Trainee Analyst-QC Jobs in Siflon Drugs & Pharmaceuticals Pvt Ltd - Hyderabad, Telangana
0 - 1 Years of Experience
Not disclosed 
Full TimeSiflon Drugs & Pharmaceuticals Pvt Ltd
Hyderabad, Telangana, India
Posted on 21-04-2026
1 Vacancy
Description
- Job Title: Trainee Analyst-QC
- Qualification: BPharm/MPharm
- Location: Siflon Drugs & Pharmaceuticals Pvt Ltd - Hyderabad, Telangana
- Work Experience: 8 to 10 Years
Job Description
- Perform analysis of raw materials, in-process samples, and finished products.
- Operate analytical instruments like HPLC, UV Spectrophotometer, pH meter, Dissolution apparatus.
- Prepare standard and sample solutions as per SOP.
- Record and document test results accurately.
- Follow GMP (Good Manufacturing Practices) and GLP (Good Laboratory Practices).
- Assist in calibration and maintenance of laboratory instruments.
- Handle routine laboratory testing activities.
- Report any OOS (Out of Specification) or abnormal results.
- Maintain cleanliness and safety in the laboratory.
Take this opportunity to join Siflon Drugs & Pharmaceuticals Pvt Ltd - Hyderabad, Telangana as a Trainee Analyst-QC in Hyderabad, Telangana and build a successful career in the healthcare industry. Apply today for this job opportunity and grow with a leading healthcare organization.
Category
Pharmaceuticals
Functional Area
Pharma Quality Control (QC)
Preferred Education
Key Skills
About Organization
Siflon Drugs & Pharmaceuticals Pvt Ltd is a pharmaceutical organization engaged in the manufacturing of veterinary formulations and animal healthcare products with a strong focus on product quality, regulatory compliance, and efficient production processes. The role involves working in a manufacturing or operational environment to support production activities and ensure adherence to industry standards. Responsibilities include assisting in production processes, monitoring process parameters, maintaining accurate batch records and documentation, and ensuring compliance with safety, hygiene, and environmental guidelines. The role also requires coordination with quality assurance and quality control teams, following Good Manufacturing Practices (GMP), and contributing to consistent product quality and operational efficiency.
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