Upstream Process Scientist - Ambr250 (Weekends)

Eurofins USA PSS Insourcing Solutions • Malvern, PA

14d

About The Position

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 organizing 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 organization 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 organized laboratory notebooks Comply with cGMP practices Analyze and present data in professional format Demonstrate clear and professional verbal and written communication. Follow appropriate SOPs and all internal documentation requirements We are considering this role for either a Tuesday-Saturday or Sunday-Thursday 9:00am-5:00pm shift.

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

Responsibilities

• 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 organizing 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 organization 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 organized laboratory notebooks
• Comply with cGMP practices
• Analyze and present data in professional format
• Demonstrate clear and professional verbal and written communication.
• Follow appropriate SOPs and all internal documentation requirements

Benefits

• 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

What This Job Offers

• Job Type: Full-time
• Career Level: Mid Level
• Number of Employees: 5,001-10,000 employees