Senior Manufacturing Engineer

F. Hoffmann-La Roche AG; Branchburg Township (NJ); On-site; USD 75,000 - 141,000; Full time

Job summary

Join a leading healthcare company as a Senior Manufacturing Engineer focused on filling and packaging processes. This role involves managing equipment projects within a GMP environment, ensuring compliance and efficiency. Ideal candidates will have a strong engineering background and experience in automated manufacturing systems.

Benefits

Discretionary annual bonus

Qualifications

• Minimum 5 years work experience in a relevant field.
• Experience with GMP manufacturing operations preferred.
• Previous experience in an FDA-regulated environment a plus.

Responsibilities

• Manage projects through design, installation, and qualification.
• Define specifications for diagnostic equipment and packaging components.
• Prepare production documents and resolve equipment functionality issues.

Skills

Technical knowledge

Problem solving

Analytical skills

Communication skills

Organizational skills

Interpersonal skills

Education

Bachelor of Science in Engineering

Tools

Microsoft Word

Microsoft Excel

Microsoft Visio

Microsoft Project

Job description

Senior Manufacturing Engineer page is loaded

Senior Manufacturing Engineer

Apply locations Branchburg time type Full time posted on Posted 2 Days Ago job requisition id 202505-113570

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

Senior Manufacturing Engineer proficient in Filling & Packaging equipment specification, procurement, installation and commissioning in a GMP environment. Ability to manage multiple equipment (new or upgrades) projects through to completion under minimal to no supervision. Understanding of equipment processes in GMP manufacturing environment. Excellent verbal/written communication skills, scheduling tasks/meetings and overall task management of equipment projects are essential pre-requisites for the position.

The Opportunity:

• Uses technical/business knowledge and expertise to support Operations in the design, scale-up, optimization, specification, procurement, installation and qualification of filling and packaging processes or equipment.

• Supports the preparation of any user/system requirements, bid package, capital justification, and factory acceptance/commissioning testing for all new filling and packaging equipment.

• Defines specifications of diagnostic equipment and packaging components in accordance with manufacturing capabilities and marketing objectives. Applies engineering principles and financial expertise to improve diagnostic manufacturing performance, promote cost reductions and achieve optimum level of quality and efficiency.

• Ability to manage equipment projects from design concept/user requirements through to installation/qualification, including collaboration with suppliers/vendors.

• Ability to evaluate filling & packaging processes to identify potential non-conformances stemming from equipment performance or supplier plastic component (e.g. bottle, cap). Collaborate with stakeholders, perform root cause investigations, recommend corrective actions and report on results.

• Prepares production documents (Packaging Records, Filling Records, Labeling Records) as needed. Investigates and resolves problems related to existing equipment functionality, and determines root cause of issues in conjunction with customer complaints.

Who You Are:

• Bachelor of Science in Engineering. Mechanical Engineering, Packaging Engineering or Industrial Engineering preferred. Minimum 5 years work experience.

• Experience with GMP manufacturing operations, equipment and equipment suppliers, preferably automated liquid filling and packaging.

• Strong technical, analytical and problem solving skills required

• Strong organizational and time management skills, ability to establish priorities to finish tasks, ability to re-prioritize tasks/projects as needed, ability to multitask, track status/progress and report/present updates as required

• Excellent interpersonal skills required to interact with stakeholders, e.g. Filling, Packaging, Quality Assurance, and Procurement.

• Excellent technical writing skills required.

• Previous good manufacturing practices (GMP) or background in an FDA-regulated environment in an engineering support role a plus.

• Proficient skills level with using Microsoft applications, including Word, Excel, Visio and MS Project.

• Previous experience with suppliers of injection-molded components and plastics processing used in FDA regulated industries.

Relocation benefits are not available for this position.

The expected salary range for this position based on the primary location of New Jersey is $75,700 to $140,500. 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

Who we are

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 .

About Us

We believe it’s urgent to deliver medical solutions right now – even as we develop innovations for the future. We are passionate about transforming patients’ lives. We are courageous in both decision and action. And we believe that good business means a better world.

That is why we come to work each 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.

We are proud of who we are, what we do, and how we do it. We are many, working as one across functions, across companies, and across the world.