Job Description

Open for hire at one of the following locations - Singapore. - Job ID: 6314

Become a member of the BioNTech Family!

As a part of our team of more than 5.000 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* QC (AS&T)

The QC Senior Manager is responsible for disciplinary and functional supervision of the laboratory construction, setup and operation for drug substance (DS) and drug product (DP) testing, and is responsible for analytical methods validation/verification/transfer, internal/external lab testing set up, procedures/processes creation for DS and DP. Ensuring cGMP-compliant, efficient, and on-time completion of analysis orders, and to provide analytical and coordinating support for assigned projects, while observing all directives and statutory regulations concerning safety, ecology, and occupational safety. Your main responsibilities are:

• Identify, prioritise, allocate and manage all activities/responsibilities of AS&T (Analytical Science and Technology) team.
• In conjunction with other QC manager, develop and implement a consistent management structure with supports: staff development, technical excellence, business improvement , quality & regulatory compliance and best practices.
• To collate and manage the execution of all routine and non-routine testing activities: DS/DP analytical method transfer and/or method validations, Cleaning validation analytical method validation and sample analysis, technical run and process performance qualification, new technology transfers.
• Assess and coordinate QC changes with respects to updates of relevant testing procedures and Pharmacopoeias revisions.
• Prepare and review analytical reports associates with APRs and PQRs in-line with agreed timelines.
• Ensure that equipment qualification and calibration activities are coordinated and performed in accordance with appropriate SOPs and schedules.
• Participates in regulatory inspections and customer audits, project team and production meetings, supports audits at external labs, participates in self inspections, and ensures implementation of the derived action plans.

What you have to offer.

• Completed bachelor degree in chemistry, biochemistry or microbiology or other relevant sciences
• At least 10 years of industry experience in an analytical, cGMP-regulated environment
• Fluent written and verbal English
• Experience supervising direct reports and organizing teams
• High degree of conscientiousness and diligence (documentation, order and cleanliness at the workstation)
• Sense of ownership and honesty (proactive handling of errors)
• Constructive, solution-oriented work habits, flexibility
• Physical stamina

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 by 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.
• BioNTech will run a background check during the hiring process

We are looking forward receiving your application.

*BioNTech does not differentiate on the basis of gender, political opinion, religion or belief, nationality, ethnic or social origin, age, sexual orientation, marital status, disability, physical appearance, health status or any other aspect of personal status. We are committed to creating a diverse and inclusive environment and are proud to be an equal opportunity employer. Most important - it\'s a match!

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