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Validation Associate Jobs in Brunswick, MD (NOW HIRING)

Lonza

Associate Director, MSAT

Walkersville, MD · On-site

$174K - $203K/yr

Associate Director, MSAT Location: This position is currently remote. A future transition to an on ... Lead process-related commissioning, qualification, validation readiness, start-up activities, and ...

Lonza

Associate Director, MSAT

Walkersville, MD · On-site +1

$174K - $203K/yr

Associate Director, MSAT Location: This position is currently remote. A future transition to an on ... Lead process-related commissioning, qualification, validation readiness, start-up activities, and ...

Carmax

Supply Associate

Frederick, MD · On-site

$20.35/hr

Valid driver's license and ability to meet CarMax driving standards. * High school diploma or ... Completion of Inventory Associate workstation certifications and assigned trainings. * Ability to ...

Carmax

Supply Associate

Sterling, VA · On-site

$18.20 - $32.60/hr

Valid driver's license with a clean driving record * Strong communication and teamwork skills to ... As an associate, you are part of an innovative movement to empower the modern customer and drive ...

Carmax

Flow Inventory Associate

Frederick, MD · On-site

$20.35/hr

Valid driver's license and ability to meet CarMax driving standards. * High school diploma or ... Completion of Inventory Associate workstation certifications and assigned trainings. * Ability to ...

Carmax

Inventory/Supply Associate

Frederick, MD · On-site

$20.35/hr

Valid driver's license and ability to meet CarMax driving standards. * High school diploma or ... Completion of Inventory Associate workstation certifications and assigned trainings. * Ability to ...

Carmax

Flow Inventory Associate

Frederick, MD · On-site

$20.35/hr

Valid driver's license and ability to meet CarMax driving standards. * High school diploma or ... Completion of Inventory Associate workstation certifications and assigned trainings. * Ability to ...

Carmax

Inventory/Logistics Associate

Frederick, MD · On-site

$20.35/hr

Valid driver's license and ability to meet CarMax driving standards. * High school diploma or ... Completion of Inventory Associate workstation certifications and assigned trainings. * Ability to ...

Virginia Tire and Auto

Warehouse Associate

Sterling, VA · On-site

$16.25 - $19.25/hr

The Warehouse Associate is responsible for the tracking, stocking, and organization of each stores ... Have and maintain a clean driving record and valid US Driver's License * Basic Math Skills * Basic ...

CarMax, Inc.

Flow Inventory Associate

Frederick, MD · On-site

$20.35/hr

Valid driver's license and ability to meet CarMax driving standards. * High school diploma or ... Completion of Inventory Associate workstation certifications and assigned trainings. * Ability to ...

Daikin Comfort

Warehouse Associate

Sterling, VA · On-site

$15.75 - $18.75/hr

Warehouse Associate The Warehouse Associate is responsible for off-loading, put-away, picking and ... Must have Valid driver's license People Management: No Physical Requirements / Work Environment:

Virginia Tire & Auto

Warehouse Associate

Sterling, VA · On-site

$16.25 - $19.25/hr

The Warehouse Associate is responsible for the tracking, stocking, and organization of each stores ... Have and maintain a clean driving record and valid US Driver's License * Basic Math Skills * Basic ...

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All JobsValidation Associate JobsValidation Associate Jobs in Brunswick, MD

Validation Associate information

See Brunswick, MD salary details

$20

$48

$72

How much do validation associate jobs pay per hour?

As of Aug 5, 2026, the average hourly pay for validation associate in Brunswick, MD is $48.13, according to ZipRecruiter salary data. Most workers in this role earn between $36.49 and $58.51 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 Brunswick, MD? The most popular types of Validation jobs in Brunswick, MD are:
What cities near Brunswick, MD are hiring for Validation Associate jobs? Cities near Brunswick, MD with the most Validation Associate job openings:
Validation Associate jobs near you
Infographic showing various Validation Associate job openings in Brunswick, MD as of June 2026, with employment types broken down into 67% Full Time, 32% Part Time, and 1% Contract. Highlights an 90% Physical, 3% Hybrid, and 7% Remote job distribution, with an average salary of $100,101 per year, or $48.1 per hour.

Manufacturing Technology Associate II

Fladger Associates

Frederick, MD • On-site

Contractor

Re-posted 24 days ago

Job description

Frederick, MD
Contract Duration: 7-36 months
Rate: Negotiable

Responsibilities:

  • Excellent employment opportunity for a Manufacturing Technology Associate II in the Frederick, MD area. (100% onsite)
  • The Manufacturing Technology Associate II play a pivotal role in channeling our scientific capabilities to make a positive impact on changing patients' lives.
  • The position may require off-shift and weekend work as well as infrequent travel.
  • Responsible for conducting or participating in technically fast paced projects within your specific area or field
  • Support the design of validation sampling/test plans and performing development studies
  • Prepare medias and buffers to support MST experiments
  • Assist to monitor and maintain lab equipment and inventory
  • Inoculate and expand cell culture to support scientific studies and resolve technical issues encountered during study execution.
  • Enter all data timely into electronic lab systems and assist in data analysis, population of presentations and reports
  • Supports technology transfer activities tracked in the site change control system, method validation/method transfer, filter validation, shipping qualification, and FAT/ SAT /Commissioning activities.

Experience:

  • Bachelor's Degree preferably in Science or Engineering.
  • At least three (3) years of experience in Scientific / Biotech / Pharmaceutical field.
  • Previous experience in Biologics working in cell culture (cell lines such as mammalian) and purification of large molecules in therapeutic antibodies, vaccines or injectables.
  • Knowledge of GMP manufacturing principles and documentation.
  • Ability to apply critical thinking to solve problems and work independently.
  • Strong interpersonal and communication skills.
  • Bachelor's Degree preferably in Science or Engineering, preferable having Biology education