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Executive Order 11246, Section 503 & VEVRAA EOE, including disability/vets
Design Powerpoint CSV Statistical Analysis Engineer
(Jobs in Providence, RI)
 
Requirement id 108797
Job title Engineer
Job location in Providence, RI
Skills required Design, MS Word, Excel, Powerpoint CSV Statistical Analysis
Open Date 30-Jul-2020
Close Date
Job type Contract
Duration 7 Months
Compensation DOE
Status requirement ---
Job interview type ---
Apply
   Email Recruiter: coolsoft
Job Description Engineer: Design, MS Word, Excel, Powerpoint CSV Statistical Analysis

Note :They need to sit on site in Providence 2-3 days a week so they will need to relo so they can be on site.

Candidate must be our W2 Employee.

Job Description : Validation Engineer Opening in Providence, RI

It combines with parent company On Assignment to make it the 2nd largest IT staffing agency in the country.

It has an opportunity for a Validation Engineer role in the Greater Providence area. This is a 6+ month contract position and the pay rate is flexible depending on experience. Here are the details:

Position: Validation Engineer

Location: Providence, RI

Rate: Negotiable based on experience

Duration: 6+ months

Position Description:

Draft and implement Quality System documentation designed to establish good validation practices within the Organization.

Design validation approaches, supported by appropriate statistical analyses, draft validation protocols, perform and/or coordinate all validation activities, analyze and assemble results, and draft validation reports.

Provide input on user and/or functional requirements of current and future processing equipment, and draft appropriate documentation. Additionally, interface with Contract Manufacturers to ensure all relevant user and functional requirements are met.

Provide support to non-engineering Staff, including those from R&D and Manufacturing, to ensure successful technology transfer and continuous improvement.

Execute assigned duties on time and within budget; pro-actively telegraph delays and other issues to relevant stakeholders.

Comply with all regulatory, corporate, and Quality System policies

Complete other projects and/or assignments as required.

Required Skills:

B.S. / M.S. in engineering or another relevant discipline.

Minimum of 5+ years of experience working within a medical device environment. Experience with device-biologic combination products is highly desirable.

Experience in the areas of Design Documentation (URS, FRS, DS, and other engineering specifications), Validation (IQ, OQ, PQ, PV, CSV, MVP, etc.), Quality Systems (Change Control, Non-Conformances, Requalification, etc)

Understanding of c.G.x.P principles and familiarization with ISO 13485, ISO 14971, and 21C.F.R.820

A strong understanding of statistical analyses is required, as are strong technical writing and presentation skills.

Proficient in Microsoft Word, Excel, PowerPoint.

Must be able to work independently with adequate supervision, multi-task, and support several projects simultaneously.

Must demonstrate strong interpersonal and teamwork skills.

A strong understanding of statistical principles is required, as are strong technical writing and presentation skills.
 
Call 502-379-4456 Ext 100 for more details. Please provide Requirement id: 108797 while calling.
 
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(Engineer: Design, MS Word, Excel, Powerpoint CSV Statistical Analysis in Providence, RI)
     
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