OECD GLP QA AUDITOR RIBOSOME RESEARCH CENTRE PVT. LTD.

0.0 years

0 Lacs

india

On-site

Company Description Ribosome Research Centre Pvt. Ltd. is a Global Contract Research Organization offering a comprehensive range of In Vitro & In Vivo Preclinical Services. Our services include Analytical Chemistry, Microbiology Services for Pharma, Medical Devices, Agrochemical, Specialty Chemicals, Cosmetics, and AYUSH Products. We are dedicated to providing a one-stop solution for all your research and development needs. Role Description This is a full-time, on-site role for an OECD GLP QA Auditor located in Kim, Surat. The OECD GLP QA Auditor will be responsible for conducting study based/process based/facility based audits to ensure compliance with Good Laboratory Practices (GLP). The a...

Posted 2 weeks ago

AI Match Score

Apply

Quality Assurance Inspector- GLP MS CLINICAL RESEARCH

8.0 - 10.0 years

0 Lacs

bengaluru, karnataka, india

On-site

Job Title: Quality Assurance (QA) Clinical Research Experience: 810 years Location: Indiranagar, Bangalore Department: Quality Assurance About the Role MSCR is seeking an experienced QA professional with strong expertise in ICH-GCP and GLP principles to ensure the highest standards of quality and compliance across clinical research and laboratory operations. The ideal candidate will be well-versed in regulatory guidelines, clinical QA processes, and GLP compliance, with proven experience in audits, CAPA management, and continuous quality improvement initiatives. Key Responsibilities Clinical QA (ICH-GCP Focus) Develop and maintain ICH/GCP-compliant processes to control the quality of work an...

Posted 3 weeks ago

AI Match Score

Apply

Quality Assurance MS CLINICAL RESEARCH

8.0 - 10.0 years

0 Lacs

bengaluru, karnataka, india

On-site

Posted 1 month ago

AI Match Score

Apply

OECD GLP QA AUDITOR RIBOSOME RESEARCH CENTRE PVT. LTD.

3.0 - 7.0 years

0 Lacs

gujarat

On-site

**Job Description** **Role Overview:** You will be working as an OECD GLP QA Auditor at Ribosome Research Centre Pvt. Ltd. in Kim. Your primary responsibility will be to conduct study-based, process-based, and facility-based audits to ensure compliance with Good Laboratory Practices (GLP). Additionally, you will review quality tools such as deviation, CAPA, and change control. Your role will also involve facing sponsor and regulatory inspections like OECD GLP, CDSCO, NABL, etc. Ensuring compliance with company standards and regulatory requirements will be crucial in this role. **Key Responsibilities:** - Conducting study-based, process-based, and facility-based audits to ensure compliance wi...

Posted 1 month ago

AI Match Score

Apply

Study Director (Acute Toxicology) JDM Scientific Research Organisation Pvt. ltd.

7.0 - 10.0 years

8 - 11 Lacs

Vadodara

Work from Office

Acute toxicity studies(Acute 6 Pack) as per OECD guidelines Acute Oral,/Dermal/Inhalation/Dermal Irritation/Eye Irritation/Skin Sensitization studies Handling animal species like Rat,Rabbit, Guinea Pig. Skilled in Dosing Prepare Reports & Study plans Required Candidate profile Exposure to OECD GLP Guidelines Knowledge of various Routes of Dosing. Skilled in preparing Reports and Study Plans.

Posted 4 months ago

AI Match Score

Apply

Start Your Job Search Today

Browse through a variety of job opportunities tailored to your skills and preferences. Filter by location, experience, salary, and more to find your perfect fit.