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Aurolife Pharma LLC

Analytical Chemist, QC

Post Date:May 19, 2017Type:Full-Time
Start Date:5/19/2017Salary:
Location:US-NJ-Dayton, NJ 08810 Job Reference:
Skills:

JOB SUMMARY

Associate Chemist will perform a variety of QC testing to assess the strength, identity and purity of test samples and/or materials. The Associate Chemist will work as a member of team to effectively plan and QC analytical testing using established (official and/or in-house) test procedures. The Associate Chemist may execute 95% - 100% of their work at the bench level. 


  1. 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.
  2. Independently plan and make adequate inventory of test reagents and solutions to perform work, assure supplies are ordered as needed to perform assigned work.
  3. Independently plan and execute testing to meet established time lines. Perform complicated testing with supervisory direction.
  4. Record data and results as specified in documentation procedures. Document work clearly and perform tests accurately.
  5. Prepare and/or Review Test Procedures, SOPs, and Protocols as assigned.
  6. Perform maintenance and calibrations on laboratory instruments/equipments with supervisory direction/training.
  7. Perform troubleshooting and investigations under the direction of a supervisor/senior QC chemist.
  8. 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. 



  1. 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.
  2. Independently plan and make adequate inventory of test reagents and solutions to perform work, assure supplies are ordered as needed to perform assigned work.
  3. Independently plan and execute testing to meet established time lines. Perform complicated testing with supervisory direction.
  4. Record data and results as specified in documentation procedures. Document work clearly and perform tests accurately.
  5. Prepare and/or Review Test Procedures, SOPs, and Protocols as assigned.
  6. Perform maintenance/minor repairs and calibrations on laboratory instruments/equipment with supervisory direction/training.
  7. 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. 

OTHER FUNCTIONS AND RESPONSIBILITIES

Perform other related duties as required and/or assigned.


QUALIFICATIONS REQUIRED
  • Minimum BS with Scientific field, Chemistry preferable
  • Minimum 1-3 years QC experience (GLP) pharmaceuticals, OTC and/or generic preferred
  • Experience with instrumental techniques (HPLC, GC, UV-Vis, and other routine QC instruments and CG) a must.
  • Ability to learn quickly
  • Preparation IQ,OQ and Protocols
  • Preparation of Calibration procedures
  • Perform minor repairs  of analytical equipment




Job Description:


A fantastic opportunity at Aurolife Pharma, LLC., a subsidiary of Aurobindo Pharma USA, Inc!

Aurolife Pharma, LLC is the manufacturing division of Aurobindo Pharma, a rapidly growing family of companies, with a consistent standing in the top 10 list of generic pharmaceutical companies, and ranked 6th among pharmaceutical companies based on Total Prescriptions Dispensed.

Not only have we received more ANDA approvals than any of our competitors, we have the lowest turnover rate of 2%, compared to an average if 19.2% among healthcare employers. 

An exciting opportunity to join our Research and Development team as a Formulation Scientist working on some of the industry's highest prescribed products. 

Pharmaceutical experience in the generic field is a strong requirement. All candidates are urged to review the requirements prior to the submission of their resume.






Contact Information
Aurolife Pharma LLC
Name: Elena Tolstikova
Ph: (732) 796-8702


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