Open for hire at one of the following locations - Singapore. - Job ID: 6323Become 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.Technical QA Expert*As Technical QA Expert* you are responsible to lead, establish, support and help ensure that Commissioning, Qualification and Validation for Facilities, Utilities and Equipment, Computerized Systems, process, analytical and microbiology methods etc in operation areas in BioNTech SGP is in alignment and compliant with global Quality, internal (Site VMP) and general GxP requirements.Your main responsibilities are:Leads, creates, executes the assigned Quality Process according to established procedures and requirementsFunction as the Quality subject matter expert and responsible to review and approve validation protocols, reports, risk assessment and other validation related documents for equipment\'s, computerized systems, HVAC & utility systems, process validation, Analytical & Microbiology methods etc.To ensure validation documents are compliance with internal procedure or regulatory requirementsResponsible to review and approve specification documents in compliance with validation requirements.Support the review of the validation related standard proceduresQuality oversight for validation maintenance programReports and presents assigned Quality Process metricsSupports or conducts training for the assigned Quality Process as appropriateServes as backup for other assigned Quality Process as appropriateComplies with applicable current GMP and regulations to execute assigned tasksFollows established procedures and requirements to execute assigned tasksParticipates in cross-functional collaboration for execution of the assigned Quality ProcessSupports regulatory inspections and auditsAdherence to safety requirementsReports any condition impacting quality and compliance to Quality Assurance ManagementParticipates in projects and improvement initiativesWhat you have to offer:Advanced Degree/Degree, Diploma in Science, Pharmacy, Pharmaceutical Science, EngineeringPreferably 8-10 years in Pharmaceutical in the field of Quality Assurance or ValidationHands on experience on validation/ qualification of manufacturing equipment\'s /systems etc.Deep knowledge on various validation regulatory guidelines such as FDA/EU cGMP, PDA Technical guide, GAMP requirements etc.Expert knowledge on Data Integrity and Compliance with cGMPDeep knowledge in Quality Assurance conceptsGood communication skillsBenefits 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:
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