140-414
Kontakt
Stephan Zoebeli, Randstad JnJ Bern
Telefon
058 231 57 94

Stellenbeschreibung

Caring for the world, one person at a time. inspires and unites the people of Johnson & Johnson. We embrace research and science - bringing innovative ideas, products and services to advance the health and well-being of people. Employees of the Johnson & Johnson Family of Companies work with partners in health care to touch the lives of over a billion people every day, throughout the world. We have more than 265 operating companies in more than 60 countries employing approximately 135,000 people.

Janssen Vaccines, one of the Janssen Pharmaceutical Companies of Johnson & Johnson, is a global biopharmaceutical company dedicated to bringing meaningful innovation to global health. We do this by discovering, developing, manufacturing and marketing products that combat major threats to the health of people worldwide. The Bern site, with its approx. 500 people of over 25 nationalities, acts as a center of expertise for development and manufacturing of innovative cell based viral- and bacterial vaccines and bacterial based therapeutic products.

Main Responsibilities

  • Execution of the practical downstream project work within a cGMP regulated environment. An implicit lead function in process planning and execution can be assigned to a Lead Technician
  • Accurate reporting and interpretation of batch manufacturing results. Conclude on results in consultation with the process engineer or the scientist/team leader contributing to campaign reporting and to process and operational improvement
  • Carry out development and manufacturing activities according to predefined study plans or batch records complying to the defined timelines
  • Carry out core DSP processes (filtration, chromatography, cross flow filtration, centrifugation, buffer preparation, filling, equipment cleaning/setup/prep, etc.) complying to cGMP regulations
  • Support and help troubleshoot purification operations
  • Support process/cleaning qualification and validation work
  • Establishment and ownership of SOPs and manufacturing protocols
  • Support safety and environmental initiatives by testing equipment prior to starting production
  • Report EHS gaps and/or incidents and initiate EHS improvements
  • Document the executed work in protocols and batch records in accordance to good documentation practice
  • Perform batch record review
  • Plan the execution of work packages and manufacturing operations as well as side activities
  • Perform manufacturing raw materials/consumables reservations in ERP system

Qualifikation

Who we are looking for

  • MSc or BSc degree in life science (pharmaceutical technology/biotechnology, food technology, chemical technology or equivalent) or technician in life science (pharmaceutical technology/biotechnology, food technology, chemical technology or equivalent) with several years of relevant professional experience
  • Flexible, adaptive and a team player
  • Ability to work independently and self-disciplined to meet the given timelines
  • Good communication in German and English
  • Previous experience or knowledge with downstream pharma processing operations is a major plus (chromatography, filtration, TFF, etc.)

This role based in Bern, Switzerland will initially be limited to approx. 12 months. If you are interested in working for a global leading health care company in a challenging role, then send us your application in English today. Or give us a call if you have any questions!