Job Description

• 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 :**

• Bachelor's 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.