Piramal Pharma Solutions Hiring 2026 – Technical Staff Jobs in Pithampur
Are you looking for an opportunity in pharmaceutical manufacturing and production?
Piramal Pharma Solutions is hiring for a Technical Staff position at its manufacturing facility in Pithampur, Madhya Pradesh.
The role focuses on granulation operations, shift supervision, cGMP compliance, manufacturing documentation, equipment handling and team coordination. It is suited to professionals who have experience working in pharmaceutical manufacturing environments.
Job Overview
| Details | Information |
|---|---|
| Company | Piramal Pharma Solutions |
| Position | Technical Staff |
| Department | Manufacturing / Production |
| Primary Area | Granulation |
| Experience | Relevant manufacturing/supervisory experience |
| Qualification | Technical or pharmacy background preferred |
| Location | Pithampur, Madhya Pradesh |
| Work Type | On-site / Full-time |
| Job ID | R00004169 |
| Last Date | October 11, 2026 |
About Piramal Pharma Solutions
Piramal Pharma Solutions is a global Contract Development and Manufacturing Organization (CDMO) and part of Piramal Pharma Limited.
The organization provides pharmaceutical development and manufacturing services across different stages of the drug lifecycle, serving both innovator and generic pharmaceutical companies.
Its capabilities include areas such as drug discovery, pharmaceutical development, clinical trial supplies, API manufacturing and finished dosage forms.
For professionals interested in regulated pharmaceutical manufacturing, the company provides exposure to structured quality systems, cGMP processes and global pharmaceutical operations.
Technical Staff – Granulation
The Technical Staff position is primarily responsible for supervising granulation activities during assigned shifts.
The person in this role will help ensure that manufacturing activities are carried out safely, efficiently and according to approved procedures.
Main Areas of Work
- Granulation operations
- Shift supervision
- Manufacturing documentation
- cGMP compliance
- Equipment and process monitoring
- Manpower allocation
- Batch record review
- Safety and hygiene
- SAP reporting
Eligibility & Experience
The original vacancy does not specify a single mandatory educational qualification. Candidates with a relevant technical, manufacturing or pharmacy background and suitable pharmaceutical manufacturing experience should review the official job description before applying.
Relevant experience in areas such as:
- Pharmaceutical production
- Granulation
- Oral solid dosage manufacturing
- Manufacturing supervision
- GMP operations
- Production documentation
can be valuable for this position.
Key Skills Required
Candidates should be comfortable with pharmaceutical manufacturing processes and shift-based operations.
Important skills include:
- Knowledge of cGMP requirements
- Understanding of Batch Manufacturing Records (BMR)
- Knowledge of ALCOA+ principles
- Granulation line operations
- Weight verification
- Product recipe selection
- Equipment qualification and validation
- Basic machine troubleshooting
- SAP documentation/reporting
- Calibration verification
- Manpower management
- EHS and workplace safety
Knowledge of HIRA, 6S, ISO 14001 and ISO 13485 practices is also relevant to the role.
Key Responsibilities
The selected candidate may be responsible for:
- Supervise granulation operations during assigned shifts
- Allocate manpower across different workstations
- Monitor line operations and production activities
- Perform weight verification and recipe selection checks
- Review Batch Manufacturing Records
- Complete manufacturing documentation according to ALCOA+ principles
- Monitor critical process parameters
- Handle minor machine parameter adjustments
- Troubleshoot routine operational issues
- Support equipment and area qualification activities
- Participate in validation activities
- Check calibration and qualification status of equipment
- Ensure proper line clearance during product changeovers
- Monitor temperature, relative humidity and pressure conditions
- Maintain cleanliness and hygiene standards
- Conduct safety checks and toolbox talks
- Report near misses and safety concerns
- Provide training and guidance to junior team members
- Update daily activities in SAP
- Take responsibility for the section when the supervisor is unavailable
Experience in Granulation Can Be Valuable
Granulation is an important stage in oral solid dosage manufacturing, where powder blends are processed to achieve suitable properties for subsequent manufacturing steps.
Because this position involves shift supervision and process monitoring, candidates who understand production equipment, batch documentation, line clearance, process parameters and GMP requirements may find the role particularly relevant to their background.
What Is ALCOA+ in Pharma Manufacturing?
For professionals applying to manufacturing roles, understanding ALCOA+ is important.
ALCOA+ principles help ensure that pharmaceutical records are reliable, traceable and suitable for regulatory review.
In practical terms, manufacturing documentation should be:
- Attributable
- Legible
- Contemporaneous
- Original
- Accurate
The additional principles extend these expectations to ensure records remain complete, consistent, enduring and available.
Benefits & Career Opportunities
The position offers an opportunity to develop experience in:
- cGMP pharmaceutical manufacturing
- Granulation operations
- Production supervision
- Validation and qualification
- EHS practices
- Manufacturing documentation
- SAP-based reporting
- Pharmaceutical quality systems
Professionals can also gain valuable experience working within a globally integrated CDMO environment.
Job Location
Piramal Pharma Solutions
Pithampur, Madhya Pradesh, India
The position is fully on-site, so applicants should be prepared to work from the Pithampur manufacturing facility.
Application Deadline
Last Date to Apply: October 11, 2026
Candidates are advised to submit their application before the deadline rather than waiting until the final day.
How to Apply
This is an online application opportunity, not a walk-in interview.
Candidates should apply through the official Piramal Pharma Solutions careers portal.
Job Reference
R00004169 – Technical Staff
When applying, highlight relevant experience in:
- Granulation
- Pharma manufacturing
- OSD production
- cGMP
- BMR documentation
- Equipment handling
- Shift supervision
Verified Job Opportunity
The vacancy is listed through the Piramal Pharma Solutions careers system under job reference R00004169.
Candidates should always verify the current status of the vacancy on the official careers portal before submitting an application.
Why Consider Piramal Pharma Solutions?
For professionals interested in pharmaceutical manufacturing, this position can provide practical exposure to granulation, production supervision, quality systems and regulated manufacturing processes.
The role also combines technical responsibilities with manpower coordination and documentation, making it relevant for candidates who want to progress toward broader production and manufacturing leadership positions.
Frequently Asked Questions
1. What is the position offered by Piramal Pharma Solutions?
The position is Technical Staff – Granulation, within the Manufacturing/Production function.
2. Where is the job located?
The position is based at Pithampur, Madhya Pradesh.
3. Is this a work-from-home position?
No. This is an on-site pharmaceutical manufacturing role.
4. What is the main responsibility of the Technical Staff?
The role involves supervising granulation operations, ensuring cGMP compliance, maintaining documentation, allocating manpower and monitoring production activities.
5. Is granulation experience important?
Yes. Experience in granulation or pharmaceutical manufacturing is highly relevant because the position involves direct supervision of granulation operations.
6. What is the job reference number?
The job reference is R00004169.
7. What is the last date to apply?
The application deadline is October 11, 2026.
8. Is this a walk-in interview?
No. Candidates should apply online through the official careers portal.
