Job Description

Open for hire at one of the following locations - Singapore. - Job ID: 6322

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 (Raw Materials and Microbiology)

Your main responsibilities are:

Responsible for operation of incoming raw materials and microbiology testing laboratories. Ensure that all QC activities are performed accordingly to the Global Quality system and SOPs. All deviations or OOX investigations are closed on time. Ensure all QC relevant KQIs meet targets and define recovery plan to mitigate performance issue

Provide leadership, direction and support to the QC teams and ensure that they are qualified, achieve a high level of competence and are motivated to carry out their duties in a safe manner

Act as key liaison with QA, PU, SCM, AS&T, MS&T to ensure effective support of new products transfer and commercialization

Perform integrated planning, priority setting and execution of activities fully synchronized with the product transfer plan, manufacturing plan, QA release timeline and supply chain shipment plan

Assist the Director QC to establish operating and capital budgets, manage operating expense budget. Ensure that the team operates in a cost effective and efficient manner and maintains an innovative approach based on productivity improvement, implementation of best practices and harmonization with technical operations

Create/ review /approve department, systems and corporate quality-related policies and procedures and provide technical and procedural training

Implement cGMP requirements, enter/approve analysis results in Quality system (e.g. LIMS)

Participate in regulatory inspections and customer audits, project team and production meetings, support audits at external labs, participate in self inspections and ensure 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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