Tuesday , November 24 2020
Home / Job / Dr.Reddys Laboratories -Hiring M.Sc for Team Member Drug Product Formulation-Apply Now

Dr.Reddys Laboratories -Hiring M.Sc for Team Member Drug Product Formulation-Apply Now

Dr.Reddys Laboratories -Hiring M.Sc for Team Member Drug Product Formulation-Apply Now

Job Description

Team member responsible for supervision & verification of buffer preparation & Formulation operation as per SOPs, Batch Production Record and cGMP procedure. To work in Shift operation as per production schedule. To ensure all documents related to FFM such as status label updation, on time completion of BPR, area/ Equipment log books, RSTs updation & archival. To Execute & review batch production record & responsible to address the QA review comments of the BPR within TAT.

Post Name:  Team Member Drug Product Formulation

Qualification: M.Sc

Experience: 5-7 years

Openings : 02

Salary: NA

Location: Bachupally, Hyderabad, Telangana, India

Contact Details :

Company : Dr.Reddys Laboratories

Click Here For Job Details & Apply Online

Apply for this position

Allowed Type(s): .pdf, .doc, .docx

About Pharmaceutical Guidanace

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

Check Also

Qualification & Validation of Equipment, Systems, Utilities in Pharmaceuticals

Qualification & Validation of Equipment Equipment qualification as required by the FDA requires verification documentation …