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Gmp Manufacturing Jobs in Texas (NOW HIRING)

TekWissen LLC

Manufacturing Associate

Houston, TX · On-site

$20 - $24/hr

Perform Environmental Monitoring (EM) activities in support of GMP manufacturing of viral therapies * Support production and aseptic processing, including cell culture and product purification, when ...

Immatics NV

Senior Manufacturing Associate

Houston, TX · On-site

Role Overview We are seeking a Senior Manufacturing Associate to support our CMC-GMP Manufacturing team. In this role, you will lead and execute complex, time-sensitive cell processing and testing ...

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How much do gmp manufacturing jobs pay per hour?

As of Sep 2, 2026, the average hourly pay for gmp manufacturing in Texas is $23.24, according to ZipRecruiter salary data. Most workers in this role earn between $18.80 and $26.88 per hour, depending on experience, location, and employer.

What is a GMP manufacturing?

A GMP Manufacturing job involves producing pharmaceutical, biotechnology, or medical device products while following Good Manufacturing Practices (GMP) regulations. Responsibilities typically include operating equipment, maintaining sterile environments, documenting processes, and ensuring product quality and compliance. These roles are essential for maintaining safety and regulatory standards in healthcare-related manufacturing industries.

What are the key skills and qualifications needed to thrive in GMP manufacturing?

To excel in GMP Manufacturing, you need a solid understanding of Good Manufacturing Practices, attention to detail, and experience in regulated production environments, often backed by a degree in life sciences or engineering. Familiarity with quality management systems, batch record documentation, and equipment such as bioreactors or chromatography columns is typically required, and certifications like GMP or Six Sigma can be beneficial. Strong teamwork, communication skills, and the ability to follow precise procedures are essential soft skills for this position. These competencies ensure safe, compliant, and efficient production of pharmaceuticals or biotechnology products within strict regulatory frameworks.

What are some common challenges faced in GMP manufacturing roles?

Employees in GMP Manufacturing often encounter challenges such as maintaining meticulous documentation, adapting to changing regulatory requirements, and adhering to strict cleanliness and safety standards. The production process must be tightly controlled and deviations must be reported and resolved promptly, which requires a high level of diligence and accountability. Additionally, working collaboratively with quality assurance, engineering, and other cross-functional teams can add complexity to daily operations. Overcoming these challenges helps ensure product quality and regulatory compliance, while also providing valuable professional experience in one of the most highly regulated industries.

What are the most commonly searched types of Gmp Manufacturing jobs in Texas?

The most popular types of Gmp Manufacturing jobs in Texas are:

What are popular job titles related to Gmp Manufacturing jobs in Texas?

For Gmp Manufacturing jobs in Texas, the most frequently searched job titles are:

What job categories do people searching Gmp Manufacturing jobs in Texas look for?

The top searched job categories for Gmp Manufacturing jobs in Texas are:

What cities in Texas are hiring for Gmp Manufacturing jobs?

Cities in Texas with the most Gmp Manufacturing job openings:

Gmp Manufacturing jobs near you
Infographic showing various Gmp Manufacturing job openings in Texas as of August 2026, with employment types broken down into 88% Full Time, 7% Part Time, 3% Contract, and 2% Nights. Highlights an 94% Physical, 2% Hybrid, and 4% Remote job distribution, with an average salary of $48,343 per year, or $23.2 per hour.

GMP Records Specialist (Sr.)

Kelly Services

Stafford, TX

Full-time

Medical, Dental, Vision, Life, Retirement

Posted 18 days ago

Job description

Kelly Scientific has an immediate opening for a GMP Documentation Specialist (Sr.) to support a state of the art cell therapy customer near Houston, TX. 
 
Job Title: GMP Records Specialist (Sr.)
Location: Stafford, TX (onsite)
Rate: Commensurate with experience
Contract Length: 12 months 
Shift: 8am-5pm | Mon-Fri
 
Position Summary/purpose
The Contract GMP Records Specialist (Senior Level) is responsible for the end-to-end management of GMP manufacturing documentation, including the review, authoring, and maintenance of batch records, SOPs, and associated technical documents. This role ensures documentation accuracy, data integrity, and compliance with cGMP and regulatory requirements to support manufacturing operations.
 
The position operates as a subject matter expert in GMP documentation, working cross-functionally with Manufacturing, Quality Assurance, and MSAT to resolve documentation issues, drive timely record completion, and improve right-first-time performance. The role also supports digital manufacturing initiatives through hands-on involvement with Manufacturing Execution Systems (MES) and/or Electronic Batch Records (EBR), including troubleshooting and continuous improvement of documentation workflows.
 
This is a senior-level contract role requiring independent execution, strong technical writing capability, and the ability to lead documentation-related improvements in a fast-paced GMP manufacturing environment.
 
  • Roles and Responsibilities of Position
    Perform end-to-end review of GMP batch records and manufacturing documentation to ensure accuracy, completeness, and cGMP compliance.
  • Drive timely resolution of documentation errors, coordinating directly with Manufacturing, QA, and MSAT.
  • Author and revise GMP documents including Master Batch Records (MBRs), Electronic Batch Records (EBRs), SOPs, and work instructions.
  • Own document changes through the change control process, including updates, impact assessment, and implementation.
  • Support execution, troubleshooting, and continuous improvement of MES/EBR systems.
  • Serve as SME for GMP documentation practices, ensuring adherence to data integrity (ALCOA+) and regulatory expectations.
  • Partner cross-functionally to resolve documentation gaps and improve right-first-time performance.
  • Maintain document tracking and support audit and inspection readiness.
  • Provide guidance to manufacturing personnel on proper documentation practices and system usage.
 
Required Qualification (Education, Experience, Knowledge, Skills)
  • Bachelor’s degree in Life Sciences, Engineering, or a related technical field.
  • 6+ years of GMP experience in pharmaceutical, biotechnology, or cell therapy manufacturing environments.
  • Extensive experience reviewing and authoring GMP documentation, including MBRs, EBRs, SOPs, and technical instructions.
  • Demonstrated ownership of document lifecycle management and change control processes.
  • Hands-on experience with MES and/or Electronic Batch Record (EBR) systems.
  • Strong knowledge of cGMP regulations, FDA expectations, and data integrity principles (ALCOA+).
  • Proven ability to work independently, manage multiple priorities, and operate in fast-paced manufacturing environments.
  • Advanced technical writing, attention to detail, and strong organizational skills.
  • Effective cross-functional communication skills with Manufacturing, QA, and MSAT.
 
Preferred Qualifications
  • Experience in cell therapy, gene therapy, or advanced biologics manufacturing.
  • Direct experience with MES/EBR platforms (e.g., Werum PAS-X, Syncade, DeltaV, or similar).
  • Familiarity with electronic Quality Management Systems (e.g., Veeva)
  • Experience supporting commercial or late-stage GMP manufacturing operations.
  • Working knowledge of deviation management, CAPA, and change control processes.
  • Experience driving continuous improvement initiatives within GMP documentation systems.
  • Exposure to regulatory inspections (FDA, EMA) and audit readiness activities.
  • Lean Manufacturing or Operational Excellence experience.
 
Ideal Candidate Profile
  • Senior GMP documentation SME with a proven track record of independently owning batch record review, authoring, and lifecycle management.
  • Hands-on MES/EBR expert capable of troubleshooting and optimizing electronic batch record workflows.
  • Highly detail-oriented with strong technical writing skills and a focus on data integrity and right-first-time execution.
  • Able to operate autonomously in fast-paced, commercial or late-stage manufacturing environments.
  • Strong cross-functional collaborator who can effectively partner with Manufacturing, QA, and MSAT.
  • Process-driven with demonstrated ability to identify gaps and implement sustainable documentation improvements
  • Comfortable supporting audits and inspections with clear, compliant, and inspection-ready documentation.

What happens next
Once you apply, you’ll proceed to next steps if your skills and experience look like a good fit. But don’t worry—even if this position doesn’t work out, you’re still in our network. That means all of our recruiters will have access to your profile, expanding your opportunities even more.
 
Helping you discover what’s next in your career is what we’re all about, so let’s get to work. Apply to be Manufacturing Support Specialist today!
 
 

As part of our promise to talent, Kelly supports those who work with us through a variety of benefits, perks, and work-related resources. Please note: The following benefits reflect Kelly's general offerings. Eligibility may vary by assignment, location, and job type. Kelly offers eligible employees voluntary benefit plans including medical, dental, vision, telemedicine, term life, whole life, accident insurance, critical illness, a legal plan, and short-term disability. As a Kelly employee, you will have access to a retirement savings plan, service bonus and holiday pay plans (earn up to eight paid holidays per benefit year), and a transit spending account. In addition, employees are entitled to earn paid sick leave under the applicable state or local plan. Click here for more information on benefits and perks that may be available to you as a member of the Kelly Talent Community.

Why Kelly® Science & Clinical?

Kelly Science & Clinical is your connection to premier scientific and clinical companies looking to hire industry experts just like you. Our team creates expert talent solutions to solve the world’s most critical challenges. Every day, we match science professionals with dream jobs that fit their skills, interests, and career goals-it’s the way we think job searching should be. Nearly 100 percent of our science recruiters have a professional background and education in science, so we know a thing or two about the science market and how to get your expertise noticed.

About Kelly

Work changes everything. And at Kelly, we’re obsessed with where it can take you. To us, it’s about more than simply accepting your next job opportunity. It’s the fuel that powers every next step of your life. It’s the ripple effect that changes and improves everything for your family, your community, and the world. Which is why, here at Kelly, we are dedicated to providing you with limitless opportunities to enrich your life-just ask the 300,000 people we employ each year.
Kelly is committed to providing equal employment opportunities to all qualified employees and applicants regardless of race, color, sex, sexual orientation, gender identity, religion, national origin, disability, veteran status, age, marital status, pregnancy, genetic information, or any other legally protected status, and we take affirmative action to recruit, employ, and advance qualified individuals with disabilities and protected veterans in the workforce. Requests for accommodation related to our application process can be directed to the Kelly Human Resource Knowledge Center. Kelly complies with the requirements of California’s state and local Fair Chance laws. A conviction does not automatically bar individuals from employment. Kelly participates in E-Verify and will provide the federal government with your Form I-9 information to confirm that you are authorized to work in the U.S.
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