QC Qualification Engineer

ABOUT THE JOB Drive and support equipment qualification as per pre-defined timeline Guide and resolve standard issues relating to current processes, systems, and qualification/validation approaches within and across various functions Review and collaborate with stakeholders to identify solutions for deviations and project discrepancies Drive QC equipment qualification (Group B and C), including drafting and execution of URS, ERES, HLRA, Vendor IOQ, In-House IOQ, PQ, QR, etc. Manage change control for equipment qualification Conduct qualification investigations as required Ensure project progression according to plan and quality expectations Perform other duties or projects assigned by the manager Comply with all HSE guidelines Detect and report potential accidents and risks, proposing solutions Participate in HSE risk assessments Participate in initial training and retraining ABOUT YOU Academic background: Degree or diploma in Science, Biology, Microbiology, Chemistry, Pharmacy, Biochemistry, or equivalent Experience in pharmaceutical quality control, quality assurance, or production (minimum 4 years in a laboratory environment within the pharmaceutical industry) Experience with QC equipment qualification Experience with MS Office applications and other standard IT applications supporting quality activities Good knowledge of GMP, quality standards, and QC testing You demonstrate strong collaboration and result-oriented skills You demonstrate strong operational excellence and digital & tech savvy skills You demonstrate strong ability to work across boundaries and apply practical solutions