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Validation Associate Jobs in Philadelphia, PA (NOW HIRING)

gpac

Associate Veterinarian

Wilmington, DE · On-site

$125K - $160K/yr

I am seeking an Associate Veterinarian for a full-service pet hospital. This practice is rated as ... Successful graduation from a Certified College of Veterinary Medicine and a valid license to ...

gpac

Associate Veterinarian

New Castle, DE · On-site

$125K - $160K/yr

I am seeking an Associate Veterinarian for a full-service pet hospital. This practice is rated as ... Successful graduation from a Certified College of Veterinary Medicine and a valid license to ...

gpac

Associate Veterinarian

Claymont, DE · On-site

$125K - $160K/yr

I am seeking an Associate Veterinarian for a full-service pet hospital. This practice is rated as ... Successful graduation from a Certified College of Veterinary Medicine and a valid license to ...

gpac

Associate Veterinarian

Elsmere, DE · On-site

$125K - $160K/yr

I am seeking an Associate Veterinarian for a full-service pet hospital. This practice is rated as ... Successful graduation from a Certified College of Veterinary Medicine and a valid license to ...

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Showing results 21-40

All JobsValidation Associate JobsValidation Associate Jobs in Philadelphia, PA

Validation Associate information

See Philadelphia, PA salary details

$21

$49

$74

How much do validation associate jobs pay per hour?

As of Aug 11, 2026, the average hourly pay for validation associate in Philadelphia, PA is $49.69, according to ZipRecruiter salary data. Most workers in this role earn between $37.69 and $60.43 per hour, depending on experience, location, and employer.

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

To thrive as a Validation Associate, you need a background in life sciences or engineering, strong analytical skills, and knowledge of regulatory compliance standards such as GMP or FDA guidelines. Familiarity with validation software, laboratory instrumentation, and documentation management systems is typically required, and certifications like Lean Six Sigma can be beneficial. Attention to detail, problem-solving abilities, and effective communication are essential soft skills in this role. These skills ensure that processes, equipment, and systems meet regulatory requirements and quality standards, which is critical for product safety and organizational compliance.

What is the difference between Validation Associate vs Quality Control Analyst?

AspectValidation AssociateQuality Control Analyst
Required CredentialsBachelor's degree in life sciences or related field; certifications like CQE or ASQ often preferredBachelor's degree in chemistry, biology, or related field; certifications like CQE or ASQ common
Work EnvironmentPharmaceutical, biotech, or medical device manufacturing facilities; focus on validation processesLaboratories, manufacturing plants; focus on testing and quality assessment
Employer & Industry UsageUsed in regulated industries requiring validation of processes and systemsCommon in quality testing, inspection, and product release processes

While both roles require a background in science and similar certifications, a Validation Associate primarily focuses on validating processes and systems to ensure compliance, whereas a Quality Control Analyst concentrates on testing products and materials to verify quality. Both roles are essential in regulated industries but serve different functions within the quality assurance framework.

What is a validation associate?

Validation Associates are professionals responsible for ensuring that processes, equipment, and systems in industries like pharmaceuticals, biotechnology, and manufacturing meet required standards and regulations. They plan and execute validation protocols to confirm that products are produced consistently and meet quality specifications. Their work involves documenting procedures, performing tests, analyzing data, and maintaining compliance with regulatory agencies such as the FDA. Validation Associates play a critical role in quality assurance and risk management within their organizations.

How does a validation associate typically collaborate with other departments during a project?

A Validation Associate frequently works cross-functionally with teams such as Quality Assurance, Manufacturing, and Research & Development. They coordinate to gather essential documents, understand process requirements, and ensure that all validation activities meet regulatory standards. Effective communication and organization are key, as Validation Associates often facilitate meetings, resolve discrepancies, and provide updates to stakeholders. This collaborative approach helps maintain compliance and supports the successful launch or improvement of products and processes.
What are the most commonly searched types of Validation jobs in Philadelphia, PA? The most popular types of Validation jobs in Philadelphia, PA are:
What are popular job titles related to Validation Associate jobs in Philadelphia, PA? For Validation Associate jobs in Philadelphia, PA, the most frequently searched job titles are:
What job categories do people searching Validation Associate jobs in Philadelphia, PA look for? The top searched job categories for Validation Associate jobs in Philadelphia, PA are:
What cities near Philadelphia, PA are hiring for Validation Associate jobs? Cities near Philadelphia, PA with the most Validation Associate job openings:
Validation Associate jobs near you
Infographic showing various Validation Associate job openings in Philadelphia, PA as of August 2026, with employment types broken down into 1% As Needed, 66% Full Time, 29% Part Time, 2% Temporary, and 2% Contract. Highlights an 97% Physical, 1% Hybrid, and 2% Remote job distribution, with an average salary of $103,364 per year, or $49.7 per hour.

Biopharm Manufacturing Assoc

Alphanumeric

King Of Prussia, PA

$22 - $24.50/hr

Contractor

Posted 4 days ago

Job description

Biopharm Manufacturing Associate II

Upper Merion (King of Prussia), PA

Alphanumeric is hiring Biopharm Manufacturing Associates II to join our client of over 20 years, a global biopharmaceutical leader committed to developing life-changing medicines that improve patients' lives.

💲 Pay Rate: $22.00?$24.50/hour

Launch or Advance Your Career in Biopharmaceutical Manufacturing

Are you passionate about science, manufacturing, and making a difference? Join a collaborative manufacturing team responsible for producing innovative biologic therapies in a highly regulated cGMP environment. You'll gain valuable experience working with advanced manufacturing technologies while contributing to medicines that impact patients around the world.

What You'll Do

As a Biopharm Manufacturing Associate II, you'll support upstream biopharmaceutical manufacturing operations by:

  • Performing production activities including fermentation, cell culture, solution preparation, filtration, chromatography, and concentration processes
  • Operating and monitoring automated manufacturing equipment
  • Completing manufacturing tasks in accordance with SOPs, batch records, and GMP documentation requirements
  • Preparing, cleaning, sanitizing, and maintaining manufacturing equipment and production areas
  • Performing autoclave operations and parts washing of process assemblies
  • Monitoring critical process parameters and assisting with troubleshooting activities
  • Supporting engineering, validation, and technology transfer activities
  • Participating in safety, compliance, deviation investigations, and continuous improvement initiatives
  • Collaborating with Manufacturing, Engineering, Quality, Validation, and Technical Operations teams
  • Maintaining accurate documentation and data integrity in accordance with cGMP requirements

Minimum Qualifications
  • Bachelor's degree in Biology, Chemistry, Biochemistry, Chemical Engineering, Biotechnology, or another scientific discipline with cGMP manufacturing experience
  • OR Associate's degree in Biotechnology or a related technical field with cGMP manufacturing experience
  • OR High School diploma/GED with at least one year of cGMP manufacturing experience
  • Strong written and verbal communication skills
  • Excellent attention to detail and documentation skills
  • Ability to work effectively in a collaborative manufacturing environment
Preferred Qualifications
  • Experience working in a pharmaceutical or biotechnology manufacturing environment
  • Knowledge of cGMP regulations and documentation practices
  • Experience with fermentation, cell culture, chromatography, filtration, or downstream manufacturing operations
  • Familiarity with SAP, Electronic Batch Records (EBR), or other manufacturing systems
  • Experience supporting validation, engineering, or technology transfer activities
  • Demonstrated troubleshooting and problem-solving abilities
Why You'll Love This Opportunity
  • Work for a global leader in biopharmaceutical innovation
  • Gain experience with advanced biologics manufacturing
  • Collaborative, team-oriented environment
  • Build valuable cGMP manufacturing experience
  • Opportunity to support life-changing therapies
  • Competitive hourly pay

Please Note: This is a 100% onsite position in Upper Merion (King of Prussia), PA.

Applicants must be legally authorized to work in the United States on a W-2 basis. We are unable to accept applications from third-party vendors or provide visa sponsorship now or in the future.

If you're ready to build your career in biopharmaceutical manufacturing and make an impact on patients' lives, we'd love to hear from you!

Education:Employment Type: CONTRACTOR

Apply