Senior Thermal MSAT Engineer for Biologics

Johnson Johnson

Wilson (NC)

On-site

USD 79,000 - 120,000

Full time

4 days ago
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Job summary

Johnson & Johnson's Manufacturing Science and Technology team in Wilson, NC seeks an Experienced Engineer - Thermal to join the MSAT Thermal Validation group. You will lead autoclave cycle development, qualification activities, and document execution.

The role requires a degree in life sciences or engineering, at least 3 years in pharmaceutical manufacturing, and proven ability to work independently under tight deadlines while coordinating with contractors and internal teams.

Qualifications

  • Degree in Life Sciences, Engineering, Biology, Biochemistry, or related field.
  • At least 3 yrs experience in the pharmaceutical manufacturing industry.
  • Excellent verbal and written communication; ability to engage with internal and external customers.
  • Proficient in MS Office, Excel, SAP.
  • Ability to work independently with tight deadlines.
  • Experience in biological Thermal Validation (minimum 2 years).

Responsibilities

  • Lead MSAT activities in Thermal Validation compliant with US/EU regulations.
  • Develop MSAT documentation and coordinate reviews and approvals.
  • Review and approve documents prepared by MSAT colleagues.
  • Field execution of MSAT protocols.
  • Coordinate MSAT activities with Manufacturing and contractors.
  • Prepare reports for completed protocols and manage change control.

Skills

Thermal validation
Communication skills
Independent work
Microsoft Office
SAP
Engineering mindset

Education

Bachelor's degree in Life Sciences, Engineering, Biology, Biochemistry, or related field

Tools

MS Office
Excel
SAP

Job description

Johnson & Johnson's Manufacturing Science and Technology team in Wilson, NC seeks an Experienced Engineer - Thermal to join the MSAT Thermal Validation group. You will lead autoclave cycle development, qualification activities, and document execution.

The role requires a degree in life sciences or engineering, at least 3 years in pharmaceutical manufacturing, and proven ability to work independently under tight deadlines while coordinating with contractors and internal teams.

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