Quality Assurance Specialist II at Pegasus Laboratories

Pensacola, Florida, United States

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Not SpecifiedCompensation

Mid-level (3 to 4 years)Experience Level

Full TimeJob Type

UnknownVisa

Pharmaceuticals, LaboratoryIndustries

Requirements

College Degree Preferred with science/engineering or equivalent discipline focus
Knowledge of cGMP’s and experience in manufacturing preferred
Knowledge and experience in writing/revising SOPs and supporting documents in QA role
Experience using MasterControl, D365, Excel
Excellent writing and verbal communication skills
Attention to detail
Proficiency with MS Word/Microsoft programs/computer skills
Ability to work well as a team
Flexibility and adaptability to changing schedule and tasks
Ability to work under limited supervision
Knowledge of MasterControl system

Responsibilities

Provide QA Compliance support across all operational areas, ensuring adherence to cGMPs, company procedures, and regulatory expectations
Manage Documentation Control functions, such as Batch Record Issuance, Review/Revise Controlled Documents, maintain archived digital and paper records
Perform Batch Record Review (BRR) and other QMS-related document reviews as assigned, ensuring completeness, accuracy, and compliance
Author, revise, and maintain SOPs, specifications, work instructions, and GMP documents to support continuous improvement and regulatory alignment
Support internal audits and inspection readiness efforts, including audit preparation, documentation requests, tracking findings, and verifying remediation activities
Monitor and maintain compliance logs and controlled records, including temperature monitoring records, calibration entries, reserve sample inventory, and other required QMS records
Support quality metrics and compliance reporting, including data collection, trending, and presenting key insights to Quality leadership
Assist in GMP training initiatives, ensuring training content accuracy and supporting onboarding of new personnel on compliance expectations
Perform other Quality Compliance duties as assigned to support the site’s state of regulatory readiness

Skills

cGMP

QMS

Batch Record Review

Documentation Control

SOP Authoring

Internal Audits

Compliance Monitoring

Data Integrity

GMP Training

Quality Metrics

Pegasus Laboratories

Pharmaceutical products for veterinary industry

About Pegasus Laboratories

Pegasus Laboratories, Inc. specializes in innovative pharmaceutical and medical products for the veterinary industry, including solutions for behavior, urinary incontinence, and seizure management. They operate in a cGMP facility with DEA approval and utilize state-of-the-art manufacturing and laboratory facilities to support their services.

8809 Ely Rd, Pensacola, FL 32514, USAHeadquarters

1986Year Founded

VENTURE_UNKNOWNCompany Stage

Industrial & ManufacturingIndustries

51-200Employees