Regulatory Affairs Officer

Vega Biotec Pvt Ltd forms part of Vega group companies involved in manufacturing and exporting of finished pharmaceutical products and having global presence in 20+ countries. We have an opening for the following post. 1. Regulatory Affairs Executive - Qualification - B.pharma/M.pharm Experience - 5-7 year's minimum in regulatory affairs Job profile: 1....

Company OverviewRenown Pharmaceuticals Pvt. Ltd., a renowned soft gelatin contract manufacturer, boasts a state-of-the-art facility in India.Job OverviewWe seek an experienced Regulatory Affairs Officer for our Vadodara office. This full-time position requires 1-3 years of experience. The salary range is competitive. Our company has over 200 employees and...

Vega Biotec Pvt Ltd forms part of Vega group companies involved in manufacturing and exporting of finished pharmaceutical products and having global presence in 20+ countries. We have an opening for the following post. 1. Regulatory Affairs Executive - Qualification - B.pharma/M.pharm Experience - 2-4 year's minimum in regulatory affairs Job profile: 1....

At Renown Pharmaceuticals Pvt. Ltd., we are seeking a highly skilled Regulatory Affairs Officer to join our team in Vadodara.About the RoleAs a Regulatory Affairs Officer, you will be responsible for ensuring compliance with regulatory requirements for product registrations, preparing and submitting regulatory documents and filings, interpreting and applying...

Regulatory Affairs Officer Job DescriptionCompany OverviewRenown Pharmaceuticals Pvt. Ltd. is a renowned soft gelatin contract manufacturer with a state-of-the-art facility in India. The company adheres to the highest quality standards and aims to be a leading producer of soft gelatin capsules in the country.Job OverviewWe seek a highly experienced...

About the Role:We are seeking an experienced Regulatory Affairs professional to join our team in a full-time capacity. The ideal candidate will have a strong background in regulatory affairs, specifically within the pharmaceutical industry.Key Responsibilities:Ensure compliance with regulatory requirements for pharmaceutical products in target marketsPrepare...

About Lifelancer, a leading talent-hiring platform in Life Sciences and IT.We are seeking an experienced Regulatory Affairs Executive to join our team.The ideal candidate will have 1-3 years of experience in quality control regulatory affairs, with a strong understanding of medical device rules and regulations.A bachelor's or master's degree in life sciences...

Regulatory Affairs Specialist Needed at PR FlexmakeJob Description:We are seeking a skilled Regulatory Affairs Specialist to join our team at PR Flexmake Private Limited.Key Responsibilities: Maintenance of Quality Management Systems and Standard Operating ProceduresDocumentation and certification for medical devicesInspecting final products for...

Job description **Company Description** Briyosis Soft Caps Pvt. Ltd. is a privately-owned contract manufacturer of custom dietary supplement formulations. Based in Vadodara, India, we are an FDA registered and WHO-GMP certified company. With our high-efficiency encapsulation lines operating 24/7, we have the capability to produce over 3 billion soft-gels...

Position Regulatory Affairs Associates Location - Vadodara KRA: As a RA Sr. Officer Reviewing artwork, PRAC variations, CEP updates for EU market. Preparation of Regulatory Strategic documents for EU/UK market. Review and compilation of deficiencies response for ROW (specially MENA, LATAM market) Compilation and submission of renewal, variation for...

Job OverviewWe are seeking a highly skilled Regulatory Affairs professional to contribute to our team's success in Vadodara. The ideal candidate will have a strong background in pharmaceutical regulations, specifically within the industry, and will hold relevant qualifications such as a B.Pharm or M.Pharm degree.Key ResponsibilitiesEnsure compliance with...

**Vega Biotec Pvt Ltd** a part of Vega group of companies having global presence and state of the art manufacturing pharmaceutical factory is having an opening for the following post. Qualification - B.Pharm/ M. Pharm Experience - 3+ years of experience in regulatory affairs for ROW market (Rest of the world) **Job Summary**: The Regulatory Affairs...

**Vega Biotec Pvt Ltd** a part of Vega group of companies having global presence and state of the art manufacturing pharmaceutical factory is having an opening for the following post. Qualification - B.Pharm/ M. Pharm Experience - 3+ years of experience in regulatory affairs for ROW market (Rest of the world) **Job Summary**: The Regulatory Affairs...

As a key member of the SUN PHARMA team, the Regulatory Affairs Manager will be responsible for ensuring compliance with various health authorities across the globe.Compile and submit registration dossiers to health authorities such as China, Canada, Europe, Australia/New Zealand, Japan, and Israel.Prepare and submit scientific advice to health...

Looking for an Enthusiastic, Efficient & Trustworthy Senior Executive - Regulatory Affairs for a Leading MNC “**Ronak Group”** **Company: Ronak Group (MNC)** Position**:Executive / Senior Executive - Regulatory Affairs** Experience: 2 to 7 Years Location: Vadodara, India We are looking for Energetic & Goal Oriented **Executive / Senior Executive -...

Company OverviewSun Pharma is a leading pharmaceutical company that offers a wide range of products and services.Job DescriptionWe are seeking an experienced Regulatory Affairs Manager to join our team in Baroda. The successful candidate will be responsible for managing the regulatory affairs function, including ensuring compliance with relevant regulations...

About the CompanyLifelancer is a leading talent-hiring platform in Life Sciences, Pharma and IT, connecting professionals with opportunities in pharma, biotech, health sciences, healthtech, data science and IT domains.Job OverviewWe are seeking a highly skilled Regulatory Affairs professional to join our team in Vadodara on a full-time basis. The ideal...

**Vega Biotec Pvt Ltd** a part of Vega group of companies having global presence and state of the art manufacturing pharmaceutical factory is having an opening for the following post. Qualification - B.Pharm/ M. Pharm Experience - Minimum 3 years in regulatory affairs for ROW market (Rest of the world) **Job Profile**: 1. Preparing dossiers as per country...

**Role & responsibilities** - EU Dossier preparation and submission to Europe market. - EU ASMF and CEP preparation and submission to Europe with post-approval activities - Handling of EDQM Agency Queries. - Brazilian DMF Preparation and Deficiency response. - China DMF Preparation and Deficiency response. - eCTD publishing in EDUCE software with PDF...

PR Flexmake Private Limited is seeking a Quality Control and Regulatory Affairs expert.Experience: 1-3 years in a similar role.The ideal candidate will have a strong understanding of medical device regulations and Quality Management Systems.Key responsibilities:Maintenance of QM, SOP, Device and Plant Master FilesQuality certification audits, documentation,...