Dear Candidate ,
As we discussed on call that Our Client THINQ Pharma having opening for QAMS for Pitampur Location.Plz go through JD and Company Detail and revert back ASAP with Updated Cv.
About Company
THINQ Pharma
THINQ Pharma is an integrated pharmaceutical company with broad global presence and world class products and services. Headquartered in Singapore and having a fully equipped Research Centre in Mumbai, India, we have a global market for 30 years Armed with a team of high skills, we provide comprehensive solutions in healthcare and wellness industries to improve people’s lives.
Website - https://thinqcro.com/
Home || Thinq harmaTHINQ represents creative amalgmation of Technology, Health, Innovation, Novelty and Quest. Technology that meets state-of-the-art. Read Morethinqcro.com
Location - Pitampur Location(Pithampur Industrial Area, Near Indo Rama Temple, Madhya Pradesh 454774)
THINQ House, A-30, Road No. 10,
MIDC, Wagle Estate,Thane - 400604, India.
Job Description: QAMS- QC
Handling Quality Management System (QMS) software for operating Change controls, Deviations, CAPA, LIR.
Ø Laboratory Incident Reports (Analytical incidences) has been adequately investigated and documented.
Ø Preparation, review and revision of specifications, IOPs/EOPs, SOPs, QCPs, GTPs etc used in Quality Control.
Ø Analytical compliance as per requirement.
Ø Preparation and revision of Elemental Impurities Risk Assessment for the product as per ICH Q3D guideline.
Ø Review of Analytical Method Validation reports, Analytical Method verification reports & Analytical Method Equivalency reports.
Ø To perform activities through Software like eDMS, DMS, SAP, QMS etc based on roles and rights provided. Ø Preparation of proposal for Regulatory submission.
Ø Co-ordinate and imparting training to comply with training management system. Ø Reprinting, Re-issuances of documents/intimation sheets etc.
Ø Ensuring on-line documentation and timely entry of operations performed in Laboratory during testing.
Ø Monitoring the usage of current approved SOPs/Specifications.
Ø Responsible to ensure use of valid chemicals, standards, reagents, correct glassware with legibility of labeled volume and meniscus, qualified and calibrated instruments/ equipment and correct test methods for analysis.
Ø APQR related work.
Ø Manual log book verification for ensuring good documentation practices. Ø Lab rounds to make ready for audits anytime.
- What are the growth prospects?
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- The Company is currently in expansion mode & is planning to expand in terms of number of stores as well as business avenues. We do see a lot many challenging opportunities coming up within organization.
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- What is the Org structure in your company?
ThinQ Pharma is a flat Organisation, with open door policy. This gives chance for a great exposure and performance related rewards even for new comers.
- What would be the salary structure?
We would like to discuss the salary structure during the personal interview round based on your fitment for the role. We are open to negotiations and it will be as per industry standards. But I can assure you that we will offer you a competitive compensation.
- Who is taking interviews?
The Interview will be taken by the HR Manager
- To whom does this position report?
Functionally you will report to. But we at Maple Digital Technology International Pvt Ltd have an open culture in which the entire will be there to support & nurture your talents.
- What will be the Team size?
There are 100+ employees are working with us
Thanks & Regards,
Naina
8319348037
Job Type: Full-time
Pay: ₹168,460.99 - ₹500,000.71 per year
