Analytical Development Testing Group Scientist
About The Position
The work we do at Eurofins Professional Scientific Services matters, and so do our employees. At Eurofins PSS, we put a focus on your professional growth. We provide our employees the ability to break into the biopharmaceutical industry and grow from the bottom up. We have the supportive teams and tools available to invest in you while also affording you work-life balance and a competitive benefits package. 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 works with the biggest companies in the world to ensure the products they supply are safe, their ingredients are authentic and labelling is accurate. Eurofins believes it is a global leader in food, environmental, pharmaceutical and cosmetics products testing and in agroscience CRO services. It is also one of the global independent market leaders in certain testing and laboratory services for genomics, discovery pharmacology, forensics, CDMO, advanced material sciences and in the support of clinical studies. If you’re looking for a rewarding career, a place to call home, apply with us today! Contributes as part of a team of AD scientists towards the execution of various analytical methods to support biological therapeutic product release and characterization testing in a compliance-based environment. Independently performs routine testing, such as but not limited to ELISA, Potency, Activity, HCP, qPCR assays - using established test methods, including associated protocol/report documentation and presentations. Conducts work in compliance with cGMP/GLP, safety, and regulatory requirements. Responsible for working on other non-lab-based tasks from time to time if assigned. Demonstrate independent judgment in technique and method selection, protocol and study design and execution, data analysis, and use of standard practices and procedures for a variety of problems of moderate scope and complexity to meet assigned objectives. Demonstrate troubleshooting capabilities. Responsible for the maintenance of lab equipment and participating in general lab upkeep. Occasional weekend work may be required to passage cells.
Requirements
- Candidate must have a Bachelor degree’s in Cell and Molecular Biology and Biochemistry with a minimum of 2 years of demonstrated work experience with plate-based assays like Binding ELISA and/or cell based assays
- Clear understanding of the concepts of the plate-based assays such as binding ELISA and cell-based cytotoxicity/ potency, their application to the pharmaceutical industry for Biologics, and proficiency with basic statistics.
- Ability to learn and cross-train on new techniques, perform multiple tasks simultaneously, keep accurate records, follow instructions, and comply with company policies.
- Excellent communication (oral and written), strong organizational skills and attention to detail
- Ability to work independently and as part of a team, self-motivation, adaptability, and a positive attitude
- Authorization to work in the United States indefinitely without restriction or sponsorship.
Nice To Haves
- Master’s degree is a plus, should demonstrate experience with plate-based assays via thesis/published literature and course-work.
- Experience with troubleshooting plate-based and cell-based assays
- Prior experience using software like SoftMax Pro and PLA.
- Experience with flow cytometer is a plus.
Responsibilities
- Contributes as part of a team of AD scientists towards the execution of various analytical methods to support biological therapeutic product release and characterization testing in a compliance-based environment.
- Independently performs routine testing, such as but not limited to ELISA, Potency, Activity, HCP, qPCR assays - using established test methods, including associated protocol/report documentation and presentations.
- Conducts work in compliance with cGMP/GLP, safety, and regulatory requirements.
- Responsible for working on other non-lab-based tasks from time to time if assigned.
- Demonstrate independent judgment in technique and method selection, protocol and study design and execution, data analysis, and use of standard practices and procedures for a variety of problems of moderate scope and complexity to meet assigned objectives.
- Demonstrate troubleshooting capabilities.
- Responsible for the maintenance of lab equipment and participating in general lab upkeep.
- Occasional weekend work may be required to passage cells.
Benefits
- comprehensive medical coverage, dental, and vision options
- Life and disability insurance
- 401(k) with company match
- Paid vacation and holiday
- Yearly goal-based bonus & eligibility for merit-based increases
Stand Out From the Crowd
Upload your resume and get instant feedback on how well it matches this job.
What This Job Offers
Job Type
Full-time
Career Level
Entry Level
Number of Employees
5,001-10,000 employees
