MCS Associate Quality Control, Biopharma; JP

Position: MCS Associate Quality Control, Biopharma (JP10321)
Job Title:MCS Associate Quality Control, Biopharma (JP10321)
Location:Thousand Oaks, CA. 91320
Employment Type: Contract
Business Unit:ATO Quality Control
Duration:18 months with likely extensions to conversion to FTE
Rate:22 - 26/hour W2.
Posting Date:05/25/2022

3 Key Consulting is hiring a
MCS Associate Quality Control
for a consulting engagement with our direct client, a leading global biopharmaceutical company.

Job Description:
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 logbooks.

Basic Qualifications:
Bachelor’s degree and 2 years of Quality Control, Quality Assurance or related experience
OR Associate’s degree and 6 years of Quality Control, Quality Assurance or related experience
OR High school diploma / GED and 8 years of Quality Control, Quality Assurance or related experience

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.

Why is the Position Open?
Supplement additional workload on team.

Top Must-Have Skill Sets:

• Pipetting
• Documentation
• Attention to Detail
• Quality Control, Quality Assurance or related experience - 2+ years
• Biology degree is ideal - science field (chemistry, biochem, biology)
• Lab experience is a must

Day to Day Responsibilities:
Testing:

• Execute routine and non-routine testing procedures and assays
• Perform data analysis of testing results and communicate results to appropriate sources
• Comply with safety guidelines
• Learn and comply with GLP, and cGMPs, which includes, but are not limited to, the maintenance of training records, laboratory notebooks, written procedures, equipment monitoring systems and laboratory logbooks.
  Material/Data Management
• Responsible for documenting, computing, compiling, interpreting, and entering data
• Responsible for the inventory management of all media, and reagents
• Ensure the timely disposal of tested samples

Employee Value Proposition:
The person in this role will work with 22 different molecules. You will be very hands on and see medicines go to patients. This position has great opportunities for growth.

Red Flags:
No experience outside of course work
Entry level position

Interview process:
Phone screening followed by in-person interview.

We invite qualified candidates to sendyour resume to Ifyou decide that you’re not interested in pursuing this position, please feel free to look at the other positions on our website are welcome to also sharethis opportunity with anyone you think might be interested in applying for this role.
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