Research Associate Cadila Pharmaceuticals Limited

2.0 - 6.0 years

0 Lacs

gujarat

On-site

As a part of this role, you will be responsible for sample preparation, daily calibration, and the maintenance of equipment, including keeping a detailed log of all activities. You will also be involved in method development, method validation, and conducting sample analysis in accordance with ICH M10 guidelines. Operating, maintaining, and calibrating LCMS equipment will be a crucial part of your responsibilities. In addition, you will be required to adhere to documentation procedures as outlined in Bio analytical SOPs and ICH M10 guidelines. This will involve thorough record-keeping and ensuring all documentation is accurate and up to date. Furthermore, you will be expected to review data and reports to ensure quality and compliance with relevant standards. Your attention to detail, ability to follow guidelines meticulously, and commitment to maintaining accurate records will be essential for success in this role. If you are looking for a position that offers diverse responsibilities in a dynamic environment, this opportunity may be the perfect fit for you.,

Posted 1 week ago

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Technical Reviewer Sgs India

3.0 - 6.0 years

3 - 6 Lacs

Gurgaon, Haryana, India

On-site

Review social audit reports as per various standards, schemes, and codes of conduct of retailers Ensure timely completion and delivery of audit report reviews within defined TAT Conduct technical reviews of social audit reports professionally Follow guidelines, SOPs, and requirements of multiple standards and schemes Maintain quality and accuracy in report assessments Align review work with internal processes and client expectations

Posted 4 weeks ago

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Technical Reviewer SGS India

3.0 - 6.0 years

5 - 11 Lacs

Gurugram

Work from Office

Opportunity for the position of Technical Reviewer (Social Audits) | Location - Gurgaon Company Profile: Established in 1878, SGS transformed grain trading in Europe by offering innovative agricultural inspection services. SGS is the world's leading inspection, verification, testing and certification MNC. We are recognized as the global benchmark for quality and integrity. With more than 96,000 employees, we operate a network of more than 2,700 offices and laboratories around the world. We cater quality services to 9 Businesses in India like Consumer & Retail Services, Oil & Gas, Industrial services, AFL, Minerals etc. Kindly visit our Global Website: www.sgs.com India Website: www.sgsgroup.in Brief Job Description: Review social Audit reports of various standards / schemes / code of conduct reports of various retailers within TAT. Key Results Areas ( KRAs) & Key Deliverables: Conduct Technical Reviews for Social audit reports professionally and in accordance with various standards /schemes / codes / SOPs requirements. Deliver audit report timely manner. Interested candidates request you to kindly share me your updated CV on fleur.dsouza@sgs.com

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Report Reviewer COD Research

3.0 - 5.0 years

7 - 9 Lacs

Ahmedabad

Work from Office

Position: Report Reviewer Department: Clinical Operations Location: Ahmedabad Key Responsibilities Prepare and finalize the visit report annotation as per protocol and study plans. Ensure finalization of the visit reports as per timeline mentioned in contract, study plans & SOPs. Effectively review trip reports as per annotated report, protocol & SOPs. Ensure the quality of reports are of the highest standards, consistent across sites and visits, errors are minimized and those issues are escalated as appropriate. To follow up on open action items and protocol deviations and coordinate with team for timely resolution of issues. To act as an extension of the CTM/CTM team for the specific purpose of visit report review To observe and escalate safety trends in patients as identified in visit reports Where required, attend project meetings and actively provide suggestions for improvement of quality of reports, provide feedback for timely and appropriate resolution of action items and report trends Ensure all necessary trainings, required to improve job performance and knowledge, are completed in a timely manner Any other responsibility assigned by HOD/Project Manager. Qualifications & experience required University Life sciences degree or related field. At least 3 to 5 years of clinical trial-related experience including on-site monitoring experience, CRO working experience is preferred. Adequate knowledge of new product development, including local regulation, GCP, clinical trial operations. Fluent written and verbal communication skills including good command of English language. Ability to handle conflicting priorities. Attention to detail and accuracy in work. Results-oriented approach to work towards delivery and output and strong problem-solving skills. Good software and computer skills, including MS Office applications including but not limited to Microsoft Outlook, Word, Excel and PowerPoint.

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