Upstream Process Scientist - Ambr250 (Sun-Thurs)

Eurofins

Malvern (Chester County)

On-site

USD 90,000 - 130,000

Full time

5 days ago
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Benefits offered by this job

Life insurance
Disability insurance
401(k) with company match
Paid vacation and holidays

Job summary

Eurofins Upstream Process Scientist position in Malvern, PA, focuses on Ambr250-based development for large molecule products within the API-Proteins group. The role emphasizes protocol-driven cell culture work and bioreactor operation, with data recording and compliant documentation.

The candidate should have a Bachelor's or Master's in biopharmaceutical fields and hands-on upstream process development experience, plus US work authorization.

Qualifications

  • Bachelor's or Master's degree in biopharmaceutical, biotechnology or pharmaceutical is required.
  • Broad knowledge in upstream process development and hands-on experience is required.
  • Authorization to work in the United States indefinitely without restriction or sponsorship is required.

Responsibilities

  • Perform upstream process development utilizing the Ambr250 system for large molecule products within the API-Proteins group.
  • Perform duties in protocol-driven work, such as cell culture, and running Ambr bioreactors.
  • Support lab work associated with development and scale-up projects within the API-Proteins area.
  • Organize records, capture results into data sheets, and contribute to technical reports in a team or individual setting to meet timelines.
  • Assist with general lab upkeep and waste disposal of large-scale cell culture/bioreactors.
  • Conduct, analyze and report data in accordance with department requirements.
  • Record experimental data and maintain organized lab notebooks.
  • Comply with cGMP practices and internal documentation.

Skills

Upstream process development
Ambr250 operation

Education

Bachelor's or Master's degree in biopharmaceutical, biotechnology or pharmaceutical

Job description

Upstream Process Scientist - Ambr250 (Sun-Thurs)

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.

  • Perform Upstream process development utilizing the Ambr250 Satorius system for large molecule based products within the API-Proteins group
  • Perform duties in a protocol-driven work, such as cell culture, and running Ambr bioreactors
  • Supporting lab work associated with development and scale-up projects within the API-Proteins area
  • Responsible for organising records, capturing results into data sheets, and contributing to technical reports in a team environment as well as contributing individually to meet project timeline and objectives
  • Assist with general lab upkeep and organisation efforts, which includes decontamination and disposal of large-scale cell culture/bioreactor wastes
  • Conduct, analysis and reporting of data in accordance with requirements set forth by the department
  • Record experimental data and accurate and highly organised laboratory notebooks
  • Comply with cGMP practices
  • Analyse and present data in professional format
  • Demonstrate clear and professional verbal and written communication.
  • Follow appropriate SOPs and all internal documentation requirements
  • Bachelors or Master’s degree in biopharmaceutical, biotechnology or pharmaceutical required
  • Broad knowledge in upstream process development and hands‑on experience
  • Authorization to work in the United States indefinitely without restriction or sponsorship

This position is Full-Time, Sun‑Thurs, 8am-5pm. Candidates currently living within a commutable distance of Malvern, PA 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

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

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