India's DMPLOI - Jobs & Networking AppBliss GVS Pharma Ltd., a USFDA and EU-GMP approved pharmaceutical manufacturing company, has announced exciting career opportunities for professionals and freshers in the Quality Control (QC) Department at its Palghar, Maharashtra facility. Candidates with a B.Sc. or M.Sc. qualification and a passion for pharmaceutical quality assurance and analytical testing are encouraged to apply.
This recruitment drive offers a great opportunity to join a reputed pharmaceutical organization known for maintaining global quality standards and regulatory compliance.
Job Details
Details
Company Name
Bliss GVS Pharma Ltd.
Department
Quality Control
Position
Trainee / Officer
Location
Palghar, Maharashtra
Qualification
B.Sc. / M.Sc.
Experience
B.Sc. – Minimum 3 Years, M.Sc. – Fresher to 4 Years
Vacancies: 10
Shift Requirement
Mandatory Shift Working
Eligibility Criteria
Educational Qualification
B.Sc. candidates with a minimum of 3 years of relevant experience.
M.Sc. candidates with 0–4 years of experience can apply.
Experience Requirements
Applicants should have exposure to pharmaceutical quality control activities such as:
Raw material analysis
Finished product testing
Instrument handling
Documentation practices
GMP and regulatory compliance
Key Responsibilities
Selected candidates may be involved in:
Routine analytical testing of pharmaceutical products
Operation of analytical instruments such as HPLC, GC, UV-Visible Spectrophotometer, and Dissolution Apparatus
Preparation and review of analytical reports
Calibration and maintenance of laboratory instruments
Compliance with cGMP, GLP, and regulatory requirements
Investigation of Out-of-Specification (OOS) and Out-of-Trend (OOT) results
Maintaining laboratory documentation and records
How to Apply
Interested candidates can send their updated CV to:
Email: chetan.pawar@blissgvs.com
Contact Number: 9673457964
Important Note
Experienced candidates should mention the following details in their email:
Current CTC
Expected CTC
Notice Period
Why Join Bliss GVS Pharma?
Opportunity to work in a USFDA & EU-GMP approved facility
Exposure to advanced pharmaceutical quality systems
Career growth in a globally recognized pharmaceutical company
Learning opportunities with modern analytical technologies
Professional and quality-driven work environment
Technical FAQs
1. What analytical instruments are commonly used in Pharmaceutical Quality Control?
Quality Control laboratories frequently use HPLC, GC, UV-Visible Spectrophotometers, FTIR, Dissolution Testers, and Karl Fischer Titrators for raw material, in-process, and finished product analysis.
2. What is the difference between Quality Assurance (QA) and Quality Control (QC)?
Quality Assurance focuses on process compliance and system implementation, while Quality Control involves laboratory testing and analysis to verify product quality.
3. What is an OOS (Out of Specification) result?
An OOS result occurs when a test result falls outside the approved specification limits. Such results require a documented investigation according to regulatory guidelines.
4. Why is HPLC important in pharmaceutical analysis?
HPLC is widely used for assay determination, impurity profiling, stability studies, and quantitative analysis because of its accuracy, sensitivity, and reproducibility.
5. What are GMP and GLP in pharmaceutical industries?
GMP (Good Manufacturing Practices) ensures products are consistently manufactured according to quality standards, while GLP (Good Laboratory Practices) governs laboratory operations, testing procedures, and data integrity.
Disclaimer: Candidates are advised to verify all recruitment details directly with the company before applying.
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