Cmc - 72+ job offers

Provide Safety induction training to all the Contractor Employees Check Fitness / Pre Medical certificate of all the Contractor Employees. Ensure Reflective jacket / uniform for all Contractor employees Daily Inspection and verification of Permit to Work to the contractors. Daily maintaining the rec

*Role Overview** The CMC RA Manager II is responsible for managing and delivering high-quality Chemistry, Manufacturing, and Control (CMC) documentation for regulatory submissions across the product lifecycle. This role involves global project management of CMC regulatory activities, ensuring compli

Eurofins

Company Description Eurofins Scientific is an international life sciences company, providing a unique range of analytical testing services to clients across multiple industries, to make life and our environment safer, healthier and more sustainable. From the food you eat, to the water you drink, to

Job Description At EY, you'll have the chance to build a career as unique as you are, with the global scale, support, inclusive culture and technology to become the best version of you. And we're counting on your unique voice and perspective to help EY become even better, too. Join us and build an e

*Sr.** **CMC Associate,** **RA** **Pharma** *Position Summary** The Senior Associate, CMC Regulatory Affairs (Global) is on-roll position responsible for supporting worldwide regulatory CMC strategies and leading post-approval activities for assigned pharmaceutical products for a global healthcare c

Senior Regulatory Affairs Consultant- CMC Biologics When our values align, there's no limit to what we can achieve. At Parexel, we all share the same goal - to improve the world's health. From clinical trials to regulatory, consulting, and market access, every clinical development solution we provid

We are looking for a Senior STEM Content Analyst with strong expertise in CMC Small Molecules and/or Biologics to join our Life Sciences team in India. The ideal candidate will have a solid background in pharmaceutical development and/or regulatory affairs across CTD/eCTD submissions and product lif

We are looking for a Senior STEM Content Analyst with strong expertise in CMC Small Molecules and/or Biologics to join our Life Sciences team in India. The ideal candidate will have a solid background in pharmaceutical development and/or regulatory affairs across CTD/eCTD submissions and product lif

*Site Name:** Bengaluru Luxor North Tower *Posted Date:** Mar 4 2026 GSK remains committed to achieving bold commercial ambitions for the future. By 2031, we aim to deliver £40 billion in annual sales, leveraging our strong performance momentum to increase our positive impact on the health of billio

We are looking for a highly skilled and experienced Regulatory Affairs Specialist to join our team at Ruputed Pharmaceutical Company, responsible for ensuring compliance with regulatory requirements in the pharmaceutical industry. The ideal candidate will have a strong background in regulatory affai

We are looking for a highly skilled and experienced Regulatory Affairs Associate to join our team at Ruputed Pharmaceutical Company in the Pharmaceutical & Life Sciences industry. The ideal candidate will have a strong background in regulatory affairs, particularly in CMC. *Roles and Responsibil

Dear Candidates We are Hiring For CMC And VMC Operator Skills- Vmc and Cmc machine Operator ,Extruder, Turning center ,Grinding machine ,Milling machine , Cmc Programming etc Salary -15-25k Share Me Updates Cv-7042740655/7042494894

*Position Description:** The purpose of Manager - CMC Regulatory, Large Molecules/Biotechnology Products, is to work cross functionally with Elanco R&D groups, manufacturing and quality to develop global regulatory strategy, oversee submission preparation and meet the reporting requirements for

*Position Description:** The purpose of Consultant, Global CMC Regulatory, is to work cross functionally with Elanco manufacturing and quality to develop regulatory strategy, oversee submission preparation and meet the reporting requirements for the maintenance of registrations/approvals of new anim

*Hiring: Regulatory CMC – Site & Regional Roles** We are hiring experienced *Regulatory CMC professionals** to support both *Site-level change management** and *regional submission activities** across a diverse portfolio including *small molecules, biologics, vaccines, and plasma-derived therapi

*Description** Sr Regulatory Consultant/ Regulatory Consultant (CMC- API - EU market) Syneos Health® is a leading fully-integrated life sciences services organization built to accelerate customer success. We partner with innovators at every point across the drug development and commercialization con

*Company Overview** Cheiron is a Stanford-based AI company building the AI-native operating system for drug development. Biopharma knowledge work is structurally fragmented. Critical decisions depend on stitching together evidence across literature, clinical trials, regulatory precedent, and patents

Elanco

Responsibilities: Life Cycle Management (LCM): Proven track record of overseeing end-to-end LCM of diverse pharmaceutical dosage forms, including otic solutions/suspensions, spot-on/pour-on solutions, collars, bee-hive strips, sterile injectables, and products derived from biotechnology/fermentation

Parexel

When our values align, there's no limit to what we can achieve. Regulatory Affairs Consultant Around 7-10 years of relevant experience in handling life cycle management (LCM) of approved/marketed drug products (Biologicals, Vaccines, ) in various markets, mainly in US, EU, Japan, Canada Switzerland,

Parexel

When our values align, there's no limit to what we can achieve. Regulatory Affairs Consultant Around 7-10 years of relevant experience in handling life cycle management (LCM) of approved/marketed drug products (Biologicals, Vaccines, ) in various markets, mainly in US, EU, Japan, Canada Switzerland,