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

• Lead the production team to achieve production schedule and volume adherence. Drive product quality improvement by identifying manufacturing issues, developing cost-effective solutions, and overseeing successful implementation into production. Work with production team to resolve manufacturing and quality problems related to methods, processes, tooling, and equipment
• Work with production and quality assurance team to create/update procedures relating to manufacturing/EHS operations and ensure compliance to good documentation practices. Lead investigations relating to deviations in manufacturing operations, writing investigation reports as well as EHS incident reporting
• Participate in new product introductions through process layout, tool development, and new equipment. Ensuring regulatory compliance through Validation & Verification - Plan execution and analysis. Work with production and quality assurance team to ensure compliance to cGMP
• Drive LEAN manufacturing implementation. Provide safe processes that comply with all local and federal regulations. Ensure that corrective action is taken to resolve observed safety concerns in all areas.
• Work with the site Process & Facility leader and his team to drive compliance in Environmental, Health & Safety efforts through coordinating safety audits, driving closure for audit CAPA, as well as leading EHS initiatives.

Who you are

• B.S. Degree in Chemical, Mechanical, Electrical, Industrial Engineering or related technical degree, or an Associates Degree and 3 years experience in production, engineering, or High School diploma with 5 years of experience in production, engineering
• 2-3 years' experience in a cGMP environment is preferred
• Proficient in MS office (word, excel and powerpoint).
• Basic understanding of EHS management system or participation/exposure in EHS processes
• Language Proficiency: Good/Excellent command in English (spoken and written). Good report writing skills
• Ability to work in a team and across functions, with good communication and project management skills
• Meticulous, analytical and possess high level of integrity and ability in ensuring compliance to site procedures/policies as well as local regulatory requirements. Demonstrate good understanding of problem solving tools/skills such as root cause analysis

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When you join us, you'll also be joining Danaher's global organization, where 80,000 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.
At Danaher, 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.
If you've ever wondered what's within you, there's no better time to find out.