Quality Control Analyst II (Manufacturing/Quality)
Swiftwater, PA 18370
12 Months, Contract
On-site
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.