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:

• Hands-on experience in HPLC, GC, PCR, Mass Spec, LC/MC
• 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:

• Bachelor's degree in Analytical Chemistry, Biochemistry, Pharmaceutical Science or related discipline
• 5-7 years of contract laboratory/research or relevant industry experience
• 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.

• 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.

EUROFINS IS A M/F, DISABLED, AND VETERAN EQUAL EMPLOYMENT OPPORTUNITY AND AFFIRMATIVE ACTION EMPLOYER.