Dr. Reddy’s Laboratories Ltd. is a leading multinational pharmaceutical company based across global locations. Each of our 24,000 plus employees comes to work every day for one collective purpose: to accelerate access to affordable and innovative medicines because Good Health Can’t Wait.
Dr. Reddy’s maintains a work environment, free from discrimination, and is an equal opportunity employer. The company is committed to equal employment opportuninty and employs all qualified persons without regard to race, colour, religion, national origin, sex, age, disability status, genetics, sexual orientation, gender identity or expression, marital status, citizenship or any other characteristic or classification protected by the applicable law(s) of the countries we operate in. We apply these principles in all aspects of employment, including recruitment, hiring, placement, promotion, termination, lay off, transfer, leaves of absence, training and compensation. If you feel you have not been treated in accordance with these principles, you should contact your local Human Resources Department. The company assures all employees that no individual filing a complaint will be discriminated against, as a result of their complaint.
Apply:
- 𝐋𝐨𝐜𝐚𝐭𝐢𝐨𝐧: Pydibhimavaram, Andhra Pradesh (70 km from Visakhapatnam)
- Ready to grow with us? Apply now: https://smrtr.io/tvwwg or DM your resume “ravipatitriveni@drreddys.com“ with subject line: Application -Team Member -QMS for Injectable Plant.
JOB DETAILS:
𝐄𝐝𝐮𝐜𝐚𝐭𝐢𝐨𝐧: B.Pharm / M.Pharm
𝐄𝐱𝐩𝐞𝐫𝐢𝐞𝐧𝐜𝐞: 3–8 years in sterile manufacturing & QMS
Knowledge of ISO & Regulatory guidelines
Hands-on with TrackWise, SAP, EDMS/ELMS
𝐘𝐨𝐮𝐫 𝐑𝐨𝐥𝐞:
Manage Change Control, Deviations, CAPA & Investigations
Ensure shop-floor compliance & regulatory adherence
Prepare/review BMR & SOPs
Coordinate audits & document control
Roles & Responsibilities:
- You will be responsible for overseeing the compliance activities in day-to-day production activities.
- You will be responsible for the incident/deviation brainstorming, investigation and closure.
- You will be responsible for implementation of CAPA actions and change proposal actions.
- You will be responsible for guiding and coaching employees, monitoring their productivity, and overseeing regular equipment safety and maintenance.
- You will be responsible for review of Documentations, BMR (Batch Manufacturing Records), BPR (Batch Production Records) and Logbooks.
- You will be responsible for ensuring product quality by maintaining cGMP (current Good Manufacturing Practices).
- You will be a training coordinator through LMS (Learning Management system).
- You will be responsible for generating the process order number.
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