Job Description

Open for hire at one of the following locations - Singapore. - Job ID: 6316Become 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* QA (QA-QC)This Senior Manager QA (QA-QC) is responsible, and ensures that operations are in alignment and compliant with Global Quality, internal and external GxP requirements. You will also ensures that raw materials are tested meeting specifications and DS and DP are produced meeting the specifications per the dossier and approved appropriately for release.He/she should have a strong commitment to drive a quality mindset culture, safety, health and environment (SHE) compliance for the site.Main responsibilities :Lead and direct the assigned Quality ProcessA key partner to the Quality Control team, ensures that general laboratory operations, commissioning and qualification, method qualifications/validations/verifications are in alignment and compliant with global, internal and external GxP requirements.Provides QA oversight of the assigned Quality Process to ensure that products are processed, manufactured, stored and distributed according to applicable current GxP and regulationsProvides QA oversight of the assigned Quality Process to ensure that facilities, equipment, materials, processes and procedures comply with applicable current GxP and regulationsImplements, maintains and reviews the assigned Quality Process according to applicable current GxP and regulationsOwns policies and procedures of the assigned Quality Process where applicable.Partners with global and communicates to functions to ensure the assigned Quality Process is executed according to established policies and proceduresReviews/approves and provides inputs for procedures, documents, records, deviations, investigations, corrective action/preventive actions, change controls and gap assessments associated with the assigned Quality ProcessEnsures deviations from assigned Quality Process are documented and investigatedEnsures QA personnel are qualified and trained to perform assigned tasksSupport technology transfer activities.Develops strategies for assigned Quality Process to be fit for purpose, including continuous improvements and ensure a state of inspection readinessSupports inspection and audit preparationsParticipates in inspections, audits and Quality Management ReviewEscalates quality and compliance risks to Head of Department, QASupports improvement initiatives, programs and projects of the assigned Quality ProcessBuild, maintain and develop a team to support the deliverables of this assigned Quality ProcessOther responsibilities may be assigned by the managerWhat you have to offer:University degree/Advanced Degree in Science (medicine, pharmacy, chemistry, biotechnology, biology or equivalent).At least 10 years\' professional working experience in Quality Management System in the pharmaceutical/biotechnology/medical device industry. Depending on the experience and technical capability of the shortlisted candidate, the role offered may be at an expert level, equivalent to a managerial level.Extensive knowledge in Quality Management System concepts and strong understanding of pharmaceutical business and regulatory governance/frameworkExperiences with collaborations with global multidisciplinary functions involved in drug development and manufacturingAbility to be agile and effectively collaborate in a dynamic, cross-functional environmentHigh degree of conscientiousness and diligenceConstructive work habits, flexibility, solution orientation, job ownership, quality awareness, and very good planning and organizational skills in a fast-paced environmentSelf-starter and learning capacitySense of ownership and honesty (proactive handling of errors)Ability to navigate through ambiguity and rapid growth and adapt to change, especially in a start-up environmentExpectation to be hands on, interactive and display practical leadershipGood communication skillsExcellent written and verbal skills.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!BioNTech - As unique as you

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