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Supervisor, Facilities and Maintenance - 12-Hr Day Shift 2-2-3
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Full-time
associate degree
Posted 9d ago
Apply by Jul 28
~40 hrs/week
Responsibilities
The Supervisor manages maintenance programs, personnel, and facility utilities while ensuring compliance with pharmaceutical regulatory standards. They are responsible for overseeing capital projects, shutdowns, and the professional development of the maintenance team.
Requirements
Candidates must possess a Military, Technical School, or Associate’s degree along with at least 3 years of supervisory experience. Expert knowledge of pharmaceutical facility operations, aseptic processing equipment, and GMP compliance is required.
Full job description
At Alcami, we deliver reliable solutions that unlock the potential of transformative medicines from discovery to commercialization, through trusted partnership with our clients, recognized industry expertise and proven regulatory track record.
Are you interested in joining our team?
Job Summary
The Supervisor, Facilities and Maintenance is accountable for driving results in a fast-paced environment by managing and overseeing the programs and personnel related to maintenance of the facility, processing equipment, critical utilities, general facility utilities. This includes routine support of day-to-day operations as well as special projects. Special projects include customer centric projects, plant shutdowns, and facility upgrades, renovations, or expansions. The Supervisor, Facilities and Maintenance facilitates implementation of projects, schedules, and provides oversight of the work during execution. All activities are conducted under the regulatory agency requirements of the pharmaceutical industry and related products that are manufactured at Alcami, such as FDA, DEA, and EU as examples.
On-Site Expectations
100% on-site position.
Day Shift: 12-Hour Rotating (2-2-3), 7:00am - 7:30pm.
Responsibilities
Provides leadership and direction to the Maintenance teams (GMP and Facilities).
Plans and supervises projects including facility/utility capital projects and other capital efforts.
Ensures GMP compliance (e.g. deviation initiation and review, CAPA assignments, compliance reports, change control generation and review).
Provides maintenance program oversight (preventative maintenance programs, repairs, spare parts program, pest control program, etc.).
Reviews and provides oversight to the facilities maintenance work order creation, which includes troubleshooting and guidance.
Responsible for utilities such as but not limited to HVAC, compressed air, WFI, Clean Steam, nitrogen, chilled water, etc.
Supervises bi-annual shutdowns.
Maintain site security, including maintaining the camera and badge reader systems at the site, maintaining the key control list and working with the Global Security Manager on implementation of security programs and site security plans.
Gather and broadcast key metrics to management.
Ensures timely completion and compliance with cGMP and all other relevant company training requirements.
Attracts, develops, and retains a high performing team to meet the current and evolving needs of the business through effective selection, training and development, coaching and mentoring and performance management.
Directly supervises team of 5-8 direct reports.
Participates in the hiring process of other employees.
Assists in hiring decisions of other employees.
Schedules and reviews the work of other employees.
Accountable for the curriculum assigned and timely completion of training of employees to meet regulatory requirements.
Coaches, mentors and develops technicians.
Prepares and delivers performance evaluations of technicians.
Make recommendations of disciplinary actions of other employees.
Other duties as assigned.
Qualifications
Military, Technical School, or Associate’s degree.
3+ years previous supervisor experience.
Knowledge, Skills, and Abilities
Expert knowledge of pharmaceutical facility operations and maintenance, and aseptic processing equipment.
Knowledge of FDA regulated industry requirements, work order/calibration software, managing personnel, and EHS required.
Excellent written and oral communication, coaching, and mentoring skills required.
Excellent ability to read and interpret engineering design, ability to read and understand equipment specifications and ability of track and trend data analysis required.
Good negotiating skills required.
Ability to supervise a Maintenance team that works multiple shifts.
Travel Expectations
Up to 10% domestic travel.
Physical Demands and Work Environment
The physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of this job. Reasonable accommodation may be made to enable individuals with disabilities to perform the essential functions. While performing the duties of this job, the employee is required to frequently talk or hear. In some case the employee is required to stand, walk, and sit. The employee is required to occasionally use hands to finger, handle, or feel; climb or balance; stoop, kneel, crouch or crawl; reach with hands and arms; taste or smell. The employee must regularly lift and/or move up to 10 pounds, occasionally lift and/or move up to 50 pounds. There is no special vision requirement for this job. The employee may occasionally work in wet or humid conditions, near moving mechanical parts, in high precarious places, near fumes, airborne particles or toxic chemicals.
Alcami is a US-based contract development and manufacturing organization headquartered in NC with 45+ years of experience advancing pharmaceuticals and biologics from development to delivery. Alcami provides fully integrated lab services, drug product manufacturing, and cGMP pharma storage and support services including environmental monitoring, calibration, and validation. Alcami’s private equity ownership includes GHO Capital, The Vistria Group, and Ampersand Capital Partners.
Offices: 2320 Scientific Park Dr, Wilmington, NC 28405, US · 4620 Creekstone Drive, Durham, NC 27703, US · 4221 Faber Place Dr, Charleston, SC 29405, US · 4260 Forest Park Ave, St. Louis, MO 63108, US · 627 Davis Dr, Suite 100, Morrisville, NC 27560, US
Sterile Fill-Finish Development & ManufacturingOral Solid Dose Development & ManufacturingLaboratory ServicesEnvironmental MonitoringPackaging & LabelingAnalytical TestingDevelopment TestingCleanroom ServicesChemistryMicrobiology
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