Supplier Quality Specialist

Cosette Pharmaceuticals, Inc.

Maintains Supplier Quality Management Program under Supplier Quality Management direction. Collaborates with teams to onboard and maintain suppliers in a hybrid pharmaceutical environment.

Posted 7/17/2026full-timeBridgewater • New Jersey • 🇺🇸 United StatesMid-LevelSenior💰 $102,000 - $128,000 per yearWebsite

Core Competencies

Role fit

Core Competencies

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Demonstrates expertise in Supplier Management Programs, Quality Control, and Quality Assurance within the pharmaceutical industry, with a strong focus on regulatory compliance and quality systems. Proficient in technical writing, risk assessments, and maintaining adherence to quality standards in a GMP environment.

Highest-signal resume keywords

Supplier Management ProgramQuality ControlQuality AssuranceRegulatory Agency Inspection ExperienceEQMS Experience

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills

Technical WritingAnalytical MethodsRoot Cause TechniquesCAPA SystemGMP TrainingQuality Management SystemsData IntegrityAnalytical ChemistryValidation PracticesDocument Control

Soft Skills

Customer FocusedGood Organizational SkillsPlanning SkillsInterdependent PartneringInitiative

Tools & Technologies

MS WordMS ExcelMS ProjectEQMS

Industry Keywords

Pharmaceutical IndustryRegulated ProductsSupplier AuditsQuality Management ReviewGood Documentation Practices

About the role

Key responsibilities & impact

Maintain Cosette Supplier Management Program under the direction of Supplier Quality Management
Drive and maintain the Cosette Supplier Management Program to include supplier records and supplier CAPA Audits and reporting
Risk assessments
Create and update quality agreements
Perform/support supplier audits
Collaborate with cross functional teams to onboard new suppliers and maintain current suppliers
Maintain metrics for adherence to the supplier audit schedule
Participate in internal, customer, and regulatory audits as needed
Support projects as requested
Travel up to 25%

Requirements

What you’ll need

Bachelor’s Degree in a scientific/technical discipline; advanced degree preferred
3+ years of experience in the pharmaceutical/regulated products industry, with a focus on Quality Control and Quality Assurance
Support of Regulatory Agency (FDA, EMA) Inspection Experience preferred
Technical Writing
Analytical Methods
Root Cause Techniques
CAPA System
GMP Training
Quality Management Review
Validation Practices
Data Integrity
Quality Management Systems
Analytical Chemistry
External Vendor Auditing Experience preferred
Experience with MS Word, Excel, and Project
Experience with eQMS required
Experience with document control/management in a regulated environment
Fundamental knowledge of quality systems in regulated environments
Customer focused, initiative, interdependent partnering
Good organizational and planning skills
Strong working knowledge of editing, proofreading, spelling, grammar, and punctuation
In-depth understanding of good documentation practices in a GMP environment
Ability to make and guide quality/compliance decisions that are data based and commensurate with risk.

Benefits

Comp & perks

medical
dental
vision
life insurance
short-term disability
long-term disability
401(k) match
flexible spending accounts
health saving account
employee assistance program
tuition reimbursement program
parental leave
wellness program
paid time off
volunteer time
holidays