Job Title: Quality Control Technician I
Location: Swiftwater, PA - on site
Type: Contract (W2)
Term: 12-months
Schedule: Monday - Friday; 8 AM - 4:30 PM ET
Pay Rate Max: $29 per hour
Sanofi's contingent workforce program, FLEXT Direct, is seeking a Quality Control Technician I for a 12-month contract.
We are seeking a detail-oriented and motivated laboratory professional to join our Quality Control Microbiology team within a highly regulated pharmaceutical manufacturing environment. This role is integral to supporting routine testing activities that directly contribute to the safety and efficacy of life-saving biological products. The successful candidate will perform scheduled testing in support of production operations, method validation, and stability programs, while maintaining strict compliance with Federal Regulations, current Good Manufacturing Practices (cGMP), and established site policies and procedures. This position offers an excellent opportunity to develop deep technical expertise in microbiological sciences within a world-class biopharmaceutical setting.
Responsibilities
- Perform routine Quality Control microbiological testing in accordance with site work instructions, cGMP, and applicable regulatory requirements
- Apply general microbiological techniques including aseptic processing and culturing of bacterial and viral isolates
- Conduct visual evaluation of vials, syringes, plates, bottles, and canisters as part of quality testing protocols
- Support method validation activities and participate in the stability testing program
- Complete all required documentation accurately and thoroughly in compliance with cGMP standards
- Assist with maintaining safety and compliance standards within the laboratory work area
- Perform cleaning and maintenance of laboratories, equipment, and ancillary areas as required
- Set up and break down laboratory equipment in preparation for and following testing activities
- Manage waste disposal in accordance with safety and regulatory guidelines
- Identify and communicate issues or trends observed during testing processes
- Develop and maintain working knowledge of appropriate compendia and regulatory guidance documents
- Attend and actively contribute to scheduled team meetings, departmental meetings, and safety meetings
- Receive required vaccinations and pass a mandatory eye exam prior to beginning work in the laboratory
Skills
- Proficiency in general microbiological laboratory techniques including aseptic technique and microbial culturing
- Knowledge of tissue culture, sterility testing, and bioburden methodologies
- Familiarity with cGMP guidelines and regulated laboratory environments
- Exceptional attention to detail with a commitment to accuracy in all laboratory and documentation activities
- Strong scientific writing skills for the preparation and completion of laboratory records and reports
- Ability to understand and apply theoretical knowledge related to laboratory processes, assays, and equipment
- Strong analytical and problem-solving skills with the ability to identify and escalate issues or trends
- Excellent interpersonal and communication skills with the ability to thrive in a collaborative team environment
- Ability to manage time effectively and execute scheduled tasks with minimal supervision
Experience
- 1–2 years of hands-on laboratory experience in a microbiological or biological sciences setting
- Prior experience in a Quality Control environment within a pharmaceutical or biopharmaceutical organization is highly desirable
- Practical experience with tissue culture, sterility testing, or bioburden assays is strongly preferred
Qualifications
- Bachelor's Degree in Microbiology, Biological Sciences, or a closely related scientific discipline is required
- Must successfully pass a mandatory eye examination as a condition of employment
- Must be willing and able to receive required vaccinations prior to working in the laboratory environment
This is a remarkable opportunity to build a meaningful career at the forefront of biopharmaceutical quality assurance, contributing directly to the development and release of vaccines and biological therapies that protect and improve lives around the world. You will work alongside a team of dedicated scientists in a dynamic, compliance-driven environment that fosters continuous learning, professional growth, and a shared commitment to public health excellence.