QC Analytical Chemist - III

sgs-job-4564

Scientific
 New York
GMP
cGMP
Quality Control
Analytical Testing
HPLC
GC
UV-Visible Spectroscopy
LIMS
Wet Chemistry
Pharmaceutical
Biopharmaceutical
Empower
Documentation
SOPs
Regulatory Compliance

Contract - 06 Months Contract + (Highest possibilities of contract extension)

Location (mandatory): Pearl River, NY 10965 (On-site) Quality Control Chemist supports a GMP-regulated Quality Control laboratory environment focused on pharmaceutical and biopharmaceutical products. This role involves performing routine analytical testing, documenting results in electronic systems, and supporting the release and stability testing of highly regulated products. The successful candidate will work in a collaborative team environment while maintaining compliance with cGMP requirements and established laboratory procedures.

Job Responsibilities:

  • Perform laboratory testing of: Raw materials Drug substances Drug products In-process samples Stability samples
  • Raw materials
  • Drug substances
  • Drug products
  • In-process samples
  • Stability samples
  • Conduct routine wet chemistry and analytical testing using laboratory instrumentation, including: HPLC GC UV-Visible Spectroscopy CGE ICE Polarimeter Osmometer pH Meter Conductivity Meter TOC Analyzer
  • HPLC
  • GC
  • UV-Visible Spectroscopy
  • CGE
  • ICE
  • Polarimeter
  • Osmometer
  • pH Meter
  • Conductivity Meter
  • TOC Analyzer
  • Accurately document and review analytical results using electronic laboratory systems (LIMS).
  • Follow all cGMP requirements, laboratory procedures, SOPs, and regulatory guidelines.
  • Participate in peer review of data and laboratory documentation.
  • Maintain laboratory equipment and ensure testing is performed according to approved methods.
  • Support internal and external audits by maintaining thorough and compliant documentation.
  • Complete required training in laboratory operations, safety procedures, and quality systems.
  • Strictly adhere to safety procedures while working with high-potency oncology products.
  • Use personal protective equipment (PPE) and respiratory protection when required.
  • Comply with OSHA and site-specific safety requirements.
  • Work in a laboratory-based, electronic paperless documentation environment utilizing LIMS.
  • Collaborate with quality, compliance, and laboratory personnel.

Skills:

  • GMP/cGMP
  • Quality Control
  • Analytical Testing
  • Wet Chemistry
  • HPLC
  • GC
  • UV-Visible Spectroscopy
  • CGE
  • ICE
  • Polarimeter
  • Osmometer
  • pH Meter
  • Conductivity Meter
  • TOC Analyzer
  • LIMS
  • Empower Chromatography Software
  • Documentation
  • SOPs
  • Regulatory Compliance
  • Data Management
  • Audit Support
  • Electronic Laboratory Systems
  • Pharmaceutical Industry
  • Biopharmaceutical Industry
  • PPE
  • OSHA
  • Attention to Detail

Education/Experience:

  • Bachelor's or Master's degree in: Chemistry Biochemistry Pharmaceutical Sciences Related scientific discipline
  • Chemistry
  • Biochemistry
  • Pharmaceutical Sciences
  • Related scientific discipline
  • Minimum 5 years of experience in a GMP/cGMP Quality Control laboratory environment.
  • Experience within the pharmaceutical or biopharmaceutical industry is required.
  • Hands-on experience with analytical instrumentation such as HPLC, GC, and UV.
  • Strong understanding of GMP documentation practices and regulatory compliance.
  • Experience working with electronic laboratory systems and data management tools.
  • Ability to follow detailed procedures and maintain a high level of accuracy.
  • 5–7 years of pharmaceutical QC laboratory experience.
  • Experience using Empower chromatography software.
  • Previous involvement in audit-ready environments.
  • Experience reviewing laboratory documentation and SOPs.

Related Jobs

Research Associate II – Digital Pathology & Slide Imaging

Scientific
 Arizona
12 Months Contract + (Highest possibilities of contract extension)

Location (mandatory): Tucson, AZ 85755 (Onsite) This is an onsite position for a Research Associate II in Research & Early Development supporting Ventana projects. The role is responsible for conducting research, development and manufacturing laboratory experimentation and other scientific activities. The primary focus is on slide imaging and image acquisition using systems such as the DP600s, 200s, VS200, and multispectral flash instruments. The individual will perform repetitive, well-defined tasks including virtual staining and assembling slide cohorts to enable the development of AI algorithms while ensuring compliance with GMP, GLP, Design Control, and company procedures.

Research & Development
Laboratory Experimentation
Slide Imaging
Image Acquisition
Virtual Staining
DP600s
VS200
Multispectral Flash Instruments
AI Algorithm Support
GMP
GLP
Design Control
Laboratory Documentation
Data Analysis
Technical Reporting
Scientific Literature Review
Bench Experiments
Troubleshooting
Cross-Functional Collaboration

Bioinformatics RA III or Scientist I (AI/ML – Assay Design)

Scientific
 California
$60/hr W2 (No PTO, No Paid Holidays)
12 Months

Location (mandatory): San Diego, CA 92121 The Bioinformatics RA III or Scientist I (AI/ML – Assay Design) is responsible for developing AI and machine learning solutions to optimize assay and primer design for diagnostic platforms. This role combines bioinformatics, molecular biology, and data science to build intelligent pipelines that analyze high-throughput PCR and sequencing data, enabling data-driven assay development and improved diagnostic performance.

Python
Bioinformatics
Machine Learning
Deep Learning
AI/ML
PCR
NGS
Primer Design
PyTorch
TensorFlow
scikit-learn
Linux
Git

Biotechnologist Associate

Scientific
 New Hampshire
12 months

Location (mandatory): Portsmouth NH Looking for a candidate with science degree and some manufacturing experience

GMP
cGMP
lab work

Manufacturing Associate - Biotech

Scientific
 California
$25-$27.50
12 Months

Location (mandatory): Vacaville CA The Manufacturing Associate is responsible for the manufacture of therapeutic proteins (API) under cGMP conditions. Level I associates are expected to execute process recipes, follow written procedures (SOPs), monitor equipment and processes, perform basic laboratory tasks, including pH, conductivity, sampling, and conduct routine sanitization tasks to maintain facility and equipment. They are expected to attain a basic understanding of cGMP compliance while training under close supervision, demonstrating aseptic technique in handling of products and materials.

GMP
Manufacturing environment
Laboratory tools

QA Documentation Specialist I

Scientific
 California
28.26
6 months

Location (mandatory): Vacaville CA We are seeking a highly motivated and experienced Quality Systems Support Specialist to join our team in Vacaville, CA. In this role, you will provide essential support to the Quality System Management process with document control and PQS integration, ensuring compliance with cGMP and global requirements.

Veeva
QMS
DMS

Quality Control Biochemistry Associate

Scientific
 North Carolina
$42/hr on W2
06 – 12 Months Contract + (Highest possibilities of contract extension)

Small Description: The Quality Control Biochemistry Associate II is responsible for contributing to key functional, tactical, strategic and operational aspects of the large molecule testing for Biochemistry group. This includes performing in-process, release testing, method transfer, validation testing and related activities associated with this testing.

Quality Control
Biochemistry
In-Process Testing
Release Testing
Method Transfer
Validation Testing
GLP
GMP
pH Testing
Appearance Testing
Osmolality Testing
Protein Concentration Testing (UV
RI
SoloVPE)
Quality Systems
Investigations
Laboratory Systems
Written Communication
Verbal Communication

SFC/HPLC Analytical Development Scientist

Scientific
 Massachusetts
40/hr
06 Months Contract + (Highest possibilities of contract extension)

Location : Cambridge, MA 02142 (Onsite) The Analytical Development team is seeking a highly creative and self-motivated candidate to join for a 6-month contract. This role will support the development of small molecule drug substances and drug products by developing innovative analytical technologies and establishing control strategies. The position will be responsible for chromatographic method development using supercritical fluid chromatography (SFC) and requires knowledge of organic chemistry, analytical chemistry, and experience working in a laboratory environment. Experience with analytical techniques such as UV, HPLC/UPLC, and LCMS is required.

Supercritical Fluid Chromatography (SFC)
HPLC
UPLC/UHPLC
LCMS
UV Detection
Analytical Method Development
Analytical Chemistry
Organic Chemistry
Pharmaceutical Analysis
Data Analysis
Technical Reporting

Environmental Monitoring Associate

Scientific
 North Carolina
06 Months Contract + (Highest possibilities of contract extension)

Location: Research Triangle Park, NC 27709 (Onsite) Responsible for performing testing and sampling of bulk gases, monitoring utility parameters, inspecting raw materials, and collaborating with cross-functional teams including Microbiology and Manufacturing to ensure quality and compliance in research and production activities.

TOC testing
Conductivity testing
Nitrate testing
Gas sampling (viable and non-viable particulates)
THC and Moisture sampling
Raw material inspection
Documentation review
Utility Monitoring
Routine Cleaning
Validation Samples

Dispensing Technician

Scientific
 New Hampshire
$34.36/hr
12 Months

Location : Portsmouth NH 03801. The Dispensing Technician Level 1 supports the manufacturing of therapeutic proteins (API) by dispensing raw materials, including liquids, powders, acids, and bases, under cGMP conditions. This night-shift role requires attention to detail, adherence to cGMP and SOPs, and active participation in safety and quality processes within a controlled Class C environment.

Dispensing
SOP
Sanitation
documentation
logo

At SGS Consulting, we go beyond resume-job matches, creating meaningful connections and pathways for individuals to thrive in defining careers.


© 2026 All rights reserved.
logologologologo