Dr.Reddys Laboratories Ltd Urgent Recruitment

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.We started in 1984 with a modest investment, 20 employees and a bold vision. 

• Important Details :
• Post of date:13/11/2024
• Selection Process: The selection will be on the basis of Interview.
• Mode of Interview: Face to face
• Interview Rounds of Interview: HR

Job Description : Greeting from Dr.Reddys Laboratories Ltd..!!!!

Vacancy details:

• Department: CSV Team Member/QC/Team Member – Packaging Development- Injectables
• Qualification: B.Tech/M.Sc/M.Pharma/Bsc
• Experience: 02 to 7 yrs
• Job Location: Duvvada/Pydibhimavaram (Vasakapatnam)

 Exciting Career Opportunity at Dr. Reddy’s Laboratories 🚀

Join our team as a CSV Team Member.

📍 Location: Visakhapatna

Experience: 3-7 Years

🔬 Key Responsibilities:

• Experience in working with sterile product facility related validations such as equipment validation, media fill, cleaning validation, process validation,
area qualification, and other miscellaneous qualifications.
• Expertise in preparation, review, and execution of documents, including URS, DQ, FDS, UTM, IQ, OQ, PQ, RQ.
• Experience in Handling incident investigations and CAPA processes.
• Experience in preparation and review of VMP and SOPs.

🎓 Qualifications: B.Tech/M.Sc/M.Pharma.

Preferably in the Formulations/Injectables.

Strong knowledge of GxP, GAMP & USFDA 21CFR part11.

If you’re ready to contribute to world-class pharmaceutical quality standards and grow your career in a dynamic environment, we want to hear from you!

📧 Interested Professionals can share your resume to dhineshtejaummadisetti01@drreddys.com

Mention subject as “CSV”

Exciting Career Opportunity at Dr.Reddy’s Laboratories 🚀

Join our team as a hashtag#Quality Control (QC) Team Member.

 Location: Visakhapatnam

Experience: 2-5 Years

🔬 Key Responsibilities:
Perform analytical testing using
HPLC GC IR UV.
Ensure strict adherence to Good Manufacturing Practices (GMP) and regulatory guidelines.
Troubleshoot and maintain analytical instruments to deliver accurate results.
Collaborate with cross-functional teams to ensure product quality and compliance.

🎓 Qualifications: B.Sc./M.Sc. in Chemistry.

Preferably in the Formulations/Injectables.

Strong knowledge of HPLC, GC analysis, Dissolution by HPLC, Assay, stability analysis, Finished products.
If you’re ready to contribute to world-class pharmaceutical quality standards and grow your career in a dynamic environment, we want to hear from you!

📧 Interested Professionals can share your resume to dhineshtejaummadisetti01@drreddys.com 

Mention subject as “QC”