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Tier-1 employer and metro location increase competition, but seniority and specialized GMP/CSV skills limit applicant pool.
GMP, CSV, and regulated manufacturing expertise makes candidate backgrounds highly industry-specific.
Explicit 8–13 years requirement and mandatory GMP/CSV/regulatory experience enforce strict shortlisting.
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Lead and develop a team providing operational support for Manufacturing Site Lab Systems ensuring reliability, data integrity, and GMP compliance.
Own system configuration, change control, validation deliverables, and maintain inspection readiness for multiple lab systems.
Collaborate globally to resolve system issues, support audits, monitor system performance, and drive continuous improvement and operational excellence.
8 - 13 years experience in Business, Engineering, IT or related field.
Hands-on experience managing computer systems from inception through maintenance in GMP regulated biotechnology or pharmaceutical environment.
Knowledge of Quality processes, laboratory and manufacturing systems, general IT architecture, and project management practices.
Willingness to work later shifts including evenings or nights as required by business needs.
Proven leadership experience in technology-driven manufacturing environments within biopharmaceuticals or pharmaceuticals under GMP regulations.
Strong expertise with Scaled Agile Framework (SAFe), computer systems validation (CSV), ITIL, and software development lifecycle in a regulated industry.
Effective collaborator with strong communication skills accustomed to working with global virtual teams and managing system transformations and continuous improvement initiatives.