Average salary: Rs1,047,000 /yearly
More statsSearch Results: 233 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
Experience :- 3 to 12
Job Description :
Sound knowledge of CTD/ECTD/ACTD dossier review of OSD/Parenteral dosage forms.
Excellent knowledge of ICH/Country...
...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...
...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...
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...
...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...
...using the advanced and latest technology in the development of drug, medicines, and pharma products. The Role
You will be responsible... ...and corporate records.
Compliance advisory to ensure regulatory and statutory requirements are met.
Ideal Profile
You have...
Rs 4 - 7 lakhs p.a.
...Specialist Responsibilities:
Ensure product quality and conformity to regulatory standards, including Medical Device Regulation (MDR) and Quality... ...for compliance.
Documentation Executive,QA,Regulatory Affair
Designation: QA & RA Associate
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...
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:...
...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...
...competitive intelligence through customer interaction key opinion leaders regulatory bodies and other sources
8. Develop strong relationships at... ...quality product development project management regulatory affairs)
~ Excellent verbal and written communication skills 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...
...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...
...a Sr. Manager - Legal at Karnavati University located in Ahmedabad. The Sr. Manager - Legal will be responsible for overseeing legal affairs, providing legal consulting, ensuring legal compliance, and preparing legal documents.
Qualifications
Expertise in Law, Legal Consulting...
Karnavati University (KU)
Ahmedabad
1 day ago
...Candidates should have minimum 5-10 years of experience in PAN INDIA marketing of bulk drugs API Job Profile:
· Responsible for looking after Marketing activities for Bulk Drugs (API).
· Grow the business by developing strategies, using current and new contacts to expand...
