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Johnson & Johnson

Makes prescription drugs and medical devices

Process Engineering-Process Validation Support

Regulatory & Quality (Life Sciences)Confirmed live in the last 24 hours
Full-timeWilson, NC, USA$79k - $120k

About the Job

Requirements

  • A degree in Life Sciences, Engineering, Biology, Biochemistry, or a related scientific field is required.
  • Excellent verbal and written communication skills, including the ability to communicate effectively with internal and external customers.
  • Computer proficiency, including Microsoft Office, Excel, and SAP.
  • At least 3 years of experience in the pharmaceutical manufacturing industry or equivalent.
  • At least 2 years of experience in biological process validation.
  • Ability to work independently with minimum supervision to meet tight deadlines.
  • Ability to interact at different organizational levels, perform under pressure, and handle conflicting interests.
  • Ability to work independently under general direction, prioritize goals, and manage time effectively.
  • Ability to adapt, remain flexible, and solve problems.
  • Ability to lead multifunctional teams and manage complexity and change.
  • Knowledge and application of industry regulations, including those of the FDA, EMEA, and other authorities.

Responsibilities

  • Conduct MSAT activities in compliance with US and EU regulations, local and global procedures, and EHS&S requirements.
  • Provide process validation support, including mixing studies, microbial hold studies, media challenges, in-line conditioning verification studies, and chemical hold studies.
  • Lead and/or provide technical guidance for process improvement projects and investigations.
  • Develop MSAT documentation, including protocols, procedures, and reports, and coordinate MSAT document review and approval.
  • Review and approve documents prepared by other MSAT colleagues.
  • Execute MSAT protocols in the field.
  • Liaise with Manufacturing to provide support for routine operations and project-based work as required.
  • Compile relevant information from contractors, suppliers, and other departments to develop technical reports.
  • Track and resolve exceptions, events, and nonconformances during MSAT activities.
  • Prioritize MSAT activities in line with Manufacturing and project schedules.
  • Coordinate MSAT activities with contractors and vendors as required.
  • Attend training required to fulfill the role of an experienced MSAT Engineer.
  • Participate in multifunctional teams for projects and investigations as required.

Desired Qualifications

  • Analytical reasoning.
  • Computerized equipment skills.
  • Knowledge of emerging technologies.
  • Gemba Kaizen.
  • Issue escalation.
  • Lean supply chain management.
  • Problem solving.
  • Process control.
  • Process engineering.
  • Process-oriented approach.
  • Product improvement.
  • Application of science, technology, engineering, and mathematics (STEM).
  • Situational awareness.
  • Supply planning.
  • Technical research.
  • Technological proficiency.
  • Validation testing.

About the Company

Johnson & Johnson

Makes prescription drugs and medical devices

Johnson & Johnson develops prescription medicines and makes medical devices for hospitals, and unlike most big drugmakers, it runs both businesses under one roof. In 2015, its Darzalex became the first antibody drug approved for multiple myeloma, a blood cancer. Its medicines treat cancer, immune diseases such as psoriasis, and mental illnesses such as depression, and patented drugs bring in most of its sales. Its MedTech unit makes heart pumps, catheters that treat irregular heartbeats, surgical sutures, and Acuvue contact lenses. It was founded in 1886 to make sterile surgical dressings, is based in New Brunswick, New Jersey, and spun off its consumer brands, such as Tylenol and Band-Aid, as Kenvue in 2023.

Company size
10,001+
Company stage
IPO
Headquarters
New Brunswick, NJ
Founded
1886

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