Development Associate I - Downstream Process Development
Lundbeck
Summary
The Development Associate I Downstream Process Development works with a team of scientists and engineers developing production processes for therapeutic biologic candidates in preclinical, clinical, and late-stage development. The primary responsibility will be to purify proteins to support the development of downstream processes. This individual plays a collaborative role within downstream team and with members of upstream, bioanalytical, analytical and formulation development groups.
Job description
Essential Functions
- Performs small-scale downstream process development experiments supporting monoclonal antibody purification, including liquid chromatography and tangential flow filtration.
- Prepares process intermediates and experimental samples for analytical testing.
- Prepares purified protein materials to support process development studies and cross-functional activities.
- Performs analytical methods, such as UV-visible spectrophotometry, turbidimetry, density, pH, and conductivity measurements.
- Collaborates closely with scientists, engineers, and other Process Development team members.
- Manages multiple laboratory activities and priorities while maintaining strong attention to detail and follow-through.
- Proactively communicates experimental progress, unexpected observations, scheduling needs, and potential challenges to teammates.
- Prepares clear, concise summaries, presentations, and reports to communicate experimental results.
- Helps maintain an organized, efficient, and safe laboratory environment.
Required Education, Experience and Skills
- Accredited bachelor's degree in a scientific or engineering discipline such as Biochemical Engineering, Chemical Engineering, Bioengineering, Biotechnology, Biochemistry, Biology, or a related field.
- Foundational knowledge of one or more of the following areas: liquid chromatography, membrane filtration, protein chemistry, biochemical engineering, or related scientific principles.
- Familiarity with common laboratory equipment such as pH, conductivity, and temperature meters; pumps; pressure gauges; balances; pipettes; and benchtop centrifuges.
- Strong verbal and written communication skills.
- Comfortable asking questions, sharing observations, and keeping teammates informed.
- Strong organizational skills, attention to detail, and the ability to plan and manage multiple priorities.
- A proactive approach to work and a willingness to take ownership of assigned responsibilities.
- Curiosity, enthusiasm for learning, and openness to feedback and coaching.
- Ability to follow standard operating procedures and established laboratory and industry safety practices.
- Proficiency with Microsoft Office applications.
- Ability to occasionally lift up to 30 pounds.
Preferred Education, Experience and Skills
- Academic, internship, research, or industry experience with protein purification or downstream processing.
- Experience with ÄKTA chromatography systems and UNICORN software.
- Exposure to pilot-scale or manufacturing-scale biotechnology operations.
- Experience presenting scientific results through laboratory meetings, research projects, internships, poster presentations, or similar settings.
Some domestic travel may be required.
Requirements
- Accredited bachelor's degree in a scientific or engineering discipline such as Biochemical Engineering, Chemical Engineering, Bioengineering, Biotechnology, Biochemistry, Biology, or a related field
- Foundational knowledge of liquid chromatography, membrane filtration, protein chemistry, biochemical engineering, or related scientific principles
- Familiarity with common laboratory equipment such as pH, conductivity, and temperature meters; pumps; pressure gauges; balances; pipettes; and benchtop centrifuges
- Strong verbal and written communication skills
- Strong organizational skills, attention to detail, and ability to plan and manage multiple priorities
- Proactive approach and willingness to take ownership of assigned responsibilities
- Ability to follow standard operating procedures and established laboratory and industry safety practices
- Proficiency with Microsoft Office applications
- Ability to occasionally lift up to 30 pounds
Benefits
- Flexible PTO
- Medical, Dental & Vision
- 401(k) Matching
- 8% Bonus Target
Company overview
Lundbeck is a global pharmaceutical company specializing exclusively in brain diseases, with over 70 years of neuroscience expertise. Founded in 1915 in Copenhagen, Denmark, the company has established itself as one of the world's leading innovators in treatments for central nervous system disorders. Lundbeck focuses on developing and commercializing therapies for conditions including depression, schizophrenia, Alzheimer's disease, Parkinson's disease, and migraine. With approximately 5,000+ employees worldwide and operations in more than 50 countries, the company maintains production facilities in Denmark, France, and Italy, with research centers in Denmark and the United States. Lundbeck's portfolio includes some of the world's most widely prescribed therapies for brain diseases, reaching over 7 million people daily. The company is publicly traded on Nasdaq Copenhagen, with the Lundbeck Foundation holding approximately 70% ownership. Lundbeck's commitment to neuroscience research and patient-centered innovation has positioned it as a key player in addressing the complex challenges of brain health globally.