Lead MS&T Scientist: Parenteral Manufacturing & Transfer

Inteldot

Manatí (PR)

On-site

USD 150,000 - 190,000

Full time

4 days ago
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Job summary

Inteldot is seeking an experienced Principal Scientist Lead to provide technical leadership in regulated pharmaceutical manufacturing. You will own end-to-end parenteral processes, drive technology transfers, DoE studies, and process optimization across multiple sites.

The role requires strong cGMP knowledge, project management, and bilingual English/Spanish communication. This position is based in Puerto Rico with flexible hours to meet business needs.

Qualifications

  • Bachelor’s degree in a related scientific discipline with strong regulatory awareness.
  • 7+ years in Technical Services, MS&T, or pharma manufacturing.
  • Experience with parenteral manufacturing, formulation, filling, sterile operations.
  • Knowledge of cGMP, FDA requirements, and regulatory expectations.
  • Experience leading tech transfers, DoE, risk assessments, and FMEA.

Responsibilities

  • Serve as SME for liquid, lyophilized, and prefilled syringe parenteral processes.
  • Lead technology transfer activities from R&D and other sites.
  • Develop and execute DoE and risk assessments for processes.
  • Support validation, process characterization, and process optimization.
  • Coordinate cross-functional teams and project plans.
  • Mentor junior scientists and drive continuous improvement.

Skills

Parenteral manufacturing
Technology transfer
DoE
FMEA
cGMP knowledge
Project management
Cross-functional leadership
Analytical skills
Bilingual English/Spanish

Education

Bachelor’s degree in pharmacy, Engineering, Chemistry, Pharmaceutical Sciences

Tools

DoE software
FMEA tools

Job description

Inteldot is seeking an experienced Principal Scientist Lead to provide technical leadership in regulated pharmaceutical manufacturing. You will own end-to-end parenteral processes, drive technology transfers, DoE studies, and process optimization across multiple sites.

The role requires strong cGMP knowledge, project management, and bilingual English/Spanish communication. This position is based in Puerto Rico with flexible hours to meet business needs.

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