Process Engineer II - Night Shift
Company: Disability Solutions
Location: Carlsbad
Posted on: April 20, 2024
Job Description:
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.The
PositionAlways innovating, we bring together dedicated people and
diverse perspectives from across our global network, empowering
each other to keep breaking new ground. We are Roche.The team,
GenMark Diagnostics is a leading provider of multiplex molecular
diagnostic solutions designed to enhance patient care, improve key
quality metrics, and reduce the total cost-of-care. At GenMark,
we're changing the diagnostics landscape, combining out-of-the-box
thinkers and game-changing technology to revolutionize patient
care. Our work atmosphere is dynamic, fast-paced, and
patient-focused. We encourage teamwork, while reinforcing the
importance of individuality, and encouraging an entrepreneurial
spiritYour OpportunityThe work schedule for this position is a
night shift from Sunday through Friday from 10 PM to 6:30 AM.As a
Process Engineer you will be driving stable, reliable production
processes for new manufacturing processes recently transferred to
production. Under minimal supervision, you will use sound and
proven engineering principles to develop and characterize
manufacturing processes, including surface treatment (i.e. plasma,
CO2 cleaning) and precision dispensing of fluids and adhesives. In
this position, you will be instrumental in creating and maintaining
process input and output specifications, performing capacity
analyses, troubleshooting, testing, and support for existing
products and new product lines. This position will sustain and
continuously improve process for existing products. Also, you
are:
- Investigating, troubleshooting, and resolving issues that arise
within the manufacturing process and effectively communicating
findings in a timely manner. Assist with problem solving and root
cause analysis using tools (ex. 5 WHY, Fishbone Diagram...etc),
DOEs (Design of Experiments), data analysis, and
development/implementation of sustainable countermeasures.
- Applying statistical methods to various production performance
datasets to monitor, track and trend, and/or assess opportunities
for improvement in capacity, yield, and/or utilization.
- Executing validation (IQ/OQ/PQ) protocols, test method
validations, test protocols, and associated activities for new or
improved processes and manufacturing equipment.
- Participating in project teams as part of product improvements,
automation, and quality improvements. Also, you are supporting
process development, characterization & improvement activities to
both new and existing product lines. To ensure project success, we
apply standard project management tools and principles
- Serving as advocate and role model for integrating change into
the organization as well as serve as departmental role model of
professional behavior and presence. You are training manufacturing
and maintenance personnel as needed.
- Document management: You will create, and approve Product
BOM's, Specs, Work Instructions and other documentation as part of
the Design Transfer for new product introductions.Who you are
- You have a Bachelor's degree in Engineering or related
technical discipline with 4+ years of related experience,
background and industry, or M.S degree with 2+ years of related
experience, background and industry. Equivalent industry experience
(5+ years) with a high school diploma is acceptable.
- You bring experience in designing/implementing manufacturing
processes, equipment and fixtures.
- It's strongly preferred that you are knowledgeable of
pharmaceutical/medical device cGMPs and FDA compliance
- Other pluses: Experience with design transfer activities for
medical devices and designing/implementing automation
equipmentBehaviors, competencies, and qualities
- Support cross-functional teams in problem solving, development
of improvement plans and root cause analysis.
- Must be proficient in the use of SolidWorks or equivalent CAD
software, Word, Excel, Visio, PowerPoint.
- Familiarity with experimental design, data analysis, and
interpretation of experiments; Proficient in the use of statistical
software such as JMP is plus.
- Strong quality orientation and a desire to deliver service
excellence. Familiarity with Lean Six Sigma or Six Sigma DMAIC
methodology is a plus.
- You have great organizational skills in a dynamic, constantly
changing environment. You are an effective communicator for
sensitive inquiries, customer inquiries or complaints as well with
management, peers, and individuals. You can work effectively,
exhibit a professional manner and establish constructive working
relationships.
- You will be able to think and work both tactically and
strategically to provide financial and operational needs to
GenMark's business.Relocation benefits are not offered for this job
posting The expected salary range for this position based on the
primary location of California is $65,200-$121,000. 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.Work EnvironmentThe essential
functions of the job are usually performed in an environmentally
controlled facility where the noise level in the work environment
is usually moderate. This position may involve a combination of
office and biotechnology laboratory environments. The employee may
be exposed to hazardous chemicals, blood borne pathogens and
automated equipment.While performing the job duties, the employee
is regularly required to sit; reach with hands and arms and talk or
hear. The employee is frequently required to stand and walk. The
employee may sometimes be required to lift and/or move up to 35
pounds. Specific vision abilities required by this job include
close vision, distance vision, color vision and ability to adjust
focus.Who we areGenMark is now a proud member of the Roche Group,
more than 100,000 people across 100 countries are pushing back the
frontiers of healthcare. As a global leader in healthcare, Roche
Diagnostics offers a broad portfolio of products, tools and
services that help in the prevention, diagnosis and management of
diseases like HPV, HIV, hepatitis and diabetes as well as other
medical conditions, such as fertility and blood coagulation. With
the addition of GenMark to the Roche Group, syndromic infectious
disease diagnostics is now added to the long list of disease states
and conditions that the Roche Group addresses. GenMark's ePlex true
sample-to-answer system offers unique solutions to address the most
significant challenges facing clinical laboratories, while
supporting hospital systems to deliver patient-centered,
value-based care. ePlex streamlines the diagnostic workflow from
physician order entry to the final test report and is the true
sample-to-answer solution designed to improve patient care, reduce
costs, and increase lab efficiency. GenMark is headquartered in
Carlsbad, California.GenMark 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.
Keywords: Disability Solutions, Escondido , Process Engineer II - Night Shift, Engineering , Carlsbad, California
Didn't find what you're looking for? Search again!
Loading more jobs...