Metrology Technician II

About the Company

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 offer formulation and compounding, fill-finish, and lyophilization services for a wide variety of liquid injectables. BioTechnique leverages our team’s expertise to create process designs tailored to our clients’ needs.

With operations spanning the globe and a multicultural team, BioTechnique is passionate about bringing together talented individuals to form something truly special. We believe in coaching and developing the next generation of industry leaders, offering tools for growth and a compensation structure that rewards your contributions.

About the Role

Our Metrology Technician II is responsible for conducting routine calibration tasks in alignment with established protocols and regulatory mandates. This position handles troubleshooting and equipment repair as needed while ensuring adherence to quality system compliance standards. This is a W2 Non-Exempt Temp position, starting with a 6-month duration and potential for extension.

Responsibilities

• Perform in-house calibrations and maintain appropriate documentation.
• Reassemble and calibrate required instruments and equipment.
• Ensure all calibration standards are properly calibrated and certified.
• Execute engineering and calibration portions of equipment qualifications.
• Assist managers in formulating tests, calibrations, repairs, and evaluation plans to maintain precision accuracy of measuring, recording, and indicating instruments.
• Schedule, calibrate, and verify calibration of instrumentation under the Metrology program.
• Assist in specifying instruments and standards and in drafting new and revised SOPs.
• Participate in training programs as required.
• Ensure compliance with company policies and procedures, including safety rules and regulations.
• Additional responsibilities as required.

Requirements

• Bachelor’s degree in engineering or a related technical field, or relevant technical certification or associate degree in a relevant discipline.
• Minimum of 3 years of experience in calibration and metrology in cGMP manufacturing.
• Experience in pharmaceutical manufacturing, biologics, aseptic processing, or a CDMO environment is preferred.
• Strong knowledge of cGMP and GDP regulatory standards and compliance.
• Experience calibrating cGMP manufacturing equipment and analytical instrumentation.
• Strong mechanical aptitude.
• Excellent attention to detail.
• Strong analytical and problem-solving skills.
• Excellent verbal, written, and interpersonal communication skills.
• Strong time management skills and ability to manage multiple priorities.
• Proficient in Microsoft Office Applications.
• Must be authorized to work in the U.S. (No C2C at this time).

Benefits

• Medical benefits.
• Sick leave benefits.