Sr. Assistant Scientist Job in Parsippany, New Jersey US

Order no :PWR5824

Title:  :Sr. Assistant Scientist/ Lab Analyst

Location: Parsippany - NJ

Duration: 1 Year

 

Job Description:

 

·         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.

·         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 Sr. Assistant Scientist : 3 – 6 yrs relevant experience with BS, 5 yrs with AS Sr. Assistant Scientist: 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.