Average salary: Rs1,047,000 /yearly
More statsSearch Results: 221 vacancies
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...
#ROW MARKET #CIS #MENA #AFRICA #LATIN #ASIA #EUROPE MARKET
Vacancy - 15
Qualification - B.Pharm/M.Pharm
Job Description :
Sound knowledge of CTD/ECTD/ACTD dossier review of OSD/Parenteral dosage forms.
Excellent knowledge of ICH/Country specific/Variation...
...4. Completion and ensure dossiers submission in targeted timeline.
5. Dispatch of registration dossiers to the National Drug
Regulatory Authorities (NDRA)/agents as applicable.
6. Actively finding solutions on queries/feedback from
NDRA/agent for supplier...
...Dear Candidate,
Greetings from Pegasus Corporate!!
Location: Ahmedabad
Opening: Manager / Sr. Manager International Regulatory Affairs
Duties
1. Market : ROW, US & Europe Market
2. Exposure : Hands on experience in :
- New US ANDA dossier Preparation, compilation...
Rs 4.8 - 5 lakhs p.a.
...Mid-Level: 4 to 6 years of experience, Full-Time position in Ahmedabad
Qualifications and Skills:
Experience in regulatory affairs within the pharmaceutical sector
Knowledge of regulatory frameworks and guidelines
Strong understanding of regulatory documentation...
Rs 40000 - Rs 50000 per month
Designation :-Legal & Global Compliance Department :-Finance
Location :-Ahmedabad, Gujarat
Educational Qualification :-LLB/LLM with CS (preferred)
Professional Experience :-3 to 6 years
Key Responsibilities:
Review, draft and negotiate a variety of Commercial...
...Join our team at Scipex Consultants, a dynamic and rapidly growing consulting firm, as a Manager - Regulatory Toxicology. This role requires a high level of expertise in toxicology , particularly for cosmetics, consumer products, and OTC products along with a dedication to...
...protocols.
- Write, and edit clinical study protocols. clinical study reports, summary documents, investigator brochures, portions of regulatory briefing documents, and development safety update reports.
- Drafting and revising pre-clinical summaries.
- Quality control...
...ensuring alignment with brand messaging and regulatory requirements. Product Lifecycle... ...Development, Marketing, Sales, and Regulatory Affairs, to ensure alignment with organizational... ...developing and distributing pioneering oncology drugs and supportive anti-cancer medicines....
...intelligence through customer interaction,key opinion leaders, regulatory bodies and other sources
Develop strong relationships at key... ...operations, quality, product development, project management, regulatory affairs)
~ Excellent verbal and written communication skills to...
Rs 2 - 10 lakhs p.a.
...identify new opportunities, market trends, and competitive threats.
# Collaborate with cross-functional teams including sales, regulatory affairs, and product development to develop marketing materials and campaigns tailored to international markets.
# Manage...
Rs 3.6 - 4.8 lakhs p.a.
...for further details call Megha on (***) ***-**** or you can send your candidature on ****@*****.***
medical devices,Drug Regulatory Affair,CDCSO,ISO,Dossier,cardiac device
Designation: Jr. Manager RA OR Sr Executive RA
Vacancies: 1
Experience: 2.0 Year(s) -...
Rs 4 - 4.2 lakhs p.a.
...responsible for ensuring that a company complies with statutory and regulatory requirements and that decisions of the board of directors are... ...of CS
Company Secretary,board meetings,Regulatory Affairs
Designation: Company Secretary
Vacancies: 1
Experience:...
Rs 12000 - Rs 25000 per month
...pacemaker systems, including hardware, firmware, and software components.
- Collaborate with clinical experts, product managers, and regulatory affairs to define product requirements and specifications.
- Conduct feasibility studies, risk assessments, and validation tests to...
...launch process, ensuring alignment with project timelines, budgets, and goals. Coordinate activities across functions, including Regulatory Affairs, Manufacturing, Supply Chain, Marketing, Sales, and Medical Affairs.
Regulatory Affairs Support: Work closely with...
...Identifying potential suppliers capable of meeting the quality, regulatory, and supply requirements for FDF in regulated markets.
Assessing... ...internal stakeholders, including quality assurance, regulatory affairs, procurement, manufacturing, and logistics teams, to ensure...
...Procedures (SOPs), Good Clinical Practice (GCP), and the applicable regulatory requirement(s).
- Checking documents of CRO/Site internal... ...- To review all data produced from IB, SOPs of Different CROs, Drug Accountability Form, Periodic Visit Checklist, Inform Consent Form...
...BOQ/BARCHART/BOM/MENPOWER SCHEDULE ETC)
Coordination with all consultant and various agencies and facilitate them in day to day affairs for plan deliverance of assigned task
Checking of quality parameters and ensure workmanship in respect of structural civil electrical...
...distribute information about our products to the physicians. You should also try to convince doctors to prescribe more of our companies drugs.
You will act as a key link between a company and healthcare experts aiming at meeting our sales targets.
If you consider...
...activities.
• Maintain the MIS sheet with respect to various agreements compliances nd other legal activities on day to day affairs.
• Intellectual property rights registration and protection.
• Filinhg of Legal documents and MIS management....
