Cookie Consent

This website uses cookies or similar technologies to enhance your browsing experience and provide personalized recommendations. By continuing to use our website, you agree to our Privacy Policy.

Quality Control Analyst II (Manufacturing/Quality)

|  Posted On: Aug 13, 2025

Swiftwater, PA 18370

12 Months, Contract

On-site

Log In and Apply

Job Summary

Job Title:  
Quality Control Analyst II (Manufacturing/Quality)

Posted Date:  
Aug 13, 2025

Duration:  
12 Months, Contract

Shift(s):  

08:00 - 17:00


We care about you! Explore Rangam’s benefits information

Talk to our Recruiter

Name:
 
Mohd Nayeem Uddin

Email:
 
mohd@rangam.com

Phone:
 
973-788-8117

Description

8AM- 5PM Mon - Fri

Onsite  

Prefer local, open to candidates willing to relocate at their own expense

Education:

  • BA Chemistry
  • Must-Have Experience with: entry level with experience in Chemistry and Pharma

 Work Experience:

  • 4 years (academia & industry)

Overview:

  • This position supports the execution of routine testing in the Quality Control Analytical Chemistry laboratory, including chemistry assays associated with Incoming Quality and Raw Materials.
  • This position requires proficiency and understanding of the theory related to processes, assays, and equipment, as well as the ability to identify issues/trends.
  • The candidate filling this position will work to ensure tasks are completed in a timely manner, while strictly adhering to client policies and procedures and cGMP.

Job responsibilities:

  • Perform QC testing while strictly adhering to client policies and safety procedures,SOP/SWI, Pharmacopeia, Federal Regulations, cGMP, and required training curricula.
  • Perform all scheduled activities defined by laboratory management to meet demands of Production, Method Development, Validation, Independent Demand, and Stability program.
  • Maintain safety and compliance of the laboratory work area.
  • Perform cleaning of laboratories, equipment, and ancillary areas as required.
  • Prepare for and operate QC equipment including pre and post-run setup and maintenance.
  • Complete required paperwork and documentation as required.
  • Troubleshoot sample discrepancies.
  • Perform peer proofing on assays.
  • Develop a working knowledge of appropriate compendia and/or regulatory guidance.
  • Attend/contribute to scheduled team meetings, department, and safety meetings.
  • Specific tasks may include:
  • Raw material testing (pharmacopeia/wet chemistry assays)
  • Water testing (TOC and Conductivity analysis)
  • pH testing for media
  • Buffer assays (titrations and photometric methods)
  • Analytical equipment setup, usage, and maintenance
  • Sample preparation and disposal
  • Coordination of contract laboratory testing
  • Chemical handling required with appropriate PPE provided. Vaccinations and vision examinations may be required based on specific job function.

Requirements:

  • Bachelor’s degree in Chemistry or equivalent
  • 2-4 years of relevant experience in cGMP controlled/pharmaceutical industry.
  • Exceptional attention to detail and strong writing skills are crucial.
  • The candidate must be able to work in a dynamic team environment with flexible schedule, including potential for weekends/holidays.

As a healthcare company and a vaccine manufacturer, client has an important responsibility to protect individual and public health. All US based roles require individuals to be fully vaccinated as required for your job responsibilities.