What are the responsibilities and job description for the Quality Complaints, Senior Associate, GMP/Medical Device (JP10448) position at 3 Key Consulting?
Job Title: Quality Complaints, Senior Associate, GMP/Medical Device (JP10448)
Location: Thousand Oaks, CA.
Employment Type: Contract
Business Unit: Product Complaints & Surveillance
Duration: 1 years with likely extensions or conversion to FTE
Notes: 100% onsite
Posting Date: 06/16/2022
3 Key Consulting is hiring Quality Complaint Senior Associate for a consulting engagement with our direct client, a leading global biopharmaceutical company.
Job Description:
Requirements:
Skills:
Strong organizational skills with the ability to manage multiple projects or assignments. Role may involve periods of prolonged sitting and standing. Role may involve lifting boxes and storage containers of up to 50lbs. Role may involve transporting samples to different buildings across campus.
Top Must-Have Skill Sets:
Day to Day Responsibilities:
Employee Value Proposition:
Career growth/ opportunity
Red Flags:
Candidate needs to have strong attention to details
Interview process:
2 WebEx interviews & 1 Onsite interview
We invite qualified candidates to send your resume to recruiting@3keyconsulting.com. If you decide that you’re not interested in pursuing this position, please feel free to take a look at the other positions on our website www.3keyconsulting.com/careers. You are welcome to also share this opportunity with anyone you think might be interested in applying for this role.
Location: Thousand Oaks, CA.
Employment Type: Contract
Business Unit: Product Complaints & Surveillance
Duration: 1 years with likely extensions or conversion to FTE
Notes: 100% onsite
Posting Date: 06/16/2022
3 Key Consulting is hiring Quality Complaint Senior Associate for a consulting engagement with our direct client, a leading global biopharmaceutical company.
Job Description:
Requirements:
- Bachelor's Degree in Life Sciences or related field or the equivalent combination of education and/or experience.
- Typically 2 plus years of related quality assurance or manufacturing experience in a GMP pharmaceutical or medical device industry.
- Evaluate documentation and operation according to company guidelines.
- Be self-motivated, attentive to details and able to prioritize and meet deadlines. Basic statistical mathematical skills including the ability to trend data.
- Basic project management skills. Independently understand, follow and implement instructions. Written and verbal communication & collaboration skills.
- Strong word processing, database and spreadsheet application
Skills:
Strong organizational skills with the ability to manage multiple projects or assignments. Role may involve periods of prolonged sitting and standing. Role may involve lifting boxes and storage containers of up to 50lbs. Role may involve transporting samples to different buildings across campus.
Top Must-Have Skill Sets:
- Attention to detail in lab environment
- Proficient in MS office
- Strong written and verbal communication skills
- Understanding GMP
- Background in quality inspection high plus
Day to Day Responsibilities:
- Receive, clean, evaluate, and file/store returned samples
- Operate equipment such as cameras, biosafety cabinets, xrays
- Manage inventory of consumables
- Interface with complaint owners and cross functional team members
- Prepare samples for shipment to other locations
Employee Value Proposition:
Career growth/ opportunity
Red Flags:
Candidate needs to have strong attention to details
Interview process:
2 WebEx interviews & 1 Onsite interview
We invite qualified candidates to send your resume to recruiting@3keyconsulting.com. If you decide that you’re not interested in pursuing this position, please feel free to take a look at the other positions on our website www.3keyconsulting.com/careers. You are welcome to also share this opportunity with anyone you think might be interested in applying for this role.
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