Scientist

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Job description

MON-FRI 8:30AM-5:00PM - ONSITE POSITION - DURATION - THREE - SIX MONTHS.

Perform Finish product Testing (Stability, development), QC release and data review.

Perform, Assay, related substances, KF, Dissolution, disintegration, Hardness.

Work on lab instruments (HPLC/GC/UPLC, KF, Dissolution, Hardness, disintegration).

Perform test and report data as per the Catalent approved procedures.

Analyst will follow the internal methods, SOPs, procedures, monographs to perform the testing.

Work on DEA controlled substance.

Conduct Laboratory investigation using the TrackWise system following SOPs and Procedures.

Perform Opex activities, data trending, SOPs revisions, as assigned.

The Scientist reports to the Quality Control & Analytical Product Development, Manager/Senior Scientist/Principal Scientist. The Scientist will be performing routine analysis of Finish products using laboratory techniques and instrumentation such as HPLC, Dissolution, Karl Fisher, pH meter. Analyst will perform Assay, Content Uniformity, Blend Uniformity, Moisture testing, related substances, dissolution on finish product.

Analyst will test In Process and FP samples and test stability samples at different ICH conditions.

Our Somerset location is the corporate headquarters for . This location houses our state-of-the-art laboratory, clinical, commercial manufacturing plant for oral dose forms in addition to be the Center of Excellence for Highly Potent Active Pharmaceutical Ingredients.

The Role

• Under the supervision of other Scientists, carry out activities in support of the manufacturing of pharmaceutical products. These activities include in-process testing, finished product testing, sample analysis, and physical evaluation of products.

• Conduct experiments which includes scope from R&D to clinical and commercial release

• Perform Assay/Related Substances, Karl Fisher, Dissolution, Hardness, Disintegration etc.

• Instrumentation techniques: HPLC,GC, UPLC, Dissolution, UV, KF

• Assist other Scientists, as necessary for timely project completion and support other lab personnel as required.

• Follow regulatory guidelines, SOPs, cGMPs and Laboratory procedures.

• All other duties as assigned.

The Candidate

• Bachelor of Science in Analytical Chemistry/Pharmaceutics with equivalent industry experience

• Master of Science in Analytical Chemistry/Pharmaceutics preferred

• 3 or more years of applicable industry experience in support of pharmaceutical product development

• Expertise in Instrumentation techniques: HPLC, GC, FTIR, UV, KF, and other wet chemistry testing.

• Experience with GMP and ICH regulations

• Requires excellent written and verbal communication

• Candidate must be comfortable in a fast-paced work environment

• Mathematical and reasoning ability

• Ability to interpret a variety of instructions furnished in written, oral, diagram, or schedule form.

• Ability to work effectively under pressure to meet deadlines.

• Individual may be required to sit, stand, walk regularly and occasionally lift 0-15 pounds.

EEO:

"Mindlance is an Equal Opportunity Employer and does not discriminate in employment on the basis of - Minority/Gender/Disability/Religion/LGBTQI/Age/Veterans."

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