Job Description: Senior Manufacturing Engineer
Responsibilities:
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Convert demonstrated pilot-scale processes to commercial manufacturing in pharmaceuticals |
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Manage employees and hands-on operation of manufacturing function |
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Ensure that as company grows, manufacturing capabilities meet or exceed all industry and customer requirements for cost, quality and responsiveness |
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Work closely with R&D on manufacturing plans, goals and future product innovations |
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Ensure systems are in place to successfully complete regulatory inspections |
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Plan & manage to continuously improve quality, reliability and efficiency |
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Ensure the operation of facilities is in compliance with cGMP's, OSHA, environmental, labor and other governmental laws and regulations |
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Develop, review and approve GMP documentation and regulatory submissions |
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Establish and maintain solid working relationship with R&D team for product extensions and modifications |
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Direct all production control, production process development, quality systems, purchasing and shipping/receiving activities |
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Partner with business development to meet with customers to discuss and set scheduling timelines for product delivery |
Requirements:
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10 years experience with managerial and technical work experience in GMP pharmaceutical production |
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Success converting lab processes into commercial manufacturing |
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Additional experience in manufacturing films preferred |
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Demonstrated outstanding communication and team skills |
Education:
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Minimum of Mechanical or Chemical Engineering degree |
If you meet the qualifications and are looking for an outstanding career opportunity, please email your resume to careers@liquidia.com.
