• Quality Oversight: To comply with regulatory standards and internal quality procedures throughout the pharmaceutical manufacturing process.
• Documentation Control: To maintain all quality-related documents, including SOPs, batch records, and quality manuals.
• Quality Systems Improvement: Suggest new opportunities for continuous improvement in quality systems and processes.
• Training and Development: maintain and Foster a culture of quality consciousness.
• Product Release: Aiding in the release of finished products, ensuring they meet quality specifications before distribution.
• Validation and Qualification: Abetting in validation and qualification activities for equipment, processes, and systems.
• Regulatory Compliance: Stay abreast of changes in regulatory requirements, communicating updates to relevant stakeholders and implementing necessary changes.
Must have a good hands on knowledge of QMS.
Job Type: Full-time
Pay: ?20,000.00 - ?45,000.00 per month
Schedule:
• Day shift
• Night shift
Application Question(s):
• How many years of Pharmaceutical Manufacturing / Production do you have
Education:
• Bachelor's (Preferred)
Experience:
• QMS: 3 years (Preferred)
Work Location: In person
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