Microbiologist Technician Intern

About the role

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. With operations spanning the globe and a multi‑cultural team, BioTechnique is 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 your professional passions, and work alongside people who will value and nurture your talents. We are firm believers in coaching and developing the next generation of industry leaders and influencers, offering a compensation and benefits structure that rewards you and providing 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.

Responsibilities

• Follow aseptic gowning procedures and wear required PPE in classified cleanroom environments.
• Independently conduct routine microbiological and environmental monitoring activities, supporting 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

• Currently pursuing a degree in a related technical field.
• Must be local to York, PA.
• Must be able to continue the internship throughout semester breaks (part‑time or a minimum of 10‑15 hours/week during academic semesters).
• 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

This is a temporary three‑month internship with a flexible Monday‑Friday part‑time shift schedule (4 hours) and full weekend shifts (8‑12 hours), with the potential for extension.