Operations Quality Pathology Customer Area Point of Contact
Operations Quality Pathology Customer Area Point of Contact
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$ 105000 - 228000
1 Vacancy
Job Description
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
As the Pathology Customer Area Single Point of Contact (SPOC) you serve as the single point of contact for the Pathology Customer Area for the Operations Quality team. You will be a key Operations Quality interface who works to enable the Pathology Customer Area business ambitions. You are capable of developing strategies and setting clear priorities to guide the focus of our Operations Quality networks chapters and squads. You will work closely with the Pathology Customer Area Lifecycle Teams (LCTs) and Functional Partners to collaborate across Networks to deliver comprehensive and successful customer solutions. You champion our Quality Management System to ensure that data-driven quality is embedded within the organization to meet customer expectations and ensure compliance with applicable global and regional regulatory requirements. You will lead one of the Operations Quality Community of Practice areas.
As the Pathology Lab Customer Area SPOC you will create an environment of innovation and collaboration. You support the operational activities of the organization by promoting and developing strong connectivity with our manufacturing sites ensuring that the organization cohesively delivers overarching product quality strategies that leverage chapters networks process excellence and our continual improvement efforts.
The Opportunity
Deliver a capability-driven organization through tactical partnerships: Support in defining the short and long-term capability needed to deliver on the Pathology Lab Customer Area strategy and execute on it ultimately advancing expertise and helping our Affiliates and LCTs to achieve their business objectives. Develop strong relationships across the DIA Networks and Chapters to enhance collaboration and shared accountability using the Q&R Hubs.
Support the delivery of mQMS: Partner with the Quality System Excellence Chapter on the strategic direction for the QMS and develop the organizational capabilities to live the mQMS as designed. Develop and lead process improvements to meet business needs taking into consideration cost compliance and complexity of change. Build and maintain partnership with Network Leaderships to ensure consistency and alignment in mQMS execution across all production sites.
Steward Knowledge Management: Champion a culture of continuous learning fostering growth opportunities that align with Roches strategic goals and drive innovation and operational excellence. Establish and sustain a system that effectively creates captures organizes shares and utilizes knowledge to drive standardization and process improvement to quality-supported production activities Implement overarching strategies to transition product quality activities from solely compliance-focused to proactively quality-focused.
Proactive Quality: Partner in the resolution of quality issues collaborating with LCTs (Local Customer Teams or cross-functional teams depending on the context) to prioritize and facilitate problem resolution ultimately ensuring customer demands are met. Communicate significant quality or regulatory issues and risks that may impact product quality or regulatory compliance in a timely manner to Executive Management. Implement overarching strategies to transition product quality activities from a solely compliance-focused approach to a proactively quality-focused one.
Who You Are:
Bachelors degree in a relevant field (Engineering Life Sciences Quality Management or similar). Advanced degree preferred.
At least five (5) years in the Medical Device/Pharma/Biopharmaceutical industry with three (3) years working in Quality Compliance Regulatory and/or Validation preferred or equivalent experience.
Demonstrated experience and knowledge of Daily Management and Continuous Improvement best practices.
Knowledge of the European US China and International cGMP regulations and demonstrated ability to adequately interpret and implement quality standards considered an advantage.
Proven ability to collaborate and build partnerships across cross-functional teams and matrix organizations preferred.
Demonstrated leadership experience in driving organizational change capability development and process standardization preferred.
Core Competencies:
Strategic Thinking: Ability to identify opportunities for improvement and create actionable plans that align with organizational goals.
Matrix Leadership: Skilled in influencing coaching and developing talent within a matrixed organization.
Problem-Solving: Analytical mindset with the ability to identify root causes develop solutions and drive continuous improvement.
Change Management: Capable of leading change initiatives to improve capabilities and processes across a dynamic environment.
Process Modelling/Engineering: Proficient in defining implementing and improving business processes
Agile - Model agile mindset and proficient in utilizing agile methodologies
Locations
You are local to Tucson Arizona.
Relocation benefits are not available.
The expected salary range for this position based on the primary location of Tucson Arizona is $105000 and $228000. 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.
Who we are
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.
Employment Type
Full-Time
