Average salary: Rs546,666 /yearly
More statsSearch Results: 7,650 vacancies
...Job Description
Job Title - Regulatory Affair Manager
Career Level : C
Lead the way for a new breed of solutions-oriented Regulators... ...approach earlier in the product lifecycle to get involved in shaping drug development
Be part of the team where you are empowered to...
Rs 3 lakh p.a.
...validations preparation & review.
- Analytical method validation review as per the ICH guideline.
- Drug Master File review
- Technical query response to the various regulatory authorities.
Ideal Profile
~ You have at least 1 year post-qualification experience in a...
...Job Title: Regulatory Affairs Specialist
Company: MakroCare
Location: Hyderabad Telangana (Onsite)
Company Description:
MakroCare... ...and overseeing regulatory submissions and communications with drug regulatory authorities. This includes ensuring compliance with...
...Job Description
Job Title: iCMC Regulatory Affairs Manager
Career Level - D
Introduction to Role:
Join our Biopharmaceuticals R&... ...Regulatory Sciences or Pharmacy
Experience in Regulatory / Drug development (Industry or Health Authority)
Breadth of knowledge...
...most impactful work of your career.
Umami Bioworks is looking to hire an inquisitive, innovative, and independent Director of Regulatory Affairs to join our R&D team in Bangalore, India .
Role:
Develop and Execute Global Regulatory Strategy: Lead the development...
...authorities deficiency
Scientific Advice
Variations and Supplements (Type IA, IA, Type IB Type
Timely review of technical and regulatory documents i.e. Specifications, batch records, method validation documents, Stability data, container closure system, DMF review....
...We are currently seeking a highly motivated and experienced professional in Regulatory Affairs specializing in Medical Devices Domain to join our team.
Positions are: Executive / Sr. Executive / Asst. Manager - Regulatory Affairs
Experience: 3 to 9 years
Location:...
...-being – a fundamental driver for many of us to show up and do our best each day.
Job Description
You will focus on leading regulatory services for global research projects of novel medicinal products in India while joining our global team of regulatory and ethics submissions...
...Basic understating about ISO 13485 and US FDA regulation (Medical Device Related)
Qualifications & experience:
Relevant regulatory and quality assurance experiences in international company for 2 years
Physical & mental requirements:
Detailed oriented....
...Regulatory Affairs Associate
Job duties of a Regulatory Affairs Specialist include:
Developing and implementing regulatory strategies for new and existing products
Preparing and submitting regulatory documentation to regulatory authorities
Liaising with regulatory...
(JOINING ASAP) We are seeking for a Regulatory Affairs Specialist who will be responsible for ensuring the delivery of regulatory activities performed in the platform/hub: About us
Responsibilities
To contribute to the production of client administrative documents...
...materials, packaging, in-process and finished product inline with ICH and USP.
Review Compilation and submission ANDAs (generic andnew drug applications) to US FDA.
Follow up with CFTs for complement of action items for deficiencies comments and prepare clear responses to...
...Regulatory Affairs Specialist
Responsibilities:
Prepare and submit regulatory documentation for new and existing medical products, including drugs, devices, and biologics.
Stay up-to-date on ever-evolving regulatory requirements and guidelines.
Liaise with regulatory...
...Position : Executive Department : Regulatory Affairs - Formulation
Location : Kandivali - West, Mumbai
Qualification - M Sc/ B Pharm/ M Pharm
Experience : 4 - 8 years and above
Role
Responsible for activities related to own submission and support...
...Executive - Regulatory Affairs (PLMDS)
at ClinChoice (View all jobs)
Chennai - India
Are you interested in working directly for a single... ...processes relating to human health submissions and selected drug and non-drug specific projects and related activities.
Support...
...: Duties & Responsibilities
Project Management:
Support Regulatory projects and Compliance standpoint on key projects within EM Regulatory... ....
Years of Experience: at least 7 years in Regulatory Affairs & RA compliance, data analysis, project Management …
Language:...
...the job
Job Description Summary
This position is responsible for the creation identification collection and entry of regulatory affairs information of medical devices. Support related regulatory affairs activities such as assessment execution and management of regulatory...
Rs 5 - 6 lakhs p.a.
...complex activities, often with competing priorities.
Most regulatory affairs positions are full time.
Regulatory Responsibility means... ...with regulatory authorities for marketing authorization.
Drug Regulatory Affair,dossier preparation ,ECTD,ACTD
Designation...
$ 62500 p.a.
...Job description
We are looking for an Associate Director or a Director, Regulatory Affairs who will be responsible for day-to-day regulatory activities of early/late phase investigational products, leads the writing and submission of IND/CTA/amendments and future marketing...
...Job description
The Director of Regulatory Affairs at DELFI Diagnostics will support the representation of DELFI with the FDA and other US and international regulatory agencies. Internally, this role will support and direct the regulatory function, regulatory activities...
