Medix™
This range is provided by Medix™. Your actual pay will be based on your skills and experience — talk with your recruiter to learn more.
Base pay range $35.00/hr - $41.00/hr
Recruitment Advisor, National Life Sciences 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.
Seniority level
Mid-Senior level
Employment type
Contract
Job function
Quality Assurance, Manufacturing, and Science
Industries
Pharmaceutical Manufacturing and Biotechnology Research
Referrals increase your chances of interviewing at Medix™ by 2x.
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Base pay range $35.00/hr - $41.00/hr
Recruitment Advisor, National Life Sciences 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.
Seniority level
Mid-Senior level
Employment type
Contract
Job function
Quality Assurance, Manufacturing, and Science
Industries
Pharmaceutical Manufacturing and Biotechnology Research
Referrals increase your chances of interviewing at Medix™ by 2x.
#J-18808-Ljbffr