QA Document Coordinator
Company: Corbion
Location: Blair
Posted on: May 4, 2024
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Job Description:
At Corbion, we exist to champion preservation in all its forms,
preserving food and food production, health, and our planet.The QA
Coordinator is responsible for several areas of the quality
management system. Other responsibilities include guiding processes
such as management of change, new product/process implementation,
and internal/external auditing, and process consultation. The
position will provide support during customer visits and third
party audits. Duties and responsibilities include the QA programs
for lactic acid and derivatives production facilities. Ensures food
safety/quality standards are met.Approx. $80MM in sales revenue
generated by Corbion - derivatives and lactic acid production.High
dollar impact of potential product recall to the
business.--Essential Job Functions ------Prepare and coordinate the
policies, procedures, and forms within the document control
system.Provide support to the engineering and technology team and
other departments for new product developments and process
improvements.Propose, write, and/or review QC and QA Standard
Operating Procedures. Maintains the plant Document Control System.
Including, development of Quality department documentation in
coordination with other Quality department team members.Assist with
tracking, reporting, and solving internal and external complaints
regarding products or deliveries alongside all departments in such
a way that problems and complaints are being solved with a focus on
long term internal and external customer satisfaction.Update the
Customer Portal in MS SharePoint, as needed, and act as a back-up
for the QA, Audit Coordinator in assisting customers.Coordinate and
conduct annual document review management processes.Provide
oversight/support for certifications held by Corbion and its
Co-manufacturers, i.e. Kosher and Halal, among others..Organize and
participate in problem solving sessions and be accountable for
timely completion of corrective and preventive actions.Actively
participate in the HACCP team and its review process.Initiate,
implement, and monitor continued improvement processes.Support
global platform objectives.Provide back-up support for the Quality
Manager, QA Audit Coordinator, or QC Supervisor as needed to
maintain QA/QC practices and ensure product availability.Executes
QESH standards per defined roles and responsibilities to ensure
personal and product safety and quality.Implements, executes and
promotes food safety of our products through the use of Good
Manufacturing Practices (GMPs), performance to Standard Operating
Procedures (SOP's), Security Measures, Housekeeping, Hazard
Analysis & Critical Control Point (HACCP), all quality, regulatory,
environmental, safety and health guidelines and regulations. These
standards are used in all daily activities to ensure the products
safety and quality are in compliance.--Knowledge, Skills &
Abilities --------BA or BS degree in a science discipline and
experience in a food or pharmaceutical facility.Minimum of four
years' experience in a food or pharmaceutical facility with similar
applications..HACCP certification preferred.Internal auditor
certification preferred.Travel and on-call availability are
required.Proficient in Microsoft Word, Excel, and
PowerPointKnowledge and experience using problem solving
techniques.Knowledge and understanding of basic quality assurance
programs and concepts.Basic knowledge and understanding of food
regulations.Excellent interpersonal, communication, organizational
and multi-tasking skills.Database experience preferred.--General
Working Environment --------The QA Coordinator is required to work
in an office environment and occasionally the laboratory; with some
tasks taking place inside of and outside of the plant.The QA
Coordinator is subject to wear the appropriate PPE including but
not limited to hard hats, safety glasses, safety boots, chemical
suits, face-shields, rubber gloves and uniform clothing.Temperature
inside and outside the facility will range between -15*F and 120*F
depending on location and the activities involved.--Usual Physical
Activities Through the course of a typical shift an individual in
this position will perform the following activities;------Prolonged
Standing, 20% of the timeWalks extensively, 20% of the timeKneels,
occasionallyAble to climb, occasionallyBends,
repetitivelySquatting, repetitivelyReaches above and below the
shoulders,Traverses multiple plant levels via stairs,
frequentlyCorrected vision, speaking ability, and hearing are
usually involved in performing written and verbal job
functions.------About CorbionCorbion is the global market leader in
lactic acid and its derivatives, and a leading supplier of
emulsifiers, functional enzyme blends, minerals, vitamins, and
algae ingredients. We use our unique expertise in fermentation and
other processes to deliver sustainable solutions for the
preservation of food and food production, health, and our planet.
For over 100 years, we have been uncompromising in our commitment
to safety, quality, innovation and performance. Drawing on our deep
application and product knowledge, we work side-by-side with
customers to make our cutting-edge technologies work for them. Our
solutions help differentiate products in markets such as food, home
& personal care, animal nutrition, pharmaceuticals, medical
devices, and bioplastics. In 2023, Corbion generated annual sales
of ---1,443.8 million and had a workforce of 2,727 FTE. Corbion is
listed on Euronext Amsterdam. For more information:
www.corbion.comCorbion is an equal opportunity employer and
committed to a diverse workplace. All applicants will be considered
equally without regard to race, color, ethnicity, veteran status,
religion, national origin, marital status, political affiliation,
age, sex, sexual orientation, handicapping condition, membership in
an organization or any other non-merit factors.Corbion provides
reasonable accommodation to applicants.EOE/M/F/Vet/DisabledCorbion
does not accept unsolicited resumes from individual recruiters or
third party recruiting agencies in response to job postings. No fee
will be paid to third parties who submit unsolicited candidates
directly to our hiring managers. All candidates must be submitted
by approved Corbion vendors who have been expressly requested to
make a submission by our Talent Acquisition team for a specific job
opening. No placement fees will be paid to any firm unless such a
request has been made by the Corbion Talent Acquisition team and
such candidate was submitted to the Corbion Talent Acquisition
Team. Job Segment:
QA, Quality Assurance, Facilities, Food Safety, Pharmaceutical,
Technology, Quality, Operations, Science----
Keywords: Corbion, Omaha , QA Document Coordinator, Other , Blair, Nebraska
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