Manufacturing Specialist Investigator (JP10551)
Company: 3 Key Consulting
Location: West Greenwich
Posted on: April 1, 2026
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Job Description:
Job Title : Manufacturing Specialist Investigator (JP10551)
Location: West Greenwich Rhode Island (Hybrid) Employment Type :
Contract Duration : 6 months with likely extensions Job posting
date : 7/14/2022 Note: This is a hybrid role (Onsite and remote) ?
3 Key Consulting is hiring a Manufacturing Specialist Investigator
for a consulting engagement with our direct client, a leading
global bio-pharmaceutical company. Job Summary: Operations is
currently seeking a Manufacturing Specialist Investigator (External
worker) in our site Investigation group. In support of companies
mission to serve patients, we are a diverse team working to
continuously improve our clinical and commercial drug Substance
Operations to ensure supply and to optimize the patient experience.
The Manufacturing Specialist Investigator - conducts technical
investigations from our clinical and commercial drug Substance
Operations. This role understands the investigation process as well
as manufacturing processes for the Rhode Island Facility. The
Manufacturing Specialist Investigator owns major and trend
deviations to support identifying root cause and will also
participate in multi-functional idealization of design solutions
(CAPAs). Also maintains close interaction with the Manufacturing
leads, engineering, Process Development, Quality Controls, Supply
Chain, and quality functions to mitigate product impact and
contribute to product/process improvement. Basic Qualifications:
Doctorate degree OR Master’s degree and 3 years of Bio
pharmaceutical Operations experience OR Bachelor’s degree and 5
years of Bio pharmaceutical Operations experience 2 years of
experience in investigation process industry experience, non
academia within biopharm environment Must have previous technical
writing experience, experience In investigation process (RCA) and
Drug Substance Experience Demonstrate understanding and application
of Drug Substance process, data mining, Microsoft office tool,
Quality and compliance. Strong technical writing and interpersonal
skills (able to influence tri functional team and organizational
leads) Ideal Candidate: Previous client Experience Demonstrated Six
Sigma proficiency specifically for root cause analysis methodology
Experience in leading continuous improvement activities by driving
the implementation of process and product quality improvement
initiatives Top Must have Skill Sets: 2 years of proven ability in
investigation process Strong technical writing Proven Six Sigma
proficiency specifically for root cause analysis methodology
Understanding and application of Drug Substance process, data
mining, quality and compliance. Day-To-Day Responsibilities: Manage
investigation process such as coordinating meetings, gathering
evidence, data mining, performing interviews Employee Value
Proposition: Growth, opportunity, experience Red Flags: No previous
experience in drug substances or investigation process Interview
Process: 1-2 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 position, please feel free
to look at other positions on our website www.3keyconsulting.com .
You are welcome to also share this posting with anyone you think
might be interested in applying for this role. Regards, 3KC Talent
Acquisition Team
Keywords: 3 Key Consulting, Salem , Manufacturing Specialist Investigator (JP10551), Healthcare , West Greenwich, Massachusetts
