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Strong employer brand plus metro location but niche pharmaceutical instrument expertise limits applicant density.
Role requires domain-specific pharma QC and regulatory experience, making cross-industry transferability low.
Multiple explicit filters: 5+ years, pharma industry, cGMP/regulatory knowledge, LIMS/SAP/TrackWise skills.
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Define and manage analytical instrument standards and lifecycle including obsolescence planning and replacement projects for global QC laboratories.
Compile and maintain instrument forecasts and inventories across QC sites, providing visibility and project tracking ratings to stakeholders.
Lead project management activities including budgeting, meetings, procedures drafting, compliance support, and health-authority inspection readiness.
Minimum Bachelor’s degree in a relevant field.
5+ years experience in Biopharm/Pharmaceutical industry with cross-functional exposure (research, analytical, quality, engineering, manufacturing, regulatory CMC, or IT).
Strong knowledge of laboratory instrument qualification, lifecycle management, and regulatory guidelines (cGMP, 21CFR, EMA Eudralex, USP).
Proficiency in LIMS, Microsoft Office, SAP, Quality Management Systems, and statistical/trending software (e.g. JMP).
Experienced in managing complex cross-site projects and engaging multiple stakeholders in matrix environments.
Demonstrates strong understanding of pharmaceutical manufacturing processes related to analytical and microbiological methods.
Skilled in risk-based decision making, issue escalation, and data analysis to maintain compliance and ensure continuous improvement.