Microbiologist Technician I

About BioTechnique

BioTechnique is a sterile injectable full service CDMO providing cytotoxic and therapeutic sterile injectable fill‑finish services. From IND applications through commercial scale production, we provide formulation and compounding, fill‑finish, and lyophilization services for a wide variety of liquid injectables. BioTechnique utilizes our team’s expertise to create a process design for our clients’ products that best suits their needs. The experience spans operations worldwide with a multicultural team, and we are passionate about bringing the best and brightest together to form something truly special. When you join our team you will be inspired in your career, explore professional passions, and work alongside people who value and nurture your talents. We believe in coaching and developing the next generation of industry leaders and influencers, offering compensation, benefits, and tools to help you grow and learn. At BioTechnique, it’s about more than just a job—it’s about your career and your future.

Your Role

We are hiring a motivated Microbiology Technician Level I to join our team. The Microbiology Technician supports BioTechnique’s Quality Control operations by executing microbiological and environmental monitoring activities in a sterile manufacturing setting. Technicians perform sampling, microbial analysis, execute disinfectant efficacy testing (DET), and documentation in compliance with GMP and industry standards. This is a temporary six‑month position with a schedule of Friday – Sunday (12‑hour shifts) and the potential for conversion to a full‑time employee (FTE). The opportunity is ideal for recent graduates, interns, or individuals beginning their careers in microbiology.

Responsibilities

• Follow aseptic gowning procedures and wear required PPE in classified cleanroom environments.
• Independently conduct routine testing and monitoring activities; support compendial compliance.
• Execute microbial testing and environmental monitoring of product samples, utilities, surfaces, air, and personnel according to SOPs and compendial standards.
• Perform disinfectant efficacy testing (DET) and related microbiological assays.
• Prepare and maintain media, sampling kits, and test solutions per SOPs and compendial requirements; support sterilization practices as applicable.
• Operate biological safety cabinets and laboratory instrumentation while following aseptic techniques.
• Perform routine cleaning and sanitization of laboratory spaces and support equipment maintenance and calibration.
• Document results accurately in validated systems (ACE, LIMS) and maintain data integrity.
• Participate in periodic lab and equipment cleaning and monthly tasks.
• Support cross‑functional collaboration with Quality Assurance, Engineering, Manufacturing, and Facilities.
• Contribute to inventory management and reagent tracking.
• Additional duties and responsibilities may be assigned from time to time.

Requirements

• 0‑2 years of experience in a quality control or manufacturing role within a regulated industry (pharmaceuticals, medical devices, biotechnology preferred).
• Strong knowledge of quality systems and regulations, including cGMP, ISO standards, and FDA/EU requirements.
• Proficiency in document control, change control, and electronic quality management systems (eQMS).
• Excellent communication and interpersonal skills with the ability to collaborate effectively with cross‑functional teams.
• Detail‑oriented with strong problem‑solving and analytical skills.
• Ability to work independently and manage multiple projects simultaneously.
• Must be authorized to work in the U.S.; no C2C at this time.

Schedule

Friday – Sunday, 12‑hour shifts (temporary six‑month assignment with potential conversion to full‑time).

Benefits

W2 temporary roles include medical and sick‑time benefits.