Who We Are
At Roche, we are passionate about transforming patients’ lives, and we are bold in both decision and action - we believe that good business means a better world. That is why we come to work every single day. We commit ourselves to scientific rigor, unassailable ethics, and access to medical innovations for all. We do this today to build a better tomorrow.
Roche is strongly committed to a diverse and inclusive workplace. We strive to build teams that represent a range of backgrounds, perspectives, and skills. Embracing diversity enables us to create a great place to work and to innovate for patients.
Your main responsibilities will include:
Representing Roche Diagnostics in external associations and authority communication on environmental regulations within North America (e.g. AdvaMed, US EPA)
Driving advocacy efforts in the field of environmental regulations within NA and LATAM in collaboration with relevant stakeholders
Establishing an internal network within NA and LATAM sites and collaborating closely with the Diagnostics global network lead
Responsible for the monitoring and internal reporting of environmental regulatory changes and requirements in NA/LATAM in collaboration with the global network lead
Providing expert advice and information to the sites according all relevant regulatory changes and requirements
Supporting in setting the implementation strategy on changes that can impact Diagnostics right to operate
Responsible for collaborating with the NA/LATAM site SHE networks and providing support as needed
Providing expert advice, facilitation and coaching to Diagnostics on environmental regulations related topics (TSCA, Prop 65, Biocide regulation, CEPA, etc)
Identifying the need and providing expert-level training, workshops and seminars for Dia in partnership with Group SHE and other appropriate SMEs
Who You Are:
Experience, Skills, Knowledge:
At least a Bachelor of Science degree in chemistry, biology or related field additional training in environmental and chemical regulations and its application is a bonus
10 years of experience or more in working on product related environmental regulations
Expert communicator, ability to influence various complex internal/external stakeholders in a matrix environment
Strong and demonstrated experience in working within industry associations and direct interaction with authorities
Experience in working in diagnostics and medical device sector
Ability to present and translate complex topics in a readily understandable fashion
Brings along a strategic vision as well as experience to build strong relationships
Ability to work independently and influence without authority. Highly developed competencies in thinking strategically, analytically and innovatively.