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Validation Associate Jobs in Indiana (NOW HIRING)

Trimedx

Inventory Validation Technician

Indianapolis, IN · On-site

$18.49/hr

Every associate matters and makes a difference It is truly a culture like no other - We hope you ... The Inventory Validation Technician works as a part of an inventory validation team and provides ...

Trimedx

Inventory Validation Technician

Indianapolis, IN · On-site

$18.49/hr

Every associate matters and makes a difference It is truly a culture like no other - We hope you ... The Inventory Validation Technician works as a part of an inventory validation team and provides ...

Micropulse, Inc.

Be Seen First

Process Validation Engineer

Columbia City, IN · On-site

$20 - $25/hr

Associates degree in manufacturing or quality engineering, or equivalent experience, required. A ... Knowledge of basic validation principles * Strong written and verbal communication skills * Good ...

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Validation Associate information

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How much do validation associate jobs pay per hour?

As of Jun 21, 2026, the average hourly pay for validation associate in Indiana is $49.48, according to ZipRecruiter salary data. Most workers in this role earn between $37.50 and $60.14 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.

How much does a validation specialist make in the US?

A validation specialist in the US typically earns between $60,000 and $85,000 annually, depending on experience, industry, and location. Entry-level roles may start around $50,000, while experienced professionals with certifications can earn over $100,000. Skills in quality assurance, regulatory compliance, and validation tools are often required for higher salaries.

What job makes $10,000 a month without a degree?

A Validation Associate typically does not earn $10,000 a month without a degree; such high earnings are uncommon for this role. Generally, jobs that can pay $10,000 monthly without a degree include specialized sales, real estate brokers, certain tech sales positions, or skilled trades with experience and commissions. These roles often require strong skills, certifications, or extensive experience rather than formal degrees.

Is QC a high paying job?

Quality Control (QC) roles, including validation associates, typically offer salaries that are average or slightly above average compared to other entry-level positions in manufacturing and healthcare industries. Compensation varies based on experience, location, and industry, with specialized skills and certifications potentially increasing earning potential.

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 are Validation Associates?

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.

Is Associate the lowest position?

In the role of Validation Associate, this position is typically an entry-level or early-career role within the validation or quality assurance departments. It is often the starting point before advancing to higher roles such as Senior Validation Associate or Validation Specialist, depending on the company's structure and experience required. The lowest position in a validation or quality team may vary by organization but often begins with entry-level titles like Validation Associate or Technician.

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 Indiana? The most popular types of Validation jobs in Indiana are:
What are popular job titles related to Validation Associate jobs in Indiana? For Validation Associate jobs in Indiana, the most frequently searched job titles are:
What job categories do people searching Validation Associate jobs in Indiana look for? The top searched job categories for Validation Associate jobs in Indiana are:
Validation Associate jobs near you

Packaging Validation Associate I - 1st Shift

Simtra BioPharma Solutions

Bloomington, IN • On-site

$14 - $17/hr

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Posted 26 days ago

Job description

Simtra BioPharma Solutions (Simtra) is a world-class Contract Development Manufacturing Organization, partnering with pharmaceutical and biotech companies to bring their sterile injectable products to market. With facilities in Bloomington, Indiana, US and Halle/Westfalen, Germany, we offer a wide range of delivery systems including pre-filled syringes, liquid/lyophilized vials, diluents for reconstitution, powder-filled vials and sterile crystallization.
Our product types include biologics and small molecules, cytotoxics, highly potent compounds, diluents for reconstitution and vaccines - which are all directly injected into patients worldwide. As such, there is a strong emphasis on quality and continuous improvement at Simtra. We hold ourselves to the highest quality and regulatory standards.
While our primary focus is cGMP manufacturing, we offer many support services including formulation and development, lyophilization optimization, global regulatory support and secondary packaging. Our teams are driven to help clients scale, innovate and bring life-changing medicines to patients worldwide.
Why join Team Simtra? Because we:
Make it HAPPEN - We bring a growth mindset to every opportunity, developing new skillsets and exceeding our expectations and those of our customers.
Make it TOGETHER - We work as one, respecting each voice and tapping into our unique strengths across teams-so we can solve problems in new ways.
Make it RIGHT - We hold ourselves to a high standard of excellence, fulfilling our commitments to the customer, their patients, and our team members.
Make it COUNT - We take pride in our day-to-day work, knowing the impact we make - taking on challenges big and small to improve patient health.
This role:
The Packaging Validation Associate I supports all aspects of the packaging process. This includes packaging development, equipment validation and general finishing operations. The position supports Packaging Development including the defining of packaging requirements, materials selection, package design, prototype development, package testing and the development of all related packaging documentation. It also supports Packaging Validation including packaging equipment design, specification development, installation, qualification, vision tuning, validation and operational support. This position reports to the Manager, Packaging Validation.
The responsibilities:
  • Manages multiple projects providing technical support for packaging operations while working in a cross-functional team environment
  • Develops and executes Validation documentation including Process Flow Diagrams, Failure Mode Effect Analysis (FMEAs), Protocols, Final Reports, Standard Operating Procedures (SOPs), etc.
  • Assists Engineering Department on Factory Acceptance Tests (FAT) and User Requirement Specifications (URS)
  • Participates in small project teams, creates timelines, tracks deliverables and communicates status updates to stakeholders.
  • Formulates and recommends validation procedures and technical work in accordance with project and business objectives
  • Participates in client and regulatory audits
  • Selects packaging materials; evaluates packaging components in terms of functionality and machinability; develops Bill of Materials (BOM), Component Specifications and Process Assembly Specifications
  • Acts as Change Control Management (CCM) Owner, Non-Conformance and OCR (Out of Control Report) author
  • Identifies and implements changes to Automated Inspection Machines
  • Reviews and approves Packaging Technical Services documents

Desired qualifications:
  • Bachelor's degree in science or engineering related area is preferred or a minimum of 5 years manufacturing experience with 2 years of leadership experience required.
  • In-depth process knowledge of related manufacturing equipment and process preferred
  • Experienced understanding of cGMPs and other regulatory guidelines applicable to the medical/pharmaceutical industry preferred
  • Ability to review Equipment Manuals including Engineering Equipment Drawings and Electrical Schematic Diagrams.
  • Proficiency in Microsoft Word, Excel, and Outlook and the ability to use enterprise software (examples include: JDE, BPLM, Trackwise, etc.)
  • Manages time effectively and independently within assigned responsibilities
  • Ability to prioritize multiple projects/workflows and manage time efficiently in order to meet established timelines
  • Operates as a self-starter having the ability to complete tasks with minimal direction from manager
  • Exhibits a sense of urgency to meet timelines and key milestones
  • Possesses good leadership skills including ability to lead cross-functional departments in the implementation of new systems and modification of existing ones

Physical / Safety Requirements:
  • Must be able to lift up to 25 lbs.
  • Duties may require overtime work, including nights and weekends
  • Use of hands and fingers to manipulate office equipment is required
  • Position requires sitting/standing for long hours, but may involve walking or standing for periods of time
  • Must wear appropriate Personal Protective Equipment as applicable
  • Must fully understand company safety rules and regulations

In return, you'll be eligible for[1]:
  • Day One Benefits
    • Medical & Dental Coverage
    • Flexible Spending Accounts
    • Life and AD&D Insurance
    • Supplemental Life Insurance
      • Spouse Life Insurance
      • Child Life Insurance
    • 401(k) Retirement Savings Plan with Company Match
    • Time Off Program
      • Paid Holidays
      • Paid Time Off
      • Paid Parental Leave and more
    • Adoption Reimbursement Program
    • Education Assistance Program
    • Employee Assistance Program
    • Community and Volunteer Service Program
    • Employee Ownership Plan
  • Additional Benefits
    • Short and Long-Term Disability Insurance
    • Voluntary Insurance Benefits
      • Vision Coverage
      • Accident
      • Critical Illness
      • Hospital Indemnity Insurance
      • Identity Theft Protection
      • Legal and more
    • Onsite Campus Amenities
      • Workout Facility
      • Cafeteria
      • Credit Union

[1] Current benefit offerings are in effect through 12/31/26
Disclaimer
This job description is intended to provide the minimum knowledge, skills and abilities necessary to perform the job. It may not be inclusive of all the duties and responsibilities of the job. Simtra reserves the right to make modifications based on business requirements.
Equal Employment Opportunity
Simtra is proud to be an equal opportunity employer. Simtra evaluates qualified applicants without regard to race, color, religion, gender, national origin, age, sexual orientation, gender identity or expression, protected veteran status, disability/handicap status or any other legally protected characteristic.
Data Privacy
To learn more about Simtra's approach to data privacy, please review the Simtra Recruitment Platform Global Privacy Policy: https://simtra.com/privacy-policy/

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