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Chemical Engineering Biotechnology Jobs (NOW HIRING)

Stark Pharma Solutions Inc

CQV Engineer

Austin, TX · On-site

Bachelor's degree in Mechanical Engineering, Chemical Engineering, Electrical Engineering, Biotechnology, Pharmaceutical Engineering, or a related engineering discipline. * 5+ years of experience in ...

Merck & Co.

$117K - $184K/yr

Analytical Method Development, Analytical Thinking, Biomedical Engineering, Biotechnology, Chemical Engineering, Chemistry, Combination Products, Container Closure Integrity Testing (CCIT), Materials ...

MSD Malaysia

$117K - $184K/yr

Analytical Method Development, Analytical Thinking, Biomedical Engineering, Biotechnology, Chemical Engineering, Chemistry, Combination Products, Container Closure Integrity Testing (CCIT), Materials ...

DPS Group

Process Engineer

Framingham, MA · On-site

Degree in Biochemical Engineering, Chemical Engineering, Biotechnology or related discipline with at least 2 plus years of GMP Lifesciences, pharmaceutical manufacturing, technology transfer ...

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How much do chemical engineering biotechnology jobs pay per year?

As of Sep 12, 2026, the average yearly pay for chemical engineering biotechnology in the United States is $87,487.00, according to ZipRecruiter salary data. Most workers in this role earn between $67,500.00 and $106,500.00 per year, depending on experience, location, and employer.

What is a chemical engineering biotechnology?

A Chemical Engineering Biotechnology job involves applying chemical engineering principles to biotechnological processes, such as pharmaceutical production, biofuels, food processing, and biomaterials. Professionals in this field work on designing and optimizing bioprocesses, scaling up production, and ensuring efficiency and safety. They collaborate with biologists, chemists, and engineers to develop sustainable and innovative solutions for industrial and medical applications.

What does a chemical engineering biotechnology do?

Professionals in Chemical Engineering Biotechnology often work on projects involving the design, optimization, and scale-up of bioprocesses for pharmaceuticals, biofuels, or specialty chemicals. Day-to-day, you may oversee experiments, manage data analysis, collaborate with R&D scientists, and ensure compliance with safety and regulatory guidelines. Many roles involve troubleshooting process issues, improving yields, and working as part of a multidisciplinary team to achieve project milestones. This dynamic work environment offers opportunities to develop both technical and leadership skills, paving the way for advancement into project management or specialist roles.

What are the key skills and qualifications needed to thrive in chemical engineering biotechnology?

To thrive in Chemical Engineering Biotechnology, a strong background in chemical engineering principles, biotechnology processes, and a relevant degree (such as a BS or MS in Chemical Engineering or Biotechnology) is essential. Familiarity with bioprocessing equipment, laboratory information management systems (LIMS), and certifications like Six Sigma or GMP compliance is commonly required. Excellent problem-solving, teamwork, and communication skills help professionals navigate complex projects and collaborate with cross-disciplinary teams. These competencies enable efficient development and scaling of biotechnological solutions while maintaining safety, quality, and regulatory standards.

Can a chemical engineer work in biotech?

Yes, chemical engineers can work in biotechnology, applying their knowledge of chemical processes, reaction engineering, and process design to develop biopharmaceuticals, biofuels, and other biotech products. They often work with bioreactors, fermentation processes, and require understanding of biological systems and regulatory standards.

What is biotechnology in chemical engineering?

Biotechnology in chemical engineering involves applying biological systems, organisms, or derivatives to develop or produce products such as pharmaceuticals, biofuels, and bioplastics. Chemical engineers in this field design processes, utilize bioreactors, and optimize conditions to scale up biological reactions for industrial use.
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Chemical Engineering Biotechnology jobs near you
Infographic showing various Chemical Engineering Biotechnology job openings in the United States as of September 2026, with employment types broken down into 1% Internship, 90% Full Time, 6% Part Time, 2% Contract, and 1% Nights. Highlights an 83% Physical, 4% Hybrid, and 13% Remote job distribution, with an average salary of $87,487 per year, or $42.1 per hour.

CQV Engineer

Austin, TX • On-site

Stark Pharma Solutions Inc
See more jobs at Stark Pharma Solutions Incexternal

Contractor

Re-posted 8 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/