About this role
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 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.
In over just 30 years, Eurofins has grown from one laboratory in Nantes, France to over 47,000 staff across a network of more than 900 independent companies in over 50 countries and operating more than 800 laboratories. Eurofins offers a portfolio of over 200,000 analytical methods to evaluate the safety, identity, composition, authenticity, origin, traceability and purity of biological substances and products, as well as providing innovative clinical diagnostic testing services, as one of the leading global emerging players in specialised clinical diagnostics testing
If you’re looking for a rewarding career, apply with us today!
Job Description
- Using GC-MS, LC-MS, and/or ICP-MS to support commercial and clinical testing of extractables and leachables for pharmaceutical manufacturing following all pertinent protocols and standard operating procedures (SOPs).
- Generate, compile, and process complex data.
- Reviews test results to ensure compliance with standards; reports any quality anomalies.
- Use processed and historical data to support conclusions and author technical summary documents of test results.
- Calibrates or verifies calibration of instruments/devices prior to use.
- Troubleshooting instrumentation and lab techniques when appropriate.
- Comply with all pertinent regulatory agency requirements.
- Follows all current cGxP (e.g. good manufacturing processes, good documentation practices, etc.)
- Participates in required training activities as both trainee and trainer.
- Maintains laboratory supplies, safety, and compliance.
- Interacts with outside vendors and/or functional peer groups in a professional manner.
- May assist in validation of methods
- Excellent communication (oral and written) and attention to detail.
- Ability to work independently and as part of a team, self-motivated, adaptability, and a positive attitude
- Ability to learn new techniques, perform multiple tasks simultaneously, keep accurate records, follow instructions, and comply with company policies
Qualifications
- Bachelor’s degree in chemistry (or other science related degree concentration) with 2+ years of industry experience, or Master's degree with any industry experience
- Experience in GC-MS, LC-MS, and/or ICP-MS
- Experience operating inside of a GMP lab space
- Strong computer, scientific, and organizational skills
- Experience writing and reviewing detailed technical documents
- Experience with an electronic laboratory information management system
- Authorization to work in the United States indefinitely without restriction or sponsorship
Additional Information
What to Expect in the Hiring Process:
- 10-15 Minute Phone Interview with Region Recruiter
- 45-60 Minute Virtual Interview with Manager and/or Group Leader
- 30 Minute Virtual Interview with Site Director
Additional Details:
The position is full-time, first shift, Monday-Friday from 8am-4:30pm. Candidates must be flexible to adapt to schedule changes that may require shift changes and/or weekend work, and overtime may be required as needed. Candidates living within a commutable distance of Rensselaer, New York, 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
- Pay is between 25.50-27.50 per hour
Eurofins USA PSS Insourcing Solutions is a Disabled and Veteran Equal Employment Opportunity employer.
Other facts
About Eurofins
It’s so much more than a specimen. It's a life.
With over 30 years of specialized expertise in infectious disease, immunology, transplant, and allergy testing for immunocompromised and critical patients, Eurofins Viracor is committed to helping medical professionals, transplant teams, reference labs and biopharmaceutical companies get results faster, when it matters most.
Eurofins Viracor is passionate about providing timely, actionable test results, never losing sight of the connection between the testing we perform and the patients our results ultimately serve.
Find out more by visiting us at www.eurofins-viracor.com/clinical
Eurofins Viracor is an equal opportunity employer.
What you'll do
- The role involves using analytical techniques such as GC-MS, LC-MS, and ICP-MS to support testing of extractables and leachables in pharmaceutical manufacturing. Responsibilities include data generation, compliance review, instrument calibration, and maintaining laboratory safety and supplies.
Ready to join Eurofins?
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