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Pharmaceutical Engineer Jobs in Texas (NOW HIRING)

CQV Engineer

Austin, TX ยท On-site

Austin, TX Duration: Long Term Position Overview We are seeking an experienced CQV Engineer to support Commissioning, Qualification, and Validation (CQV) activities for pharmaceutical and medical ...

Strong expertise in pharmaceutical engineering systems, including facilities, utilities, equipment, commissioning, qualification, and lifecycle maintenance * Direct involvement with quality ...

Platform Engineer

Austin, TX ยท On-site

$150 - $190/hr

Provide technical guidance and education to developers on platform tools and best practices ... Experience with regulated industries (pharmaceutical, medical device, finance) * Background with ...

Provide technical guidance and education to developers on platform tools and best practices ... Experience with regulated industries (pharmaceutical, medical device, finance) * Background with ...

Pharmacist

Mexia, TX ยท On-site

$46.75 - $56.25/hr

Pharmacist Mexia, TX Company Summary This healthcare organization is dedicated to improving the ... Engineering, Government & Critical Infrastructure. Contracting Vehicles: GSA 621i VA FSS ...

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Pharmaceutical Engineer information

See Texas salary details

$31

$35

$38

How much do pharmaceutical engineer jobs pay per hour?

As of Aug 23, 2026, the average hourly pay for pharmaceutical engineer in Texas is $35.83, according to ZipRecruiter salary data. Most workers in this role earn between $34.04 and $37.64 per hour, depending on experience, location, and employer.

What does a pharmaceutical engineer do?

Pharmaceutical engineers design and manufacture pharmaceutical products. As a pharmaceutical engineer, the focus of your work may be on chemical research, manufacturing design, field testing, quality assurance, packaging and labeling, product delivery, or regulations compliance. Your job duties include collaborating with other engineers and manufacturing personnel, and ensuring all procedures follow Good Manufacturing Practice Regulations established by the Food and Drug Administration (FDA). You need extensive science experience, strong analytical and problem-solving skills, and the ability to work well with a team.

What are the key skills and qualifications needed to thrive as a pharmaceutical engineer, and why are they important?

To thrive as a Pharmaceutical Engineer, you need a strong background in chemical or biomedical engineering, pharmaceutical sciences, and process development, typically supported by a relevant bachelor's or master's degree. Familiarity with Good Manufacturing Practice (GMP) regulations, process simulation software, and quality assurance systems is essential. Exceptional problem-solving, attention to detail, and teamwork skills help you excel in cross-functional environments. These skills ensure safe, efficient drug production and regulatory compliance, which are vital for patient safety and business success.

How do pharmaceutical engineers typically collaborate with cross-functional teams during drug development projects?

Pharmaceutical engineers work closely with scientists, quality assurance specialists, regulatory teams, and manufacturing staff throughout the drug development process. They play a key role in translating laboratory-scale processes into safe, efficient, and scalable manufacturing solutions. Effective communication and teamwork are crucial, as engineers must ensure that all technical, safety, and compliance requirements are met while balancing project timelines and budgets. This collaborative environment offers valuable opportunities to broaden your expertise and develop leadership skills, especially as you take on more responsibility in project management or process optimization roles.

What is the difference between Pharmaceutical Engineer vs Chemical Engineer?

AspectPharmaceutical EngineerChemical Engineer
CredentialsBachelor's in Pharmaceutical Engineering, Chemical Engineering, or related field; often requires industry-specific certificationsBachelor's in Chemical Engineering; professional engineer (PE) license optional
Work EnvironmentPharmaceutical manufacturing facilities, labs, quality controlChemical plants, refineries, research labs
Industry UsagePrimarily in pharmaceutical and biotech industriesBroader industries including chemicals, energy, and materials
Job FocusDesigning and optimizing drug manufacturing processes, ensuring compliance with regulationsDesigning chemical processes, scaling up production, safety analysis

While both roles require a background in chemical processes, Pharmaceutical Engineers focus specifically on drug manufacturing and regulatory compliance within the pharmaceutical industry. Chemical Engineers have a broader scope, working across various chemical production sectors. The choice depends on your industry interest and specialization goals.

What are the most commonly searched types of Pharmaceutical Engineer jobs in Texas?

The most popular types of Pharmaceutical Engineer jobs in Texas are:

What cities in Texas are hiring for Pharmaceutical Engineer jobs?

Cities in Texas with the most Pharmaceutical Engineer job openings:

What are popular job titles related to Pharmaceutical Engineer jobs in TX?

For Pharmaceutical Engineer jobs in TX, the most frequently searched job titles are:

Infographic showing various Pharmaceutical Engineer job openings in Texas as of August 2026, with employment types broken down into 94% Full Time, 3% Part Time, and 3% Contract. Highlights an 85% Physical, 6% Hybrid, and 9% Remote job distribution, with an average salary of $74,532 per year, or $35.8 per hour.

CQV Engineer

Stark Pharma Solutions Inc

Austin, TX โ€ข On-site

Contractor

Re-posted 17 days ago


Job description

Hi,

My name is Sravani Dasari from Stark Pharma Solutions Inc. We are hiring talent for our client and are currently working on a CQV Engineer position. Please send me your updated resume if you have relevant experience and are interested in this opportunity. The detailed job description is as follows.

Job Title: CQV Engineer
Location: Austin, TX
Duration: Long Term

Position Overview

We are seeking an experienced CQV Engineer to support Commissioning, Qualification, and Validation (CQV) activities for pharmaceutical and medical device manufacturing facilities. This role will focus on equipment qualification, utility validation, process validation, and ensuring compliance with GMP, FDA, and industry regulations. The ideal candidate will have extensive experience with IQ/OQ/PQ execution, validation documentation, deviation investigations, and cross-functional collaboration throughout the validation lifecycle.

Key Responsibilities

  • Execute Commissioning, Qualification, and Validation (CQV) activities for manufacturing equipment, utilities, facilities, and process systems.
  • Develop, review, approve, and execute Installation Qualification (IQ), Operational Qualification (OQ), and Performance Qualification (PQ) protocols and reports.
  • Perform equipment, utility, and system qualification activities in accordance with GMP, FDA, and company standards.
  • Support commissioning activities for new manufacturing equipment and facility expansions.
  • Ensure compliance with GMP, FDA regulations, cGMP guidelines, and internal quality management systems.
  • Analyze validation data, investigate deviations, support root cause analysis, and implement CAPA activities.
  • Collaborate with Engineering, Manufacturing, Validation, Quality Assurance, and Regulatory teams to ensure successful project execution.
  • Prepare, review, and maintain validation documentation, traceability matrices, SOPs, and technical reports.
  • Support internal audits, regulatory inspections, and client audits by providing validation documentation and technical expertise.
  • Drive continuous improvement initiatives to enhance validation processes, compliance, and operational efficiency.

Required Qualifications

  • Bachelor's degree in Mechanical Engineering, Chemical Engineering, Electrical Engineering, Biotechnology, Pharmaceutical Engineering, or a related engineering discipline.
  • 5+ years of experience in Commissioning, Qualification & Validation (CQV), Equipment Qualification, or Validation Engineering within the pharmaceutical, biotechnology, or medical device industry.
  • Strong hands-on experience with Installation Qualification (IQ), Operational Qualification (OQ), and Performance Qualification (PQ).
  • Thorough understanding of GMP, cGMP, FDA regulations, ISPE guidelines, and validation lifecycle methodologies.
  • Experience preparing and executing validation protocols, reports, risk assessments, and technical documentation.
  • Hands-on experience with equipment commissioning, qualification, and process validation activities.
  • Knowledge of deviation management, change control, CAPA, and quality systems.
  • Strong analytical, troubleshooting, documentation, and problem-solving skills.
  • Excellent communication and interpersonal skills with the ability to work effectively in cross-functional teams.
  • Experience supporting regulatory audits and inspections is preferred.
  • Familiarity with clean utilities, HVAC systems, computerized systems validation (CSV), cleaning validation, or facility qualification is an added advantage.

I am actively connecting with professionals for current and upcoming opportunities. If you are open to exploring new roles or would like to stay informed about relevant positions, please send me your updated resume along with the best number and time to reach you.

Please follow Stark Pharma Solutions on LinkedIn for the latest job updates: https://www.linkedin.com/company/99455976/