7 Quality Complaints, Senior Associate, GMP/Medical Device (JP10448) Jobs in Thousand Oaks, CA

SORT BY

SET JOB ALERT

OFF

Details...

Quality Complaints, Senior Associate, GMP/Medical Device (JP10448)

3 Key Consulting

Thousand Oaks, CA | Full Time

$102k-123k (estimate)

3 Months Ago

Quality Complaints, Senior Associate, GMP/Medical Device (JP10448)

3 Key Consulting

Thousand Oaks, CA | Full Time

$97k-116k (estimate)

9 Months Ago

Quality Complaints, Senior Associate, GMP/Medical Device (JP10246)

3 Key Consulting

Thousand Oaks, CA | Full Time

$97k-116k (estimate)

9 Months Ago

Quality Assurance Associate, Biopharma Medical Device (JP9524)

3 Key Consulting

Thousand Oaks, CA | Full Time

$97k-116k (estimate)

9 Months Ago

Engineer, Biotech Medical Device Complaints Investigator (JP10155)

3 Key Consulting

Thousand Oaks, CA | Full Time

$106k-129k (estimate)

3 Months Ago

Engineer, Complaints Technical Investigator Medical Device (JP12260)

3 Key Consulting

Thousand Oaks, CA | Full Time

$98k-119k (estimate)

7 Months Ago

Engineer, Biotech Medical Device Complaints Investigator (JP10155)

3 Key Consulting

Thousand Oaks, CA | Full Time

$98k-119k (estimate)

9 Months Ago

Quality Complaints, Senior Associate, GMP/Medical Device (JP10448)

3 Key Consulting Thousand Oaks, CA

$97k-116k (estimate)

Full Time | Business Services 9 Months Ago

Save

3 Key Consulting is Hiring a Quality Complaints, Senior Associate, GMP/Medical Device (JP10448) Near Thousand Oaks, CA

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:

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/ opportunityRed Flags:
Candidate needs to have strong attention to detailsInterview 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.