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Piramal Pharma Limited Announces Walk-In Interview for Quality Control and Assurance Positions in Pithampur
Piramal Pharma Limited, a prominent pharmaceutical company with a global presence, has announced a walk-in interview for multiple positions at its manufacturing facility in Pithampur, Indore, Madhya Pradesh. The company is seeking experienced professionals for various roles in Quality Control (QC) and Quality Assurance (QA) departments.
Available Positions
The pharmaceutical giant is looking to fill four key positions:
1. QC Executive: RM/FG/Stability
Experience Required: Minimum 3 years
Qualifications: B. Pharma/M. Pharma/M.Sc (Chemistry)
Candidates for this role should possess comprehensive knowledge of analyzing Finished Goods (FG), Raw Materials (RM), Stability, and Pharmaceutical Manufacturing (PM) samples using various QC instruments including LCMS, HPLC, GC, Dissolution analyzers, and Malvern 3000. Familiarity with Laboratory Information Management Systems (LIMS) is considered an added advantage.
2. Lab-QA Manager
Experience Required: Minimum 10 years in OSD (Oral Solid Dosage) unit
Qualifications: B. Pharma/M. Pharma/M.Sc (Chemistry)
This senior position requires candidates with extensive exposure to Analytical Data Review and electronic data management of QC instruments. Strong knowledge of QC investigations, laboratory incidents, and Out-of-Specification (OOS)/Out-of-Trend (OOT) procedures is essential.
3. QA Executive
Experience Required: Minimum 3 years in OSD unit
Qualifications: B. Pharma/M. Pharma/M.Sc (Chemistry)
The ideal candidate should have solid experience in Process Validation, Technology transfer activities within OSD units, and comprehensive knowledge of Quality Management Systems (QMS), including incidents, change control, and deviation management.
4. QC Manager
Experience Required: Minimum 10 years in OSD unit
Qualifications: B. Pharma/M. Pharma/M.Sc (Chemistry)
This managerial position requires candidates with proven expertise in Analytical Method Validation/Verification and Method Transfer. Proficiency with QC instruments and strong knowledge of laboratory investigations, including OOS/OOT cases, is mandatory.
Interview Details
Venue: Piramal Pharma Limited, Pithampur, Madhya Pradesh – 453446
Date: Saturday, November 15, 2025
Time: 9:00 AM to 3:00 PM
Contact Person: Vijayraj Singh Chauhan
Contact Number: 6260322279
About Piramal Pharma Limited
Piramal Pharma Limited is a well-established pharmaceutical company with global operations. The company’s Pithampur facility in Indore, Madhya Pradesh, represents one of its key manufacturing units, focusing on quality pharmaceutical production and adhering to international standards.
Interested candidates meeting the specified qualifications and experience requirements are encouraged to attend the walk-in interview with updated resumes and relevant documents. This presents an excellent opportunity for pharmaceutical professionals looking to advance their careers with a globally recognized pharmaceutical organization.
FAQ:
1. What analytical instruments should QC candidates be proficient in?
QC candidates should have hands-on experience with advanced analytical instruments such as HPLC, GC, LCMS, Dissolution Tester, and Malvern 3000. Familiarity with Laboratory Information Management Systems (LIMS) is also desirable for data management and compliance.
2. What key skills are expected from QA candidates in OSD units?
QA professionals should demonstrate strong knowledge in Process Validation, Technology Transfer, and Quality Management Systems (QMS). They must be capable of handling incidents, deviations, CAPA, and change control systems effectively while ensuring regulatory compliance.
3. What is the difference between OOS and OOT investigations in QC?
OOS (Out of Specification) refers to test results that fall outside predefined acceptance criteria.
OOT (Out of Trend) involves results that are within specifications but show an unusual trend or drift from historical data.
Both require root cause analysis, documentation, and corrective/preventive actions in line with cGMP and regulatory guidelines.
4. What knowledge is required for Analytical Method Validation/Verification?
Candidates for managerial QC roles must be proficient in developing, validating, and verifying analytical methods as per ICH Q2 (R2) guidelines. This includes accuracy, precision, linearity, range, specificity, robustness, and system suitability testing for various dosage forms.
5. What are the essential elements of Data Integrity and Electronic Data Management in QA/QC?
Professionals should understand ALCOA+ principles (Attributable, Legible, Contemporaneous, Original, Accurate, Complete, Consistent, Enduring, and Available). Experience in handling electronic data review, audit trails, and compliance with 21 CFR Part 11 is crucial for maintaining data integrity in laboratory systems.
