Scientist - Test Method Validation

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.

Branchburg is the molecular diagnostics manufacturing engine within Global Operations and a Polymerase Chain Reaction (PCR) center of excellence. As the largest DIA manufacturing site in North America, our teams deliver a broad portfolio of PCR-based in-vitro diagnostic tests. Our operations include reagent and active diagnostic ingredient (ADI) production, filling and packaging. Our 63-acre site with ~1400 people is currently under expansion, fueled by our culture of agility, innovation and transformation. Each day we focus on delivering the value of Roche Diagnostics to patients around the world.

The Opportunity:

• Prepare validation documents utilizing established and published procedures or batch records and technical and theoretical understanding while managing schedules and work flow to accomplish assigned objectives or schedules.
• Assumes responsibility for the accuracy, quality, and timeliness of validation documents. Summarizes batch or experimental results, and reviews conclusions with supervisor/project leader. Communicates results of validation activities. Keeps supervisor/project leader informed of work status, particularly of significant findings and results in critical problem areas.
• Analyzes and interprets test results, experimental data using various data analysis software, spreadsheets and or applying quantitative methods. Uses technical writing skills to produce reports and documents. May present findings at internal meetings.
• Assumes accountability for batch record, hard copy or electronic lab notebook documentation, ensuring experimental methods and results are represented accurately and consistently, and according to established formats.
• May troubleshoot issues related to validation execution. With guidance, analyzes and brainstorms alternative approaches to solve problems, makes recommendations and finds solutions to solve problems.
• Establishes as appropriate internal/ cross-functional/ customer relationships
• Other duties as assigned by management.

Who You Are:

• Bachelor's degree or equivalent combination of education and work experience required
• 3 years of relevant industry experience or general laboratory experience required
• Strong technical writing skills, required.
• Demonstrates potential for technical proficiency, engineering creativity, collaboration with others, and independent thought.
• Demonstrated troubleshooting and problem solving skills including the use of designed experiments.
• Strong teamwork and communication skills.
• Experience with Microsoft Office, JMP and statistical analysis, analytical testing and PCR technology, preferred.

Relocation benefits are not available for this job posting.

The expected salary range for this position based on the primary location of New Jersey is $64,100 to $119,100. 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

#BBGManufacturing#

A healthier future drives us to innovate. Together, more than 100'000 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.

Let's 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 company's 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.