JOB SUMMARY The Quality Assurance Associate Specialist is responsible for preparing and completing ... for GMP compliance. WHAT YOU WILL DO * You will prepare and complete the CARESS ACT list for FDA.
JOB SUMMARY The Quality Assurance Associate Specialist is responsible for preparing and completing ... for GMP compliance. WHAT YOU WILL DO * You will prepare and complete the CARESS ACT list for FDA.
JOB SUMMARY The Quality Assurance Associate Specialist is responsible for preparing and completing ... for GMP compliance. WHAT YOU WILL DO * You will prepare and complete the CARESS ACT list for FDA.
JOB SUMMARY The Quality Assurance Associate Specialist is responsible for preparing and completing ... for GMP compliance. WHAT YOU WILL DO * You will prepare and complete the CARESS ACT list for FDA.
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 ...
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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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... 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 ...
Formulation Associate 2nd & 3rd
Lee, MA · On-site
$19.58 - $36.59/hr
... GMP compliance and written SOP and batch records. Duties and Responsibilities * Operate glass ... Formulation Associate I - Zero to two (0-2) years' experience in a GMP environment performing and ...
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Formulation Associate 2nd & 3rd
Lee, MA · On-site
$19.58 - $36.59/hr
... GMP compliance and written SOP and batch records. Duties and Responsibilities * Operate glass ... Formulation Associate I - Zero to two (0-2) years' experience in a GMP environment performing and ...
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QA Batch Record Reviewer (3-11:30pm; Pharma Exp. Required)
Newtown, PA · On-site
$50K - $60K/yr
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 ...
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QA Batch Record Reviewer (3-11:30pm; Pharma Exp. Required)
Newtown, PA · On-site
$50K - $60K/yr
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 ...
Senior Manufacturing Associate
Plainville, MA · On-site
$31/hr
If Senior Manufacturing Associate sounds like something you would be interested in, and you meet ... GMP compliance * Support equipment troubleshooting, maintenance, and continuous improvement ...
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Senior Manufacturing Associate
Plainville, MA · On-site
$31/hr
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 ...
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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 ...
The QA Specialist ensures accurate records, strong GMP compliance, andeffective execution of key ... Associate's or Bachelor's degree in a science-related field (Food Science, Biology, Chemistry, etc ...
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The QA Specialist ensures accurate records, strong GMP compliance, andeffective execution of key ... Associate's or Bachelor's degree in a science-related field (Food Science, Biology, Chemistry, etc ...
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 ...
Quality Assoc I
Lawrenceburg, IN · On-site
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 ...
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Quality Assoc I
Lawrenceburg, IN · On-site
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 ...
Associate Director / Senior Manager, Quality Assurance Allakos Inc. is a clinical-stage company ... Maintain appropriate development phase GMP compliance for release testing, and stability * Reviews ...
Associate Director / Senior Manager, Quality Assurance Allakos Inc. is a clinical-stage company ... Maintain appropriate development phase GMP compliance for release testing, and stability * Reviews ...
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 ...
Metrologist
Durham, NC · On-site
... 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 ...
Metrologist
Durham, NC · On-site
... 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 ...
FAB QA TECHNICIAN 1ST SHIFT
Tolleson, AZ · On-site
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 ...
FAB QA TECHNICIAN 1ST SHIFT
Tolleson, AZ · On-site
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 ...
Facilities Associate
Frederick, MD · On-site
$17 - $22.75/hr
Facilities Associate - Essential Support for Facility Operations Location: Onsite (Frederick, MD ... * Assist in ensuring GMP compliance across facility spaces, helping maintain cleanliness ...
Facilities Associate
Frederick, MD · On-site
$17 - $22.75/hr
Facilities Associate - Essential Support for Facility Operations Location: Onsite (Frederick, MD ... * Assist in ensuring GMP compliance across facility spaces, helping maintain cleanliness ...
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
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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
The Associate Director will collaborate with cross-functional teams to identify opportunities for ... GMP Compliance, Good Manufacturing Practices (GMP), Medical Devices, Quality Management Systems ...
The Associate Director will collaborate with cross-functional teams to identify opportunities for ... GMP Compliance, Good Manufacturing Practices (GMP), Medical Devices, Quality Management Systems ...
Metrologist
Durham, NC · On-site
... 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 ...
Metrologist
Durham, NC · On-site
... 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 ...
Sr. QA Specialist, Operations
Plantation, FL · On-site
$81K - $112K/yr
... ensuring GMP compliance during manufacturing operations while exercising independent quality ... Associate or Bachelor's degree preferred. · Strong knowledge of cGMP, aseptic manufacturing, and ...
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Sr. QA Specialist, Operations
Plantation, FL · On-site
$81K - $112K/yr
... ensuring GMP compliance during manufacturing operations while exercising independent quality ... Associate or Bachelor's degree preferred. · Strong knowledge of cGMP, aseptic manufacturing, and ...
Gmp Compliance Associate information
See salary details
$12.50 - $17.15
5% of jobs
$17.15 - $21.81
19% of jobs
$22.20 is the 25th percentile. Wages below this are outliers.
$21.81 - $26.46
9% of jobs
$26.46 - $31.12
15% of jobs
The median wage is $31.58 / hr.
$31.12 - $35.77
16% of jobs
$40.11 is the 75th percentile. Wages above this are outliers.
$35.77 - $40.43
12% of jobs
$40.43 - $45.08
4% of jobs
$45.08 - $49.74
7% of jobs
$49.74 - $54.39
5% of jobs
$54.39 - $59.05
5% of jobs
$59.05 - $63.70
2% of jobs
$12
$35
$63
How much do gmp compliance associate jobs pay per hour?
What is the difference between Gmp Compliance Associate vs Quality Assurance Associate?
| Aspect | Gmp Compliance Associate | Quality Assurance Associate |
|---|---|---|
| Certifications | GMP certifications, relevant compliance training | GMP certifications, QA-specific training |
| Work Environment | Regulatory compliance, documentation review, audits | Product quality testing, process validation, audits |
| Industry Usage | Pharmaceutical, biotech, medical devices | Pharmaceutical, 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.

Shiseido rating
7.2
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
About Shiseido
Sourced by ZipRecruiter
Company size
5,001 - 10,000 Employees
Headquarters location
New York, NY, US
Year founded
1872