United Pharma Technologies Inc
We are seeking a skilled Analytical Chemist to support laboratory testing activities within a regulated pharmaceutical environment. The ideal candidate will have hands‑on experience with analytical techniques, GMP documentation, and pharmaceutical testing to support product development, release, and stability programs.
Key Responsibilities
Perform routine and non‑routine analytical testing of raw materials, in‑process samples, and finished pharmaceutical products
Execute testing using techniques such as HPLC, GC, UV‑Vis, FTIR, Dissolution, Karl Fischer, and related methods
Support method validation, verification, and transfer activities per ICH guidelines
Conduct stability testing and maintain stability chambers as required
Prepare, review, and maintain GMP‑compliant documentation, including test results, protocols, and reports
Investigate OOS, OOT, and deviations, and support CAPA activities
Follow SOPs, cGMP, FDA, and data integrity requirements
Maintain laboratory instruments, logs, and calibration records
Support audits and inspections as needed
Required Qualifications
Bachelor’s degree in Chemistry, Analytical Chemistry, or related scientific discipline
2–5+ years of experience in an analytical laboratory within the pharmaceutical or biotech industry
Strong hands‑on experience with HPLC (mandatory)
Working knowledge of cGMP, GLP, USP, ICH, and FDA regulations
Experience with laboratory documentation and electronic systems (LIMS preferred)
Strong attention to detail and data integrity
Preferred / Nice‑to‑Have
Experience with method development and validation
Exposure to stability programs
Experience with LC‑MS or GC‑MS
Familiarity with regulatory inspections and audits
Seniority level
Mid‑Senior level
Employment type
Contract
Job function
Pharmaceutical Manufacturing
Location: Salt Lake City Metropolitan Area Salary: $32.00–$42.00
#J-18808-Ljbffr
Key Responsibilities
Perform routine and non‑routine analytical testing of raw materials, in‑process samples, and finished pharmaceutical products
Execute testing using techniques such as HPLC, GC, UV‑Vis, FTIR, Dissolution, Karl Fischer, and related methods
Support method validation, verification, and transfer activities per ICH guidelines
Conduct stability testing and maintain stability chambers as required
Prepare, review, and maintain GMP‑compliant documentation, including test results, protocols, and reports
Investigate OOS, OOT, and deviations, and support CAPA activities
Follow SOPs, cGMP, FDA, and data integrity requirements
Maintain laboratory instruments, logs, and calibration records
Support audits and inspections as needed
Required Qualifications
Bachelor’s degree in Chemistry, Analytical Chemistry, or related scientific discipline
2–5+ years of experience in an analytical laboratory within the pharmaceutical or biotech industry
Strong hands‑on experience with HPLC (mandatory)
Working knowledge of cGMP, GLP, USP, ICH, and FDA regulations
Experience with laboratory documentation and electronic systems (LIMS preferred)
Strong attention to detail and data integrity
Preferred / Nice‑to‑Have
Experience with method development and validation
Exposure to stability programs
Experience with LC‑MS or GC‑MS
Familiarity with regulatory inspections and audits
Seniority level
Mid‑Senior level
Employment type
Contract
Job function
Pharmaceutical Manufacturing
Location: Salt Lake City Metropolitan Area Salary: $32.00–$42.00
#J-18808-Ljbffr