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Biotech Quality Control Jobs in Rosenberg, TX (NOW HIRING)

Danaher

Senior Engineer, Process Validation

Houston, TX · On-site +1

$100K - $130K/yr

... biotechnology? At Aldevron, one of Danaher's 15+ operating companies, our work saves lives-and we ... , QA and RA, and during client audits and regulatory inspections, kaizens and workshop events.

Danaher

Senior Engineer, Process Validation

Houston, TX · On-site +1

$100K - $130K/yr

... biotechnology? At Aldevron, one of Danaher's 15+ operating companies, our work saves lives-and we ... , QA and RA, and during client audits and regulatory inspections, kaizens and workshop events.

TekWissen LLC

Scientist

Houston, TX · On-site

$20 - $25/hr

... Biotechnology, Life science ingredients, Nutrition, Microbial Control, Agriculture, Materials ... Maintenance of quality systems and cGMP compliance for the business by ensuring that all team ...

TekWissen LLC

Scientist

Houston, TX · On-site

... Biotechnology, Life science ingredients, Nutrition, Microbial Control, Agriculture, Materials ... Maintenance of quality systems and cGMP compliance for the business by ensuring that all team ...

TekWissen LLC

Supply Chain Project Manager

Houston, TX · On-site

$35 - $45/hr

... Biotechnology, Life science ingredients, Nutrition, Microbial Control, Agriculture, Materials ... meet compliance and quality expectations. Required Skills * Bachelor's degree in business ...

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All JobsBiotech Quality Control JobsBiotech Quality Control Jobs in Rosenberg, TX

Biotech Quality Control information

See Rosenberg, TX salary details

$27.2K

$72.6K

$115.5K

How much do biotech quality control jobs pay per year?

As of Jul 20, 2026, the average yearly pay for biotech quality control in Rosenberg, TX is $72,564.00, according to ZipRecruiter salary data. Most workers in this role earn between $54,000.00 and $89,200.00 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 job categories do people searching Biotech Quality Control jobs in Rosenberg, TX look for? The top searched job categories for Biotech Quality Control jobs in Rosenberg, TX are:
What cities near Rosenberg, TX are hiring for Biotech Quality Control jobs? Cities near Rosenberg, TX with the most Biotech Quality Control job openings:
Biotech Quality Control jobs near you
Infographic showing various Biotech Quality Control job openings in Rosenberg, TX as of July 2026, with employment types broken down into 1% Locum Tenens, 1% As Needed, 85% Full Time, 6% Part Time, 1% Temporary, and 6% Contract. Highlights an 81% Physical, 2% Hybrid, and 17% Remote job distribution, with an average salary of $72,564 per year, or $34.9 per hour.
Analytical Chemistry Investigation Specialist

Analytical Chemistry Investigation Specialist

Eagle

Houston, TX

Full-time

Re-posted 2 days ago

Job description

What We're Looking For
We are seeking a highly skilled and detail-oriented Investigation Specialist with expertise in Analytical Chemistry to join our team. This role is responsible for leading and supporting investigations related to laboratory deviations, out-of-specification (OOS) results, and other quality-related issues. The ideal candidate will possess strong analytical capabilities, a thorough understanding of laboratory operations, and the ability to interpret complex scientific data to drive effective root cause analysis and corrective actions.

What You Will Do

  • Lead, conduct, and document investigations into laboratory deviations, non-conformances, OOS/OOT (Out-of-Trend) results, and quality events.

  • Perform detailed root cause analysis using analytical data, laboratory records, and supporting documentation.

  • Analyze and interpret complex analytical chemistry data to identify trends, anomalies, and potential risks.

  • Develop, recommend, and track corrective and preventive actions (CAPAs) to ensure timely and effective resolution.

  • Prepare clear, concise, and compliant investigation reports in accordance with internal procedures and regulatory requirements.

  • Collaborate cross-functionally with Quality Assurance, Production, R&D, and Regulatory Affairs to support investigations and implement solutions.

  • Ensure investigations are completed within established timelines and meet compliance standards.

  • Support internal and external audits by providing documentation and subject matter expertise as needed.

  • Identify recurring issues or trends and contribute to continuous improvement initiatives.

  • Maintain a strong understanding of current regulatory guidelines and industry best practices related to analytical chemistry and quality systems.

Who You Are

  • Bachelor’s degree in Chemistry, Analytical Chemistry, or a related scientific discipline (Master’s degree preferred).

  • 3–5+ years of experience in a regulated laboratory environment (e.g., pharmaceutical, biotechnology, or related industry).

  • Strong knowledge of analytical techniques such as HPLC, GC, UV-Vis, FTIR, or similar instrumentation.

  • Experience with OOS, deviation investigations, and CAPA processes.

  • Familiarity with GMP (Good Manufacturing Practices) and relevant regulatory requirements (e.g., FDA, ICH).

  • Excellent problem-solving, critical thinking, and analytical skills.

  • Strong written and verbal communication skills with the ability to clearly document findings.

  • High attention to detail and strong organizational skills.

  • Ability to manage multiple priorities and meet deadlines in a fast-paced environment.

  • Experience in method validation, method transfer, or stability testing.

  • Prior involvement in regulatory inspections or audits.

  • Knowledge of statistical analysis tools and trending methodologies.

  • Laboratory and office-based role with regular interaction across multiple departments.

  • May require occasional extended hours to support critical investigations or deadlines.

Who We Are

Serving customers since 2004, Eagle offers the highest quality in preparation testing for sterility, bacterial endotoxins, microbial detection, beyond-use dating (BUD) determination and active ingredient potency. State-of-the-art equipment, combined with the experience and knowledge of our team, makes Eagle the best choice for all testing needs. The Eagle team is committed not only to performing the best quality control testing, but also working relentlessly with our customers on solutions if tests receive unexpected results. Learn more at www.eagleanalytical.com. 

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