Shilpa Medicare Ltd -Interview for QC, Regulatory Affairs- US/ EU/ Canada/ RoW on 03Feb 2024(Saturday)

Shilpa Medicare Ltd -Interview for QC, Regulatory Affairs- US/ EU/ Canada/ RoW on 03Feb 2024(Saturday)

 

Walk-ins for QC Formulations, RAD Formulations on 3rd Feb 2024 at Shilpa Medicare Ltd, Hyd

Date: 03.02.2024

Department: Quality Control- Formulation, Regulatory Affairs- US/EU/Canada, Regulatory Affairs-RoW

Designation: Trainees/ Executives/ Sr Executive/ Asst/ Dy Manager

Qualification: M Pharm, B Pharm. MSc And UG

Experience: 0-12 Yrs

Key Skills:

Method validation/Method transfer Analysis of RM, PM, FP & GLP Stability

Need for US/Europe/Canada Region. End to End Activities

Preparation, compilation and

review of dossiers Row region in CTD/country specific format. Etc

Date: 03.02.2024(Saturday)

Time : 10.00 AM to 04.00 PM

 VENUE:Shilpa Medicare Ltd.
Address: Plot no 79. Road No 15. Survey No 125 IDA Mallpur, Nacharam. Uppal, Mandal, Telangana 500076

DOCUMENTS REQUIRED:

  1. Updated Resume,
  2. Recent Increment Letter /Offer Letter with CTC break up
  3. Latest 3 Months Payslips & 6 Months Bank statement
  4. Copies of all education certificates

5.Copy of Aadhar 6.Copy of pan card

Candidates Who are Unable to attend the interview can Mail your updated resumes to karthik.kumar@vbshilpa.com Should have relevant experience for above said positions.

Job Category: pharma
Job Type: Full Time
Job Location: Hyderabad

Apply for this position

Allowed Type(s): .rtf

About Pharmaceutical Guidanace

Ms. Abha Maurya is the Author and founder of pharmaceutical guidance, he is a pharmaceutical Professional from India having more than 18 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

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