QC Analytical Chemist - Night Shift

Eurofins PSS Insourcing Solutions

City of Albany (NY)

On-site

USD 33,000 - 43,000

Full time

6 hours ago

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Benefits offered by this job

Comprehensive medical coverage, dental

Vision options

Life and disability insurance

401(k) with company match

Paid vacation and holidays

Yearly goal-based bonus & merit-based

Job summary

Eurofins PSS Insourcing Solutions is hiring a QC Analytical Chemist to support GMP testing of pharmaceutical in-process, raw materials, intermediates, APIs, and stability samples. The role includes investigations of invalid results and method transfer activities, requiring high attention to detail and strong organizational skills.

The candidate will work with techniques such as LC, NMR, GC, ICP-OES, IR, RI, UV-Vis, and TGA, while following GMP/ICH guidelines. US work authorization is required.

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: NMR, GC, ICP-OES, IR, RI, UV-Vis, TGA
Knowledge and in-depth understanding of GMPs, ICH, and 21 CFR guidelines
Authorization to work in the United States indefinitely without restriction or sponsorship
Preferred Qualifications: At least a year of GMP experience

Responsibilities

Conduct testing and review in accordance with approved methods, specifications, protocols, and compendial requirements
Follow 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, Titration, TGA, and more
Reference standard qualification and management
Elemental impurities and residual solvent testing and review

Education

BS in Chemistry / Pharmaceutical Sciences / Life Sciences or related degree

MS in Chemistry / Pharmaceutical Sciences / Life Sciences or related degree

Tools

Conductivity

Titration

NMR

ICP-OES

UV-Vis

TGA

Job description

The work we do at Eurofins Professional Scientific Services matters, and so do our employees. At Eurofins PSS, we put a focus on your professional growth. We provide our employees the ability to break into the biopharmaceutical industry and grow from the bottom up. We have the supportive teams and tools available to invest in you while also affording you work-life balance and a competitive benefits package.

Eurofins Scientific is an international life sciences company, providing a unique range of analytical testing services to clients across multiple industries, to make life and our environment safer, healthier and more sustainable. From the food you eat, to the water you drink, to the medicines you rely on, Eurofins works with the biggest companies in the world to ensure the products they supply are safe, their ingredients are authentic and labelling is accurate. Eurofins believes it is a global leader in food, environmental, pharmaceutical and cosmetics products testing and in agroscience CRO services. It is also one of the global independent market leaders in certain testing and laboratory services for genomics, discovery pharmacology, forensics, CDMO, advanced material sciences and in the support of clinical studies.

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