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Mylan Laboratories Conducts Walk-In Interview for Quality Assurance Positions in Bengaluru
Mylan Laboratories Limited, a prominent subsidiary of Viatris Company, has announced a walk-in interview opportunity for Quality Assurance professionals at its Injectable Manufacturing Facility located in Hosur. The pharmaceutical major is seeking qualified candidates to strengthen its quality management team.
Interview Details
The walk-in interview is scheduled for January 10th, 2026, between 10:00 AM and 3:00 PM. This presents an excellent opportunity for pharmacy graduates seeking to advance their careers in pharmaceutical quality assurance within a globally recognized organization.
Position Overview
Department: Quality Assurance
Focus Areas: IPQA / QMS / Compliance / Documentation
Facility: Injectable Manufacturing Unit, Hosur
The Quality Assurance team plays a critical role in ensuring that all pharmaceutical products meet stringent regulatory standards and quality specifications. Selected candidates will be involved in various aspects of quality management, including in-process quality assurance, quality management systems, regulatory compliance, and documentation control.
Eligibility Criteria
Educational Qualifications:
– M.Pharm (Master of Pharmacy)
– B.Pharm (Bachelor of Pharmacy)
– M.Sc. in relevant disciplines
Experience Required: 2 to 8 years of relevant experience in pharmaceutical quality assurance
Walk-In Venue
Location: Injectables Operations Office
Complete Address:
Plot No. 289, 290, 291,
Bommasandra Jigani Link Road Industrial Area,
Near APC Circle,
Jigani Hobali, Anekal Taluk,
Bengaluru – 560105
About Mylan Laboratories
Mylan Laboratories Limited operates as part of Viatris, a global healthcare company formed through the combination of Mylan and Upjohn. The company is committed to empowering people worldwide to live healthier at every stage of life. With a diverse portfolio spanning branded and generic medicines, complex generics, and biosimilars, Viatris maintains a significant presence in the global pharmaceutical landscape.
The Hosur facility specializes in injectable pharmaceutical manufacturing, adhering to international quality standards and regulatory requirements. Working at this facility offers professionals exposure to world-class manufacturing practices and quality systems.
What Candidates Should Bring
Prospective candidates attending the walk-in interview should carry:
– Updated resume (multiple copies)
– Original educational certificates and mark sheets
– Experience certificates from previous employers
– Valid photo identification
– Passport-size photographs
Career Opportunities
This recruitment drive represents a significant opportunity for pharmacy professionals to join a multinational pharmaceutical organization. Quality Assurance roles at Mylan offer:
– Exposure to international quality standards
– Work in a regulated manufacturing environment
– Professional development opportunities
– Competitive compensation packages
– Career growth within a global organization
FAQ:
1. What Quality Assurance activities are expected in an Injectable Manufacturing facility?
Quality Assurance in injectables involves In-Process Quality Assurance (IPQA), aseptic area monitoring, batch manufacturing record (BMR) review, line clearance, media fill oversight, environmental monitoring (EM), sterility assurance, and ensuring compliance with cGMP, USFDA, EU-GMP, and WHO guidelines.
2. What regulatory guidelines should QA professionals be familiar with for this role?
Candidates should have strong knowledge of cGMP, USFDA 21 CFR Parts 210 & 211, EU-GMP, ICH guidelines (Q7, Q9, Q10), Schedule M, and Data Integrity (ALCOA+) principles, especially as they apply to injectable dosage forms.
3. What role does QA play in handling deviations, CAPA, and change control?
QA is responsible for deviation investigation, root cause analysis, CAPA implementation, change control evaluation, and ensuring that corrective actions are effective and compliant with regulatory expectations. Documentation accuracy and timely closure are critical.
4. How is documentation control managed in the Quality Assurance department?
QA oversees SOP issuance and control, document revision management, BMR/BPR review, logbook verification, data integrity compliance, and archival of quality documents in line with regulatory and audit requirements.
5. What experience is preferred for IPQA roles in injectable plants?
Hands-on experience in aseptic operations, cleanroom behavior, visual inspection, process validation support, environmental monitoring, and audit readiness is preferred. Exposure to regulatory audits and customer inspections is an added advantage.
