Regulatory Affairs Officer

**Vacancy**: For Regulatory affairs officer **Job description** **Roles and Responsibilities** 2) To check artworks for regulated/ semi regulated countries. 3) To co-ordinate for documents and samples for regulatory submissions with manufacturing locations LL & TP 4) Handling of queries pertaining to regulatory submissions from various regulatory...

The **Regulatory Affairs Specialist** stays with the same company for an average of 10 to 15 years; the rate of turnaround is therefore low. Networking is very much encouraged, through joining various associations to participate in conferences and exhibitions, and also to access current literature. Presently, there is a strong demand for Regulatory Affairs...

Greetings, We have an excellent opportunity for Regulatory Affairs officer. Location : Malad Experience :1 + year Role: We are seeking a skilled and licensed Regulatory officer to join our team. The products, managing purchase orders, and ensuring proper follow-up procedures. The officer will play a crucial role in maintaining compliance with...

Seeking Drug Regulatory Affairs for a Company into Pharma Industry **Key Responsibilities**: - Research and stay updated on regulatory requirements and guidelines - Coordinate with cross-functional teams to gather necessary documentation and information for regulatory filings - Review and assess product labeling, packaging, and promotional materials to...

**Responsibilities** - Support in creating regulatory and quality policy plan as needed internally and externally - Work with internal personnel and external agencies to implement relevant regulatory requirements - Maintain and submit regular follow up documentation to regulatory/ quality agencies and participate in audits as needed - Document review and...

Looking for RA Executive having min 2 years of Experience **Salary**: ₹40,000.00 - ₹50,000.00 per month Schedule: - Day shift **Experience**: - Regulatory Affairs: 2 years (required) Work Location: In person **Speak with the employer** +91 8002870884

Job Req ID: 39631- Location: Pune, IN- Function: Other- About: - Vodafone Idea Limited is an Aditya Birla Group and Vodafone Group partnership. It is India’s leading telecom service provider. The Company provides pan India Voice and Data services across 2G, 3G and 4G platform. With the large spectrum portfolio to support the growing demand for data and...

Dear Candidates Greetings from Randstad India ! We have an openingfor the role of Executive Regulatory Affairs with a leading pharmacompany in India. Interested candidates can drop your resume to the mailid The details arebelow: Qualification: B.Pharm / M. PharmExperience: 48 years Market:Canada Location: Pune Review of compilation...

**JOB DESCRIPTION OF REGULATORY AFFAIRS** **TOTAL YEARS OF EXPERIENCE**: 2-4 YEARS - Handling dossier, COPP submission and query Handling for South East Asian Country, East Africa, Latin America, Central America, Europe. - In depth knowledge about regulatory requirements for above region - Need to work independently - Need to have knowledge about legal...

Role Description The RA Executive will be responsible for handling regulatory affairs related to the company's products, filing of DMF, Dossier compilation, co-ordination with third party auditors and authorities, and handling the licensing process. - Knowledge of the regulatory environment and laws in India and around the world - Experience in DMF...

Designation : Regulatory SpecialistExperience : 7+Location : PuneQualificationsBachelor of Science in science and/or engineering field8 - 12years of regulatory experience in medical device industry (equivalent industry/educational experience may be considered)Thorough working knowledge of applicable FDA, ISO, EU and/or other region-specific medical device...

Designation : Regulatory Specialist Experience : 7+ Location : Pune Qualifications Bachelor of Science in science and/or engineering field 8 - 12years of regulatory experience in medical device industry (equivalent industry/educational experience may be considered) Thorough working knowledge of applicable FDA, ISO, EU and/or other region-specific medical...

Designation : Regulatory SpecialistExperience : 7+Location : PuneQualificationsBachelor of Science in science and/or engineering field8 - 12years of regulatory experience in medical device industry (equivalent industry/educational experience may be considered)Thorough working knowledge of applicable FDA, ISO, EU and/or other region-specific medical device...

Designation : Regulatory SpecialistExperience : 7+Location : PuneQualificationsBachelor of Science in science and/or engineering field8 - 12years of regulatory experience in medical device industry (equivalent industry/educational experience may be considered)Thorough working knowledge of applicable FDA, ISO, EU and/or other region-specific medical device...

Ensuring compliance with all regulatory requirements - Maintaining regulatory documentation database - Assisting with the preparation and submission of all regulatory reports - Providing accurate reviews of data and reports - Ensuring accurate and timely submissions to regulatory agencies - Advising others on regulatory and compliance matters Pay:...

Designation : Regulatory SpecialistExperience : 7+Location : PuneQualifications- Bachelor of Science in science and/or engineering field- 8 - 12years of regulatory experience in medical device industry (equivalent industry/educational experience may be considered)- Thorough working knowledge of applicable FDA, ISO, EU and/or other region-specific medical...

Regulatory documentation work under supervision of senior Regulatory staff for a Pharma manufacturing and Export company in Navi Mumbai having its various manufacturing locations in India and exporting its products worldwide. **Salary**: From ₹15,000.00 per month **Benefits**: - Provident Fund Schedule: - Day shift Supplemental pay types: - Yearly...

Maintaining regulatory documentation database Ensure compliance with regulations Prepare and file regulatory submissions Develop or conduct employee regulatory training Liaising and negotiating with regulatory authorities Studying scientific and legal documents Undertake and manage regulatory inspections Coordinate compliance committee Pay:...

**Eligibility**: - Masters in Chemistry or Bachelors in Food Tech. - A minimum of 3 -4 years of experience in Food Ingredients, Food or Analytical Laboratory company - Your past profile could be of Quality Assurance (QA), Product / Regulatory Documentation or Quality Management (QM). - SAP experience is must - Good communication skills in English are...

**About Apotex Inc.** Apotex Inc. is a Canadian-based global health company that produces high-quality, affordable medicines for patients around the world. Apotex employs almost 7,200 people worldwide in manufacturing, R&D, and commercial operations. Apotex medicines are accessible to patients in more than 75 countries globally. Through vertical...