DeltaV Decommissioning

Job Title: DeltaV Decommissioning/Validation Engineer

Company: Novozen Health Care LLC.

Location: North Chicago, IL

Employment Type: Contract

Job Responsibilities:

Our client is a large pharmaceutical manufacturing company looking to onboard an experienced DeltaV Decommissioning / Validation Engineer to support a major facility expansion and redevelopment project. The site is decommissioning existing manufacturing systems and equipment that will either be upgraded as part of the expansion or removed/demolished to make way for new equipment and infrastructure.

This individual will primarily own the authoring and execution of decommissioning protocols associated with DeltaV-controlled equipment and systems. The project includes approximately 100–150 protocols, making strong GMP documentation and protocol execution experience critical.

Project:

• Author and execute DeltaV decommissioning protocols for existing manufacturing systems and equipment.

• Support decommissioning activities involving tanks, bioreactors, process skids, and associated controls.

• Execute decommissioning of DeltaV control modules, equipment controls, and associated PI points/tags.

• Support some DeltaV Batch activities, although the majority of the scope will center around control modules and equipment-level controls.

• Coordinate with engineering, validation, automation, and project stakeholders to ensure systems are properly documented and decommissioned.

• Support D3-related protocol activities as needed; a dedicated D3 technical specialist will be available, so prior D3 expertise is not required.

Required Qualifications:

• Strong hands-on experience with Emerson DeltaV in a GMP manufacturing environment.

• Experience authoring and executing validation/decommissioning protocols.

• Knowledge of DeltaV control modules, equipment controls, and system architecture.

• Experience with Impact Assessments, Risk Assessments, and Change Controls.

• Understanding of GMP validation and documentation practices.

• 3+ years of strong GMP pharmaceutical/biotech experience.

• Ability to independently manage a high volume of protocol generation and execution.

Pay Scale:

Anticipated hourly pay range: Specific range such as ($50/Hr to $60/Hr).

Benefits:

Employees hired into this position are eligible for the following benefits, subject to the applicable plan terms and eligibility requirements.

Health Insurance:

Medical, dental, and vision insurance options are available through a third-party provider. Employees are responsible for paying the full cost of their insurance premiums.

Retirement Benefits:

A 401(k) retirement savings plan is available. No employer matching or other employer contributions are provided.

Paid Time Off (PTO) : No PTO other than that required by applicable state and local laws.