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Biotech Quality Control Jobs in Arizona (NOW HIRING)

BioLab Holdings, Inc.

Quality Inspector I

Mesa, AZ · On-site

Description BioLab Holdings is a biotechnology company committed to raising the standard of caring ... Process Support: • Follow established quality control processes and tissue handling procedures ...

New

RD Partners

Biospecimen Coordinator I

Tucson, AZ · On-site

$30/hr

Execute sample labeling and perform final quality control checks to verify labeling accuracy. · ... We provide job opportunities within major pharmaceutical, biopharmaceutical, biotechnology, and ...

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All JobsBiotech Quality Control JobsBiotech Quality Control Jobs in Arizona

Biotech Quality Control information

See Arizona salary details

$28.4K

$75.8K

$120.7K

How much do biotech quality control jobs pay per year?

As of Jul 18, 2026, the average yearly pay for biotech quality control in Arizona is $75,784.00, according to ZipRecruiter salary data. Most workers in this role earn between $56,400.00 and $93,200.00 per year, depending on experience, location, and employer.

Does QA or QC pay more?

In biotech quality control, Quality Assurance (QA) roles typically pay slightly more than Quality Control (QC) positions due to their broader responsibilities in process oversight and compliance. Both roles require attention to detail and knowledge of industry regulations, but QA positions often involve more strategic planning and documentation, which can influence salary differences.

What are the typical daily responsibilities of someone working in Biotech Quality Control?

On a daily basis, a Biotech Quality Control professional performs routine testing and analysis of raw materials, intermediates, and finished products to ensure they meet established specifications. This involves preparing samples, operating analytical equipment, maintaining accurate records, and documenting results in compliance with regulatory guidelines. Quality Control staff also collaborate closely with production, quality assurance, and research teams to troubleshoot issues and support process improvements. Regular internal audits and participation in team meetings are common, making communication and teamwork key parts of the job.

How to become a biotech quality control specialist?

To become a biotech quality control specialist, candidates typically need a bachelor's degree in biology, chemistry, or a related field. Relevant skills include knowledge of laboratory techniques, quality assurance processes, and familiarity with regulatory standards like GMP. Certifications such as ASQ CQE or training in laboratory management can enhance job prospects.

What is the highest paying job in biotech?

In biotech quality control, senior roles such as Director of Quality Assurance or Vice President of Quality typically have the highest salaries, often exceeding six figures. These positions require extensive experience, leadership skills, and knowledge of regulatory standards like GMP and ISO.

What is a Biotech Quality Control job?

A Biotech Quality Control (QC) job involves ensuring that biological products, processes, and facilities meet regulatory and quality standards. QC professionals conduct testing, analyze data, and document results to verify product safety and efficacy. They work with laboratory techniques such as PCR, HPLC, and microbiological testing. The role is critical in maintaining compliance with industry regulations like GMP and FDA guidelines.

What are the key skills and qualifications needed to thrive in the Biotech Quality Control position, and why are they important?

To excel in Biotech Quality Control, candidates typically need a background in biology, chemistry, or related sciences, with strong knowledge of laboratory techniques and regulatory requirements. Familiarity with laboratory information management systems (LIMS), Good Manufacturing Practices (GMP), and common analytical instruments such as HPLC or PCR is highly valued. Attention to detail, problem-solving abilities, and effective communication are crucial soft skills for this role. These competencies are vital for ensuring that biotech products consistently meet quality and compliance standards essential for patient safety and regulatory approval.

What does quality control do in biotech?

In biotech, quality control (QC) involves testing and inspecting products, raw materials, and processes to ensure they meet safety, efficacy, and quality standards. QC teams use analytical techniques and documentation to identify deviations and maintain compliance with regulatory requirements such as GMP. This role is essential for ensuring product consistency and regulatory approval.
What are the most commonly searched types of Biotech Quality Control jobs in Arizona? The most popular types of Biotech Quality Control jobs in Arizona are:
What are popular job titles related to Biotech Quality Control jobs in Arizona? For Biotech Quality Control jobs in Arizona, the most frequently searched job titles are:
What job categories do people searching Biotech Quality Control jobs in Arizona look for? The top searched job categories for Biotech Quality Control jobs in Arizona are:
What cities in Arizona are hiring for Biotech Quality Control jobs? Cities in Arizona with the most Biotech Quality Control job openings:
Biotech Quality Control jobs near you
Quality Control Associate

Quality Control Associate

Dawar Consulting, Inc.

Tucson, AZ

$23 - $25/hr

Full-time

Medical, Dental, Vision, Retirement

Posted 26 days ago

Job description

Our client, a world leader in biotechnology and life sciences, is seeking a "Quality Control Associate" based in Tucson, AZ.

Job Duration: Long-Term Contract (Possibility Of Extension)
Rate: $25.75/hr on W2
Company Benefits: Medical, Dental, Vision, Paid Sick Leave, 401K

Summary: The QC Associate supports raw material, in‑process, and finished goods testing in an ISO 13485/cGMP environment. This role performs routine inspections, documents results, maintains lab equipment, and ensures compliance with quality and safety standards. The individual will work with complex systems, support investigations (OOS/non‑conformance), maintain inspection‑ready labs, and generate QC documentation for Device History Records.

Key Responsibilities:
  • Perform testing of raw materials, in‑process samples, and finished goods
  • Document results, complete batch records, and generate qualification reports
  • Conduct data analysis and support OOS/non‑conformance investigations
  • Maintain QC lab, equipment, and records per cGMP and OP requirements
Requirements:
  • HS Diploma + 7 years experience, OR Associate’s + 3 years, OR Bachelor’s + <1 year
  • Hands‑on lab experience; strong data analysis and troubleshooting skills
  • Accurate pipetting, attention to detail, and ability to meet deadlines
  • Experience in regulated environments (GLP, cGMP, ISO) preferred
  • Ability to lift 25 lbs and work on feet for extended periods

If interested, please share your updated resume at hr@dawarconsulting.com/lakshmi@dawarconsulting.com