Deccan Nutraceuticals Pune Jobs For QA Reviewers For API / Bulk Drugs


About Company

Deccan Nutraceuticals Pvt Ltd (DNPL) is a fully owned subsidiary of Alkaloids Corporation (Kolkata). Alkaloids Corporation was established in 1967 and has 4 manufacturing subsidiaries -1 in Pune (DNPL), 2 in Hyderabad and 1 in Vizag. For more information, kindly visit www.alkaloidscorp.com.
Deccan Nutraceuticals Pvt Ltd (DNPL) was established in 2001 and is located 30 km from pune station. It is involved in the manufacture of bulk drugs/APIs. The company has been audited successfully by USFDA (4 times) and by EDQM (1 time) and sells most of its products in US and Europe.

Education
Diploma / B.Tech/B.E. in Chemical, B.Sc in Chemistry, B.Pharma in Pharmacy, 
M.Tech in Chemical, MS/M.Sc(Science) in Chemistry

Designation & Department: 

QA Reviewers For API / Bulk Drugs


Experience Required: 4 - 9 Years

Vacancies: 04

Job Location: Pune

Job Description


We have vacancies for QA Reviewers in Manufacturing and QC sections.

1. JD of Manufacturing Dept Reviewers:

1.1 Responsible for review of Manufacturing Department (Production, Warehouse and Maintenance) documents such as SOP's, Batch Manufacturing & Packaging Records, Equipment Cleaning Records, Master Formula Records, log books and their traceability;

1.2 Responsible for review of Process and Cleaning Validation, Equipment 

Qualifications protocols and reports;
1.3 Responsible for review of Change Controls and Deviations in Manufacturing Departments;

1.4 Participate in audits and investigations;

1.5 Responsible for despatch documentation and coordination.

2.JD of QC Dept Reviewers:

2.1 Responsible for review of routine QC documents like Analytical Work Sheets, log books, calibration records;

2.2 Responsible for review of qualification documents;

2.3 Responsible for online review of electronic data of instruments like HPLC, GC, IR, TOC, Polarimeter etc.

Required Candidate profile

The candidate must have an eye for perfection. He / She must have worked as a Reviewer in the past in a regulated pharma company and should have the skill to identify discrepancy / errors / omissions in documents.

Interested candidates can send their CV on

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