Analytical Chemist

  • location: Parsippany, NJ
  • type: Contract
  • salary: $21.83 - $25.68 per hour
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job description

Analytical Chemist

job summary:
  • Working with some supervision, applies established knowledge of laboratory techniques such as HPLC, dissolution, moisture by KF, GC, TLC, and others to perform pharmaceutical product stability testing
 
location: Parsippany, New Jersey
job type: Contract
salary: $21.83 - 25.68 per hour
work hours: 9 to 5
education: Bachelors
 
responsibilities:
  • Candidate will be responsible for understanding and performing routine analytical testing for stability samples, evaluating and documenting results in a timely manner.
  • Understands and follows all SOPs and written test procedures.
  • Performs testing within established standard test times and maintains quality and productivity at acceptable levels as communicated by the supervisor.
  • Candidate will execute troubleshooting of instrumentation and will be expected to maintain laboratory equipment in good working condition.
  • Candidate will perform laboratory investigation steps with appropriate approvals and with guidance from supervisor.
  • Candidate will understand the investigation process and begin to assist in preparation of laboratory investigation documents.
  • Keeps supervisor fully informed of all results and project status on a daily basis and reports critical information in a timely manner.
  • Should have some ability to multi-task.
  • Will be expected to perform other tasks as assigned by the supervisor (e.g. assist other colleagues with laboratory investigations, training of other analysts as assigned.
 
qualifications:
  • 3 - 6 yrs relevant experience with Bachelor's Degree, 5+ yrs with Associate's Degree
  • Good working knowledge of dissolution and chromatographic techniques, especially HPLC, is necessary and a requirement.
  • Working knowledge of both computer and/or data handling acquisition systems is necessary and required. Candidate must have good oral and written communication skills. cGMP experience is required.
  • Previous pharmaceutical, quality control / stability experience preferred.
  • Ability to work in a fast-paced environment
 
skills: HPLC, SOP, Analytical Chemistry, GMP (Good Manufacturing Practice)
Equal Opportunity Employer: Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status.

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