|Reference # : ||18-37197
||Title : ||Quality Systems Specialist - III //La Verne, CA with A Big Pharmaceutical Company|
|Position Type : ||Contract|
|Experience Level : ||
||Start Date / End Date : ||07/16/2018 / 01/13/2019
| Description |
|Job Title: Quality Systems Specialist - III|
Work Location: La Verne, CA
Length of Assignment: 6 Months
Position Type: Contract Full Time
Client: A Big Pharmaceutical Company
• Responsible for reviewing, editing and approving technical documentation supporting Commercial Operations, Quality Control as well as Validation activities such as QC instrument qualification, I/O/PQ documents, and computerized systems assessments while ensuring compliance with applicable regulatory requirements.
• Support the data integrity program, including performing routine data integrity audits.
Knowledge and Skills requirements:
• Work independently on assignments that are complex in nature where analysis of situations or data requires an in depth evaluation of different factors. Normally receives minimal instruction on routine work and receive general instructions on new assignments.
• Interacts with appropriate departments to establish priorities and deadlines for technical documentation. Demonstrates strong knowledge of current Good Manufacturing Practice (FDA, EU, and ICH) requirements and quality systems, with the ability to assess compliance risks.
Demonstrates analytical problem solving skills, ability to explain complex concepts with clarity and simplicity, perform detail-oriented work with a high degree of accuracy.
**Minimum 6 years experience required
**Minimum of a Bachelors Degree Required
If you are interested in this job than please send me your most updated resume on firstname.lastname@example.org or you can reach me at #973-507-7579