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Danaher Corporation Production Specialist 2 - Team Lead (Serum, 2nd Shift) in Logan, Utah

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 levels

  • Review and approve safety, quality and production records throughout shift.

  • Monitor, report and investigate defects

  • Ensure completion of daily visual management and communications to team

  • Confirm equipment is in good working order

  • Read work procedures and schematics, and provides instruction to others when required

  • Manage and conduct associate training and cross-training

  • Write/Update Standard Work, Job Breakdown sheets, other process documents

  • Conduct 5S, standard work and safety audits

  • Audit that required tools are available and in good working order and escalate if additional action is required

  • Monitor the daily production flow and adjust workloads and resources appropriately

  • Ensure all necessary components are present to complete production

  • Monitor and escalate QA/RA and EHS procedures and policies as required

  • Ensure manufacturing documentation used during the production process is of the correct and most current revision

  • Check and review of final product paperwork for completion and accuracy

  • Other duties as assigned, and may be asked to be included in quality activities, training sessions, and employee activity teams

  • Participates in quality control inspections when required

  • Comply with EHS regulations and policies

Quality Specific Goals

  • Aware 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/position

  • Complete all planned Quality & Compliance training within the defined deadlines

  • Identify and report any quality or compliance concerns and take immediate corrective action as required

  • Knowledge 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 specification

  • Ensures the creation of accurate, complete and timely records Aware 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 are

  • High school diploma or local equivalent

  • 1 year of related manufacturing experience

  • Ability to communicate, receive and understand instructions regarding duties to be performed

  • Ability to provide instructions regarding policies and procedures

Desired Characteristics

  • 3 years of related manufacturing experience

  • Associates degree in chemistry, biology or related field

  • Experience in LM/Serum/DPM production

  • Prior leadership experience

  • Prior experience working in a medical device manufacturing environment

  • Experience 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 (https://www.danaher.com/how-we-work/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 (http://www.dol.gov/ofccp/regs/compliance/posters/pdf/eeopost.pdf) .

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 (http://www.dol.gov/ofccp/regs/compliance/posters/pdf/eeopost.pdf) .

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