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Danaher Corporation IPT Consumables Supervisor in Sunnyvale, California

ESSENTIAL JOB RESPONSIBILITIES:

  • Manages the Consumables IPT department daily work activities including: Team schedule, ensuring training, general guidance to direct reports and across functional groups, and serves as resource for technical / administrative problems.

  • Hires, trains, motivates, leads, develops, and evaluates staff. Takes corrective action as necessary on a timely basis and in accordance with company policy.

  • Ensures Quality Control systems are compliant with corporate and site procedures, as well as industry standards.

  • Supports development of analytical methods. Works in conjunction with other departments to develop, qualify, and transfer testing analytical methods as applicable.

  • Ensures maintenance of testing equipment – qualification, calibration and maintenance.

  • Drafts, reviews, and approves Standard Operating Procedures (SOP), sampling plans, specifications, protocols and reports related to product/processes, equipment, method, validation. This includes deviation investigation and reporting.

  • Develops and implements statistical tools for monitoring and review.

  • Identifies and implements improvement opportunities for established processes, procedures, and training to support CAPA, Change Control, Deviation, Risk Management, and Investigation processes.

  • Lead investigations for failures during testing; perform troubleshooting, process development or improvement activities.

TRAINING RESPONSIBILITIES:

  • Complete all assigned and required training satisfactorily and on time

MINIMUM REQUIREMENTS:

Education and Experience:

  • High school degree with 8+ years of experience or Bachelor’s degree with 5+ years of experience OR Master’s degree with 3+ years of experience.

Knowledge and skills:

  • Experience with managing people and providing leadership.

  • Thorough knowledge of cGMP regulations related to Quality Control required.

  • Experience with analytical method, and Microbiology testing.

  • Proven track record in method validation / qualification and qualification of equipment / systems.

  • Experience with facility / laboratory expansions.

  • Experience in a QC support in high pace manufacturing setting.

PREFERRED REQUIREMENTS:

  • Experience working in a GMP/ISO/FDA manufacturing environment

  • Experience using analytical scales, Pipettes and working with hazardous chemicals

  • Flexibility with the work schedule including modified shift times and weekends

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 (https://www.danaher.com/how-we-work/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 (https://www.dol.gov/agencies/ofccp/posters) .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 applyassistance@danaher.com to request accommodation. If you’ve ever wondered what’s within you, there’s no better time to find out.

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