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Quality Specialist
2 weeks ago
West Greenwich, Rhode Island, US

Job Description

Manager is open to Post Grad candidates that has technical writing experience from school.

Job Details: Responsible for supporting the deviation of major event related large molecule Bulk Drug Substances (BDS) manufactured at


 Rhode Island (ARI). Primary responsibilities of this position include support the investigation process, perform investigation, project manager the owning deviations, CAPA generations, lead functional team, communicate with management when situation is holding the progress of the deviations. Skills: ; knowledge of process and faculty equipment, and the ability to interpret and apply Good Manufacturing Practices (GMP); quality assurance or manufacturing experience in the pharmaceutical industry; written and spoken fluency required in specific language needed

Max Rate Not to Exceed (If this differs from the job posting template): 
(No Value)

Why is the Position Open? 
Supplement additional workload on team

Top 3 Must Have Skill Sets: 
2-3 years of Technical Writing

1+ years
Project management knowledge

Day to Day Responsibilities: 
Call meetings, lead functional team, technical write deviations, work cross functionally with multiple teams (PD, Mfg, QA, QC, SC, Warehouse).

Employee Value Proposition: 
* Candidate will have the opportunity to work in a challenging yet rewarding environment. * This can be assigned special projects related to operational excellent
* From investigation stand point, this candidate will learn the operational process in the biotech operations (QC, Engineering, Warehouse)

Possible Extension: 

Red Flags: 
No experience in Pharmaceutical industry.
No experience with technical writing

Interview Process: 
Initial phone interview followed by an in person, and (potentially) panel forum.

Job Requirements

management, writing, manager, assurance, Bulk, call, CAPA, Communicate, deviation, drug


Job Code: 824557

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Recruiter N. Indraneel
Phone +9737747831

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