Company Information: Located in Clifton, New Jersey, CS Analytical is an FDA regulated testing laboratory that specializes in container and package testing for the pharmaceutical, biotechnology and medical device industries. Please visit to learn more about the services we perform.

Position Overview:  Working in an FDA regulated Laboratory that adheres to a strict quality system, you will work as a quality department associate alongside some of the world’s leading experts on Container and Package Testing. In this support role under the supervision of the Director of Quality, you will assist with all administrative and functional tasks in support of the laboratory. Examples of expected work include data review of laboratory workflows, drafting of reports using MS Word, MS Excel and other word processing software, management of quality specific procedures and processes that support the efficient operation of the laboratory.

Desired Skill Set:             

  1. Previous work experience in a cGMP Laboratory setting. Direct experience working in a quality role is a plus.
  2. A science oriented educational background or previous experience working in a science related field.
  3. Good computer skills to include MS suite of products (Word and Excell).
  4. Be a good team player that interacts well with co-workers and enjoys working in  a fast-paced, but pleasant work setting.

This is NOT a remote position – You will be working onsite at our Clifton, NJ facility

This position is ideal for a local (Clifton) person that is looking for a flexible part-time professional position of for someone who has been out of the workforce and looking to return to work at this time.

Expectations are a minimum of approximately 20 hours weekly, scheduled 5 days per week / 4 hours per day. Work hours each day are flexible between 8am -6pm

To Apply, please send a cover letter and resume to CAREERS@CSANALYTICAL.COM