Facilities Engineer II
Job in
Charlottesville, Albemarle County, Virginia, 22904, USA
Listing for:
Afton Scientific. LLC
Full Time
position
Listed on 2026-05-16
Job specializations:
-
Manufacturing / Production
Pharmaceutical Manufacturing, Manufacturing Engineer, Validation Engineer, Operations Engineer
Salary/Wage Range or Industry Benchmark: 70000 - 90000 USD Yearly
USD
70000.00
90000.00
YEAR
Job Description & How to Apply Below
Afton Scientific is a privately held, PE-backed sterile fill‑finish contract development and manufacturing organization (CDMO) headquartered in Charlottesville, Virginia. For over 20 years, Afton has provided aseptic manufacturing services for biologics and small‑molecule injectables, supporting clients from clinical trials through commercial supply. The company operates FDA‑inspected, cGMP‑compliant manufacturing facilities and is currently executing a $200M+ expansion (Avon IV) that will add high‑speed isolator‑based filling lines and significantly increase capacity.
Afton serves pharmaceutical and biotech companies across oncology, metabolic/obesity therapeutics, immunology, infectious disease, and rare disease markets. Our location in central Virginia places us within a one‑day drive of approximately 50% of the U.S. population, a strategic advantage for cold‑chain and time‑sensitive pharmaceutical logistics.
The Facilities Engineer II plays a key role in ensuring compliant operations within a GMP pharmaceutical manufacturing environment. This position provides hands‑on support across a broad range of service areas involving pharmaceutical process equipment, including, but not limited to fill lines, isolators, parts washers, autoclaves, and other production‑related machinery. Working in a highly technical setting, Facilities Engineer IV must have experience maintaining safe, reliable production activities.
The role requires strong critical‑thinking skills and the ability to evaluate business impacts before acting, helping prevent unintended outcomes such as safety incidents, equipment failures, or other operational risks. The position also demands sound independent judgment and the ability to thrive in a dynamic, small‑company environment where priorities can shift quickly. The ideal candidate has a proven history of delivering results in a fast‑paced sterile manufacturing setting, while fostering a positive mindset and contributing to a strong, collaborative team culture.
Key Responsibilities Provide technical expertise to production teams, resolving issues as they arise and collaborating closely with Engineering and other support functions.Support daily production operations within the manufacturing area and serve as the first responder for equipment malfunctions.Partner with Facilities Department to maintain appropriate inventory levels of critical spare components and develop/update preventive maintenance (PM) instructions for production equipment.Assist in coordinating and executing calibration and preventive maintenance activities.Complete all required documentation including work orders and GMP records accurately, clearly, and on time.Troubleshoot equipment issues, working with equipment owners, engineers, and external vendors to drive timely resolution.Proactively engage with support teams to develop solutions for recurring or emerging equipment challenges.Foster strong working relationships within the Facilities team and with internal and external customer departments.Collaborate with Manufacturing, Operations, Environmental Health & Safety, and other cross‑functional groups to meet production goals.Support onboarding and technical training of Manufacturing personnel on process equipment.Assist MST team with new product introductions and technology transfer activities.Support the revision and management of manufacturing documents such as Batch Records and SOPs.Adapt quickly to changes in production schedules and reprioritize tasks to minimize operational disruptions.Participate in periodic on‑call rotations to monitor and respond to equipment issues.Qualifications
High school diploma with at least six (6) years of experience performing maintenance on manufacturing equipment, or an associate’s degree or higher in Pharmaceutical Sciences, Engineering, or a related field (preferred).Experience working in sterile fill and finish manufacturing environments.Strong understanding of GMP standards, regulatory requirements, and industry best practices.Ability to work independently while following established procedures, guidelines, and operational practices.Background in continuous process…
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