Specialist Manufacturing (JP9662)
Company: 3 Key Consulting
Location: West Greenwich
Posted on: April 2, 2026
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Job Description:
Job Title: Specialist Manufacturing (JP9662) Location: West
Greenwich, RI. 02817 Employment Type: Contract Business Unit: ARI
Manufacturing Support Duration: 7 months (with likely extensions
and/or conversion to permanent) Posting Date: 1/12/2022 Notes:
Working on site with the opportunity to work remotely in some
instances. 3 Key Consulting is hiring a Specialist Manufacturing
for a consulting engagement with our direct client, a leading
global biopharmaceutical company. Job Description: Operations is
one of three foundational functions at our client with a mission to
manufacture and deliver safe and effective medicine to patients
around the world. The Operations Program at the Rhode Island site
is divided into five functions: Supply Chain, Process Development,
Quality, Manufacturing, and Facilities & Engineering. We are
currently seeking highly motivated, hardworking individuals who
will directly support Manufacturing operations in their newest Next
Generation Biomanufacturing plant. Along with key business partners
and functional groups, this position will focus on directly
supporting manufacturing operations and new product introductions.
The primary responsibilities for this role may include, but are not
limited to the following: Support of manufacturing operations.
Management of Manufacturing process documentation per required
process in accordance with agreed timelines and in adherence with
format, content and style guidelines, giving consideration to
usability and ensuring accuracy, consistency and quality.
Initiating and owning quality records (e.g. change controls,
deviations, CAPAs). Why is the Position Open? Additional workload
on team. Top Must Have Skills: GMP experience. Technical writing
experience. Development of regulated or process documents with the
ability to deliver high quality documentation. Day to Day
Responsibilities: Support of manufacturing operations. Management
of Manufacturing process documentation per required process in
accordance with agreed timelines and in adherence with format,
content and style guidelines, giving consideration to usability and
ensuring accuracy, consistency and quality. Initiating and owning
quality records. Basic Qualifications: Bachelor’s degree in
Engineering, Science or related field. Preferred Qualifications: 3
or more years of experience in Cell Culture or Purification
execution and/or support. Single use technology experience.
Proficient on Microsoft Office Suite. Ability to work independently
and as a team player. Excellent collaboration and problem solving
skills. Ability to work virtually. Ability to understand, apply and
evaluate basic chemistry, biology and physical principles.
Experience with Manufacturing execution and automation systems.
Experience with lab equipment/testing. Experience in influencing
and negotiation. Employee Value Proposition: Great Biotech/pharma
to work for. Grow their skillset. Red Flags: Inexperience in GMP
and technical writing Interview process: Video Skype Panel
Interview We invite qualified candidates to send your resume to
resumes@3keyconsulting.com . If you decide that you’re not
interested in pursuing this particular position, please feel free
to take a look at the other positions on our website
www.3keyconsulting.com/careers. You are also welcome to share this
opportunity with anyone you think might be interested in applying
for this role. Regards, 3KC Talent Acquisition Team
Keywords: 3 Key Consulting, Pawtucket , Specialist Manufacturing (JP9662), Engineering , West Greenwich, Rhode Island
