Quality Control Associate - LIMS

Roles & Responsibilities

Design, create master data and execute dry runs for verification.

Design logics and verification through dry runs.

Investigation, addressing master data revisions and acknowledging the changes through ticketing system and as per change control action plan.

Ability to do process mapping & Gap identification in the existing process flows.

STP/SOP’s revision as per the LIMS requirements.

Execution of test scripts to enable qualification of instruments & new modules.

Effective communication with end users, CFT’s, line QA regarding the master data.

Lead the investigation, complete the root cause analysis, assess the impacted master data and propose an appropriate CAPA.

Periodic uptake of queries from end users and co-ordinating within the team members for resolutions.

End user training & support.

Support in regulatory audits.

Educational Qualification

A B.Pharm. or Post-Graduation (Life Sciences)

Minimum Work Experience

4 years of industrial experience with specific operational experience in Manufacturing, Quality Control, Quality Assurance or Engineering & Development

About the Department

Biologics

Currently operates in the Global Biosimilars business - a segment that is poised for attractive and sustained growth over the next 10–15-year time horizon...

" Benefits Offered

At Dr. Reddy’s, we actively help to catalyze your career growth and professional development through personalized learning programs. The benefits you will enjoy at Dr. Reddy’s are on par with the best industry standards...

" Our Work Culture

Ask any employee at Dr. Reddy’s why they come to work every day and they’ll say, because Good Health Can’t Wait. This is our credo as well as the guiding principle behind all our actions...

For more details, please visit our career website at https://careers.drreddys.com/#!/

"