Microbiologist Technician III

PSC Biotech; York (York County); On-site; USD 60,000 - 78,000; Full time

Benefits offered by this job

Medical benefits

Sick time

Job summary

BioTechnique in York, United States is seeking a Microbiology Technician Level III to support Quality Control in a sterile manufacturing environment. You will perform sampling, microbial analysis, DET, and documentation in GMP-compliant processes.

This is a six-month temporary role with a Friday–Sunday 12-hour shift pattern, with potential to convert to full-time. W2 assignment includes medical and sick time benefits and mentorship of junior staff.

Qualifications

• 5–7 years in quality control or manufacturing in regulated environments.
• Strong knowledge of cGMP, ISO, FDA/EU requirements.
• Proficient with document control, change control, and eQMS.
• Excellent communication and cross-functional collaboration.
• Detail-oriented with strong analytical and problem-solving skills.
• Authorized to work in the U.S.; no C2C.

Responsibilities

• Perform sampling, microbial analysis, DET, and environmental monitoring in sterile manufacturing.
• Operate biosafety cabinets and lab instrumentation with aseptic technique.
• Prepare media, kits, test solutions; support sterilization as needed.
• Document results in ACE/LIMS and maintain data integrity.
• Mentor junior team members and support QA, Engineering, Manufacturing, Facilities.

Skills

GMP practices

Documentation

Cross-functional collaboration

Analytical skills

Communication skills

Tools

ACE

LIMS

eQMS

Job description

York, United States | Posted on 09/10/2026

The Experience

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.

Your Role

We are hiring a motivated Microbiology Technician Level III 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 . In addition, this role will be responsible for overseeing and mentoring junior team members.

This is a temporary six-month position with the schedule of Friday - Sunday (12 hour shifts), with the potential for conversion to a full-time employee (FTE).

• Follow aseptic gowning procedures and wear required PPE in classified cleanroom environments.
• Independently conducts routine testing and monitoring activities; supports compendial compliance.
• Execute microbial testing and environmental monitoring of product samples, utilities, surfaces, air, and personnel according to SOPs and compendial standards.
• Execute 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.
  
• Mentor and oversee junior team members.
• Additional duties and responsibilities may be assigned from time to time.
  

Requirements

• 5-7 years of experience in a quality control or manufacturing role within a manufacturing environment, preferably in a regulated industry (e.g., pharmaceuticals, medical devices, biotechnology).
• 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.
  

W2 Temp roles include our Medical and Sick Time benefits

Equal Opportunity Employment Statement

PSC is committed to a policy of Equal Employment Opportunity with respect to all employees, interns, and applicants for employment. Consistent with this commitment, our policy is to comply with all applicable federal, state and local laws concerning employment discrimination. Accordingly, the Company prohibits discrimination against qualified employees, interns and applicants in all aspects of employment including, but not limited to: recruitment, interviewing, hiring (or failure or refusal to hire), evaluation, compensation, promotion, job assignment, transfer, demotion, training, leaves of absence, layoff, benefits, use of facilities, working conditions, termination and employer-sponsored activities and programs, including wellness, social and recreational programs. Employment decisions will be made without regard to an applicant’s, employee’s, or intern’s actual or perceived: race, color, religion, sex (including pregnancy, gender identity, and sexual orientation), national origin, age (40 or older), disability, genetic information, or any other status protected by law.