Sign upLog in

Technical Writer - Life Science

IntelliPro Group Inc.

Research Triangle Park, NC

Apply
JOB DETAILS
SKILLS
Analysis Skills, Biology, Biotech and Pharmaceutical, Campaigns, Communication Skills, Cross-Functional, Current Good Manufacturing Practice (cGMP), Customer Support/Service, Data Sets, Diversity, Documentation, Drug Manufacturing, Drug Products, FDA Requirements, Genetics, Leadership, Manufacturing, Project/Program Management, Realtime Transport Protocol, Service Delivery, Team Player, Technical Writing, Writing Skills
LOCATION
Research Triangle Park, NC
POSTED
Today
Job Title: Technical Writer
Duration: 06 months with possible extension
Office: Research Triangle Park, NC 27709
Pay rate: $60/hr. on W2

Job Summary:
  • As a member of Manufacturing Sciences, the Technical Writer will provide written documentation expertise to the clinical and commercial manufacturing campaigns run at the Parenteral Facility RTP Pharma Site. The focus of this position will be as a key leader for investigations and project implementation for Manufacturing Sciences using their technical expertise on fill/finish, visual inspection, and packaging.
  • The incumbent will be tasked with writing PPQ Protocols, PPQ Reports, data verification activities for confirmation of source data for reports, preliminary writing for sections of the filing.  Creating the Master Sample Matrix (MSM) for Manufacturing personnel to be used for on the production floor activities.

Qualifications Required:
  • Life Science background with at least 5 years’ experience.
  • Good communication and project management skills appropriate for leadership of tech transfer projects
  • Working knowledge in technical understanding of Parenteral Filling Operations (e.g. Filling Isolator, Lyophilizer, Visual Inspection) including transfer of such processes into full-scale drug product manufacturing facilities
  • Excels at working in a team environment
  • Comfortable analyzing scientific datasets/analytical skills with excellent written skills
  • Ability to work independently and support a large cross-functional group
  • Some knowledge of cGMP, FDA/EMA regulations, Process Performance Qualification, Continued Process Verification.

About Us:
Founded in 2009, IntelliPro is a global leader in talent acquisition and HR solutions. Our commitment to delivering unparalleled service to clients, fostering employee growth, and building enduring partnerships sets us apart. We continue leading global talent solutions with a dynamic presence in over 160 countries, including the USA, China, Canada, Singapore, Japan, Philippines, UK, India, Netherlands, and the EU.
IntelliPro, a global leader connecting individuals with rewarding employment opportunities, is dedicated to understanding your career aspirations. As an Equal Opportunity Employer, IntelliPro values diversity and does not discriminate based on race, color, religion, sex, sexual orientation, gender identity, national origin, age, genetic information, disability, or any other legally protected group status. Moreover, our Inclusivity Commitment emphasizes embracing candidates of all abilities and ensures that our hiring and interview processes accommodate the needs of all applicants. Learn more about our commitment to diversity and inclusivity at https://intelliprogroup.com/.

Compensation: The pay offered to a successful candidate will be determined by various factors, including education, work experience, location, job responsibilities, certifications, and more. Additionally, IntelliPro provides a comprehensive benefits package, all subject to eligibility.

Powered by JazzHR

About the Company

I

IntelliPro Group Inc.

Resume Resources

Free Resume TemplatesFree Resume Builder