10.0 - 12.0 years

0 Lacs

india

On-site

Cargill's size and scale allows us to make a positive impact in the world. Our purpose is to nourish the world in a safe, responsible and sustainable way. Cargill is a family company providing food, ingredients, agricultural solutions and industrial products that are vital for living. We connect farmers with markets so they can prosper. We connect customers with ingredients so they can make meals people love. And we connect families with daily essentials from eggs to edible oils, salt to skincare, feed to alternative fuel. Our 160,000 colleagues, operating in 70 countries, make essential products that touch billions of lives each day. Join us and reach your higher purpose at Cargill. This po...

Posted 1 day ago

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Senior Quality Engineer ( Noida NSEZ ) Sr Jobs Solutions

8.0 - 13.0 years

1 - 4 Lacs

noida

Work from Office

10 hours duty No Canteen Face to Face interview only 2D Autocad drawings In process inspections & documenting inspection audit & verifications self caliberations of gauges, fixtures in the factory Man & team handling , system adherence

Posted 1 month ago

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Quality assurance & Regulatory Affairs Acumont Solutions

6.0 - 11.0 years

7 - 15 Lacs

Hyderabad, Chennai, Bengaluru

Work from Office

Hiring QA & RA with an leading IVD Company in Hyderabad Exp: 6+ Yrs in QA & RA, ISO 13485 Mandatory Stability & immediate joiner with Biotech background Candidate With medical Device background can apply share resume at sarika.bhandari@acumont.com

Posted 3 months ago

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Auditor COD Research

3.0 - 6.0 years

4 - 8 Lacs

ahmedabad

Work from Office

Position : Auditor Department : Quality Assurance Location : Ahmedabad Key Responsibilities Plan & conduct the Study audits as per audit plan in compliance with internal procedures, protocol and applicable regulatory requirements Plan and conduct Investigator site audit, file/document audit for Clinical Trial Projects to ensure compliance with SOPs, Protocol, ICH GCP, quality system and applicable regulatory requirements. Review study documents like Protocol, Study plans, Informed Consent Document, Case Report Form, Clinical Study Report, Data Management etc. to ensure compliance, correctness and adequacy with ICH GCP and other applicable regulatory requirements Assist in facilitating the sp...

Posted Date not available

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