Supervisor Manufacturing Operations, 2nd shift 3:00 PM - 11:30 PM

Roche fosters diversity, equity and inclusion, representing the communities we serve. When dealing with healthcare on a global scale, diversity is an essential ingredient to success. We believe that inclusion is key to understanding people's varied healthcare needs. Together, we embrace individuality and share a passion for exceptional care. Join Roche, where every voice matters.

A healthier future. It's 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.

That's what makes us Roche.

The Supervisor of Manufacturing is a strategic thinker who works well in a team environment, has leadership experience, and is able to implement business strategy and development. You will supervise the daily packaging operation at RMD Branchburg. You will manage a team of 12 Direct Reports and share the responsibility of overseeing the packaging department of a staff of 40-50 employees who conduct the labeling and packaging of diagnostic reagents into final kits. Responsibilities include managing the schedule and work assignments for the packaging and labeling areas, as well as the scheduling of automated packaging and labeling equipment to meet production demands.

This position is a second shift position and is eligible for Shift Differential.

Working Hours: 3:00 PM - 11:30 PM

• You will resolve scheduling conflicts and production issues in order to meet production and replenishment demands. Leads project-based activities (e.g., new product transfers product validation activities) to support departmental and company goals. Maintains control of work group expenses within limits of DOA.

• You will be responsible for the accuracy, quality and timeliness of Packaging operations and product supply. Keeps the manager(s) informed of product and project status, particularly of significant observations and results in critical areas. Ensures that Packaging group performs work according to established internal safety guidelines and procedures, and as specified by appropriate external regulatory agencies (e.g., OSHA, FDA, ISO).

• You will serve as a technical resource for the specific area of supervision assigned. Individual is a mentor to the members of the work group and resolves issues encountered in the logistics and planning processes to improve performance. Provides definition and plans for timely achievement of overall product or project goals and to the expeditious transfer of technologies.

• You will lead investigations, write the investigation reports, and advance through the quality system. Makes recommendations, provides or implements process improvements and document improvements. Prepares complex reports, presentations, protocols and other documents.

• You will lead Change Management initiatives within the packaging operations. Ensures all area personnel are trained in job specific SOPs and that all operations are performed in a manner compliant with Master Records and associated SOPs. Writes and/or revises documents (e.g., SOPs, Variances, Rework Orders, Change Requests) to comply with cGMP/ QSR practices.

• Identify opportunities for efficiency gains focusing on Cost & Process improvements. Utilize and implement digital solutions for the department. Defines and monitors project timelines, ensuring timely achievement of overall project goals and establishing priorities.

• Possess knowledge of Overall Equipment Effectiveness (OEE) and managing manufacturing productivity.

• You will manage staff; provide staff with coaching, training and opportunities to develop skills, and provide ongoing, constructive and timely feedback on performance and progress toward goals and expectations. Participates in routine training activities to maintain/enhance own technical skill level and supervisory abilities. Other duties as assigned by management.

• You have an Associate's Degree. A Bachelor's Degree or Master's Degree is preferred.

• You have 6 years of relevant experience in production, manufacturing or related fields. Supervisory/management or leading/directing people is preferred.

Are equivalencies acceptable?

Yes. Equivalent combination of education and work-related experience.

Knowledge, Skills and Abilities

• In-depth understanding of GMP, ISO, QSR requirements is required.

• Strong problem-solving skills.

• Ability to communicate effectively in small group settings.

• Ability to summarize complex information and present the same to senior staff.

• Ability to manage conflicts.

• Ability to make decisions.

Travel Requirements: 10%

Relocation benefits are not available for this posting.

The expected salary range for this position based on the primary location of Branchburg, New Jersey is $80,900.00 - $150,300.00 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

At Roche, more than 100,000 people across 100 countries are pushing back the frontiers of healthcare. Working together, we've become one of the world's leading research-focused healthcare groups. Our success is built on innovation, curiosity and diversity.

Roche is an equal opportunity employer and strictly prohibits unlawful discrimination based upon an individual's race, color, religion, gender, sexual orientation, gender identity/expression, national origin/ancestry, age, mental/physical disability, medical condition, marital status, veteran status, or any other characteristic protected by law.

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.