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Associate Chemist
Ref No.: 18-33503
Location: Dayton, New Jersey
Position Type:Contract
Shift:Second
Job Category:Manufacturing/Operations
Benefits:Medical Insurance
HIRING AN ASSOCIATE CHEMIST
Client Location: Dayton, NJ
***TEMP TO PERM POSITION
Shift: 8:30 am - 5 pm Monday - Friday
Pay Rate: Based on Experience

Description:

Chemist-A will perform a variety of QC testing to assess the strength, identity and purity of test samples and/or materials. The Chemist-A will work as a member of team to effectively plan and QC analytical testing using established (official and/or in-house) test procedures. The Chemist-A may execute 95% - 100% of their work at the bench level.
  • Involve in complete life cycle of Laboratory Information and Management Software (LIMS) implementation, and day-to-day support
  • Perform assigned sampling, physical, chemical tests and assay on raw materials, active pharmaceutical ingredients, in-process, finished and stability products, using various wet chemicals, physical and instrumental techniques (HPLC, GC, UV-Vis, IR, Particle Size Analyzer, KF Autotitrator, Bulk Density, and other routine QC instruments) as per as per USP monograph / In-house / any other Compendial monographs.
  • Independently plan and make adequate inventory of test reagents and solutions to perform work, assure supplies are ordered as needed to perform assigned work
  • Independently plan and execute testing to meet established time lines. Perform complicated testing with supervisory direction.
  • Record data and results as specified in documentation procedures. Document work clearly and perform tests accurately
  • Prepare and/or Review Test Procedures, SOPs, and Protocols as assigned
  • Prepare the Method Transfer/Method verification protocols. Execution of the method transfer/validation/verification activities and reports preparation.
  • Perform the testing activity of all Exhibit batch's required raw materials (Active/inactive/Packaging materials), finished product dosage forms and stability sample testing
  • Provide the necessary document to Support for the ANDA filing
  • Perform maintenance/minor repairs and calibrations on laboratory instruments/equipment with supervisory direction/training.
  • Perform troubleshooting and investigations under the direction of a supervisor/senior QC chemist.
  • Comply with all regulatory/in-house requirements (may include but not limited to safety, house keeping, laboratory chemical waste, cGMP, cGLP, documentation) when performing the assigned activity.
Qualifications:
  • Minimum BS with Scientific field
  • BS with Chemistry is one of the subjects would be preferable
  • Minimum 2 –3 years QC experience in pharmaceuticals preferable
  • QC experience in Generic Pharmaceutical industries would be preferable
  • Ability to learn quickly


To Apply for immediate consideration please send resume to Michael Estaris at Michael.Estaris@onboardusa.com and reference job #18-33503 in the Subject Line and indicate the best times to contact you (please include nights and weekends if needed).
**Candidates must complete background and drug screenings before starting any assignment.
On-Board Services provides equal employment opportunities (EEO) to all employees and applicants for employment without regard to race, color, religion, sex, national origin, age, disability or genetics.