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2.0 - 6.0 years
0 Lacs
meerut, uttar pradesh
On-site
Your main responsibility will involve developing and implementing safety policies and procedures to ensure the protection of employees from injury and illness. You will be required to conduct regular inspections of working conditions and safety equipment to identify potential risks. In the event of accidents, you will investigate the incidents, assist injured individuals, and work towards improving safety measures in the area. Monitoring compliance with safety regulations by employees is also an essential aspect of this role. Additionally, you will be responsible for preparing and delivering training on emergency procedures, workplace safety, and other relevant topics. It will be your duty to maintain records, ensuring that material safety data sheets are up to date and easily accessible. Developing environmental management plans that adhere to all environmental regulations and laws will also fall under your purview. As a part of this position, you will manage and train other health and safety staff members while responding to incident reports and conducting field investigations. The role requires a total work experience of 2 years, and the work location is in-person. The application deadline for this full-time position is 04/10/2025.,
Posted 3 days ago
2.0 - 5.0 years
5 - 12 Lacs
mumbai, hyderabad, ahmedabad
Work from Office
Detailed Job Role Ensure regulatory compliance, prepare documentation for approvals, monitor regulatory changes and communicate with authorities. KRA (Key Responsibility Areas) Documentation submission, monitoring compliance, advising teams, record management KPI (Key Performance Indicators) Submission success rate, audit results, documentation accuracy, response time Job Summary: We are seeking a detail-oriented Regulatory Affairs Executive to ensure regulatory compliance, prepare documentation for approvals, and liaise with regulatory authorities. The ideal candidate will monitor regulatory changes, advise internal teams, and maintain accurate records to support product approvals and compliance. Key Responsibilities: Prepare and submit regulatory documentation for product approvals and registrations. Monitor regulatory changes and ensure organizational compliance. Advise internal teams on regulatory requirements and product compliance. Maintain records of submissions, approvals, and communications with authorities. Support audits and inspections by regulatory bodies. Collaborate with R&D, QA, and production teams to ensure regulatory alignment. Key Performance Indicators (KPIs): Success rate of regulatory submissions Compliance during audits and inspections Accuracy and completeness of documentation Timeliness of responses to regulatory queries Skills & Competencies: Strong knowledge of pharmaceutical regulations and submission processes Attention to detail and strong documentation skills Analytical and problem-solving abilities Effective communication and collaboration skills Proficiency in regulatory tracking tools and MS Office Education - B.Pharm,M.Pharm, M.Sc (Life Sciences)
Posted 4 days ago
5.0 - 9.0 years
0 Lacs
hyderabad, telangana
On-site
As a Quality Control Manager, you will be responsible for understanding customer and stakeholder requirements in order to develop effective quality control processes. You will devise specifications for products and processes, set raw material requirements for suppliers, and monitor their compliance. Additionally, you will conduct an assessment of the company's production processes and develop in-house quality policies to ensure compliance with both local and global production standards. Collaboration with quality personnel will be essential for the implementation of systems, procedures, and standards of operation. You will also be responsible for conducting quality audits to ensure adherence to quality policies, as well as training quality assurance personnel to build a strong work unit. Establishing procedures for sampling, recording, and reporting data will be a key part of your role. This is a full-time position that requires a minimum of 5 years of experience in quality control, preferably in the glass manufacturing industry. The work location is in person. If you have the required experience and expertise in quality control processes, we encourage you to apply for this exciting opportunity.,
Posted 1 month ago
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