Manager, Regulatory Salary at Basf Se BETA

Job Description Hilltop Holdings is looking to hire a Regulatory Reporting Manager. The Regulatory Reporting Manager is considered an experienced professional responsible for producing and submitting multiple regulatory filings in compliance with legal and regulatory requirements, the organization's policies and procedures, and accepted accounting principles. This position will prepare reports for bank and bank holding companies' regulatory agencies, focusing on quarterly Call and FRY-9C reports and other regulatory submissions. The position will have an elevated level of visibility within the organization with opportunities to work directly regularly with Management and will also interact very closely with other groups throughout Hilltop, including Risk, Legal, Treasury, Accounting, SEC Reporting, and Accounting Policy. Other responsibilities include various support tasks associated with earnings release, 10-Q/10-K disclosures, internal controls on Regulatory data integrity, data qual

This is a new hire for a company who has over 10 years experience in Biologics focusing on producing therapies using antibodies. Looking at Oncology, Infectious Disease and Haematology, this company strives to offer the best antibody based medicine to patients globally. They are hiring for an experienced CMC Regulatory Affairs Senior Manager. The candidate who would fit this role would be someone skilled in the below: CMC specialist in Drug Product development and manufacturing of injectable biologics (e.g., vials, prefilled syringes, auto injectors). Lead US (BLA) & EU (MAA) CMC strategy & authoring for drug development through to commercialization worldwide. Lead engagement with regulatory agencies and commercial partners.

Position Overview We are seeking a seasoned regulatory affairs professional to lead the post-market compliance operations within our regulatory team. This role focuses on overseeing critical post-market functions including incident reporting, global compliance submissions, and product surveillance. The successful candidate will be responsible for managing a team, engaging with international regulatory bodies, and driving continuous improvement in regulatory processes. Key Responsibilities Post-Market Compliance & Surveillance Lead all post-market surveillance activities, ensuring compliance with regional and international regulatory standards. Review and approve documentation related to adverse event reporting, device malfunctions, and corrective actions. Oversee development and execution of post-market surveillance strategies and risk assessments. Coordinate and conduct health hazard evaluations in collaboration with cross-functional subject matter experts. Ensure proper execution and

About the job Senior Manager Regulatory Affairs Senior Manager Regulatory Affairs A well-known large consumer products corporation is hiring for Regulatory Affairs Manager. Responsibilities include: Ensure completion of appropriate documents during the development life cycle and launch Ensure compliances with policies and product regulations Ensure compliances with standardization of consumer communications Responsible for all US regulatory submissions, supplement notifications, and application of any changes in the regulations for submissions Requirements Atleast 4-5 years relevant experience Degree in Science Product development experience strongly preferred If you are interested in the above opportunity please apply. Only relevant candidates will be contacted. workforcesolutionsvirensglobal... Locations: America, Europe, Asia & Australia

This is a new hire for a company who has over 10 years experience in Biologics focusing on producing therapies using antibodies. Looking at Oncology, Infectious Disease and Haematology, this company strives to offer the best antibody based medicine to patients globally. They are hiring for an experienced CMC Regulatory Affairs Senior Manager. The candidate who would fit this role would be someone skilled in the below: CMC specialist in Drug Product development and manufacturing of injectable biologics (e.g., vials, prefilled syringes, auto injectors). Lead US (BLA) & EU (MAA) CMC strategy & authoring for drug development through to commercialization worldwide. Lead engagement with regulatory agencies and commercial partners.

GOSECO International Executive Search® has been exclusively retained on behalf of one of our global clients to conduct the search for their Manager of Regulatory and Compliance in Guadalajara, Jalisco, Mexico. COMPANY OVERVIEW Our client is an international leader in 7+ countries across three continents in advanced manufacturing and product development across highly regulated industries, including medical devices, aerospace, and high-tech electronics. From Olympic stadiums to surgical suites, their products power some of the most mission-critical applications on Earth. POSITION SUMMARY The Manager of Regulatory and Compliance will play a pivotal leadership role in ensuring regulatory excellence and inspection readiness at one of their most strategic sites worldwide. This is your opportunity to step into a high-impact leadership role at a global technology company that's shaping the future of advanced electronics and medical device manufacturing, take the reins of a mature compliance fu

Job Description Responsible for managing Regulatory Publishing staff who format and publish electronic documents, build Regulatory submission deliverables such as INDs, CTAs, BLAs, MAAs, including their amendments and supplements, in accordance with applicable Regulatory Agency regulations, guidelines, and/or specifications (eg, FDA, EMA, ICH, etc). Job Duties •Manages staff who electronically format, publish electronic documents and builds Regulatory submission deliverables. Ensures quality, accuracy, and submission-readiness per Regulatory agency guidance and specifications, and internal procedures. •Provides guidance to multidisciplinary teams on developing submission structure strategies in accordance with applicable Regulatory Agency regulations, guidelines, and/or specifications (eg, FDA, EMA, ICH, etc) •Provides guidance on good documentation and submission practices •Assist with developing and maintaining Regulatory document processing and Regulatory submission publishing stand

Job Title: Senior Manager, Regulatory Strategy Location: Azusa, CA Position Type: Full-time Exciting opportunity to join a dynamic and innovative Cosmetics company - the team is committed to excellence and continuous improvement in all aspects of the business, but most importantly QC/Regulatory. As the team expands operations, they seek a highly qualified and experienced Senior Manager, Regulatory Strategy to join the team. Job Summary: The Senior Manager, Regulatory Strategy will play a crucial role in ensuring our compliance with regulatory requirements, optimizing our product development processes, and guiding strategic decision-making. Reporting to the VP of QC/Regulatory Affairs, this position requires a candidate with strong leadership skills, a deep understanding of regulatory frameworks, and the ability to collaborate cross-functionally to achieve regulatory compliance objectives. Key Responsibilities: Regulatory Strategy Development: Develop and implement comprehensive regulat