Downstream Process Development Engineer at Eurofins

Upper Gwynedd Township, Pennsylvania, United States -

Full Time

Start Date

Immediate

Expiry Date

16 Sep, 26

Salary

0.0

Posted On

18 Jun, 26

Experience

2 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

Skills

Purification, Filtration, Column Chromatography, HPLC, FPLC, TFF, Centrifugation, Membrane Filtration, GMP, Downstream Processing, Biochemical Testing, Analytical Testing

Industry

Medical and Diagnostic Laboratories

Description

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 Employee Responsibilities: Perform lab-scale downstream processing of vaccine products and process intermediates Perform assays on vaccine products, process intermediates, and related experimental samples using biochemical/analytical tests Prepare solutions/reagents Set-up process equipment for lab-scale experiments Maintain records and experimental results following good manufacturing practices (GMP) Qualifications Bachelor's degree in Engineering with 2 years of industry experience or Masters in Engineering Authorization to work in the United States indefinitely without restriction or sponsorship The Ideal Candidate would possess: Experience with Purification and Filtration, Column Chromatography, HPLC, FPLC, TFF, Centrifugation, Membrane Filtration Strong computer, scientific, and organizational skill Excellent communication (oral and written) and attention to detail Ability to work independently and as part of a team, self-motivation, adaptability, and a positive attitude Ability to learn new techniques, perform multiple tasks simultaneously, keep accurate records, follow instructions, and comply with company policies Proven ability to work independently in hands-on laboratory setting Additional Information Position is full-time and permanent, Monday-Friday, 8am-5pm with over time as needed. Candidates currently living in a commutable distance to West Point, PA are encouraged to apply. On-site work is expected in order to be effective in this role. 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.

Responsibilities

Perform lab-scale downstream processing and biochemical assays on vaccine products and intermediates. Maintain detailed experimental records in compliance with Good Manufacturing Practices (GMP).