MSAT - Scientist ll

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 that 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.

The MSAT - Scientist ll is responsible for assessing potential application of company products to meet customer needs pre and/or post-sales and prepares detailed product specifications for the development and implementation of customer products/applications/solutions in alignment with manufacturer stated specifications. Builds mini-applications with process simulation, product demo/training (at conferences, seminars, trade shows, or customer sites) for customer. May assist with optimizing products to meet customer needs and workflow requirements.

This position reports to the Manager-MSAT and is part of the MSAT and will be fully remote.

· Provide technical support for (market segment) products. This will include some or all of the following:

· Support the filter business unit by providing technical consultation, filter sizing recommendations, process optimization, trouble shooting, and customer training.

· Technical consultation involving scale up/scale down testing plans and data review, sizing and compatibility recommendations, and troubleshooting customer technical issues and field investigations.

· Trouble shooting customer complaints and field investigations

· Paid technical services, e.g. Technical training, etc.

· Technical Consultation, e.g. Process development and optimization, etc.

· Take responsibility for assigned projects of moderate complexity, typically in only selected areas of coverage

· Perform role of a project manager, to ensure projects assigned are completed in a timely manner.

· Prepare trial proposals/protocols based on information supplied by customer. Confirm customer acceptance.

· Provide support for technical discussions when required.

· Interpret laboratory data and prepare specific test reports. Confirm customer acceptance.

· Close out of project reports and present results to customers face to face.

· Maintain close customer liaison during projects. This will involve some or all of the following:

· Update customer of project status in particular if there are problems/issues with the project.

· Answer customer technical questions in a timely manner.

· Travel to customer sites for technical meetings and/or to perform field trial work.

· Give presentations and trainings to operators, engineers, and potential heads of departments.

· Establish project priorities and decide appropriate action required to meet required target.

· Schedule work into the laboratory in conjunction with the Manager/Supervisor.

· Update manager of status of assigned projects, including completion, delays or problems.

· Maintain up to date knowledge of current Biopharm (Biologicals, Vaccines, Proteins)/Pharmaceutical (Therapeutic Oral doses, Topical products, Ophthalmic products, Antibiotics, etc.)

· Active Product Ingredient processing technology and industry trends (PDA, ISPE, ACS, etc.), current regulatory trends (FDA/EMA/PIC/s, etc.), issues and guidelines related to the products being supported.

· Develop expertise by regular communication with other Cytiva groups. Attend training courses as required

• Master’s Degree in Life Science/Engineering (E.g. Biology, Genetics, Biochemistry, Bioprocess engineering, Life Sciences, etc.) with 2 - 4 years relevant work experience.
• Bachelor’s Degree Life Science/Engineering (E.g. Biology, Genetics, Biochemistry, Bioprocess engineering, Life Sciences, etc.) with 5 years relevant work experience.
• Experience in monoclonal antibody, vaccines development, immunoassay, or recombinant protein is highly desirable
• Familiarity with GLP and GMP practices
• Experience of process development and optimization using QbD will be plus.
• Excellent verbal, writing and reading skills in English & Korean is a must.

Travel, Motor Vehicle Record & Physical/Environment Requirements: if applicable for role

• Local travel in Korea to customer sites is expected to be at least up to 50% of the time. Oversea travel is expected if required.
• Fluent level of English & Korean in written and verbal communications 한국어 및 영어로의 서면 및 구두 의사소통능력이 높으신 분
• Ability to travel abroad upon business needs 해외여행에 결격사유가 없으신 분
• Must have a valid driver’s license with an acceptable driving record within territory or locations 운전을 하여 담당하는 국내 고객사에 방문할 수 있는 분
• If foreign national, legal work permit is required to pursue employment contract by Korean immigration law 대한민국에서의 근무가 가능한 비자가 있는 분
• Candidates who have undergone a pre-assignment health examination and have been confirmed to be suitable for the job performance based on the health examination results 배치 전 건강검진을 실시하며, 건강검진 결과가 해당 업무 수행에 적합하다고 확인된 분

Cytiva, a Danaher operating company, offers a broad array of comprehensive, competitive benefit programs that add value to our lives. Whether it’s a health care prog