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Quality Assurance Biotech Jobs in Spring, TX (NOW HIRING)

RIGUP -Midstream Oil & Gas

Piping Designer

Houston, TX · On-site

... and QA/QC workflows. * Project Controls & Scope Management: Monitor project scope, track earned ... Experience specifically within pharmaceutical, biotech, advanced manufacturing, or oil & gas ...

Radiomedix, Inc.

Radiochemist

Humble, TX · On-site

Radiochemist RadioMedix Inc., a Biotechnology Company headquartered in Houston, Texas, is seeking ... quality assurance procedures under 21 CFR 211, and ICH guidelines. Research * Develop ...

Radiomedix, Inc.

Radiochemist

Humble, TX · On-site

Radiochemist RadioMedix Inc., a Biotechnology Company headquartered in Houston, Texas, is seeking ... quality assurance procedures under 21 CFR 211, and ICH guidelines. Research * Develop ...

RXinsider LTD.

Microbiologist II - Sterile

Houston, TX · On-site

$65 - $90/hr

... biotech clients, contributing expertise and innovative solutions. * Support the training and ... Communicate effectively across departments, including Quality Assurance, Client Care, and other ...

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Quality Assurance Biotech information

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$11

$26

$55

How much do quality assurance biotech jobs pay per hour?

As of Sep 4, 2026, the average hourly pay for quality assurance biotech in Spring, TX is $26.07, according to ZipRecruiter salary data. Most workers in this role earn between $16.68 and $30.58 per hour, depending on experience, location, and employer.

What is a quality assurance biotech?

A Quality Assurance (QA) Biotech job involves ensuring that biotechnology products meet regulatory and company standards for safety, efficacy, and quality. QA professionals develop and implement quality systems, conduct audits, review documentation, and ensure compliance with Good Manufacturing Practices (GMP) and other regulations. They collaborate with various departments, including manufacturing, R&D, and regulatory affairs, to maintain product integrity. Their role is critical in preventing defects, ensuring consistent processes, and maintaining compliance with industry standards.

What are the key skills and qualifications needed to thrive in quality assurance biotech?

To thrive as a Quality Assurance Biotech, you need a solid understanding of biotechnology processes, quality control methodologies, and regulatory standards such as GMP, often supported by a degree in biology, chemistry, or a related field. Familiarity with laboratory information management systems (LIMS), documentation software, and industry certifications like ASQ or GMP training is highly beneficial. Attention to detail, strong analytical thinking, and effective communication skills are valued soft skills in this role. These abilities ensure precise compliance with regulatory requirements, facilitate collaboration with cross-functional teams, and help maintain the integrity and safety of biotech products.

What are the most common challenges faced by quality assurance professionals in the biotech industry?

Quality Assurance professionals in biotechnology often encounter challenges related to staying up-to-date with evolving regulatory requirements and ensuring that all processes consistently meet strict quality standards. Additionally, managing thorough documentation and collaborating across various departments—such as research, manufacturing, and regulatory affairs—can be complex. Those in the role may also need to respond quickly to deviations or quality events, requiring both proactive problem-solving and excellent organizational skills. However, overcoming these challenges is highly rewarding, as it directly contributes to maintaining the safety and efficacy of biotech products.

What job categories do people searching Quality Assurance Biotech jobs in Spring, TX look for?

The top searched job categories for Quality Assurance Biotech jobs in Spring, TX are:

What cities near Spring, TX are hiring for Quality Assurance Biotech jobs?

Cities near Spring, TX with the most Quality Assurance Biotech job openings:

Quality Assurance Biotech jobs near you
Infographic showing various Quality Assurance Biotech job openings in Spring, TX as of August 2026, with employment types broken down into 1% As Needed, 81% Full Time, 14% Part Time, 3% Contract, and 1% Nights. Highlights an 92% Physical, 1% Hybrid, and 7% Remote job distribution, with an average salary of $54,216 per year, or $26.1 per hour.

Quality Control Project Lead - Cell Therapy

Lonza

Houston, TX • On-site

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Posted 29 days ago

Lonza rating

8.3

Company rating: 8.3 out of 10

Based on 42 frontline employees who took The Breakroom Quiz

24th of 86 rated pharmaceutical

Job description

Quality Control Project Lead - Cell Therapy
Location: Houston, Texas - Onsite
Schedule: Monday-Friday, 8:00 AM-4:30 PM
As a Quality Control Project Lead, you will play a critical role in supporting late-stage cell therapy programs as they progress through Phase III, PPQ, and commercial launch activities. This position serves as the primary Quality Control representative for assigned client programs, partnering closely with QC laboratories, Program Management, Quality Assurance, Manufacturing, and customers to ensure successful technology transfers, analytical readiness, and project execution.
What you will get:
A competitive compensation package. In addition, below you will find a comprehensive summary of the benefits package we offer:
  • Performance-related bonus
  • Medical, dental and vision insurance
  • 401(k) matching plan
  • Life insurance, as well as short-term and long-term disability insurance
  • Employee assistance programs
  • Paid time off (PTO)

Compensation for this role will be determined by the candidate's qualifications, skills, experience, and relevant knowledge.
What you will do:
  • Lead Quality Control activities supporting client programs through technology transfer, process development, qualification, validation, and commercial readiness efforts.
  • Serve as the primary QC representative on cross-functional project teams, communicating testing status, timelines, risks, and analytical requirements to internal stakeholders and customers.
  • Coordinate new product introductions and support implementation of new methods, assays, and processes within the QC organization.
  • Author, review, and approve technical documentation including transfer plans, assay transfer protocols, reports, specifications, sampling plans, stability reports, comparability reports, and bridging studies.
  • Collaborate with BioAnalytical Services and laboratory teams to support method qualification, validation, and analytical lifecycle management activities.
  • Provide technical support for investigations, deviations, out-of-specification events, CAPAs, audits, and regulatory compliance activities.
  • Support stability programs by coordinating protocol initiation, tracking testing milestones, and ensuring timely reporting of results and project deliverables.
  • Act as a liaison between customers and internal teams, ensuring expectations, commitments, and project timelines are effectively managed and communicated.

What we are looking for:
  • Bachelor's degree in a scientific discipline required.
  • Experience in Quality Control within a regulated biopharmaceutical, biotechnology, cell therapy, or related GMP environment.
  • Strong knowledge of cell therapy product development, technology transfer, analytical methods, validations, and product-specific qualification requirements.
  • Experience supporting new product introductions and cross-functional project execution.
  • Demonstrated technical writing experience, including preparation and review of scientific reports and GMP documentation.
  • Customer-facing experience with the ability to effectively manage client relationships and stakeholder communications.
  • Strong organizational, planning, and project management capabilities with proven ability to manage multiple priorities simultaneously.
  • Experience with analytical techniques such as flow cytometry, ELISA, PCR, cell viability, or cell-based assays preferred.
  • Excellent verbal and written communication skills, attention to detail, and ability to influence cross-functional teams.

About Lonza
At Lonza, our people are our greatest strength. With 30+ sites across five continents, our globally connected teams work together every day to manufacture the medicines of tomorrow. Our core values of Collaboration, Accountability, Excellence, Passion and Integrity reflect who we are and how we work together. Everyone's ideas, big or small, have the potential to improve millions of lives, and that's the kind of work we want you to be part of.
Innovation thrives when people from all backgrounds bring their unique perspectives to the table. At Lonza, we offer equal employment opportunities to all qualified applicants regardless of race, religion, color, national origin, sex, sexual orientation, gender identity, age, disability, veteran status, or any other characteristic protected by law.
Ready to shape the future of life sciences? Apply now.

What Lonza employees say

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About Lonza

Sourced by ZipRecruiter

Industry

Biotechnology research and development and pharmaceutical and medicine manufacturing

Company size

10,000+ Employees

Headquarters location

Bern, KS, US

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