- 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
The ideal candidate would possess:
- Hands-on experience in HPLC, CAD, GC, Karl Fisher, Empower
- Strong computer, scientific, and organizational skills
- Excellent communication (oral and written) and attention to detail
- Ability to work independently and as part of a team, self-motivation, adaptability, and a positive attitude
- Ability to learn new techniques, perform multiple tasks simultaneously, keep accurate records, follow instructions, and comply with company policies
Basic Minimum Qualifications:
- Experience with method development and validation with HPLC
- Bachelor's degree in Analytical Chemistry, Biochemistry, Pharmaceutical Science or related discipline
- 3-5 years of contract laboratory/research or relevant industry experience
- Authorization to work in the United States indefinitely without restriction or sponsorship
- 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.
- Position Salary Range- $55,000- $70,000 based on education/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 is a M/F, Disabled, and Veteran Equal Employment Opportunity and Affirmative Action employer.
