QC Analytical Chemist

Eurofins US Network

City of Albany (NY)

On-site

USD 32,000 - 40,000

Full time

9 days ago

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Benefits offered by this job

Comprehensive medical coverage

Dental and vision options

401(k) with company match

Paid vacation and holidays

Job summary

Eurofins Professional Scientific Services in Albany, NY is seeking a QC Analytical Chemist to support GMP testing of pharmaceutical in-process, raw materials, intermediates, APIs, and stability samples. The role requires attention to detail, organization, and reliability.

The position involves method transfer, investigations of invalid results, and collaboration with cross-functional teams. It offers full-time hours, rotating shift patterns, and eligible benefits in a fast-paced lab environment.

Qualifications

BS in Chemistry, Pharmaceutical Sciences, Life Sciences, or related degree with at least a year of GMP/GLP testing experience
At least a year of industry experience with LC, Conductivity, and Titration
Proven experience utilizing NMR, GC, ICP-OES, IR, RI, UV-Vis or 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

Responsibilities

Conduct testing and review in accordance with approved methods, specifications, protocols and compendial requirements
Follow GMP protocols, 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

Skills

GMP/GLP testing

LC chromatography

Education

BS in Chemistry/Pharma/Life Sciences

Tools

NMR

ICP-OES

UV-Vis

TGA

Job description

Albany, NY, USA

Full-time

Company 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

Qualifications

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

Additional Information

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 6am-6pm on a rotating schedule - the following shifts are available: