Stellar walk-in Production, QA, QC, ADL, IPQA, Engineering
- H2: Company Overview
- H2: Job Role & Responsibilities
- H3: Production Department
- H3: Engineering Department
- H3: Quality Control (QC)
- H3: Microbiology Department
- H3: Quality Assurance (QA)
- H3: IPQA Department
- H3: DQA Department
- H3: Analytical Development Laboratory (ADL)
- H3: Formulation & Development (F&D)
- H3: HR/Admin Department
- H2: Eligibility / Qualifications
- Educational Qualifications
- Relevant Courses
- Experience Requirements
- H2: Location & Salary
- H2: Application Process
- Walk-In Interview Schedule
- Walk-In Interview Schedule
- H2: Frequently Asked Questions (FAQs)
- 1. Is OSD formulation experience mandatory?
- 2. Are freshers eligible to apply?
- 3. Which departments have vacancies?
- 4. What qualifications are accepted?
- 5. Can candidates apply through email?
- 6. What is the job location?
- Summary
Stellar Formulations Hiring QA QC Production Jobs
Stellar Formulations hiring for Production, QA, QC, ADL, IPQA and Engineering roles in Vadodara. BPharm, MPharm, MSc candidates can apply.
Pharmaceutical professionals seeking OSD formulation jobs in Gujarat have an excellent opportunity with Stellar Formulations Industries Pvt. Ltd. The company is conducting a walk-in interview drive for multiple vacancies across Production, Quality Assurance, Quality Control, IPQA, DQA, ADL, Engineering, HR/Admin, Microbiology, and Formulation & Development departments.
This hiring drive is open to freshers and experienced professionals with qualifications including B.Pharm, M.Pharm, M.Sc Chemistry, M.Sc Microbiology, BE, B.Tech, Diploma Engineering, MBA HR, MSW, and MLW. Candidates with exposure to solid oral dosage (OSD) manufacturing, pharmaceutical quality systems, regulatory compliance, validation, analytical development, and formulation development are encouraged to attend.
The primary keyword for this job posting is OSD Formulation Jobs.
H2: Company Overview
Stellar Formulations Industries Pvt. Ltd. is a pharmaceutical manufacturing company focused on the development and production of high-quality solid oral dosage formulations. The company operates modern manufacturing facilities and follows current Good Manufacturing Practices (cGMP) to ensure quality, safety, and regulatory compliance.
With growing demand in the pharmaceutical manufacturing sector, Stellar Formulations continues to expand its workforce across production, quality assurance, analytical development, microbiology, engineering, and formulation development functions. Candidates joining the organization gain exposure to regulated pharmaceutical manufacturing environments, quality systems, validation processes, and drug development operations.
For all positions, prior exposure to OSD formulation manufacturing is preferred.
H2: Job Role & Responsibilities
H3: Production Department
Positions Available
- Executive
- Trainee Officer
Key Responsibilities
- Execute manufacturing activities in OSD production areas.
- Handle batch manufacturing records and production documentation.
- Monitor manufacturing processes and equipment performance.
- Ensure compliance with GMP requirements.
- Coordinate production schedules and shift activities.
- Maintain process efficiency and product quality standards.
H3: Engineering Department
Positions Available
- Executive QMS
- Senior Officer (Mechanical)
- Senior Officer (Electrical)
Key Responsibilities
- Handle preventive and breakdown maintenance.
- Manage equipment qualification and utility systems.
- Maintain engineering documentation and QMS records.
- Support HVAC, electrical, and mechanical operations.
- Ensure regulatory compliance for engineering systems.
- Coordinate maintenance planning and execution.
H3: Quality Control (QC)
Positions Available
- Executive (AMV)
- Senior Officer
- Senior Officer (Documentation)
Key Responsibilities
- Perform analytical testing of raw materials and finished products.
- Conduct analytical method validation activities.
- Prepare and review laboratory documentation.
- Operate analytical instruments as per SOP requirements.
- Ensure compliance with GLP and GMP standards.
- Support audit and regulatory inspection readiness.
H3: Microbiology Department
Position Available
- Senior Officer
Key Responsibilities
- Conduct microbiological testing and environmental monitoring.
- Maintain microbial laboratory documentation.
- Perform water testing and microbial analysis.
- Ensure compliance with pharmaceutical microbiology procedures.
- Support quality and validation programs.
H3: Quality Assurance (QA)
Positions Available
- Manager
- Assistant Manager
- Senior Officer (Documentation)
Key Responsibilities
- Oversee quality systems and GMP compliance.
- Review SOPs, protocols, and validation reports.
- Handle deviation investigations and CAPA management.
- Ensure audit readiness and regulatory compliance.
- Support qualification and validation activities.
- Manage documentation control processes.
H3: IPQA Department
Positions Available
- Senior Officer
- Officer
Key Responsibilities
- Conduct in-process quality checks.
- Perform line clearance activities.
- Monitor manufacturing compliance.
- Review batch records and shop floor documentation.
- Ensure adherence to GMP requirements.
H3: DQA Department
Positions Available
- Executive
- Senior Officer
Key Responsibilities
- Handle documentation quality assurance activities.
- Review controlled documents and records.
- Maintain document management systems.
- Support quality compliance initiatives.
H3: Analytical Development Laboratory (ADL)
Positions Available
- Senior Officer
- Officer
Key Responsibilities
- Develop and validate analytical methods.
- Conduct stability and analytical studies.
- Support formulation development projects.
- Prepare analytical reports and protocols.
- Ensure compliance with regulatory expectations.
H3: Formulation & Development (F&D)
Position Available
- Senior Officer
Key Responsibilities
- Support formulation development activities.
- Conduct product optimization and scale-up studies.
- Prepare development reports and documentation.
- Participate in technology transfer activities.
- Collaborate with analytical and manufacturing teams.
H3: HR/Admin Department
Position Available
- Officer
Key Responsibilities
- Manage HR operations and employee records.
- Coordinate recruitment and onboarding.
- Support employee engagement activities.
- Maintain administrative documentation and compliance records.
H2: Eligibility / Qualifications
Educational Qualifications
Candidates with the following qualifications are eligible to apply:
- B.Pharm
- M.Pharm
- M.Sc Chemistry
- M.Sc Microbiology
- BE
- B.Tech
- Diploma (Mechanical/Electrical)
- MBA HR
- MSW
- MLW
Relevant Courses
Pharmacy, Pharmaceutical Sciences, Pharmaceutical Technology, Quality Assurance, Quality Control, Analytical Chemistry, Industrial Chemistry, Organic Chemistry, Microbiology, Formulation Development, Regulatory Affairs, Validation Studies, Mechanical Engineering, Electrical Engineering, Human Resource Management, Industrial Relations, Manufacturing Technology.
Experience Requirements
- Production Executive: 5–7 Years
- Production Trainee Officer: 0–1 Year
- Engineering Executive QMS: 5–7 Years
- Engineering Senior Officer: 3–5 Years
- HR/Admin Officer: 1–3 Years
- QC Executive (AMV): 5–7 Years
- QC Senior Officer: 3–5 Years
- QA Manager: 12–15 Years
- QA Assistant Manager: 9–12 Years
- QA/IPQA/DQA Positions: 1–7 Years
- ADL Positions: 1–5 Years
- F&D Senior Officer: 3–5 Years
H2: Location & Salary
Location: Vadodara, Gujarat
Salary: Approx. ₹2.8 LPA – ₹18 LPA (Based on qualification, experience, designation, and interview performance)
H2: Application Process
Interested candidates can attend the walk-in interview directly with:
- Updated Resume
- Current Salary Proof
- Passport Size Photographs
Walk-In Interview Schedule
Date: 30 May 2026
Venue: Stellar Formulations Industries Pvt. Ltd., 83-A, Alindra GIDC Estate, Savli Taluka, Vadodara
Time: 9:30 AM – 5:00 PM
Walk-In Interview Schedule
Date: 31 May 2026
Venue: AURUM Building, ISKCON Temple Road, Opp. Aastha Hospital, Near D-Mart, Vasna Road, Vadodara, Gujarat
Time: 9:30 AM – 5:00 PM
Candidates unable to attend the walk-in interview may send their updated CV to:
Email: hr.savli_u1@stellarformulations.in
Contact: +91 6357130094 / +91 6357313009
H2: Frequently Asked Questions (FAQs)
1. Is OSD formulation experience mandatory?
Yes, the company has specifically mentioned that OSD formulation exposure is essential for all positions.
2. Are freshers eligible to apply?
Yes. The Production Trainee Officer position is open for candidates with 0–1 year of experience.
3. Which departments have vacancies?
Production, Engineering, QA, QC, IPQA, DQA, ADL, Microbiology, F&D, and HR/Admin departments are hiring.
4. What qualifications are accepted?
B.Pharm, M.Pharm, M.Sc Chemistry, M.Sc Microbiology, BE, B.Tech, Diploma, MBA HR, MSW, and MLW qualifications are accepted depending on the role.
5. Can candidates apply through email?
Yes. Candidates unable to attend the walk-in drive can email their resume to hr.savli_u1@stellarformulations.in.
6. What is the job location?
The positions are based at Stellar Formulations’ manufacturing facility in Vadodara, Gujarat.
Summary
| Category | Details |
|---|---|
| Company | Stellar Formulations Industries Pvt. Ltd. |
| Department Vacancies | Production, Engineering, QA, QC, IPQA, DQA, ADL, Microbiology, F&D, HR/Admin |
| Qualification | B.Pharm, M.Pharm, M.Sc Chemistry, M.Sc Microbiology, BE, B.Tech, Diploma, MBA HR, MSW, MLW |
| Experience | 0–15 Years |
| Location | Vadodara, Gujarat |




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