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Pharma Validation Engineer Jobs in Florida (NOW HIRING)

Manufacturing Engineer

Orlando, FL ยท On-site

$68K - $87K/yr

Hi, My name is Sravani Dasari from Stark Pharma Solutions Inc. We are hiring talent for our client ... Collaborate with Manufacturing, Production, Quality Assurance, Validation, Engineering, and ...

... science, engineering, or equivalent experience; 6+ years of experience in computer system validation in a life sciences environment, including pharma, biotech, medical device, or clinical

... science, engineering, or equivalent experience; 6+ years of experience in computer system validation in a life sciences environment, including pharma, biotech, medical device, or clinical

... science, engineering, or equivalent experience; 6+ years of experience in computer system validation in a life sciences environment, including pharma, biotech, medical device, or clinical

... science, engineering, or equivalent experience; 6+ years of experience in computer system validation in a life sciences environment, including pharma, biotech, medical device, or clinical

... science, engineering, or equivalent experience; 6+ years of experience in computer system validation in a life sciences environment, including pharma, biotech, medical device, or clinical

... science, engineering, or equivalent experience; 6+ years of experience in computer system validation in a life sciences environment, including pharma, biotech, medical device, or clinical

... science, engineering, or equivalent experience; 6+ years of experience in computer system validation in a life sciences environment, including pharma, biotech, medical device, or clinical

... science, engineering, or equivalent experience; 6+ years of experience in computer system validation in a life sciences environment, including pharma, biotech, medical device, or clinical

... science, engineering, or equivalent experience; 6+ years of experience in computer system validation in a life sciences environment, including pharma, biotech, medical device, or clinical

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Pharma Validation Engineer information

See Florida salary details

$16

$38

$58

How much do pharma validation engineer jobs pay per hour?

As of Aug 12, 2026, the average hourly pay for pharma validation engineer in Florida is $38.86, according to ZipRecruiter salary data. Most workers in this role earn between $29.47 and $47.26 per hour, depending on experience, location, and employer.

What does a pharma validation engineer do?

A typical day for a Pharma Validation Engineer involves developing and executing validation protocols for manufacturing equipment, laboratory instruments, or processes, ensuring they meet all regulatory and quality standards. You might collaborate closely with QA teams, production staff, and external vendors to troubleshoot issues, review data, and document results for compliance audits. Preparing detailed reports, participating in cross-functional meetings, and staying updated with current regulatory changes are also common responsibilities. This dynamic environment offers opportunities to work on diverse projects and continually expand your technical expertise while supporting product safety and efficacy.

What skills and qualifications are needed to be a pharma validation engineer?

To thrive as a Pharma Validation Engineer, you need a solid background in engineering or life sciences, with expertise in validation protocols, regulatory compliance (such as FDA or EMA guidelines), and Good Manufacturing Practices (GMP). Experience with validation software (like ValGenesis or MasterControl), statistical analysis tools, and relevant certifications (such as Six Sigma or ISPE) is highly valued. Strong attention to detail, project management abilities, and effective communication skills are crucial for this role. These competencies ensure validation activities meet strict regulatory standards, support product quality, and facilitate seamless cross-functional collaboration in the pharmaceutical industry.

What is a pharma validation engineer?

A Pharma Validation Engineer ensures that manufacturing processes, equipment, and systems in the pharmaceutical industry comply with regulatory standards such as FDA, GMP, and ISO. They develop validation protocols, conduct tests, analyze data, and generate reports to ensure consistent product quality and safety. Their role is critical in minimizing risks, maintaining compliance, and supporting regulatory audits.

What are the most commonly searched types of Pharma Validation Engineer jobs in Florida? The most popular types of Pharma Validation Engineer jobs in Florida are:
What are popular job titles related to Pharma Validation Engineer jobs in Florida? For Pharma Validation Engineer jobs in Florida, the most frequently searched job titles are:
Infographic showing various Pharma Validation Engineer job openings in Florida as of August 2026, with employment types broken down into 48% Full Time, and 52% Contract. Highlights an 100% In-person job distribution, with an average salary of $80,821 per year, or $38.9 per hour.

Manufacturing Engineer

Stark Pharma Solutions Inc

Orlando, FL โ€ข On-site

$68K - $87K/yr

Contractor

Posted 28 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 Manufacturing 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: Manufacturing Engineer
Location: Orlando, FL
Duration: Long Term

Position Overview

We are seeking a motivated Manufacturing Engineer with 0–1 year of experience to support manufacturing operations within the pharmaceutical, biotechnology, or medical device industry. This entry-level role is ideal for recent graduates or candidates with internship or co-op experience who are eager to build a career in regulated manufacturing. The selected candidate will assist with process improvements, manufacturing support, equipment qualification, documentation, and quality compliance while working closely with cross-functional teams.

Key Responsibilities

  • Support daily manufacturing operations to ensure safe, efficient, and compliant production.
  • Assist in monitoring and improving manufacturing processes to enhance productivity and product quality.
  • Support equipment installation, qualification, troubleshooting, and maintenance activities.
  • Assist with process validation, equipment qualification (IQ/OQ/PQ), and manufacturing documentation.
  • Prepare and maintain SOPs, work instructions, batch records, and engineering documentation.
  • Collaborate with Manufacturing, Production, Quality Assurance, Validation, Engineering, and Regulatory teams.
  • Collect and analyze manufacturing data to identify process improvement opportunities.
  • Assist with deviation investigations, CAPA activities, and change control documentation.
  • Ensure compliance with GMP, cGMP, FDA regulations, ISO standards, and company quality procedures.
  • Participate in Lean Manufacturing and continuous improvement initiatives.

Required Qualifications

  • Bachelor's degree in Mechanical Engineering, Manufacturing Engineering, Industrial Engineering, Chemical Engineering, Biomedical Engineering, Biotechnology, or a related engineering discipline.
  • 0–1 year of experience through internships, co-op programs, academic projects, or entry-level roles in pharmaceutical, biotechnology, medical device, or regulated manufacturing environments.
  • Basic understanding of manufacturing processes and engineering principles.
  • Familiarity with GMP/cGMP, FDA regulations, ISO 13485, or regulated manufacturing practices is preferred.
  • Basic knowledge of process validation, equipment qualification, and quality systems is a plus.
  • Strong analytical, troubleshooting, and problem-solving skills.
  • Excellent written and verbal communication skills.
  • Ability to work effectively in a cross-functional team environment.
  • Proficiency in Microsoft Office applications.
  • Eagerness to learn and grow in a regulated manufacturing environment.

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/