Senior Manager* C&Q & Compliance Engineering

  • BioNTech Careers
  • Singapore
  • Executive Middle Management
  • Production, manufacturing
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Become a member of the BioNTech Family!

As a part of our team of more than 4.000 pioneers, you will play a key role in developing solutions for some of the most crucial scientific challenges of our age. Within less than a year, we were able to develop our COVID-19 mRNA vaccine following the highest scientific and ethical standards – writing medical history.
 
We aim to reduce the suffering of people with life-changing therapies by harnessing the potential of the immune system to develop novel therapies against cancer and infectious diseases. While doing so, we are guided by our three company values: united, innovative, passionate. Get in touch with us if you are looking to be a part of creating hope for a healthy future in many people's lives.

Senior Manager* C&Q & Compliance Engineering

Along with the growth of BioNTechs global footprint, we are staffing a new site engineering
team. The site engineering is in charge to host and execute the local repair, maintenance,
calibration, qualification and automation.
The site engineering team ensures equipment availability in GMP compliant manner. The
mRNA manufacturing suites and its periphery are automated (PCS 7 SIEMENS for Pro-
cess, BMS, EMS, MES) and host standard biotech unit operations (AHUs, Bioreactors,
TFF, Filtration skids, etc. pp.)

Your main responsibilities are:
  • Responsible to lead a team of external compliance and C&Q engineers from service suppliers
  • Business owner for site specific engineering SOPs
  • Execution of commissioning and qualification for equipment, utilities and clean rooms
  • Definition and Implementation of Change Controls, CAPAs
  • Deviation management
  • Build and grow the compliance team on site
  • SPOC for audits

What you have to offer.

Education:
  • Completed academic degree (B.Sc./M Sc.) with major in process engineering, mechanical engineering, or biotechnology
Professional experience:
  • At least 3-5 years of engineering experience in the pharmaceutical industry
Languages: 
  • English fluent spoken and written
Competencies:
  • High degree of GMP know-how for pharmaceutical operations
  • Extensive Commissioning, Qualification and Validation knowledge and professional experience required
  • Very good planning and organizational skills
  • Ability to work without supervision and to demonstrate job ownership
  • Pronounced team and communication skills
  • Analytical and concept-based thinking and acting
  • GMP-related experience is a must
  • Strong industry network to equipment vendors etc.

Benefits for you.

We offer a competitive compensation package which will be determined by the contract type and selected candidate’s qualifications and experience.
 

How to apply.

Apply now and simply send us your application documents including Curriculum Vitae, copy of ID, copies of degree certificates and professional certificates, motivation letter as well as your contact details using our online form.

Please note: 
  • Only applications sent via our online form shall be considered.
  • Only Candidates with the right qualifications and relevant experience shall be shortlisted and 
  • Incomplete applications shall be rejected
  • Please note that BioNTech will run a background check during the hiring process (criminal record certificate) in case you do not provide one.
We are looking forward receiving your application.

*BioNTech does not differentiate on the basis of gender, race or ethnicity, religion, color, sexual orientation or identity, disability, age and other protected statuses as given by applicable law. We are committed to creating a diverse environment and are proud to be an equal opportunity employer. Most important – it’s a match!