Scientist, Data Review

About the role

The Quality Assurance Associate position is an entry-level position involved in day-to-day activities in a laboratory setting under prescribed processes (protocols, standard operating procedures, methods, etc.).

Responsibilities

• Review scientific reports under cGMP guidelines to ensure regulatory requirements have been met, the data is whole and accurate, and the report is of high quality.
• Affixing to internal audits.
• Working closely with lab operations staff on a day-to-day basis and having the authority and responsibility for final report sign-off.
• Performing other duties as assigned.

Qualifications

• Experience in a laboratory setting or GMP pharmaceutical setting.
• Good organizational skills; ability to follow direction and good communication skills are required.
• 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.

Benefits

• Full-time position, Monday - Friday 8:00am - 4:30pm.
• Candidates currently living within a commutable distance of Columbia, MO 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.