Quality Assurance Supervisor at Pegasus Laboratories

Pensacola, Florida, United States

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Not SpecifiedCompensation

Mid-level (3 to 4 years), Senior (5 to 8 years)Experience Level

Full TimeJob Type

UnknownVisa

Pharmaceuticals, Animal Health, ManufacturingIndustries

Requirements

Bachelor’s degree in chemistry, biology, or related field
Minimum 5 years of quality assurance experience in a regulated environment (e.g., pharmaceutical, biotechnology, or medical device), including at least 1–2 years in a leadership or supervisory capacity
Strong understanding of cGMP, FDA, EMA, Health Canada, and other regulatory requirements
Proven experience managing audits, CAPAs, document control, and batch record review
Strong analytical, problem-solving, and decision-making abilities
Excellent written and verbal communication skills
Proficiency in quality systems and tools (e.g., QMS, MasterControl, deviation tracking, document management platforms)
Proficiency in computer systems and tools (e.g., Microsoft Office, ERP inventory systems (Microsoft Dynamics 365), labeling software (Loftware))
Professional certifications (e.g., ASQ, Six Sigma) are a plus

Responsibilities

Oversee daily QA operations including raw material/packaging component inspection and release, production floor inspections, label issuance, document control, batch record review and release, deviation management, and change control processes across 2 shifts
Ensure compliance with all applicable regulations (GMP, FDA, EMA, Health Canada, VICH) and company quality standards
Manage and participate in internal, supplier, customer and regulatory audits; oversee timely resolution of audit findings and implementation of corrective and preventive actions (CAPA)
Exercise independent judgment to initiate or halt production operations based on quality, safety, and/or regulatory concerns
Support and respond to urgent business needs, including corrective actions and critical quality-related decisions
Conduct, monitor, and improve training programs to ensure all employees maintain required knowledge and competency levels
Supervise, mentor, and manage the workload of QA team members while supporting their professional growth
Lead investigations into quality deviations, non-conformances, and customer complaints; ensure thorough root cause analysis and effective CAPA implementation
Drive process improvement initiatives to enhance product quality, ensure compliance, and increase operational efficiency
Collaborate cross-functionally with Production, QC, Technical Services, and other departments to ensure alignment with quality objectives
Collaborate with internal and external stakeholders to identify and resolve quality risks, issues, or concerns
Maintain and track quality metrics to monitor trends, identify improvement areas, and report key performance indicators (KPIs) to management
Effectively lead and participate in meetings across all organizational levels with strong communication and interpersonal skills

Skills

cGMP

GMP

FDA

EMA

Health Canada

VICH

CAPA

Deviation Management

Change Control

Batch Record Review

Audits

Document Control

Quality Training

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