Process Engineer - CIP​/SIP​/Autoclave

Process Engineer - CIP/ SIP/ Autoclave

What you will do:

In this vital role you will be joining the Facilities & Engineering (F&E) group to partner closely with the corporate engineering team to design, build, commission, and qualify new equipment and systems needed for drug substance production as well as developing domain expertise to support operations upon start-up.

Site design, construction, start-up, and operational readiness:
Support the commissioning and qualification of manufacturing systems in alignment with GMP requirements and interact with regulatory inspectors.

Demonstrate technical expertise and provide lifecycle support for CIP skid systems, SIP circuits, autoclaves, transfer panels, process tanks, valves, instrumentation, and associated automation platforms.

The role will support commissioning, qualification, startup readiness, routine manufacturing operations, troubleshooting, and continuous improvement initiatives with a focus on CIP, SIP and autoclave systems.

Ensure systems are installed and operate safely and comply with pertinent environmental health/safety practice, rules and regulations.

Interact with regulatory inspectors as a manufacturing systems owner to communicate and demonstrate appropriate regulatory compliance of operating systems.

Assist with new product/technology introductions by performing engineering assessments, implementing equipment modifications, and supporting engineering runs.

Site Operations:
Provide system support for biopharmaceutical process equipment – specifically CIP/SIP and/or autoclave systems.

Assist in identifying and implementing engineering-based improvements or upgrades to equipment or facility systems.

Experience with CIP circuit design/validation and SIP.

Support the development of business cases for improvements, identification of design requirements, and translation of these requirements into process equipment/system design, specifications, and supporting the construction, startup, and validation of improvements.

Develop equipment maintenance programs, ensure the availability of spare parts, and coordinate maintenance activities to ensure systems are in proper working order.

We are all different, yet we all use our unique contributions to serve patients. The engineering professional we seek enjoys challenges and is motivated to help serve patients with these qualifications.

Master’s degree OR Bachelor’s degree and 2 years of Engineering experience OR Associate’s degree and 6 years of Engineering experience OR High school diploma / GED and 8 years of Engineering experience

Bachelor’ s degree in Chemical or Mechanical Engineering or similar engineer discipline. 3+ years' of relevant work experience with 2+ years' experience in Biopharmaceutical operations/manufacturing environment Direct knowledge of design and troubleshooting with GMP Biopharmaceutical Production facility equipment/systems with direct experience with Solution Prep, Upstream, and Downstream purification equipment such as weigh and dispense equipment, solution preparation vessels, cell culture reactors, centrifugation, chromatography, viral filtration skids, and UFDF skids as well as other equipment needed to support these processes such as autoclaves, clean in place (CIP) systems, washers, clean steam, water for injection, etc.

Ability to analyze problems, develop and propose engineering solutions in a scientific manner using data-driven techniques and analyses (e.g., Data Analytics, Root Cause Analysis (RCA), Statistical Process Control (SPC), Six Sigma, Predictive Maintenance, etc.) Experience working in a regulated environment (e.g. cGMP, OSHA, EPA, etc.) and familiarity with GMP quality…