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Required skill set See below

• 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

• Maintenance of QC testing laboratory operations and supporting quality records in line with GLP
• Run critical validation experiments on newly developed methods for characterization of technologies in the bio-process portfolio
• Accountable for the on-time delivery of data in support of in-process, release and stability activities
• Ensure data integrity and GMP compliance requirements are followed within the laboratories
• Participate in continuous improvement activities by identifying and appropriately escalating process and product quality gaps, providing solutions when possible

Who you are

• A high school degree with 10+ years of experience, an A.S. with 5+ years of experience, a B.S. with 3+ years of experience, or a M.S. with 1+ years experience
• 1 - 10 years of lab experience in a manufacturing environment, with QC experience preferred
• Knowledge of relevant analytical techniques used in manufacturing (analytical testing, trouble shooting and method validation)
• Experienced in scientific principals and techniques used in QC laboratories preferable but not mandatory
• Experience of working within an ISO 9001, 13485 and/or cGMP (GLP) QMS environment is preferred
• Demonstrated ability to solve problems, develop plans and advance to completion on time and in full

• Diverse technical understanding and ability to apply skills/knowledge to new technology
• 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.