Chemist I, II, III

Irvine Pharmaceutical Services, Inc., a fully cGMP compliant contract testing laboratory, provides expert analytical testing services for the Pharmaceutical, Biotechnology and Medical Device industries. For more information, please visit our website, http://www.irvinepharma.com/.

 

R&D Chemist: Hands-on experience using analytical instrumentation including HPLC, GC, UV within a cGMP

environmentOrganize, coordinate, and execute project assignments and interpret results in a timely manner

within a cGMP environmentMethod development and validation experience  is a plusPlan and execute laboratory experiments, technical activities, and professional services in a timely

manner while coordinating all necessary resourcesExperience in one or more of these instruments are required: HPLC, GC, UV

 

Biopharma Chemist:Hands-on experience using analytical instrumentation including HPLC, LC/MS, ELISA, CE, Gel

Electrophoresis, and PCROrganize, coordinate, and execute project assignments and interpret results in a timely manner

within a cGMP environmentExperience with Biopharmaceutical analysis, analytical method development and validation for

proteins and peptides, as well as dosage form design, including lyophilized and non-lyophilized

inject able dosage forms, and capsule and tablet dosage form is highly desirable. Experience in one

  or more of these instruments are required.

 

QC Chemist:Perform wet chemistry and analytical testing utilizing HPLC, GC, AA, UV-Vis, and other lab

instrumentsOrganize, coordinate, and execute project assignments and interpret results in a timely manner

within a cGMP environmentExperience in one or more of these instruments are required: HPLC, GC, AA and UV-Vis Good comprehension of USP, EP and other compendial methods and procedures is required

 

Stability Chemist:Perform testing of drug products using wet chemistry techniques and instrumental analysis including

HPLC, UV Spectrophotometer, and Gas ChromatographyOrganize, coordinate and execute project assignments and interpret results in a timely manner within

  a cGMP environmentAnalyze raw material using USP/NF/FCC testing methodsSignificant knowledge with cGMP regulatory requirements and ICH guidelines are required (especially

ICH guidelines for stability studies) Experience in one or more of these instruments are required: HPLC, UV Spectrophotometer, and Gas

Chromatography

 

Inhalation Chemist: Perform testing of inhalation/nasal products within a cGMP environmentOrganize, coordinate and execute project assignments and interpret results in a timely mannerAssist with troubleshooting instruments and methodsExhibit an understanding of cGMP regulatory requirements, ICH guidelines, and inhalation testing

  requirement USP

 

 

Requirements: B.S. Degree with a minimum of 2+ years hands-on experience using analytical instrumentationKnowledge of GMP and regulatory issues relevant to product development (FDA, ICH, USP)Must be proactive, creative, willing to learn (quickly), well-organized, a team player, and able to

  work independentlyPossess excellent communication skills

 

For Consideration:

Please apply your resume with salary history and a brief outline of your skills and greatest achievements in the body of the email. Due to volume of resumes we receive, only those selected for interviews will be contacted.