Chemveda Life Sciences Pvt. Ltd- Walk-In Drive for Analytical R&D Department On 3rd October 2021
Walk-In Drive On 3rd October 2021 For Analytical R&D Department (PDMO & CRO) @ Chemveda Life Sciences, Hyderabad
Department: Analytical R&D
Designation: Research Associate/ Senior Research Associate
Qualification: M.Sc. (Analytical Chemistry/ Organic chemistry)
Experience: 3-9 years
Work Location: Hyderabad
Key Skills and Competencies:
Should Support to the Process Research team and should have at least one of the below req. Skillset:
•LC-MS/MS -Performing Development for Genotoxic Impurities. (Performing Validations will be an advantage).
•GC/ GC-HS- GC Method development for in-process samples, residual solvents and content methods.
•HPLC Method development and In-Process Validations-> HPLC Routine analysis, execution of method developments, mini Validations, method transfers.
> Knowledge on Review of analytical data. Preparation and review of Analytical weekly updates.
> Preparation of documents like SOPs, Spec and MOAs, Protocols and Reports.
JH> Standards qualifications, Analysis of impurities, Physical Characterizations, Residue Content, Stability Studies etc
•HPLC &Documentations-HPLC Routine analysis (RAW Materials, In-Process and Intermediates) and Calibrations.
Time and Venue Details: Walk-In Drive On 3rd October 2021 from 10:00 AM to 12:00 PM ,Venue: Chemveda Life Sciences Pvt. Ltd ,Plot# B-11/1, IDA Uppal, Hyderabad
Note: Interested Candidates who can not attend the Interview On the Walk-In date can Share the profile On [email protected]
Candidate need to have six months of a time gap between successive attempts of the Interview.
Required Candidate Profile :
Qualification: M.Sc (Analytical Chemistry/ Organic chemistry)
Experience: 3-9 years of relevant experience in Analytical R&D.
Kindly Cary the below Documents:
Last three months payslips, recent hike letter. (Photocopy).
Passport size Photo.
1 photocopy of your Photo ID Proof (Pan Card/ Passport/ Drivers License).
Mr. Shiv Kumar is the Author and founder of pharmaceutical guidance, he is a pharmaceutical Professional from India having more than 14 years of rich experience in pharmaceutical field.
During his career, he work in quality assurance department with multinational company’s i.e Zydus Cadila Ltd, Unichem Laboratories Ltd, Indoco remedies Ltd, Panacea Biotec Ltd, Nectar life Science Ltd. During his experience, he face may regulatory Audit i.e. USFDA, MHRA, ANVISA, MCC, TGA, EU –GMP, WHO –Geneva, ISO 9001-2008 and many ROW Regularities Audit i.e.Uganda,Kenya, Tanzania, Zimbabwe. He is currently leading a regulatory pharmaceutical company as a head Quality. You can join him by Email, Facebook, Google+, Twitter and YouTube