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6.0 - 11.0 years
4 - 9 Lacs
Bharuch, Ahmedabad, Vadodara
Work from Office
Hiring for RA Executive / AM For Pharmaceutical-Formulation Qualification: Bsc/B.PHARMA Experience: 7 to 15 Years CTC: 10.0 LPA Send CV on sdpbharuch@gmail.com sub With : RA Vadodara Free Job Share with your Friends & Colleagues!! Required Candidate profile Join Our WhatsApp Group: https://chat.whatsapp.com/EMLcH2RoVs1AzcbRKmZkjZ Follow Our WhatsApp Channel: https://whatsapp.com/channel/0029VaDwTZoHgZWddec9BL0y
Posted 3 days ago
12.0 - 16.0 years
0 Lacs
haryana
On-site
As the DM- Regulatory Affairs at Olympus Medical Systems India Private Limited, your primary responsibility will be to oversee Indian regulatory affairs activities related to Gastrointestinal (GI) & Olympus products. You will also be responsible for advising and consulting with stakeholders about compliance with CDSCO, BIS, WPC, and other applicable regulatory bodies. Your role will involve implementing best practices and contributing to both the strategic and operational functions of the regulatory affairs team. Your key responsibilities will include assessing regulatory intelligence to assist in the development of local, regional, and global regulatory strategies. You will evaluate the regulatory environment and provide internal advice throughout the product lifecycle to ensure product compliance. Anticipating regulatory obstacles and emerging issues, you will develop solutions and identify requirements and potential obstacles for market access distribution. Furthermore, you will assist in the development of regulatory strategy, update strategy based upon regulatory changes and evaluate proposed products for regulatory classification and jurisdiction. You will determine requirements for regulatory submission, approval pathways, and compliance activities while providing regulatory information and guidance for product development and planning. In addition, you will compare regulatory outcomes with initial product concepts, negotiate with regulatory authorities, and identify the need for new regulatory procedures. You will help train stakeholders on current and new regulatory requirements, provide regulatory input on global regulatory requirements to product development teams, and advise stakeholders of regulatory requirements for quality, preclinical, and clinical data. You will also be responsible for assessing the acceptability of quality, preclinical, and clinical documents for submission filing, evaluating proposed changes for regulatory filing solutions, and monitoring the progress of the regulatory authority review process. Communication and interaction with regulatory authorities before and during the development and review of regulatory submissions will be crucial aspects of your role. To be considered for this position, you are required to have a qualification of M. Pharma/B Pharma along with a PG Diploma in Drug Regulatory Affairs. The preferred experience includes 12 to 15 years of working experience in a customer-oriented position in an international organization. Proficiency in MS Office, particularly Excel, and fluency in oral and written communication in English are essential. Key competencies for this role include business acumen, customer focus (internal and external), execution excellence, domain expertise, effective communication, developing organizational talent, and team leadership. By applying your expertise and knowledge, you will play a vital role in ensuring regulatory compliance and contributing to the success of Olympus Medical Systems India's regulatory affairs team.,
Posted 5 days ago
10.0 - 15.0 years
18 - 20 Lacs
Bengaluru
Work from Office
1. Property Identification & Sourcing Conduct market research to identify potential land parcels suitable for villa and high-rise apartment development, ensuring alignment with company goals. 2. Site Evaluation & Feasibility Analysis Assess the viability of properties by analyzing location, zoning regulations, legal clearances, and infrastructure availability. 3. Landlord & Broker Coordination Build and maintain strong relationships with property owners, brokers, and developers to negotiate the best acquisition terms. 4. Due Diligence & Documentation Oversee the verification of property titles, ownership records, legal disputes, encumbrances, and compliance with local laws. 5. Negotiation & Deal Closure Lead negotiations with property owners, ensuring favorable purchase terms and finalizing agreements in line with the company's budget and project plans. 6. Liaison with Legal & Regulatory Authorities Work closely with legal teams, government agencies, and consultants to ensure smooth approvals, permits, and compliance with all statutory requirements. 7. Reporting & Stakeholder Communication Prepare and present reports on market trends, potential acquisitions, and ongoing negotiations to senior management. 8. Signing & Handover Coordination Oversee the execution of agreements, registration formalities, and smooth transition of acquired land for project commencement.
Posted 1 week ago
1.0 - 3.0 years
1 - 3 Lacs
Hyderabad, Chennai, Bengaluru
Work from Office
Environmental Health Officer Job Title : Environmental Health Officer Location : Chennai, Hyderabad, Bangalore Experience : 1-3 Summary: Ensures that construction and real estate projects comply with health, safety, and environmental regulations. Key Responsibilities: Conduct site inspections and audits. Monitor compliance with health and safety laws. Investigate incidents and recommend corrective actions. Provide training on environmental health practices. Prepare reports and liaise with regulatory authorities. Skills & Qualifications: Degree in Environmental Health, Public Health, or Safety Management. Certification in occupational health and safety (e.g., NEBOSH). Strong knowledge of environmental regulations. Attention to detail and investigative skills.
Posted 1 week ago
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