Average salary: Rs923,750 /yearly
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Job Title
Regulatory Affairs Manager
Job Description
Job Description
Business Title: Manager - Regulatory affaire
In this role, you have the opportunity to make life better.
Looking at the challenges the world is facing today Philips...
Job Description
JOB DESCRIPTION
Regulatory Affairs 3-4 years Experience Medical Devices & Drug productsSummary:
Under general supervision responsible for the coordination and the preparation of documents/packages for regulatory submissions. Review and evaluate technical...
...Regulatory Consultant
Syneos Health® is a leading fully integrated biopharmaceutical solutions... .... We translate unique clinical, medical affairs and commercial insights into outcomes to... ...medical writing-related field. Moderate pharmaceutical/medical device related experience....
...Should have good knowledge and experience of BIS (Bureau of Indian Standardization).
Regulatory Affairs:
1. Proactive planning for all regulatory submission as per business requirement & new requisition received from Spain.
2. Compilation and review of the registration...
...framework or protocols for strategic analysis
Experience
4-7 years of experience in similar/allied role in Advisory organization or Pharmaceutical Industry
Educational Qualifications
Graduate/Post- graduate with a management degree from a reputed institute
Pharm/M....
Rs 10 - 13 lakhs p.a.
...Qualification:
MBBS/BDS/PhD/Master’s in Pharmaceuticals, with relevant post-qualification... ...Good to have:
Should understand the regulatory climate relevant to OTC/Rx space esp. in... ...Designation: CDMA | Clinical Development Medical Affairs
Vacancies: 5
Experience: 5.0 Year(s...
Rs 2.5 - 6.5 lakhs p.a.
...the work progress to your line manager in 1:1 in weekly/ monthly meetings and other stakeholders appropriately as and when advised
Regulatory,R&D,Drug Regulatory Affair
Designation: Data Scientist - Regulatory
Vacancies: 1
Experience: 1.0 Year(s) - 7.0 Year(s)...
...procedures, work-instructions etc. as needed.
• Bridge gaps when new regulatory systems with clinical requirements go live (e.g., EUDAMED)
•... ...of various clinical forums including SCAN (Stryker Clinical Affairs Network) and EUMDR clinical monthly meetings.
Education & Work...
...Oppo India is hiring for Manager - Public Affairs. Experience - 10-12 Years
Education - Graduate/Post Graduate - Full Time
Location... ...as ICEA, CII, MAIT, PHD Chamber of commerce etc. to monitor regulatory changes and represent the interest of the company.
Develop and...
...Responsibilities
Job Responsibilities
Provides vision, leadership, and strong strategic direction to the Division of Student Affairs in supporting the academic mission of the University.
Provides strong, creative, energetic, and strategic leadership to design and...
...Regulatory Reporting-
Role Description
Role will provide Execution Support to IRR-PRA Workstreams
Key Responsibilities • Support management in the execution of IRR standards for Large Exposure Returns in scope of PRA Workstreams. • Support where required the successful...
Rs 20 - 30 lakhs p.a.
...Primary Role Description:
Compliance Manager is responsible for driving compliance culture and ensuring checks and controls for regulatory requirements.
Key Roles & Responsibilities:
· To identify new laws and regulations applicable to the Company and achieve its implementation...
Rs 7 - 11 lakhs p.a.
...Description : Design, build and configure applications to meet business process and application requirements. Must have Skills : SAP EHS Regulatory Compliance Good to Have Skills : No Technology Specialization Job Requirements : Key Responsibilities : a Candidate should be able...
...Hiring for a Leading Hospital Brand for Head of Content/Editor - Strong Pharmaceuticals OR Healthcare Background
~ Gurugram Location
~6 Days Working
~ Must Have experience in Journalism Background
~ Should have strong Pharmaceuticals OR Healthcare Background...
...Job Title: Lead Medical Affairs
Location: Gurgaon India and Bangalore
Experience: 2 to 3 years in medical affairs with a hospital... ...teams including product management marketing sales and regulatory affairs to ensure alignment on medical strategy and messaging....
Job Description :- Minimum 7 years in Pharmaceutical/Biotechnology/Medical Device industry or equivalent- Experience with requirements gathering, design and specification development of eCRFs, edit checks, and understanding of database structures and programming languages- Knowledge...
...be directly responsible for the following:
Management of a complete and consistent traceability data model framework for in scope regulatory returns including system changes and enhancements, thereby, ensure data integrity across the return.
Govern delivery through KPIs...
...Director - Regulatory Compliance Solution (Anti Bribery Anti-Corruption)- CPG050797
Genpact (NYSE: G) is a global professional services and solutions firm delivering outcomes that shape the future. Our 125,000+ people across 30+ countries are driven by our innate curiosity...
...to drugs and always derive and communicate the changes to the relevant and responsible managers of the organization
Should be well verse with the Labelling requirements as per the Drugs Act
Skills Required : "quality", "Regulatory", "q
Experience : 3 to 5 Years
...Senior Manager - Regulatory Reporting CTB - BFS028693
With a startup spirit and 115,000+ curious and courageous minds, we have the expertise to go deep with the world’s biggest brands—and we have fun doing it. We dream in digital, dare in reality, and reinvent the ways companies...
...Business Analyst
Regulatory Operations is a wide-reaching team responsible for transaction reporting for our derivatives businesses, covering all asset classes across the North Americas and APAC regions. In parallel with delivering regulatory changes, the team also provides...
...of choice for our clients outside and our network inside the pharmaceutical and biotech industry? Are you a curious and committed person... ...Industry, Patents search, Clinical trials, and Regulatory affairs….
· Ability to work collaboratively in a team environment...
...professional mastery of a specialized field of regulatory expertise that typically requires a... ...or equivalent experience within a pharmaceutical and/or medical device company, or similar... ...Advanced Degree (Masters in Regulatory Affairs) preferred. Demonstrate knowledge and skills...
...General Counsel,you will handle all corporate, compliance, and regulatory matters, including contract negotiation and management; advising... ...meet statutory requirements and advise on corporate governance affairs.
Regulatory Affairs: Monitor and analyze changes in laws that...
...Proven expertise in management consulting in the life sciences, pharmaceutical/biotech consulting industry or equivalent industry role... ...with one or more R&D operational roles (clinical operations, regulatory, safety or similar discipline) either in industry or consulting...
...leading source of analysis on international business and world affairs. We deliver our information through a range of formats, from newspapers... ...informed about emerging cyber threats, industry trends, and regulatory requirements to ensure the relevance and accuracy of awareness...
...interested in working at one of the World’s Best Workplaces, apply now !
Need another reason to apply? Here are 10 reasons to join our Regulatory Affairs/Quality Assurance team:
Objective –
This position is responsible for two areas:
1.Driving government affairs and market...
...Compliance and Reporting:
o Ensure compliance with all regulatory requirements and company policies.
o Provide regular and... ...related field. MBA is a plus.
·Minimum [X] years of experience in pharmaceutical sales, with a focus on PCD.
·Proven track record of...
...leading source of analysis on international business and world affairs. We deliver our information through a range of formats, from newspapers... ...strategies and policies.
Ensure compliance with applicable regulatory and legal requirements, as well as industry standards and best...
...documentation is consistent with eTMF specifications, ICH-GCP guidelines, regulatory requirements, and applicable SOPs
Address eTMF questions... ...clinical research and TMF experience at a biotechnology, pharmaceutical company or CRO required
~ Previous experience working in...