18.0 - 25.0 years

0 Lacs

pune, maharashtra, india

On-site

Schaeffler is a dynamic global technology company and its success has been a result of its entrepreneurial spirit and long history of private ownership. Does that sound interesting to you As a partner to all of the major automobile manufacturers, as well as key players in the aerospace and industrial sectors, we offer you many development opportunities. Your Key Responsibilities Hand on experience in working closely with customer for technical agreements. Anaylitical Knowledge & Experience with problem solving techniques & methodology Well versed in conducting system, process & product audits within plants. Brief knowledge on application base relating to product commodities Conversant with 8...

Posted 2 days ago

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QA Doc Controller Ferring Pharmaceuticals

2.0 - 6.0 years

0 Lacs

hyderabad, telangana

On-site

You will be responsible for the issuance, control, and retrieval of documents. Your duties will also include scanning and uploading approved paper-based documents in Veeva Vault, as well as maintaining master copies for SOPs. Additionally, you will be involved in conducting and organizing training sessions, maintaining Vendor audit and Technical agreement planners, and preparing/reviewing SOPs, Protocols, and other cGMP documents. You will also be tasked with tracking Change control, CAPA, Deviation, OOS/OOT, and coordinating with stakeholders for timely closure. Location: Ferring India Laboratories,

Posted 1 week ago

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Team Member - QA Cipla

3.0 - 5.0 years

0 Lacs

india

On-site

Division Department Sub Department 1 Job Purpose Review the compliance level of site for deficiency response, prepare master validation protocol and report as per company quality policy and applicable regulatory guidelines Key Accountabilities (1/6) Collate, review and provide required work plans on received deficiencies to HO in order to respond to regulatory authorities in a timely manner Collect data from all SPOCs with respect to received work plan for review Escalate any delays in receiving response from unit with respect to work plan Review of collected data for work plan fulfilment Send data to HO for compilation of deficiency response Take follow up with HO to receive updated dossier...

Posted 2 months ago

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QA Doc Controller Ferring Pharmaceuticals

2.0 - 6.0 years

0 Lacs

hyderabad, telangana

On-site

As a Document Controller at Ferring India Laboratories, your role involves handling the issuance, control, and retrieval of documents. You will be responsible for scanning and uploading approved paper-based documents in Veeva Vault. Additionally, maintaining master copies for SOPs, including issuance, control, and retrieval of SOPs will be a key part of your responsibilities. Your key responsibilities will include: - Managing and conducting training sessions - Organizing training programs - Maintaining vendor audit and technical agreement planners - Preparing and reviewing SOPs, Protocols, and other cGMP documents - Tracking Change control, CAPA, Deviation, OOS/OOT, and coordinating with sta...

Posted 2 months ago

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