Danopharm Walk-in QC Production
- Company Overview
- Job Role & Responsibilities
- 1. Trainee – Production
- 2. Officer – Quality Control
- 3. QC Reviewer
- 4. Officer / Operator – Production
- Eligibility / Qualifications
- Location & Salary
- Application Process
- Why Consider a Career in API Manufacturing?
- Frequently Asked Questions (FAQs)
- 1. How many vacancies are available?
- 2. Is pharma experience mandatory?
- 3. What analytical instrument knowledge is required?
- 4. Are freshers eligible?
- 5. Is there any salary limit?
- Job Summary
BSc ITI QC Production Jobs Ankleshwar
B.Sc/ITI QC & Production vacancies at Danopharm Ankleshwar. 12 openings for fresher & experienced candidates. Walk-in Mon–Sat.
Danopharm Chemicals Pvt. Ltd. has announced multiple openings in Production and Quality Control at its Ankleshwar manufacturing facility. The company is hiring Trainee Production, Production Officer/Operator, QC Officer, and QC Reviewer roles. Candidates with pharmaceutical API or chemical manufacturing experience are encouraged to apply or attend the walk-in interview.
If you are searching for pharma jobs in Ankleshwar, QC officer vacancy in API plant, GMP production operator jobs, HPLC reviewer careers, or B.Sc chemistry jobs in Gujarat pharma industry, this opportunity offers strong growth in a bulk drug manufacturing environment.
Company Overview
Danopharm Chemicals Pvt. Ltd., established in 1995, is an Indian manufacturer of pharmaceutical bulk drugs and intermediates. The company operates a GMP-compliant manufacturing facility in Ankleshwar, Gujarat, one of India’s largest pharmaceutical and chemical hubs.
The plant is equipped for handling complex chemical reactions and supports global markets through high-quality API production and contract manufacturing services. Danopharm focuses on scientific innovation, regulatory compliance, and process efficiency, making it a stable platform for professionals seeking long-term careers in API manufacturing and quality control.
Working here provides exposure to:
- Bulk drug (API) manufacturing processes
- GMP-compliant plant operations
- Wet lab and analytical QC systems
- HPLC data review and documentation control
- Global export-oriented manufacturing standards
Job Role & Responsibilities
1. Trainee – Production
Qualification: B.Sc / ITI (AOCP)
Experience: Fresher
Vacancy: 01
Key Responsibilities:
- Assist in API production activities under supervision
- Follow plant SOPs and GMP documentation practices
- Support chemical process handling and material transfer
- Maintain safety compliance while handling solvents and intermediates
Candidates must have completed ITI AOCP or B.Sc in a relevant science discipline.
2. Officer – Quality Control
Qualification: B.Sc / M.Sc
Experience: Minimum 2 Years
Vacancies: 06
Key Responsibilities:
- Perform sampling activities as per SOP
- Conduct wet lab analysis and routine testing
- Maintain GMP-compliant laboratory documentation
- Ensure data accuracy and traceability
- Support audit preparation and regulatory compliance
Experience in API QC laboratory operations is essential.
3. QC Reviewer
Qualification: B.Sc / M.Sc
Experience: Minimum 5 Years
Vacancy: 01
Key Responsibilities:
- Review HPLC analytical data and chromatograms
- Verify laboratory documentation and reports
- Ensure compliance with GMP and data integrity guidelines
- Support OOS investigations and audit queries
Strong experience in HPLC reviewing within pharmaceutical API manufacturing is mandatory.
4. Officer / Operator – Production
Qualification: B.Sc / Diploma / ITI
Experience: Minimum 1 Year
Vacancies: 04
Key Responsibilities:
- Handle plant operations and chemical process equipment
- Maintain GMP documentation and batch records
- Assist in manpower coordination and shift activities
- Ensure safe handling of chemicals and adherence to SOPs
Prior pharma or chemical industry experience is required.
Eligibility / Qualifications
Relevant Courses (comma-separated):
B.Sc Chemistry, M.Sc Chemistry, ITI AOCP, Diploma in Chemical Engineering, Diploma in Mechanical Engineering
Experience Requirements:
- Fresher for Trainee Production
- 1–2+ years for Production Officer
- 2+ years for QC Officer
- 5+ years for QC Reviewer (HPLC review mandatory)
Industry Background Required: Pharmaceutical API or Chemical Manufacturing
Immediate joiners are preferred. No salary bar for the right candidate based on skills and experience.
Location & Salary
Work Location: GIDC Ankleshwar, Bharuch District, Gujarat
Industry: Pharmaceutical API & Bulk Drug Manufacturing
Ankleshwar is one of India’s major pharmaceutical and chemical industrial zones, offering long-term growth in API production and quality control roles.
Salary: As per industry norms. Compensation will be aligned with experience, analytical skills, and plant exposure. Experienced HPLC reviewers and QC professionals typically receive competitive packages in API manufacturing sectors.
Application Process
Walk-In Interview Timings:
Monday to Saturday
11:00 AM to 03:00 PM
Address:
C-1/7130, 7131, 7132, 7133 & 7102
GIDC Ankleshwar – 393002
District Bharuch, Gujarat
Interested candidates may also email resumes to:
hr@danopharm.com
Documents to Carry:
- Updated Resume
- Salary Slip (if applicable)
- Educational Certificates
- Experience Certificates
Shortlisted candidates will undergo technical and HR evaluation.
Why Consider a Career in API Manufacturing?
API and bulk drug manufacturing professionals gain:
- Deep exposure to chemical process operations
- Strong regulatory and GMP compliance experience
- Advanced analytical instrument handling (HPLC, wet lab)
- Career growth into senior QC and production management roles
- Opportunities in global pharmaceutical supply chains
Experience in Ankleshwar-based API companies significantly enhances career prospects in India’s pharmaceutical sector.
Frequently Asked Questions (FAQs)
1. How many vacancies are available?
A total of 12 positions across Production and QC departments.
2. Is pharma experience mandatory?
Yes, pharma or chemical industry experience is required except for the Trainee role.
3. What analytical instrument knowledge is required?
HPLC review experience is mandatory for QC Reviewer roles.
4. Are freshers eligible?
Yes, freshers are eligible for Trainee Production (ITI AOCP/B.Sc only).
5. Is there any salary limit?
No salary bar for suitable and experienced candidates.
Job Summary
| Company | Danopharm Chemicals Pvt. Ltd. |
|---|---|
| Vacancies | Trainee Production; Production Officer/Operator; QC Officer; QC Reviewer |
| Required Education | B.Sc, M.Sc, ITI (AOCP), Diploma |
| Experience | Fresher to 5+ Years (Role Based) |
To apply for this job email your details to hr@danopharm.com
