QC Analytical Chemist - 3rd Shift

LabRulez

City of Albany (NY)

On-site

USD 49,000 - 62,000

Full time

14 hours ago

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Benefits offered by this job

Comprehensive medical coverage

Dental and vision options

Life and disability insurance

401(k) with company match

Paid vacation and holidays

Yearly goal-based bonus

Merit-based increases

Job summary

Eurofins PSS is hiring a QC Analytical Chemist to support GMP testing of pharmaceutical in-process, raw materials, intermediates, APIs, and stability samples in Albany. You will ensure accuracy, follow GMP/ICH guidelines, and assist with investigations.

Requires 3+ years GMP/GLP experience, LC/Conductivity/Titration, and proficiency with NMR, GC, ICP-OES, IR, RI, UV-Vis, RI, and TGA. Excellent organizational skills and attention to detail are essential.

Qualifications

BS in Chemistry or Life Sciences with 3+ years GMP/GLP testing experience.
MS in Chemistry, Life Sciences, or related field with 1+ years GMP/GLP testing experience.
At least 1 year of industry LC, Conductivity, and Titration experience.
Experience with NMR, GC, ICP-OES, IR, RI, UV-Vis, or TGA.
Knowledge of GMPs, ICH, and 21 CFR guidelines.

Responsibilities

Conduct testing and review per approved methods, specifications, protocols, and compendial requirements.
Follow GMP regulations, including 21 CFR Parts 210 and 211, and applicable ICH guidelines.
Test pharmaceutical samples including in-process, raw materials, intermediates, API, stability.
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, TGA.

Skills

GMP/GLP testing experience

Liquid Chromatography (LC)

NMR

ICP-OES

UV-Vis

Titration

ICH guidelines

21 CFR Part 210/211 knowledge

Education

Bachelor's degree in Chemistry or Life Sciences

Master's degree in Chemistry or Life Sciences

Tools

NMR

ICP-OES

UV-Vis

TGA

Job description

Analytical chemist, Quality Control (QC), Spectroscopy, Liquid chromatography, Gas chromatography, AAS, ICP/OES, ICP/MS, NMR, Molecular spectroscopy UV-Vis, RAMAN, FTIR

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.

In over 35 years, Eurofins has grown from one laboratory in Nantes, France to 61,000 staff across a decentralised and entrepreneurial network of ca. 900 laboratories in 61 countries. Eurofins companies offer a portfolio of over 200,000 analytical methods to evaluate the safety, identity, composition, authenticity, origin, traceability and purity of biological substances and products.

In 2025, Eurofins generated total revenues of EUR 7.296 billion, and has been among the best performing stocks in Europe over the past 20 years.

QC Analytical Chemist - 3rd Shift

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 3+ years of GMP/GLP testing experience; OR MS in Chemistry, Pharmaceutical Sciences, Life Sciences, or related degree with 1+ years 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

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 10:00pm-8:30am and the following shifts are available:

Excellent full-time benefits include: