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Process Development Associate Iii Jobs in Washington

... Development Associate who can combine rigorous underwriting skills with active involvement ... Minimum 3 years of relevant experience; 5+ years preferred * Proven ability to build complex Excel ...

... Development Associate who can combine rigorous underwriting skills with active involvement ... Minimum 3 years of relevant experience; 5+ years preferred * Proven ability to build complex Excel ...

... Development Associate who can combine rigorous underwriting skills with active involvement ... Minimum 3 years of relevant experience; 5+ years preferred * Proven ability to build complex Excel ...

As a Business Development Associate at KME.digital, you'll play an active role in helping our organization surpass quarterly revenue goals, track and maintain sales processes, and engage in community ...

As a Business Development Associate at KME.digital, you'll play an active role in helping our organization surpass quarterly revenue goals, track and maintain sales processes, and engage in community ...

You'll assist with developing scopes of work, reviewing contracts, and processing check requests ... The ideal Land Development Associate is a self-starter with very strong organizational skills and ...

Ability to learn and apply ACEEE's business processes and systems, including Salesforce and ... (3) weeks of vacation in the first year and four (4) weeks thereafter, 11 federal holidays and ...

Laboratory Associate III Job Code: LA1652 ABOUT US We are welcoming a new era in healthcare where ... Processes requisitions for testing. * Prepares and distributes reports. Safety: Adheres to all ...

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Process Development Associate Iii information

What are the key skills and qualifications needed to thrive as a Process Development Associate III, and why are they important?

To thrive as a Process Development Associate III, you need a strong background in bioprocess engineering or related sciences, typically with a bachelor's or master's degree and relevant industry experience. Familiarity with laboratory equipment, bioprocessing systems, statistical analysis software, and documentation tools is essential, and certifications such as Six Sigma or Lean are often valued. Strong problem-solving abilities, attention to detail, and effective communication skills help drive process improvements and enable collaboration across teams. These skills are crucial for optimizing manufacturing processes, ensuring product quality, and supporting successful technology transfer within biopharmaceutical organizations.

What is the difference between Process Development Associate Iii vs Process Development Associate Ii?

AspectProcess Development Associate IiiProcess Development Associate Ii
Required CredentialsBachelor's degree in Chemistry, Biology, or related field; 2+ years experienceBachelor's degree; 1+ year experience
Work EnvironmentLaboratory and manufacturing settings, collaborative teamsLaboratory-focused, supporting process experiments
Employer & Industry UsagePharmaceutical, biotech, and biotech manufacturing companiesSimilar industries, often within same companies or teams
Common Search & Comparison IntentUnderstanding role progression and responsibilitiesClarifying experience levels and job expectations

The Process Development Associate Iii typically has more experience and responsibilities than the Process Development Associate Ii, including leading experiments and contributing to process improvements. Both roles require a strong background in science and laboratory work, but the Iii level often involves more independent work and project involvement within pharmaceutical or biotech settings.

What are Process Development Associate III roles and responsibilities?

A Process Development Associate III is responsible for developing, optimizing, and scaling up manufacturing processes, often within the biotechnology or pharmaceutical industries. They work closely with scientists and engineers to design experiments, analyze data, and implement improvements that enhance product quality and efficiency. This role typically involves hands-on laboratory work, documentation, troubleshooting, and ensuring compliance with regulatory standards. Process Development Associate IIIs may also mentor junior associates and contribute to cross-functional project teams. Their work is critical to moving products from research to full-scale production.

What are some common challenges faced by a Process Development Associate III, and how are they typically addressed?

Process Development Associate III professionals often encounter challenges such as troubleshooting complex process deviations, balancing multiple projects with tight timelines, and adapting to evolving regulatory requirements. These challenges are typically addressed through close collaboration with cross-functional teams (such as Quality Assurance and Manufacturing), continuous skill development, and utilizing robust documentation and data analysis tools. Proactive communication and participation in process improvement initiatives also help in overcoming obstacles and ensuring successful project outcomes.
What are popular job titles related to Process Development Associate Iii jobs in Washington? For Process Development Associate Iii jobs in Washington, the most frequently searched job titles are:
What job categories do people searching Process Development Associate Iii jobs in Washington look for? The top searched job categories for Process Development Associate Iii jobs in Washington are:
What cities in Washington are hiring for Process Development Associate Iii jobs? Cities in Washington with the most Process Development Associate Iii job openings:
Infographic showing various Process Development Associate Iii job openings in Washington as of June 2026, with employment types broken down into 86% Full Time, 7% Temporary, and 7% Contract. Highlights an 43% In-person, 43% Hybrid, and 14% Remote job distribution.

Senior Associate, Process Development

Kolon TissueGene, Inc.

Rockville, MD

Other

Retirement, PTO

Posted 7 days ago


Job description

ABOUT KOLON TISSUEGENE

Kolon TissueGene, Inc. (KTG) is a clinical-stage biopharmaceutical company developing TG-C, a first-in-class cell and gene therapy for osteoarthritis — a disease with significant unmet need and no approved disease-modifying treatment in the U.S. We are a small, high-conviction team preparing for our most pivotal chapter: commercial launch. Every person we hire shapes how we get there.


ABOUT THE ROLE

The Senior Process Development Associate will independently design, execute, and document process development studies that support our clinical manufacturing programs. This role requires hands-on laboratory experience and the ability to plan, execute, analyze, and document PD activities with minimal supervision.


This is not a manufacturing technician role, and it is not an entry-level PD position. We're looking for someone who can run projects independently and contribute meaningfully to protocol development, batch records, and process optimization — bringing both technical depth and ownership to everything they do.


WHAT YOU WILL DO

  • Independently design and execute process development studies, including experimental plans, study protocols, and batch records
  • Perform and oversee scale-up or scale-out studies, process optimization runs, and special/non-routine PD runs
  • Analyze and interpret experimental data with scientific rigor
  • Review results, troubleshoot issues, and recommend process improvements to enhance robustness and efficiency
  • Contribute to documentation packages with accuracy and attention to detail
  • Collaborate cross-functionally with Manufacturing, Analytical Development, and Research; maintain compliance with GMP expectations where applicable


WHAT WE ARE LOOKING FOR

REQUIRED

  • Bachelor’s degree required, with a strong preference for a STEM field; laboratory coursework and hands-on lab training required.
  • 3–5 years of relevant Process Development or closely related experience — this role requires independent PD capability, not entry-level lab support.
  • Demonstrated experience independently designing PD studies, executing experiments, and reviewing and interpreting data.
  • Strong hands-on laboratory experience with a solid grounding in cell culture techniques and core PD laboratory methods.
  • Upstream processing experience required.
  • Experience generating and maintaining technical documentation (experimental plans, protocols, batch records, reports).

PREFERRED

  • GMP manufacturing exposure.
  • Biologics experience.
  • Cell therapy or gene therapy experience (preferred but not mandatory).
  • Downstream processing experience — a strong plus.
  • Broader exposure beyond a single modality.


WHY KTG

First-in-Class Science TG-C is a cell and gene therapy advancing toward U.S. commercialization for osteoarthritis — a disease with no approved disease-modifying treatment. Your work in the lab directly supports a potential paradigm shift in how this condition is treated.

Real Ownership You will run your own studies end-to-end — from experimental design through documentation — with the autonomy that comes from being trusted to deliver.

Direct Access to Leadership On a small, mission-driven team, you will work closely with PD leadership, Manufacturing, Analytical Development, and Research — with no layers between your work and the program's direction.

Culture of Rigor & Curiosity We value deep scientific thinking, intellectual honesty, and continuous improvement, and we invest in the tools and training to help you grow your expertise.


BENEFITS

  • Onsite yet flexible work schedules
  • Premium-free global health insurance (50% dependent coverage)
  • 401k with immediate eligibility
  • Long-term incentive bonuses
  • On-site gym & wellness perks
  • Extra PTO accrual every year
  • Global and local training opportunities


WORK ENVIRONMENT

This is a full-time, onsite role based at our Rockville, MD headquarters. Work is performed in a general and biological laboratory environment; proper gowning and PPE (lab coat, safety glasses, gloves, hair and shoe covers) are required where applicable.


PHYSICAL REQUIREMENTS

Ability to sit for extended periods at a computer workstation.

Extensive keyboarding involving repetitive finger motion.

Ability to communicate via telephone and video conference.

Ability to lift, push, or carry up to 25 lbs occasionally.


DISABILITY ACCOMMODATION & VETERAN SELF-IDENTIFICATION

We invite all applicants to voluntarily self-identify as a person with a disability and/or a protected veteran. This information is collected for federal compliance purposes only and will not affect hiring decisions. To request a reasonable accommodation at any stage of the application or interview process, contact us at hr@tissuegene.com. All requests are handled confidentially and in accordance with applicable law.


Kolon TissueGene, Inc. is an equal opportunity employer.

We celebrate diversity and are committed to creating an inclusive environment for all employees. All qualified applicants will receive consideration without regard to race, color, religion, gender, identity, sexual orientation, national origin, disability, or veteran status.