Hillsboro Technical Operations (HTO) is a drug product & finished goods manufacturing organization responsible for the reliable delivery of Roche’s commercial portfolio & pipeline products.  The Operations organization at HTO is divided into 2 value streams, which combine to produce millions of units of life-saving medicine every year to patients around the world.

The Opportunity:

Please note we have multiple positions available. The manufacturing organization works a 24x7 operation with day, swing, and night shifts. We work a compressed work schedule, front/half back/half. The schedule for these positions are DAYS either 6:00am - 6:30pm Sunday through Tuesday (alternating Wednesdays) or Thursday through Saturday (every other Wednesday) or NIGHTS either 6:00pm - 6:30am Sunday through Tuesday (alternating Saturdays) or 6:00pm through 6:30am Wednesday through Fridays (alternating Saturdays).

Under the direction of the Process Unit Lead or other qualified Operations Specialist, you will perform a wide variety of tasks and operations that are required to formulate, fill, inspect and package sterile pharmaceutical products in a state-of-the-art, automated production and packaging facility.

You will perform equipment change over, setup and perform test runs for various-sized vials and packages as required.

You will perform equipment troubleshooting or coordinate with cross functional teams to resolve equipment failures.

You will execute production recipes, check-in equipment, and perform material movements using automated computer software applications (SAP and MES systems). You will use these systems to ensure inventory control of materials.

You will interface with other automated process control systems (DeltaV) as a routine part of your normal duties.

You will monitor process performance using trend analysis and document issues such as unplanned downtime.

You will help ensure effective communication across shifts, within the value stream and use communication to collaborate with external support groups.

You will help ensure compliance of a GMP facility to regulatory standards. You will triage and help determine the root cause of production deviations to ensure patient safety for therapeutic drugs. You work closely with quality assurance to document the impact, root cause and corrective actions associated with these deviations.

You will support the Operations Specialist, Maintenance, and/or outside services in the repair, maintenance, and calibration of Genentech systems

You will drive to develop and maintain a LEAN culture dedicated to providing the best results for our internal and external customers

You will perform preparation of sterile components

You will identify process optimizations and assist in the development of plant SOPs and training materials

Prior to start-up, during processing, and at the completion of the manufacturing process, you will perform all documentation and clerical functions to provide the proper accountability and traceability of components and finished product.

At the start and finish of each shift, you will report and make recommendations regarding equipment, supplies, required repairs, process concerns, safety concerns, and areas for improvement in reliability, yield, and efficiency

You will assist in cleaning, setting up, sterilizing, and disassembling various processing equipment in the production area

You will perform training of other Technicians

You will conduct environmental monitoring activities in the manufacturing areas as required.

You will work effectively and efficiently in a team-oriented environment to ensure maximum, high-quality output; adhering to all plant safety policies and procedures and proactively identify unsafe conditions.

Who You Are:

You have a High School Diploma

You have 5-9 years previous experience operating complex mechanical equipment or in a related discipline

You are computer literate, including the ability to interface with computer systems and PLC-based logic.

Preferred/Desired:

You have an Associates Degree in Electro-Mechanical Discipline or a Bachelors degree in engineering or related field

You have previous experience with biopharmaceutical drug product manufacturing; Formulation, Filling, Conveying, Sealing, Inspection and Packaging of products/containers

Work Environment/Physical Demands/ Safety Considerations:

 Able to lift 45 pounds and stand for extended periods of time

Must pass a vision acuity and color discrimination test

Must complete periodic physical examinations to identify medical conditions that pose a risk to Grade C or higher operation

Perform cleaning and housekeeping duties as required.

The expected salary range for this position based in Oregon is $50,000 - $92,000. Actual pay will be determined based on experience, qualifications, geographic location, and other job-related factors permitted by law.  A discretionary annual bonus may be available based on individual and Company performance. 

This position also qualifies for the benefits detailed at the link provided below.

Benefits

Genentech is an equal opportunity employer, and we embrace the increasingly diverse world around us. Genentech prohibits unlawful discrimination based on race, color, religion, gender, sexual orientation, gender identity or expression, national origin or ancestry, age, disability, marital status and veteran status.