Laboratory Analyst

• 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.

• Candidates MUST HAVE 3+ years with relevant pharmaceutical experience.

• Candidates MUST be able to complete an initial 1 year Project based assignment.

• Extension past this time is probable but not guaranteed.

• Some OT may be required and will be paid.

• No Travel required.

• All work to be performed onsite in Parsippany.

• 3 – 6 yrs. relevant experience with Bachelor's Degree, 5+ yrs. with Associate's Degree;

• Good working knowledge of dissolution and reverse phase 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.

Thanks

Warm Regards

Ricky Bansal