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Full Time Downstream Process Development Scientist Jobs in Spokane, WA

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Full Time Downstream Process Development Scientist information

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$20

$39

$62

How much do full time downstream process development scientist jobs pay per hour?

As of Aug 6, 2026, the average hourly pay for full time downstream process development scientist in Spokane, WA is $39.09, according to ZipRecruiter salary data. Most workers in this role earn between $28.70 and $46.68 per hour, depending on experience, location, and employer.

What does a full time downstream process development scientist do?

A Full Time Downstream Process Development Scientist is responsible for designing, optimizing, and scaling up processes that purify biological products such as proteins, antibodies, or vaccines after they are produced in cells or microbes. This role involves developing and improving techniques like filtration, chromatography, and centrifugation to ensure high purity and yield of the final product. The scientist also conducts experiments, analyzes data, and collaborates with cross-functional teams to transfer processes from the lab to manufacturing. Their work is critical for producing safe and effective biopharmaceuticals on a large scale.

What is the difference between Full Time Downstream Process Development Scientist vs Downstream Process Engineer?

AspectFull Time Downstream Process Development Scientist
Primary FocusDesigning, optimizing, and developing downstream purification processes for biopharmaceuticals
Required CredentialsBachelor's or Master's in Biotechnology, Biochemistry, or related field; experience in process development
Work EnvironmentLaboratories, R&D settings, collaborative teams in biotech or pharma companies
Typical ResponsibilitiesProcess scale-up, method validation, troubleshooting, documentation

While both roles involve downstream bioprocessing, the Full Time Downstream Process Development Scientist focuses on process development and optimization, whereas the Downstream Process Engineer typically handles process implementation and manufacturing support. The scientist role emphasizes research and development, while the engineer role is more operational. Candidates often hold similar degrees and certifications, but their daily tasks and focus areas differ.

What are some typical challenges faced by a full time downstream process development scientist, and how can they be addressed?

Downstream Process Development Scientists often encounter challenges such as optimizing protein purification processes to achieve high yield and purity, troubleshooting unexpected impurities, and scaling up processes from laboratory to manufacturing scale. These tasks require strong problem-solving skills, meticulous attention to detail, and effective collaboration with upstream teams, analytical scientists, and manufacturing staff. Addressing these challenges involves staying current with new purification technologies, maintaining robust documentation, and participating in cross-functional meetings to ensure seamless process integration and regulatory compliance.

What are the key skills and qualifications needed to thrive as a full time downstream process development scientist, and why are they important?

To thrive as a Full Time Downstream Process Development Scientist, you need a strong background in biochemical engineering, protein purification, and analytical techniques, typically supported by a degree in biochemistry, biotechnology, or a related field. Proficiency with chromatography systems (e.g., HPLC, FPLC), filtration technologies, and knowledge of regulatory and quality systems like GMP is essential. Strong problem-solving abilities, teamwork, and effective communication skills help you collaborate with cross-functional teams and troubleshoot process challenges. These skills are crucial for developing robust purification processes that ensure product quality, regulatory compliance, and efficient production in biopharmaceutical environments.
What are the most commonly searched types of Downstream Process Development Scientist jobs in Spokane, WA? The most popular types of Downstream Process Development Scientist jobs in Spokane, WA are:
What job categories do people searching Full Time Downstream Process Development Scientist jobs in Spokane, WA look for? The top searched job categories for Full Time Downstream Process Development Scientist jobs in Spokane, WA are:
What cities near Spokane, WA are hiring for Full Time Downstream Process Development Scientist jobs? Cities near Spokane, WA with the most Full Time Downstream Process Development Scientist job openings:
Full Time Downstream Process Development Scientist jobs near you

Process Engineer, Sr.

Jubilant HollisterStier Spokane

Spokane, WA • On-site

$105K - $136K/yr

Full-time

Medical, Dental, Vision, Life

Re-posted 22 days ago

Job description

Join a Leader in Pharmaceutical Manufacturing - And Build What's Next
As Spokane's Largest Manufacturing Company, Jubilant HollisterStier LLC is a well-established force in the pharmaceutical and biopharmaceutical industries, providing a complete range of manufacturing services that support lifechanging medicines around the world.
We are nationally recognized for our expertise in producing sterile injectable vials and lyophilized products, and our Allergy business is a global leader in allergenic extracts that support treatments for allergies and asthma. Jubilant HollisterStier is proudly part of the global, Jubilant Pharma family. established force in the pharmaceutical and biopharmaceutical industries, providing a complete range of manufacturing services that support lifechanging medicines around the world.
For the Builders, Innovators, and Doers - This Is Your Place
If you are someone who thrives on solving complex problems, improving systems, and building real solutions, you'll feel at home here. At Jubilant HollisterStier, your ideas matter - and your impact is felt globally.
Why builders choose us:
  • Immediate impact: Your work directly supports essential medicines and allergenic therapies used worldwide.
  • Benefits start on day one: Medical, Dental, Vision, FSA/HSA, Life, AD&D, and Disability benefits begin immediately because your well-being shouldn't have a waiting period.
  • A career you can grow: We provide opportunities for growth, promotion, and annual raises, with midpoint compensation reserved for high performance and longevity.
  • A culture of improvement: We value people who thrive on continuous improvement, innovation, and hands on contribution.
  • A stable industry leader: Backed by Jubilant Pharma, we pair long term stability with forward looking innovation.

If you want to build something meaningful with a team that values your drive, skills, and ideas - you belong here.
Job Description:
The Senior Process Engineer provides expertise primarily in the areas of pharmaceutical process engineering and technical transfer. This position will manage large scale projects and multi-disciplinary teams. The process engineer will also provide technical direction for complex projects and exhibit superior communication skills with all levels of employees. The individual will be responsible for refining department and site processes and provide leadership and guidance to others.
  • Design, optimize and implement site manufacturing processes to improve efficiency, quality and sustainability.
  • Oversee and assess existing processes and workflows.
  • Establish and track process metrics to monitor process stability and discover areas for improvement.
  • Technical Transfer of new products from both internal and external clients.
  • Ownership of product process from initial quote to product retirement.
  • Evaluate incoming processes for robustness, efficiency and fit within JHS-Spokane.
  • Perform appropriate development work to define CPPs and CQAs to allow strong execution upon transfer to Manufacturing.
  • Author validation study documents that demonstrate manufacturing processes are capable of consistently making acceptable product.
  • Develop and execute validation studies to test and qualify new and improved manufacturing processes.
  • Troubleshooting, oversight and/or sampling of events within Manufacturing will require occasional off-shift at-location support.
  • Generate reports summarizing results of studies to document data collected; utilize data obtained to qualify site processes.
  • Review data summaries generated by other departments, assess the data for potential trends or conditions that may adversely impact the quality of the sterile products being manufactured, and ensure that corrective action measures are implemented when required/warranted.
  • Participate in or perform deviation investigation and evaluation of impact.
  • Implement effective CAPAs.
  • Responsible for optimizing gross profit margin and minimizing deviation rate.
  • Provide necessary reviews for regulatory and client audits and provide responses to audit observations.
  • In-depth understanding of cGMP's, European regulatory requirements, relevant USP chapters, and scientific principles associated with clean room operations and room classifications as they apply to media fills, sterilization and depyrogenation (dry heat and steam), endotoxin reduction, and microbiological monitoring and control.
  • Minimal travel (< 10%).

Level Specific:
  • Expected to perform job functions autonomously and effectively.
  • Expected to be an authority in pertinent scientific principles and applicable existing and new guidance.
  • Expected to be an authority on technical aspects of site processes.
  • Expected to provide leadership and guidance to others on these topics, as well as update and improve site practices and policies accordingly.

Qualifications:
  • A Bachelor's of Arts or Science with a major in Biology, Chemistry, Physics, or Engineering is required.
  • 5-10 years related Pharmaceutical experience or FDA regulated Industry Experience required.
  • Supervisory or other Leadership Experience required.
  • Project Management experience required.
  • Master's Degree counts as 2 yrs experience.
  • Statistical Analysis desired.
  • Lean Manufacturing Principles desired.
  • Microsoft Office experience required.
  • Extended periods of sitting or standing required.
  • Ability to lift 40 lbs. unassisted required.

Location: Spokane, WA - On Site, Full-Time
Shift: Monday-Friday 5x8hr
Relocation Available
Compensation & Benefits That Start on Day One - Because Your Well Being Matters
Hiring Wage: Hiring Wage: $98,700.00 - $157,900annually depending on experience, with opportunity for growth, promotion and annual raises with opportunities for growth, promotion, and annual raises.
At Jubilant HollisterStier, we don't believe in waiting periods. From the moment you join us, you and your family have access to a full suite of benefits designed to support your health, stability, and long-term success.
Starting on your first day, you receive:
  • Medical, Dental & Vision coverage
  • Flexible Spending Accounts (FSA) & Health Savings Accounts (HSA)
  • Life & AD&D Insurance
  • Short-Term & Long-Term Disability Insurance
  • Employee Assistance Program

Unlock Your Potential
If you're seeking a dynamic and rewarding career, we welcome your application today. Apply online:
Careers - Jubilant HollisterStier
Jubilant HollisterStier is an EEO/AA Employer. All qualified applicants will receive consideration without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or protected veteran status.
If you require assistance applying for a position, contact:
JHS-TalentAcquisition@jubl.com
Our Promise: Caring, Sharing, Growing
We are committed to enhancing value for customers and stakeholders by delivering innovative and economically efficient solutions, always with care for the environment and society.

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