About this role
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 methodsExcellent communication (oral and written) and attention to detail.Ability to work independently and as part of a team, self-motivated, adaptability, and a positive attitudeAbility to learn new techniques, perform multiple tasks simultaneously, keep accurate records, follow instructions, and comply with company policies Bachelor’s degree in chemistry (or other science related degree concentration) with 2+ years of industry experience, or Master's degree with any industry experienceExperience in GC-MS, LC-MS, and/or ICP-MSExperience operating inside of a GMP lab spaceStrong computer, scientific, and organizational skillsExperience writing and reviewing detailed technical documentsExperience with an electronic laboratory information management systemAuthorization to work in the United States indefinitely without restriction or sponsorship What to Expect in the Hiring Process:
10-15 Minute Phone Interview with Region Recruiter45-60 Minute Virtual Interview with Manager and/or Group Leader30 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 optionsLife and disability insurance401(k) with company matchPaid vacation and holidayYearly goal-based bonus & eligibility for merit-based increasesPay is between 25.50-27.50 per hourEurofins USA PSS Insourcing Solutions is a Disabled and Veteran Equal Employment Opportunity employer.