Senior Manufacturing Formulator

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 Senior 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 Senior 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.

Additionally a Senior Manufacturing Formulator 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 Formulator 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

Production

• Acts as subject matter expert in the formulation and production of stocks and bulk solutions by performing calculations completing material requests and transactions and utilizing lab equipment in controlled areas.

• Identifies improvements as work is performed to improve cycle time quality safety and delivery of products.

• Performs in-process testing of reagents as detailed in manufacturing formulas troubleshoots and develops 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.

• Performs planning input and execution of validations protocols and scientist investigations. Initiates and leads process improvement projects.

• Contributes to the manufacturing schedule by supporting 3 or more reagent product lines (detection molecular special stains antibody bulk reagents).

• Acts as subject manager expert in validated production systems as part of manufacturing documentation and inventory management.

• Communicates and collaborates with planning quality control material conveyance and other production teams to expedite work.

• 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.

• Assists with batch record reviews.

Safety and Quality

• 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.

• Recognizes and initiates safety improvement projects communicates and partners with SHE group and Leadership to implement.

• Ensures audit readiness (OSHA NMPA FDA etc.); may be required to represent their team during internal audits/inspections.

• 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.

• Escalates all quality and production deviations to leadership.

• Leads and owns non-conformance investigations reworks and corrective actions.

• Owns initiates monitors reviews and provides feedback on document changes including redlines.

• Adheres to 95% or above internal training compliance.

• Maintains calibrated equipment assesses the need for new /replacement equipment and coordinates purchase and ioq/certification process.

Teamwork and Collaboration

• Proactively collaborates with peers on shift and with other function to ensure we exceed daily targets.

• Assists in the successful onboarding of new employees and contractors including facilitating OJT.

• Supports the leaders to maintain and cultivate the organizations culture.

• Collaborates with the team and leaders to achieve departmental goals.

• Communicates outside the department with manufacturing and associated organizations.

• Partners with internal and external functions to address escalations in a timely and effective manner.

• May collaborate with cross-functional teams on new production processes.

Continuous Improvement

• Acts as subject matter expert in 6S activities; Identifies owns and implements process improvements and continuous improvement initiatives utilizing lean tools.

• Participates in the collection of data population and trending of daily metrics (e.g. Safety Quality Cost Delivery) to identify gaps and support operational excellence initiatives and improvements.

• Identifies areas for improvement and can convey ideas to maintenance engineering or area leaders .Troubleshoots problems engages appropriate support functions and assists in implementing preventative measures.

Qualifications for the Role:

Associates degree 3 years of work experience required.

Bachelors degree 2 years of experience preferred.

Experience in a regulated industry required.

Experience in GxP required.

Relocation benefits are not available for this job posting.

Pay transparency

The expected salary range for this position based on the primary location of Tucson is 49800.00 - 92400.00 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.

Benefits

A healthier future drives us to innovate. Together more than 100000 employees across the globe are dedicated to advance science ensuring everyone has access to healthcare today and for generations to come. Our efforts result in more than 26 million people treated with our medicines and over 30 billion tests conducted using our Diagnostics products. We empower each other to explore new possibilities foster creativity and keep our ambitions high so we can deliver life-changing healthcare solutions that make a global impact.

Lets build a healthier future together.

Roche is an equal opportunity employer. It is our policy and practice to employ promote and otherwise treat any and all employees and applicants on the basis of merit qualifications and competence. The companys policy prohibits unlawful discrimination including but not limited to discrimination on the basis of Protected Veteran status individuals with disabilities status and consistent with all federal state or local laws.

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.