Search Results: 7,967 vacancies
...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....
...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...
...-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....
Rs 3 lakh p.a.
...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 similar role.
What's on Offer?...
...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...
...undertaking and overseeing product trials and regulatory inspections
Keeping up to date with... ...about regulations to manufacturers/scientists
Writing comprehensible, user-friendly... ...to switch their career into Regulatory Affairs can apply. They must be having the knowledge...
...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...
...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...
$ 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...
RA US injectable JD:
Knowledge on manufacture and testing of sterile products and Knowledge of environmental conditions during sterile product manufacturing.
Review and clearance of pre-exhibit batch R&D documents like formula clearance w.r.t Q1/Q2, IIG, specifications...
...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...
...Job Description
Job TitleHead of Regulatory Affairs IGTS-MoSJob Description Head of Regulatory Affairs IGTS-MoS
Critical RA leader of the IGTS MoS Category (Image Guided Therapy Systems Mobile Surgery). Also, a member IGTS MoS Leadership Team and advise senior management...
...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...
...Executive - Regulatory Affairs (PLMDS)
at ClinChoice (View all jobs)
Chennai - India
Are you interested in working directly for a single sponsor while having the security and additional career opportunities that working for a global CRO can bring? Our team says it’...
...Markets and Global Markets businesses with an ambition to become a licensed capital markets business in India.
This Head of Regulatory Affairs & Corporate Governance will have the huge responsibility of the overall middle-back office management and infrastructure development...
Rs 5 - 6 lakhs p.a.
...work frequently with other employees and team members to coordinate complex activities, often with competing priorities.
Most regulatory affairs positions are full time.
Regulatory Responsibility means a duty or responsibility, assigned to an individual by...
#ROW MARKET #CIS #MENA #AFRICA #LATIN #ASIA #EUROPE MARKET
Vacancy - 15
Qualification - B.Pharm/M.Pharm
Experience :- 3 to 12
Job Description :
Sound knowledge of CTD/ECTD/ACTD dossier review of OSD/Parenteral dosage forms.
Excellent knowledge of ICH/Country...
...proven end to end expertise from clone development, manufacturing, clinical development, regulatory approvals to commercialization in developed and emerging markets. Global Regulatory Affairs
The Global Regulatory Affairs (GRA) at Biocon consists pool of talented...
...Position Overview:
~ Handling assigned activities in the regulatory department.
Experience:
~5-8 years
Qualification:
~ B. Pharm, M.Pharm preferred.
Responsibilities:
Identify the required documentation for EU regulatory submissions and compilation...
