Job Description

• Perform various type of testing using chromatographic systems, HPLC, GC, IC
• 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

Qualifications

-Minimum Required: Bachelors, Science discipline
-Chromatography Experience: BS: 4+ years; MS: 2 years
-Familiarity with United States Pharmacopeia testing requirements and techniques preferred
-Experience with HPLC and GC analysis, with ability to maintain and troubleshoot instruments
-Ability to author reports/investigations and execute protocols with limited support
-Capable of generating scientifically valid data in accordance with GMP practices
-Ability to work autonomously on projects after training is completed is essential

Additional Information

Position is full-time, Monday - Friday 8:30am - 5pm. Candidates currently living within a commutable distance of Jacksonville, FL 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.