Regulatory affairs - Thane, Maharashtra, India

We are seeking an experienced Regulatory Affairs Executive – API to manage regulatory documentation and submissions for active pharmaceutical ingredients (APIs). Compile, prepare, and review regulatory documents including DMF, DCP, EDMF, and CEP for API products. · Ensure timely ...

This role is for one of the Weekday's clients seeking an experienced Regulatory Affairs Executive – API to manage regulatory documentation and submissions for active pharmaceutical ingredients (APIs). The role focuses on ensuring compliance with global regulatory requirements thr ...

We are seeking an experienced Regulatory Affairs Executive - API to manage regulatory documentation and submissions for active pharmaceutical ingredients (APIs). The role focuses on ensuring compliance with global regulatory requirements through accurate preparation, review, and ...

This role is for one of the Weekday's clients. We are seeking an experienced Regulatory Affairs Executive - API to manage regulatory documentation and submissions for active pharmaceutical ingredients (APIs). The role focuses on ensuring compliance with global regulatory requirem ...

We are seeking a detail-oriented Assistant or RAQA Executive to support Regulatory Affairs and Quality Assurance activities for laboratory equipment and/or medical devices. · ...

Lead regulatory submissions for Inhalation projects in US market. · Ensure timely responses to product deficiencies raised by US regulatory authorities. · ...

Lead regulatory submissions for Inhalation projects in the US market and ensure timely responses to product deficiencies raised by US regulatory authorities. · ...

Lead regulatory submissions for Inhalation projects for the US market. · ...

This is a Regulatory Specialist role in the Global Regulatory Affairs Service Center Team in Mumbai. · ...

You execute the regulatory affairs strategy for your respective category or categories and geographical area using your technical and regulatory knowledge. · ...

The role involves maintaining regulatory databases and supporting document compilation. · Maintaining and updating database to track the submissions. · Support for document compilation for Applicant's part. · Preparation of Letter of Access. · ...

We are looking for a RA-Executive to join our team. The role will be responsible the role also includes participation in investigations such as deviations, OOS/OOT, and supporting departmental responsibilities in the absence of the reporting authority, along with any duties assig ...

We have an urgent opening coming up with one of the leading Pharmaceutical organization Mumbai (Kandivali West) for the role of Regulatory Affairs. · Should be well versed with Regulatory Affairs Guidelines of South East Asia Africa Middle East LATAM ROW. · Knowledge of Preparati ...

Officer de Asuntos Regulatorios · CDSCO Submissions · GMP & GDP Implementation · ...

The Regulatory Affairs Manager will oversee all functions of the department including scheduling activities, dossier preparation and review, regulatory submissions and approvals, task management and timeliness, compliance assurance, team leadership and development. · ...

This is a Regulatory Specialist role in the Global Regulatory Affairs Service Center Team in Mumbai (GRASC – Team). The person will be reporting to the Manager Regulatory Affairs. · Author Safety Data Sheets for multiple geographies across the globe as per applicable hazard commu ...

Olive PharmaScience Ltd is seeking a full-time Regulatory Affairs Executive/Senior Executive at our Corporate Office in Mumbai. The ideal candidate will prepare regulatory submissions while ensuring compliance with local and international regulations. · ...

Candidates should have 5 -13 years of experience in pharmaceutical regulatory affairs . · ...

Prepare regulatory dossiers for new products and submissions. · ...

This is a Regulatory Specialist role in the Global Regulatory Affairs Service Center Team in Mumbai.The GRASC – Team is an integral part of the Diversey regulatory function. · Handle key regulatory activities like compliance workflows, creation of SDS, labels, product registratio ...