Upstream Process Development Scientist (Sunday-Thursday)

SmartRecruiters, Inc.; Malvern (Chester County); On-site; USD 90,000 - 130,000; Full time

Benefits offered by this job

Medical, dental, vision coverage

Life and disability insurance

401(k) with company match

Paid vacation and holidays

Job summary

Eurofins Scientific is seeking an Upstream Process Development Scientist (Sunday-Thursday) to lead development, optimization, and scale-up of upstream bioprocesses for biologics, vaccines, or related products. The role collaborates with Manufacturing, Analytical Sciences, and Quality to ensure robust processes and regulatory compliance.

The candidate will design studies, analyze data, and drive process improvements, with a focus on cell culture and bioreactor operations.

Qualifications

• Excellent communication skills (oral and written).
• Strong computer, scientific, and organizational skills.
• Ability to work independently and as part of a team; self-motivation and adaptability.

Responsibilities

• Design, develop, optimize, and scale upstream bioprocesses (cell culture, bioreactor operations).
• Plan and execute studies to improve growth, productivity, and product quality.
• Analyze data and identify critical process parameters for scale-up and tech transfer.
• Collaborate with Manufacturing, Analytical Sciences, Quality, and Process Engineering.
• Author/review study protocols, reports, SOPs, and regulatory documents.
• Troubleshoot deviations and implement corrective actions; support continuous improvement.
• Foster a collaborative, team-oriented work environment.

Skills

Communication skills (oral & written)

Computer and scientific skills

Teamwork and independence

Self-motivation and adaptability

Education

Bachelor's or Master’s Degree in Chemical Engineering or related

Advanced degree in Biotechnology/Biology/Chemistry/related

Tools

eLN

Job description

Upstream Process Development Scientist (Sunday-Thursday)

• Full-time

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.

The Upstream Process Development Scientist is responsible for the development, optimization, characterization, and scale-up of upstream bioprocesses supporting the production of biologics, vaccines, cell therapies, or other biotechnology products. This role applies scientific expertise in cell culture, fermentation, media development, and bioreactor operations to improve process performance, product quality, and manufacturing efficiency. The scientist collaborates closely with cross-functional teams, including Process Development, Manufacturing, Analytical Sciences, and Quality, to support technology transfer, process validation, and commercial manufacturing activities. The position requires strong technical knowledge, data analysis capabilities, and a commitment to maintaining compliance with applicable quality and regulatory standards. This role may also contribute to continuous improvement initiatives, troubleshooting efforts, and the implementation of innovative bioprocess technologies.

Essential Duties and Responsibilities

• Design, develop, optimize, and scale upstream bioprocesses, including mammalian cell culture, and bioreactor operations, to support research, clinical, and commercial manufacturing objectives.
• Plan and execute process development studies to improve cell growth, productivity, product quality, and overall process robustness using sound scientific and engineering principles.
• Analyze experimental data, and identify critical process parameters to support process understanding, scale-up, and technology transfer activities.
• Collaborate with cross-functional teams, including Manufacturing, Analytical Sciences, Quality, and Process Engineering, to advance development programs and support manufacturing operations.
• Author and review study protocols, technical reports, process descriptions, regulatory documentation, and standard operating procedures (SOPs) in compliance with applicable quality standards.
• Troubleshoot process deviations and technical challenges, implement corrective actions, and support continuous improvement initiatives to enhance process performance and operational efficiency.
• Foster a collaborative, engaged, and team-oriented work environment

Required Education, Experience, Skills and Certifications

• Bachelor's or Master’s Degree in Chemical Engineering, Biochemical Engineering, Biotechnology, Biology, Biochemistry, Microbiology, Pharmaceutical Sciences, or related scientific discipline.
• Excellent communication skills (oral and written)
• Strong computer, scientific, and organizational skills
• Ability to work independently and as part of a team, self-motivation, adaptability, and a positive attitude

Preferred Education, Experience, Skills and Certifications

• Advanced degree in Biotechnology, Biology, Chemistry, Biochemistry, or a related scientific discipline.
• Familiar with cell passaging including vial thaw, inoculation and harvest processes for 5L and 10L bioreactors.
• Certified Biomanufacturing Professional (CBP)
• Lean Six Sigma Green Belt or Black Belt
• GMP or Bioprocess Manufacturing Training Certification
• Proficient with recording data via eLN, following SOPs and validation reports.
• Familiar with GMP and GLP standards.

Work Authorization Requirements

• Must be authorized to work in the USA indefinitely without restrictions

This position is Full-Time,Sunday-Thursday8am-5pm. Candidates currently living within a commutable distance of Malvern, PAare 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

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

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