Scientist, Process Development

At QIAGEN, we are driven by a simple but powerful vision: making improvements in life possible.

We're dedicated to revolutionizing science and healthcare for the better. From our entrepreneurial roots to our current global presence, we've grown into a force for positive change. With thousands of employees across six continents, collaboration is our greatest strength. We're always striving to identify talented individuals to join our exceptional teams.

We have played a pivotal role in shaping modern science and healthcare, and we're just getting started. If you're someone who thrives on new challenges, and wants to make a tangible difference in people's lives, then QIAGEN is the place for you.

At QIAGEN, every day is an opportunity to make a real-life impact.

Join us, grow with us, and together, let's shape the future of biological discovery.

- Responsible for Design Transfer from R&D to Operations team

- Development of the reasonable manufacturing process through Validation, Scale up, Optimization, and Automation

- Improvement of manufacturing process for cost efficiency and better quality

- Statistical research and analysis on manufacturing data

- Design experimental work independently or with minimal supervision

- Product implementation to manufacturing system

- Presentation of research outcome at meetings

- Publication of Standard Operating Procedure

- Cross-functional communications and collaboration with R&D, Engineer, QC, QA, GPM, and manufacturing teams

- Training Operators on any new process or on the changes

- MS/PhD degree in Molecular Biology, Biochemistry, Bioengineering, or related Life Sciences field

- Minimum 5-years hands-on experience in a molecular biology laboratory or in relevant industry environment

- Hands-on experience in Next-Gen-Sequencing, RT-PCR, miRNA, gene expression, molecular cloning, analytical chemistry, protein purification, bioinformatics, and bioengineering.

- Excellence in designing of scientific experiments, analyzing the data, and the presentation

- Excellence in the statistical analysis from scientific, manufacturing, or sales data

- Excellent skills in MS-office software especially in MS-Excel

- Excellence in time management skill

- Ability to read and follow technical procedures. Ability to publish SOP.

- Experience in a regulated manufacturing condition is a plus.

- Experience in a process validation is a plus.

- Must be fluent in English and possess exceptional verbal and writing skills

- Ability to effectively present information and promptly respond to questions from managers and colleagues

- Must be organized, motivated, and a team player

- Bonus/Commission
- Local benefits
- Referral Program
- Volunteer Day
- Internal Academy (QIALearn)
- Employee Assistance Program and internal QIAGEN communities
- Hybrid work (conditional to your role)

Our people are the heartbeat of everything we do. Passion drives us as we push boundaries to innovate and evolve.We inspire with our leadership and make an impact with our actions.We cultivate a collaborative, supportive environment where each individual and team can flourish. We champion accountability and encourage entrepreneurial thinking.

QIAGEN is committed to creating an inclusive environment and is proud to be an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, sex, age, national origin, religion, sexual orientation, gender identity, status as a veteran, disability or any other status protected by applicable law.

QIAGEN complies with applicable laws regarding the confidentiality of employee health information and the reasonable accommodation of individuals with disabilities and/or sincerely held religious beliefs. Candidates who require accommodation should contactrecruting@qiagen.com. This policy is part of QIAGEN's ongoing efforts to support public health efforts and to ensure the safety and-well-being of its employees, customers, business partners, and community.