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Production Support Coordinator

Cepheid - Sunnyvale, CA

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Job Description

At Cepheid, we are passionate about improving health care through fast, accurate diagnostic testing. Our mission drives us, every moment of every day, as we develop scalable, groundbreaking solutions to solve the world''s most complex health challenges. Our associates are involved in every stage of molecular diagnostics, from ideation to development and delivery of testing advancements that improve patient outcomes across a range of settings. As a member of our team, you can make an immediate, measurable impact on a global scale, within an environment that fosters career growth and development.Cepheid is proud to work alongside a community of six fellow Danaher Diagnostics companies. Together, we''re working at the pace of change on diagnostic tools that address the world''s biggest health challenges, driven by knowing that behind every test there is a patient waiting.Learn about the Danaher Business System which makes everything possible.This position is part of Cepheid Diagnostics and will be located in Sunnyvale, this role, you will have the opportunity to:Perform in process review and final verification of manufacturing documentation prior to submission.Work with SAP and other inventory management system.Performs material transactions in SAP and DHR review for release in compliance with standards for good manufacturing practices.Monitors and provide updates on DHR review and release priority.Perform Data entry (Raw materials, IPT spreadsheet).Archive DHRs turn in to QA.Log DHR errors and coordinate with production supervisors for the correction.Update work request schedule spreadsheet for manufacturing.SAP transaction for Work request material used charge out.Perform inventory cycle count for all manufacturing.Monitor of Kanban card system, which includes updating Kanban cardsEnsures employee training plan and training documents are up-to-date.Work on assignments that are complex in nature which considerable judgment and initiative are required in resolving problems and making recommendations.Follow established documentation outlining the job processing requirements in compliance with standards for GMPs.The essential requirements of the job include:At least 2 years of related experience.High School diploma/GED or equivalent experience.Degree preferred but not required in lieu of experience.Ability to lift 25 lbs.Experience in clean room assembly or Manufacturing in the medical device, pharmaceutical or biotech industry, or equivalent combination of education and experience.Experience in operating manufacturing and packaging equipment preferred.Experience with GMP, QSR, SOP''s and clean room operations.Experience in small-scale manufacturing process equipment and documentations.Understand Good Manufacturing Practice (GMP) and Good Documentation Practice (GDP).Must be a team player and able to demonstrate the willingness and the ability to provide assistance to co-workers.Must be able to perform basic math skills (multiplication, division, ratios, and percentages).Must be able to understand SOPs and demonstrate understanding through verbal and/or written format.Ability to multitask, organize and troubleshoot.Ability to work in a high-volume fast pace environment.Ability to follow and understand company/department policies.Effective verbal and written communication skills.Solid communication and problem resolution skills.Attention to detail.Must be computer literate with SAP, Windows, Work and Excel.Basic Computer Skills: Microsoft Excel & Word.Ability to solve practical and analytical problems.Ability to manage the pressure associated with a deadline-oriented atmosphere and customer issues.Ability to work on assignments requiring considerable judgment and initiative.Understands implications of work and makes recommendations for solutions.Ability to work closely with department support groups such as Engineering, Manufacturing Automation, Manufacturing Support, Planning and Stockroom groups regarding materials, processes and equipment.Cepheid, a Danaher company, offers a broad array of comprehensive, competitive benefit programs that add value to our lives. Whether it''s a health care program or paid time off, our programs contribute to life beyond the job.Check out our benefits at .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 require all US and Puerto Rico employees to be fully vaccinated against COVID-19 as a condition of employment, subject to reasonable accommodation as required by law.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 [Click Here to Email Your Resumé] to request accommodation.If you''ve ever wondered what''s within you, there''s no better time to find out.

Created: 2021-11-29

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