Quality Engineer - Cumberland, RI (Mainly Remote)-(REF11622N)
ProPharma Group
Remote
engineer
remote
medical
operating
engineer
deviations
regulatory
regulatory compliance
compliance
pharmacovigilance
lifecycle
biotechnology
australia
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November 24, 2022
ProPharma Group
Seattle, Washington
FULL_TIME
Company Description
ProPharma Group is an industry leading, single source provider for regulatory compliance, pharmacovigilance, and medical information services across the full development lifecycle for pharmaceutical, biotechnology, and medical device companies. Operating around the world with offices in Australia, Canada, Germany, Japan, the Netherlands, Sweden, United Kingdom, and the United States, ProPharma Group's fully integrated service offerings will provide clients with a comprehensive suite of global support services that are required to be competitive in today's dynamic markets. We build successful long-term relationships with clients by providing leading industry knowledge, experience, and proven processes.
Job Description
Client is looking for a Quality Engineer resource for a 3 month project. This will be mainly remote but may require an occasional visit on-site.
Scope
All candidates must be legally eligible to work in the United States.
We are an equal opportunity employer. M/F/D/V
***ProPharma Group does not accept unsolicited resumes from recruiters/third parties. Please, no phone calls or emails to anyone regarding this posting.***
ProPharma Group is an industry leading, single source provider for regulatory compliance, pharmacovigilance, and medical information services across the full development lifecycle for pharmaceutical, biotechnology, and medical device companies. Operating around the world with offices in Australia, Canada, Germany, Japan, the Netherlands, Sweden, United Kingdom, and the United States, ProPharma Group's fully integrated service offerings will provide clients with a comprehensive suite of global support services that are required to be competitive in today's dynamic markets. We build successful long-term relationships with clients by providing leading industry knowledge, experience, and proven processes.
Job Description
Client is looking for a Quality Engineer resource for a 3 month project. This will be mainly remote but may require an occasional visit on-site.
Scope
- Review data that is going into BLA to ensure reports are accurate.
- This will include nonclinical, CMC, and design history file documentation.
- Looking for a quality engineer with some device experience.
- Approx. 30 hours/week
- Minimum 7 years experience required.
- Qualified candidates will possess a Bachelor's degree in scientific or engineering discipline along with 7 plus years related industry experience.
- Proficient in Microsoft Word, Excel, Power Point and Project.
- General knowledge of quality system elements and cGMP regulations.
- Experience providing support to clients with quality issues such as OOS results, deviations and non-conformances arise. Also, provide advisement for the implementation of proper CAPA to resolve deviations and non-conformances.
- Ability to write and revise Standard Operating Procedures.
- Effective written and oral communication skills; ability to write, type, express or exchange ideas; ability to convey information/instructions accurately.
- Carry out duties and responsibilities with limited supervision.
- Flexibility to work occasional weekends and evenings.
- Ability to walk, stand and move about for long periods of time; work with equipment in the field including basic hand tools, lift and manipulate reasonable weights (approximately 35 lbs.), ability to sit and type for long periods of time.
- Ability to plan and manage own work
- Must be willing to travel regionally and/or nationally throughout the US.
All candidates must be legally eligible to work in the United States.
We are an equal opportunity employer. M/F/D/V
***ProPharma Group does not accept unsolicited resumes from recruiters/third parties. Please, no phone calls or emails to anyone regarding this posting.***
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