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Downstream Purification Lead Jobs (NOW HIRING)

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How much do downstream purification lead jobs pay per hour?

As of Sep 14, 2026, the average hourly pay for downstream purification lead in the United States is $26.43, according to ZipRecruiter salary data. Most workers in this role earn between $18.99 and $31.01 per hour, depending on experience, location, and employer.

What does a downstream purification lead do?

A Downstream Purification Lead oversees the purification processes in biopharmaceutical manufacturing, ensuring that proteins or other biological products are efficiently separated and purified after initial production. They manage teams, troubleshoot process issues, implement improvements, and ensure compliance with industry regulations and quality standards. Their role is critical for delivering high-purity products for clinical or commercial use, and they often collaborate with upstream production, quality control, and regulatory teams.

What are the key skills and qualifications needed to thrive as a downstream purification lead?

To thrive as a Downstream Purification Lead, you need expertise in bioprocess engineering, protein purification techniques, and a relevant degree in biotechnology, biochemistry, or a related field. Familiarity with chromatography systems, filtration technologies, and regulatory compliance (such as GMP) is crucial, along with experience using laboratory information management systems (LIMS). Strong leadership, problem-solving abilities, and effective communication help manage teams and resolve process challenges efficiently. These skills are vital to ensure high-yield, high-purity product output while maintaining safety and compliance in biomanufacturing environments.

What are some common challenges faced by a downstream purification lead, and how can they be addressed?

A Downstream Purification Lead often faces challenges such as maintaining process consistency, troubleshooting equipment issues, and ensuring product quality under tight timelines. Balancing multiple projects and adapting to evolving regulatory requirements can also be demanding. Effective solutions include rigorous documentation, proactive communication with upstream and analytical teams, and ongoing training in emerging purification technologies. Building strong cross-functional relationships and fostering a culture of continuous improvement can help navigate these complexities successfully.

What are popular job titles related to Downstream Purification Lead jobs?

For Downstream Purification Lead jobs, the most frequently searched job titles are:

Infographic showing various Downstream Purification Lead job openings in the United States as of September 2026, with employment types broken down into 88% Full Time, 10% Part Time, and 2% Contract. Highlights an 88% Physical, 3% Hybrid, and 9% Remote job distribution, with an average salary of $54,972 per year, or $26.4 per hour.

Process Engineer II - Downstream - Site Based, Redmond, WA

Redmond, WA • On-site

$86K - $90K/yr

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Re-posted 22 hours ago


Job description

About Us: this is who we are

At Just Evotec Biologic, we believe that curiosity is the spark that drives innovation and success. As a forward-thinking team, we thrive on challenging the status quo, learning from each other, and pushing the boundaries of what's possible. We're on a mission to create a place where curiosity isn't just encouraged-it's celebrated.

Are you someone who asks questions, seeks answers, and isn't afraid to go deeper? #BeCureious with us and see where your curiosity can take you!

The Role:

We're looking for a passionate and curious Process Engineer II to join our team. If you're excited by new challenges, solving complex problems, and learning every step of the way, you might just be the perfect fit. In this role, you'll have the opportunity to drive impactful projects, collaborate with bright minds, and explore uncharted territories.

As a Process Engineer II at Just Evotec Biologic, you'll have the freedom to ask the hard questions, think outside the box, and find creative solutions that push us forward. It's a role where your curiosity will fuel both your personal growth and the success of the team.

The Process Engineer II Downstream for Site MSAT is part of a fast-paced, collaborative, and multidisciplinary team. The role reports to Downstream Lead for site MSAT, and is responsible to support all aspects of downstream processing for multiple clinical-scale cGMP manufacturing trains employing the innovative Just-Evotec continuous processing platform in 24/7 operations.

Roles and responsibilities:

  • Represents site MSAT on project teams as technical subject matter expert (SME) and interface with global MSAT, Operations and Quality functions.

  • Develop process understanding and expertise.

  • Authors, reviews and owns process related documentation (technical documents, test protocols, batch records, process descriptions, SOPs, etc)

  • Authors, reviews change controls including managing change implementation of the change as the assigned change agent.

  • Utilize technical skills and process knowledge to participate and/or lead investigations related to process/ New product implementation. Collaborate with impacted groups to drive implementation of CAPAs from approval to closure & effectiveness check.

  • Monitors and reports on process performance data analysis.

  • Ability to share 24/7 on call support activities during production.

  • Apply Operational Excellence principles to lead continuous improvement for downstream process improvements.

Position Requirements:

  • Masters (or Bachelors) degree in Engineering with 2+ (5+) years of pharmaceutical/biotech experience including a minimum of 2-4 years of supporting downstream purification activities for biopharmaceutical products.

  • Proven record of accomplishment and self-directed leadership in GMP pharmaceutical or biotechnology is required.

  • Technical purification and solution preparation operations using disposable-based manufacturing technologies.

  • Demonstrated capabilities to work with high-performing teams, drive change, and influence internal and external stakeholders.

  • Good interpersonal, team, and collaborative skills are required.

  • Excellent verbal and written communication skills in English; ability to interface with all levels of the organization.

  • Experience in leading risk assessment and risk management for pharmaceutical products and processes. Experience in applying principles of Quality by Design.

The base pay range for this exempt position at commencement of employment is expected to be $86,250 to $90,000; Base salary offered may vary depending on the individual's skills, experience and competitive market value. Additional total rewards include discretionary annual bonus, comprehensive benefits to include Medical, Dental and Vision, short-term and long-term disability, company paid basic life insurance, 401k company match, flexible work, generous paid time off and paid holiday, wellness and transportation benefits.

Evotec (US) Inc. is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, gender, age, disability, genetic information, gender expression, gender identity, national origin, religion, sexual orientation, or veteran status.