Swiss Hiring Engineering, Production, QA, QC & Warehouse
- Company Overview
- Job Role & Responsibilities
- Engineering Department
- Production Department
- Quality Assurance Department
- Quality Control – Microbiology
- Warehouse Department
- Eligibility / Qualifications
- Eligible Courses (comma-separated)
- Location & Salary
- Application Process
- Why Build Your Career in Parenteral Manufacturing
- Frequently Asked Questions (FAQs)
- Is parenteral manufacturing experience mandatory?
- Are multiple departments hiring simultaneously?
- How can I apply?
- Is GMP knowledge required?
- Summary Table
Pharma Engineering Production QA QC Jobs | Bavla
Swiss Parenterals hiring Engineering, Production, QA, QC & Warehouse roles in Bavla, Ahmedabad. 1–10 yrs exp.
Swiss Parenterals Ltd. is inviting applications from experienced pharmaceutical professionals for multiple departments at its parenteral (injectable) manufacturing facility in Bavla, Ahmedabad. The company is hiring across Engineering, Production, Quality Assurance, Quality Control (Microbiology), and Warehouse functions. Candidates must have prior exposure to a regulated injectable or parenteral manufacturing plant.
This is a strong opportunity for professionals searching for injectable plant jobs in Gujarat, pharma engineering vacancies, QA executive injectable roles, QC microbiology jobs, sterile production operator openings, and warehouse executive pharma careers in a GMP-compliant environment.
Company Overview
Swiss Parenterals Ltd. is a well-established pharmaceutical manufacturer specializing in sterile injectable formulations. The company operates from its Bavla, Ahmedabad facility and adheres to stringent GMP and regulatory compliance standards required for parenteral manufacturing.
Injectable manufacturing demands strict environmental control, sterility assurance, water system validation, HVAC monitoring, and detailed documentation systems. Swiss Parenterals emphasizes quality systems, deviation control, CAPA management, and regulatory audit readiness to meet domestic and export market requirements.
Professionals joining Swiss gain hands-on exposure to aseptic manufacturing, environmental monitoring systems, QMS documentation, sterile utilities, and audit-facing operations aligned with global pharmaceutical standards.
Job Role & Responsibilities
Swiss Parenterals is hiring across multiple technical departments. All candidates must have prior exposure to parenteral or sterile manufacturing plants.
Engineering Department
1. Engineering – Executive (Plant Maintenance)
Experience: 4–5 Years
- Handle preventive and breakdown maintenance of mechanical and electrical equipment
- Troubleshoot plant machinery and utilities
- Maintain maintenance records and SOP documentation
- Coordinate with production and QA teams for uninterrupted operations
2. Engineering – Operator (Plant Maintenance)
Experience: 1–3 Years
Qualification: ITI Fitter preferred
- Perform mechanical fitting and routine maintenance activities
- Support breakdown maintenance
- Ensure GMP compliance in engineering areas
3. Engineering – Utilities (Chiller / Air Compressor / Nitrogen Plant)
Experience: 2–4 Years
- Operate and monitor utility systems
- Maintain logbooks and operating parameters
- Ensure uninterrupted supply to production areas
- Report abnormalities and follow safety SOPs
4. Engineering – Water System Operator
Experience: 2–4 Years
- Operate and maintain primary water systems
- Monitor critical parameters
- Maintain records as per SOPs
5. Engineering – HVAC Operator
Experience: 2–4 Years
- Maintain temperature and humidity in sterile areas
- Monitor HVAC parameters
- Ensure compliance with GMP standards
Production Department
1. Production Manager
Experience: 8–10 Years
- Oversee pharmaceutical production operations
- Manage manpower and batch planning
- Ensure GMP compliance and documentation accuracy
- Coordinate with QA/QC and regulatory teams
2. Production Officer – Filling & Capping
Experience: 1–2 Years
- Handle aseptic filling of injectable products
- Maintain BMR documentation
- Ensure cleanroom compliance and GMP adherence
3. Production Officer – Washing
Experience: 1–2 Years
- Manage equipment washing activities
- Maintain cleaning records
- Coordinate with QA for compliance verification
4. Production – Documentation (Sr. Officer / Executive)
Experience: 3–4 Years
- Handle BMR/BPR documentation
- Support outside production line documentation activities
- Ensure deviation and compliance tracking
5. Production Operators (Vial Washing / Tunnel / Autoclave / Filling / Capping / Labeling / Carton Coding)
Experience: 2–4 Years
- Operate sterile processing equipment
- Manage sterilization cycles (Autoclave)
- Handle vial washing and tunnel operations
- Perform dry powder filling and vial capping
- Operate labeling and carton coding machines
- Maintain accurate batch documentation and SOP adherence
Quality Assurance Department
1. QA – QMS (Executive to Assistant Manager)
Experience: 4–7 Years
- Manage Deviation, CAPA, Change Control, OOS
- Handle SOP documentation and review
- Support regulatory audits
- Ensure QMS compliance in injectable manufacturing
2. QA – IPQA (Sr. Officer to Executive)
Experience: 2–4 Years
- Perform line clearance and in-process checks
- Review BMR/BPR documentation
- Verify critical process parameters
- Support shop-floor compliance and audit readiness
Quality Control – Microbiology
QC Micro Executive
Experience: 3–4 Years
- Conduct Environmental Monitoring (EM)
- Perform sterility testing
- Analyze PW/WFI water systems
- Maintain aseptic practices and GMP documentation
- Support regulatory audit inspections
Warehouse Department
Warehouse Executive
Experience: 2–4 Years
- Handle receipt, storage, and issue of materials
- Maintain stock records and GRN entries
- Ensure FIFO compliance
- Coordinate with purchase, production, and maintenance teams
- Maintain adherence to SOPs and safety guidelines
Eligibility / Qualifications
Eligible Courses (comma-separated)
B.Pharm, M.Pharm, B.Sc Microbiology, M.Sc Microbiology, B.Sc Chemistry, M.Sc Chemistry, ITI Fitter, Diploma Mechanical Engineering, Diploma Electrical Engineering, BE Mechanical Engineering, BE Electrical Engineering
Candidates must have relevant experience in sterile injectable or parenteral pharmaceutical plants.
Location & Salary
Job Location: Bavla, Ahmedabad, Gujarat
Swiss Parenterals’ Bavla facility operates as a regulated injectable manufacturing plant with strong compliance standards.
Salary: As per company standards and experience level. Compensation will align with expertise in parenteral manufacturing and regulatory exposure.
Application Process
Interested candidates may share their updated CV at:
For additional information, candidates can refer to the official website: www.swiss.in
Candidates should clearly mention the department and designation applied for in the email subject line.
Why Build Your Career in Parenteral Manufacturing
Parenteral or injectable manufacturing is one of the most technically demanding segments of the pharmaceutical industry. It requires expertise in sterile processing, environmental control, water systems, HVAC validation, QMS documentation, and regulatory audit support.
Professionals in this domain benefit from:
- Exposure to aseptic manufacturing practices
- High regulatory compliance standards
- Strong career progression in QA, QC, Engineering, and Production
- Experience with environmental monitoring and sterility assurance
- Opportunities in export-driven pharmaceutical markets
These openings are ideal for candidates seeking injectable plant jobs in Gujarat, pharma QA executive vacancies, QC microbiology roles, sterile production operator jobs, engineering maintenance pharma careers, and warehouse executive pharma positions.
Frequently Asked Questions (FAQs)
Is parenteral manufacturing experience mandatory?
Yes. Candidates must have prior exposure to sterile or injectable pharmaceutical plants.
Are multiple departments hiring simultaneously?
Yes. Engineering, Production, QA, QC Microbiology, and Warehouse departments are hiring.
How can I apply?
Send your updated CV to hrl@swiss.in or recruitment@swiss.in mentioning the applied position.
Is GMP knowledge required?
Yes. Strong understanding of GMP, SOPs, and documentation is essential for all roles.
Summary Table
| Company | Swiss Parenterals Ltd. |
|---|---|
| Vacancies | Engineering Executive/Operator, Production Manager/Officer/Operator, QA QMS/IPQA Executive, QC Micro Executive, Warehouse Executive |
| Required Education | B.Pharm, M.Pharm, B.Sc, M.Sc, Diploma, BE, ITI |
| Experience | 1–10 Years (Parenteral Plant Required) |








To apply for this job email your details to hrl@swiss.in