summary.

Bern, Bern
Temporary
12 months+

specialism
life sciences
contact
Stephan Zoebeli
reference number
127140-671

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job details

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

Performing qualification, verification and co-validation activities.
Responsible for writing and conducting study plans, method validation and writing scientifically sound documents and reports
Being compliant with general guidelines and processes in QC in accordance with current GMP guidelines. This includes all steps of the analysis under cGMP from the sample collection point to the release of the results by the authorized person
Timely and effective completion of lab events, investigations and CAPAs including writing, executing and reviewing related documents
Supervising and coordination equipment maintenance activities.
Periodic review and evaluation of microbiological assays (cGMP) according to given timelines
Supporting planning activities
Performing laboratory duties to support department objectives
Support the Quality department in internal and external audits and requests
Provide support to analytical development, process development and other stakeholders when the need arises

Main Responsibilities

Performing qualification, verification and co-validation activities.
Responsible for writing and conducting study plans, method validation and writing scientifically sound documents and reports
Being compliant with general guidelines and processes in QC in accordance with current GMP guidelines. This includes all steps of the analysis under cGMP from the sample collection point to the release of the results by the authorized person
Timely and effective completion of lab events, investigations and CAPAs including writing, executing and reviewing related documents
Supervising and coordination equipment maintenance activities.
Periodic review and evaluation of microbiological assays (cGMP) according to given timelines
Supporting planning activities
Performing laboratory duties to support department objectives
Support the Quality department in internal and external audits and requests
Provide support to analytical development, process development and other stakeholders when the need arises

qualifications
Who we are looking for
- PhD/University degree in natural sciences or applied sciences
- Relevant Laboratory experience
- Work experience in Pharma, Biotech or Vaccines industry is a plus
- Experience in microbiological method validation and verification and equipment qualification
- Preferably familiar with compendial testing and related industry guidelines
- Demonstrates innovative spirit, strong interpersonal skills and project management abilities
- Ability to work in a dynamic environment according to tight and challenging timelines
- Team player
- Very Good German & English communication (verbal & written)
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, progressive, and collaborative environment, then send us your application today. Or give us a call if you have any questions!

Stephan Zoebeli

+41 58 231 57 94
Randstad JnJ Bern

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Scientist QC Microbiology // Johnson & Johnson.

job details

qualifications

get in touch.

Stephan Zoebeli

the application process.

apply with randstad.

we'll contact you.

getting you registered.

compliance, reference and background check.

the perfect job for you.

the interview.

start your new job.

ongoing support.

related jobs.

Operator DSP // Johnson & Johnson

Pharmatechnologe*in USP // Johnson & Johnson

Senior Technician Monitoring // Johnson & Johnson

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