Work Your Magic with us! Start your next chapter and join MilliporeSigma.
Ready to explore, break barriers, and discover more? We know you’ve got big plans – so do we! Our colleagues across the globe love innovating with science and technology to enrich people’s lives with our solutions in Healthcare, Life Science, and Electronics. Together, we dream big and are passionate about caring for our rich mix of people, customers, patients, and planet. That's why we are always looking for curious minds that see themselves imagining the unimaginable with us.
This role does not offer sponsorship for work authorization. External applicants must be eligible to work in the US.
Your Role
The Manufacturing team at our Spruce site, supports production of antibody products for use in in vitro diagnostic (/VD) immunohistochemistry (IHC). All Production Lab Techs are expected to effectively perform the job functions defined in the "Essential Functions" and possess the skills and abilities in the "Knowledge, Skills, & Abilities sections below.
Level III Production Lab Tech are expected to be highly proficient in at least three of the work areas outlined in the "Work Areas and Specific Tasks" listed below and will train others in those areas. Level III Production Lab Techs will assume a leadership role in at least one Work Area and will be the go-to person for troubleshooting in area(s) of expertise. Level III Production Lab Techs performing Label and Documentation duties will perform all tasks in that area and will be proficient with Quality Systems or another Production-specific skill. Specific responsibilities include:
Perform area clearance tasks and maintaining separation of productPerform standard and new operating proceduresCollect and record data on documents and batch records where requiredUtilize computer hardware and software for data entry and record keeping where requiredEnsure compliance with all Quality and Regulatory specificationsSupport process improvement through identification and reporting of areas needing improvement and assisting in improvement projectsEffectively utilize Quality Management Systems (QMS) and other applicable databasesFamiliarity with and proper use of safety equipment and Personal Protective Equipment (PPE)Demonstrate attention to detail and complete work according to daily scheduleVerify data against standardPrint and apply product labels based on established production planFill and package product based on an established production planFill and package product using standardized techniques and practicesStocks inventory as necessaryDemonstrated ability to learn and understand safe laboratory practicesSupport 6S programs to maintain a Lean work environmentWork occasional overtime and weekends as needed to meet production requirementsComply with applicable established cGMP, FDA, OSHA, EPA, and Quality System regulationsReport all deviations from established procedural documents to the appropriate supervisor/managersAdditional duties as defined by management and business needsParticipate in production failure investigationsAttend and participate in scheduled meetingsCompose emails to groups according to good business writing standardsEffectively present DMS Board to management and coworkersFollow regulatory and standard requirements as applicable to the site, i.e., MDSAP, ISO 13485, IVDR, and compliance with the site Quality ManualOther duties as assigned or required to support the businessCustomer service: Respond promptly to internal customer needs from other departmentsProfessionalism: Approach others in a tactful manner, react well under pressure, treat others with respect and consideration, present a professional image in all business mattersProductivity: Meet productivity standards, strive to increase productivity without sacrificing quality and safetyQuality: Look for ways to improve and promote quality, demonstrate accuracy and thoroughnessContinuous improvement: Regularly submit suggestions for improvement (SFls)Ethics: Treat people with respect, keep commitments, work with integrity and ethics, uphold organizational valuesDiversity: Promote a harassment-free environment, show respect and sensitivity for cultural differencesTeamwork: Exhibit objectivity and openness to others' views, give and welcome feedback, supports others' efforts to succeedProblem solving: Identify and resolve problems in a timely manner, develop alternative solutionsSafety: Observe safety procedures, report potentially unsafe conditions, use equipment and materials properly and according to usage guidelinesPlanning/organizing: Manage time and priorities work to meet deadlines, effectively multitask with various interruptionsJudgment: Make timely decisions, exhibit sound and accurate judgment
Who You Are
Minimum Qualifications:
High school diploma or GED required2+ years of within a production or manufacturing environment
Preferred Qualifications:
2+ years of experience with general laboratory equipmentWorking knowledge of SAP, SAP NEXT, or other ERP systems Knowledge of GMP facility, FDA QSRs, and ISO 13485Experience in an FDA regulated biotechnology or pharmaceutical environmentThe ability to learn, understand, and carry out safe laboratory practicesProficiency with Quality Management Systems (QMS) Knowledge of the metric systems Ability to communicate effectively with all levels within the organization and with outside contacts
RSREMD
What we offer: We are curious minds that come from a broad range of backgrounds, perspectives, and life experiences. We celebrate all dimensions of diversity and believe that it drives excellence and innovation, strengthening our ability to lead in science and technology. We are committed to creating access and opportunities for all to develop and grow at your own pace. Join us in building a culture of inclusion and belonging that impacts millions and empowers everyone to work their magic and champion human progress!
Apply now and become a part of our diverse team!
If you would like to know more about what diversity, equity, and inclusion means to us, please visit https://www.emdgroup.com/en/company/press-positions.html