A Process Control Engineer designs, operates and maintains process control systems in manufacturing companies. Works to ensure that production, quality assurance and safety requirements are met in manufacturing operations. Operates and maintains process control equipment and provides preventative maintenance. May create or maintain automation processes for a company.
Bachelor's degree in Chemical / Biochemical Engineering, Pharmaceutical Science, or Chemistry/Biology, or other related science or engineering field.
Required Experience and Skills:
Minimum of 6 years post-bachelor's degree experience in a GMP functional area or support of a GMP functional area, such as Operations, Technical Operations, Technology, or Engineering Min 3 years of experience supporting sterile / aseptic drug product filling (vials, syringes, etc.) Prior experience and competency with change control Statistics experience Strong communication and teamwork skills Demonstrated ability to independently manage projects/work to schedule/deadlines Travel may be required but not to exceed 25%(NC/Indiana)
Preferred Experience and Skills:
Experience with isolator filling.
Key Skills:
•External Manufacturing Technical Operations Contractor role supporting Drug Product operations. The assignment is planned for one year, with a possible one-year extension. Both remote and hybrid options available. The role can be remote, but West Point is the preferred location; local candidates may be expected to come onsite a few days(1-2days) per week. The ideal candidate should have around 6 years of experience and strong technical operations experience in sterile liquids, injectables, vials, and syringes not solid dosage. Key skills include change control ownership/execution, organization, planning, statistical understanding, cross-functional communication, teamwork, and ability to work independently. The role will involve process-related technical change controls across multiple sites, including work with SOPs, procedures, systems, emails, meetings, and stakeholder coordination. Travel will be up to 25%, mainly to North Carolina and Indiana. This role will primarily support the commercial manufacture of Drug Product (Form / Fill) at the client's External Partner network sites inclusive of the responsibilities below.
Responsibilities include:
Author, review, and maintain GMP technical documentation with clarity, accuracy, and compliance to applicable regulatory and quality requirements.
Documents include:
Change control ownership and execution Protocols and technical reports Continued Process Verification (CPV) plans, data sets, trend analyses, and periodic reports Perform statistical data extraction and analysis to support proactive process analysis.
Typical activities:
Pull and validate production, quality, and process control data from relevant GMP sources or approved data trending systems Apply statistical process control (SPC), capability analysis, and other appropriate methods Create visualizations and summary metrics to support assessment outputs Contribute to continuous improvement initiatives, including data-driven process optimization and documentation standardization Floor support as needed for Person-In-Plant activities at External Partner Nesco Resource offers a comprehensive benefits package for our associates, which includes a MEC (Minimum Essential Coverage) plan that encompasses Medical, Vision, Dental, 401K, and EAP (Employee Assistance Program) services. Nesco Resource provides equal employment opportunities to all employees and applicants for employment and prohibits discrimination and harassment of any type without regard to race, color, religion, age, sex, national origin, disability status, genetics, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state, or local laws.
