JOB REQUIREMENTS: Duties and Responsibilties of Job: The Membrane
Manufacturing Supervisor position is a shift-based role, responsible for
the coordination of production activities overseeing shift personnel in
the Membrane facility. The Supervisor will be accountable for the
achievement of production targets, department metrics, and objectives
ensuring productivity, financial delivery, quality, service, and safety.
The Supervisor will take responsibility for assuring thoroughness of
training, mentoring and motivating of employees, as well as establishing
performance standards, monitoring employees\' performance against those
standards, and appropriately communicating evaluations of performance to
employees. As part of this project, this position is heavily involved in
the development of the facility, systems, and personnel that will bring
the LFM in Sheboygan Falls to fruition. This will include development of
a shift structure, role and responsibility, training plan, system
implementation, facility design, and many other elements of facility
operations. Responsibilities: include: Troubleshoot process, product,
quality, and safety issues to achieve long term solutions, including
technical support and contact with external MilliporeSigma personnel and
customers on process/product subjectsOversee statistical performance of
processes and process equipment to ensure minimal variability in product
qualityLead and coordinate day-to-day production and processesSupport
process development related to new products and qualifications,
including scheduling qualification work to determine process windows
prior to qualifications Participate and lead design efforts including
establishing process design basis, development of process options, and
optimization of selected designsResponsible for development,
introduction and operation of process monitoring & control systems and
procedures, including analysis of this data to identify trends and
weaknessesMaintain and develop process documentation and procedures,
documenting and tracking all process changes and modificationsReport
process performance to management personnelSupport the training of
production personnel on process and product principlesInitiate, review,
and approve change requests to products and processesWork independently
as a technical specialistLead and coordinate risk mitigation initiatives
such as impact, FMEA and risk assessments Investigate Quality and EHS
issues using Root Cause Analysis methodology, and implement robust
corrective and preventative actions and issue response flow
checklistsInvestigate and report on improved technology regarding
membrane products and processes through journal, patent and networking
with membrane experts within the organizationEnsure that process
information is documented in the membrane process information documents,
to reflect increased process knowledge and understandingParticipate in
business development activitiesSupport quality review boardEnsure
compliance with GMP and ISO requirementsContribute to a safe working
environment by following and developing corporate and departmental
safety regulationsMiscellaneous duties and tasks as assigned Who you
are: Minimum Qualifications: Bachelor\'s degree in chemistry, Biology,
Chemical Engineering or other scientific discipline2+ years of
experience in either paper making, medical device manufacturing,
membrane manufacturing, chemical manufacturing, or other manufacturing
environment Preferred Qualifications: Master\'s degree in chemistry,
Biology, Chemical Engineering or other scientific discipline2+ years of
leadership experienceUnderstanding of ISO9001/14001/45001Familiarity
with OSHA, EPA, FDA regulationsExperience with Microsoft Office and
statistical software (MINITAB/JMP)Knowledge of 6-Sigma techniques and
meth To view the full job description please use the link below.
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