Jobs: regulatory affairs

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...

Position: Regulatory Affairs Assistant - Cosmetic Industry Department: Regulatory Affairs Experience Required: 0-2 years Location: Santej, Ahmedabad Salary Range: 2.2 LPA - 3 LPA Roles & Responsibilities: 1. Handling Legal Documents and Regulatory Affairs: - Assist in the preparation, review, and submission of regulatory documents. - Maintain and...

**Executive Regulatory Affairs (API Pharma)** **Qualification**: M.Sc. - Organic & preferably diploma or must have worked in Regulatory Affairs department of Pharmaceutical Organization / API **Experience** : 8 - 10 years in Quality Assurance department (QA) of Pharmaceutical Industry & regulatory Affairs department ,preferably from API Pharma...

**Regulatory Affairs Executive Job Description** **Job Summary**: The Regulatory Affairs Executive will work with product development and manufacturing management to ensure that the product development process meets all applicable regulatory requirements. **Duties/Responsibilities**: - Works in the regulatory affairs department on assigned projects. -...

Sunrise Remedies Job Opening for Regulatory Affairs (RA). **Experience**: Minimum 2 Years **Industries**: Pharmaceutical Company **Education**: B.Sc. / M.Sc / B.Pharm / M.Pharm **Job Location**: Santej Ahmedabad. **Key Responsibilities**: - Regulatory Affairs Specialists assist in obtaining and maintaining government approval for drugs, medical devices,...

Hiring for a **REGULATORY AFFAIRS OFFICER ** for our **Ahmedabad **location. Freshers with good knowledge should apply **Key Responsibilities**: - Assist in the preparation, compilation, and submission of regulatory documents, such as drug master files (DMFs), technical dossiers, and regulatory filings, to health authorities and regulatory agencies. -...

Regulatory affairs professionals play a critical role in the drug development process, working closely with other stakeholders to ensure that pharmaceutical products meet regulatory requirements at every stage of development. Some of their key responsibilities include ( CTD/ ACTD DOSSIER PREPRATION ( MARKET ASEAN, CIS ROW ) **Regulatory Strategy...

DETAILS: Experience in regulatory affairs for ROW market EXPERIENCE: 2-3 years EDUCATION: B. Pharm/ M. Pharm LOCATION: Ahmedabad, India

Works in the regulatory affairs department on assigned projects. - Coordinates with product development and/or research and development teams to request, develop, and prepare required data and reports to be submitted to regulatory bodies and agencies. - Collaborates with key staff from Planning, Product Development, Operations, and Legal departments as...

_**Duties/Responsibilities**:_ - Works in the regulatory affairs department on assigned projects. - Coordinates with product development and/or research and development teams to request, develop, and prepare required data and reports to be submitted to regulatory bodies and agencies. - Collaborates with key staff from Planning, Product Development,...

We are looking for a motivated and experienced Regulatory Affairs Specialist to join our team As a Regulatory Affairs Specialist, you will be responsible for the day-to-day monitoring of the companys regulatory activities to ensure compliance with all regulations. You will be a key member of our regulatory affairs team, which is responsible for the companys...

We are looking for a motivated and experienced Regulatory Affairs Specialist to join our team As a Regulatory Affairs Specialist, you will be responsible for the day-to-day monitoring of the companys regulatory activities to ensure compliance with all regulations. You will be a key member of our regulatory affairs team, which is responsible for the companys...

**Description** Drug Regulatory Affairs - Job description - Prepare CTD, ACTD Dossiers and file regulatory submissions. - Perform assessments of new or revised products. - Manage complaint documentation (including investigation and closure). - Respond to inquiries from regulatory bodies. - Should be technically well versed with requirements for medicines...

**Regulatory Affairs** **This is us**: Ovesco Endoscopy is a research-based medical device company specializing in flexible endoscopy. We develop, produce, and sell highly innovative instruments and systems for the treatment of gastrointestinal diseases. We offer comprehensive procedures and accompany our customers all the way from training to...

**Roles and Responsibilities** **Position :Regulatory Affairs Executive** **Qualification**:Graduation+ PG diploma in Regulatory Affairs**Experience **:0to 2 Years**Location **:Dombivali, Mumbai(Experienced or fresh) will be required for the expansion of the Regulatory department. The expansion of the department is necessary to cater to the requirements...

Managing regulatory affairs of the organization its subsidiaries/associates Liaising with regulatory bodies like State and Central FDA,DCI Well conversant with Drug law/feed supplement regulation Co-ordination with purchase, marketing departments Preparation of Applicant part and Restricted part DMFs (USDMF, EUDMF and ROW). **Salary**: From ₹171,172.50...

Company DescriptionSwiss Pharma Pvt. Ltd. is one of India's leading pharmaceutical companies based in Ahmedabad. With a focus on exports to regulated and semi regulated markets, Institution & Tender Business and Contract Development and Manufacturing Organizations (CDMO), Swiss Pharma is known for manufacturing various dosage forms, including injections,...

**Opening for Regulatory Affairs Officer** **Qualification: MSc. Organic Chemistry** **Experience Required: 3**-5 Yrs in Pharmaceuticals (API Manufacturing) **Job Role**: 1 Be the point of contact and support on regulatory matters. 2 Prepare draft for regulatory / submission dossiers. 3 Generate, collect, compile & Review the regulatory submission...

**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...

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,...