India's DMPLOI - Jobs & Networking AppMylan Laboratories Limited, a part of Viatris, has announced a Walk-In Interview Drive for experienced professionals in the Quality Control (QC) Department at its Injectable Manufacturing Facility located in Hosur, Tamil Nadu. This opportunity is ideal for candidates with a strong background in sterile injectable quality control and analytical testing.
The company is seeking qualified professionals who can contribute to maintaining high-quality standards in pharmaceutical manufacturing while ensuring compliance with global regulatory requirements.
Walk-In Interview Details
Details
Company
Mylan Laboratories Limited (A Viatris Company)
Department
Quality Control
Interview Date
13th June 2026 (Saturday)
Time
10:00 AM to 12:00 PM
Qualification
M.Sc. Chemistry
Experience
5 to 8 Years
Industry Experience
Sterile Injectable Manufacturing
About the Opportunity
The Quality Control team plays a critical role in ensuring that pharmaceutical products meet predefined quality specifications before release. Professionals joining Mylan’s injectable facility will be involved in analytical testing, method compliance, laboratory investigations, documentation, and adherence to cGMP guidelines.
Candidates with experience in sterile injectable environments and exposure to regulatory audits will be highly valued.
Key Responsibilities
Perform routine and stability sample analysis.
Conduct testing using analytical instruments such as HPLC, GC, UV-Visible Spectrophotometer, and Dissolution Systems.
Review analytical data and laboratory documentation.
Participate in OOS, OOT, and laboratory investigations.
Ensure compliance with cGMP, GLP, and data integrity requirements.
Support regulatory inspections and internal audits.
Maintain laboratory records and calibration documentation.
Skills Required
Strong knowledge of pharmaceutical quality control operations.
Hands-on experience with HPLC, GC, and other analytical instruments.
Understanding of sterile injectable manufacturing processes.
Familiarity with USP, IP, EP, and regulatory guidelines.
Experience in laboratory investigations and documentation practices.
Knowledge of data integrity and quality systems.
Why Join Mylan Laboratories?
Mylan, now a part of Viatris, is recognized globally for delivering high-quality medicines and healthcare solutions. Employees gain exposure to advanced pharmaceutical technologies, international regulatory standards, and career growth opportunities within a globally respected organization.
Technical FAQs
1. What analytical instruments are commonly used in Injectable Quality Control laboratories?
Quality Control laboratories typically use HPLC, GC, UV-Visible Spectrophotometers, FTIR, TOC analyzers, pH meters, and Particle Counters for testing raw materials, in-process samples, and finished injectable products.
2. What is an OOS (Out of Specification) result?
An OOS result occurs when a test result falls outside the predefined acceptance criteria or specification limits. It requires a structured investigation to determine the root cause and assess product impact.
3. Why is data integrity important in pharmaceutical QC?
Data integrity ensures that laboratory data is accurate, complete, consistent, and reliable throughout its lifecycle. Regulatory agencies expect compliance with ALCOA+ principles to maintain product quality and patient safety.
4. What are critical quality tests performed for sterile injectable products?
Critical tests include sterility testing, bacterial endotoxin testing (BET), particulate matter analysis, assay, related substances, pH testing, osmolarity, and appearance evaluation.
5. What is the role of HPLC in pharmaceutical Quality Control?
HPLC is widely used for assay determination, impurity profiling, stability studies, content uniformity testing, and method validation. It provides accurate and reliable quantitative analysis of pharmaceutical products.
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