- 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 :
- Bachelors degree in chemistry (or other science related degree concentration) with 2 years of industry experience or Masters 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-4pm. Candidates must be flexible to adapt to schedule changes requiring 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 Lancaster Laboratories Professional Scientific Services (PSS) is a global award-winning insourcing solution that places our people at our clients sites dedicated to running and managing laboratory services while eliminating headcount co-employment and project-management worries.
We infuse our 55-year track record of scientific and laboratory operations expertise as well as HR and a great place to work best practices to recruit hire train and manage highly qualified scientists to perform laboratory services using our clients quality systems and equipment.
To learn more about Eurofins Lancaster Laboratories please explore our website .
Eurofins USA PSS Insourcing Solutions is a Disabled and Veteran Equal Employment Opportunity employer.
Remote Work :
No
Employment Type :
Full-time