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Part Time Pharmaceutical Validation Jobs in Renton, WA

Collabera Digital

Senior Biostatistician

Seattle, WA · On-site

$150K - $160K/yr

ADaM/TLF & FDA Submission Expert (Part-Time) Location: Hybrid as needed 2 days/week in Seattle, WA ... Review and validate AI-generated ADaM/TLF outputs against CDISC standards and FDA submission ...

Bruker

Title QC Inspector

Bothell, WA

$41K/yr

Address 3350 Monte Villa Parkway Type Employee Full Time/Part Time Full Time Overview As one of the ... Perform lot validation testing while monitoring and adjusting testing frequencies. * Support review ...

New

Labcorp

Phlebotomist Float

Seattle, WA

$21.87 - $32.28/hr

... researchers, pharmaceutical companies and health systems make confident decisions and improve ... Valid Driver's License and clean driving record * Be at least 21 years old * Able to pass a ...

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Part Time Pharmaceutical Validation information

See Renton, WA salary details

$25

$58

$87

How much do part time pharmaceutical validation jobs pay per hour?

As of Aug 17, 2026, the average hourly pay for part time pharmaceutical validation in Renton, WA is $58.49, according to ZipRecruiter salary data. Most workers in this role earn between $44.33 and $71.11 per hour, depending on experience, location, and employer.

What is a part time pharmaceutical validation?

A part time pharmaceutical validation job involves ensuring that equipment, processes, and systems in a pharmaceutical environment operate according to regulatory standards and company requirements, but on a part-time or flexible schedule. Responsibilities typically include documenting procedures, conducting tests, and reporting results to confirm that products are consistently produced with the desired quality. Part-time roles may be ideal for students, retirees, or professionals seeking work-life balance while contributing to pharmaceutical quality assurance. These positions require attention to detail, regulatory knowledge, and strong analytical skills. They often support full-time validation teams, especially during audits or when new equipment is introduced.

What are the typical responsibilities for someone in a part time pharmaceutical validation role?

In a part-time pharmaceutical validation role, your primary responsibilities often include assisting with the qualification of equipment, processes, and systems to ensure compliance with regulatory guidelines. You'll likely be involved in executing validation protocols, documenting results, and supporting investigations when deviations occur. Collaboration is key, as you'll work closely with quality assurance, production, and engineering teams to maintain high standards. The part-time nature of the role may mean flexible hours, but attention to detail and clear communication remain essential.

What are the key skills and qualifications needed to thrive as a part time pharmaceutical validation professional, and why are they important?

To thrive as a Part Time Pharmaceutical Validation professional, you need a background in life sciences or engineering, strong knowledge of validation protocols, and familiarity with regulatory standards like GMP. Experience with validation software tools, documentation management systems, and possibly certifications such as Six Sigma or relevant GxP training are typically required. Attention to detail, analytical thinking, and effective communication are crucial soft skills for identifying issues and collaborating with cross-functional teams. These competencies ensure compliance, product quality, and efficient validation processes in a regulated pharmaceutical environment.

What is the difference between Part Time Pharmaceutical Validation vs Part Time Quality Control Analyst?

AspectPart Time Pharmaceutical ValidationPart Time Quality Control Analyst
Required CredentialsValidation certifications, GMP knowledgeQC certifications, laboratory skills
Work EnvironmentManufacturing, validation labsLaboratories, testing facilities
Employer & Industry UsagePharmaceutical manufacturing companiesPharmaceutical and biotech companies
Common Search & ComparisonYesYes

Part Time Pharmaceutical Validation focuses on ensuring manufacturing processes meet quality standards through validation protocols, while Part Time Quality Control Analysts perform testing and analysis of products. Both roles require industry-specific certifications and are integral to pharmaceutical quality assurance, but they differ in daily tasks and focus areas.

What cities near Renton, WA are hiring for Part Time Pharmaceutical Validation jobs?

Cities near Renton, WA with the most Part Time Pharmaceutical Validation job openings:

Part Time Pharmaceutical Validation jobs near you

Senior Biostatistician

Collabera Digital

Seattle, WA • On-site

$150K - $160K/yr

Full-time, Part-time

Medical, Dental, Vision, Retirement, PTO

This job post has expired today. Applications are no longer accepted.

Job description

About Ascendion
Ascendion is a full-service digital engineering solutions company. We make and manage software platforms and products that power growth and deliver captivating experiences to consumers and employees. Our engineering, cloud, data, experience design, and talent solution capabilities accelerate transformation and impact for enterprise clients. Headquartered in New Jersey, our workforce of 6,000+ Ascenders delivers solutions from around the globe. Ascendion is built differently to engineer the next.
Ascendion | Engineering to elevate life
We have a culture built on opportunity, inclusion, and a spirit of partnership. Come, change the world with us:
  • Build the coolest tech for world's leading brands
  • Solve complex problems - and learn new skills
  • Experience the power of transforming digital engineering for Fortune 500 clients
  • Master your craft with leading training programs and hands-on experience

Experience a community of change makers!
Join a culture of high-performing innovators with endless ideas and a passion for tech. Our culture is the fabric of our company, and it is what makes us unique and diverse. The way we share ideas, learning, experiences, successes, and joy allows everyone to be their best at Ascendion.
About the Role:
Now Hiring: ADaM/TLF & FDA Submission Expert (Part-Time)
Location:Hybrid as needed 2 days/week in Seattle, WA
Ascendion is hiring anADaM/TLF & FDA Submission Expertto support a confidential Fortune 500 technology client developing next-generation AI solutions for clinical trial data and regulatory submissions.
This is a unique opportunity for an experienced clinical data professional with deep expertise inADaM, TLFs, CDISC standards, and FDA submissionsto help validate AI-generated clinical trial outputs. You'll work alongside engineering and clinical teams to ensure AI-generated deliverables meet real-world regulatory and submission standards.
Key Responsibilities
  • Provide hands-on expertise inADaM dataset structureandTLF (Tables, Listings & Figures)development.
  • Review and validate AI-generated ADaM/TLF outputs againstCDISC standardsandFDA submission requirements.
  • Support the preparation and review ofFDA submission packages, includingDefine.xmland associated documentation.
  • Identify compliance gaps, inconsistencies, and submission risks while providing actionable feedback.
  • Partner with engineering and clinical teams to translate regulatory requirements into AI development guidance.
  • Ensure submission-ready data meets quality, compliance, and regulatory expectations.

Required Qualifications
  • Proven hands-on experience building and/or submittingADaM datasetsandTLF packagesfor clinical trial submissions.
  • Strong knowledge ofCDISC ADaM,SDTM, and FDA submission standards.
  • Experience supportingFDA submission packagesfor clinical trials.
  • Strong analytical, problem-solving, and written communication skills.
  • Ability to review technical outputs and identify regulatory compliance issues.

Preferred Qualifications
  • Experience working withAI-assisted clinical dataor AI-generated outputs.
  • Experience inGxP-regulatedenvironments.
  • Background in pharmaceutical, biotechnology, or CRO organizations.
  • Experience collaborating with cross-functional teams, including biostatistics, clinical programming, regulatory affairs, and engineering.

Why Join?
  • Work on cutting-edgeAI solutions transforming clinical trial data and regulatory submissions.
  • Collaborate with a leading Fortune 500 technology company.
  • Flexiblepart-timeengagement with a highly specialized, high-impact project.
  • Opportunity to shape the future of AI in clinical research and regulatory compliance.

If you have hands-on expertise inADaM, TLFs, FDA submissions, CDISC, Define.xmlwe'd love to hear from you!
Salary Range: The salary for this position is between $150,000 - $160,000 annually. Factors which may affect pay within this range may include geography/market, skills, education, experience and other qualifications of the successful candidate.
Benefits: The Company offers the following benefits for this position, subject to applicable eligibility requirements: [medical insurance] [dental insurance] [vision insurance] [401(k) retirement plan] [long-term disability insurance] [short-term disability insurance] [personal days accrued each calendar year. The Paid time off benefits meet the paid sick and safe time laws that pertains to the City/ State] [12-15 days of paid vacation time] [6-8 weeks of paid parental leave after a year of service] [9 paid holidays and 2 floating holidays per calendar year] [Ascendion Learning Management System] [Tuition Reimbursement Program]
Want to change the world? Let us know.
Tell us about your experiences, education, and ambitions. Bring your knowledge, unique viewpoint, and creativity to the table. Let's talk!
Preferred Skills
ADaM DataSets
  • TLF
  • FDA Submisson

Apply