Intas Pharmaceuticals Ltd Walk-In Interview for QA Department
IF YOU HAVE THE AMBITION, WE HAVE THE POSITION
Join a leading global pharmaceutical organisation
As one of the world's leading pharmaceutical companies, Intas is committed to fulfilling the unmet global medical needs through comprehensive, progressive and affordable medical products. To fuel its ever- expanding vision, Intas Pharmaceuticals is looking for elite professionals aiming to take their careers to the next level through the following positions.
WALK-IN INTERVIEW
Position: QA LEAD ROLE
Qualification: M.Pharm, B.Pharm
Experience: 1 to 5 Years
Job Description:
• To ensure compliance for QA functions being supported from India-QA team To Co-ordinate with CMOs for resolving queries related to batch release and compliance activities
Review and approval of CRF, deviation, Investigation, OOS, Market complaints and CAPA.
Review and approval of master batch documents (BMR/BPR) on the behalf of Accord MAH.
To participate in performing GMP compliance audit at CMOs sites as per the schedule. To support the
Accord as lead auditor in the function of GMP audit and compliance.
To review and approve Complaint investigation Report, To ensure the complaint response time is
maintained and critical complaints are tracked and escalation to senior management where needed.
To address complaint response time management including Agency complaints
Review and approve the periodic trend of CRF /Temp. excursion and market complaint and to escalate to
senior management.
Leading the team of OA India team for quality function. Establishes quality and reliability standards with other members of management QPs, and with QA team.
Implement Quality Management System (QMS) as per the organization need. To participate monthly QMS meeting and to update on the department functions and outcome.
• Maintains product quality and release by enforcing quality assurance policies and procedures and GMP requirements.
• To plan and develop strategy for new product and launch support for test and release aspects through coordination with CMO/BTS and BRS. To plan the AMT and monitor timely closure of the activities.
To establish the relationship with the CMO and to be a bridge between Accord and CMO and to lead the quality function with CMO
Completes quality assurance operational requirements by scheduling and assigning employees, following
up on work results.
•Perform audits of API sites, Contract Testing Laboratory, Release site, Manufacturing site and Warehouse and ensure recommendations are complied with.
Ensure POR team function as intended. To approve schedule, OOT report and monitor compliance.
Please carry your updated resume all educational, experience & salary documents Candidates who have appeared for an interview at Intas in the last six months are requested not to apply
Only candidates having experience in globally regulated plants (USFDA, MHRA, etc.) should apply
All candidates must adhere to COVID-19 guidelines during the interview process (Wearing of mask Social Distancing, Sanitization of Hands, etc.)
Date: 10" Dec, 2022 (Saturday) &
13 Dec, 2022 (Tuesday)
Time: 10:00 am to 01:00 pm
Venue: Intas Pharmaceuticals Ltd. Corporate House, Near Spla bridge. S.G. Highway, Thaltej, Ahmedabad, Gujarat, India-380054.
JOB LOCATION INTAS CORPORATE OFFICE, AHMEDABAD
Please Note: Intas Pharmaceuticals Ltd. does not directly or indirectly charge any fee for job application, processing, training or testing. Do not participate in any such invitations
INTAS PHARMACEUTICALS LTD.
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