Save Job Back to Search Job Description Summary Similar JobsRegional exposureWell-know established medTech companyAbout Our ClientThis organisation operates within the medical devices industry and is located in KL.Job DescriptionEnsure compliance with regulatory standards and guidelines for products and processes across SEA region.Develop and maintain quality assurance documentation and systems.Coordinate with cross-functional teams to implement regulatory requirements.Monitor and assess changes in regulatory policies and update internal processes accordingly.Prepare and submit regulatory filings and documentation as needed.Conduct internal audits to ensure adherence to quality standards.Provide guidance on regulatory and quality matters to relevant teams.Support continuous improvement initiatives in regulatory and quality processes.The Successful ApplicantA successful Senior RAQA Specialist should have:A strong background in regulatory affairs and quality assurance within the medical devices industry.Knowledge of relevant regulatory standards and guidelines.Experience in preparing and submitting regulatory documentation.Ability to work collaboratively with cross-functional teams.Excellent organisational and communication skills.Attention to detail and a proactive approach to problem-solvingWhat's on OfferBasic benefits package included.Permanent position in the life sciences industry.This is a role for professionals in Sea to advance their careers in regulatory and quality assurance. Interested candidates are encouraged to apply.ContactMichelle LimQuote job refJN-082026-7085535Phone number+603 2302 4057Job summaryFunctionLife SciencesSpecialisationRegulatory AffairsWhat is your area of specialisation?Healthcare / PharmaceuticalLocationKuala LumpurContract TypePermanentConsultant nameMichelle LimConsultant contact+603 2302 4057Job ReferenceJN-082026-7085535
