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

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 ...

Lilly

Site Compliance Leader

Houston, TX

... change control review board, etc.) Ensure adequate quality oversight for material and supplier ... Minimum of 12+ years of experience in quality assurance within a biotechnology or pharmaceutical ...

Aerotek

GMP Weekend Supervisor

Houston, TX · On-site

$29 - $30/hr

... contamination control protocols. * Support daily manufacturing operations by performing tasks ... Prior experience in pharmaceutical, biotech, or food and beverage production environments.

EDG Inc

Sr. Automation Professional - Batch

Houston, TX · On-site

$99K - $130K/yr

... Biotech, Pharma, Food and Beverage, Beauty Care, and related industries. The Sr. Automation ... quality requirements. o Serve as lead for batch automation, MES integration, and electronic ...

GlobalPundits

Electrical Design Engineer

Houston, TX

... control, and report on material key quantities; provide analysis and forecasts Provide technical ... quality assurance program Manufacturing, pharmaceutical or biotechnology Advanced knowledge of:

Delan Associates, Inc

Mechanical Design Engineer

Houston, TX · On-site

$72K - $98K/yr

... control, and report on material key quantities; provide analysis and forecasts Provide technical ... under a nuclear quality assurance program o Manufacturing, pharmaceutical or biotechnology ...

Delan Associates, Inc

Mechanical Design Engineer

Houston, TX · On-site

$72K - $98K/yr

... control, and report on material key quantities; provide analysis and forecasts Provide technical ... under a nuclear quality assurance program o Manufacturing, pharmaceutical or biotechnology ...

Braskem

Process Engineer

Houston, TX

Work closely with Automation to prepare all process control descriptions for improvements or new ... Help resolve chronic Quality issues and Customer Complaints. * Support RCA analysis for all Process ...

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

Biotech Quality Control information

See Spring, TX salary details

$27.1K

$72.4K

$115.2K

How much do biotech quality control jobs pay per year?

As of Jun 12, 2026, the average yearly pay for biotech quality control in Spring, TX is $72,369.00, according to ZipRecruiter salary data. Most workers in this role earn between $53,800.00 and $89,000.00 per year, depending on experience, location, and employer.

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.

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 are the most commonly searched types of Biotech Quality Control jobs in Spring, TX? The most popular types of Biotech Quality Control jobs in Spring, TX are:
What are popular job titles related to Biotech Quality Control jobs in Spring, TX? For Biotech Quality Control jobs in Spring, TX, the most frequently searched job titles are:
What job categories do people searching Biotech Quality Control jobs in Spring, TX look for? The top searched job categories for Biotech Quality Control jobs in Spring, TX are:
What cities near Spring, TX are hiring for Biotech Quality Control jobs? Cities near Spring, TX with the most Biotech Quality Control job openings:
Biotech Quality Control jobs near you
Infographic showing various Biotech Quality Control job openings in Spring, TX as of June 2026, with employment types broken down into 5% Full Time, 90% Part Time, and 5% Nights. Highlights an 94% Physical, 1% Hybrid, and 5% Remote job distribution, with an average salary of $72,369 per year, or $34.8 per hour.
Manufacturing Deviation Investigator

Manufacturing Deviation Investigator

TekWissen LLC

Houston, TX • On-site

$20 - $24/wk

Contractor

Posted 12 days ago

Job description

Overview:  
  
TekWissen is a global workforce management provider headquartered in Ann Arbor, Michigan that offers strategic talent solutions to our clients world-wide.   Our client is a leading biotechnology company that combines technological insight with world-class manufacturing, scientific expertise, and process excellence and helps their customers to deliver new and innovative medicines that help treat a wide range of diseases. Our client specializes in pharmaceutical ingredients, Bioscience, Biopharmaceuticals, Custom manufacturing, Biotechnology, Life science ingredients, Nutrition, Microbial Control, Agriculture, Materials Science, Personal Care, and cell and gene therapy.  
  
Job Title:       Manufacturing Deviation Investigator / Sr. Quality Records Investigator
Location:       Houston, TX - 77047
Duration:       6 Months    
Job Type:       Contract    
Work Type:   Onsite 
 Shift:             Monday to Friday - 08:00 AM to 05:00 PM
 
 
Summary
 
The Deviation Investigator/Initiator Level III is responsible for the initiation, investigation and completion of Minor and low/medium severity Major process deviations unassisted, and the supervised completion of high severity Major and Critical process deviations with the aim at identification of root cause, determining Product Quality Impact (PQI) and implementation of corrective actions to prevent recurrence.
 
 
Responsibilities
  • Technical writing for the educated but uninformed reader, translate difficult and complex scientific events into a brief and cohesive report as a finished product.
  • Accurately capture immediate actions and containment of the event, address comments from both internal and external clients on the compiled final report.
  • Gathering Data from various sources across the site, performance of Root Cause Analysis (RCA) to determine the most likely cause of the deviation investigation, assessment of event for impact to Safety Identity Strength Quality Purity (SISQP), perform trending analysis, identification of Corrective and Preventative Actions to reduce deviation recurrence, performance of Risk Assessments, Causing Mapping, Interviewing.
  • Management of multiple projects and timelines concurrently.
  • Ability to adhere to standard timeline, and escalate actions appropriately for resolution in a timely manner.
  • Participation in the Daily Management meetings to update leadership or current deviation statuses.
  • Routine interaction with the customer, including compilation of Power Points to communicate investigational current status, Alignment meetings, facilitated reviews, CAPA discussions, Comments resolution.
  • Work on the manufacturing floor for data gathering, observing of processes for investigations, and performance of associate interviews.
  • Meeting Facilitation and participation, aligning internal review team and area subject matter experts on an agreed to investigational path forward.
  • Complex Conflict resolution, problem solving in a cross functional setting, and ability to keep the meeting on track to achieve objectives of varying difficulty.
  • Attendance and occasional leadership of the daily management system and participating/leading the deviation review board.
  • Perform other duties as assigned. 
Required Skills 
  • Prior experience in Technical writing and documentation
  • Prior experience in performing in Deviation investigation and root cause analysis (RCA)
  • Strong hands on experience with CAPA (Corrective and Preventive Actions) creation and follow-through
  • Understanding of cGMP and pharmaceutical/biotech manufacturing
  • Quality systems and deviation lifecycle management
TekWissen® Group is an equal opportunity employer supporting workforce diversity. 

TekWissen is an emerging global human capital, recruitment and IT services organization. Operating since 2009, we draw upon more than a decade of staffing experience to deliver critical talent acquisition solutions and IT engagements for our clients. We’re founded on a culture that is passionate about delivering tailored solutions, that create lasting partnerships.

Our global footprint covers six countries: United States, Canada, Australia, India, United Kingdom and the Philippines. This allows us to work in close partnership with organizations and manage everything from global talent needs with demanding resourcing strategies, to single sites with lower recruitment volumes.

TekWissen® is an equal opportunity employer supporting workplace diversity. 

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About TekWissen

Sourced by ZipRecruiter

TekWissen is an emerging global human capital, recruitment and IT services organization. Operating since 2009, we draw upon more than a decade of staffing experience to deliver critical talent acquisition solutions and IT engagements for our clients. We’re founded on a culture that is passionate about delivering tailored solutions, that create lasting partnerships.

Industry

Recruiting and staffing services

Company size

501 - 1,000 Employees

Headquarters location

Ann Arbor, MI, US

Year founded

2009

Social media

Twitter

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