Senior Manufacturing Process Engineer
Company: Abbott Laboratories
Location: Scarborough
Posted on: April 7, 2026
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Job Description:
Abbott is a global healthcare leader that helps people live more
fully at all stages of life. Our portfolio of life-changing
technologies spans the spectrum of healthcare, with leading
businesses and products in diagnostics, medical devices,
nutritionals and branded generic medicines. Our 115,000 colleagues
serve people in more than 160 countries. Senior Manufacturing
Process Engineer Working at Abbott At Abbott, you can do work that
matters, grow, and learn, care for yourself and your family, be
your true self, and live a full life. You’ll also have access to: -
Career development with an international company where you can grow
the career you dream of. - Employees can qualify for free medical
coverage in our Health Investment Plan (HIP) PPO medical plan in
the next calendar year. - An excellent retirement savings plan with
a high employer contribution - Tuition reimbursement, the Freedom 2
Save student debt program, and FreeU education benefit - an
affordable and convenient path to getting a bachelor’s degree. - A
company recognized as a great place to work in dozens of countries
worldwide and named one of the most admired companies in the world
by Fortune. - A company that is recognized as one of the best big
companies to work for as well as the best place to work for
diversity, working mothers, female executives, and scientists. The
Opportunity Abbott Rapid Diagnostics is part of Abbott’s
Diagnostics family of businesses, bringing together exceptional
teams of experts and industry leading technologies to support
diagnostic testing which provides important information for
treatment and management of diseases and other conditions. The
position of Senior Manufacturing Process Engineer is within our
Infectious Disease Developed Markets business unit located at
Scarborough, Maine. In this role you will support all Manufacturing
Equipment and equipment quality/cost savings initiatives, improving
efficiency through material and process improvement, reducing
material processing costs, and participating in new product design.
What You’ll Work On - Owns and is responsible for processes based
on product specifications and in consideration to process and test
method capabilities - Evaluates and drives process and design
alternatives based on Design for Manufacturability (DFM)
principles. - Solves highly technical and complex problems using
problem solving and statistical tools and make sound design
recommendations. - Manages program compliance with Quality
requirements (i.e. Design Control, Process validation etc.). -
Maintains knowledge of new developments in manufacturing and design
technologies. - Can identify and propose and own solutions for work
environment issues (i.e. OSHA regulations, etc.). - Supports all
Company initiatives as identified by management and in support of
Quality Management Systems (QMS), Environmental Management Systems
(EMS), and other regulatory requirements. - Designs and leads
tests, collects anaylzes and formats data, supporting engineering
studies (DOEs). - Engages in start up of new equipment, defining
and executiing validation protocols based on requirements. -
Communicates effectively and participate on cross functional
development teams. - Leads in technical design reviews for process
equipment and product design and requirements documents. -
Responsible for utilizing and maintaining the effectiveness of the
quality system, including supporting Quality Incidents and CAPA
investigations and actions. - Analyzes raw material specifications
to ensure appropriate features and limits are in place to support
company manufacturing process. - Evaluates and owns change actions
assocaited with company initiated raw material changes and
coordinates appropriate testing and validation as required. - Works
to reduce costs in all areas of manufacturing by analyzing current
equipment for process suitability and provides detailed plans for
improvement. - Creates and revises manufacturing documents,
specifications, standard operating procedures (SOPs), safety
instructions, validation protocols, risk assessments, and
procedures and other technical documents to insure compliant,
efficient and safe processes. - Conducts operational procedure
audits to ensure compliance with SOPs, ISO, FDA and cGMP
requirements. - Researches engineering solutions to a diverse set
of challenges in production and development. - Complies with U.S.
Food and Drug Administration (FDA) regulations, other regulatory
requirements, Company policies, operating procedures, processes,
and task assignments. - Mentors junior engineers and maintenance
technicians to ensure continual improvement, safety, and
compliance. - Leads change through Agile PDM. Required
Qualifications - Bachelor's degree (BS) in Engineering or
equivalent combination of education and experience. - 7 years
engineering experience in a manufacturing environment. - Technical
experience in mechanical, biomedical, industrial or chemical
engineering. - Experience in performing engineering calculations,
controlled tests, statistical analyses. - Experience in Microsoft
Suites software. (Microsoft Excel, PowerPoint, Power BI, etc.) -
Experience with change management principles and practices.
PREFERRED QUALIFICATIONS: - Proficient with cGMP and ISO 13485
regulations and practices. - Proficient with statistical analysis
software. (Minitab or JMP preferred) Apply Now Learn more about our
health and wellness benefits, which provide the security to help
you and your family live full lives: www.abbottbenefits.com Follow
your career aspirations to Abbott for diverse opportunities with a
company that can help you build your future and live your best
life. Abbott is an Equal Opportunity Employer, committed to
employee diversity. Connect with us at www.abbott.com, on Facebook
at www.facebook.com/Abbott, and on Twitter @AbbottNews. The base
pay for this position is $78,000.00 – $156,000.00. In specific
locations, the pay range may vary from the range posted.
Keywords: Abbott Laboratories, Portland , Senior Manufacturing Process Engineer, Engineering , Scarborough, Maine