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Pharmaceutical Process Development Jobs in Pennsylvania

The Richmond Group

Senior Process Engineer

Allentown, PA · On-site

$102K - $132K/yr

... used in pharmaceutical and biotech applications. They are investing in expanding their capabilities, which includes building a team to conduct process development, commercialization, and ...

PSC Biotech

MSAT Engineer

York, PA

$71K - $92K/yr

Pharmaceutical process development * Senior MSAT Engineer * 8+ years pharmaceutical industry experience * Strong experience supporting sterile injectable products * Must be authorized to work in the ...

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Pharmaceutical Process Development information

What is pharmaceutical process development?

Pharmaceutical process development is the series of activities involved in designing, optimizing, and scaling up the manufacturing processes for pharmaceutical products. It includes transforming laboratory procedures into reliable, efficient, and reproducible processes that meet regulatory standards for quality and safety. This phase is crucial for ensuring that medications can be produced consistently and at a larger scale while maintaining product efficacy and compliance with industry regulations.

What are the key skills and qualifications needed to thrive in pharmaceutical process development?

To thrive in Pharmaceutical Process Development, you need a solid background in chemical engineering, pharmaceutical sciences, or a related field, often supported by an advanced degree. Familiarity with process analytical technology (PAT), Good Manufacturing Practice (GMP) standards, and software like MATLAB or SIMCA is typically required. Strong problem-solving, teamwork, and communication skills help professionals navigate complex projects and cross-functional collaborations. These skills are crucial for ensuring efficient, compliant, and innovative drug development processes that meet regulatory requirements and industry standards.

What are the typical challenges faced when transitioning a pharmaceutical process from laboratory scale to full-scale manufacturing?

One of the main challenges in pharmaceutical process development is ensuring that processes developed at laboratory or pilot scale remain robust, efficient, and compliant when scaled up to full manufacturing. Variables such as mixing, temperature control, and material properties can behave differently at larger volumes, potentially impacting product quality or yield. Process developers often work closely with manufacturing, quality assurance, and engineering teams to troubleshoot issues and optimize protocols, making strong cross-functional collaboration skills essential. Addressing regulatory requirements during scale-up is also critical to ensure that the process meets all quality and safety standards.

What is the difference between Pharmaceutical Process Development vs Pharmaceutical Manufacturing Technician?

AspectPharmaceutical Process DevelopmentPharmaceutical Manufacturing Technician
Primary FocusDesigning, optimizing, and scaling up manufacturing processes for new or existing drugsOperating equipment, assembling products, and ensuring production runs smoothly
Work EnvironmentLaboratories, R&D facilities, pilot plantsProduction floors, manufacturing plants
Required CredentialsBachelor's degree in pharmacy, chemistry, or related field; experience in process developmentHigh school diploma or equivalent; on-the-job training

Pharmaceutical Process Development focuses on creating and refining manufacturing processes, while Pharmaceutical Manufacturing Technicians handle the day-to-day production tasks. Both roles are essential in the drug development and manufacturing pipeline, but they differ in scope, responsibilities, and work environment.

How to get into pharmaceutical process development?

To enter pharmaceutical process development, candidates typically need a bachelor's degree in chemical engineering, pharmaceutical sciences, or a related field. Gaining experience through internships or entry-level roles in manufacturing or R&D, along with knowledge of process design, GMP regulations, and process optimization tools, is beneficial. Advanced roles may require a master's or Ph.D. and familiarity with process simulation software.

What are popular job titles related to Pharmaceutical Process Development jobs in Pennsylvania?

For Pharmaceutical Process Development jobs in Pennsylvania, the most frequently searched job titles are:

What job categories do people searching Pharmaceutical Process Development jobs in Pennsylvania look for?

The top searched job categories for Pharmaceutical Process Development jobs in Pennsylvania are:

Pharmaceutical Process Development jobs near you
Infographic showing various Pharmaceutical Process Development job openings in Pennsylvania as of August 2026, with employment types broken down into 1% As Needed, 86% Full Time, 11% Part Time, and 2% Contract. Highlights an 86% Physical, 3% Hybrid, and 11% Remote job distribution.

Downstream Process Development Engineer

Eurofins USA PSS Insourcing Solutions

West Point, PA • On-site

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

This job post has expired today. Applications are no longer accepted.

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 laboratories work with the biggest companies in the world to ensure the products they supply are safe, their ingredients are authentic and labelling is accurate.

The Eurofins network of companies is the global leader in food, environment, pharmaceutical and cosmetic product testing and in agroscience Contract Research Organisation services. It 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. It also has a rapidly developing presence in highly specialised and molecular clinical diagnostic testing and in-vitro diagnostic products.

In over 30 years, Eurofins has grown from one laboratory in Nantes, France to 58,000 staff across a decentralised and entrepreneurial network of 900 laboratories in over 54 countries. Eurofins companies offer a portfolio of over 200,000 analytical methods to evaluate the safety, identity, composition, authenticity, origin, traceability and purity of biological substances and products.

In 2021, Eurofins generated total revenues of EUR 6.72 billion, and has been among the best performing stocks in Europe over the past 20 years.

Job Description
  • Perform lab-scale downstream processing of vaccine adjuvant & Lipid Nanoparticle (LNP) products and process intermediates
  • Perform assays on vaccine adjuvant & LNP products, process intermediates, and related experimental samples using biochemical/analytical tests
  • Prepare solutions/reagents
  • Set-up process equipment for lab-scale experiments
  • Maintain records and experimental results following good manufacturing practices (GMP)
Qualifications

Minimum Qualifications:

  • Bachelor's degree in Engineering with 8+ years of industry experience or Masters in Engineering with 6+ years of industry experience or PhD in Engineering with 2+ years of industry experience.
  • Authorization to work in the United States indefinitely without restriction or sponsorship

The Ideal Candidate would possess:

  • Experience with adjuvant and LNP process unit operations including Extrusion, Tee-mixing, Multi-Inlet-Vortex-Mixing (MIVM), Homogenization/Microfluidization, Filtration, Tangential Flow Filtration (TFF)
  • Scale up experience related to liposome and LNP formation unit ops including, but not limited to, Extrusion, Teemixing, Microfluidization/Homogenization
  • Experience handling potent compound lipids (OEB4 & 5) and working in isolators and Ventilated Booth Enclosures (VBEs)
  • Strong computer, scientific, and organizational skill
  • Excellent communication (oral and written) and attention to detail
  • Ability to work independently and as part of a team, self-motivation, adaptability, and a positive attitude
  • Ability to learn new techniques, perform multiple tasks simultaneously, keep accurate records, follow instructions, and comply with company policies
  • Proven ability to work independently in hands-on laboratory setting

Additional Information

Position is full-time and permanent, Monday-Friday, 8am-5pm with over time as needed. Candidates currently living in a commutable distance to West Point, PA are encouraged to apply. On-site work is expected in order to be effective in this role.

  • 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

Eurofins USA PSS Insourcing Solutions is a Disabled and Veteran Equal Employment Opportunity employer.

Apply