Piramal Pharma Walk-In Interview 2026 – QC & QA Jobs in Pithampur
Are you an experienced pharmaceutical Quality Control or Quality Assurance professional looking for your next career opportunity?
Piramal Pharma Limited is conducting a walk-in interview from 15 to 18 September 2026 at its Pithampur facility near Indore, Madhya Pradesh.
The recruitment drive includes several positions across Quality Control, Method Validation, Raw Materials, QC Review, IPQA and QA. Candidates with B.Pharm or M.Sc qualifications and relevant pharmaceutical experience can apply.
This is particularly relevant for professionals with experience in OSD manufacturing, analytical testing, HPLC, GC, LC-MS, method validation, QMS and IPQA.
Piramal Pharma Walk-In Job Overview
| Details | Information |
|---|---|
| Company | Piramal Pharma Limited |
| Departments | QC, QA & IPQA |
| Qualification | B.Pharm / M.Sc |
| Experience | 3–10+ years, depending on role |
| Job Location | Pithampur, Madhya Pradesh |
| Interview Location | Pithampur Industrial Area |
| Interview Dates | 15–18 September 2026 |
| Interview Time | 9:00 AM – 3:00 PM |
| Work Type | On-site |
About Piramal Pharma
Piramal Pharma Limited is a global pharmaceutical company with businesses spanning contract development and manufacturing, complex hospital generics and consumer healthcare.
The company operates multiple development and manufacturing facilities and serves customers across international markets. Its Pithampur operations provide opportunities for professionals interested in oral solid dosage manufacturing, quality systems and analytical operations.
For experienced QC and QA professionals, this recruitment drive offers exposure to a regulated pharmaceutical manufacturing environment and global quality standards.
Piramal Pharma Open Positions
1. QC Executive / Senior Executive
Department: Quality Control
Experience: Minimum 3 years
Qualification: B.Pharm / M.Sc
Preferred Expertise
- HPLC
- GC
- LC-MS
- Dissolution testing
- Analytical testing
- Pharmaceutical laboratory operations
Candidates should be comfortable working in a regulated QC environment and maintaining accurate analytical documentation.
2. QC Manager – Method Validation & Transfer
Experience: Minimum 10 years
Qualification: B.Pharm / M.Sc
The position involves leading analytical method validation and transfer activities while managing a QC team.
Key Areas
- Analytical method validation
- Method transfer
- Documentation and compliance
- Team leadership
- Troubleshooting analytical activities
3. QC Manager – Raw Materials
Experience: Minimum 10 years
Qualification: B.Pharm / M.Sc
This role focuses on managing the Raw Materials QC section supporting OSD manufacturing operations.
Responsibilities Include
- Managing raw material testing activities
- Supervising QC personnel
- Ensuring compliance with specifications
- Reviewing analytical documentation
- Maintaining laboratory quality standards
4. QC Reviewer – Senior Executive / Deputy Manager
Experience: Minimum 6 years
Qualification: B.Pharm / M.Sc
This position is suitable for professionals experienced in QC data review and quality systems.
Key Focus Areas
- QC data review
- OOS and OOT investigations
- Incident handling
- QMS activities
- Analytical documentation review
5. IPQA / QA – Executive / Senior Executive
Experience: Minimum 9 years
Qualification: B.Pharm / M.Sc
Professionals with experience in OSD manufacturing and IPQA operations can apply.
Relevant Experience
- IPQA activities
- BMR/BPR preparation and review
- Cleaning validation
- Equipment qualification
- Manufacturing floor compliance
- cGMP requirements
Eligibility Criteria
Candidates should meet the qualification and experience requirements for their preferred position.
Educational Qualification
- B.Pharm
- M.Sc
Experience
Experience requirements vary by position:
- QC Executive/Sr. Executive: 3+ years
- QC Reviewer: 6+ years
- IPQA/QA: 9+ years
- QC Manager positions: 10+ years
Relevant experience in pharmaceutical manufacturing, OSD operations, QC laboratories or QA/IPQA is important for these positions.
Skills Required
Depending on the position, candidates should have experience with:
- HPLC and GC
- LC-MS
- Dissolution testing
- Analytical method validation
- Method transfer
- Raw material testing
- Stability testing
- QC data review
- OOS/OOT investigations
- QMS
- IPQA
- BMR/BPR documentation
- Cleaning validation
- Equipment qualification
- cGMP and regulatory compliance
Key Responsibilities
Selected professionals may be responsible for:
- Performing and reviewing pharmaceutical analytical testing
- Ensuring laboratory activities comply with approved procedures
- Managing analytical method validation and transfer
- Reviewing QC data and laboratory records
- Handling OOS, OOT and quality incidents
- Supporting IPQA activities on the manufacturing floor
- Preparing and reviewing BMR/BPR documentation
- Supporting cleaning validation and equipment qualification
- Maintaining inspection-ready documentation
- Working with production, QA and other cross-functional teams
Salary & Benefits
Piramal Pharma has not specified a salary figure in the provided recruitment details. Compensation is expected to depend on experience, qualifications and the position offered.
Potential career advantages include:
- Growth within a global pharmaceutical organization
- Exposure to regulated manufacturing operations
- Experience with advanced analytical technologies
- Leadership opportunities in QC and QA
- Professional learning and development
- Exposure to international quality standards
Piramal Pharma Walk-In Interview Details
🗓️ Interview Dates
15 September to 18 September 2026
⏰ Interview Time
9:00 AM to 3:00 PM
📍 Venue
Piramal Pharma Limited
Pithampur Industrial Area, Sector-2
Pithampur, Madhya Pradesh – 454775
📍 Job Location
Pithampur, Madhya Pradesh
Documents to Carry
Candidates attending the walk-in should carry:
- Updated Resume/CV
- Educational certificates
- Experience certificates
- Latest salary slip, if applicable
- Government-issued ID proof
- Relevant employment documents
Experienced candidates should also be prepared to discuss their current responsibilities, technical expertise and previous pharmaceutical projects.
How to Apply
Candidates who meet the eligibility requirements can attend the walk-in interview directly at the Pithampur venue.
You can also contact the recruitment team through:
Email: Noopur.pandit@piramal.com
Email: Akanksha.gupta@piramal.com
Contact: +91 91091 44429
Mention your preferred position and relevant experience when contacting the recruitment team.
Interview Preparation Tips
Before attending the interview, revise the technical areas related to your target position.
For QC Candidates
Prepare topics such as:
- HPLC and GC
- Method validation
- Dissolution
- Stability testing
- OOS/OOT
- Data integrity
- Pharmacopoeial requirements
For QA/IPQA Candidates
Revise:
- GMP
- QMS
- Deviations
- CAPA
- BMR/BPR
- Cleaning validation
- Equipment qualification
- IPQA activities
- Audit readiness
Also be ready to explain your actual hands-on experience rather than relying only on theoretical answers.
Why Consider Piramal Pharma?
Piramal Pharma provides professionals with an opportunity to work in a structured pharmaceutical manufacturing environment.
For QC and QA professionals, the Pithampur recruitment drive can provide exposure to:
- OSD manufacturing
- Analytical laboratory operations
- Quality systems
- Regulatory compliance
- Global pharmaceutical standards
- Cross-functional manufacturing activities
Senior candidates can also explore opportunities involving team leadership and quality management.
Frequently Asked Questions
1. When is the Piramal Pharma walk-in interview?
The walk-in interview is scheduled from 15 September to 18 September 2026, between 9:00 AM and 3:00 PM.
2. Where is the interview being conducted?
The interview will be held at Piramal Pharma Limited, Pithampur Industrial Area, Sector-2, Madhya Pradesh.
3. What qualifications are required?
The listed positions accept B.Pharm and M.Sc candidates.
4. Are freshers eligible?
No. The positions listed in this drive require relevant professional experience, starting from approximately 3 years, depending on the role.
5. What QC skills are preferred?
Experience with HPLC, GC, LC-MS, dissolution testing, method validation, data review and pharmaceutical QC operations is relevant.
6. What experience is required for QA/IPQA positions?
The listed IPQA/QA roles require around 9 years or more of relevant experience.
7. Can candidates with OSD experience apply?
Yes. OSD manufacturing, analytical testing and IPQA experience are particularly relevant to the listed positions.
8. How can I contact the recruitment team?
Candidates can contact Noopur.pandit@piramal.com, Akanksha.gupta@piramal.com, or +91 91091 44429.
9. Is there any recruitment fee?
Candidates should never pay a recruitment fee. Verify any communication directly with Piramal Pharma before sharing sensitive personal or financial information.
