Analytical Support Scientist at Eurofins

St. Louis, Missouri, United States -

Full Time

Start Date

Immediate

Expiry Date

12 May, 26

Salary

0.0

Posted On

11 Feb, 26

Experience

2 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

Skills

Sample Management, Mechanical Force Testing, Component Characterization, Data Compilation, Report Authoring, Laboratory Support, Biotherapeutics Development, HPLC, CGE, iCE, Spectroscopy, ISO Test Methods, Regulatory Compliance, Data Verification, Electronic Laboratory Notebooks, General Maintenance

Industry

Medical and Diagnostic Laboratories

Description

Company Description 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! Job Description This is a laboratory-based position performing sample management, mechanical force testing, and other component/material characterization testing. Furthermore, this position may assist in data compilation, data presentations, report authoring, and department documentation support. RESPONSIBILITIES: The responsibilities of this position include, but are not limited to: Work closely with other engineers in the evaluation, development, qualification and implementation of new components and container closure systems Support the formulation and process development groups to comply with regulatory requirements and guidance documents related to components and container closure systems Author and/or review engineering and development documentation such as component drawings, specifications, assembly drawings, tolerance stack analyses, risk analyses, etc. Execute designated test methods and protocols associated with component/device Provide general laboratory support, including ordering/replacement of reagents and consumables, general maintenance of equipment, continuous improvement activities, and participating in periodic lab inspections. This position will be responsible for preparing data summary presentations, providing data verification support, compiling data, and using lab-based systems for data collection such as electronic laboratory notebooks. Flexibility in support of additional biotherapeutics development activities including biophysical & biochemical characterization using techniques such as HPLC Capillary Gel electrophoresis (CGE), Imaged Capillary Electrophoresis (iCE) Spectroscopy techniques, light obscuration, microflow imaging Qualifications Minimum Qualifications: Bachelor's Degree or higher in appropriate Science & Engineering disciplines, e.g. Chemistry, Biochemistry; Biomedical etc. A minimum of 2+ years relevant experience with the Pharmaceutical Parenteral Packaging Development Authorization to work in the United States indefinitely without restriction or sponsorship Preferred Qualifications: • Familiarity with eLN, Bluehill Software, ISO test methods, including ISO 11040 and ISO 80369, US/EP Pharmacopoeia and other standards, regulations and guidance associated with components, container closure systems and drug delivery devices. • Strong computer skills and experience with lab-based computer systems • Familiarity with standard biotherapeutics analytical techniques such as HPLC, CGE, iCE, Spectroscopy Additional Information Position is Full Time, Monday-Friday, 8am-5 pm. Candidates currently living within a commutable distance of Saint Louis, MO are encouraged to apply Excellent full-time benefits include: 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 Eurofins USA PSS Insourcing Solutions is a Disabled and Veteran Equal Employment Opportunity employer.

Responsibilities

The role involves performing sample management and mechanical force testing, as well as assisting in data compilation and report authoring. The position also includes supporting the evaluation and development of new components and container closure systems.