KBI Biopharma

Supervisor, Maintenance - Night Shift - Boulder

Boulder, CO
KBI Biopharma is a global leader in providing comprehensive contract services for protein therapeuti

Job Description

Supervisor, Maintenance - Night Shift

Posted: Saturday, 8/5/2023
Schedule and coordinate maintenance work with Manufacturing Scheduler and process equipment owners to ensure on time compliance. Allocate daily work to maintenance technicians. Review and close work performed by maintenance technicians. Train maintenance technicians on equipment maintenance execution and ensure training for all maintenance technicians are current. Perform maintenance activities on GMP manufacturing environment. Evaluate equipment performance. Generate and resolve deviations as they pertain to the maintenance program. Work within a team environment that actively supports, participates, and embraces an empowered team culture including significant interaction with Quality Assurance, Manufacturing Operations, Engineering, and other support groups. Must be able to provide “On-Call” response to support plant operations during off-hours as required.
Shift is 8 Hours (Grave shift). Hours are 11:00PM to 7:30 AM, Sunday night through Friday morning, or Monday night to Saturday morning.
  • Schedule and coordinate maintenance work with Manufacturing Scheduler and lab owners to ensure on time compliance.
  • Allocate daily work to maintenance technicians. Review and close work performed by maintenance technicians.
  • Train maintenance technicians on equipment maintenance execution and ensure training for all maintenance technicians are current.
  • Will evaluate equipment performance. Generate and resolve deviations as they pertain to the maintenance program. Support internal and external audits. Develop and execute Corrective Action Plans (CAPA) as required.
  • Perform corrective and preventative maintenance of architectural systems, structural/civil systems, mechanical systems, electrical systems, plumbing systems, process equipment and utility equipment training on and following approved procedures where applicable.
  • Troubleshoot and repair facilities, equipment, and systems, including mechanical, electrical, pneumatic, or hydraulic circuits (motors, pumps, compressors, boilers, chillers, and purified and domestic water systems) using manuals, SOPs, specifications, and other workplace aids.
  • Provide recommendations and assist with implementation of methods, procedures and techniques for improving maintenance of existing/new systems as well as assisting with system failure root cause investigations.
  • Prepare documents to include maintenance, quality, and other documents/reports as deemed appropriate following good documentation practices potentially inclusive of deviations, corrective actions preventative actions (CAPA), change controls, and SOP revisions.
  • Monitor the work of others to include contracted suppliers and service providers.
  • Includes hazardous and non-hazardous waste handling
Experience:
High School diploma or equivalent, preferably including hands-on or vocational school training, and a minimum of ten (10) years of experience as a general maintenance mechanic in a manufacturing environment, or an equivalent combination of training and experience, or A.S./A.A. Degree in Mechanical/Utilities Technology, or Licensed Journeyman, with a minimum of five (5) years of work experience. Five years of direct personnel management experience.
Minimum Requirements
(Include education, experience, special skills and licenses or certifications required.)
Prior experience with general utility systems, boilers, electrical, HVAC and refrigeration systems. Universal CFC Refrigerant License preferred. Prior experience in a cGMP pharmaceutical manufacturing environment preferred.
  • High School diploma and a two-year degree in Engineering, Life Sciences, other related technical field or equivalent military training and 10 years of applicable Maintenance experience or the equivalent combination of education and experience
  • Some direct personnel management experience.
  • Prior experience in a cGMP pharmaceutical manufacturing environment preferred
  • Strong understanding of Standard Operating Procedures
  • Familiar working within Computerized Maintenance Management Systems to schedule and document work performed
  • Knowledge of general OSHA safety requirements a plus
  • Must be able to read P&ID's and electrical schematics
  • Must be able to use Word, Excel and Outlook
  • Must be able to communicate effectively with colleagues and internal customers and all levels of management
Salary Range: 75K - 90K; Shift Differential Available
Salary range provided per current averages and expectations. The salary and job title for this opening will be based on the selected candidates qualifications and experience and may be outside this range. KBI has a robust total rewards strategy which includes an annual bonus structure for all employees, medical, dental, and vision coverage, paid PTO and holidays, Sabbatical program, 401K matching with 100% vesting in 60 days and employee recognition programs.
KBI Biopharma, Inc. (KBI) is committed to providing a safe and healthy workplace. Any employee entering a KBI site located in the US must either (1) have provided proof of full vaccination (as defined by the CDC) with a COVID-19 vaccination which has been granted FDA approval or Emergency Use Authorization; or (2) perform weekly COVID-19 testing with negative test results.
KBI Biopharma, Inc. is an EEO/AA employer and actively seeks to diversify its work force. Therefore, all qualified applicants, regardless of race, color, national origin, religion, gender, gender identity, sexual orientation, age, disability or veteran status, are strongly encouraged to apply.
I understand that neither the completion of this application nor any other part of my consideration for employment establishes any obligation for KBI Biopharma, Inc. to hire me. If I am hired, I understand that either KBI Biopharma, Inc. or I can terminate my employment at any time and for any reason, with or without cause and without prior notice. I understand that no representative of KBI Biopharma, Inc. has the authority to make any assurance to the contrary.
I attest with my signature below that I have given to KBI Biopharma, Inc. true and complete information on this application. No requested information has been concealed. I authorize KBI Biopharma, Inc. to contact references provided for employment reference checks. If any information I have provided is untrue, or if I have concealed material information, I understand that this will constitute cause for the denial of employment or immediate dismissal.

KBI Biopharma At A Glance

KBI Biopharma is a global leader in providing comprehensive contract services for protein therapeutics development. Our services help clients succeed through broad development and commercialization activities from analytical, formulation, process development to cGMP manufacturing With each of our 500+ client partners, we have worked closely to personalize and rapidly accelerate their drug development programs. Built upon a foundation of world-class analytical capabilities, we deliver efficient process development and clinical and commercial cGMP manufacturing services for mammalian, microbial, and cell therapy programs.
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