Supervisor, Vaccine Production (CEF)
 Biomune Company | |||||||||
 United States, Kansas, Lenexa | |||||||||
| 8906 Rosehill Rd (Show on map) | |||||||||
 Jun 13, 2025 | |||||||||
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Supervisor, Vaccine Production (CEF) The success of a company depends on the passionate people we partner with. Together, let's share our talents. Your Location: Lenexa, KS
The Supervisor, CEF is responsible for supervision and leadership of front-line Chicken Embryo Fibroblast (CEF) manufacturing processes of the Mareks Focus Factory. This role will oversee processes which may include, but are not limited to, ovoscopy, centrifugation, trypsinization, autoclaving, assembling and disassembling materials, working with pressurized vessels and aseptic practices. The Supervisor will provide support to the Focus Factory Leader by serving as a front-line leader within the department and directing the assigned team to ensure the manufacture of quality products, in a safe environment, delivered on time.
Development & Leadership * Instill a culture of Safety, Quality & Continuous Improvement through role model behavior and accountability * Hire, train, motivate, and develop team to support current and near-term business needs o Create an environment of accountability in their area of responsibility o Set performance objectives for direct reports o Create development plans for direct reports o Create improvement plans and monitor progress, as needed Safety * Demonstrate a strong safety mindset and set a high standard for self and team * Ensure safety standards, procedures, and processes are known and followed by team * Proactively identify safety risks during implementation of new equipment or processes * Report all accidents, incidents and near misses within 24 hours o Active participant in root cause investigations o Drive implementation of correction and preventive actions Quality * Accountable for implementation and adherence of production batch records, labeling and standard operating procedures (SOP) * Accountable for input and support for the update, review and approval of documentation in their area of responsibility o SOP o Production Batch Records o Qualification Protocols o New Product/Product Transfer Documentation * Support timely and thorough investigations of product or process deviations o Active participant in root cause investigations o Drive implementation of correction and preventive actions Operations * Support daily production scheduling and staff assignment o Ensure resourcing is adequate through appropriate training o Support validation, product study or process improvement initiatives * Escalate and communicate risk or changes to production goals * Accountable for inventory accuracy through timely workorder completion and cycle counts * Anticipate and resolve problems that may impact schedules o Support problem solving at appropriate level * Create a culture of continuous improvement o Identify process improvements through active supervision and Tier communication o Utilize key performance indicators to prioritize improvement areas o Support implementation of process improvements Assist other departments as required
* Shape solutions out of complexity - Is open and curious of other's perspectives. Organized analytical thinker with high level of energy * Client focus - Has in mind client's satisfaction * Collaborate with empathy - Has a positive attitude towards collaboration * Engage and develop - Clarifies short-term directions. Demonstrates continuous leadership ability and qualities. * Drive ambition and accountability - Proactively manages own and others work. Self-motivated and can work with minimal supervision * Influence others - Communicates transparently
* Flexibility to complete necessary tasks with last-minute change to the production plan and establishment of new priorities. * Confident trainer. * Excellent communication skills, both verbal and written. * Flexible to complete necessary tasks with last-minute changes to the production plan and establishment of new priorities. * Excellent communication skills, both verbal and written * Exercise rapid learning ability * Strong attention to detail is a must * Excellent computer skills; familiarity with Microsoft Office and Google Suites * Strong math skills
Education - Bachelor's degree in a scientific field required (i.e., chemistry, general biology, cellular biology, microbial biology, etc.); equivalent, closely related work experience (4+ years) may be considered in lieu of a degree Work Experience - 2+ years of experience in the biologics industry required; additionally, 2+ of managerial/supervisory experience in the biologic/pharma industry strongly preferred. Other (consider certifications, specialized knowledge and/or training, etc.) - Knowledge of Quality Systems; investigations/CAPAs/ performing gap assessments
* Able to read, write legibly and communicate in English * Standing for long periods of time * Frequent repetitions of bending, twisting, lifting arms above head, wrist, and shoulder movements * Visual inspection * Dexterity: Frequent fine motor movement * Lifting 50 lbs. * Daily dressing and operating in clean room required garments and PPE
* Potential for work in -196C storage tanks for more than one hour
N/A This job description is intended to convey information essential to understanding the scope of the job and general nature and level of work performed by job holders within this job. This job description is not intended to be an exhaustive list of qualifications, skills, duties and responsibilities or working conditions associated with the job. This job description is not an employment contract. Ceva reserves the right to modify job duties and/or job descriptions at any time to meet the needs of the business. *VEVRAA Federal Contractor 669B #USCEVAYour Education - Bachelor's degree in a | |||||||||