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Documentation Administrator
3 weeks ago
Location: Newton, MA
Pay Rate: $32.29
Duration: 3 months+
Hours: 9:00 a.m. to 5:00 p.m.
Responsibilities:
" Disposition non-conforming material (NCMR).
" Lead and/or participate in product complaint investigations leading to root cause.
" Propose, lead, initiate and follow-up on Corrective Action and Preventive Actions (CAPA).
" Ensuring that all changes and associated documents are managed in accordance with internal and external standards, policies, and procedures.
" Ensuring the accuracy (Quality) of documents with regards to: numbering formatting, revisions, and content per approved changes.
" Incoming part inspection; ~ 70% Mechanical, 30% Electrical.
" In-process Inspection.
Required Experience
" HS diploma/GED
" 2-5 yrs. combined experience of Document Control, Inspection, and/or Quality Assurance experience
" Working knowledge of SAP PLM (1-2 yrs.)
" Proficient with MS WORD and EXCEL
" Strong organizational skills, detail oriented, and the ability to meet changing deadlines on a fast-moving environment
" Ability to communicate effectively within a technical environment
" Team player who is customer driven
" No travel required.
Preferred Experience
" Prior Medical Device/Biotech experience
" Prior experience with a Document Control Platform such as Arena or Agile
" Ability to work semi-independently within a regulated environment
Benefits:(employee contribution)
Health insurance
Health savings account
Dental insurance
Vision insurance
Flexible spending accounts
Life insurance
Retirement plan
All qualified applicants will receive consideration for employment without regard to age, race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or status as a protected veteran.
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