Piramal Pharma Solutions is hiring for the position of Senior Executive – QC at its Pithampur, Madhya Pradesh location. This is a full-time opportunity for professionals interested in pharmaceutical quality control, laboratory analysis, stability testing and GMP/GLP-compliant documentation.
The selected candidate will be responsible for analyzing stability samples and finished products, operating analytical instruments according to approved methods, maintaining laboratory records, handling QC samples and reporting deviations or laboratory incidents. The role also includes supporting stability activities and maintaining chemical-store documentation.
Piramal Pharma Solutions Senior Executive QC Recruitment 2026 – Job Highlights
| Particular | Details |
|---|---|
| Company | Piramal Pharma Solutions |
| Position | Senior Executive – QC |
| Department | Quality Control |
| Location | Pithampur, Madhya Pradesh |
| Job Type | Full Time |
| Key Area | Pharmaceutical Quality Control |
| Experience | Not Specified |
| Qualification | Not Specified |
| Requisition ID | R00004349 |
| Application Deadline | October 29, 2026 |
| Salary / CTC | Not Specified |
About Piramal Pharma Solutions
Piramal Pharma Solutions is a Contract Development and Manufacturing Organization (CDMO) providing pharmaceutical development and manufacturing services across the drug lifecycle.
Its capabilities include drug discovery, process and pharmaceutical development, clinical trial supplies, commercial API and finished dosage manufacturing, as well as specialized services involving highly potent APIs and antibody-drug conjugation.
The company’s integrated operations support pharmaceutical innovators and generic companies across multiple markets.
Job Description
The Senior Executive – QC will work within the Quality Control laboratory and support analytical testing, stability activities and laboratory documentation.
The position requires adherence to GLP and GMP requirements while ensuring that analytical activities are performed accurately and that laboratory records and raw data are maintained appropriately.
The role involves working with analytical instruments such as HPLC, Dissolution, UV Spectrophotometer and Karl Fischer Apparatus according to approved methods and configurations.
Key Responsibilities
Quality Control Sample Analysis
- Analyze stability samples according to applicable cGMP requirements.
- Perform testing of finished-product samples.
- Ensure analytical activities generate accurate and reliable results.
- Complete relevant analytical documentation alongside testing activities.
- Handle QC samples from receipt through storage and final disposition.
Analytical Instrument Operations
- Perform approved analytical methods using:
- HPLC
- Dissolution apparatus
- UV Spectrophotometer
- Karl Fischer Apparatus
- Operate instruments according to approved methods and configurations.
- Follow established laboratory procedures and analytical requirements.
- Do not make unauthorized changes to analytical methods, report formats or method configurations.
Stability Management
- Support analysis of stability samples.
- Maintain stability incubators and chambers.
- Prepare monthly stability testing plans.
- Ensure stability samples are appropriately received, stored and processed.
- Support proper documentation of stability-related analytical activities.
Laboratory Documentation
- Maintain analytical records concurrently with laboratory activities.
- Maintain raw analytical data in accordance with applicable procedures.
- Complete online entries in instrument and equipment usage logbooks.
- Maintain QC laboratory records.
- Maintain relevant records such as laboratory notebooks and Certificates of Analysis (COAs).
- Ensure documentation meets applicable GLP and GMP requirements.
Deviation and Laboratory Incident Reporting
- Immediately report deviations to the Section Head or Head of QC.
- Report laboratory incidents when identified.
- Escalate Out of Trend (OOT) results according to applicable procedures.
- Escalate Out of Specification (OOS) results promptly.
- Support appropriate documentation of quality-related events.
Chemical Store and Sample Management
- Maintain the Bin Card for the chemical store.
- Support appropriate receipt, inward processing and storage of QC samples.
- Ensure samples are properly controlled throughout the testing process.
- Complete sample disposition activities after analysis.
GMP and GLP Compliance
- Follow applicable Good Laboratory Practice (GLP) requirements.
- Maintain compliance with Good Manufacturing Practice (GMP) expectations.
- Ensure laboratory documentation and analytical activities follow approved procedures.
- Support maintenance of an inspection-ready laboratory environment.
Additional Responsibilities
- Perform other QC-related duties assigned by the Section Head.
- Support laboratory operations and quality objectives as required.
Educational Qualification / Eligibility Criteria
The provided vacancy does not specify a particular educational qualification for the Senior Executive – QC position.
Candidates should review the official job listing and recruitment communication for the latest qualification requirements before applying.
Experience Requirements
The provided vacancy does not mention a specific number of years of experience.
The responsibilities indicate that candidates should be familiar with pharmaceutical QC laboratory operations, analytical testing, stability samples, laboratory documentation and GMP/GLP requirements.
Required Technical Skills
Relevant technical knowledge for this position includes:
- Quality Control laboratory operations
- Pharmaceutical analytical testing
- Stability sample analysis
- Finished-product analysis
- HPLC
- Dissolution testing
- UV Spectrophotometry
- Karl Fischer analysis
- Stability chamber management
- QC sample management
- Laboratory documentation
- Raw-data management
- Laboratory notebooks
- Certificates of Analysis
- OOS handling
- OOT handling
- Deviation reporting
- GMP compliance
- GLP compliance
Required Soft Skills
The role also requires:
- Strong attention to detail
- Accurate documentation
- Ability to follow approved procedures
- Timely reporting of deviations and laboratory events
- Organizational skills
- Ability to maintain laboratory records
- Ability to work according to quality requirements
- Effective communication with QC leadership
Work Location and Job Type
Location: Pithampur, Madhya Pradesh, India
Job Type: Full Time
The provided vacancy does not specify a remote or hybrid arrangement. Given the laboratory-based responsibilities, the position involves on-site QC activities.
Salary / CTC
The salary or CTC has not been specified in the provided recruitment details.
Candidates should confirm compensation and other employment terms through the official Piramal Pharma Solutions recruitment process.
Selection Process
The detailed selection procedure has not been provided in the vacancy. Candidates should follow the official recruitment process and complete any interviews, assessments or other stages communicated by Piramal Pharma Solutions.
How to Apply for Piramal Pharma Solutions Senior Executive QC Recruitment 2026
Interested candidates can apply online through the official Piramal Pharma Solutions careers portal.
- Open the official job listing.
- Review the responsibilities and eligibility requirements.
- Prepare an updated CV highlighting relevant QC and analytical laboratory experience.
- Submit the application through the official careers portal.
- Complete any additional recruitment steps requested by the company.
Important Details Before Applying
- The position is Senior Executive – QC.
- The job location is Pithampur, Madhya Pradesh.
- This is a full-time position.
- The role is focused on pharmaceutical Quality Control laboratory activities.
- Responsibilities include stability and finished-product sample analysis.
- HPLC, Dissolution, UV Spectrophotometer and Karl Fischer instruments are mentioned.
- Candidates must follow approved methods and must not make unauthorized changes to methods or configurations.
- GLP and GMP compliance is an important part of the position.
- OOS, OOT, deviations and incidents must be reported appropriately.
- Stability chambers and monthly stability planning are part of the responsibilities.
- Laboratory notebooks, COAs, raw data and instrument logbooks must be maintained.
- The vacancy does not specify salary, qualification or years of experience.
- The stated application deadline is October 29, 2026.
- Job requisition ID: R00004349.
Frequently Asked Questions
1. What position is Piramal Pharma Solutions hiring for?
The company is hiring for Senior Executive – QC.
2. Where is the job located?
The position is based in Pithampur, Madhya Pradesh.
3. What department is this position associated with?
The position is within Quality Control (QC).
4. What are the main responsibilities?
The role includes stability and finished-product analysis, analytical instrument operation, QC sample management, laboratory documentation, stability activities and GMP/GLP compliance.
5. Which analytical instruments are mentioned?
The vacancy mentions HPLC, Dissolution, UV Spectrophotometer and Karl Fischer Apparatus.
6. Does the role involve stability testing?
Yes. Stability sample analysis, stability chamber maintenance and preparation of monthly stability plans are included.
7. Does the position involve OOS and OOT handling?
Yes. Deviations, incidents, Out of Trend (OOT) and Out of Specification (OOS) results must be reported to the appropriate QC leadership.
8. Is GMP knowledge required?
The position requires implementation and adherence to GMP and GLP requirements in the QC laboratory.
9. Does the job involve laboratory documentation?
Yes. Responsibilities include analytical records, raw data, instrument usage logbooks, laboratory notebooks and Certificates of Analysis.
10. Is a specific qualification mentioned?
The provided vacancy does not specify a particular educational qualification.
11. Is a specific experience requirement mentioned?
No specific number of years of experience is provided in the vacancy.
12. What is the salary?
The salary or CTC has not been disclosed in the provided job information.
13. What is the last date to apply?
The stated application deadline is October 29, 2026.
14. What is the job requisition number?
The requisition ID is R00004349.
Important Note
Job availability, eligibility criteria, experience requirements, salary and other employment conditions may change. Candidates should verify the latest information on the official Piramal Pharma Solutions careers portal before applying.