This site uses cookies. By continuing to browse the site you are agreeing to our use of cookies. Find out more here.

Close Message for pharmaceutical industry jobs
NonStop Recruitment

Please note, at the end of July 2022 we will close the specialist jobs board services at and

Until then the services will run as normal, but then any contact data that we have on file will be permanently deleted.

Looking ahead, you might be interested in joining us at a new careers event, Working in and around #MedComms, on 19 September at Heathrow. We’d love to see you there.


Sister sites:
Our sister site Our sister site

MedComms Networking

MedComms Networking is a global initiative that facilitates networking and dialogue amongst individuals working in and around the pharmaceutical industry and MedComms, focusing on specialist medical education, medical communications and medical publishing activities. Why not sign up to our weekly newsletter and please, help spread the word amongst all relevant others.

MedComms Networking on Facebook

MedComms Networking on Linkedin

MedComms Networking on Twitter

MedComms Networking Youtube Channel

Partner sites:

At Burntsky Limited we work with a number of job aggregators in order to maximise the reach of the jobs posted with us including but not limited to:

JooblePartner Jooble
Jobs in UK

Job Details
This job has expired. Click here to view similar jobs.

MS&T Bioconjugation Process Expert - Swiss Biotech

Business Type: Biotechnology Company
Job Type: Biotechnology
Job Level: Experienced (non manager)
Position: Full Time
Salary: CHF80.000 - CHF120.000 per annum + 13% bonus
Location: Ireland (Eire)
Reference: 200406.2
Closing Date: 16/06/22
Job Details:

Join a global leader in life sciences operating across three continents. The site you''ll join in Switzerland is growing exponentially. For our Biologics organization, we are currently looking for an MS&T Bioconjugation Process Expert. We have a strong track record in the manufacturing of BioConjugates from early clinical to large scale commercial supplies. Our dedicated Protein Conjugation Plant facility (PCP) is recognized as a center of excellence for Antibody Drug Conjugates (ADC) as well as other classes of BioConjugates. We are experiencing an increased demand in this area and as part of our dedicated model, new BioConjugation suites will be built out within a pre-existing shell. In this context, a dedicated MSAT (Manufacturing Science & Technology) group for BioConjugation technologies was created.

In the position of MS&T Bioconjugation Process Expert, you will make a difference by being responsible for the successful supervision, support and life cycle management of BioConjugates processes running in our facilities. You will play a crucial role in the network between the different departments as manufacturing, development, quality assurance and control. Become part of this exciting opportunity and apply now!


  • Competitive salary (90-120.000 CHF base)
  • Rewarding bonus structure (10-13% yearly bonus)
  • Canton privileges for families and children (generous family allowance, up to 550€ per child allowance)
  • Visa sponsorship (extended to family members)
  • Pension contributions (60%)
  • Relocation package
  • Settling allowance
  • Facilitation of opening a bank account
  • Additional employee-only benefits
  • Opportunity of unparalleled growth
  • Learn cross-functionally from other departments
  • International and cosmopolitan environment
  • Global experience

Key criteria for an interview invitation:

  • European nationality (mandatory)
  • Biotech experience of 3-5+ years
  • GMP experience preferable (or GMP like)
  • In an MSAT function already (preferable)
  • Mammalian/Microbial expression cell line experience
  • Proficient English

Key responsibilities:

  • Support of the commercial and clinical re-supply BioConjugates GMP campaigns in our protein Conjugation Plant (small scale and large scale PCP) facilities
  • Plan and supervise MSAT activities on project level to ensure that the processes deliver the required products with the required quality in a safely, timely and in a cost effective manner

You will be responsible for:

  • The preparation of GMP clinical re-supply and commercial campaigns as part of a project team (tech transfer, scale up, GMP documentation, equipment)
  • Leading process troubleshooting on the manufacturing floor as needed
  • Change control management
  • Process validation activities
  • Annual product review (APQR)
  • Representing the facility during process specific inspections and audits as SME for area of responsibility

Key requirements:

  • Master or PhD (preferred) in Biotechnology, chemical engineering, organic chemistry or related disciplines
  • Significant experience in biopharma manufacturing and / or process development, preferably in the area of BioConjugates or DSP (Mammalian or Microbial)
  • cGMP experience and deep understanding of Bioprocess technology
  • Excellent communication skills for interaction with customers and within the project organization
  • Fluent in English and in German
  • Creative, agile, open-minded

Posted: 19/05/2022 | NPJ Ref: 306230 | NPJ Original URL
line graphic

Compatible with:

JobMate   Broadbean   Idibu

Site optimised for Internet Explorer 8+ / Firefox 3+
View a complete Jobs Listing