Piramal Pharma Solutions is inviting applications for the position of Executive – Quality Control at its Pithampur, Madhya Pradesh location. This is a full-time opportunity within the Quality Control function of Piramal Pharma Solutions.
The selected candidate will be responsible for supporting quality control testing, analytical activities, laboratory documentation, sample management, and compliance with applicable cGMP, GLP, GMP, and data integrity requirements.
Candidates interested in this opportunity should review the eligibility requirements and job responsibilities carefully before applying through the official Piramal Pharma Solutions careers portal.
Piramal Pharma Solutions Recruitment 2026 – Job Highlights
| Particulars | Details |
|---|---|
| Company | Piramal Pharma Solutions |
| Job Title | Executive – Quality Control |
| Department | Quality Control |
| Job Type | Full Time |
| Location | Pithampur, Madhya Pradesh |
| Requisition ID | R00004372 |
| Application Deadline | October 30, 2026 |
| Experience | Not specified in the provided job description |
| Qualification | Not specified in the provided job description |
| Salary / CTC | Not specified |
| Work Mode | On-site / Laboratory-based role |
| Industry | Pharmaceutical / CDMO |
About Piramal Pharma Solutions
Piramal Pharma Solutions (PPS) is a contract development and manufacturing organization (CDMO) that provides development and manufacturing services across different stages of the pharmaceutical product lifecycle.
The company operates through a global network of facilities across North America, Europe, and Asia. Its services include drug discovery, process and pharmaceutical development, clinical trial supplies, commercial API and finished dosage manufacturing, as well as specialized capabilities such as highly potent API development and antibody-drug conjugation.
Job Description
The Executive – Quality Control will support day-to-day analytical and laboratory activities while ensuring that testing and documentation are performed in accordance with applicable quality standards.
The position involves testing pharmaceutical samples, supporting analytical method-related activities, maintaining laboratory records, managing raw data, and following GLP/GMP and data integrity requirements.
Executive – Quality Control: Role Overview
The key focus areas of this position include:
- Quality control testing of pharmaceutical and related samples.
- Analytical method validation, verification, and transfer activities.
- Preparation and standardization of laboratory solutions and reagents.
- Maintaining analytical records and laboratory documentation.
- Proper handling and storage of raw analytical data.
- Vendor approval sample analysis.
- Compliance with GLP and GMP requirements.
- Maintaining QC laboratory records and supporting quality-related activities.
Key Responsibilities
1. Pharmaceutical Sample Testing
The candidate will perform analysis of:
- Finished products
- In-process samples
- Hold-time samples
- Raw materials
- Stability samples
- Other quality control samples as assigned
Testing and associated documentation must be performed in accordance with applicable cGMP requirements.
2. Analytical Method Activities
Support analytical method-related activities for new projects, including:
- Method transfer
- Method validation
- Method verification
These activities are intended to support the implementation of appropriate analytical procedures for new projects.
3. Preparation of Laboratory Solutions
The role includes preparing and standardizing laboratory materials such as:
- Volumetric solutions
- Reagents
- Indicator solutions
Preparation and standardization should be performed as required for laboratory testing activities.
4. Analytical Documentation and Raw Data
Maintain documentation concurrently during analytical activities. Responsibilities include:
- Recording analytical results.
- Maintaining analytical records.
- Ensuring proper storage of raw data.
- Making required online entries in instrument and equipment usage logbooks.
5. Vendor Approval Samples
The Executive – Quality Control will also be responsible for carrying out analysis of samples associated with vendor approval activities as required.
6. GLP and GMP Compliance
Follow applicable Good Laboratory Practices (GLP) and Good Manufacturing Practices (GMP) requirements during laboratory operations.
7. QC Laboratory Records
Maintain and control important QC laboratory records, including:
- Laboratory notebooks
- Chromatograms
- Certificates of Analysis (COA)
- Other applicable laboratory documentation
Proper record maintenance is an important part of maintaining laboratory traceability and data integrity.
Educational Qualification
The provided job description does not mention a specific educational qualification for the Executive – Quality Control position.
Candidates should therefore verify the latest qualification requirements on the official Piramal Pharma Solutions careers page before submitting an application.
Experience Requirements
The provided vacancy information does not specify a minimum number of years of professional experience.
Applicants should refer to the official job posting for any experience requirements or additional eligibility conditions applicable to the position.
Required Skills
Based on the responsibilities listed in the vacancy, candidates should be comfortable working with:
- Pharmaceutical quality control testing
- cGMP requirements
- GLP practices
- Laboratory documentation
- Analytical records
- Raw data management
- QC laboratory records
- Analytical method validation
- Analytical method verification
- Analytical method transfer
- Reagent and solution preparation
- Instrument/equipment logbooks
- Stability and finished-product analysis
- Data integrity requirements
Work Location and Work Environment
Location: Pithampur, Madhya Pradesh
This is a full-time Quality Control position involving laboratory and quality-related activities. The provided posting does not mention a remote or hybrid work arrangement.
Salary / CTC
The salary or CTC for the Executive – Quality Control position has not been specified in the provided vacancy details.
Candidates should refer to the official recruitment communication or discuss compensation details with the employer during the recruitment process.
Selection Process
The provided job posting does not specify the complete selection process.
Candidates should check the official Piramal Pharma Solutions recruitment communication for information regarding screening, interviews, assessments, or other selection stages, if applicable.
How to Apply for Piramal Pharma Solutions Recruitment 2026
Interested and eligible candidates can apply online through the official Piramal Pharma Solutions careers portal.
Application Deadline: October 30, 2026
Job Requisition ID: R00004372
Apply Online – Executive – Quality Control
Steps to Apply
- Open the official application page.
- Review the job requirements carefully.
- Complete the online application form.
- Enter your educational and professional information accurately.
- Upload the required documents or resume, if requested.
- Review the information before submitting the application.
- Keep the application/reference details for future communication.
Important Details Before Applying
- The position is based in Pithampur, Madhya Pradesh.
- This is a full-time Executive – Quality Control opportunity.
- The application deadline is October 30, 2026.
- The job requisition number is R00004372.
- The provided posting does not specify salary or CTC.
- Specific educational and experience requirements are not included in the supplied job description.
- The role involves laboratory testing, analytical documentation, method-related activities, and GLP/GMP compliance.
- Applicants should verify the latest vacancy status and requirements through the official employer careers portal.
Frequently Asked Questions
1. What is the job title at Piramal Pharma Solutions?
The position is Executive – Quality Control.
2. Where is this Piramal Pharma Solutions job located?
The position is based in Pithampur, Madhya Pradesh.
3. What is the job type?
It is a full-time position.
4. What is the requisition ID?
The requisition ID is R00004372.
5. What is the last date to apply?
The application deadline mentioned in the supplied posting is October 30, 2026.
6. What will the Executive – Quality Control do?
The role involves QC testing of finished products, in-process samples, raw materials, stability samples and other materials, along with laboratory documentation, analytical method activities, sample analysis and GLP/GMP compliance.
7. Does the role involve analytical method validation?
Yes. The job description includes analytical method transfer, validation and verification activities for new projects.
8. Does the position involve laboratory documentation?
Yes. The role includes maintaining analytical records, raw data, instrument/equipment logbooks, laboratory notebooks, chromatograms and Certificates of Analysis.
9. Is salary mentioned for this vacancy?
No. The salary or CTC is not specified in the provided job posting.
10. Is the required qualification mentioned?
A specific educational qualification is not provided in the supplied vacancy details. Candidates should check the official posting for the latest eligibility information.
11. Is previous experience mandatory?
The supplied job description does not state a minimum experience requirement. Applicants should verify the official listing for any applicable experience criteria.
12. How can candidates apply?
Candidates can apply online through the official Piramal Pharma Solutions careers portal using the application link provided above.
Important Note
Recruitment details, eligibility requirements, application deadlines, and vacancy status may change at the employer’s discretion. Candidates should verify all information, including qualification, experience, salary, and other recruitment conditions, on the official Piramal Pharma Solutions careers portal before applying.