Quality Control Technician II (Pharmaceutical)

HireTalent - Staffing & Recruiting Firm; Swiftwater (Monroe County); On-site; USD 50,000 - 70,000; Full time

Job summary

A leading company in the pharmaceutical sector is seeking a Quality Control Technician II to join their team in Swiftwater, PA. The ideal candidate will have a background in Life Sciences or Engineering and experience in instrument commissioning within a cGMP laboratory environment. Responsibilities include supporting installation of Air Particle Counters, optimizing Environmental Monitoring practices, and maintaining regulatory-compliant documentation. Strong technical skills and attention to detail are essential for this role.

Qualifications

• 1–3 years of GMP lab experience.
• Required vaccinations (flu).

Responsibilities

• Supporting installation and qualification of Air Particle Counters.
• Optimizing Environmental Monitoring practices.
• Executing testing and qualification protocols under cGMP.

Skills

Technical Aptitude

Attention to Detail

Communication

Education

Bachelor’s in Life Sciences

Bachelor’s in Engineering

Tools

Air Particle Counters

Environmental Monitoring Systems

MS Office

Job description

Quality Control Technician II (Pharmaceutical)

We are seeking a technical professional with 1–3 years of experience to work onsite full-time in Swiftwater, PA. The ideal candidate will have a background in Life Sciences or Engineering, with experience in instrument commissioning and qualification, preferably within a cGMP laboratory environment. Strong technical aptitude, attention to detail, and communication skills are essential. Familiarity with Air Particle Counters (APCs) and Environmental Monitoring (EM) systems is desired.

Responsibilities include:

1. Supporting installation and qualification of Air Particle Counters
2. Optimizing Environmental Monitoring practices
3. Executing testing and qualification protocols under cGMP
4. Collaborating with cross-functional teams for troubleshooting and validation
5. Maintaining regulatory-compliant documentation
6. Using MS Office tools for data tracking and reporting

Qualifications:

• Bachelor’s in Life Sciences or Engineering
• 1–3 years of GMP lab experience
• Required vaccinations (flu)

Nice to Have:

• Experience in Biotech or Pharmaceutical manufacturing
• Experience with QC instruments in regulated labs