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Associate Director Purification Jobs (NOW HIRING)

... purification trains. With a focus on innovation and reliability, this leader drives technical ... The Associate Director serves as the suite's technical owner in client forums, translating product ...

Execute & Troubleshoot Complex Purification Campaigns Lead hands-on execution of mass-directed and ... associates, and technicians - equipping them to independently master preparative chromatography ...

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Associate Director Purification information

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$30.5K

$102.7K

$173K

How much do associate director purification jobs pay per year?

As of Sep 14, 2026, the average yearly pay for associate director purification in the United States is $102,728.00, according to ZipRecruiter salary data. Most workers in this role earn between $70,000.00 and $141,000.00 per year, depending on experience, location, and employer.

What does an associate director purification do?

An Associate Director of Purification oversees the development, optimization, and operation of purification processes in biopharmaceutical manufacturing. This role typically involves managing teams responsible for the purification of proteins, antibodies, or other biologics, ensuring processes meet regulatory standards and production goals. They collaborate with other departments, troubleshoot issues, and drive continuous improvement efforts. Additionally, they play a key role in technology transfer, process validation, and ensuring compliance with Good Manufacturing Practices (GMP).

What key skills and qualifications are needed to thrive as an associate director purification?

To thrive as an Associate Director Purification, you need advanced expertise in protein purification, process development, and a degree in biochemistry, chemical engineering, or a related fieldβ€”often at the Ph.D. level. Familiarity with large-scale chromatography systems, filtration technologies, and regulatory compliance (such as cGMP) is crucial, along with experience in data analysis tools. Strong leadership, problem-solving, and cross-functional communication skills set outstanding candidates apart in this role. These capabilities ensure the efficient development and scaling of purification processes, regulatory adherence, and successful management of teams and projects in biopharmaceutical manufacturing.

What are some typical challenges an associate director purification faces when scaling up purification processes from lab to manufacturing?

Associate Directors of Purification often encounter challenges such as ensuring process consistency and product quality during scale-up, managing cross-functional communication between R&D and manufacturing teams, and troubleshooting unexpected impurities or yield loss at larger scales. They must also navigate regulatory requirements and validate new equipment or procedures. Strong project management and problem-solving skills are essential, as is the ability to lead teams through complex technical transfers while meeting tight timelines.

What is the difference between Associate Director Purification vs Senior Scientist Purification?

AspectAssociate Director PurificationSenior Scientist Purification
CredentialsAdvanced degree (PhD/MSc), extensive industry experienceMaster's or PhD, significant laboratory experience
Work EnvironmentLeadership role overseeing teams and projectsHands-on laboratory research and process development
Employer UsageBiotech and pharmaceutical companies, managing purification processesResearch-focused roles within same industries
Search IntentLeadership, project management, strategic oversightTechnical expertise, experimental work

The Associate Director Purification typically holds a leadership position with strategic responsibilities, overseeing purification teams and projects. In contrast, the Senior Scientist Purification focuses more on technical research and process development. Both roles require advanced degrees and industry experience, but their focus and scope differ significantly.

What are popular job titles related to Associate Director Purification jobs?

For Associate Director Purification jobs, the most frequently searched job titles are:

Infographic showing various Associate Director Purification job openings in the United States as of September 2026, with employment types broken down into 1% As Needed, 67% Full Time, 29% Part Time, 1% Temporary, 1% Contract, and 1% Nights. Highlights an 96% Physical, 1% Hybrid, and 3% Remote job distribution, with an average salary of $102,728 per year, or $49.4 per hour.

Senior Manager/Associate Director, Drug Substance MSAT

Full-time

Posted 25 days ago


Job description

Position OverviewThe Associate Director, Drug Substance MSAT, leads end-to-end process stewardship (Upstream and Downstream) for an assigned manufacturing suite (DSM1 or DSM2). The role executes MSAT strategy, builds and develops a team of scientists and engineers, and optimizes large scale cell culture operations across seed/production bioreactors and purification trains. With a focus on innovation and reliability, this leader drives technical stewardship through tech transfer execution, process performance qualification (PPQ) execution, commercialization, as well as continuous improvement initiatives. This leader partners closely with the rest of the MSAT leadership team, Manufacturing, QA, Automation, and Engineering to improve systems and working methods. The Associate Director serves as the suite's technical owner in client forums, translating product requirement needs into clear plans, stage gates, and flawless execution to enable compliant, on time Drug Substance delivery.Company OverviewFUJIFILM Biotechnologies is building the future of bioproduction in Holly Springs, North Carolina. By end of 2025, we'll open North America's largest end-to-end CDMO biopharmaceutical manufacturing facility, offering drug substance production, fill-finish, and packaging under one roof.We're looking for passionate, mission-driven people to help us realize this exciting vision and deliver the next vaccine, cure, or therapy. We offer a dynamic work environment and we're proud to cultivate a culture that will fuel your purpose, energy, and drive-what we call Genki. Ready to shape the future of medicine? Let's transform healthcare together!Holly Springs, North Carolina, combines small-town warmth with proximity to Raleigh's thriving tech scene, making it the perfect blend of community and opportunity.Fujifilm is globally headquartered in Tokyo with over 70,000 employees across four key business segments of healthcare, electronics, business innovation, and imaging. We are guided and united by our Group Purpose of "giving our world more smiles." Visit: https://www.fujifilm.com/us/en/about/region/careersJob DescriptionWhat You'll Do:Assigns and coaches upstream/downstream scientists, engineers, and team members; directs upstream/downstream technical leads for TT execution and readiness activities; reviews performance and concerns, partners with HR as needed for resolutionOwns product and process stewardship by leading end to end technical strategy execution for assigned products in the suite from new product introduction through commercialization, covering upstream (seed/production bioreactors) and downstream (purification trains)Sets direction in defining and maintaining the process control strategy by translating product critical quality attributes into upstream/downstream critical process parameters, acceptable ranges, and control plansEnsures process flow diagram, change controls, and associated documents remain currentEnsures floor presence, safety, and compliance as well as successful manufacturing process comparability and validation runsDrives continuous improvement projects to improve manufacturability, reliability, efficiency, quality, cost, and complianceEstablishes systems and procedures to enable proactive process monitoring, analysis, and reporting of manufacturing process data (within batch and batch-to-batch)Promotes professional development, psychological safety, accountability, personal ownership, and proactive problem-solving; runs effective tier huddles; recognizes contributions and shares learnings (Yokoten)Oversees critical manufacturing investigations and deviations; reviews trends, capability, and alarms; determines true root cause; initiates, oversees, and verifies corrective and preventive actions (CAPAs); authors and approves change controlsAuthors Chemistry, Manufacturing, and Control (CMC) sections of regulatory filings; supports the CMC review of regulatory submissions, site inspections, and health authority inquiries, as requiredPartners with Client, Process Development, Quality, Manufacturing, and Engineering on large-scale platform development, technology innovation, scale-up, and manufacturability as part of tech transfer (TT), as neededCoordinates cross-functional delivery by collaborating with Manufacturing, Quality, Automation, Engineering, Supply Chain, and other support groups to align schedules, resources, and decisions under tiered governance; utilizes clear decision rights (D.A.I model)Functions as a senior leader to support supplier technical evaluations, risk assessments, raw material evaluations, and qualificationsAdministers company policies such as time off, shift work, and inclement weather that directly impact employeesCompletes required administrative tasks (e.g., timecard approvals, time off approvals, expense reports, etc.)Participates in the recruitment process and retention strategies to attract and retain talent, as neededPerforms other duties, as assignedMinimum Requirements: Master's degree in an Engineering or Scientific field with 9+ years of experience ORBachelor's degree in an Engineering or Scientific field with 11+ years of experience8+ years of people management/leadership experience9+ years of CMC experience leading pre-approval and post-approval activities for biologic product, including process development and Good Manufacturing Practices (GMP)Preferred Requirements:12+ years of experience in similar role with large projects from conceptual design phase to operations8+ years of experience leading technical departmentsTechnical leadership experience with drug substance manufacturing facilitiesPrior drug substance development and manufacturing experience including process validation, process transfer, commercialization, manufacturing support, and troubleshooting drug substance operationsExperience communicating and collaborating with a global teamEEO InformationFujifilm is committed to providing equal opportunities in hiring, promotion and advancement, compensation, benefits, and training regardless of nationality, age, gender, sexual orientation or gender identity, race, ethnicity, religion, political creed, ideology, national, or social origin, disability, veteran status, etc.ADA InformationIf you require reasonable accommodation in completing this application, interviewing, completing any pre-employment testing, or otherwise participating in the employee selection process, please direct your inquiries to our HR Department (FDBN_PNC@fujifilm.com). Salary: . Date posted: 08/20/2026