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...
...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...
...submission.
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’s...
...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...
Rs 15 - 18 lakhs p.a.
...Handling of CAPA and tracking
Handling queries of Customer & Regulatory Affairs
Preparation, review and approve of various master documents... ...and archive.
Prepare the Regulatory related documents i.e. Drug Master file and other regulatory
required compliance...
...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....
...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 - 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 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 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...
...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...
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...
...accurate filing of tax returns, including GST, income tax, and other regulatory filings.
Bank Reconciliations : Manage bank accounts,... ...portion of this role will involve liaising with banks and financial institutions to manage the company's financial affairs effectively....
...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...
...Act as a trusted advisor to GCC management with respect to legal, regulatory and compliance risks on major business decisions, projects and... ...collaboration with other risk and control functions including legal affairs, ethics & compliance, regulatory affairs, government affairs,...
...Founded in 1968 Oriel STAT A MATRIX is a leading global organization providing consulting and training services to the Regulatory Affairs and Quality Assurance functions within the Life Science industry. We are proud of our focus on client outcomes: we achieve superior client...
...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...
...accommodation,
tickets, etc.)
Provide full administrative and secretarial support to the MD to ensure smooth
management of day to day affairs and most effective use of time.
Chasing input and feedback for all open actionable points.
Organise meetings and ensure all...
...Responsibilities:
Develop and execute strategic marketing communication plans in collaboration with the Head of Marketing & Clinical Affairs and Vice President of Global Strategy.
Oversee and supervise the work of SEO agencies, ensuring alignment with organizational...
