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

QuVa Pharma

Facility & Manufacturing Engineer

Sugar Land, TX · On-site

$65K - $84K/yr

Our Facility / Manufacturing Engineer plays a vital role in ensuring the highest quality and safety ... Quva Pharma's multiple production facilities and industry-first dedicated remote distribution ...

Unicon Pharma Inc.

Core Technician I - Houston, TX

Houston, TX · On-site

$18.25 - $24/hr

Coordinates EM equipment needs with QC EM team for Manufacturing processes * Drafting, completion and revision of manufacturing documents including Batch Records and EM forms * Buffer and component ...

Unicon Pharma Inc.

Core Technician I - Houston, TX

Houston, TX · On-site

$18.25 - $24/hr

Coordinates EM equipment needs with QC EM team for Manufacturing processes * Drafting, completion and revision of manufacturing documents including Batch Records and EM forms * Buffer and component ...

Unicon Pharma Inc.

Core Technician I - Houston, TX

Houston, TX · On-site

$18.25 - $24/hr

Coordinates EM equipment needs with QC EM team for Manufacturing processes * Drafting, completion and revision of manufacturing documents including Batch Records and EM forms * Buffer and component ...

Unicon Pharma Inc.

Core Technician I - Houston, TX

Houston, TX · On-site

$18.25 - $24/hr

Coordinates EM equipment needs with QC EM team for Manufacturing processes * Drafting, completion and revision of manufacturing documents including Batch Records and EM forms * Buffer and component ...

Unicon Pharma Inc.

Core Technician I - Houston, TX

Houston, TX · On-site

$18.25 - $24/hr

Coordinates EM equipment needs with QC EM team for Manufacturing processes * Drafting, completion and revision of manufacturing documents including Batch Records and EM forms * Buffer and component ...

Unicon Pharma Inc.

Core Technician I - Houston, TX

Houston, TX · On-site

$18.25 - $24/hr

Coordinates EM equipment needs with QC EM team for Manufacturing processes * Drafting, completion and revision of manufacturing documents including Batch Records and EM forms * Buffer and component ...

Unicon Pharma Inc.

Core Technician I - Houston, TX

Houston, TX · On-site

$18.25 - $24/hr

Coordinates EM equipment needs with QC EM team for Manufacturing processes * Drafting, completion and revision of manufacturing documents including Batch Records and EM forms * Buffer and component ...

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All JobsQuality Control Pharma JobsQuality Control Pharma Jobs in Rosenberg, TX

Quality Control Pharma information

See Rosenberg, TX salary details

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How much do quality control pharma jobs pay per hour?

As of Aug 18, 2026, the average hourly pay for quality control pharma in Rosenberg, TX is $18.71, according to ZipRecruiter salary data. Most workers in this role earn between $16.11 and $20.58 per hour, depending on experience, location, and employer.

What is quality control in the pharmaceutical industry?

Quality Control (QC) in the pharmaceutical industry refers to the processes and procedures used to ensure that pharmaceutical products meet required standards of quality, safety, and efficacy. QC professionals test raw materials, in-process samples, and finished products using various analytical techniques to verify that they comply with regulatory specifications. The goal is to detect and prevent defects, ensuring that only products that pass rigorous standards are released to the market. QC is essential for maintaining public health and regulatory compliance in the pharmaceutical sector.

What are the key skills and qualifications needed to thrive as a quality control professional in the pharmaceutical industry?

To thrive as a Quality Control professional in pharma, you need a strong background in chemistry, biology, or a related science, along with knowledge of Good Manufacturing Practices (GMP) and relevant regulations. Familiarity with laboratory instruments (e.g., HPLC, GC), LIMS software, and quality assurance certifications such as ASQ or ISO standards is typically required. Attention to detail, analytical thinking, and effective communication help professionals excel in ensuring product quality and regulatory compliance. These skills ensure that pharmaceutical products are consistently safe, effective, and compliant with industry standards.

What are some of the common challenges faced by quality control professionals in the pharmaceutical industry?

Quality Control professionals in pharma often face challenges such as staying updated with evolving regulatory standards, managing tight timelines for product release, and ensuring accuracy in complex analytical testing. They must also coordinate closely with production and R&D teams to address any discrepancies or deviations quickly. Maintaining meticulous documentation and effectively handling audits are essential parts of the role, making attention to detail and strong communication skills particularly important.

What is the difference between Quality Control Pharma vs Quality Assurance Pharma?

AspectQuality Control PharmaQuality Assurance Pharma
Primary FocusTesting and inspecting raw materials, in-process, and finished products for complianceDeveloping and maintaining quality systems and processes to prevent defects
CertificationsGMP, GLP, relevant laboratory certificationsGMP, ISO 9001, quality management system certifications
Work EnvironmentLaboratories, testing facilitiesQuality departments, documentation, audits
Common Employer RolesPharmaceutical companies, contract labsPharmaceutical companies, regulatory agencies

While both roles aim to ensure product quality, Quality Control Pharma focuses on testing and inspection, whereas Quality Assurance Pharma emphasizes establishing systems and processes to prevent issues. Understanding these differences helps in choosing the right career path or job focus within the pharmaceutical industry.

Is Quality Control Pharma a good career?

Quality Control Pharma involves testing and inspecting pharmaceutical products to ensure they meet safety and quality standards. It requires attention to detail, knowledge of laboratory techniques, and often involves certifications such as GMP training. The role offers stable employment opportunities in the pharmaceutical industry with potential for career advancement.

What are popular job titles related to Quality Control Pharma jobs in Rosenberg, TX?

For Quality Control Pharma jobs in Rosenberg, TX, the most frequently searched job titles are:

What job categories do people searching Quality Control Pharma jobs in Rosenberg, TX look for?

The top searched job categories for Quality Control Pharma jobs in Rosenberg, TX are:

What cities near Rosenberg, TX are hiring for Quality Control Pharma jobs?

Cities near Rosenberg, TX with the most Quality Control Pharma job openings:

Quality Control Pharma jobs near you
Infographic showing various Quality Control Pharma job openings in Rosenberg, TX as of August 2026, with employment types broken down into 1% As Needed, 74% Full Time, 18% Part Time, 6% Contract, and 1% Nights. Highlights an 86% Physical, 2% Hybrid, and 12% Remote job distribution, with an average salary of $38,914 per year, or $18.7 per hour.

Facility & Manufacturing Engineer

QuVa Pharma

Sugar Land, TX • On-site

$65K - $84K/yr

Full-time

Medical, Dental, Vision, Retirement, PTO

Re-posted 7 days ago

QuVa Pharma rating

7.7

Company rating: 7.7 out of 10

Based on 10 frontline employees who took The Breakroom Quiz

54th of 86 rated pharmaceutical

Job description

Our Facility / Manufacturing Engineer plays a vital role in ensuring the highest quality and safety standards of our pharmaceutical products. Once you complete our training, your responsibilities will include providing MEP support around the design, building and implementation of new facility projects and production equipment. Your attention to detail and adherence to precise procedures will guarantee that our medications meet the highest standards of safety, efficacy, and quality, providing patients with the best possible care and outcomes. Turn your passion for precision and your commitment to quality into a meaningful impact on healthcare across the US.
What the Facility/Manufacturing Engineer Does Each Day:
  • Provides technical skills and expertise to support operations and ensure mechanical elements for manufacturing are designed and operating as required
  • Generates and executes (as applicable) Validation Project Plans, Validation protocols -Installation Qualifications/Operational Qualifications/Performance Qualifications (IQ/OQ/PQ) and summary reports and Standard Operating Procedures (SOPs) as required for pharmaceutical manufacturing
  • Develop and write specifications for production equipment from aseptic processing to labeling and packaging
  • Support design of production equipment and responsible for commissioning/qualification
  • Maintaining site level facility drawings including revising where required
  • Supports development of site and departmental metrics to gauge ongoing performance of organization and identification of opportunities for continual process improvement

Our Most Successful Facility/Manufacturing Engineers:
  • Are team players
  • Have strong technical writing skills and verbal/written communication skills, including presentation skills
  • Utilize analytical, critical thinking and structured root cause analysis techniques for problem solving
  • Demonstrate expertise in project management
  • Creatively meet challenges and develop innovative approaches

Minimum Requirements for this Role:
  • Bachelor of Science in Mechanical Engineering or equivalent engineering degree with 2+ years' experience in a manufacturing environment or Associated degree in Mechanical Engineering or equivalent engineering degree with 5+ years' experience in a manufacturing environment
  • Able to successfully complete a drug and background check
  • Equipment/Instrument Calibration Principals
  • Direct experience working on large scale MEP systems
  • Honeywell EBI BMS
  • Cleanroom Design, Operation and Maintenance
  • Experience with pharmaceutical grade compressed air systems
  • Knowledge with local and state regulatory requirements
  • Must be currently authorized to work in the United States on a full-time basis; Quva will not sponsor applicants for work visas

Any of the Following Will Give You an Edge:
  • PC literate with a working knowledge of MS Project, Visio, AutoCAD and SolidWorks
  • 2 years of experience in a regulated industry

Benefits of Working at Quva:
  • Comprehensive health and wellness benefits including medical, dental and vision
  • 401k retirement program with company match
  • 17 paid days off plus 8 paid holidays per year
  • National, industry-leading high growth company with future career advancement opportunities

About Quva:
Quva provides industry-leading health-system pharmacy services and solutions, including 503B sterile injectable outsourcing services and AI-based data software solutions that help power the business of pharmacy. Quva Pharma's multiple production facilities and industry-first dedicated remote distribution capabilities provide ready-to-administer sterile injectable medicines critical to patient care. Quva BrightStream partners with health systems to aggregate, normalize, and analyze large amounts of complex data across their sites of care, and through proprietary machine learning, transforms data into actionable insights supporting revenue optimization, script capture, inventory management, drug shortage control, and more. Quva's overall progressive and integrated platform helps health-systems transform pharmacy management to achieve greater value and deliver highest-quality patient care.
Quva is an equal opportunity employer and is committed to creating and maintaining a work environment that is free from all forms of discrimination and harassment. Quva's Equal Opportunity Policy prohibits harassment or discrimination due to age, ancestry, color, disability, gender, gender expression, gender identity, genetic information, marital status, medical condition, military or veteran status, national origin, race, religious creed, sex (including pregnancy, childbirth, breastfeeding, and any related medical conditions), sexual orientation, and any other characteristic or classification protected by applicable laws. All employment with Quva is "at will."
California Consumer Privacy Act (CCPA) Notice for Applicants and Employees
Equal Opportunity Employer
This employer is required to notify all applicants of their rights pursuant to federal employment laws.
For further information, please review the Know Your Rights notice from the Department of Labor.

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