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Laboratory Analyst

Integrated Resources Inc

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.

Vacancy posted 4 days ago
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