Quality Control Job at Piramal Pharma | Apply Now
A rare chance has emerged through Piramal Pharma careers for aspiring Quality Control professionals in Pithampur. This role seeks candidates with 1–3 years of experience in quality control, offering an opportunity to contribute to a leading contract development and manufacturing organization.
About The Company
Piramal Pharma is a prominent contract development and manufacturing organization (CDMO) that provides comprehensive development and manufacturing solutions across the drug life cycle. The company is dedicated to delivering high-quality services and products to its clients in the pharmaceutical sector, ensuring compliance with stringent regulatory standards.
- Position: Executive – Quality Control
- Department: Quality Control
- Location: Pithampur, MP
Piramal Pharma Careers: Job Description
The selected candidate will work as a Quality Control analyst responsible for the analysis of AMV/AMT, finished products, stability samples, and raw materials as per cGMP and USFDA requirements. The role also involves the preparation of protocols, reports, and related documentation as per GDP. Candidates exploring Piramal Pharma careers should ensure their analytical and documentation experience aligns with these responsibilities.
Key Responsibilities
- Perform analysis of AMV/AMT, finished products, stability samples, and raw materials as per cGMP and USFDA requirements.
- Prepare protocols, reports, and other related documentation as per GDP.
- Handle receipt, inward, storage of QC samples, and disposition of samples after analysis.
- Maintain concurrent documentation of analytical records and storage of raw data.
- Make online entries in instrument and equipment usage logbooks.
- Report any deviation, incident, OOT, or OOS instantly to the Section Head or Head QC.
- Carry out any additional responsibility assigned by the section head.
- Implement GLP/GMP requirements in the QC laboratory.
- Control and maintain QC laboratory records, including laboratory notebook and COA records.
- Support the site DICO (Data Integrity Compliance Officer) for monitoring and implementation of actions related to data integrity awareness at site.
Eligibility Criteria
- Hands-on experience on HPLC, GC, FTIR, Dissolution Test apparatus, KF, LC-MS/MS, AAS, Malvern PSD analyzer/analyser, etc.
- Sound knowledge of cGMP, GLP, GDP, ICH, and ALCOA++.
- Ability to perform analytical testing and maintain documentation as per regulated quality standards.
This opportunity at Piramal Pharma presents a significant step for qualified candidates in the Quality Control domain. Interested individuals are encouraged to apply before the deadline to seize this chance to advance their careers in a reputable organization. Candidates interested in Piramal Pharma careers are encouraged to review the role requirements before applying.
