Job description

Company Description
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.

Job Description
Supervise and assist in the conduct of regulatory studies performed at Product Safety Labs (PSL).

Responsibilities include:

 Supervise study conduct.
 Assist in protocol development, design and implementation.
 Responsibilities as stated in GLP regulations.
 Data interpretation and report writing.
 Client liaison

Management Responsibilities:

• Overall, day-to-day laboratory operation including supervision of technical staff assigned to your studies.
• Scheduling and coordinating initiation and conduct of studies.
• Ensure that the study schedule and financial aspects of each study that you are responsible for are accurately tracked on a regular basis.

Technical Responsibilities:
Overall responsibility for the technical conduct of all studies and interpretation, analysis, documentation and reporting of results. Specifically:

• Establish test protocols and corresponding SOP's.
• Develop experimental design and supervise implementation of experiments (tests).
• Obtain sponsor approval of protocols and institute any necessary deviations from the test protocol with sponsor approval.
• Ensure all experimental data is properly recorded and that observations of unanticipated responses of the test system are accurately recorded and verified.
• Ensure tests are conducted in accordance with the test protocol and SOP.
• Supervise conduct of all phases of the study, including participation in study conduct.
• Ensure that GLP regulations are followed.
• Interpretation, calculation, analysis, documentation and reporting of results.
• Instruct, train and supervise scientists in all procedures.
• Maintain liaison with sponsors, advising them of test results; and assisting with protocol development.
• Maintain liaison with regulatory agencies in conjunction with: test protocols, and past or present studies submitted for regulatory approval, compliance with GLP's and appropriate test guidelines.
• Ability to safely wear a respirator required
• Any other duties assigned.

Qualifications

• At least a Bachelor of Science degree or equivalent experience in a field related to their area of responsibility (e.g., toxicology, animal science, chemistry, biology, microbiology).
• Intimate working familiarity and/or ability to quickly learn and develop such familiarity with all government regulations dealing with testing particularly EPA, FDA, DOT, OECD, and GLP regulations in addition to ISO standards.
• Hands-on working knowledge of the tests that will be under their responsibility.
• Good administrative skills and leadership ability. Must communicate effectively and write well.

Additional Information
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.

Job Type: Full-time

Benefits:

• 401(k)
• 401(k) matching
• Dental insurance
• Health insurance
• Life insurance
• Paid time off
• Vision insurance

Schedule:

• 8 hour shift
• Day shift
• Monday to Friday

Ability to commute/relocate:

• Township of South Brunswick, NJ 08810: Reliably commute or planning to relocate before starting work (Required)

Application Question(s):

• Do you have previous GLP experience working with animals?

Work Location: In person

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