Jobs
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.
As part of our recruitment process, we may use automated tools or AI-enabled technologies to assist with resume screening and candidate matching. These tools help our recruitment team review applications more efficiently, but they do not make hiring decisions. All final decisions are made by human reviewers.