Associate Scientist QC Raw Materials

vor 4 Wochen

Bern, Bern, Schweiz Randstad Vollzeit

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 Johnson & Johnson 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 120,000 people.

Johnson & Johnson Innovative Medicine is a global pharmaceutical 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. 600 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:

After the respective training, you are expected to coordinate and conduct analytical testing on Raw materials, intermediates and other GMP samples, in details following competencies and responsibilities are required:

Being responsible for completion (i.e., execution and documentation) of different analytical tests according to internal (TMDs) and/or external (e.g., EP, USP, ISO) requirements. Analytical tests encompass EP/USP ion ID tests, FTIR, TLC, Appearance of solution, pH, Osmolality, Density, Refractometry, Manual titrations, Conductivity, ...)Being responsible for raw material sampling, when the need arisesWrite scientifically-sound technical documents and reportsSupport laboratory management, e.g., planning activities covering end-to-end raw materials processSupport a timely and effective completion of lab events, investigations, change controls and CAPAs, including writing, execution and review of related documentsBeing responsible for writing and conducting study plans and method verification/validation plans and reportsMaintain laboratory equipment by supporting in their periodic maintenance and calibration tasks executionOperate efficiently analytical instruments in QC Raw Materials labPerform laboratory duties to support QC-department objectivesSupport QC department in internal and external audits and requests when the need arisesBeing responsible for compliance within the quality goals for this positionHelp to build and expand a strong team, enhancing the current expertise and be ready to reflect changing and dynamic business needsProvide support to other stakeholders when the need arises
Qualifikationen Who we are looking for: Bachelor or Master level University/Higher educational degree in natural sciences, applied sciences or equivalentWork experience in Pharma, Biotech or Vaccines industry is a major plusProfound working understanding of laboratory operations and practicesExperience in method validations/verifications and equipment qualificationGood writing skills for scientifically sound technical documents, instructions, protocols and reportsSelf-dependent way of working and taking ownership of assigned task to plan and deliver according agreed timelinesFamiliar with compendial testing and related industry guidelinesDemonstrate innovative spirit, strong interpersonal skills and project management abilitiesAbility to work in a dynamic environment according to tight and challenging timelinesAdvanced IT skillsGood verbal and written skills in English (German is a plus)This job based in Bern, Switzerland will initially be limited to 12 months. If you are interested in working with a global leading pharmaceutical company in a dynamic, inclusive and collaborative environment, then send us your application today. Or give us a call if you have any questions

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