Analytical Chemist III

Joulé

Pearl River, NY

JOB DETAILS
SALARY
$35–$41.43 Per Hour
SKILLS
Analytical Chemistry, Biotech and Pharmaceutical, Chromatography, Current Good Manufacturing Practice (cGMP), Data Management, Documentation, Drug Products, Equipment Maintenance/Repair, External Audit, GMP (Good Manufacturing Practices), Internal Audit, Laboratory, Laboratory Equipment, Laboratory Management, Laboratory Systems, Laboratory Testing, Outsourcing, Quality Control, Regulatory Compliance, Service Delivery, Standard Operating Procedures (SOP), Testing
LOCATION
Pearl River, NY
POSTED
1 day ago

Job Title: Analytical Chemist III
Location: Pearl River, NY
Type: Contract
Compensation: $35-$41.43
Work Model: Onsite – onsite
Hours: 40.0

Overview
Leading pharmaceutical company looking for an experienced Analytical Chemist III. Ideal candidates should have Bachelor’s or master’s degree with at least 5 years of experience in a GMP/cGMP Quality Control laboratory environment.


Responsibilities
• Perform laboratory testing of:

o Raw materials
o Drug substances
o Drug products
o In-process samples
o Stability samples

• Conduct routine wet chemistry and analytical testing using laboratory instrumentation, including:

o HPLC
o GC
o UV-Visible Spectroscopy
o CGE
o ICE
o Polarimeter
o Osmometer
o pH Meter
o Conductivity Meter
o 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.


Requirements
• Bachelor’s or master’s degree in:

o Chemistry
o Biochemistry
o Pharmaceutical Sciences
o 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.

Preferred Qualifications
• 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.

System One, and its subsidiaries including Joulé and Mountain Ltd., are leaders in delivering outsourced services and workforce solutions across North America. We help clients get work done more efficiently and economically, without compromising quality. System One not only serves as a valued partner for our clients, but we offer eligible employees health and welfare benefits coverage options including medical, dental, vision, spending accounts, life insurance, voluntary plans, as well as participation in a 401(k) plan.
System One is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex (including pregnancy, childbirth, or related medical conditions), sexual orientation, gender identity, age, national origin, disability, family care or medical leave status, genetic information, veteran status, marital status, or any other characteristic protected by applicable federal, state, or local law.



Ref: #558-Scientific


About the Company

J

Joulé

With extensive scientific, clinical, and healthcare industry experience, Joulé recruiters excel at placing talent across core specialty areas:

  • Scientific staffing for hard-to-find skills

Working across every scientific discipline, Joulé places biologists, chemists, scientists, technicians and other specialists.

  • Clinical lifecycle recruiting

From research to regulations, safety to statistics, Joulé helps clients manage every stage of the clinical development lifecycle.

  • Equipment calibration, maintenance and validation

Laboratory and facility support comes with a total quality commitment backed by ISO 9001:2008 certification.

  • National healthcare recruitment

Trust Joulé’s extensive experience in physician, advanced practice provider and executive direct placement search.

COMPANY SIZE
500 to 999 employees
INDUSTRY
Biotechnology/Pharmaceuticals
WEBSITE
https://www.jouleinc.com/