Technology Innovation Engineer - Process Engineering

At Johnson & Johnsonwe believe health is everything. Our strength in healthcare innovation empowers us to build aworld where complex diseases are prevented treated and curedwhere treatments are smarter and less invasive andsolutions are our expertise in Innovative Medicine and MedTech we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow and profoundly impact health for more at

As guided by Our Credo Johnson & Johnson is responsible to our employees who work with us throughout the world. At Johnson & Johnson we respect the diversity and dignity of our employees and recognize their merit.

Supply Chain Engineering

Process Engineering

Scientific/Technology

Johnson & Johnson is currently seeking a Experienced Engineer - Thermal to join our Manufacturing Science and Technology team located in Wilson NC.

J&J is expanding our manufacturing capacity with $2 billion investment to support strongportfolio growth and continue delivering breakthrough innovation and transformational medicinesfor patients. The new facility will expand production of innovative biologic medicines in areas including oncology immunology and neuroscience.J&Js significant supply chain investment ensures a resilient and reliable future supply of medicines to meet accelerating demand for our current portfolio of medicines and our future innovations.

Manufacturing Science and Technology (MSAT) manages the process technology platform strategy for the production of biotherapeutics in the new BioProcessing Facility in Wilson North Carolina. We are responsible for Process & Cleaning Validation Standardization of Equipment for New Product Introduction and Life Cycle Management (LCM) of our commercial production processes.

Performing autoclave Cycle Development Performance Qualifications Controlled Temperature Equipment (refrigerators/ freezers) and Re-Qualification executions.
Develop MSAT documentation (e.g. strategies plans protocols procedures reports) and co-ordinate MSAT document review and approval
Review and approve documents prepared by other MSAT colleagues.
Field execution of MSAT protocols.
Liaise with Manufacturing to provide support where required with routine operations / project based work.
Compile relevant information from contractors suppliers and other departments to develop technical reports
Representing the JBI MSAT site team on platform technical teams.
Initiate and implement change control activities in accordance with site procedures.
Prioritize MSAT activities in line with Manufacturing / the particular project schedule.
Co-ordinate MSAT activities with contractors and vendors as required.
Attend identified training required to fulfill the role of a Senior MSAT Engineer.
Participate in multi-functional teams (project investigations) as required.
Mixing Studies Microbial Hold Studies Media Challenges) Cleaning Validation supporting process improvement projects Supporting New product Introduction/ process validation GMP documentation generation (e.g. protocols / SOPs / WIs / Technical Documents Exception/Event Investigations).

Degree in Life Sciences Engineering Biology Biochemistry or related scientific field is required.
Excellent verbal and written communication skills including ability to effectively communicate with internal and external customers.
Excellent computer proficiency e.g MS Office Excel SAP.
At least 3 yrs experience in the pharmaceutical manufacturing industry or equivalent.
Must be able to work independently with minimum supervision to meet tight deadlines.

Excellent verbal and written communication skills including ability to effectively communicate with internal and external customers.
Also beneficial would be experience in Projects Process Validation Support (e.g. Mixing Studies Microbial Hold Studies Media Challenges) Cleaning Validation supporting process improvement projects Supporting New product Introduction/ process validation.
Proven knowledge and application of industry regulations including those of FDA HPRA EMEA and other authorities.
All qualified applicants will receive consideration for employment without regard to race color religion sex sexual orientation gender identity age national origin disability protected veteran status or other characteristics protected by federal state or local law. We actively seek qualified candidates who are protected veterans and individuals with disabilities as defined under VEVRAA and Section 503 of the Rehabilitation Act.
If you are an individual with a disability and would like to request an accommodation please email the Employee Health Support Center () or contact AskGS to be directed to your accommodation resource.

Analytical Reasoning Computerized Equipment Skills Emerging Technologies Gemba Kaizen Issue Escalation Lean Supply Chain Management Problem Solving Process Control Process Engineering Process Oriented Product Improvements Science Technology Engineering and Math (STEM) Application Situational Awareness Supply Planning Technical Research Technologically Savvy Validation Testing

Subject to the terms of their respective policies and date of hire Employees are eligible for the following time off benefits: for employees who reside in the State of Washington 56 hours per calendar year Holiday pay including Floating Holidays 13 days per calendar year Work Personal and Family Time - up to 40 hours per calendar year Parental Leave 480 hours within one year of the birth/adoption/foster care of a child Condolence Leave 30 days for an immediate family member: