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Associate Director, Experimental Process Development *PC 1519

Miltenyi Biotec Inc
dental insurance, 401(k)
United States, Maryland, Gaithersburg
1201 Clopper Road (Show on map)
Jan 22, 2026
Description

Your Role:

Miltenyi Biotec is seeking a visionary and strategic Associate Director of Experimental Process Development to spearhead the establishment of a robust lipid nanoparticle (LNP) platform for therapeutic delivery, while continuing to advance our lentiviral vector (LVV) pipeline. This role places LNP innovation at the core of our next-generation delivery strategy, driving the development of scalable, high-quality manufacturing processes for both viral and non-viral modalities.

As the Associate Director, you will lead a team of five scientists and work in close collaboration with the broader Miltenyi Bioindustry Process Development organization. The ideal candidate will bring deep technical expertise in nanoparticle and/or viral vector technologies, strong strategic vision, and a collaborative mindset to expand platform capabilities and accelerate translation into impactful therapeutic solutions.

Essential Duties and Responsibilities:



  • Lead and mentor a team of scientists in the design and optimization of lipid nanoparticle (LNP) platforms, while advancing upstream and downstream processes for viral vectors including lentivirus and AAV.
  • Drive scientific and technological innovation to improve LNP formulation, encapsulation efficiency, stability, scalability, and to enhance viral vector productivity, purity, and robustness.
  • Develop and execute strategic process-development plans that accelerate LNP platform maturation and support integrated viral vector development in alignment with organizational objectives.
  • Partner cross-functionally with Analytical Development, Manufacturing, Quality, and other Bioindustry teams to ensure seamless integration of LNP and viral vector workflows.
  • Evaluate emerging technologies in nanoparticle engineering, nucleic acid delivery, and viral vector production, and incorporate high-impact approaches into development pipelines.
  • Ensure compliance with regulatory, quality, and safety standards across all LNP and viral vector R&D activities.
  • Present scientific findings, program updates, and strategic recommendations to senior leadership and external collaborators.
  • Foster a culture of scientific excellence, innovation, and continuous improvement within the platform development organization.


Requirements:



  • Ph.D. or master's degree in Biochemical Engineering, Molecular Biology, or related field and 10+ years of experience in bioprocess development, with a focus on viral vectors and/or LNPs.
  • Proven leadership experience managing scientific teams and cross-functional projects.
  • Strong understanding of GMP principles, tech transfer, and regulatory expectations.
  • Demonstrated ability to translate scientific innovation into scalable processes.
  • Excellent communication, strategic thinking, and problem-solving skills.
  • Ability to generate and implement new ideas that push the boundaries of current technologies.
  • Capable of setting long-term vision and aligning team efforts with business objectives.
  • Skilled in building partnerships across departments and sites.
  • Balance creativity with operational discipline to deliver results.


Physical Demands:

The physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. While performing the duties of this job, the employee is regularly required to walk; use hands to finger, handle, or feel; reach with hands and arms, talk, and hear. The employee is required to stand; climb or balance and stoop, kneel, crouch. The employee must occasionally lift and/or move up to 50 pounds. Specific vision abilities required by this job include close vision, color vision, peripheral vision, depth perception and ability to adjust focus. Must have ability to handle more than one task at a time and must work at a rapid pace while maintaining attention to detail.

Work Environment:

The work environment characteristics described here are representative of those an employee encounters while performing the essential functions of this job. This job is performed in a temperature-controlled facility without exposure to extreme hot or cold temperatures. Generally, this job is performed in a clean laboratory setting and routinely uses standard medical and research equipment such as centrifuges, biosafety cabinets, microscopes, incubators, chromatography devices and columns, tangential-flow filtration devices and filters, peristaltic pumps and metering fill pumps, pipettes and computers. While performing the duties of this job, the employee is frequently exposed to blood, viruses, bacteria, body fluids and other tissues. Employees entering and leaving the laboratory must wear appropriate clothing and protective equipment such as lab coats, glasses and gloves. The noise level in the work environment is usually moderate.

The hiring range for this position is expected to fall between $165,300 - $194,400/year, reflecting the range candidates can reasonably expect to be considered for at time of offer, based on factors such as experience, internal equity, and qualifications.

The salary of the finalist(s) selected for this role will be set based on a variety of considerations, including but not limited to internal equity, experience, education, specialization, skills, abilities, and training. The above range represents the Company's good faith and reasonable estimate of possible compensation at the time of posting.

In addition to your salary, the Company offers a comprehensive benefits package, including health, vision, and dental insurance, as well as a 401(k) plan. All benefits are subject to eligibility requirements. Certain positions may also be eligible for additional compensation such as bonuses or commissions.

Miltenyi Biotec, Inc. is an EO Employer - M/F/Veteran/Disability/Sexual Orientation/Gender Identity.

Miltenyi Biotec, Inc. participates in E-Verify.

Are you ready to start revolutionizing biomedical research? When you join Miltenyi Biotec, you join a family that is passionate about making a real impact - one breakthrough at a time. For over 30 years, we have played a pivotal role in the design, development, manufacture, and integration of products for sample preparation, cell separation, cell analysis, imaging, and cell culture needs. These developments have led to cutting-edge cell and gene therapies - transformative methods that mobilize the body's own cells and genetic blueprint to tackle diseases such as cancer and autoimmune conditions. Today, our more than 18,000 solutions play a vital role in paving the way for the medicine of tomorrow.

Equal Opportunity Employer

This employer is required to notify all applicants of their rights pursuant to federal employment laws.
For further information, please review the Know Your Rights notice from the Department of Labor.
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