Project Manager Global Regulatory Affairs - Vapi

Regulatory Affairs Executive · The Regulatory Affairs Executive will be responsible for managing and coordinating regulatory documentation and compliance activities for radiology and imaging systems such as X-Ray, C-Arm, Digital Radiography (DR), and CT equipment. · ...

We're Hiring | Regulatory Affairs – CMC (Cell & Gene Therapy) · Prepare, review, and manage CMC sections for regulatory submissions (IND, CTA, BLA, MAA) · ...

Regulatory Affairs Executive is responsible for preparing regulatory documentation and ensuring compliance with regulatory requirements in Micro Orgo Chem. · ...

This company is a rapidly growing manufacturer of Active Pharmaceutical Ingredients (API), trusted by overseas and Indian customers for its quality and reliability. · ...

We are looking for a Regulatory Affairs professional with strong CMC expertise in Cell & Gene Therapy (CGT) to join our growing team. · ...

+Job summary · We are seeking an experienced · Regulatory Affairs professional · to lead and execute global regulatory strategies for biologic products across multiple development stages.+ResponsibilitiesDevelop and implement global regulatory strategies for biologic products acr ...

Develop global regulatory strategies for biologic products across all development phases. Prepare high-quality regulatory submissions including INDs/IMPDs, BLA/MAA. · ...

Key Responsibilities: · Lead and oversee end-to-end medical device testing in line with international standards, risk management frameworks, and design principles. · Organize, manage, and evaluate product data to prepare comprehensive technical files. · Prepare regulatory dossier ...

We're Hiring: Officer / Executive / Assistant Manager – Regulatory Affairs Are you passionate about regulatory compliance and medical innovation? Join Meril, a global leader in medical device technology, and play a key role in delivering safe and effective healthcare solutions. · ...

Join Meril, a global leader in medical device technology · Lead and oversee end-to-end medical device testing · Organize product data to prepare technical files · Collaborate with cross-functional teams on innovative product development ...

+ Job Title: Clinical Executive · To support and execute clinical studies, trials, and observational research activities while developing high-quality clinical documentation, scientific outputs, and regulatory-ready evidence. · ...

To prepare, review, and control technical, quality, and validation documentation for Women's Health & Fertility / IVF medical devices, supporting R&D and Production activities. Ensure compliance with ISO 13485, IEC , and applicable regulatory requirements. · ...

Job summaryChief of Staff · Stakeholder Engagement: Identify and establish strong relationships with key external stakeholders. · Government and Regulatory Affairs: Keep abreast of all relevant laws, regulations, · Crisis Management: Act as a mediator in case of any disputes or ...

Job summary · Land Acquisition Manager. · ResponsibilitiesStakeholder Engagement: Identify and establish strong relationships with key external stakeholders. · Government and Regulatory Affairs: Keep abreast of all relevant laws, regulations, and policies that impact the company' ...

The Liaisoning Manager is responsible for identifying and establishing strong relationships with key external stakeholders and ensuring compliance with government regulations and policies. · ...

The Liaisoning Manager will be responsible for establishing strong relationships with key external stakeholders, managing government and regulatory affairs, supporting business development initiatives, coordinating projects, handling crisis management situations. · ...

The General Manager will oversee timely commissioning of Green Field Project & manufacturing operations for Pharma Intermediates & API's Products. Responsibilities include managing plant operations, ensuring quality & regulatory affairs. · ...

To prepare technical documentation for medical devices supporting R&D activities ensuring compliance with ISO requirements. · - Control document lifecycle including creation review approval revision distribution archival. · - Maintain document traceability version control data in ...

To support and execute clinical studies, trials, and observational research activities while developing high-quality clinical documentation, scientific outputs, and regulatory-ready evidence. · ...

To plan, execute, and manage high-quality medical and scientific events while ensuring seamless infrastructure readiness, regulatory compliance, and cost-effective delivery. · Plan and execute medical and scientific programs including CMEs, surgeon trainings, cadaver labs, produc ...