Instrumentation Specialist

Pre-Startup

During the plant start-up project you will be on the User Team and be responsible for establishing the site’s calibration program across the production and qc lab areas including procedures and training. In addition, you will partner with instrumentation & control engineers to establish a metrology program for the site. You will also have the potential to support FAT for production equipment. To accomplish this, you will partner and collaborate with our partner organizations (Engineering and MSAT, Quality, Supply Chain, Technical Development, Regulatory, CMO, Strategy). Initially, you will perform a mix of remote and onsite work (first at the General Planner’s office, later at construction site/plant). You will transition to local full time on-site work once the site buildings are built and equipment delivered. Travel of up to 30% of the time is expected during the project phase.

Post-Startup

You will provide in the field execution of calibration activities on GMP assets and support the metrology program/lab at the site. This will include both planned preventative calibration and repairs / troubleshooting. Supporting troubleshooting of PLC/automation is expected. This will be done while adhering to applicable SOPs, complying with cGMP, and adhering to Federal, State, Local, and Genentech safety standards. You will perform timely detailed documentation following Good Documentation Practices in electronic (e.g. SAP) and paper based systems. You will create and facilitate continuing education for the calibration staff to increase technical skills through formal and informal training, coaching and mentorship. You will provide assistance with identification of spare parts and BOM improvements to improve service delivery and reduce equipment downtime. You will need to Read and Understand P&lDs, work from Standard Operating Procedures (SOPs) and have basic computer skills using word processors, spreadsheets, databases, and email. You will provide inputs to master data needed to support the calibration program in SAP S4/HANA. You will support Quality Record management through gathering information and providing SME. Proficient in Quality Management System(s) which include owning quality events (ex. deviations and planned change events). You will need to understand controlled, classified environments, aseptic processing principles, and maintain associated qualifications for access.

Who you are

• High School diploma or equivalent with 7+ years of related work experience in an industrial / manufacturing setting with demonstrated strong mechanical aptitude.
• An A.A., A.S., A.A.S., or Trade School Certificate is preferred with 5+ years of related work experience.
• Specifically, experience with maintaining high performance pharmaceutical packaging lines.
• You have an ability to organize and solve complex, unique or unprecedented problems through the regular use of ingenuity and innovation; consistently demonstrating courage and drive to ensure optimal business results.
• You are proficient in using AI and other digital tools to solve complex challenges
• You have familiarity with cGMP's, Health Authority regulations, and Quality Systems.
• Strong interpersonal, communication (written and verbal), project management, and time management skills

Work Environment/Safety Considerations

Candidates must be flexible to work overtime and adjust working schedule beyond normal work week. Work schedule may be subject to change based on the phase of the project and/or commercial demand. May work in the clean room environment that requires gowning in the form of hospital scrubs, bunny suits, gloves, and steel toe boots. Potential to work near hazardous materials, chemicals, and equipment as per company safety procedures and guidelines. Active role which includes lifting up to 35 lbs, navigating stairs/ladders/scaffolding, transporting equipment to the location of instruments, and working away from a desk for the majority of working shift. Be able to work extensive hours while standing