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Pharmaceutical Process Development Jobs in Pennsylvania

Merck & Co.

D. in Chemical Engineering, Biochemistry, Pharmaceutical Sciences, or a related scientific ... process development.Deep expertise spanning the full product lifecycle, from early development ...

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Pharmaceutical Process Development information

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.

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 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.
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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, 77% Full Time, 19% Part Time, 2% Contract, and 1% Nights. Highlights an 91% Physical, 3% Hybrid, and 6% Remote job distribution.

Gene Therapy Drug Product Development Scientist

Eurofins Scientific

Philadelphia, PA • On-site

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Posted 20 days ago

Eurofins rating

7.4

Company rating: 7.4 out of 10

Based on 180 frontline employees who took The Breakroom Quiz

69th of 120 rated laboratories

Job description

Company Description

The work we do at Eurofins Professional Scientific Services matters, and so do our employees. At Eurofins PSS, we put a focus on your professional growth. We provide our employees the ability to break into the biopharmaceutical industry and grow from the bottom up. We have the supportive teams and tools available to invest in you while also affording you work-life balance and a competitive benefits package.

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 believes it is a global leader in food, environmental, pharmaceutical and cosmetics products testing and in agroscience CRO services. It is also one of the global independent market leaders in certain testing and laboratory services for genomics, discovery pharmacology, forensics, CDMO, advanced material sciences and in the support of clinical studies.

If you're looking for a rewarding career, a place to call home, apply with us today!

Job Description

Eurofins PSS is seeking a Drug Product Formulation Scientist to permanently work at a client site to support drug product formulation, biophysical characterization, and process development for gene therapy research. The successful employee will thrive in a high throughput environment, working with small-scale drug product manufacturing process development and scale-up activities.

Position Responsibilities:

  • Drug product formulation, delivery, and process development activities in support of AAV gene therapy research in a small-scale manufacturing facility
  • Utilize biophysical characterization techniques, administration, and instrumentation
  • Analytical characterization via operation and troubleshooting of HPLC, HIAC, HALO, and other instrumentation on raw materials and drug products
  • Collaborate with multiple teams throughout study timeline
  • Data analysis, interpretation, reporting, and presentation
Qualifications

Basic Minimum Qualifications:

  • BS in a life sciences discipline (Biology, Molecular Biology, Pharmaceutical Sciences, etc.) with at least 2 years of pharmaceutical industry experience working in drug product formulation development.
  • Must have experience with a mixture of biophysical characterization techniques (XRD, DLS, DSC, etc.) and analytical techniques (HPLC, ELISA, etc.)
  • Ability to understand and follow report protocols and coordinate with multiple cross-functional teams
  • Must be eligible to work in the United States indefinitely without restriction or sponsorship

Preferred Qualifications:

  • Experience with HIAC and HAOL is highly preferred
Additional Information

The position is full-time, first shift, Monday-Friday with overtime as needed. Candidates living within a commutable distance of Philadelphia, PA are encouraged to apply.

Excellent full-time benefits include:

  • 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.

What Eurofins employees say

Pay

Benefits

Hours and flexibility

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About Eurofins

Sourced by ZipRecruiter

Industry

Scientific research and development services, biotechnology research and development and environmental consulting services

Company size

10,000+ Employees

Headquarters location

Leacock, PA, US

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