Quality Assurance Associate

Job Title: MCS Associate Quality Assurance

Location: Thousand Oaks, CA

Duration: 12 Months Contract

Description:

Fully onsite at Thousand Oaks

Standard business hours

Under general supervision, this position will perform routine procedures and testing in support of the lab. This position will be responsible for one or more of the following activities: - Performing routine laboratory procedures - Routine analytical testing - Documenting, computing, compiling, interpreting, and entering data - Maintaining and operating specialized equipment - Initiating and / or implementing changes in controlled documents. Must learn and comply with safety guidelines and cGMPs/CFRs which includes, but is not limited to, the maintenance of training records, laboratory documentation, written procedures, building monitoring systems and laboratory log books.

Preferred Qualifications

• Ability to adhere to regulatory requirements, written procedures and safety guidelines? Ability to evaluate documentation/data according to company and regulatory guidelines? Ability to organize work, handle multiple priorities and meet deadlines? Strong written and oral communication skills? Must be detail orientated? Must be flexible and adaptable to changing priorities and requirements? Demonstrate understanding of regulatory requirements, safety guidelines and factors impacting compliance? Demonstrates understanding of when and how to appropriately escalate.? May identify, recommend and implement improvements related to routine job functions.? Must learn and comply with safety guideline and cGMPs.
• Basic Qualifications
• Bachelor degree OR Associate degree and 4 years of directly related experience OR High school diploma / GED and 6 years of directly related experience

Top 3 Must Have Skill Sets:

• Team player
• Quality mindset
• MUST be willing to learn and follow direction in a GMP environment as it relates to SOP guidance/ etc.

Day to Day Responsibilities:

-General inspection of received shipments of raw materials, components, and labels

-Sampling of chemical raw materials and preparation of sample shipments

-Quality inspection and dimensional analysis for component and label batches

-Review of GMP shipment paperwork

-GMP controlled document review

-Receiving operations oversight and consultation (Purposeful Presence on the Floor)

-Initiation of deviation records

Employee Value Proposition:

Unique industry experience, opportunity

Possible Extension:

Yes