What are the responsibilities and job description for the HPLC QC Chemist - 247994 position at Medix™?
Join the GMP analytical lab of a growing CDMO team in Cranbury, NJ.
The QC Chemist will conduct GMP quality control analytical product testing for release, stability etc. as well as method development and validation for a range of products, primarily oral solid dosage pharmaceuticals.
Position is Contract-to-Hire.
Job Duties:
- Perform HPLC, Karl Fischer, GC (gas chromatography), Dissolution, moisture and other analytical testing for routine and non-routine analyses of raw materials, in-process materials, environmental samples, product release, and stability samples.
- Participate in analytical method development and method validation.
- Participate in assay development and assay validation.
- Troubleshoot analytical methods and equipment, including HPLC.
- Peer-review laboratory records.
- Conduct deviation investigations as needed.
- Collaborate with peers and leadership on expanding, developing, and continuously improving the Analytical lab procedures and workflows.
Qualifications:
- Bachelor’s of Science Degree with 3-8 years of analytical (HPLC) GMP testing experience.
- Ability to independently run HPLC and Karl Fischer testing.
- Quality control analytical testing including product release testing, stability, etc.
- Helpful / Preferred: to have experience with HPLC troubleshooting, method validation and method development
- Excellent written and verbal communication skills including ability to author SOPs and Work Instructions.
Please note, visa sponsorship is not available for this opening at this time.
Salary : $35 - $41