ONSITE Monday-Friday, at RTP Manufacturing facility
Site-based role supporting biologics manufacturing--looking for a highly detailed and focused individual who demonstrates a beginning to intermediate level of technical process knowledge, technical writing ability, and subject matter expertise with manufacturing processes and equipment.
Starts as a 6-month contract that can be extended up to 18 months or converted to a permanent role with our client.
This contract role would provide great experience for anyone interested in growing their pharma/tech writing career.
WHAT YOU WILL DO:
Manufacturing documentation of equipment and instrumentation, procedure development, writing, and document revisions
Independently work and collaborate with cross-functional stakeholders to create and/or revise process instructions including master production records (MPRs) and procedures
What you bring:
? Intermediate to advanced level of technical writing skill
? Prior experience in cGMP mfg - Cell Culture, Purification, or Harvest/Cell Clarification
? Project management and project execution
? Technical knowledge of Biologic manufacturing equipment and processes
Education & Experience:
Preferred: Associates or bachelor's degree or equivalent skilled trades or vocational training
Minimum Requirements: High School Diploma along with pharmaceutical experience and/or related life science industries
What we offer for you:
Medical, dental, vision benefits and 401k plan with Randstad
Career experience, growth and potential to extend and/or convert to a permanent position
40 hour work week-Mon-Fri and pay range of $36.00-38.00/hour
This position will provide opportunities to collaborate and innovate with groups of individuals who are all passionate about transforming patient lives.
APPLY NOW and grow your career - let's have a conversation and determine if this would be a great fit for you!