Akums Drugs & Pharmaceuticals Limited Released Job Openings On 05/07/2022.Akums Drugs & Pharmaceuticals Ltd., is largest contract manufacturing company engaged in manufacturing of pharmaceutical formulation, ayurvedic/herbal preparations, hormones, nutraceuticals and more.
Vacancy Details:
Akums Drugs & Pharmaceuticals Limited Recruiting B.Pharma,M.Pharma,M.Sc with 12-15 years of Experience for Quality Assurance – Other Position.Complete Details for the Quality Assurance – Other as follows.
Important Details :
- Location :Haridwar
- No of Vacancies:NA
- Details of Salary: Not Disclosed by Recruiter
- Opening date for online Application: 05/07/2022
- Mode of application :Online
- How To Apply: At the End of the Article We Have Provided Source Link,Please Go through that and Follow Necessary Steps
Related Job : QC,QA,TSD,SRP,EHS,IT,Engineering,Fire Safety Immediate Openings At Venkata Narayana Active Ingredients
IQVIA,Cognizant,Dr. Reddys,Troikaa,Hikal,Aurobindo,Hetero Latest Openings
Job Description/Skills Required
- Review verification and monitoring of the laboratory and its compliance.
- Review of all laboratory OOS, OOT, change control, deviation & Laboratory incident.
- Verification of good laboratory practices and good documentation practices in the laboratory.
- Review STS and STP of Raw material, Packing material, In-process & Finished products, Stability data.
- Verification of all electronic data and audit trails of all instrument in the quality control laboratory.
- Review Analytical method validation protocol & report.
- Review Audit compliance for Quality Control department.
- Audit trial review and software related activities.
- Review analyst qualification and instrument qualification, calibration. Review & ensuring that Calibration and Qualification of all Quality Control instrument is done as per pre-determined schedule.
- Monitoring of Preventive maintenance of all Instruments/ Equipments.
- Review of outside party calibration, qualification with certificate.
- Review Micro related activities.
- Aware about regulatory requirements.
- Monitor Good Laboratory Practices (GLP) & Good Documentation Practices (GDP) in Laboratory.
- To review the calibration data, working standard qualification data and analytical reports of Finished product, semi-finished, Stability & others samples tested in Quality Control department.
- Trained all persons on various analytical techniques as well as on the various aspects of GLP and GMP practices, effective quality control processes, Skill development and update all persons about the Audits Critical observations & DI Challenges.
- Monitor stock of spare parts of Instruments as per requirement.
- Monitor Primary Standard, Reference Standard, Impurities, HPLC columns, and Chemical / reagents.
Click here for Official notification and ApplyÂ
