Regulatory Affairs Executive(Female)

Required Regulatory Affairs Executive in Pharma Industry. Industry Background:Pharma (HO) Post: Regulatory Affairs Executive Gender: Preferably Female. Qualification : - M. Sc / B. Sc / M. Pharm / B. Pharm. Degree / Diploma in Regulatory Affairs. **Position 4 : Regulatory Executive (preferably female)** **Eligibility**: - M. Sc / B. Sc / M. Pharm / B....

**Job Description Form** **Fields** **Required Information** **Job Title** **Executive - Agriculture Regulatory Affairs** Reports To Manager CTC Budget 3-4 LPA Position Type New position Location Marol, Mumbai Job Overview Planning, undertaking, and overseeing regulatory work for local & export related products in Agri and Scientific...

Apply for Executive Regulatory Affairs, Regulatory Intelligence, Career Progress Consultants in Mumbai for 3 - 6 Year of Experience on

Apply for Executive Regulatory Affairs, Regulatory Intelligence, Career Progress Consultants in Mumbai for 3 - 6 Year of Experience on TimesJobs.com.

**Designation**: Executive - Agriculture Regulatory Affairs **Location**: Marol, Mumbai **Experience**: 2 - 5 Years **Qualification**: B.sc Agri/ M.sc Agri/ Diploma in regulatory affairs - Responsible for licensing & registration of agricultural products locally with state Agri department for sales permission, Product inclusions in the State sale...

At Ultratech India Limited, we believe employees are at the heart of all that matters. Connected in purpose by career, life, and health. The best people produce the best products and thus Ultratech is constantly on the lookout for bright and ambitious team players who have a strong commitment towards the organization. **Regulatory Affairs Executive**: ...

DESCRIPTIONVACANCYREGULATORY AFFAIRS EXECUTIVE(Pharma Company is manufacturing veterinary products)Job Location: Mumbai MaharashtraEligibility : M. Sc / B. Sc / M. Pharm / B. Pharm. Degree / Diploma in Regulatory Affairs. Should have good knowledge of preparing registration of Drugs & Feed Supplements in different countries Minimum 2 years experience in the...

VACANCYREGULATORY AFFAIRS EXECUTIVE(Pharma Company is manufacturing veterinary products)Job Location: Mumbai MaharashtraEligibility : M. Sc / B. Sc / M. Pharm / B. Pharm. Degree / Diploma in Regulatory Affairs. Should have good knowledge of preparing registration of Drugs & Feed Supplements in different countries Minimum 2 years experience in the same...

**We are Urgently looking for Regulatory Affairs - API** **Company name - Archerchem Healthcare Pvt Ltd** **Responsible for all regulatory affairs for API regulatory filings** **DMF compiling and filings** **Online filing of DMF as required.** **Customer queries to respond and resolve** **CEP filings to be done** **Education** **UG: B.Sc in...

**Job Description Form** **Fields** **Required Information** **Job Title** **Executive - Agriculture Regulatory Affairs** Reports To Manager Position Type New position Location Marol, Mumbai Job Overview Planning, undertaking, and overseeing regulatory work for local & export related products in Agri and Scientific support Responsibilities and...

Mumbai, Vile Parle VACANCY REGULATORY AFFAIRS EXECUTIVE (Pharma Company is manufacturing veterinary products) Job Location: Mumbai Maharashtra Eligibility: - M. Sc / B. Sc / M. Pharm / B. Pharm. Degree / Diploma in Regulatory Affairs. - Should have good knowledge of preparing registration of Drugs & Feed Supplements in different countries - Minimum 2 years...

The Sr. Manager, Regulatory Affairs will be responsible for overseeing regulatory activities related to clinical trials conducted by the clinical research organization. This position will play a crucial role in ensuring compliance with regulatory requirements and providing strategic regulatory guidance to internal teams and clients. The Sr. Manager,...

The Sr. Manager, Regulatory Affairs will be responsible for overseeing regulatory activities related to clinical trials conducted by the clinical research organization. This position will play a crucial role in ensuring compliance with regulatory requirements and providing strategic regulatory guidance to internal teams and clients. The Sr. Manager,...

The Sr. Manager, Regulatory Affairs will be responsible for overseeing regulatory activities related to clinical trials conducted by the clinical research organization. This position will play a crucial role in ensuring compliance with regulatory requirements and providing strategic regulatory guidance to internal teams and clients. The Sr. Manager,...

The Sr. Manager, Regulatory Affairs will be responsible for overseeing regulatory activities related to clinical trials conducted by the clinical research organization. This position will play a crucial role in ensuring compliance with regulatory requirements and providing strategic regulatory guidance to internal teams and clients. The Sr. Manager,...

We have job opportunity in our leading manufacturing company of Medical devices Position: - Regulatory Affairs Executive Experience: - 2 to 4 Yrs The JD as follows: - Maintain regulatory files. Maintain and update regulatory authorizations, such as IDEs, Medical device licenses, and CE dossiers for certifications etc. - Documenting technical file for...

MAIN PURPOSE OF ROLE Specialist professional individual contributor with comprehensive knowledge in the area of Regulatory Affairs. Ability to execute highly complex or specialized projects. Adapts precedent and may make significant departures from traditional approaches to develop solutions. MAIN RESPONSIBILITIES As the Specialist in the Regulatory Affairs...

We are currently seeking a highly motivated and experienced professional in Regulatory Affairs specializing in Medical Devices to join our team.Job Titles: Executive / Senior Executive / Assistant Manager - Regulatory AffairsExperience: 3 to 9 yearsLocation: Andheri east, MumbaiWorking Days: 6 days (Mon-Sat) - WFOResponsibilities:1. Dossier collation and...

Key Responsibilities: - Should have 2 Years of Experience in Regulatory Affairs - Coordinate with Plant and associated departments to facilitate the dossier requirements. - Review of PVP PVR, Stability, PDR, BMR, and other directly or indirectly linked Quality Section in CTD/ACTD - Experience in handling markets like African Countries, the Philippines,...

Provide expert regulatory input to strategic decision making; including portfolio review, prioritization, and external communications, Product packaging, Artwork etc.  Provide expert regulatory input to in-licensing evaluations and due diligence activities  Provide advice about regulations to manufacturers/scientists  Ensure that quality...