Chemveda Life Sciences is a mid-sized, fast-growing service provider to the pharmaceutical, biotechnology, agrochemical industries, and the academia. As a contract research orginization (CRO), Chemveda is boosting its value creation along and beyond the drug discovery services and drug development services continuum, with an emphasis on churning out cost and timeline efficiencies for its global clientele.
Chemveda harnesses its scientific and technological expertise to deliver full-suite drug discovery chemistry services support ranging from lab scale chemical synthesis, to Process R&D, and large-scale custom chemical development of drug substances, key intermediates, and starting materials across multiple chemistry classes. Lately, we have been investing in developing in-house expertise in the most sought-after scientific platforms in order to answer the existing and evolving challenges in basic and applied research.
0 years
Not Disclosed
Time and Venue
29 May , 10.00 AM – 12.00 PM
Chemveda life Sciences Admin Building,1st Floor, Plot No. B-11/1, IDA Uppal, Hyderabad-500 072, India.
Job description
Greetings from Chemveda life Sciences
We have vacancy in DQA
Walk-In Date – 29th May 2024 ( Wednesday)
Timings – 10.00 AM to 12.00 PM
Venue Details:-
Chemveda life Sciences
Admin Building,1st Floor,
Plot No. B-11/1, IDA Uppal,
Hyderabad-500 072,
India.
Note – Females Not Eligible
Roles and Responsibilities:-
1. To monitor the Quality Systems for their effective implementation and compliance during the development of Projects at R&D and AR&D.
2. Tofollowo a controlled document system for projects in Research & Development, Analytical Research & Development, Development Quality Assurance and other relevant departments.
3. Responsible to receive reviewing and archive all records relevant to Technology transfer
4. To review Technical report along with R&D and finalise the Technical report for Technology transfer discussion.
6. To review of Spec & MOA.
7. To review and verify completeness of Technology transfer documents through checklist.
8. Coordinating with Contract Manufacturing Organisations for document closures.
9. To share Technology transfer documents to Manufacturing QA.
10. To review of R&D and AR&D LNBs for completeness and as per GDP.
11. Good knowledge on Guidelines.
Desired Candidate Profile:-
1. 0 6 Months of experience in the Pharmaceutical Industry.
2. Must be Proficient in written, verbal, and Computer skills.
2. Should be self-motivated and result-oriented.
3. Should be a keen learner, proactive, and have good analytical skills.
4. Ability to multitask and prioritize responsibilities.
Qualification – M.Pharma (2023,2024 Passed outs)
Preferred for Male
if anyone is unable to attend an interview kindly share your profiles to ramasatish.uppuluri@chemvedals.com
Role:
Quality Assurance – OtherIndustry Type:
Pharmaceutical & Life SciencesDepartment:
Quality AssuranceEmployment Type:
Full Time, PermanentRole Category:
Quality Assurance – Other
Education:
M.Pharma in Pharmacy
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