Controls Engineer

Overview

Valspec—a global provider of system validation and lifecycle services—provides commissioning and qualification of computerized systems for clients in the Life Sciences industry. Established in 1999, Valspec’s mission is to provide a wide spectrum of services that help its clients meet their capital project and lifecycle maintenance goals. Valspec’s projects are critical to the industry and to the people who rely on its products. Many projects ensure that life-changing drugs are available to those who need them; others streamline production to meet demand at a lower cost, allowing for the discovery of new and innovative therapies. SENIOR AUTOMATION ENGINEER (AUTOMATION, INFORMATION & OPERATIONS TECHNOLOGY SOLUTIONS) This is a great opportunity for anyone seeking to get closer to family in New York, New Jersey, Pennsylvania, or Maryland. The ideal candidate is a tech savvy professional with a proven track record in the SDLC (system development life cycle) of automated computer systems within biopharmaceutical environments. We are pursuing both individuals who can join our team long term and SMEs (subject matter experts) who would like to join us on a consulting basis. Responsibilities

Specification, design, and configuration of programmable logic controllers (PLC), distributed control systems (DCS), manufacturing execution systems (MES), and data historians (OSI PI). Work as part of an internal project team or at a client site, interacting with cross-functional groups to propose and assess modifications to equipment and processes to improve operational efficiency. Prepare and execute engineering documentation, operating / maintenance procedures, commissioning and validation test plans for multiple process and utility systems. Project Overview

Special project to increase production capabilities of vaccine. Implementation of DeltaV Batch system utilizing the PCSD libraries and DeltaV Live. Full lifecycle activities including development of software design specifications, design workshops, configuration, testing, SFATs, skid vendor FATs, and site commissioning. Duration

12 Months+ Travel Requirements

Much of the work can be performed remotely with the exception of the start-up commissioning phase. The ideal candidate is willing to relocate, at least temporarily, if called in. Expenses will be reimbursed at cost. Requirements

5+ years of experience in control systems design and implementation; broad SDLC experience in automated systems (process controls, MES, and / or data management). S88 Batch experience required. Strong process knowledge and understanding of engineering documents, process control (PLC / DCS / SCADA), networks, control systems and application engineering. Working knowledge of structured methodologies for manufacturing systems and programming skills. Experience with Emerson DeltaV and / or Allen Bradley controllers and interfaces is strongly preferred. Prior experience in biotechnology, pharmaceutical, or FDA-regulated environments; experience in development and execution of IQ, OQ, PQ validation protocols for new or upgraded factory floor systems. Able to be onsite when needed. Benefits and Environment

Valspec offers a standout culture, a professional environment, and competitive benefits including premium medical, 401K match, tuition reimbursement, and other incentives. Eligibility and Compliance

Candidates must be legally eligible to work in the United States without company sponsorship. We are not interested in working on a corp-to-corp basis at this time. Valspec is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to sex, race, color, religion, national origin, age, sexual orientation, gender identity, disability, protected veteran status or any other protected class. We are committed to a professional environment free of discrimination or harassment and a Drug-Free Workplace. Important Notices

For government reporting purposes, we ask candidates to respond to voluntary self-identification surveys. Completion is voluntary and will be kept confidential. Any information provided will be maintained in a confidential file and used solely for compliance reporting. This includes EEOC and VEVRAA-related inquiries as applicable. Disclosures and cautions : This description reflects current responsibilities and requirements and may change without notice.

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