Technician Ii, Instrument/Calibration

Janssen Biotech, Inc. is recruiting for an Instrument Calibration Technician to be located in Malvern, Pennsylvania.

• Shift Differential and Overtime Pay (Depending on the designated work schedule)
• This role is eligible for a $3,000 sign-on bonus for qualified/eligible candidates
• Relocation Package offered for qualified/eligible candidates

At the Janssen Pharmaceutical Companies of Johnson & Johnson, we are working to create a world without disease. Transforming lives by finding new and better ways to prevent, intercept, treat and cure disease inspires us. We bring together the best minds and pursue the most promising science. We are Janssen. We collaborate with the world for the health of everyone in it. Learn more at www.janssen.com and follow us @JanssenGlobal. Janssen Biotech, Inc. is part of the Janssen Pharmaceutical Companies.

Thriving on a diverse company culture, celebrating the uniqueness of our employees and committed to inclusion. Proud to be an equal opportunity employer.

This position is responsible for performing Metrology/Calibration procedures and the execution of scheduled tasks within a cGMP environment. Applicant will be maintaining the highest standards in compliance within company policies, procedures and all applicable regulations. Additionally, will be responsible for encouraging site pride and J&J citizenship.

Key Responsibilities:

• Working knowledge of equipment including, but not limited to PLC control systems and HMI’s
• Familiarity with electrical theory, thermal energy principals, mechanical maintenance techniques, and electromechanical theory.
• Investigates, troubleshoots, and provides repairs to equipment, instruments and instrumentation systems as assigned
• Execute calibration and repair of instrumentation used in cGMP and non GMP systems and maintain all calibration standards

Additional responsibilities/duties:

• Complies with all company and/or site policies and procedures
• This is not an exhaustive or comprehensive listing of job functions. May perform other duties as assigned.
• Recommends and leads, and implements improvements
• Ensures regulatory and job training remains current by promptly completing required training
• May assist in training other associates as needed
• Participate in PM development and optimization
• Participate in Maintenance projects as required including but not limited to Root Cause Analysis, FMEA’s, and Non- Conformance investigations
• Independently performs duties
• Identifies gaps in processes,
• Carries out all duties in compliance with all company, state and federal regulations and guidelines including FDA, EPA, OSHA, DEA and TSA.
• Support “Operator Asset Care” program for manufacturing areas
• May lead small departmental projects and serve as subject matter expert on project teams
• Independently troubleshoots and resolves complex problems;
• Retrieves and analyzes data from sources such as control systems;
• Is available for other duties as required
• Complete all GMP documentation to support Maintenance activities and supply legible and complete documentation of work orders as required
• Demonstrates willingness to learn new skills as required
• Order basic supplies as needed

Qualifications

• Basic computer knowledge is required. Knowledge in SAP is preferred.
• Must interpret a variety of instructions furnished in written, oral, diagram or schedule form.
• While performing the duties of this job, the employee is regularly required to stand; walk; use hands to finger, handle, or feel; climb, bend and stoop; and reach with hands and arms.
• Works independently on routine and complex issues
• Basic mechanic skills are preferred.
• Position requires ability to lift up to 20 lbs. and to perform gowning procedures to work in manufacturing core.
• Troubleshooting knowledge is highly preferred.
• Experience with Electronic Batch records is preferred.
• Trade / Technical School certification or Certification in Craft required. Military equivalent of Trade / Technical School certification is accepted.
• A minimum of an Associate’s Degree or Technical Degree is required. Bachelor's or higher degree is preferred.
• Take on practical problems and deal with myriad concrete variables in situations where only limited standardization exists.
• Is aware of and understands departmental and site level operations
• 6+ years of related industrial experience
• Must follow detailed procedures and work instructions in a GMP environment.
• Requires availability to work in Malvern, PA.
• Ability to make innovation part of the site agenda and be an active driver of innovation; think outside of the box and challenge others to do the same is required.
• A minimum of two (2) years Biotech/Pharmaceutical or regulated industry experience is prefered.
• Serves as technical expert within area of expertise and has conceptual and basic working knowledge of maintenance disciplines outside technical expertise;

Johnson & Johnson is an Affirmative Action and Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, age, national origin, or protected veteran status and will not be discriminated against on the basis of disability.

For more information on how we support the whole health of our employees throughout their wellness, career and life journey, please visit www.careers.jnj.com .