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Chemical Engineering Biotechnology Jobs (NOW HIRING)

This client is a German multinational Pharmaceutical and biotechnology company and one of the ... Collaborate with plant engineering resources to scope, document and define implementation plans for ...

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$38 - $42/hr

Preferred Qualifications/Educational background in Chemical Engineering, Biomedical Engineering, Biotechnology correlated technical field of study in biotechnology, life sciences or related ...

Bachelor's, Master's, or PhD in Biochemistry, Chemistry, Biology, Chemical Engineering, Biotechnology, or a related field. Preferred Qualifications * 5+ years in the biotechnology industry with ...

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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Chemical Engineering Biotechnology information

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$40K

$87.5K

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How much do chemical engineering biotechnology jobs pay per year?

As of Jul 4, 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 are some typical projects or daily tasks for professionals in Chemical Engineering Biotechnology roles?

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 is a Chemical Engineering Biotechnology job?

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 are the key skills and qualifications needed to thrive in the Chemical Engineering Biotechnology position, and why are they important?

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.

More about Chemical Engineering Biotechnology jobs
What cities are hiring for Chemical Engineering Biotechnology jobs? Cities with the most Chemical Engineering Biotechnology job openings:
What are the most commonly searched types of Chemical Engineering Biotechnology jobs? The most popular types of Chemical Engineering Biotechnology jobs are:
What states have the most Chemical Engineering Biotechnology jobs? States with the most job openings for Chemical Engineering Biotechnology jobs include:
Infographic showing various Chemical Engineering Biotechnology job openings in the United States as of June 2026, with employment types broken down into 50% Full Time, and 50% Contract. Highlights an 100% In-person job distribution, with an average salary of $87,487 per year, or $42.1 per hour.

Validation Engineer

Stark Pharma Solutions Inc

Concord, NC • On-site

Contractor

Posted 9 hours ago


Job description

Job Title: Validation Engineer
Location: Concord, NC
Duration: Long Term

Job Summary

We are seeking a motivated and detail-oriented Validation Engineer to support validation activities within a GMP-regulated biopharmaceutical manufacturing environment. The Validation Engineer will be responsible for equipment qualification, process validation, utility validation, and cleaning validation activities to ensure compliance with FDA, cGMP, and industry standards.

The ideal candidate will collaborate with Manufacturing, Quality Assurance, Engineering, and Regulatory teams to support production operations, maintain validated systems, and ensure regulatory compliance across the facility.

Key Responsibilities

  • Develop, execute, and review validation protocols and reports including IQ, OQ, and PQ documentation
  • Support equipment qualification activities for biopharmaceutical manufacturing equipment and laboratory systems
  • Perform process validation for upstream and downstream manufacturing processes
  • Execute cleaning validation and utility qualification activities including HVAC, purified water, compressed gases, and cleanroom systems
  • Ensure compliance with FDA, cGMP, GDP, and company quality standards
  • Support computerized systems validation (CSV) activities when required
  • Participate in deviation investigations, root cause analysis, CAPA, and change control processes
  • Collaborate with cross-functional teams during equipment installation, commissioning, and technology transfer projects
  • Maintain validation lifecycle documentation including SOPs, Validation Master Plans (VMP), and risk assessments
  • Assist during internal audits and regulatory inspections by providing validation documentation and technical support
  • Identify and implement continuous improvement opportunities within validation and manufacturing processes

Required Qualifications

  • Bachelor’s degree in Chemical Engineering, Mechanical Engineering, Biomedical Engineering, Biotechnology, or related field
  • 3+ years of validation experience in biopharmaceutical, pharmaceutical, or regulated manufacturing industries
  • Strong understanding of cGMP, FDA regulations, and validation principles
  • Experience with IQ/OQ/PQ protocol execution and report generation
  • Knowledge of process validation, cleaning validation, and utility qualification
  • Familiarity with deviation management, CAPA, and change control systems
  • Strong technical writing and documentation skills
  • Excellent communication, analytical, and problem-solving abilities