Job description

Wondering what’s within Beckman Coulter Diagnostics? Take a closer look.
At first glance, you’ll see that for more than 80 years we’ve been dedicated to advancing and optimizing the laboratory to move science and healthcare forward. Join a team where you can be heard, be supported, and always be yourself. We’re building a culture that celebrates backgrounds, experiences, and perspectives of all our associates. Look again and you’ll see we are invested in you, providing the opportunity to build a meaningful career, be creative, and try new things with the support you need to be successful.

Beckman Coulter Diagnostics is proud to work alongside a community of six fellow Diagnostics Companies at Danaher. Together, we’re working at the pace of change to improve patient lives with diagnostic tools that address the world’s biggest health challenges.

The QC Manager, Process Engineering for Beckman Coulter Diagnostics is responsible for the quality control testing and inspection for all MicroScan consumable products, in-process and final product.

This position is part of the Microbiology Operating Company located in West Sacramento and will be on-site. At Beckman Coulter, our vision is to relentlessly reimagine healthcare, one diagnosis at a time.

You will be a part of the Operations team and report to the Director of Technical Operations responsible for he quality control testing and inspection for all MicroScan consumable products, in-process and final product. If you thrive in a leadership role and want to work to build a world-class multi-functional team and inspiring change—read on.

In this role, you will have the opportunity to:
Strong team orientation and unqualified support of divisional and leadership goals.

Provide technical support and oversight for Operations (Design of experiments, technical writing, analytical testing (HPLC, UV-Vis Spectroscopy, and bioassay)

Supports Operations projects (validation and design changes)

Lead and resolve Internal Non-conformance investigations (assessment of non-conforming product, root cause analysis, corrective, and preventative actions)

Lead and resolve customer manufacturing related CAPA and Post Launch Risk Assessments

The essential requirements of the job include:
Bachelor’s degree in science or related field with 9+ years experience OR Master's Degree in field with 7+ years experience

Background in manufacturing, quality control, R&D, process engineering, or failure investigation

Demonstrated leadership skills (independent action, effective delegation, motivation techniques, ability to resolve interpersonal issues, making “judgment calls” based on experience, etc.).

Effectiveness and timeliness of communication, both vertically and horizontally within the organization. This includes the ability to communicate tactfully, appropriately and professionally in all situations or settings.

Creativity and ingenuity in originating new ideas and concepts.

Minimal direct supervision or follow-up required. Able to act independently (within the scope outlined) and report later.

Demonstrated dedication to quality principles in a cGMP manufacturing environment

It would be a plus if you also possess previous experience in:

Knowledge of analytical testing and/or microbiology preferred

Quality System Regulation (QSR’s, ISO 13485:2003) / Aseptic Techniques / Contamination Control

Project Management / Design of Experiments / Process Validation

When you join us, you’ll also be joining Danaher’s global organization, where 80,000 people wake up every day determined to help our customers win. As an associate, you’ll try new things, work hard, and advance your skills with guidance from dedicated leaders, all with the support of powerful Danaher Business System tools and the stability of a tested organization.

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