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Associate Director Downstream Process Development Jobs

Lundbeck

Downstream Development Associate II

Bothell, WA · On-site

$38 - $45/hr

Summary: Performs downstream process development experiments and supporting activities, which enable both early and late-stage manufacturing process design for therapeutic monoclonal antibody ...

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How much do associate director downstream process development jobs pay per hour?

As of Sep 9, 2026, the average hourly pay for associate director downstream process development in the United States is $33.68, according to ZipRecruiter salary data. Most workers in this role earn between $27.64 and $41.35 per hour, depending on experience, location, and employer.

What does an associate director downstream process development do?

An Associate Director of Downstream Process Development leads teams responsible for developing, optimizing, and scaling up purification processes for biologics or pharmaceuticals after the initial production phase. They oversee activities such as chromatography, filtration, and formulation to ensure that products meet quality, safety, and regulatory standards. This role involves strategic planning, cross-functional collaboration, troubleshooting, and ensuring that the processes are efficient and compliant for large-scale manufacturing. Additionally, they mentor junior staff, manage budgets, and often interact with regulatory agencies.

What are the key skills and qualifications needed to thrive as an associate director downstream process development?

To thrive as an Associate Director Downstream Process Development, you need advanced knowledge in bioprocess engineering, protein purification, and a relevant advanced degree (typically Ph.D. or M.S.) in biochemistry or a related field. Experience with chromatography systems, process analytical technologies (PAT), and regulatory compliance (GMP) is typically required. Strong leadership, project management, and cross-functional communication skills help drive team performance and successful technology transfer. These skills and qualities are essential to ensure efficient development, scale-up, and regulatory approval of biopharmaceutical products.

What are some of the primary challenges faced by an associate director downstream process development, and how can they be addressed?

One of the main challenges in this role is overseeing the scale-up and transfer of downstream bioprocesses from development to manufacturing while maintaining product quality and meeting regulatory requirements. This often involves troubleshooting process inconsistencies, adapting to evolving project priorities, and ensuring effective cross-functional communication with teams such as upstream development, quality assurance, and manufacturing. Success in this position relies on strong leadership, proactive risk management, and the ability to mentor and guide team members through complex technical and operational issues.

What are popular job titles related to Associate Director Downstream Process Development jobs?

For Associate Director Downstream Process Development jobs, the most frequently searched job titles are:

Infographic showing various Associate Director Downstream Process Development job openings in the United States as of September 2026, with employment types broken down into 1% Internship, 1% As Needed, 82% Full Time, 14% Part Time, and 2% Contract. Highlights an 87% Physical, 2% Hybrid, and 11% Remote job distribution, with an average salary of $70,060 per year, or $33.7 per hour.

Downstream Development Associate II

Bothell, WA • On-site

Lundbeck
Pharmaceutical Product Wholesalers • 5 - 10K employees
Learn more about Lundbeckexternal

$38 - $45/hr

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

This job post has expired today. Applications are no longer accepted.

Key responsibilities

  • Performs downstream process development experiments for monoclonal antibodies, including liquid chromatography and filtration activities.

  • Prepares experimental samples and purified protein products to support downstream and upstream process development activities.

  • Organizes and analyzes data, and prepares reports and presentations based on experimental results.

Job description

Do you want to join a team where the mission is meaningful, the challenges are complex, and you can directly see the results of your hard work? Lundbeck Seattle BioPharmaceuticals (Lu-SBP), located in Bothell, Washington, is the Process Development Center of Excellence for Biologics within the global Lundbeck CMC organization. Since integrating into Lundbeck in October 2019, Lu-SBP has supported commercial launch of Lundbeck's first biologic product (Vyepti) and advancement of a growing biologics pipeline in collaboration with our Copenhagen-based Process Science & Validation Team. The Lu-SBP team leads and supports the development of new product candidates from cell line development through commercial validation of Drug Substance and Drug Product manufacturing processes. Join us on our journey to advance brain health and transform lives.

Summary:

Performs downstream process development experiments and supporting activities, which enable both early and late-stage manufacturing process design for therapeutic monoclonal antibody production via yeast and mammalian expression systems.

Essential Functions:

  • Performs small-scale downstream process development experiments for monoclonal antibodies, as applied to liquid chromatography and tangential/normal flow filtration.
  • Prepares experimental intermediate samples for further analytical testing, including purification via miniature liquid chromatography and ultrafiltration devices.
  • Prepares purified protein product to support upstream process development and supply further downstream process development activities.
  • Performs analytical methods, such as UV-visible spectrophotometry, turbidimetry, density measurement, size exclusion and protein A affinity HPLC, and biolayer interferometry.
  • Organizes and analyzes primary data and prepares concise presentations and reports.

Required Education, Experience, and Skills:

  • Accredited bachelor's degree and a minimum of 2+ years of biotechnology/pharmaceutical industry experience or equivalent combination of education and experience totaling 4 years.
  • Basic understanding of the principles of liquid chromatography, membrane filtration, sedimentation/centrifugation, aqueous physical chemistry, and protein chemistry.
  • Familiar with basic laboratory equipment, including pH, conductivity, & temperature meters, pumps, pressure gauges, weight scales, pipette dispensers, and tabletop centrifuges.
  • Excellent verbal communication skills to interact collaboratively with Process Development teammates.
  • Well-developed organizational skills and the ability to take a proactive approach to job responsibilities.
  • Ability to comply with FDA GMP documentation regulations and industry standard safety practices.
  • Proficiency in Microsoft Windows 10/Office.
  • Must be able to lift to 30 pounds on occasion.

Preferred Qualifications, Skills and Competencies

  • An accredited B.S. degree in science or engineering (i.e. Biochemical Engineering, Chemical Engineering, Biotechnology Engineering, Biochemistry, Biotechnology or equivalent).
  • Experience with analytical techniques such as HPLC, UPLC, and/or CE a plus.
  • Experience with pilot scale operations a plus.
  • Experience with MPLC systems such as the Akta/Unicorn platform a plus.

 

The range displayed is specifically for those potential hires who will work or reside in the state of Washington, if selected for this role, and may vary based on various factors such as the candidate's qualifications, skills, competencies and proficiency for the role. Salary Pay Range: $38/hour - $45/hour and eligibility for an 8% bonus target based on company and individual performance. Additional benefits for this position include flexible paid time off (PTO), health benefits to include Medical, Dental and Vision and company match 401k. Additional benefits information can be found on our site.

Why Lundbeck

Lundbeck offers a robust and comprehensive benefits package to help employees live well and protect their health, family, and everyday life. Information regarding our benefit offering can be found on the U.S. career site.
 

Lundbeck is committed to working with and providing reasonable accommodations to disabled veterans and other individuals with disabilities during our employment application process. If, because of a disability, you need a reasonable accommodation for any part of the application process, please visit the U.S. career site.

Lundbeck is proud to be an equal opportunity workplace. We are committed to equal employment opportunity regardless of race, color, religion, sex, sexual orientation, gender identity, age, national origin, disability, protected veteran status, and any other characteristic protected by law, rule, or regulation. Lundbeck participates in E-Verify.

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