Qualifications: Minimum of a High School diploma and 6 months to one year experience.
Strong competence using Microsoft Word and Excel especially with various
formatting features preferred. Must be detail oriented, well organized with
exceptional communication skills. Ability to review documents for long
periods of time and recognize errors.
? Adherence to laboratory health and safety
? Adherence to Standard Operating Procedures (SOPs)
? Adherence to applicable company policies and guidelines
? Adherence to federal and/or local regulations as applicable
This position will be primarily responsible for reviewing all laboratory documents, records and
logs for accuracy and adherence to SOPs, GLP guidelines, and established laboratory policies.
? Reviews run folders, notebooks and other study documentation.
? Keep detailed documentation of noted QC findings for each document reviewed.
? Assure that all QC findings and deviations are corrected and/or addressed in a timely manner
and consistent with good documentation practices and SOPs.
? Assure that all run folders move through the internal process including QAU in sufficient time
to meet client timelines.
? Work as a liaison between support groups as assigned.
? Strong organizational skills.
? Effectively communicate with lab personnel or Project Managers to resolve any discrepancies,
? Other duties as assigned.
? Knowledge of GLP.
? Ability to multi-task and participate in multiple studies concurrently.
? Ability to produce high quality data while working under the pressure of strict deadlines.
? Overtime and weekend work as required.
? Work may require the use of PPE (personal protective equipment).
Attention To Detail
Personal Protective Equipment
Product Quality Assurance