JOB REQUIREMENTS: 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 eleme nts 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 m odificationsReport
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 fo llowing 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
***** APPLICATION INSTRUCTIONS: Apply Online:
https://www.aplitrak.com/?adid=YmJnZW5lcmljLjc3OTcwLjg3NzBAZW1kbWlsbGlwb3JlY29tcC5hcGxpdHJhay5jb20