C

Cellectis

Develops allogeneic CAR-T cell therapies

Metrology / Facilities Technician

Validation, Compliance & Quality SystemsConfirmed live in the last 24 hours
Full-timeRaleigh, NC, USANo salary listedIn-person

About the Job

Requirements

  • An associate degree in a related Engineering or Science discipline, or an equivalent combination of education and experience.
  • At least five years of experience in pharmaceutical calibrations/metrology or another highly regulated industry.
  • Experience working in a regulated environment, such as cGMP, OSHA, or EPA, and familiarity with GMP quality systems and processes including change control, non-conformances, corrective and preventative actions, and qualifications/validation.
  • Knowledge of instrumentation, controls, process improvement methodologies, root cause analysis, pharmaceutical processes, and utilities.
  • In-depth knowledge of metrology principles, standards, and best practices.
  • Demonstrated experience in measurement instrumentation theory and method development.
  • Demonstrated experience calibrating pharmaceutical or other highly regulated instrumentation.
  • Ability to work in a highly regulated commercial pharmaceutical manufacturing environment and comply with procedurally driven activities.
  • Experience scheduling and supervising external calibration and service vendors.
  • Experience with or working knowledge of a computerized maintenance management system.
  • Ability to work effectively in a cross-functional team environment and demonstrate leadership and team management skills.
  • Ability to use good judgment to resolve routine and non-routine issues or make recommendations.
  • Ability to execute daily tasks with minimal instruction and new assignments with general instruction.
  • Basic working knowledge of programmable logic controllers, heating, ventilation, and air conditioning, and building monitoring systems is a plus.
  • Working knowledge of Microsoft Word and Excel.
  • Ability to participate in an on-call rotation and work nights and weekends as needed to support facilities operations.
  • Ability to recognize workplace hazards, take appropriate safety measures, and wear personal protective equipment suited to the work environment.

Responsibilities

  • Execute GMP instrumentation maintenance and calibration activities not directly performed by end users through standard operating procedures or work instructions.
  • Calibrate, troubleshoot, maintain, and repair instrumentation in accordance with established procedures.
  • Adhere to cGMPs, written procedures, good documentation practices, and regulatory expectations for instrument calibrations.
  • Support equipment owners with calibration specifications, problem solving, instrument selection, and failure investigations.
  • Complete calibration activities on time, to standard, and with minimal impact on operations.
  • Coordinate with other departments during planning and process improvement to meet operational objectives and milestones.
  • Support other technicians through training, problem solving, and improvement projects.
  • Improve calibration methods, standards, and specifications to meet stakeholder and site needs.
  • Manage documentation change requests for calibration-related standard operating procedures and vendor calibration records, ensuring accuracy and consistency.
  • Partner with Metrology/Facilities Mechanics and the Site Coordinator to maintain active spare-parts inventory.
  • Interface with external customers and the FDA during audits and inspections.
  • Perform duties in accordance with applicable safety regulations, monitor environmental, health, and safety aspects of the job, and understand risks and liabilities associated with facilities maintenance and repair activities.
  • Perform other responsibilities and duties assigned by the Company.

Desired Qualifications

  • Basic working knowledge of programmable logic controllers, heating, ventilation, and air conditioning, and building monitoring systems.

About the Company

Cellectis

Develops allogeneic CAR-T cell therapies

Cellectis develops immunotherapy treatments for cancer using gene-edited allogeneic CAR T cells. Its products rely on donor-derived T cells that are edited to remove T cell receptor activity and engineered to express a chimeric antigen receptor (CAR) that targets cancer cells. The goal is to create off-the-shelf CAR T therapies that are available quickly and at a lower cost than patient-specific (autologous) CAR T treatments. Cellectis works through research and development, clinical trials, and partnerships with other pharma companies, such as Sanofi, and generates revenue from licensing, milestone payments, and potential future product sales. The company differentiates itself by offering off-the-shelf solutions rather than custom-made therapies, aiming to broaden access to advanced cancer treatment.

Company size
201-500
Company stage
IPO
Headquarters
Paris, France
Founded
2000

Recently Posted Jobs

Explore more opportunities at Cellectis

See more jobs