Johnson & Johnson

Eng Process Engineering

Johnson & Johnson • $80K — $95K *
Pharmaceuticals & Biotech
Less than 5 years of experience
Job Overview by Ladders

Qualifications

  • Bachelor's degree in Chemical, Mechanical, Bioprocess Engineering, or related field; required
  • MS/MBA/Ph.D. PE Certificate preferred
  • 0 to 2+ years of process/plant engineering experience in GMP MFG large molecule biologics facilities
  • Track record of successful program execution and team outcomes
  • Ability to lead and/or support multiple projects simultaneously

Responsibilities

  • Support the deployment of MTO aspirations by providing engineering design for GMP biologics manufacturing facility systems
  • Drive innovative engineering solutions in support of manufacturing technology
  • Coordinate with Technical Operations to align projects with engineering standards
  • Interact with external partners to develop and execute project plans as SME and process systems owner
  • Provide ownership of bioprocess manufacturing equipment and review critical documentation
  • Explore technology and manufacturing challenges to synthesize business needs into solutions
  • Lead multi-functional teams on projects and resolve inter-functional issues

Benefits

  • Opportunity to work in a newly expanded facility with a significant investment in manufacturing capabilities
  • Collaborative and diverse team environment
  • Engagement in innovative biologic medicines for critical health areas
  • Professional development opportunities in a leading medical company
  • Potential for international and domestic travel
Full Job Description

Job Function:

Supply Chain Engineering

Job Sub Function:

Process Engineering

Job Category:

Scientific/Technology

All Job Posting Locations:

Wilson, North Carolina, United States of America

Job Description:


An internal pre-identified candidate for consideration has been identified. However, all applications will be considered.


We are searching for the best talent for anEng Process Engineering.

Johnson and Johnson Innovative Medicine (J&JIM), is recruiting for a Process Engineer for the Large Molecule Drug Substance (LMDS) project. This position is to be located in Wilson, NC!


J&J is expanding our manufacturing capacity with $2 billion investment to support strong portfolio growth and continue delivering breakthrough innovation and transformational medicines for 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.

Are you interested in joining a diverse team delivering outstanding results to our customers? Apply now for this exciting opportunity!

We, the MTO are responsible for supplying medicines to markets around the world. With Quality as our primary focus, our group strives to provide access and affordability through innovation and strong collaboration with our R&D and Commercial partners to deliver life changing solutions for patients in need.

Position summary:

  • Support the deployment of the MTO aspiration to innovate to safely supply quality products and services competitively, faster, always. Responsible for providing engineering design and start-up of GMP large molecule biologics manufacturing facility systems, and equipment. Provide integrated equipment, utility, and facility engineering expertise with an operational focus in support of technology transfer and manufacturing projects to support right first time execution and start up.
  • Drive innovative solutions in engineering support, and process technology. Coordinate with Technical Operations platform to ensure project alignment with technology standards and engineering specifications for manufacturing technology. This is intended to be a general job description and should not be construed as all-inclusive.

Key Responsibilities:

  • Extensive interaction with external partners (A&E, construction firms, equipment vendors) to develop, organize and execute project plans as SME and process systems owner. The incumbent should demonstrate the following: detail and goal oriented, teamwork, customer-focus, thorough understanding of GMPs and regulatory requirements.
  • Serve as Process Engineering Expert to develop business based technology solutions and provide integrated equipment, utility, and facility engineering expertise with an operational focus to support execution of strategic and key CAPEX manufacturing projects, driving right first time start up and execution.
  • Provide system ownership for bioprocess manufacturing equipment including review or URS, P&ID, C&Q, automation and architectural drawings and documentation.
  • Explore and understand Technology and Manufacturing challenges and synthesize business needs, manufacturing requirements, engineering elements, and technology inputs, etc. into business solutions.
  • Provide technical leadership of multi-functional teams on many projects/ process improvements and resolves inter-functional issues.
  • High degree of collaboration with internal (manufacturing, quality, engineering) to develop standards and define project needs and priorities; as well as recruiting project team members.
  • The incumbent must also have a thorough understanding of business requirements, effective communication skills, leadership, and interdependent partnering, conflict and risk management.

Qualifications :

Education:

  • Minimum of a Bachelors or equivalent University Degree in Chemical, Mechanical, Bioprocess Engineering or related field; required;
  • MS/MBA/Ph.D. PE Certificate preferred

Experience and Skills:

  • Preferably 0 to 2+ years of process/plant engineering experience in GMP MFG large molecule biologics facilities.
  • The ability to lead and/or support multiple projects simultaneously
  • Track record of successful program execution and team outcomes
  • FPX certification and Six Sigma and/or Lean experience are a plus

Other:

  • Ability to travel up to 10%; international and domestic


#LI-Onsite

Required Skills:

Preferred Skills:

Analytical Reasoning, Computerized Equipment Skills, Corrective and Preventive Action (CAPA), Emerging Technologies, Execution Focus, Gemba Kaizen, Issue Escalation, Lean Supply Chain Management, Process Control, Process Engineering, Process Oriented, Product Improvements, Project Engineering, Safety-Oriented, Science, Technology, Engineering, and Math (STEM) Application, Situational Awareness, Technical Research, Technologically Savvy

About Johnson & Johnson

Scio Diamond creates single-crystal Type IIa diamonds for the jewelry market and for industrial applications. It employs a patent-protected chemical vapor deposition (CVD) process in a precisely controlled laboratory setting to produce diamonds. It was founded in 2009 and is headquartered in Greenville, South Carolina.

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Learn more about Johnson & Johnson
Size
141,700 employees
Market Cap
$462.7 billion
Industry
Net Income
$14.7 billion
Founded
1886
5 Year Trend
+5.5%
Revenue
$82.5 billion
NASDAQ

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