Quality Control Jobs at Lonza
Looking for the latest Quality Control Jobs in the pharmaceutical industry? Here’s an excellent opportunity from Lonza Jobs for the position of QC Analyst at its Rewari, Haryana facility. If you have a degree in Pharmacy, Chemistry, or Life Sciences with experience in analytical testing and GMP-regulated laboratories, this is your chance to join one of the world’s leading pharmaceutical manufacturing companies. Explore the complete eligibility, responsibilities, qualifications, and application details below and take the next step in your Life Science Jobs career.
About Lonza
Lonza is one of the world’s leading pharmaceutical, biotechnology, and life sciences companies, operating across more than 30 manufacturing and research sites globally. The company partners with healthcare innovators to develop and manufacture medicines that improve patient lives worldwide. Known for its commitment to innovation, quality, sustainability, and employee development, Lonza Jobs provide excellent opportunities for professionals seeking long-term careers in pharmaceutical manufacturing, biotechnology, and Life Science Jobs.
Job Details:
- Job Title: QC Analyst
- Location: Rewari, Haryana, India
Position Overview
The QC Analyst is responsible for performing quality control activities to ensure the safety, quality, and regulatory compliance of pharmaceutical products within a Good Manufacturing Practice (GMP) environment. The role involves analytical testing, laboratory operations, quality systems management, documentation, and continuous improvement initiatives while collaborating with cross-functional teams to support product quality and regulatory compliance.
Key Responsibilities
- Performs laboratory activities, including sampling, testing, and release of raw materials, packaging materials, and finished pharmaceutical products.
- Reviews and approves analytical results and Certificates of Analysis (CoA) to ensure accurate and timely material disposition using SAP.
- Manages quality systems, including Out-of-Specification (OOS) investigations, Out-of-Trend (OOT) assessments, deviations, change controls, and Annual Product Quality Reviews (APQR).
- Ensures compliance with current Good Manufacturing Practices (cGMP), Good Laboratory Practices (GLP), regulatory guidelines, and internal quality procedures.
- Maintains and reviews laboratory documentation, including Standard Operating Procedures (SOPs), Standard Test Procedures (STPs), and Document Management System (DMS) records.
- Oversees laboratory operations, including instrument qualification, calibration, validation, stability studies, and reagent and chemical inventory management.
- Supports internal audits, regulatory inspections, vendor qualification activities, and coordination with external analytical laboratories.
- Identifies and implements continuous improvement initiatives to enhance laboratory efficiency, quality, and compliance.
- Promotes adherence to Environmental Health and Safety (EHS) policies and laboratory safety practices.
- Collaborates with manufacturing, quality assurance, regulatory, and other cross-functional teams to ensure timely product release and quality compliance.
Required Qualifications
- Bachelor’s degree in Life Sciences discipline.
- 1–3 years of experience in Quality Control within the pharmaceutical or other regulated manufacturing industries.
Technical Skills
- Strong knowledge of current Good Manufacturing Practices (cGMP) and Good Laboratory Practices (GLP).
- Experience managing pharmaceutical quality systems, including OOS, OOT, deviations, change control, CAPA, and APQR.
- Hands-on experience with analytical laboratory techniques and instrumentation, including High-Performance Liquid Chromatography (HPLC), Gas Chromatography (GC), UV-Visible Spectroscopy, and dissolution testing.
- Familiarity with laboratory instrument qualification, validation, calibration, and stability testing programs.
- Experience using SAP for material management, laboratory documentation, and batch disposition.
- Understanding of regulatory requirements governing pharmaceutical quality control laboratories.
Core Competencies
- Strong analytical and problem-solving abilities.
- High attention to detail and commitment to data integrity.
- Excellent organizational and time management skills.
- Ability to manage multiple priorities in a regulated environment.
- Effective written and verbal communication skills.
- Strong stakeholder management and cross-functional collaboration.
- Leadership and decision-making capabilities.
- Commitment to continuous improvement, quality excellence, and regulatory compliance.
