Regulatory Affairs Manager Jobs in Beijing

Working with UsChallenging. Meaningful. Life-changing. Those arent words that are usually associated with a job. But working at Bristol Myers Squibb is anything but usual. Here uniquely interesting work happens every day in every department. From optimizing a production line to the la More...

Job DescriptionResponsibilities:Collaborate closely with global colleagues to prepare dossiers for veterinary medicine product registration in China (e.g. variations renewals GMO applications) providing guidance on Chinese regulatory requirements and conducting regulatory assessments. More...

At Cision we believe in empowering every individual to make an impact. Here your voice is heard your ideas are valued and your unique perspective fuels our collective success. As part of our global team youll thrive in an environment that champions curiosity collaboration and innovati More...

You will lead medical device regulatory affairs activities in China for Apple Health. You will demonstrate the ability to develop a variety of solutions to RA/QA challenges and will exercise independent judgment in settling and communicating appropriate regulator action and engagement More...

Do you thrive in regulatory environments and have a passion for building trusted relationships with government and internal stakeholders Are you looking for a role where your bilingual skills and attention to detail can make a meaningful difference in a global mission-driven organisat More...

-Product registration related including new extension and changes:Document requirementSample ordering and type testingDossier preparationSubmissionFollowing up CMDE evaluation proceduresSolving various problems in whole processMaintaining database like RA database MDRiMFiling dossiers More...

At least bachelor degree on medical pharmaceutical biology or related regulatory legal or medical management master degree is preferred.At least 12-15 years working experience and 5 years leadership experience in regulatory science or other related areas in healthcare industry.Solid k More...

Job DescriptionResponsibilities:Work closely with Global colleagues to prepare dossiers and documents for product registration in China. Provide guidance and regulations required by the Chinese authorities for the documentation preparations. Independently undertake theproject.Work clo More...

Manage regulatory activities across a designated product range within the OTC portfolio seeking guidance as requiredBuild strategic regulatory insights into product registration strategies to ensure fast introduction of new products (including new indications) by securing import licen More...

JOB DESCRIPTION:EXPERIENCE:Over 5 years working experience in regulatory affairs or R&D for pharmaceuticals including more than 3 years in regulatory affairs.Solid registration project management skills;Effective problem solving and planning capabilities;Good knowledge of NMPA/C More...

Job DescriptionPosition title: Senior Manager Regulatory Affairs CMCDepartment: Regulatory AffairsReport to: Associate Director Regulatory Affairs CMCLocation: Beijing ChinaResponsibilitiesLead Regulatory CMC Policy & Intelligence efforts to effectively navigate the regulatory lan More...

JOB DESCRIPTION:Works in a strategic role and demonstrates organizational influence1. Product registrations /Submissions-Develops and directs regulatory plans for product and/or geographic groups assigned and ensures they are in-line with business needs-Reviews regulatory data packa More...

When our values align theres no limit to what we can achieve.At Parexel we all share the same goal - to improve the worlds health. From clinical trials to regulatory consulting and market access every clinical development solution we provide is underpinned by something special - a dee More...

Job DescriptionResponsibilities:Work closely with Global colleagues to prepare dossiers and documents for product registration in China. Provide guidance and regulations required by the Chinese authorities for the documentation preparations. Independently undertake theproject.Work clo More...

The Senior Manager Regulatory Affairs In Vitro Diagnostics and Companion Diagnostics works with internal and external partners to develop and implement regulatory strategies for In Vitro Diagnostics (IVD)/Companion Diagnostics (CDx) to support business objectives with limited manageme More...

PurposeDescribe the primary goals objectives or functions or outputs of this position.To deliver successful regulatory submissions and approvals to ensure that products within an assigned portfolio comply with local regulatory requirement and to support the commercialisation of produc More...