Eurofins USA BioPharma Services
Job Description
Perform various type of testing using chromatographic systems, Karl Fischer (Coulometric and Volumetric), UV/Spec, various wet chemistry analyses, HPLC, IC, IR, ICP, AA, TGP, DSC, PDA, auto-titrators, TLC, and dissolution apparatus
Execute specialized analyses and method transfer and feasibility testing
Document work as required for GMP compliance
Perform tests accurately
Troubleshoot method and instrumentation problems
Use office and instrumentation specific computer software
Produce written reports (e.g., SOP, OMC, client reports)
Develop and execute validation plans
Carry out method transfers and feasibility studies
Train technical staff
Some travel to client sites for technical meetings could be required
Qualifications: Qualifications
The Ideal Candidate would possess:
1-2 years of transferable laboratory experience
Experience using EMPOWER and HPLC in industry
Experience with validation in industry
_
Minimum Qualifications: _
Bachelor's or Master's degree in chemistry or other related degree concentration, or equivalent directly-related experience (two years of directly related industry experience is equivalent to one full-time year of college in related major)
3 years
related pharmaceutical experience in a cGMP environment
Authorization to work in the United States indefinitely without restriction or sponsorship
Additional Information
Position is full-time, Monday-Friday 8am-5pm. Candidates within a commutable distance of Lancaster, PA are encouraged to apply.
Excellent full-time benefits including:
Comprehensive medical coverage, dental, and vision options.
Life and disability insurance
401(k) with company match
Paid vacation and holidays
Eurofins USA BioPharma Services is a Disabled and Veteran Equal Employment Opportunity employer.
Perform various type of testing using chromatographic systems, Karl Fischer (Coulometric and Volumetric), UV/Spec, various wet chemistry analyses, HPLC, IC, IR, ICP, AA, TGP, DSC, PDA, auto-titrators, TLC, and dissolution apparatus
Execute specialized analyses and method transfer and feasibility testing
Document work as required for GMP compliance
Perform tests accurately
Troubleshoot method and instrumentation problems
Use office and instrumentation specific computer software
Produce written reports (e.g., SOP, OMC, client reports)
Develop and execute validation plans
Carry out method transfers and feasibility studies
Train technical staff
Some travel to client sites for technical meetings could be required
Qualifications: Qualifications
The Ideal Candidate would possess:
1-2 years of transferable laboratory experience
Experience using EMPOWER and HPLC in industry
Experience with validation in industry
_
Minimum Qualifications: _
Bachelor's or Master's degree in chemistry or other related degree concentration, or equivalent directly-related experience (two years of directly related industry experience is equivalent to one full-time year of college in related major)
3 years
related pharmaceutical experience in a cGMP environment
Authorization to work in the United States indefinitely without restriction or sponsorship
Additional Information
Position is full-time, Monday-Friday 8am-5pm. Candidates within a commutable distance of Lancaster, PA are encouraged to apply.
Excellent full-time benefits including:
Comprehensive medical coverage, dental, and vision options.
Life and disability insurance
401(k) with company match
Paid vacation and holidays
Eurofins USA BioPharma Services is a Disabled and Veteran Equal Employment Opportunity employer.