Production Specialist 2 Team Lead (LVLM, 2nd Shift)

Company: Leica Biosystems
Location: Logan
Posted on: June 9, 2021

Job Description:

Be part of something altogether life-changing Working at Cytiva in the Life Sciences industry means being at the forefront of providing new solutions to transform human health. Our incredible customers undertake life-saving activities ranging from fundamental biological research to developing innovative vaccines, new medicines, and cell and gene therapies. At Cytiva you will be able to continuously improve yourself and us working on challenges that truly matter with people that care for each other, our customers, and their patients. With associates across 40 countries, Cytiva is a place where every day is a learning opportunity so you can grow your career and expand your skills in the long term. Cytiva is proud to work alongside a community of nine fellow Danaher Life Sciences companies. Together, we re pioneering the future of science and medicine, developing products that enable researchers in the fight to save lives. What you ll do The Production Specialist 2 Team Lead is responsible for ensuring the day-to-day work in the assigned area is completed. They may provide input or recommendations to supervisory personnel on associate performance and discipline. They are responsible for execution of the daily, weekly and monthly forecasted production priorities required to meet output quotas and group performance goals.Motivate and lead a shift of associates to achieve safety, quality, production, and performance goals.Drive continuous improvement by using day-to-day problem-solving tools and root cause analysis to eliminate reoccurring issues.Assist in implementation of process improvements to increase quality and productivity levelsReview and approve safety, quality and production records throughout shift.Monitor, report and investigate defectsEnsure completion of daily visual management and communications to teamConfirm equipment is in good working orderRead work procedures and schematics, and provides instruction to others when requiredManage and conduct associate training and cross-trainingWrite/Update Standard Work, Job Breakdown sheets, other process documentsConduct 5S, standard work and safety auditsAudit that required tools are available and in good working order and escalate if additional action is requiredMonitor the daily production flow and adjust workloads and resources appropriatelyEnsure all necessary components are present to complete productionMonitor and escalate QA/RA and EHS procedures and policies as requiredEnsure manufacturing documentation used during the production process is of the correct and most current revisionCheck and review of final product paperwork for completion and accuracyOther duties as assigned, and may be asked to be included in quality activities, training sessions, and employee activity teamsParticipates in quality control inspections when requiredComply with EHS regulations and policies Quality Specific GoalsAware of and comply with the Quality Manual, Quality Management System, Quality Management Policy, Quality Goals, and applicable laws and regulations as they apply to this job type/positionComplete all planned Quality & Compliance training within the defined deadlines Identify and report any quality or compliance concerns and take immediate corrective action as requiredKnowledge and understanding of production process, work instructions, documentation configuration control, non-conforming and rework documentation requirements and operates within them to ensure that the product conforms to its specificationEnsures the creation of accurate, complete and timely recordsAware of and comply with Stop Order, Concessions, ESD, Calibration, Preventative Maintenance, Material Identification & Segregation, and Good Documentation Practices, as associated with this job type/position Who you areHigh school diploma or local equivalent1 year of related manufacturing experienceAbility to communicate, receive and understand instructions regarding duties to be performedAbility to provide instructions regarding policies and procedures Desired Characteristics3 years of related manufacturing experienceAssociates degree in chemistry, biology or related fieldExperience in LM/Serum/DPM productionPrior leadership experiencePrior experience working in a medical device manufacturing environmentExperience in GMP work environment When you join us, you ll also be joining Danaher s global organization, where 68,000 people wake up every day determined to help our customers win. As an associate, you ll try new things, work hard, and advance your skills with guidance from dedicated leaders, all with the support of powerful Danaher Business System tools and the stability of a tested organization. Danaher is committed to a diverse and inclusive culture where everyone feels they belong and all voices are heard. We believe in our associates and the unique perspectives they bring to every challenge, which is why we ll empower you to push the boundaries of what s possible. If you ve ever wondered what s within you, there s no better time to find out. Danaher Corporation and all Danaher Companies are equal opportunity employers that evaluate qualified applicants without regard to race, color, national origin, religion, sex, age, marital status, disability, veteran status, sexual orientation, gender identity, or other characteristics protected by law. The EEO is the Law poster is available here. When you join us, you ll also be joining Danaher s global organization, where 69,000 people wake up every day determined to help our customers win. As an associate, you ll try new things, work hard, and advance your skills with guidance from dedicated leaders, all with the support of powerful Danaher Business System tools and the stability of a tested organization. Danaher Corporation and all Danaher Companies are committed to equal opportunity regardless of race, color, national origin, religion, sex, age, marital status, disability, veteran status, sexual orientation, gender identity, or other characteristics protected by law. We value diversity and the existence of similarities and differences, both visible and not, found in our workforce, workplace and throughout the markets we serve. Our associates, customers and shareholders contribute unique and different perspectives as a result of these diverse attributes. The EEO posters are available here. We will ensure that individuals with disabilities are provided reasonable accommodation to participate in the job application or interview process, to perform crucial job functions, and to receive other benefits and privileges of employment. Please contact us at or to request accommodation. If you ve ever wondered what s within you, there s no better time to find out.

Keywords: Leica Biosystems, Logan , Production Specialist 2 Team Lead (LVLM, 2nd Shift), Other , Logan, Utah