Sanolet Lifecare Pvt. Ltd., a growing pharmaceutical manufacturing company specializing in dry powder injection formulations, has announced multiple job openings for experienced professionals and freshers at its Ahmedabad manufacturing facility. The company is inviting applications from qualified candidates for various departments including Quality Assurance (QA), Quality Control (QC), Production, Packing, Store, and Dispatch.
This recruitment drive presents an excellent opportunity for pharmaceutical professionals seeking career growth in a GMP-regulated manufacturing environment.
Available Positions
1. Quality Assurance (QA)
Designation: Officer to Sr. Executive
Experience: 3–7 Years
Vacancies: 02
Key Responsibilities:
Handling QMS activities
Validation and qualification documentation
Managing CAPA, OOS, and OOT investigations
Preparation of SOPs, protocols, and reports
2. Quality Control (Chemical)
Designation: Officer to Sr. Executive
Experience: 3–5 Years
Vacancies: 01
Key Responsibilities:
Operation of HPLC, TOC, and UV Spectrophotometer
GLP/GDP compliance
Analytical testing and documentation
3. Production
Designation: Sr. Executive
Experience: 5–7 Years
Vacancies: 01
Key Responsibilities:
Production supervision
GMP/GDP compliance
Workforce management
Documentation and process control
4. Quality Control (Microbiology)
Designation: Jr. Officer (Male)
Experience: Fresher – 1 Year
Vacancies: 01
Key Responsibilities:
Environmental monitoring
Water sampling
Microbiological testing
Laboratory documentation
5. Packing
Designation: Officer
Experience: 2–3 Years
Vacancies: 01
Key Responsibilities:
Packing operations management
Productivity monitoring
Daily production reporting
Team coordination
6. Store
Designation: Officer to Sr. Executive
Experience: 2–5 Years
Vacancies: 01
Key Responsibilities:
Material inward and dispensing
Inventory management
QMS documentation
Pharmaceutical warehouse operations
7. Dispatch
Designation: Officer
Experience: 1–3 Years
Vacancies: 01
Key Responsibilities:
Finished goods dispatch
Dispatch documentation
Logistics coordination
GMP/GDP compliance
Eligibility Criteria
Candidates with Dry Powder Injection manufacturing experience will be preferred.
Freshers can apply for the QC Microbiology position.
Good knowledge of GMP, GDP, and pharmaceutical documentation practices is required.
Strong communication and teamwork skills are desirable.
Employee Benefits
Transportation facility available from Gota and CTM, Ahmedabad.
Subsidized canteen facility.
Career growth opportunities in a regulated pharmaceutical manufacturing environment.
Attractive joining benefits for selected candidates.
How to Apply
Interested candidates can send their updated CV to:
hr@sanolet.co.in
Company Address
Sanolet Lifecare Pvt. Ltd.
Plot No. 10, Survey No. 151, Inside Varmora Plastech,
P.O. Vasna Chancharwadi, Bavla-Changodar Highway,
Ahmedabad – 382213, Gujarat, India.
Technical FAQs
1. What is CAPA in Pharmaceutical Quality Assurance?
CAPA (Corrective and Preventive Action) is a systematic approach used to investigate quality issues, identify root causes, implement corrective actions, and prevent recurrence to maintain regulatory compliance.
2. Why is HPLC widely used in Pharmaceutical Quality Control?
HPLC (High-Performance Liquid Chromatography) is used for the identification, quantification, and purity analysis of pharmaceutical compounds with high accuracy, precision, and sensitivity.
3. What is the difference between OOS and OOT results?
OOS (Out of Specification): Test results that fall outside predefined specifications.
OOT (Out of Trend): Results that remain within specifications but show unusual variation from historical trends.
4. What is Environmental Monitoring in Microbiology?
Environmental Monitoring (EM) is the process of assessing microbial contamination levels in cleanrooms, manufacturing areas, air, surfaces, and personnel to ensure sterile manufacturing conditions.
5. Why are GMP and GDP important in pharmaceutical manufacturing?
GMP (Good Manufacturing Practices) ensures products are consistently manufactured according to quality standards, while GDP (Good Documentation Practices) ensures data integrity, traceability, and regulatory compliance throughout the product lifecycle.

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