Operations Technician-USA

Cryoport Systems is the life science industry’s most trusted provider of supply chain solutions for temperature-sensitive materials, serving biopharmaceutical, IVF and surrogacy and animal health organizations around the world. Cryoport Systems' proprietary Cryoport Express® shippers, Cryoportal® Logistics Management Platform, leading-edge Smartpak™ Condition Monitoring System and geo-sensing technology paired with unparalleled logistics expertise and 24/7/365 customer support, make Cryoport Systems the end-to-end temperature controlled supply chain partner that you can trust.

Position Summary
The Operations Technician Bioservices role is responsible for ensuring all operational activities are executed accurately and timely, following specific procedures and processes as defined in Work Instructions. This role involves the receipt, inventory, storage, withdrawal, packaging, labeling, and shipment of biological materials, therapeutic products, clinical agents, and materials from multiple commercial and government clients. The Operations Technician Bioservices may also participate in the assembly of various types of kits and label printing, involving materials stored at temperatures ranging from ambient (room temperature) to below freezing (including cryogenic) with potentially hazardous properties.

Primary Responsibilities (include but are not limited to):

• Receipt and inventory management of biological materials (including therapeutic drug products), data entry, relocation, retrieval, packaging, and logistics operations according to standard operating procedures
• Packaging and labeling of pharmaceutical product at all temperatures (including low and ultra-low temperatures) according to standard operating procedures
• Assembly of a range of kit types according to strictly defined client specifications
• Liaising with Program Managers to provide support regarding the scheduling of work, assisting in writing and updating SOPs and other project-related activities
• Assist in deviation investigations and change control documentation
• Scheduling of project work and accounting for deadlines, available resources, and business need
• Disseminating information from and providing feedback to Project Managers.
• Coordinate stock management and receipt of kit production, packaging, and labeling materials.
• Manage stock levels of kit materials, packaging, and labeling components
• Assist with Quality Control tasks such as verification, validation and calibration procedures as required
• Ensure project work areas are kept clean and free of any possible safety hazards
• Understands and uses the inventory management, temperature monitoring, and site infrastructure systems
• Primary responder to all equipment alarms and active member of the site On-Call team, responding to all alarms including out-of-hours (24/7 on a rotating cycle with other team members)
• Being available for infrequent overtime work as necessary, willingness to attend site, out-of-hours in the case of an emergency or extraordinary work requirement
• Document alarms in response to the temperature monitoring systems
• Work around hazardous substances and follow safety guidelines to minimize exposure
• Assure compliance to cGMP requirements and company quality systems
• Maintain cGMP training records and participate in staff quality training
• Ensure all job-related paperwork is correct, error-free, and completed in real-time per instructions

Competencies & Personal Attributes

• Exhibits professional behavior, language, and appearance at all times
• Follows policy (when escorting client sponsors through the facility), acts courteously and displays a positive attitude
• Maintains a professional manner when problems/conflicts arise
• Possesses a good understanding of quality management
• Previous experience working with materials at ultra-low & cryogenic temperatures is desirable
• Health, Safety and Environmental (HSE) experience/qualification is desirable
• Flexible and adaptable with excellent interpersonal skills (at all levels)
• Able to analyze problems and define solutions
• Attention to detail with a “right-first-time” mentality
• Able to work under pressure and support others within the team
• Builds customer commitment
• Supports operational excellence (30/30)
• Focuses on priorities (80/20)
• Teamwork, collaboration, and accountability (90/10)
• Emphasis on business growth
• Passion for and alignment with Cryoport’s mission
• A change agent and strong collaborator who is not afraid of challenging the status quo
• An individual who brings strong core values, quality, ethics, and integrity to the job
• A collaborative team player who embraces and champions the culture
• Strong work ethic and ability to deliver results and meet commitments in a dynamic environment
• Exceptional and dynamic communications skills with the ability to inspire and influence people at all levels, build consensus and commitment, and effectively drive change throughout the organization at a rate that fits the corporate culture
• Exceptional organizational and planning skills with strong analytical abilities

Qualifications And Education Requirements

• Degree level, or equivalent experience, in a relevant discipline is preferred
• Minimum 1-2 years’ experience working in a GMP/GxP environment
• Hands-on experience working with biological and pharmaceutical materials and drug products
• Hands-on experience working in clinical packaging and labeling is desirable.

Compensation: $25 hr.

Cryoport Systems is an Equal Opportunity Employer offering competitive compensation with a generous benefits package that includes health insurance, a 401K with company match and stock equity (Nasdaq: CYRX).To learn more about Cryoport Systems, please visit