- Develop qualify and validate analytical test methods for drug product intermediates and excipients
- Design and execute analytical development studies
- Write analytical method validation protocols and reports
- Write and maintain applicable SOPs
- Provide analytical support to QC Process Engineering and Manufacturing as applicable
- Perform externally generated data review
- Assist in development stability study design and protocol writing
- Assist management during regulatory inspections and internal audits
Qualifications :
The ideal candidate would possess:
- Experience with variety of analytical techniques method development and validation
- Hands-on experience in HPLC GC LCMS and GCMS is a plus
- Ensure adherence to highest quality and efficiency standards in laboratory operations
- Excellent communication (oral and written) and attention to detail
- Capability to work well on a team and be able to troubleshoot and problem solve in cross functional team setting
- Independently engage and collaborate with coworkers customers and management
- 1-5 years of contract laboratory/research or relevant industry experience is a plus
Basic Minimum Qualifications:
- Bachelors degree in biology biochemistry chemistry or other related degree concentration
- Authorization to work in the United States indefinitely without restriction or sponsorship
Additional Information :
Position is full-time Monday - Friday 8:00am - 5:00pm. Candidates currently living within a commutable distance of San Diego CA are encouraged to apply.
Pay range: $27.50/h - $31.5/h depending on related experience.
- 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
Develop qualify and validate analytical test methods for drug product intermediates and excipientsDesign and execute analytical development studiesWrite analytical method validation protocols and reportsWrite and maintain applicable SOPsProvide analytical support to QC Process Engineering and Manufa...
- Develop qualify and validate analytical test methods for drug product intermediates and excipients
- Design and execute analytical development studies
- Write analytical method validation protocols and reports
- Write and maintain applicable SOPs
- Provide analytical support to QC Process Engineering and Manufacturing as applicable
- Perform externally generated data review
- Assist in development stability study design and protocol writing
- Assist management during regulatory inspections and internal audits
Qualifications :
The ideal candidate would possess:
- Experience with variety of analytical techniques method development and validation
- Hands-on experience in HPLC GC LCMS and GCMS is a plus
- Ensure adherence to highest quality and efficiency standards in laboratory operations
- Excellent communication (oral and written) and attention to detail
- Capability to work well on a team and be able to troubleshoot and problem solve in cross functional team setting
- Independently engage and collaborate with coworkers customers and management
- 1-5 years of contract laboratory/research or relevant industry experience is a plus
Basic Minimum Qualifications:
- Bachelors degree in biology biochemistry chemistry or other related degree concentration
- Authorization to work in the United States indefinitely without restriction or sponsorship
Additional Information :
Position is full-time Monday - Friday 8:00am - 5:00pm. Candidates currently living within a commutable distance of San Diego CA are encouraged to apply.
Pay range: $27.50/h - $31.5/h depending on related experience.
- 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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