Dishman Walk-In QA, QC, Production, R&D

Dishman Walk-In QA, QC, Production, R&D

Dishman Walk-In – QA, QC, Production, R&D – Ahmedabad

Dishman Carbogen Amcis hiring QA, QC, Production & R&D professionals in Ahmedabad. 2–15 years experience. Walk-in 21 Dec 2025.

Dishman Carbogen Amcis has announced a large-scale walk-in interview drive at its Corporate House in Ahmedabad for experienced professionals across Quality Assurance, Quality Control, Production (Formulation – Softgel), and Research & Development functions. This hiring drive supports Dishman’s growing API and formulation operations at its Bavla and Naroda manufacturing plants.

The walk-in is designed for mid-level to senior pharmaceutical professionals with hands-on experience in regulated manufacturing, quality systems, analytical laboratories, and R&D process development. Candidates seeking long-term, compliance-driven careers in a global pharmaceutical organization will find this opportunity highly relevant.


Company Overview

Dishman Carbogen Amcis is a globally integrated pharmaceutical company specializing in API manufacturing, formulations, contract research, and development services. With a strong footprint across India, Europe, and global regulated markets, the company is recognized for its scientific depth, compliance culture, and technology-driven operations.

Dishman operates USFDA, EU-GMP compliant facilities and supports global innovators and generic pharmaceutical companies through end-to-end solutions, from research and development to commercial manufacturing. Careers at Dishman offer exposure to complex molecules, advanced analytical platforms, and international regulatory standards.


Job Role & Responsibilities

Multiple roles are open across Quality, Production, and R&D functions. Selected candidates will be responsible for ensuring product quality, regulatory compliance, and efficient manufacturing or research execution.

Quality Assurance – API & Formulation (Bavla)

  • Manage quality documentation including issuance, retrieval, distribution, and archival
  • Review executed batch manufacturing records, ECRs, and analytical documentation
  • Handle sampling activities for finished products, stability, and hold-time samples
  • Monitor packing and repacking operations and maintain compliance records
  • Verify dispatch activities and approve QR codes
  • Conduct plant rounds and ensure compliance with cGMP, GLP, and data integrity practices
  • Prepare and review Product Quality Reviews (PQR)
  • Draft and review SOPs, equipment qualification protocols, and reports
  • Manage change control, deviations, and CAPA implementation
  • Prepare and review validation protocols and reports (process and cleaning)
  • Handle vendor qualification, equipment qualification, and external calibration records

Quality Control – API (Naroda)

  • Perform wet lab analysis and routine analytical testing
  • Operate and troubleshoot laboratory instruments including HPLC, GC, UV, IR, KF, and analytical balances
  • Ensure compliance with GDP and GLP requirements
  • Handle laboratory QMS activities such as OOS, deviations, and incident management
  • Maintain accurate analytical documentation and laboratory records

Quality Control – AMV (Bavla)

  • Perform analytical method validation and stability studies
  • Troubleshoot sophisticated QC instruments such as HPLC, UPLC, GC, GC-MS, and dissolution systems
  • Support day-to-day analytical operations and investigation activities

Production – Formulation (Softgel)

  • Execute softgel manufacturing operations including gelatin and medicament preparation
  • Handle PEG-based products and high-potency molecules
  • Perform encapsulation operations and troubleshooting
  • Manage online documentation, SAP entries, and batch record review
  • Perform calibration of IPQC instruments
  • Support QMS activities including change control, deviations, and CAPA

Production – Packaging & Operators (Softgel)

  • Operate and troubleshoot BQS blister packing machines
  • Handle primary and secondary packing activities
  • Perform online documentation including BMR, BPR, and equipment logs
  • Manage calibration of IPQC instruments and packing equipment
  • Support serialization, carton coding, and export packaging requirements

Research & Development Roles

Research Associate / Analytical Associate / Research Scientist

  • Conduct process development for API synthesis
  • Perform experimental work for product development and improvement
  • Support technology transfer, scale-up, and troubleshooting at pilot and commercial levels
  • Operate analytical instruments such as HPLC and GC for method development
  • Finalize synthetic routes based on feasibility, literature, and raw material availability

Eligibility / Qualifications

Required Education

M.Sc. Chemistry, M.Sc. Organic Chemistry, M.Sc. Analytical Chemistry, B.Pharmacy, M.Pharmacy, B.Sc., Diploma Engineering, ITI

Experience

  • Quality Assurance: 3–10 years
  • Quality Control (API): 2–8 years
  • Quality Control (AMV): 5–12 years
  • Production (Softgel): 2–10 years
  • R&D Roles: 2–15 years

Location & Salary

  • Job Locations: Bavla Plant, Naroda Plant (Gujarat)
  • Interview Venue: Dishman Corporate House, Bopal Ambli Road, Ahmedabad
  • Salary: Competitive and aligned with industry standards, based on role and experience

Walk-In Interview Details

  • Date: 21st December 2025 (Sunday)
  • Time: 10:00 AM to 04:00 PM
  • Venue:
    Dishman Corporate House
    Bopal Ambli Road, Ahmedabad

Application Process

Eligible candidates can directly attend the walk-in interview.

Candidates unable to attend may share their updated resume at:

Email: hrd@dishmangroup.com


Why Build Your Career at Dishman Carbogen Amcis

Dishman offers professionals the opportunity to work on complex APIs, advanced formulations, and high-end research projects within a globally regulated environment. Exposure to international clients, advanced technologies, and strong quality systems makes Dishman an ideal organization for long-term career growth in pharmaceuticals.


Frequently Asked Questions (FAQs)

Who can attend this walk-in interview?

Experienced professionals from Quality, Production, and R&D functions meeting the specified criteria can attend.

Is this walk-in open for freshers?

No. Most roles require prior industry experience.

Can I apply if I cannot attend in person?

Yes. Candidates may email their resumes to the HR contact provided.

Where will I be posted after selection?

Selected candidates will be placed at Bavla or Naroda plants based on role requirements.


Summary Table

Company Dishman Carbogen Amcis
Vacancies Multiple
Required Education M.Sc. Chemistry, M.Sc. Organic Chemistry, M.Sc. Analytical Chemistry, B.Pharm, M.Pharm, Diploma Engineering, ITI
Experience 2–15 years (Role-dependent)
Dishman Walk-In QA, QC, Production, R&D
Dishman Walk-In QA, QC, Production, R&D
Dishman Walk-In QA, QC, Production, R&D
Dishman Walk-In QA, QC, Production, R&D
Dishman Walk-In QA, QC, Production, R&D
Dishman Walk-In QA, QC, Production, R&D
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