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
- Apply GMP/GLP in all areas of responsibility, as appropriate
- Applies the highest quality standard in all areas of responsibility
- Demonstrates and promotes the company vision
- Demonstrates strong client service skills, teamwork, and collaboration
- Proactively plans and multitasks to maximize productivity
- Meets all quality and productivity metrics and demonstrates strong teamwork and collaboration
- Regular attendance and punctuality
- Experience with cGMP practices
- Supporting lab work associated with development and scale-up projects within the large molecule group
- Demonstrate a working experience with aseptic technique
- Perform duties in a protocol-driven work, such as passaging and sampling cell cultures, and running Ambr bioreactors,
- Use analytical instruments to monitor bioreactors
- Assist with general lab upkeep and organization efforts, which includes decontamination and disposal of large scale cell culture wastes
- 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.
- Occasional weekend work might be required. Analyze and present data in professional format;
- Demonstrate clear and professional verbal and written communication;
- Conduct, analysis and reporting of data in accordance with requirements set forth by the department;
- Ensure maintenance of detailed documentation of assay development and qualification;
- Record experimental data and accurate and highly organized laboratory notebooks;
- Follow appropriate SOPs and all internal documentation requirements.
Qualifications
- Broad knowledge in upstream process development and hands-on experience is desired.
- Bachelors or Master’s degree in biopharmaceutical, biotechnology or pharmaceutical required.
Additional Information
Position is full-time, Tuesday-Saturday 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.
