VP Manufacturing - Biotechnology
Sterling Life Sciences - Miami, FL

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1) Manage all cGMP compliant manufacturing operations, including cell culture, bioreactor operations, protein purification and final filling2) Supervise materials management and facilities operations, including equipment and physical plant maintenance, validation, calibration, metrology, cleaning and related services3) Direct the activities of the responsible department managers to ensure projects are performed and completed in a manner that is acceptable to clients and company4) Ensure that Operations Department follow cGMP, SOPs and safety procedures as required and also ensure that all Operation?s employees are properly trained for their job functions and that the training is documented in CGMP training records5) Collaborate with Business Development, Process Development, Project Management, RA/QA/QC, existing and prospective clients to meet the requirements of each project6) Prepare and maintain department budgets, schedules for development, manufacturing, materials management and facilities activities and also prepare, review and approve written procedures, SOP?s, validation and other documents

1) University degree is required (preference will be given to those with degree in relevant field, though all candidates are welcome and encouraged to apply)2) Appropriate full-time work experience is mandatory (no students or fresh graduates please)3) Recent experience in the biotechnology industry is strongly preferred4) Preference will be given to people who have recent experience in Manufacturing Operations