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Associate Qc Biotech Jobs (NOW HIRING)

Since 1980, we've helped pioneer the world of biotech in our fight against the world's toughest ... Associate Quality Control What you will do Let's do this. Let's change the world. In this vital ...

Since 1980, we've helped pioneer the world of biotech in our fight against the world's toughest ... Associate Quality Control What you will do Let's do this. Let's change the world. In this vital ...

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How much do associate qc biotech jobs pay per hour?

As of Jun 8, 2026, the average hourly pay for associate qc biotech in the United States is $25.46, according to ZipRecruiter salary data. Most workers in this role earn between $18.51 and $31.01 per hour, depending on experience, location, and employer.
What are the most commonly searched types of Qc Biotech jobs? The most popular types of Qc Biotech jobs are:
Infographic showing various Associate Qc Biotech job openings in the United States as of May 2026, with employment types broken down into 1% As Needed, 66% Full Time, and 33% Part Time. Highlights an 97% Physical, 1% Hybrid, and 2% Remote job distribution, with an average salary of $52,962 per year, or $25.5 per hour.
Associate Quality Control - (JP9845)

Associate Quality Control - (JP9845)

3 Key Consulting

Thousand Oaks, CA

Other

Posted 11 days ago


Job description

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 toresumes@3keyconsulting.com. 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 websitewww.3keyconsulting.com/careers. You are also welcome to sharethis opportunity withanyone you think might be interested in applying for this role.