Piramal Pharma Limited Walk-In Drive| Production, TSD/Process Engineering & Mechanical API Jobs

Piramal Pharma Limited has announced a Walk-In Drive for experienced professionals in the API Manufacturing Division. The recruitment is for Production (API), TSD/Process Engineering (API), and Mechanical (API) positions at the company’s Digwal, Telangana manufacturing facility. Candidates with relevant qualifications and API industry experience are invited to attend the interview.

Walk-In Interview Details

Particular Details

Company

Piramal Pharma Limited

Job Type

Walk-In Interview

Walk-In Date

Sunday, 26 July 2026

Time

10:00 AM – 4:00 PM

Interview Venue

Hotel Rockdale, Waltair Main Road, Near Seven Hills Hospital, Beside ICICI Bank, Visakhapatnam – 530002

Job Location

Digwal, Telangana

Available Positions

1. Executive – Production (API)

Qualification:

B.Sc / M.Sc

B.Tech / B.E. (Chemical Engineering)

Experience:

2–4 Years

Key Responsibilities:

API Production Operations

Batch Manufacturing Record (BMR) execution

Batch Packaging Record (BPR) documentation

GMP compliance

Process monitoring and documentation

2. Executive / Senior Executive – TSD / Process Engineering (API)

Qualification:

B.Tech / M.Tech / B.E. (Chemical Engineering)

Experience:

2–5 Years

Required Skills:

API Technology Transfer

Process Engineering

Batch Monitoring

Scale-up Activities

Pilot Plant Operations

Validation & Trial Batches

Process Flow Diagram (PFD)

Piping & Instrumentation Diagram (P&ID)

Process Mapping

HAZOP Studies

Process Troubleshooting

GMP Documentation

Deviation Closure

Investigation Reports

BMR & ECR Documentation

3. Executive – Mechanical (API)

Qualification:

B.Tech (Mechanical Engineering)

Experience:

3–6 Years

Required Skills:

API Plant Equipment Maintenance

Preventive & Breakdown Maintenance

Equipment Modifications

Good Manufacturing Practices (GMP)

Safety Standards

SAP Knowledge

Good Engineering Practices (GEP)

Who Should Apply?

Candidates who have:

Experience in API manufacturing plants.

Strong understanding of GMP documentation.

Knowledge of production, process engineering, validation, or mechanical maintenance.

Relevant educational qualifications and required experience.

Documents to Carry

Updated Resume/CV

Passport-size Photographs

Educational Certificates

Experience Certificates

Latest Salary Slip (if available)

Government Photo ID Proof

PAN Card & Aadhaar Card

Email ID

Candidates who are unable to attend the walk-in interview can send their updated CV to:

Kedarnath.mattam@piramal.com

Why Join Piramal Pharma?

Piramal Pharma Limited is a globally recognized pharmaceutical company offering career opportunities in API manufacturing, process engineering, and pharmaceutical operations. Employees gain exposure to advanced manufacturing technologies, regulatory compliance, technology transfer projects, and continuous professional development.

Technical FAQs

1. What is the role of BMR and BPR in API manufacturing?

Batch Manufacturing Record (BMR) documents every manufacturing step, while Batch Packaging Record (BPR) records packaging activities to ensure complete GMP compliance and product traceability.

2. What is Technology Transfer (TSD) in pharmaceuticals?

Technology Transfer involves transferring a manufacturing process from R&D or one manufacturing site to another while ensuring consistent product quality, process reproducibility, and regulatory compliance.

3. Why are PFD and P&ID important in API plants?

A Process Flow Diagram (PFD) provides an overview of the manufacturing process, while a Piping & Instrumentation Diagram (P&ID) shows equipment, pipelines, valves, and instrumentation used for operation and maintenance.

4. What is HAZOP in pharmaceutical manufacturing?

HAZOP (Hazard and Operability Study) is a structured risk assessment method used to identify process hazards, operational risks, and safety improvements before production begins.

5. What is the importance of GMP documentation?

GMP documentation ensures manufacturing activities are properly recorded, supports regulatory compliance, improves product quality, enables investigations, and maintains complete traceability throughout the production lifecycle.