Sign upLog in

QC Chemist

Atrium

Monroe Township, NJ

Apply
JOB DETAILS
SALARY
$36–$38 Per Hour
SKILLS
Analysis Skills, Artificial Intelligence (AI), Assays, Biochemistry, Biology, Biotech and Pharmaceutical, Capsules, Chemistry, Contract Manufacturing, Corrective and Preventative Action (CAPA) Systems, Current Good Manufacturing Practice (cGMP), Documentation, Dosage Forms, Drug Manufacturing, FDA (Food and Drug Administration), Fourier-Transform Infrared Spectroscopy (FTIR), GMP (Good Manufacturing Practices), Genetics, High Performance Liquid Chromatography (HPLC), ICH Regulations, Identify Issues, Interviewing Skills, Laboratory, Laboratory Information Management System (LIMS), Manufacturing, Product Testing, Quality Assurance, Quality Control, Regulations, Short Messaging Service (SMS), Team Player, Time Management, Titration
LOCATION
Monroe Township, NJ
POSTED
1 day ago
Client Overview:
Our client is a pharmaceutical contract manufacturing site specializing in cGMP solid oral dosage production, and they are seeking an experienced QC Chemist to join their Laboratory team.

Salary/Hourly Rate:
$36/hr - $38/hr

Position Overview:
The QC Chemist role is a lab-based position focused on supporting batch release and stability programs within a cGMP environment. The role demands strong operational QC expertise in solid oral dosage forms (tablets and capsules) and the ability to work effectively in a fast-paced setting.

Responsibilities of the QC Chemist:
  • Execute batch release and stability testing, including assay and impurity analysis.
  • Operate, troubleshoot, and maintain HPLC/UPLC and other analytical instruments.
  • Ensure GMP-compliant documentation and maintain audit-ready records.
  • Support investigations related to out-of-specification/out-of-trend results and CAPA implementation.
  • Manage stability sample handling and data trending.
  • Collaborate with Quality Assurance and Manufacturing teams to meet production timelines.
Required Experience/Skills for the QC Chemist:
  • 6+ years of hands-on pharmaceutical QC laboratory experience in a cGMP environment.
  • Proven expertise with solid oral dosage forms (tablets and capsules).
  • Recent experience operating HPLC/UPLC instruments.
  • Skilled in analytical techniques including GC, UV, FTIR, dissolution, and Karl Fischer titration.
  • Experience supporting OOS/OOT investigations, deviations, and CAPA processes.
Preferred Experience/Skills for the QC Chemist:
  • Familiarity with regulatory standards and systems such as Empower, LIMS, ALCOA+, FDA, ICH, and cGMP.
  • Knowledge of assay, dissolution, impurity testing, and finished product release.
  • Ability to work efficiently in a fast-paced environment.
Education Requirements:
  • Bachelor's degree in a scientific field (Chemistry, Biology, Biochemistry, etc.) is required.
Benefits:
  • Atrium Care Package available, upon eligibility (including healthcare plans, discount programs, and paid time off).
Job Wrapping ID: #LI-AJ3

About Atrium:What you do matters. Guided by our Applicant-Centric™ approach, we foster an environment of collaboration, high performance, and innovation where your talents are valued, and your achievements are celebrated. Join us and become part of an inclusive team committed to your growth and success. By applying to this job, you agree to receive calls, AI-generated calls, text messages, and/or emails from Atrium and its affiliates, and contracted partners. Frequency varies for text messages. Message and data rates may apply. Carriers are not liable for delayed or undelivered messages. You can reply STOP to opt out on any message you receive. For more details, please review our Terms of Use and Privacy Policy . As a woman-owned firm, we value diversity. We are an equal opportunity and affirmative action employer and will consider all applications without regard to race, sex (including gender, pregnancy, sexual orientation and gender identity), age, color, religion or creed, national origin or ancestry, veteran status, disability (physical or mental), genetic information, citizenship or any other characteristic protected by law. We will ensure that individuals with disabilities are provided reasonable accommodation to participate in the job application or interview process, to perform essential job functions, and to receive other benefits and privileges of employment. Candidates who apply for roles through the Atrium website will be added to our candidate pool and may be considered for additional roles of a similar title. Please contact us to request an accommodation.
EOE/M/F/D/V/SO

Position ID: 399526

About the Company

A

Atrium

Founded in 1995, Atrium is a global WBENC certified leader in Extended Workforce Management and Talent Solutions that partners with the world’s largest brands to reimagine how work gets done. Guided by our Applicant-Centric™ philosophy, we approach hiring from the perspective of the candidate. By getting to know you and listening to what truly motivates you, we build lasting relationships and find our applicants jobs they love.

COMPANY SIZE
250 to 500 employees
INDUSTRY
Staffing/Employment Agencies
FOUNDED
1995
WEBSITE
https://www.atriumglobal.com

Resume Resources

Free Resume TemplatesFree Resume Builder