Senior Manufacturing Engineer

Danaher CorporationPensacola, FL
Onsite

About The Position

Bring more to life. Are you ready to accelerate your potential and make a real difference within life sciences, diagnostics and biotechnology? At Cytiva, one of Danaher’s 15+ operating companies, our work saves lives—and we’re all united by a shared commitment to innovate for tangible impact. You’ll thrive in a culture of belonging where you and your unique viewpoint matter. And by harnessing Danaher’s system of continuous improvement, you help turn ideas into impact – innovating at the speed of life. Working at Cytiva 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 who care for each other, our customers, and their patients. Take your next step to an altogether life-changing career. Learn about the Danaher Business System, which makes everything possible.

Requirements

  • Bachelor's degree in chemical engineering, chemistry, polymer science, or a related technical field, with over 10+ years of experience in process, product, manufacturing, quality engineering, R&D, or product development.
  • Hands-on experience in manufacturing high-quality web-based polymeric materials like membranes, polymer films, polymeric fibers, or nonwoven synthetic fabrics.
  • Proficiency in analytical and statistical methods.
  • Experience in program/project management and leadership, capable of driving impactful business projects.

Nice To Haves

  • Six Sigma Green Belt certification preferred.
  • Knowledge of validation activities such as equipment and process qualifications (IQ, OQ, PQ).
  • High-level knowledge and skill to utilize a data-driven approach to assist in determining root cause and countermeasure.
  • Experience working in a medical device manufacturing environment.

Responsibilities

  • Assist the manufacturing operations in problem-solving, continuous process improvements, setting up and/or revising manufacturing testing equipment, and coordinating new program launches.
  • Mentor and provide training to other production personnel.
  • Solve process and equipment problems, document causes, and implement solutions to prevent recurrence.
  • Participate in Environment, Health, and Safety initiatives, ensuring compliance with policies during changes.
  • Identify and suggest improvements to reduce process variation, waste, downtime, and training gaps.
  • Investigate and resolve work-in-process issues using Lean Manufacturing and other methodologies.
  • Assist in transferring new products from development to production, ensuring smooth implementation.

Benefits

  • Comprehensive, competitive benefit programs that add value to our lives.
  • Health care program
  • Paid time off
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