Process Engineering- Process Validation Support

At Johnson & Johnson, we believe health is everything. Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through 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 humanity. Learn more at jnj.com

As guided by Our Credo, Johnson & Johnson is responsible to our employees who work with us throughout the world.  We provide an inclusive work environment where each person is considered as an individual.  At Johnson & Johnson, we respect the diversity and dignity of our employees and recognize their merit.

Johnson & Johnson is currently seeking a Experienced Engineer- Process Validation Support (PVS) to join our Manufacturing Science and Technology team located in Wilson, NC.  

Manufacturing Science and Technology (MSAT) manages the process technology platform strategy for the production of biotherapeutics in the new Bio-Processing 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.

We have a great opportunity for an experienced MSAT Engineer to join our Process Validation Support team.

The experienced MSAT Engineer will be responsible for the following:

• →Conduct MSAT activities in compliance with US and EU regulations, local and global procedures and EHS&S requirements.
• →Process Validation Support (e.g. Mixing Studies, Microbial Hold Studies, Media Challenges, In-Line Conditioning Verification Studies, Chemical Hold Studies) area.
• →Leading and/or providing technical guidance for process improvement projects and investigations.
• →Develop MSAT documentation (e.g. 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.
• →Track and resolve exceptions/events/nonconformances during MSAT activities.
• →Prioritize MSAT activities in line with Manufacturing / the project schedule.
• →Co-ordinate MSAT activities with contractors and vendors as required.
• →Attend identified training, required to fulfill the role of an experienced MSAT Engineer.
• →Participate in multi-functional teams (project, investigations) as required.

• 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.

Additional Description for Pay Transparency: