Regulatory Affairs Assistant
7 days ago
**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 annually. Our 100,000 square feet facility encompasses production, laboratory, and warehousing space, and we adhere to FDA cGMP standards to ensure product quality and safety.
**Role Description**
This is a full-time on-site role for a Regulatory Affairs Executive at Briyosis Soft Caps. The Regulatory Affairs Executive will be responsible for managing regulatory documentation, ensuring compliance with regulatory requirements, preparing dossiers, and overseeing all regulatory affairs activities within the company.
**Qualifications**
- B.pharm/M.pharm
- Regulatory Affairs experience with a focus on dietary supplements
- Knowledge of regulatory requirements and compliance standards
- Experience in dossier preparation for regulatory submissions
- Strong attention to detail and ability to manage regulatory documentation
- Excellent communication and interpersonal skills
- Ability to work independently and within a team
- Proficiency in relevant software and tools used in regulatory affairs
- Relevant certifications or qualifications in regulatory affairs or related field
- Experience working in a manufacturing environment is a plus
**Job Types**: Full-time, Permanent
Pay: ₹12,000.00 - ₹15,000.00 per month
**Benefits**:
- Paid sick time
- Provident Fund
Schedule:
- Day shift
Supplemental Pay:
- Yearly bonus
**Experience**:
- total work: 1 year (preferred)
Work Location: In person
-
Regulatory Affairs Executive
5 days ago
Jarod, Vadodara, Gujarat, India Briyosis Soft Caps Pvt Ltd Full timeCompany DescriptionBriyosis 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 annually. Our 100,000...
-
Regulatory Affairs Executive
7 days ago
Vadodara, Gujarat, India Amico Formulations LLP Full time**POST**:RA OFFICER/EXECUITVE **LOCATION: JAROD, VADODARA** **EXPERIENCE**: 2-3 YEARS Experience in handling regulatory affairs for ROW market mainly Latin American, African & Asian countries for Pharma Formulations. Preparation, compilation & Review of Registration documents that include Administrative & Technical. Reviewing the technical documents...
-
Vadodara, Gujarat, India Neujin Solutions Full time ₹ 5,00,000 - ₹ 12,00,000 per yearAs a Junior Regulatory Affairs Executive, you will have the opportunity to work with a dynamic team of professionals in the field of regulatory affairs.Key ResponsibilitiesConducting technical writing tasks to prepare necessary documentation for regulatory submissionsCollaborating with manufacturers of medical and diagnostic devices in product design,...
-
Executive - Regulatory Affairs
2 weeks ago
Vadodara, Gujarat, India Sun Pharmaceutical Industries Full timeJob Title Executive - Regulatory Affairs Business Unit R D1 Regulatory Affairs Job Grade G12A Location Baroda At Sun Pharma we commit to helping you Create your own sunshine - by fostering an environment where you grow at every step take charge of your journey and thrive in a supportive community Are You Ready to Create Your Own Sunshine As you enter the Sun...
-
Assistant Manager Regulatory affairs
4 weeks ago
Vadodara, India Biotech Healthcare Full timeRole Objective Key objective of this role is to prepare, review, and maintain regulatory documents in compliance with international standards and country-specific requirements. The role ensures timely preparation and updating of Technical Master Files, supports product registrations, manages post-market surveillance activities, and contributes to audit...
-
Regulatory Affairs Executive
2 weeks ago
Vasna Road, Vadodara, Gujarat, India Vega Biotec Pvt. Ltd Full time**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...
-
Regulatory Affairs Executive
5 days ago
Vasna Road, Vadodara, Gujarat, India Vega Biotec Pvt. Ltd Full time**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...
-
Regulatory Affairs Executive
7 days ago
Sola, Ahmedabad, Gujarat, India WEST-COAST PHARMACEUTICAL WORKS LTD Full time**West coast pharma is looking for Regulatory Affairs Head - Male preferred** Qualification: B.PHARM/M.PHARM Experience: 5 to 10 years only **Regulatory Affairs Head - Pharmaceuticals Job Role**: The Regulatory Affairs Head leads the regulatory strategy and compliance for pharmaceutical products. They oversee submission of dossiers to health authorities,...
-
Regulatory Affairs Associate
1 week ago
Ambli, Ahmedabad, Gujarat, India Rishika Health Full time**Job Description**: Prepare, review and submit regulatory dossiers for product registrations. Ensure all necessary documentation is accurate, complete and meets regulatory requirements. Collaborate with cross-functional teams to ensure compliance with global regulatory standards. Conduct regulatory research and stay updated on international regulatory...
-
Senior Regulatory Affairs Professional
1 week ago
vadodara, India beBeeGlobal Full timeRegulatory Affairs Specialist - Global Regulatory ExpertResponsible for handling global regulatory submissions, ensuring compliance with health authorities and regulations.Conduct dossier gap analysis to identify document and data gaps across all CTD modules (1–5).Prepare and submit regulatory dossiers in multiple formats including eCTD, ACTD, and...