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Company Description QUALITY PROFESSIONAL PHARMA SERVICES LTD is a pharmaceutical services organization headquartered on Doncaster Road in Barnsley, United Kingdom. The company focuses on delivering high-quality, compliant solutions to clients in the life sciences and healthcare sectors. Team members work in a regulated environment that emphasizes precision, documentation integrity, and continuous improvement. The organization values collaboration, accountability, and professional development, offering opportunities to contribute to safe and effective healthcare products. As the company grows, it is expanding its quality-focused operations and leadership capabilities in key locations such as Bengaluru.
Role Description The Assistant Manager QC (Quality Control) is a full-time, on-site role based in Bengaluru. The role involves overseeing day-to-day laboratory quality control activities, including review and approval of analytical test results, monitoring of routine and stability testing, and ensuring adherence to relevant pharmacopeial and regulatory standards. The Assistant Manager QC coordinates with cross-functional teams such as Production, Quality Assurance, and Regulatory Affairs to address quality issues and support timely product release. Responsibilities include guiding and mentoring QC analysts, managing laboratory documentation, supervising calibration and maintenance of instruments, and supporting investigations, deviations, out-of-specification (OOS), and change control processes. The role also contributes to internal audits, supports external inspections, drives continuous improvement initiatives, and helps implement updated quality systems and best practices.
Qualifications
- Strong foundation in pharmaceutical quality control principles, including cGMP, GLP, and relevant regulatory guidelines (e.g., ICH, WHO, local regulatory requirements).
- Hands-on experience with analytical techniques and instruments commonly used in QC labs (e.g., HPLC, GC, UV/Vis, dissolution, titration, and related methods).
- Proficiency in documentation practices, data integrity standards, and electronic or paper-based quality systems, including preparation and review of SOPs, test methods, and reports.
- Experience in handling deviations, OOS/OOT results, investigations, CAPA, and change control within a structured quality management framework.
- Demonstrated ability to lead, train, and mentor QC team members, manage workload, and coordinate with cross-functional stakeholders.
- Strong analytical thinking, problem-solving, and decision-making skills, with attention to detail and accuracy in a regulated environment.
- Effective verbal and written communication skills in English, with the ability to clearly present quality data, trends, and recommendations.
- Bachelor’s or Master’s degree in Pharmacy, Chemistry, or a related scientific discipline; prior experience in a pharmaceutical QC leadership or senior analyst role is preferred.
- Comfort working on-site in a laboratory and production-adjacent environment in Bengaluru, following all safety and
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