Gland Pharma-Walk-In Interview for Quality Assurance On 20th Dec’ 2023

Gland Pharma-Walk-In Interview for Quality Assurance On 20th Dec’ 2023

Walk-in Interviews | Quality Assurance | 20th December 2023 (Wednesday) @ Gland Pharma Unit 2, Pashamylaram | Immediate Joiners Preferred | Parenteral Experience Mandatory | 3 – 6 Years Experienced Candidates.

Injectable pharma experience is Mandatory for Quality Assurance 

Job Description:
•Review of complete batch records prior to batch release.
•Review and evaluation of new products introducing to the facility.
•Preparation and a review of Media fill Protocols and Reports.
•Preparation and Review of Process Validation Protocols and Reports.
•Preparation and Review of APR’s and APDR’s summary reports.
•Documentation Experience is Mandatory.
•Should have experience in CSV – Computer System Validations.

Willing to work in any shifts

Date: 20th Dec’ 2023
Time: 09:00 AM to 11:30 AM
Venue Details: Gland Pharma Unit 2, Plot No: 42-52., Phase III, TSIIC. Pashamylaram. Patancheru, Hyderabad, Medak, Telangana, India.

Mandatory Documents: 10th, 12th, UG, PG marks memo, Last three months’ Salary slips, Latest Increment Letter/CTC letter, Last three months Bank Statement
Education – B.Sc, B.Pharma, M.Sc, M.Pharma candidates can apply.
Please Note: Candidates interviewed within the last 6 months are not eligible. Non Local candidates with relevant skillsets and experience can mail their resumes to Hrd.pmy@glandpharma.com`/ Suryateja.velaga@glandpharma.com

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

Apply for this position

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

ABHA

Abha is the Author  of pharmaceutical guidance, she is a pharmaceutical professional having more than 22 years of rich experience in pharmaceutical field. During her career, she works in the quality assurance department with multinational companies i.e Zydus Cadila Ltd, Unichem Laboratories Ltd, Indoco remedies Ltd. During his experience, she faces many regulatorily audits 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. She is currently leading a regulatory pharmaceutical company as a Head Quality. You can join him by Email, Facebook, Google+, Twitter, and YouTube