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

RIGUP -Midstream Oil & Gas

Piping Designer

Houston, TX · On-site

  • Medical

  • Dental

  • Vision

... 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

Houston, 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

Houston, 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 ...

Amazon

Area Manager II - Katy, TX

Katy, TX · On-site

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

... Quality Assurance, Human Resources to develop plans to meet business objectives - Lift up to 49 ... biotech, electronics, energy, instrumentation, machinery, defense/aerospace, medical, cosmetics ...

Amazon

Area Manager II

Houston, TX · On-site

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

... Quality Assurance, Human Resources to develop plans to meet business objectives * Lift up to 49 ... biotech, electronics, energy, instrumentation, machinery, defense/aerospace, medical, cosmetics ...

Danaher

Senior Engineer, Process Validation

Houston, TX · On-site +1

$100K - $130K/yr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

... 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

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

... 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.

Arc Technologies Group

IT/OT Consultant

Houston, TX

  • Medical

  • Dental

  • Vision

  • Retirement

... biotechnology, and healthcare. At Arc Technologies Group, we have a passion for learning and ... D, quality assurance, and manufacturing, to deliver IT/OT solutions that meet business needs ...

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Quality Assurance Biotech information

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How much do quality assurance biotech jobs pay per hour?

As of Aug 13, 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, 78% Full Time, 15% Part Time, 5% Contract, and 1% Nights. Highlights an 87% Physical, 4% Hybrid, and 9% Remote job distribution, with an average salary of $54,216 per year, or $26.1 per hour.

QC Senior Specialist, Raw Materials(W)

Cellipont Bioservices

Spring, TX • On-site

$75K - $103K/yr

Full-time

Medical, PTO

Re-posted 21 days ago

Job description

Job Summary Cellipont Bioservices is growing, and we are looking for a QC Sr Specialist, Raw Materials who believes in the potential of bridging clients discoveries to patient cures and who wants to challenge the status quo and take Cellipont and its clients to the next level. The QC Sr Specialist, Raw Materials works in a fast-paced environment providing quality control support for the receipt of raw materials, as well as raw material documentation and qualification. The QC Sr Specialist, Raw Materials will be responsible raw material specification review and approval, drafting/approval of raw material sampling plan and risk assessments, as well as coordinating raw material qualification program for commercialization of cell therapy products. The QC Sr Specialist, Raw Materials is also responsible for ensuring all activities are executed timely and cost effectively to ensure customer and stakeholder satisfaction. This role will also require the individual to demonstrate strong ability to work cross-functionally and possess strong leadership skills. The Role Lead QC activities associated with incoming raw material life cycle management, including new material assessment, drafting/approval of raw material specifications and sampling plans.Performs testing of incoming raw materials and components according to specifications and procedures. Performs routine investigations in support of out of specification testing results. Manage raw material qualification program for raw materials in a phase-dependent manner. Coordinate outsourced testing and sample shipments with contract testing laboratories (CTLs) if required.Support quality systems associated with raw material investigations, deviations, and/or CAPAs. Assesses and executes actions related to change controls and vendor change notifications, as pertains to QC.Assist in drafting and approval of raw material risk assessments, as required. Maintain and evaluate raw materials processes and procedures. Identify and initiate opportunities for continuous improvement. The Candidate BS or A.S in a Life Sciences discipline with a minimum of 4 years of relevant GMP industry experience.Previous experience working in groups which support receipt, inspection, or release or materials in a pharmaceutical or biotechnology facility is a plus. Familiarity with USP and EP pharmacopeias, and pharmaceutical raw material compendial testing.Knowledge and ability to apply basic scientific principles to solve operational and quality tasks.Knowledge of FDA regulations is a plus. Self-starter with the ability to produce results in a fast-paced environment to meet client deadlines under minimal supervision. Excellent oral and written communication skills. Position BenefitsOpportunities for career growth within an expanding teamDefined career path and annual performance review & feedback processCross-functional exposure to other areas of within the organization Robust benefit package designed for unique Health & Wellness needs, including coverage for your furry family members401K strong employer match Tuition ReimbursementEmployee Referral BonusesFlexible work schedules and PTO based on role/level, increasing 1 PTO day each year and paid holidaysGain experience in the cutting-edge cell therapy space "At Cellipont Bioservices, we look for candidates with an innate desire to serve. Our "family" approach ensures you will get the mentorship you need to develop a satisfying career here!"Notice to Agency and Search Firm RepresentativesCellipont Bioservices is not accepting unsolicited resumes from agencies and/or search firms for this job posting. Resumes submitted to any Cellipont Bioservices employee by a third party agency and/or search firm without a valid written & signed search agreement, will become the sole property of Cellipont Bioservices. No fee will be paid if a candidate is hired for this position as a result of an unsolicited agency or search firm referral. Thank you.