Product Safety Labs (PSL) was established in 1972 and over the years has built a tradition of serving Sponsors with outstanding values and unique services which leads to strong relationships.  This is all driven by our talented group of leaders. 

PSL is led by an experienced team that is dedicated to the pursuit of meeting our Sponsors' needs while continuing to maintain operational excellence.  Each member of the team brings experience and wealth of industry knowledge that continues to set PSL apart from the competition.  Collectively, the team contributes to the three key service areas - Toxicology, Pharmacology and Analytical Chemistry.

GENERAL  DESCRIPTION:

To fulfill the requirements for provision of Quality Assurance (QA) functions as outlined in FDA and EPA Good Laboratory Practice (GLP) standards.

QUALIFICATIONS:

QA auditors will have experience in a laboratory regulated by FDA/EPA GLP standards.  Experience in other quality standards such as cGMP or GCP will also be considered. 

Experience with acute toxicology, analytical chemistry, and/or general laboratory procedures is preferred.  B.S. degree in biology, toxicology, animal science or related field and/or AALAS certification at the Technician level is also preferred.  Experience in computer system validation and electronic data capture is desirable but is not required.

The individual holding this position must be of the highest integrity and have a very strong sense of responsibility.  Attention to detail is essential.  He/she must be well organized, tactful, be able to work independently and maintain all records, documents, and schedules associated with quality assurance procedures and studies.  Communication skills, especially written, are necessary.  Proficiency with MSWord and Excel is required. 

SPECIFIC RESPONSIBILITIES:

• Assist in performance of all Quality Assurance functions as outlined in the GLPs and PSL SOPs. Assist the Quality Assurance Director as needed during inspections by EPA, FDA or clients.  Prepare records and assemble copies of documents requested by inspectors when advance notice is given and Sponsor and/or Laboratory Director approval is obtained. 
• Conduct in-process study inspections and general facility inspections in the toxicology and chemistry laboratories as directed.
• Audit raw data and proofread report and tables against raw data for accuracy and for typing corrections.  Audit final report to verify corrections.
• Amend and update Standard Operating Procedures as required using word processing system. File all QAU-related paperwork as directed.
• Select intervals for inspection for any regulatory test under the auditor's responsibility or as directed by QA Director, Laboratory Director, or President.  Perform such inspections in accordance with the test schedule.  When the time for conduct of intervals requiring inspection falls outside of normal working hours, this will be brought to the attention of the Study Director or QA Director in order that a suitable arrangement may be made. 
• Ability to safely wear a respirator required.
• Other duties as assigned.

ACCOUNTABILITY: Director of Quality Assurance

Position is full-time, Monday - Friday first shift, weekends and holidays as needed.  Candidates currently living within a commutable distance of Dayton, NJ 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

PSL is a M/F, Disabled, and Veteran Equal Employment Opportunity and Affirmative Action employer.