Description:

Project Overview:

• Quality Associate and Project Management resources in support of the project on implementing a new policy in Process Development

• Quality and process support to help facilitate transition of projects from a research environment to a validated process.

• Provide SOPs, documents, and templates in order to facilitate process development and progress from phase I to II to III

Responsibilities

o Will write any new SOPs, documents, and/or templates needed to complete the project

o Will work with all stakeholders to ensure a mutually agreed upon process

Skills:

translational medicine, translational science, Technical writing, Process Development, GMP, r&d

Additional Skills & Qualifications:

Experience working between the R&D and clinical / regulated GMP production space. This is translational medicine or translation science experience.

Quality systems with technical writing and process development documentation experience (SOPs, creating templates, job aids, etc.).

Experience Level:

Expert Level

About Actalent:

Actalent connects passion with purpose. Our scalable talent solutions and services capabilities drive value and results and provide the expertise to help our customers achieve more. Every day, our experts around the globe are making an impact. We’re supporting critical initiatives in engineering and sciences that advance how companies serve the world. Actalent promotes consultant care and engagement through experiences that enable continuous development. Our people are the difference. Actalent is an operating company of Allegis Group, the global leader in talent solutions.

The company is an equal opportunity employer and will consider all applications without regards to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.