Senior Process Development Manager, Drug Synthesis

Piramal Pharma Limited

Riverview (MI)

On-site

USD 120,000 - 170,000

Full time

6 days ago
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Job summary

Piramal Pharma Solutions Ash Stevens, LLC, Riverview facility, seeks a Manager, Process Development to lead the design and optimization of API synthesis processes. You will supervise planning, ensure contract terms and cGMP requirements are met, and provide technical input to senior management and clients.

You will collaborate with QA/QC, Safety, Engineering, and Operations, generating development reports, coordinating client communications, and directing laboratory or plant activities to meet

Qualifications

  • Ph.D. in Organic Chemistry, Medicinal Chemistry, or Chemical Engineering.
  • Minimum ten (10) years' experience in research and chemical development of drugs and fine chemicals.
  • Wide knowledge of classic and modern synthetic methods.
  • Up to five (5) years of successful track record building and managing research teams.
  • Familiar with project management tools and best practices.

Responsibilities

  • Assess new projects to identify best chemical routes and resources for development.
  • Organize the department to meet timeliness, specifications, and FDA requirements.
  • Conduct literature searches and lab work to identify routes and optimal solutions.
  • Develop in-process methods to monitor chemical processes.
  • Provide technical opinions to elaborate economical, cGMP-compliant processes.
  • Interact with QA, QC, Engineering, Safety, and Operations to align project needs.
  • Prepare technical reports and participate in site management meetings.

Skills

Team leadership
Process development
cGMP knowledge
Project management

Education

Ph.D. in Organic Chemistry, Medicinal Chemistry, or Chemical Engineering

Job description

Piramal Pharma Solutions Ash Stevens, LLC, Riverview facility, seeks a Manager, Process Development to lead the design and optimization of API synthesis processes. You will supervise planning, ensure contract terms and cGMP requirements are met, and provide technical input to senior management and clients.

You will collaborate with QA/QC, Safety, Engineering, and Operations, generating development reports, coordinating client communications, and directing laboratory or plant activities to meet

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