
Regulatory Affairs Officer
2 weeks ago
This role is for one of the Weekday's clients
Salary range: Rs Rs ie INR 3-8 LPA)
Min Experience: 3 years
Location: India, Hyderabad
JobType: full-time
Requirements
Key Responsibilities:
Drug Master Files (DMF):
- Prepare, compile, and review US DMFs (Type II), EU ASMFs, and other region-specific dossiers.
- Manage lifecycle activities such as updates, deficiency responses, and annual reports.
- Collaborate with internal teams to gather technical documents for submissions.
Regulatory Documentation & Submissions:
- Compile CTD/eCTD dossiers for global regulatory submissions (USFDA, EDQM, WHO, TGA, etc.).
- Ensure adherence to current international regulatory guidelines and standards.
- Maintain accurate records, document control systems, and submission archives.
Cross-Functional Collaboration:
- Coordinate with QA, QC, R&D, and Production teams for necessary documentation and technical inputs.
- Support preparation and review of product specifications, stability data, and Certificates of Analysis (COAs).
Audits & Inspections:
- Provide assistance during regulatory audits and inspections by international authorities and clients.
- Address regulatory queries and observations in a timely manner.
Regulatory Intelligence:
- Monitor and interpret updates in global regulatory guidelines (USFDA, EMA, ICH, etc.).
- Provide inputs on regulatory strategies, product classification, and compliance requirements.
Required Skills & Qualifications:
- Bachelor's or Master's degree in Pharmacy, Life Sciences, or a related field.
- 3-7 years of experience in Regulatory Affairs, preferably in pharmaceuticals, nutraceuticals, or herbal formulations.
- Strong understanding of DMF/ASMF preparation and submission processes.
- Familiarity with global regulatory frameworks (USFDA, EMA, TGA, WHO, etc.).
- Excellent documentation, communication, and organizational skills.
- High attention to detail with the ability to manage deadlines effectively
-
Hyderabad, Telangana, India beBeeregulatory affairs officer Full time ₹ 40,00,000 - ₹ 80,00,000Job Summary:","Regulatory Affairs Specialist: Artwork Management and Compliance"],
-
Regulatory Affairs
2 weeks ago
Hyderabad, Telangana, India Clininfotech Full time ₹ 1,04,000 - ₹ 1,30,878 per yearWe are seeking a Regulatory Affairs Executive Freshers To Work in the MNC For Hyderabad LocationThe ideal candidate should have hands-on experience in compiling and reviewing ACTD and CTD dossiers for various regulatory submissions. Required Candidate profileB.Pharm & M.Pharm With Knowledge of Regulatory Affairs CTD ECTD DMF and Regulatory Guidelines are...
-
Regulatory Affairs
2 weeks ago
Hyderabad, Telangana, India Biological E Full time ₹ 9,00,000 - ₹ 12,00,000 per yearRegulatory Affairs Job OpportunityDesired Experience : 3- 9 yearsJob Location : Genome Valley, Shameerpet, HyderabadPreferred Industry : Vaccines / BiotechDesignation: Senior Executive/ ExecutiveQualification: M. Pharmacy/ M. Sc/ B. PharmacyJob Responsibilities:Responsible for Regulatory submission to Indian NRA, Emerging Markets, Regulated Markets and World...
-
Hyderabad, Telangana, India beBeeRegulatory Full time ₹ 32,00,000 - ₹ 48,00,000Job Role: Regulatory Affairs Officer">We are seeking a skilled and detail-oriented Regulatory Affairs Officer to join our team in Hyderabad, India.">The successful candidate will be responsible for:">">Generating new artwork in collaboration with artists and maintaining accurate records">Revising existing artworks and communicating changes to various...
-
Regulatory Affairs CMC
2 weeks ago
Hyderabad, Telangana, India Vipsa Talent Solutions Full time ₹ 6,00,000 - ₹ 12,00,000 per yearRegulatory Affairs CMCExperience: 6-11 yearsEducation: Science GraduateLocation: HyderabadSkills: Regulatory Affairs, US market, CMC
-
Regulatory Affairs Associate
2 weeks ago
Hyderabad, Telangana, India Vipsa Talent Solutions Full time US$ 60,000 - US$ 1,20,000 per yearRegulatory Affairs AssociateExperience: 3-6 yearsEducation: Science GraduateLocation: HyderabadSkills: Regulatory Affairs, EU market, Formulation, RA, European market, Post and Pre approval
-
US Regulatory Affairs Professional
1 week ago
Hyderabad, Telangana, India beBeeRegulatory Full time ₹ 1,20,00,000 - ₹ 1,50,00,000Regulatory Affairs Specialist OpportunityWe are seeking a highly skilled Regulatory Affairs professional to support our team in the US market.Key Responsibilities:Prepare and review regulatory submissions, including ANDAs, NDAs, supplements, amendments, deficiency responses, annual reports, and PADER in eCTD format.Maintain compliance with US FDA and ICH...
-
Regulatory Affairs Specialist
1 week ago
Hyderabad, Telangana, India beBeeRegulatory Full time ₹ 9,00,000 - ₹ 12,00,000Job Title:Regulatory Affairs Specialist - CMCJob Description:This position involves supporting submissions to regulatory authorities and managing the lifecycle of products. We are seeking a highly skilled Regulatory Affairs Specialist to join our team.Key Responsibilities:Prepare, review, and compile high-quality regulatory submissions in electronic format,...
-
Regulatory Affairs CMC Associate
1 week ago
Hyderabad, Telangana, India Ztek Consulting Full timeJob Description – Regulatory Affairs CMC Associate (US Market)We are seeking a Regulatory Affairs Associate to support US FDA submissions and lifecycle management activities.Key Responsibilities:- Prepare, review, and compile regulatory submissions (ANDAs, NDAs, supplements, amendments, deficiency responses, annual reports, PADER) in eCTD format.- Maintain...
-
Regulatory Affairs Coordinator
7 days ago
Hyderabad, Telangana, India beBeeRegulatory Full time ₹ 6,00,000 - ₹ 10,00,000Job SummarySeeking a highly skilled Regulatory Affairs Specialist to prepare, review, and maintain regulatory documents ensuring compliance with international guidelines and country-specific requirements.Key ResponsibilitiesScreen and analyze documents received for product registration requests as per country-specific guidelines.Prepare, compile, and review...