Specialist, Direct Materials
Specialist, Direct Materials
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Not Disclosed
Salary Not Disclosed
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
A healthier future. Its what drives us to innovate. To continuously advance science and ensure everyone has access to the healthcare they need today and for generations to come. Creating a world where we all have more time with the people we love.
Thats what makes us Roche.
The Opportunity:
You lead the execution of direct material-related operational and change management activities for the global Roche manufacturing network.
You manage direct material (DM) introductions changes and qualification activities.
You manage DM databases documents websites and data repositories.
You oversee DM-related material assessments write protocols and reports as applicable.
You execute DM business processes develop process improvement solutions as needed and guide alignment for the network.
You work independently with limited direction and in a team environment with key customers/stakeholders including: Quality Process Development Manufacturing Sciences Regulatory and External Suppliers.
You communicate effectively and efficiently with all levels of the organization and identify and manage issues and conflicts in a positive manner. Additionally you present at department cross-department and project team meetings and create training materials to train stakeholders on DM business processes tools and requirements.
Who You Are:
You hold a Bachelors degree and/or advanced degree in Life Sciences or a related field.
You have a minimum of 5 years experience in biotechnology/pharmaceutical manufacturing process development and/or project management in a related industry.
You are familiar with and knowledgeable about cGMP and quality compliance as well as bio manufacturing processes and direct materials.
You are proficient in Google applications (e.g. gMail gCal gSites gDocs gSheet gSlides) and Quality and Document Management Systems (e.g. Veeva Trackwise).
You have experience with change management and project management along with strong attention to detail and a desire to deliver high-quality work with the ability to manage multiple tasks
You participate in teamwork at the network level suggesting project/process improvements demonstrating strong interpersonal organizational and problem-solving skills flexibility and the ability to prioritize and multitask while working with minimal supervision in a team environment.
Relocation benefits are not available for this position
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.
Required Experience:
Unclear Seniority
Employment Type
Full-Time
