Senior MSAT - Tech Transfer for New Drug Products

Simtra BioPharma Solutions

Bloomington (IN)

On-site

USD 90,000 - 130,000

Full time

14 days+
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Benefits offered by this job

Medical & Dental Coverage
401(k) Retirement Savings with Company
Time Off Program
Education Assistance Program
Employee Assistance Program

Job summary

Simtra BioPharma Solutions in Bloomington, IN, is seeking a MSAT Senior Associate to lead onboarding and process development for new drug products. You will work with cross-functional teams across program management, sales, supply chain, R&D, and more, coordinating development and transfer to commercial operations.

You will design processes, supervise development studies, and contribute to PPQ strategies, while supporting daily manufacturing and driving process improvements.

Qualifications

  • Bachelor’s degree required, preferably in a science or engineering field.
  • Deep knowledge of aseptic processing, sterile filtration, and clinical manufacturing.
  • Experience: 5 years pharmaceutical manufacturing with 3+ years MSAT/Tech Transfer.
  • Proficient in MS Office and enterprise software (e.g., JDE, Trackwise).

Responsibilities

  • Lead onboarding and process development for new drug products with cross-functional teams.
  • Develop technical transfer documents and PPQ strategies.
  • Support daily manufacturing operations and drive process improvements.
  • Own deviations, CAPAs, change control, and product release evaluations.

Skills

MSAT/Tech Transfer
Aseptic processing
Process development
Cross-functional collaboration
Regulatory knowledge

Education

Bachelor's degree

Tools

JDE
BPLM
MiniTab
Trackwise

Job description

Simtra BioPharma Solutions in Bloomington, IN, is seeking a MSAT Senior Associate to lead onboarding and process development for new drug products. You will work with cross-functional teams across program management, sales, supply chain, R&D, and more, coordinating development and transfer to commercial operations.

You will design processes, supervise development studies, and contribute to PPQ strategies, while supporting daily manufacturing and driving process improvements.

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