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The Senior Manufacturing Operator collaborates to produce reliable medical device products and supplies with effective operations in an empowered organization. As part of a dynamic team, the Senior Manufacturing Operator's, responsibilities include performing electro-mechanical assembly, in-line testing, reagent filling, kitting, and/or packing functions in a regulated environment, through the manual assembly or operation of automated equipment.
Additionally, a Senior Manufacturing Operator supports production by proactively recognizing, and elevating safety, equipment, and product-related issues, contributing to the achievement of production goals. They utilize validated software systems to maintain processes, batch records, and inventory control, ensuring all production related documentation is in compliance with quality system regulations. They are responsible for training new employees, sharing best practices, and ensuring team members are qualified to perform the work. A Senior Manufacturing Operator influences, motivates and provides guidance to team members, serves as back-up Process Lead, communicates and collaborates with leadership as needed. They also have excellent communication and organizational skills, and the ability to identify opportunities that would drive the business forward while complying with quality processes and objectives.
This is an essential position supporting the organizational goals requiring attendance on weekends, holidays and during emergency or exceptional conditions.
The Opportunity
Acts as subject matter expert (SME) in the process of assembly, filling, labeling & packaging equipment of varying complexity and in accordance with production manufacturing records, operating procedure requirements to produce finished intermediates and final kits while meeting production targets. Has the ability to adapt to support other functional areas with minimal training.
Interfaces with highly complex systems and controls in a regulated manufacturing environment, (e.g. receive, process, build product/materials, facilitate material availability, perform SAP transactions/confirmations).
Operates equipment to achieve OEE, set up time, cycle times and standard work; Troubleshoots equipment-related problems on multiple production lines.
Identifies defects and non-conforming parts, and performs in-process inspections; tests products, and troubleshoots routine test failures to the subassembly level with support and consultation from experienced technical personnel.
Assists with specific equipment repairs. Performs basic preventative and unplanned maintenance ensuring completeness of appropriate documentation and escalates to appropriate support team(s) accordingly.
Partners with Process Lead to understand and execute production schedule; Ensures daily end of shift reports/pass downs are completed to ensure proper communication and synergies between shifts and teams and collaborates, aligns, provides feedback and assists in the development and execution of protocol/validations.
Other duties as assigned by management.
Who You Are
You hold a High School Diploma and 4 years of experience in a regulated environment, utilizing hand tools and test equipment, validating software systems used to maintain quality, inventory, and processes, diagnosing and correcting equipment problems.
Preferred Requirements
Associate’s Degree with relevant work experience, in GMP environment utilizing hand tools and test equipment, validating software systems used to maintain quality, inventory, and processes, diagnosing and correcting equipment problems.
Behaviors, competencies, and qualities of the ideal Senior Manufacturing Operator
Strong critical thinking, problem solving and analytical skills.
Ability to deal with a variety of concrete variables in situations where thorough standardization exists.
Ability to work with cross-functional teams.
Ability to be agile and accurate in a high-volume, fast paced environment.
Strong organizational skills, planning skills and attention to detail.
Strong communication skills - written, verbal.
Excellent time management skills to manage multiple tasks and competing timelines.
The expected salary range for this position based on the primary location of Tucson, AZ is 47,040.00 - 87,360.00 USD Annual . 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.
Are you ready to apply?
Relocation benefits are not available for this position.
At Roche, more than 100,000 people across 100 countries are pushing back the frontiers of healthcare. Working together, we’ve become one of the world’s leading research-focused healthcare groups. Our success is built on innovation, curiosity and diversity.
Ventana Medical Systems, Inc. (Ventana), a member of the Roche Group, innovates and manufactures instruments and reagents that automate tissue processing and slide staining for cancer diagnostics. Our integrated staining, workflow management and digital pathology solutions optimize laboratory efficiency to reduce errors and support diagnosis for pathology professionals. Together with Roche, Ventana is driving personalized healthcare through accelerated drug discovery and companion diagnostics.
Roche is an equal opportunity employer and strictly prohibits unlawful discrimination based upon an individual’s race, color, religion, gender, sexual orientation, gender identity/expression, national origin/ancestry, age, mental/physical disability, medical condition, marital status, veteran status, or any other characteristic protected by law.
If you have a disability and need an accommodation in relation to the online application process, please contact us by completing this form Accommodations for Applicants .
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