Associate Quality Control JP

Position: Associate Quality Control - (JP9845)
Job Title: Associate Quality Control - (JP9845)
Location: Thousand Oaks, CA.
Employment Type: Contract
Business Unit: ATO Quality Control Chemistry and Biochemistry
Duration: 1+ years (with likely extensions)
Notes: Onsite. Entry-level
Posting Date: 2/18/22

3 Key Consulting is hiring a 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 Quality Control Chemistry group. 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.

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

Top Must-Have Skill Sets:

• Must have bachelor’s degree & 1-3 years of industry experience, open to the industry - manufacturing, cosmetics, pharma, biotech etc.
• Must have cGMP Experience & Experience in general compendia testing
• Flexible hours

Day to Day Responsibilities:

• 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.
• General Lab housekeeping

Basic Qualifications:

• Must have bachelor’s degree & 1-3 years of industry experience, open to the industry - manufacturing, cosmetics, pharma, biotech etc.
• Must have cGMP Experience & Experience in general compendia testing.

Red Flags:

• Travel Distance
• Lack of flexibility

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

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