- 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.
Remote Work :
No
Employment Type :
Full-time
Perform various type of testing using chromatographic systems HPLC GC ICExecute specialized analyses and method transfer and feasibility testingDocument work as required for GMP compliancePerform tests accuratelyTroubleshoot method and instrumentation problemsUse office and instrumentation specific ...
- 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.
Remote Work :
No
Employment Type :
Full-time
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