Facilities Supervisor
Xellia

Cleveland, Ohio

This job has expired.


This position will have the overall responsibility for the facilities maintenance including management and supervision of all supporting services required to properly maintain a state of operations readiness for a sterile drug manufacturing site. This includes, but not limited to the areas of utilities areas and buildings, warehouse and manufacturing working areas, grounds and exterior building maintenance. The supervisor will supervise activities of individuals responsible for all related functional areas and ensure the highest quality standards and regulatory compliance are maintain.

Key Responsibilities

  • Responsible for directing and overseeing work activities involved facilities maintenance, janitorial, pest control, landscaping, security and any other contracted service required to maintain the facility in good state and meeting regulatory requirements.
  • Support capital projects execution activities and small renovations activities associated with the facility.
  • Oversee the security personnel to maintain building access control as per stablished procedures.
  • Evaluate and engages with service providers to provide required facility maintenance, repair and regular services required to maintain a state of operational readiness and meet regulatory requirements.
  • Provide appropriate training and mentoring to the facilities staff.
  • SME for facility and grounds maintenance expertise during customer or regulatory agency related audits.
  • Responsible for the implementation, monitoring and maintenance of the pest control program, contact with outside service provided, trend analysis / KPI's, training of the site staff on awareness of control program and maintain up to date requirements with regards to the best pest management practices.
  • Other related duties as assigned to meet departmental and Company objectives.
  • Partner with Quality to ensure processes and products are in compliance with all local, state, and federal rules and regulations. Oversee that processes are in cGMP compliance, and establish systems that identifies opportunities for improvement and makes constructive suggestions for change to improve process effectiveness to heighten quality. Develop knowledge of and understand regulatory requirements such as 21CFR part 210 and 211, cGMP's, FDA, OSHA and other regulatory agencies.
  • Personnel engaged in the manufacture, processing, packing, or holding of a drug product shall wear clean clothing appropriate for the duties they perform. Protective apparel, such as head, face, hand, and arm coverings, shall be worn as necessary to protect drug products from contamination.

Requirements

  • BA required with applicable experience, BS in science or engineering preferred.
  • At least 10 years of facility engineering and/ or facility management expertise, preferably in a sterile pharmaceutical manufacturing environment or similar FDA regulated environment.
  • Exhibit a continuous improvement mindset with attention to details and the ability to train, influence peers. Be able to make sound decisions when faced with competing priorities.
  • Expertise in CMMS applications such as AMMS, Maximo, etc.
  • Excellent verbal and written communication skills.
  • Must be detail oriented.
  • Must be knowledgeable in Microsoft Office products.

Physical Requirements of the Role

Position is exposed to plant environment. This role is continuously sitting and typing. Frequently talking and using eye and hand coordination. Occasionally requiring lifting and carrying less than 25 lbs. Standing, walking, bending over and repetitive use of legs are done occasionally. Any person shown at any time (either by medical examination or supervisory observation) to have an apparent illness or open lesions that may adversely affect the safety or quality of drug products shall be excluded from direct contact with components, drug product containers, closures, in-process materials, and drug products until the condition is corrected or determined by competent medical personnel not to jeopardize the safety or quality of drug products. All personnel shall be instructed to report to supervisory personnel any health conditions that may have an adverse effect on drug products.

Xellia Pharmaceuticals is owned by Novo Holding A/S and is a specialty pharmaceutical company leading in the development, manufacture and supply of anti-infective treatments. Headquartered in Copenhagen, Denmark, Xellia has global facilities in Europe, North America, and Asia, currently employing over 1700 people. With over 100 years of industry experience in developing last resort treatments for infectious diseases, Xellia is focused on the supply of products which not only save lives, but also improve and enhance patients' quality of life. Together with us, you can help lead the fight against bacterial infections.

Read more about Xellia Pharmaceuticals here


This job has expired.

Get Hired Faster

Subscribe to job alerts and upload your resume!

*By registering with our site, you agree to our
Terms and Privacy Policy.

More Pharmaceuticals jobs


Zoetis
Louisville, Illinois
Posted about 2 hours ago
Zoetis
Union City, Georgia
$182,000.00 - $279,000.00 per year
Posted about 2 hours ago
Zoetis
Parsippany-Troy Hills, New Jersey
Posted about 2 hours ago
View Pharmaceuticals jobs ยป