Chemical Mix Associate Technician

Roche•Tucson, AZ

1d•Onsite

About The Position

At Roche you can show up as yourself, embraced for the unique qualities you bring. Our culture encourages personal expression, open dialogue, and genuine connections, where you are valued, accepted and respected for who you are, allowing you to thrive both personally and professionally. This is how we aim to prevent, stop and cure diseases and ensure everyone has access to healthcare today and for generations to come. Join Roche, where every voice matters. The Position The Manufacturing Formulator collaborates to produce reliable medical device products and supplies with effective operations in an empowered organization. As part of a dynamic team, the Manufacturing Formulators, responsibilities include performing weigh, mix and in process testing of chemical reagents in a regulated environment, through the manual processing or operation of automated equipment. Manufacturing Formulator recognizes and elevates safety, equipment, and product problems, contributing to the achievement of production goals. Utilizes validated software and systems to maintain processes, batch records, and inventory control. Ensures all production related documentation is in compliance with quality system regulations. May be responsible for low complexity training of new employees and sharing best practices. They must have good communication and organizational skills and the ability to identify opportunities that would drive the business forward. This is an essential position supporting the organizational goals requiring attendance on weekends, holidays and during emergency or exceptional conditions.

Requirements

H.S. Diploma
Associate's Degree
2 years Relevant work experience with H.S. Diploma.
1 year Relevant work experience with Associate's Degree.
Knowledge of basic and some specialized laboratory techniques.
Experience in accurate and precise manual pipetting and measuring techniques.
Experience with handling corrosive and hazardous materials.
Demonstrated experience with Lean / Continuous Improvement.
Experience with Google products (gMail, gSheets, gDoc, etc).
Experience with ERP systems.
Ability to read, write and comprehend English.
Ability to work with cross-functional teams.
Ability to be agile and accurate in a high-volume environment.
Strong organizational skills, planning skills and attention to detail.
Strong communication skills - written, verbal.
Strong critical thinking, problem solving and analytical skills.
Excellent time management skills to manage multiple tasks and competing timelines.
Ability to use the technology associated with the industry.
Ability to use precision tools.
Ability to have prompt, regular and reliable worksite attendance.
Ability to work effectively with a respirator and other required PPE.
High degree of initiative with the ability to work under general supervision.

Nice To Haves

Experience in regulated industry.
Experience in GDP/GMP.

Responsibilities

Production Follows work instructions to formulate and document production of stocks and bulk solutions by performing calculations, completing material requests and transactions, and utilizing lab equipment in controlled areas.
Performs in-process testing of reagents as detailed in manufacturing formula and standard operating procedures.
Supports team members with verifications including concentrations/titers, line clearance, and line closeout.
Fulfills reservations by proactively checking open reservations, requesting material, pulling material aliquot and properly labeling material.
Contributes to the manufacturing schedule by supporting at least 2 reagent product lines (detection, molecular, special stains, antibody, bulk reagents).
Utilizes validated production systems as part of manufacturing documentation and inventory management.
May assist in the execution of validations, protocols, and scientist investigations.
Maintains Right to Operate and ensures that all processes are performed in a safe and healthy manner.
Addresses and escalates any potentially unsafe hazards; Ensures timely reporting of safety hazards, incidents and near misses using safety reporting tools.
Navigates and understands the quality system and escalates issues.
Accurately performs tasks in a regulated environment (OSHA, NMPA, FDA, etc.).
Performs and documents all transactions and production instructions with accuracy related to the proper receipt, quarantine, storage, and disbursement of materials as it relates to FDA, OSHA, QSR, ISO, Good Manufacturing Practices and other Roche policies and procedures.
Assists with non-conformance investigations, reworks, and corrective actions.
Participates in the review of and provides feedback on document changes, including redlines.
Adheres to 95% or above internal training compliance.
Maintains calibrated equipment.
Proactively collaborates with peers on shift and with other functions to ensure daily targets are achieved.
Assists in the successful onboarding of new employees and contractors.
May collaborate with cross-functional teams on new production processes.
Performs 6S activities, gathers/meets cycle times and develops/follows standard work; identifies and implements process improvements and continuous improvement initiatives utilizing lean tools.
Participates and contributes in tier meetings.
Participates in process improvement projects.
May participate in the collection of data for daily metrics purposes and to support operational excellence nitiatives and improvements.
Other duties as assigned by management.