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Gmp Compliance Associate Jobs (NOW HIRING)

Warehouse Associate I

Brooks, KY · On-site

$15.75 - $18.75/hr

Warehouse Associate I Location: Brooks KY Duration: 2+ Months Job Type: Contract Maximum ... Attention to detail and GMP compliance * Safe material handling and warehouse practices Must-Have ...

... GMP compliance, and collaborating with Engineering, Quality, and other departments. May train associates and perform material handling as needed. Key Responsibilities * Assemble, integrate, and test ...

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In addition to batch record review, this position will also support GMP compliance video review as ... Associate degree or higher in Life Sciences, Chemistry, Biology, Pharmaceutical Sciences, or a ...

If Senior Manufacturing Associate sounds like something you would be interested in, and you meet ... GMP compliance * Support equipment troubleshooting, maintenance, and continuous improvement ...

Opportunity to gain experience in medical device production and GMP compliance * Access to Adecco ... For instant consideration for this Final Assembly Associate position with Adecco in Skaneateles ...

GMP Audits * Identify and report any nonconformances and process deviations. * Maintain cGMP compliant documentation of Production and Quality records. * Assist with Stability, Reserve, and USP ...

GMP Audits * Identify and report any nonconformances and process deviations. * Maintain cGMP compliant documentation of Production and Quality records. * Assist with Stability, Reserve, and USP ...

... compliance with GMP regulations and internal procedures. Summary of Key Responsibilities ... Associate's Degree in a relevant technical discipline with 5+ years of GMP pharmaceutical or ...

Responsibilities:Monitor SOP's, SSOP?s, and GMP compliance of associates, perform HACCP procedures to comply with federal regulationsWork with USDA and present records to them at the agency?s ...

QA Associate

Pearl River, NY · On-site

$55K - $95K/yr

About the Role The QA Associate supports production-related quality activities to ensure processes ... Review microbiology data, records, and reports for accuracy, completeness, and GMP compliance

... compliance with GMP regulations and internal procedures. Summary of Key Responsibilities ... Associate's Degree in a relevant technical discipline with 5+ years of GMP pharmaceutical or ...

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Gmp Compliance Associate information

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$12

$35

$63

How much do gmp compliance associate jobs pay per hour?

As of Jun 10, 2026, the average hourly pay for gmp compliance associate in the United States is $35.41, according to ZipRecruiter salary data. Most workers in this role earn between $23.08 and $43.99 per hour, depending on experience, location, and employer.

What is the difference between Gmp Compliance Associate vs Quality Assurance Associate?

AspectGmp Compliance AssociateQuality Assurance Associate
CertificationsGMP certifications, relevant compliance trainingGMP certifications, QA-specific training
Work EnvironmentRegulatory compliance, documentation review, auditsProduct quality testing, process validation, audits
Industry UsagePharmaceutical, biotech, medical devicesPharmaceutical, biotech, manufacturing

Gmp Compliance Associates focus on ensuring regulatory adherence and compliance documentation, while Quality Assurance Associates concentrate on product quality and process validation. Both roles are essential in regulated industries and often collaborate to maintain high standards and compliance.

What are the most commonly searched types of Gmp Compliance jobs? The most popular types of Gmp Compliance jobs are:
Infographic showing various Gmp Compliance Associate job openings in the United States as of June 2026, with employment types broken down into 66% Full Time, 33% Part Time, and 1% Contract. Highlights an 98% Physical, 1% Hybrid, and 1% Remote job distribution, with an average salary of $73,648 per year, or $35.4 per hour.
Associate Specialist, Quality Assurance

Associate Specialist, Quality Assurance

Shiseido

East Windsor, NJ • On-site

Other

Posted 25 days ago


Shiseido rating

7.2

Company rating: 7.2 out of 10

Based on 11 frontline employees who took The Breakroom Quiz


Job description

WHERE YOU WILL WORK

Without compromising our steadfast commitment to Quality, Safety and Sustainability our manufacturing and packaging facility produces in excess of 70MM units per year.   This is a demonstration of our can-do attitude, collaborative spirit, focus on innovation and continuous improvement mindset.   Always People First! 

JOB SUMMARY

The Quality Assurance Associate Specialist is responsible for preparing and completing the CARES act report for FDA, is responsible for BOM review and approval, Bulk and Finished Good, Responsible for Releasing Finished Goods (OTC, Non-OTC etc.) reviewing Batch records, specifications, procedures, protocols, and records for GMP compliance. 

WHAT YOU WILL DO 

  • You will prepare and complete the CARESS ACT list for FDA.
  • You will complete BOM review and approval, set up the system specifications for Finished Goods, FG, and Bulk working closely with different departments
  • You will be responsible for Releasing Finished Goods (OTC, Non-OTC, etc.)
  • You will prepare master production records for all OTC products.
  • You will review raw material, packaging material, in-process material and finished product specifications for GMP compliance - Reconciliation of OTC Batch Records.
  • You will perform review of Production batch records and control records for OTC products and initiate investigation for any unexplained discrepancy found during review. Prepare Certificate of Manufacturing and Compliance and release OTC products for shipment.
  • You will aid in investigations as required.
  • You will file and maintain batch production and control records for OTC product.
  • You will conduct/review Annual Product Review of OTC products.  Record the observations that needs follow up with AIC team.
  • You will provide GMP Training to other departments as needed
  • You will research and prepare data as needed for monthly quality metrics reporting
  • You will assist in any projects/tasks assigned by the Manager.

WHO YOU ARE 

  • You have a bachelor's degree (B. A.) from a four-year college or university, preferably in Engineering or Science
  • You have two years' knowledge of pharmaceutical GMP documentation requirements and quality assurance experience in a regulated industry.
  • You have a good understanding of 21CFR (Part210-211), ICH guidelines
  • You have experience with SAP systems
  • You are an expert in Excel and PowerPoint presentation.
  • You have good verbal and written communication skills

PHYISCAL REQUIREMENTS

The physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of this job, if applicable. Reasonable accommodation may be made to enable individuals with disabilities to perform the essential functions. 

Employees must be able to wear personal protective equipment (PPE) as required by the area of work or tasks being performed. Required PPE may include, but is not limited to, eye protection, hearing protection, safety shoes, gloves, or additional protective clothing.

Standing

Under 1/3

Walking

Under 1/3

Sitting

Over 2/3

Use hands to finger, handle or feel

Not Applicable

Climb or balance

Under 1/3

Reach with hands and arms

Under 1/3

Stoop, Kneel, Crouch, or Crawl

Not Applicable

Up to 10 pounds

Under 1/3

Up to 25 pounds

Under 1/3

Up to 50 pounds

Not Applicable

Up to 100 pounds

Not Applicable

If this sounds like you, we want you on our team.  Apply today and let's create something beautiful!

Your Dreams. Our Future.  

#NYLaw #LI-Onsite


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