Integrity Bio, Inc. - Camarillo, CA
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Integrity Bio, Inc. is looking for a Manufacturing Engineer with experience in the development, tech transfer, & scale up of parenteral formulation, filling/finish, & freeze-drying operations, who is motivated, creative & a respected team player. The ideal applicant should have a solid underst&ing of cGMP, aseptic processing & biotech technologies to join our Manufacturing Group. If you enjoy working in a friendly, innovative, dynamic, fast paced environment, you should consider working for our organization.
C&idate will provide scientific & technical expertise in support of clinical manufacturing process development including UFDF (TFF) formulations, lyophilization, & fill/finish of vials & syringes.
Propose creative solutions for improvements & in solving manufacturing issues.
Proactively manage the implementation of process improvements to address project objectives in a cGMP regulated manufacturing facility.
Effectively present complex technical information to internal & external stake holders.
Provide leadership to approximately 6 manufacturing technicians along with fostering teamwork, alignment with company as well as department goals & priorities.
Demonstrate leadership in daily activities.
Independently manage multiple cross-functional projects.
Contribute to scientific field of expertise with external presentation & publications.