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Process Development Associate Jobs in Louisville, KY

Brady

Manufacturing Engineer

Louisville, KY · On-site

$67K - $87K/yr

Influences key associates to promote participation and cooperation in process development/improvement initiatives. * Ensures conformance with and application of policies and procedures. * Designs ...

Brady Worldwide, Inc.

Manufacturing Engineer

Louisville, KY · On-site

$67K - $87K/yr

Influences key associates to promote participation and cooperation in process development/improvement initiatives. * Ensures conformance with and application of policies and procedures. * Designs ...

Samtec

Process Engineer (HDR)

New Albany, IN

Associates may be asked to perform additional tasks depending on strengths and capabilities.* Required/Preferred Experience: * 5+ Years' Experience in Process Engineering, development and ...

Samtec

Process Engineer (HDR)

New Albany, IN · On-site

Associates may be asked to perform additional tasks depending on strengths and capabilities.* Required/Preferred Experience: * 5+ Years' Experience in Process Engineering, development and ...

samtec

Process Engineer (HDR)

New Albany, IN · On-site

Associates may be asked to perform additional tasks depending on strengths and capabilities.* Required/Preferred Experience: * 5+ Years' Experience in Process Engineering, development and ...

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Process Development Associate information

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$32

$47

How much do process development associate jobs pay per hour?

As of Aug 11, 2026, the average hourly pay for process development associate in Louisville, KY is $32.36, according to ZipRecruiter salary data. Most workers in this role earn between $26.54 and $39.71 per hour, depending on experience, location, and employer.

What is the difference between Process Development Associate vs Process Engineer?

AspectProcess Development AssociateProcess Engineer
Required CredentialsBachelor's in Chemistry, Chemical Engineering, or related field; often some experience in process developmentBachelor's or Master's in Chemical Engineering or related; more emphasis on engineering principles
Work EnvironmentLaboratory and pilot plant settings, focused on process research and developmentManufacturing plants, production lines, and process optimization environments
Employer & Industry UsagePharmaceutical, biotech, and chemical industries; entry to mid-level rolesChemical, manufacturing, and process industries; more senior roles in process optimization

The Process Development Associate primarily focuses on developing and optimizing new processes in lab and pilot settings, often working closely with R&D teams. In contrast, the Process Engineer applies engineering principles to scale up processes, improve manufacturing efficiency, and troubleshoot production issues. While both roles require a background in chemical or process engineering, the Process Development Associate is more research-oriented, whereas the Process Engineer emphasizes process implementation and optimization in production environments.

What are the key skills and qualifications needed to thrive as a process development associate?

To thrive as a Process Development Associate, you need a strong background in biochemistry, chemical engineering, or a related field, often supported by a bachelor’s or master’s degree. Experience with laboratory instrumentation, process optimization tools, and familiarity with regulatory standards such as GMP are typically required. Attention to detail, problem-solving abilities, and effective teamwork are vital soft skills for excelling in this role. These competencies are crucial for ensuring efficient process design, regulatory compliance, and successful scale-up in manufacturing environments.

What are the primary challenges faced by a process development associate when scaling up laboratory processes to manufacturing scale?

A Process Development Associate often encounters challenges in translating small-scale laboratory protocols into large-scale manufacturing processes. Variations in equipment, raw material quality, and environmental conditions can impact reproducibility and efficiency. Addressing these issues requires strong troubleshooting skills, attention to detail, and close collaboration with cross-functional teams such as manufacturing, quality assurance, and engineering to ensure smooth technology transfer and consistent product quality.
What are popular job titles related to Process Development Associate jobs in Louisville, KY? For Process Development Associate jobs in Louisville, KY, the most frequently searched job titles are:
What job categories do people searching Process Development Associate jobs in Louisville, KY look for? The top searched job categories for Process Development Associate jobs in Louisville, KY are:
Process Development Associate jobs near you
Infographic showing various Process Development Associate job openings in Louisville, KY as of August 2026, with employment types broken down into 100% Full Time. Highlights an 91% In-person, and 9% Remote job distribution, with an average salary of $67,316 per year, or $32.4 per hour.

Synthetic DNA Process Development Scientist

Eurofins USA Genomic Services

Louisville, KY

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Re-posted 3 days ago

Job description

Company Description

Eurofins Scientific is an international life sciences company, providing a unique range of analytical testing services to clients across multiple industries, to make life and our environment safer, healthier and more sustainable. From the food you eat, to the water you drink, to the medicines you rely on, Eurofins works with the biggest companies in the world to ensure the products they supply are safe, their ingredients are authentic and labelling is accurate.

Eurofins is the global leader in food, environment, pharmaceutical and cosmetic product testing and in agroscience Contract Research Organisation services. Eurofins is one of the market leaders in certain testing and laboratory services for genomics, discovery pharmacology, forensics, advanced material sciences and in the support of clinical studies, as well as having an emerging global presence in Contract Development and Manufacturing Organisations. The Group also has a rapidly developing presence in highly specialised and molecular clinical diagnostic testing and in-vitro diagnostic products.

In over just 30 years, Eurofins has grown from one laboratory in Nantes, France to 55,000 staff across a decentralised and entrepreneurial network of 900 laboratories in over 50 countries. Eurofins offers a portfolio of over 200,000 analytical methods to evaluate the safety, identity, composition, authenticity, origin, traceability and purity of biological substances and products.

Job Description

Synthetic DNA Process Development Scientist Include but are not Limited to the Following:

We are seeking a highly skilled and motivated Organic Chemist with expertise in oligonucleotide synthesis and purification to support process development and manufacturing. This role focuses on developing, optimizing, and scaling chemical processes for high-throughput and high-quality oligonucleotide production.

  • Design, develop, and optimize chemical synthesis processes for nucleotides and oligonucleotides
  • Process development and scale-up from R&D to manufacturing
  • Develop and improve oligonucleotide purification processes (e.g., HPLC, ion-exchange, desalting)
  • Troubleshoot synthesis and purification challenges to improve yield and purity
  • Collaborate with manufacturing, QC, and engineering for process transfer
  • Evaluate new chemistries and technologies
  • Author SOPs, batch records, and technical reports
  • Ensure compliance with quality systems
  • Mentor lab technicians
Qualifications

Basic Minimum Education Qualifications:

  • Ph.D. or Master’s degree in Organic Chemistry or related field (required)

Basic Minimum Work Requirements:

  • Minimum 5 years of industrial experience in chemical synthesis
  • Hands-on experience with solid-phase oligonucleotide synthesis
  • Hands-on experience in oligonucleotide purification process development
  • Strong analytical skills (HPLC, LC-MS)
  • Experience scaling processes to manufacturing
  • Experience in GMP or regulated environments, preferred
  • Familiarity with automated DNA/RNA synthesizers, strongly preferred
  • Knowledge of modified nucleotides, strongly preferred
  • Experience in high-throughput oligo production, strongly preferred
  • Authorization to work in the United States indefinitely without restriction or sponsorship.

The Ideal Candidates Possess the Following:

  • Fast-paced, collaborative environment
  • Ability to manage multiple priorities
  • Occasional off-hours support as needed

Additional Information

Position is full-time working Monday - Friday 8:00am - 5:00pm, with overtime and weekend work as needed.  Candidates currently living within a commutable distance of Louisville, KY are encouraged to apply.

  • Excellent full-time benefits including comprehensive medical coverage, dental, and vision options
  • Life and disability insurance
  • 401(k) with company match
  • Paid vacation and holidays

#LI-KS1 

Eurofins USA Genomic Services is a Disabled and Veteran Equal Employment Opportunity employer.