The Dishman Group continually invests in the pharmaceutical industry, ensuring our businesses can provide pharmaceutical customers with high-value, high-quality products and services today and in the future. Our focus is to add value to the global pharmaceutical industry by serving as a reliable partner. We strongly believe that our business is successful only when our customers are successful.

Walk in Interview for Bavla Plant, Ahmedabad

Production Formulation (Softgel)

Production – Softgel (Officer / Sr. Officer) 
Experience : 02 to 05 Years
Qualification : B.Pharm/ M.Pharm
Should be well versed with cGMP/GDP, and Schedule M guidelines Expertise Manufacturing of gelatin and medicament (experience in handling PEG based product and high potent molecule is required). Trouble shooting during manufacturing.
Well versed with Encapsulation methodology, handle trouble shooting of encapsulation activity, Online Documentation, Document review and preparation, and QMS
To perform calibration activity of all IPQC instruments Should be fluent in English and well versed with SAP entries.

Production – Packaging – (Formulation – Softgel) (Executive) 
Experience : 02 to 07 Years
Qualification : B.Pharm/ M.Pharm
•  Should be well versed with cGMP/GDP and Schedule M guidelines.
•  Online Documentation, Document review and preparation Well versed in QMS
•  Expertise in BQS blister packing machine and secondary packing and troubleshooting of the BQS machine related to softgelatin capsules packing.
• Must have knowledge of online blister coding, export packaging requirements, and palletisation for export
• Should be fluent in English and well versed with SAP entries.

Quality Assurance (API & Formulation)
Designation : Officer/ Executive/ Senior Executive/ Assistant Manger (QA – Formulation)
Experience : 03 to 10 Years
Qualification : M.Sc. Chemistry/ B.Pharm/ M.Pharm
• Carry out line clearance activity of shop floor and online review of all related documents regarding line clearance.
• Carry out all the in-process activity of the shop floor and maintaining online document of all the shop floor activity.
• Preparation and Review of PVP, CVP and SOPs.
• Carry out and involvement in validation (process validation & cleaning validation) activity of shop floor and maintaining the documents related to validation activity.
• Carry out all the sampling of different stages of the batch manufacturing process and filling of protocol and sending of all samples to QC (Quality Control).
• Handling of Hold time study sample and send to QC (Quality Control) as per define schedule.
• Handling of Control sample and maintaining its record.
• Ensure batch manufacturing & packed as per standard approved BMR/ BPR.

Officer/ Executive/ Senior Executive/ Assistant Manger (QA – API)
Experience : 03 to 10 Years
Qualification : M.Sc Chemistry / B.Pharm / M.Pharm
• Prepare and review Standard Operating Procedures (SOPs).
• Review Batch Manufacturing Records (BMR), Batch Packing Records (BPR), Engineering Change Requests (ECR), and Process Flow • Diagrams (PFD). Oversee Process Performance Qualification (PPQ) and Cleaning Validation. Handle and document Deviations and manage Change Control activities. Investigate Out of Specification (OOS) and Out of Trend (OOT) results related to manufacturing.
• Prepare and review Risk Assessment reports and also prepare and review Annual Product Quality Reviews (APQR).
• Review Line Clearance activities and Qualification documents.
• Perform sampling activities and Participate in Technology Transfer processes and Assist in product release activities.
• Ensure compliance with Safety, Health, and Environmental norms, including proper use of personal protective equipment (PPE).
• Should be fluent in English

Walk in Interview
Date : 25/01/2026, Sunday
Time : 10:00 am to 04.00 pm N
Venue : HOTEL GINGER, Behind Honda Showroom, Opp. Empress Mall, N.H 8, Salvav Vapi, Gujarat 396191

If unable to attend interview, please share resume on [email protected]