Job Description

Quality Controller Assurance Analyst for pharmaceutical testing lab

Quality assurance professionals in the pharmaceutical industry have a wide range of responsibilities. Their main duties include developing and implementing quality management systems, conducting audits, SOP preparation and inspections, reviewing and approving standard operating procedures, and ensuring compliance with regulatory requirements. They also play a key role in investigating and resolving quality issues and implementing corrective actions to prevent reoccurrence.

Another important responsibility of quality assurance professionals is to stay up-to-date with the latest industry trends and regulatory changes. This involves continuously monitoring and analyzing new regulations, guidelines, and best practices to ensure that the quality assurance processes and systems are in line with the current standards. By staying informed, they can proactively adapt and improve the quality assurance practices to meet the evolving requirements of the pharmaceutical industry.

Responsible for review of all analytical reports, usage log books IQ, OQ, PQ and external and internal calibration reports of Laboratory instruments and Analytical method validation/verification protocols & reports.

• Issuance of raw data sheets (Analytical reports, Calibration reports, etc.), usage log books and review of the same.
• Responsible for SOP, SOP annexures and log book formats preparation, implementation, issuance, retrieval and archival.
• Responsible for handling of QMS (Incidents, Change controls, deviations investigations related to Quality control and closing the same in stipulated times.
• Maintenance of laboratory procedures in accordance with Good Laboratory Practice (GLP) and Good Document Practice (GDP)
• Responsible for conducting Induction programme and training to new employees.
• Responsible for conducting periodic internal audit.
• Responsible for allotting equipment ID and maintenance of calibration schedule of instruments.
• Responsible for data handling, storage, archival and retrieval of documents.
• Responsible for review and compilation of stability data.
• Responsible for regular QA checks in laboratory.

Job Type: Full-time

Pay: ?15,000.00 - ?30,000.00 per month

Schedule:

• Day shift

Education:

• Education: Diploma in Pharmacy (D.Pharm) / Bachelor of Pharmacy (B. Pharm) or Bachelor Degree (B.Sc) Chemistry / Master Degree (M.Sc) Chemistry or Any Related Degree

Experience:

• Experience : 1 - 2 Years
• Quality assurance: 1 to 2 years (Required)
• Industry Type: Manufacturing / Production / Quality

Work Location: In person

Speak with the employer
+91 81448 82555 (Call or Send CV -WhatsApp)

Job Types: Full-time, Permanent

Pay: ?15,000.00 - ?25,000.00 per month

Schedule:

• Day shift

Supplemental Pay:

• Performance bonus

Experience:

• total work: 1 year (Preferred)

Work Location: In person