Piramal Pharma Solutions is hiring for Analytical Data Reviewer & QA(QMS) Manager

About Company:

Piramal Pharma Solutions (PPS) is a Contract Development and Manufacturing Organization (CDMO) offering end-to-end development and manufacturing solutions across the drug life cycle. We serve our customers through a globally integrated network of facilities in North America, Europe, and Asia. This enables us to offer a comprehensive range of services including drug discovery solutions, process & pharmaceutical development services, clinical trial supplies, commercial supply of APIs, and finished dosage forms. We also offer specialized services such as the development and manufacture of highly potent APIs, antibody-drug conjugations, sterile fill/finish, peptide products & services, and potent solid oral drug product. Our track record as a trusted service provider with experience across varied technologies makes us a partner of choice for innovator and generic companies worldwide.

Vacancy Details:

Job Description:

Piramal Pharma Solutions

We’re Hiring!

Walk-In Drive @ Panchkula, India

Roles:

Manager – Analytical Data Reviewer

Department: Central Quality

Experience: 8 to 14 years

Qualification: B. Pharma / M. Pharma / M. Sc(Chemistry)

Experience: Strong exposure to analytical data review and electronic data review from QC instruments such as HPLC, GC, dissolution apparatus, and Malvern 3000 .

Thorough understanding of Quality Control investigations, including Lab Incidents, OOS, and OOT

Relevant experience in Oral Solid Dosage (OSD) formulations and/or Active Pharmaceutical Ingredient processes (API)

Manager – QA (QMS)

Department: Central Quality Experience: 8 to 14 years

Qualification: B. Pharma / M. Pharma / M. Sc (Chemistry)

Experience:

Knowledge of Quality Control investigations including OOS, OOT, Lab Incidents, and deviations

Expertise in Root Cause Analysis and Risk Assessment

Hands-on experience with analytical instruments and various QC techniques

Proficient in drafting Quality Technical Agreements (QTA)

Skilled in compendia assessments, data trending, Annual Product Quality Review (APQR)

Exposure to Process Validation, Cleaning Validation, and Equipment Qualification

Relevant experience in Oral Solid Dosage (OSD) formulations and/or Active Pharmaceutical Ingredient (API) processes

Note: This role will support one of our sites in North America and will require the candidate to work as per the US time zone.

How to Apply?

Walk-in venue: Hotel KC Cross Road, Site No. 1, Maheshpur Rd, Opposite Bus Stand, Sector 10, Budanpur, Panchkula, Haryana 134113

Date and Time: Sunday, 8th June 2025 | 9 AM – 3 PM

Job Location: Kurla, Mumbai, India

In case of any queries, contact Anuj Yagik – 6260600524/ Anuj.Yagik@piramal.com


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