QC Analytical Chemist - 2nd Shift

Eurofins

City of Albany (NY)

On-site

USD 29,000 - 48,000

Full time

4 days ago
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Benefits offered by this job

Medical coverage
Dental coverage
Vision options
Life insurance
401(k) with match
Paid vacation

Job summary

Eurofins USA PSS Insourcing Solutions is seeking a QC Analytical Chemist to support GMP testing of in-process materials, raw materials, intermediates, APIs, and stability samples. The role includes investigations of invalid results and method transfer activities.

The position requires a BS or MS in Chemistry or related field with GMP/GLP experience, 1 year of LC/Conductivity/Titration experience, and familiarity with multiple analytical techniques.

Qualifications

  • BS in Chemistry/Pharmaceutical Sciences or Life Sciences with GMP/GLP testing experience
  • MS in Chemistry/Pharmaceutical Sciences or Life Sciences with at least 6 months GMP/GLP experience
  • At least 1 year of industry experience with LC, Conductivity, and Titration
  • Experience using at least two of the listed analytical techniques/instruments
  • Knowledge of GMPs, ICH, and 21 CFR guidelines
  • Ability to work in the United States without sponsorship or restrictions

Responsibilities

  • Conduct testing and review per approved methods and compendial requirements
  • Follow GMP regulations and ICH guidelines
  • Test samples (in-process, raw materials, intermediates, APIs, stability)
  • Participate in method transfer, qualification, and verification
  • Support investigations for OOS, OOT, and invalid results
  • Utilize analytical techniques (NMR, GC, LC, ICP-OES, IR, RI, UV-Vis, TGA)
  • Reference standard qualification and management
  • Perform elemental impurities and residual solvent testing and review

Skills

LC testing
Titration
NMR/GC/ICP-OES
GMP/ICH knowledge
US work authorization

Education

BS in Chemistry/Pharma
MS in Chemistry/Pharma (optional)

Tools

NMR
GC
LC
ICP-OES
IR
RI
UV-Vis
TGA

Job description

Eurofins PSS is currently hiring for a QC Analytical Chemist to support GMP testing of pharmaceutical in-process, raw materials, intermediates, APIs, and stability samples. In addition, the successful candidate will support investigations of invalid results and method transfer activities. This individual will have high attention to detail and possess excellent organizational skills.

Key Responsibilities:
  • Conduct testing and review in accordance with approved methods, specifications, protocols, and compendial requirements
  • Follow protocols for GMP regulations, including 21 CFR Parts 210 and 211, and applicable ICH guidelines
  • Testing of pharmaceutical samples including in-process, raw materials, intermediates, API, stability, and more.
  • Participate in method transfer, qualification, and verification studies
  • Support investigations for OOS, OOT, and invalid results
  • Utilize various analytical techniques including: NMR, GC, LC, ICP-OES, IR, RI, UV-Vis, Conductivity, Specific Rotation, Titration, TGA, and more
  • Reference standard qualification and management
  • Elemental impurities and residual solvent testing and review
Basic Minimum Qualifications:
  • BS in Chemistry, Pharmaceutical Sciences, Life Sciences, or related degree with at least a year of GMP/GLP testing experience; OR MS in Chemistry, Pharmaceutical Sciences, Life Sciences, or related degree with at least 6 months of industry GMP/GLP testing experience
  • At least a year of industry experience with Liquid Chromatography (LC), Conductivity, and Titration
  • Proven experience utilizing at least two of the following techniques and/or instruments: Nuclear Magnetic Resonance (NMR), Gas Chromatography (GC), Inductively Coupled Plasma Optical Emission Spectroscopy (ICP-OES), Infrared Spectroscopy (IR), Refractive Index (RI), Ultraviolet-Visible (UV-Vis), Thermogravimetric Analysis (TGA)
  • Knowledge and in-depth understanding of GMPs, ICH, and 21 CRF guidelines
  • Authorization to work in the United States indefinitely without restriction or sponsorship
Preferred Qualifications:
  • At least a year of GMP experience

This position is a permanent, full-time role with overtime as needed. Candidates currently living within a commutable distance of Albany, NY are encouraged to apply. The position will work 6pm-6am on a rotating schedule (Sunday, Monday, Tuesday - 36 hours & Wednesday, Thursday, Friday - 48 hours).

Excellent full-time benefits include:
  • Comprehensive medical coverage, dental, and vision options
  • Life and disability insurance
  • 401(k) with company match
  • Paid vacation and holidays
  • Eligibility for yearly goal-based bonus & merit-based increases
  • Compensation: $21.50-$34.75 per hour (plus a 10% 2nd shift differential) based on education and related experience

Eurofins USA PSS Insourcing Solutions is a Disabled and Veteran Equal Employment Opportunity employer.

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