12 Specialist Product Quality Jobs in Thousand Oaks, CA
SORT BY
J
A
A
A
S
A
A
3
3
A
R
A
Specialist Product Quality
$95k-120k (estimate)
Full Time
2 Weeks Ago
Advanced Bio-Logic Solutions Corp is Hiring a Specialist Product Quality Near Thousand Oaks, CA
Description:
Note:
***Remote*** any time zone
Ideal candidate:
"This posting is for Contingent Worker, not an FTE"
Note:
***Remote*** any time zone
Ideal candidate:
- B.S. in biochemistry, chemistry, biology, or a related protein or synthetic biotechnology sciences field or an equivalent level of biopharmaceutical experience with responsibility in a quality, analytical development, process development, or manufacturing environment- at least 10 years exp.
- Familiar with pharmaceutical sciences, quality, compliance and regulatory requirements, associated with biologics and synthetic chemical manufacturing and QC testing.
- Previous experience using VEEVA, Track wise and quality systems.
- Knowledge of biopharmaceutical bulk and drug product development, manufacturing, and/or Quality Control Testing.
- Some understanding and experience owning deviations and/or change control in GMP setting.
- Experience with Owning or QA approving GMP documents and records.
- Experience with Product Quality monitoring - APR (Annual Product Review), product monitoring, process monitoring, specifications/In Process controls, or IND/CTA/MA filings.
- Doesn't have filing knowledge not a deal breaker.
- Doctorate degree OR Master degree and 3 years of experience OR Bachelor degree and 5 years of experience OR Associate degree and 10 years of experience OR High school diploma / GED and 12 years of experience
- Familiar with pharmaceutical sciences, quality, compliance and regulatory GMP requirements, associated with biologics and synthetic chemical manufacturing and QC testing.
- B.S. in biochemistry, chemistry, biology, or a related protein or synthetic biotechnology sciences field or an equivalent level of biopharmaceutical experience with responsibility in a quality, analytical development, process development, pharmaceutics, regulatory, or manufacturing environment.
- Previous experience using VEEVA, Track wise and other quality systems.
- Knowledge of biopharmaceutical bulk and drug product development, manufacturing, and/or Quality Control Testing
- Strong project management skills.
- General knowledge of cGMP and filing regulations, practices, and trends pertaining to the manufacture and testing of biopharmaceuticals.
- Previous experience working on a cross-functional team in a matrix environment.
- Excellent written and verbal communication skills, including facilitation and presentation skills.
- Own deviation or change control records for the Product Quality department, leading cross-functional investigation or change planning teams.
- QA review and approve product specifications, deviation, and change control records.
- Use of business tools such as Teams and Smartsheet's, as well as GMP systems such as VEEVA and Track Wise.
"This posting is for Contingent Worker, not an FTE"
Job Summary
JOB TYPE
Full Time
SALARY
$95k-120k (estimate)
POST DATE
04/17/2024
EXPIRATION DATE
06/15/2024
Show more
Similar Jobs
Popular Articles
Top 10 Things to Avoid Putting on a Job Application
Read Article
How to Describe Your Education in a Resume
Read Article
How to Write a Memorable Cover Letter in 5 Ways
Read Article
4 Personal Finance Tips to Make During Job Transition
Read Article
4 Best Camera Setups for Interview
Read Article
Keeping a Job Search Journal: 9 Types of Journaling You Can Do
Read Article
