Swiss Hiring QC, QA, R&D & Production
- Company Overview
- Job Role & Responsibilities
- Quality Control (FG / HPLC / Microbiology)
- Quality Assurance (IPQA / QMS)
- FR&D (Formulation Research & Development)
- AR&D (Analytical Research & Development)
- Production (Granulation / Compression / Capsule)
- Eligibility / Qualifications
- Required Education
- Experience Requirements
- Additional Requirements
- Location & Salary
- Job Location:
- Salary:
- Application Process
- Why You Should Apply
- FAQs
- How many vacancies are available?
- What qualifications are required?
- Is experience mandatory?
- Is there any test or trial?
- How can I apply?
- Summary Table
Swiss Garnier Life Sciences Hiring 35+ Pharma Professionals Across QC, QA, R&D & Production Roles in Himachal Pradesh
Swiss Garnier Life Sciences, a fast-growing pharmaceutical manufacturing organization, is actively hiring across multiple departments including Quality Control (QC), Quality Assurance (QA/IPQA/QMS), Formulation R&D (FR&D), Analytical R&D (AR&D), and Production. With over 35+ vacancies for roles such as Executive, Jr. Executive, and Production Operators, this opportunity is ideal for experienced professionals with 2 to 10 years of experience in regulated pharmaceutical environments.
The hiring is based at their manufacturing facility in Una, Himachal Pradesh. Candidates with qualifications like B.Pharm, M.Pharm, M.Sc, ITI, and Diploma are eligible depending on the role.
Company Overview
Swiss Garnier Life Sciences is part of the Swiss Garnier Group of Companies, known for its strong presence in pharmaceutical formulation manufacturing. The company operates from its facility in Himachal Pradesh and focuses on delivering high-quality, compliant pharmaceutical products aligned with global regulatory standards.
With a growing footprint in both domestic and export markets, the organization emphasizes quality systems, regulatory compliance, and innovation in formulation and analytical development. Employees gain exposure to GMP-regulated environments, advanced analytical techniques, and cross-functional pharmaceutical operations.
Working here allows professionals to build expertise in areas such as:
- Pharmaceutical quality control and analytical testing
- Regulatory-compliant manufacturing practices
- Formulation development and product lifecycle management
- Quality assurance systems including IPQA and QMS
Job Role & Responsibilities
Quality Control (FG / HPLC / Microbiology)
- Perform finished goods (FG) analysis and release testing
- Operate and maintain HPLC systems for analytical testing
- Conduct microbiological testing including environmental monitoring
- Maintain documentation as per GLP and GMP standards
- Support stability studies and analytical validations
Quality Assurance (IPQA / QMS)
- Perform in-process quality assurance (IPQA) checks
- Handle QMS activities including CAPA, deviation, and change control
- Ensure compliance with SOPs and regulatory guidelines
- Participate in internal and external audits
FR&D (Formulation Research & Development)
- Develop and optimize pharmaceutical formulations
- Support product scale-up and technology transfer
- Maintain documentation for development batches
AR&D (Analytical Research & Development)
- Develop and validate analytical methods
- Support regulatory submissions with analytical data
- Conduct method transfer and stability analysis
Production (Granulation / Compression / Capsule)
- Operate manufacturing equipment for OSD production
- Ensure batch execution as per BMR and SOPs
- Maintain safety and quality compliance during production
- Trial is mandatory for operator-level roles
These roles directly contribute to ensuring pharmaceutical product quality, regulatory compliance, and efficient manufacturing operations.
Eligibility / Qualifications
Required Education
Candidates must meet the following educational qualifications based on the role:
B.Pharm, M.Pharm, M.Sc (Chemistry, Microbiology, Biotechnology), ITI, Diploma, 12th Science
Experience Requirements
- QC / QA / R&D roles: 2 to 5 years
- Production Operator roles: 5 to 10 years
Additional Requirements
- Strong understanding of GMP, GLP, and regulatory guidelines
- Hands-on experience in pharmaceutical manufacturing or laboratory environments
- Trial assessment mandatory for operator positions
Location & Salary
Job Location:
- Swiss Garnier Life Sciences, Industrial Area Mehatpur, Una, Himachal Pradesh
Salary:
- Salary is competitive and based on experience and skill set
Application Process
Interested candidates can apply by sending their updated resume via email or contacting directly:
recruitment.sg1@swissgarnier.com
Contact: 9318909212
Candidates are advised to:
- Clearly mention department and role in subject line
- Highlight relevant experience in QC, QA, R&D, or Production
- Be prepared for technical screening and operator trials (if applicable)
Why You Should Apply
- Multiple openings across high-demand pharma domains
- Opportunity to work in GMP-compliant manufacturing setup
- Exposure to analytical instruments, regulatory systems, and formulation development
- Strong career growth in quality assurance, quality control, and R&D sectors
FAQs
How many vacancies are available?
There are 35+ openings across QC, QA, R&D, and Production departments.
What qualifications are required?
B.Pharm, M.Pharm, M.Sc, ITI, Diploma, and 12th Science depending on the role.
Is experience mandatory?
Yes, roles require 2 to 10 years of relevant pharmaceutical experience.
Is there any test or trial?
Yes, operator roles require a practical trial assessment.
How can I apply?
Send your resume to the provided email ID or contact the HR team.
Summary Table
| Company | Swiss Garnier Life Sciences |
|---|---|
| Vacancies | QC Executive, QA IPQA Executive, QMS Executive, FR&D Executive, AR&D Executive, Production Operator |
| Required Education | B.Pharm, M.Pharm, M.Sc (Chemistry, Microbiology, Biotechnology), ITI, Diploma, 12th |
| Experience | 2–10 years |

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