Nectar Lifesciences Ltd Walk In Interview 2022. Nectar Lifesciences Ltd Notification full details below..Interested and eligible candidates Submit Resume. Nectar Lifesciences Ltd, we go much beyond addressing the financial needs of our customers. We give them reasons to strengthen their trust in us, at every step. This belief has paid us rich dividends, bringing with it steady growth, rapid expansion and an opportunity for you to propel your career further.
Vacancy details:
- Post Name: QA Sr. Manager/Validation Manager/QA Analytical Data Reviewer
- Qualification: MSc/B Pharma/M Pharma
- Experienced:10- 17 years
- Openings: NA
Job Description: Nectar Lifesciences Ltd Hiring For QA Sr. Manager/Validation Manager/QA Analytical Data Reviewer !
Important Details :
- Location: Visakhapatnam, Hyderabad/Secunderabad, Mandideep, Ahmedabad
- Post of date:12/09/2022
- Selection Process: The selection will be on the basis of Interview.
- Interested candidates can send their CV on hr@neclife.com, rakesh.sharma@neclife.com
Job description
For Senior Manager QA :
1) MSc/B Pharma/M Pharma having 15 to 20 Years experience in Sterile manufacturing ( API & Injectables)
2) Good experience for QMS i.e investigations , market complaints, OOS, deviations etc
3) Good knowledge on GMP SOPs, regulatory guidelines as per US and Europe.
4) Good experience on aseptic practices , media fill, smoke study for Sterile manufacturing and QA controls
For Validation Manager :
1) MSc/B Pharma/M Pharma having 12 to 15 Years experience in Sterile manufacturing ( API & Injectables)
2) Good experience for validations & Qualifications i.e Process Validations, Equipement qualifications, cleaning validations etc
3) Good knowledge on regulatory guidelines requirements for US and Europe market
4) Good experience on aseptic practices , media fill, smoke study for Sterile manufacturing and process controls
For QA analytical data Reviewer :
1) MSc/B Pharma having 8 to 10 Years experience in Quality Control as doer and reviewer.
2) Good experience for QMS i.e Lab investigations,market complaints analytical part,OOS, deviations etc
3) Good knowledge on GLP, 21 CFR Part 11 as per US and Europe guidelines.
4) Good experience on Chromatography, Laboratory instruments, review of QC raw data, Instrument calibrations etc
