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Product Process Development Scientist Jobs (NOW HIRING)

... development, and communicates relevant observations. * May introduce advanced scientific methods ... May initiate productive collaborations within and outside of the department or company. * Advises ...

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R&D Scientist

Newark, DE · On-site

$65K - $85K/yr

The R&D Scientist will explore and develop novel base materials for stationary phase in ... Collaborate with production team to improve production process and product quality and consistency.

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Product Process Development Scientist information

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$46K

$82.7K

$120.5K

How much do product process development scientist jobs pay per year?

As of Aug 6, 2026, the average yearly pay for product process development scientist in the United States is $82,657.00, according to ZipRecruiter salary data. Most workers in this role earn between $69,000.00 and $94,500.00 per year, depending on experience, location, and employer.

What skills and qualifications are needed to thrive as a product process development scientist?

To thrive as a Product Process Development Scientist, you generally need a strong background in chemistry, chemical engineering, or related sciences, often supported by an advanced degree. Familiarity with laboratory instrumentation, process modeling software, and quality management systems, as well as relevant certifications like Six Sigma, is typically required. Strong problem-solving skills, attention to detail, and effective teamwork and communication abilities make candidates stand out. These skills and qualities are essential for designing scalable, efficient, and compliant product processes that meet organizational goals and regulatory standards.

What does a product process development scientist do?

A Product Process Development Scientist is responsible for designing, optimizing, and implementing processes to manufacture new products, typically in industries such as pharmaceuticals, food, or chemicals. They work closely with research teams to scale up lab findings to production-level processes, ensuring efficiency, quality, and regulatory compliance. Their role involves problem-solving, documentation, and continuous improvement of production methods to achieve cost-effective and high-quality results.

How does a product process development scientist typically collaborate with cross-functional teams during new product development?

Product Process Development Scientists work closely with R&D, quality assurance, manufacturing, and sometimes marketing teams to ensure new products are developed efficiently and meet quality standards. They often translate laboratory-scale formulations into scalable processes suitable for full production, requiring frequent communication with engineers and production staff. Regular meetings and project updates are common, and collaboration is key to troubleshooting process challenges, optimizing workflows, and ensuring compliance with regulatory requirements. This cross-functional teamwork is essential for bringing new products from concept to market-ready stages.

What is the difference between Product Process Development Scientist vs Manufacturing Process Engineer?

AspectProduct Process Development ScientistManufacturing Process Engineer
CredentialsBachelor's or Master's in Engineering, Chemistry, or related field; often requires experience in product developmentBachelor's or Master's in Engineering, Chemical Engineering, or related; focuses on manufacturing processes
Work EnvironmentResearch labs, product development teams, R&D facilitiesManufacturing plants, production lines, process optimization settings
Industry UsageConsumer goods, pharmaceuticals, biotech, electronicsAutomotive, chemicals, consumer products, pharmaceuticals

The Product Process Development Scientist primarily focuses on developing and optimizing new products and their processes in R&D settings, while the Manufacturing Process Engineer concentrates on scaling up, maintaining, and improving manufacturing processes on the production floor. Both roles require technical expertise but differ in their focus on development versus manufacturing operations.

More about Product Process Development Scientist jobs
Infographic showing various Product Process Development Scientist job openings in the United States as of August 2026, with employment types broken down into 100% Full Time. Highlights an 95% In-person, and 5% Remote job distribution, with an average salary of $82,657 per year, or $39.7 per hour.

Senior Scientist II, Biologics Drug Product Development

AbbVie

North Chicago, IL • On-site

$109K/yr

Full-time

Medical, Dental, Vision, Retirement, PTO

Re-posted 26 days ago


AbbVie rating

8.7

Company rating: 8.7 out of 10

Based on 100 frontline employees who took The Breakroom Quiz

14th of 86 rated pharmaceutical


Job description

Company Description
AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas - immunology, oncology, neuroscience, and eye care - and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at www.abbvie.com. Follow @abbvie on X, Facebook, Instagram, YouTube, LinkedIn and Tik Tok.
Job Description
Biologics Drug Product Development (Bio DPD), a part of Development Sciences within AbbVie's R&D, is a global organization that is responsible for drug product formulation and process development, and definition of the product presentation for biologics (proteins, conjugates, peptides, neurotoxins etc.) and genetic medicine (AAV, LNPs, Cell Therapy).
AbbVie is seeking a highly motivated candidate for the position of Senior Scientist II, located in North Chicago, IL. We are seeking an accomplished scientist with a proven track record in biologics drug product process development, modeling, scale-up and tech transfer. This position will be an integral part of the product development and CMC teams and will have strong collaborations with several stakeholders, including discovery research, analytical research and development, bioprocess development, combination products development, product development science and technology, pilot plants and third-party manufacturers.
Key Responsibilities:
  • Lead the design and execution of biologics drug product formulation and process development, characterization and robustness studies.
  • Support scale-up and technology transfer activities to internal and external manufacturing sites.
  • Initiate and/or support scientific initiatives to drive innovation, continuously enhance capabilities and platforms, and improve business processes.
  • Effectively and timely communicate development plans, risks, and mitigation plans to stakeholders and line management.
  • Represent Bio DPD in the cross-functional Product Presentation and Device Strategy Team (PPDST) and the CMC Team.

Qualifications
Qualifications
  • PhD in Pharmaceutics, Pharmaceutical Sciences, Chemistry, Chemical Engineering, or related disciplines with 4+ years of relevant industry experience.
  • Proven ability to solve critical scientific problems.
  • Experience with biologics (proteins, conjugates, peptides and/or neurotoxins), parenteral synthetic molecules and/or genetic medicine (AAV, LNPs, cell therapy) drug product process development.
  • Experience with sterile manufacturing unit operations (freeze-thaw, compounding, mixing, filtration and filling, lyophilization), characterization, scale-down models, simulation, scale-up, technology transfer, and batch record authoring.
  • Hand-on experience with authoring regulatory filings for biologics and sterile parenteral products
  • Experience leading drug product development as the functional lead within cross-functional teams

Preferred Qualifications:
  • Biologics drug product formulation development
  • Understanding of relevant cGMP and regulatory guidance for biologics and sterile parenteral products
  • Experience in managing third party manufacturers of sterile parenteral products
  • Experience with quality risk management and control strategies for biologics and sterile parenteral products

Key Competencies:
  • Deep scientific knowledge and significant hands-on experience with drug product process development and tech transfer
  • Effectively communicates to influence without authority, drives technical excellence, and inspires continuous improvement.
  • Builds strong relationships with peers and cross-functional partners to enable higher performance.
  • Connects ideas from disparate fields, integrates data and information quickly, and takes risks to achieve the highest performance.
  • Raises the bar and is never satisfied with the status quo.
  • Creates a learning environment, open to suggestions and experimentation for improvement.
  • Embraces the ideas of others, nurtures innovation and manages innovation to reality.

Additional Information
Applicable only to applicants applying to a position in any location with pay disclosure requirements under state or local law:
  • The compensation range described below is the range of possible base pay compensation that the Company believes in good faith it will pay for this role at the time of this posting based on the job grade for this position. Individual compensation paid within this range will depend on many factors including geographic location, and we may ultimately paymore or less than the posted range. This range may be modified in the future.
  • We offer a comprehensive package of benefits including paid time off (vacation, holidays, sick), medical/dental/vision insurance and 401(k) to eligible employees.
  • This job is eligible to participate in our short-term incentive programs.

Note: No amount of pay is considered to be wages or compensation until such amount is earned, vested, and determinable. The amount and availability of any bonus, commission,incentive, benefits, or any other form of compensation and benefits that are allocable to a particular employee remains in the Company's sole and absolute discretion unless and untilpaid and may be modified at the Company's sole and absolute discretion, consistent with applicable law.
AbbVie is an equal opportunity employer and is committed to operating with integrity, driving innovation, transforming lives and serving our community. Equal Opportunity Employer/Veterans/Disabled.
US & Puerto Rico only - to learn more, visit https://www.abbvie.com/join-us/equal-employment-opportunity-employer.html
US & Puerto Rico applicants seeking a reasonable accommodation, click here to learn more:
https://www.abbvie.com/join-us/reasonable-accommodations.html

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About AbbVie

Sourced by ZipRecruiter

AbbVie's mission is to discover and deliver innovative medicines that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas: immunology, oncology, neuroscience, eye care, virology, women's health, and gastroenterology, in addition to products and services across its Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at www.abbvie.com. Follow @abbvie on Twitter, Facebook, Instagram, YouTube, and LinkedIn.

Industry

Scientific research and development services

Company size

10,000+ Employees

Headquarters location

North Chicago, IL, US

Year founded

2013