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BioSpace

Sr. Director - API Manufacturing Quality Control

BioSpace, Houston, Texas, United States, 77246

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Sr. Director - API Manufacturing Quality Control

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Sr. Director - API Manufacturing Quality Control

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BioSpace . Overview

Lilly is constructing an advanced manufacturing facility for production of API molecules. This is a leadership role on the startup of a greenfield site to enable GMP manufacturing operations. The Sr. Director – QC provides strategic and administrative leadership for the quality control and analytical sciences laboratories at the Lilly API site, developing capabilities and processes to support site operations and Lilly’s pipeline. Responsibilities

Build and lead a high-performing Quality Laboratory Operations team Ensure GMP compliance across all lab activities Deliver the “lab of the future” vision with integrated digital, paperless processes Collaborate with local and global quality teams to standardize lab design, processes, and systems Participate in site and quality leadership teams Drive strategic decisions and successful business outcomes Coordinate lab-related planning and budget management Promote cross-functional integration and communication Maintain a safe, compliant work environment Serve as a liaison for corporate communications Compliance Oversight

Ensure consistent quality and compliance across laboratories Manage regulatory and internal inspections Personnel Development

Lead HR planning, performance management, and talent development Recruit and build site capabilities for a high-functioning QC lab organization Ensure strong administrative and technical leadership within the team Basic Qualifications

Bachelor’s degree in a relevant field (STEM preferred) 10+ years of supporting complex analytical testing (mass spectrometry, bioassay, protein characterization) 5+ years of supervisory/leadership experience Additional Preferences

Knowledge of QC operations, new product introduction, and process development Expertise in analytical lab quality and compliance requirements Experience with regulatory submissions Proficient in Microsoft Office and other computer systems Strong technical writing and communication skills Effective interpersonal skills with ability to lead leaders and influence cross-functionally Commitment to maintaining a safe work environment Lilly is an equal opportunity employer

and is committed to providing reasonable accommodations to applicants with disabilities. If you require accommodation to submit a resume, please use the Lilly workplace accommodation process. Lilly reserves the right to amend compensation and benefits programs at its discretion. Actual compensation will depend on education, experience, skills, and location. The anticipated wage for this position is $151,500 - $222,200. Full-time employees are eligible for a company bonus and a comprehensive benefits program.

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