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Posted on 30 Nov, -0001
- Determining and agreeing on in-house quality procedures, standards and specifications. Inspecting and setting standards for quality on a regular basis.
- Performing Quality Control review of documents, case report forms, protocols, informed consents, policies, procedures and reports of undertaken clinical studies.
- Ensuring tests are carried out as per appropriate standard specification and verifying the correctness of results. Conducting stability studies as per the regulatory requirements.
- Responsible for reviewing implementation, tracking and archival of SOPs, their distribution, monitoring and control. Evaluating and taking corrective actions whenever required.
- Performing Internal Audit on site - specific files, master files and various others as per the local and international guidelines and regulatory requirements.
- Responsible for approving sampling instructions, specifications, test methods and other quality control procedure.
- In-depth knowledge of Quality control of medical supplies;
- Ability to develop and institutionalize quality control processes;
- People Management skills;
- Knowledge of the India medical supplies (drugs and equipment) industry.
- Industry - PHARMACEUTICAL / MEDICAL DEVICES / CRO
- Functional Area - Quality - QC / QA / QMS / TQM / Lean / Six Sigma
- Job Role - QC Manager
- Employment type - Full Time
- Work Mode - In Office
- Any Graduate - Any Specialization
- MPharma - Any Specialization
- Any Doctorate - Any Specialization
Name - HR
Designation - HR
- ric.pharmaceuticals@gmail.com
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