Sr. Executive/Asst. Manager - Production (QMS)
1 Nos.
144845
Full Time
5.0 Year(s) To 12.0 Year(s)
6.00 LPA TO 10.00 LPA
Production / Quality / Maintenance
Pharma/Biotech/Clinical Research
B.Pharma - Pharmacy; B.Sc - Chemistry; M.Pharma - Pharmacy
Job Description:
Position: Sr. Executive/Asst. Manager - Production (QMS)
Location: Ahmedabad
Experience: 5 - 12 Years
Industries: Pharma
Responsibilities
- Ensure effective implementation of QMS requirements within the Production department.
- Prepare, Review, initiate, investigate, and monitor deviations, incidents, OOS/OOT, change controls, CAPA, and risk assessments related to Production.
- Coordinate with QA, QC, Engineering, Warehouse, and other cross-functional teams for timely investigation and closure of quality events.
- Review and ensure compliance of BMR/BPR, SOPs, logbooks, formats, and other GMP documentation.
- Support preparation and review of Annual Product Quality Review (APQR/PQR) data related to Production.
- Monitor CAPA effectiveness and ensure timely closure of commitments.
- Conduct and support self-inspections, internal audits, customer audits, and regulatory inspections.
- Ensure timely implementation of audit observations and track action plans to closure.
- Participate in QRM/FMEA activities for manufacturing processes, equipment, and quality risks.
- Identify opportunities for process improvement, compliance enhancement, and reduction of recurring deviations.
- Review production trends, deviations, yields, rejections, reconciliation, and other quality-related performance indicators.
- Ensure adherence to data integrity, ALCOA+ principles, GDP, GMP, and documentation practices.
- Provide GMP/QMS training to Production personnel and monitor training effectiveness.
- Support implementation and periodic review of SOPs, Work Instructions, Master Documents, and other controlled documents.
- Ensure timely investigation and closure of market complaints, product quality issues, and regulatory commitments related to manufacturing.
- Maintain QMS trackers, dashboards, and periodic management reports.
- Ensure effective implementation of change management and assessment of changes impacting product quality and regulatory compliance.
- Coordinate with QA for batch review, investigation closure, and product disposition-related activities.
- Promote a strong quality culture and right-first-time approach within Production
Required Skills:
- Strong knowledge of Pharmaceutical QMS and GMP.
- Good investigation and root-cause analysis skills.
- Knowledge of 5 Why, Fishbone, FMEA, CAPA, and risk assessment.
- Good documentation and report-writing skills.
- Strong analytical and problem-solving capability.
- Effective coordination with cross-functional teams.
- Good communication and interpersonal skills.
- Ability to manage multiple QMS activities and meet timelines.
- Proficiency in MS Excel, Word, PowerPoint, and QMS/SAP systems.
Required Qualification: - B.Pharm/M/Pharm/B.Sc/M.Sc - Chemistry
Salary :- Upto 10.00 LPA
If you are interested for this opening please send updated resume on same mail with following details.
Total No. of Years Experience :-
Current CTC :-
Expected CTC :-
Notice Period :-
Company Profile
It is one of the leading pharma formulation client of quality hr services.
Apply Now
- Interested candidates are requested to apply for this job.
- Recruiters will evaluate your candidature and will get in touch with you.