Akums Drugs & Pharmaceuticals Ltd. is the largest contract manufacturing company engaged in the manufacturing of pharmaceutical formulation, ayurvedic/herbal preparations, hormones, nutraceuticals, and more. Quality, innovations & customer satisfaction are virtues at Akums. The approach is technologically driven to serve the emerging needs in the ever-expanding market. The 9 states of art facilities are dedicated to separate dosage forms across therapeutic segments. The infrastructure is equipped with sophisticated and ultra-modern equipment & machines, with huge manufacturing capacities in all sections. In our continuous pursuit of Healthier today and tomorrow, we are working towards redesigning global healthcare.
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When we work at Akums we work in a family. We are committed to providing a warm, friendly, and open working environment that encourages ideas and innovation. The focus is to allow everyone at Akums to enhance their creativity and think differently to create value. We have a deep belief in transparency and perennial growth for each one.
Nurturing an employee-centric work philosophy, we believe Â in unleashing the hidden potential of every dedicated member and in Â bringing out the best in each one by facilitating holistic growth.
Designation: Sr Executive/Asst Manager QA/Validation
Location: Haridwar, Uttrakhand, India
- Responsible for review of investigation related to Non-compliance, Deviation, Incident, NCR, OOS, OOT, laboratory incidents investigation and Risk Assessment report etc. in consultation with respective departments
- Responsible for participation in RCA (Investigation) of Incident, Deviation, NCR, Market complaints, Risk Assessment & Corrective & Preventive Action (CAPA).
- Responsible for Review and providing the inputs for further enhancement of all departmental SOPs.
- Monitoring of SOP / Logbook issuance, control, and retrieval in co-ordination with respective section Head / Department Head.
- To provide Training as per department Annual Training Calendar (ATC) or time to time Need-Based training (NBT) as per requirement.
- Responsible for monitoring of Qualification and Validation/Calibration activities, Quality Management System, Documents, and Data control
- Responsible for Review and timely completion of HVAC/Area qualification and equipment qualification in plant 4.
- Qualification of service providers and miscellaneous items.
- Responsible for compliance of Internal/external/Self-inspection/Regulatory audits.
- Responsible for Approval of Bound log book issuance slip, Document numbering & Issuance format, etc.
- Responsible for review of Audit data raw data and MetaData in the Quality control area
- Any other responsibilities assigned by senior from time to time.
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