Quality Compliance Associate (Pharma/Medical Device)

Aequor; Fort Worth (TX); On-site; USD 65,000 - 90,000; Full time

Job summary

Aequor is seeking a Quality Assurance Compliance Associate to support site compliance with cGMP, Health Authority, and ISO standards in Fort Worth, TX. The role includes coordinating labeling artwork changes and collaborating with cross-functional teams to drive improvements.

The ideal candidate holds a Bachelor’s Degree (or equivalent) with strong communication, attention to detail, and knowledge of manufacturing systems such as SAP, LIMS, and Veeva.

Qualifications

• Bachelor’s Degree (or equivalent years of related experience).
• Excellent communication skills, in both verbal and written form.
• Highly attentive to details and comfortable speaking up.
• Self-driven and action oriented.
• Knowledge of manufacturing applications (e.g. SAP, LIMS, Veeva).

Responsibilities

• Provide tactical site support to ensure compliance with cGMP, Health Authority, Alcon Quality Manual, and ISO standards.
• Independently review and coordinate labeling artwork changes driven by lifecycle management, package engineering, and supplier quality teams.
• Collaborate with cross-functional teams to drive problem-solving and innovation through scientific principles.
• Apply specialized knowledge to make significant decisions and perform tasks to achieve objectives in Quality Assurance Compliance.
• Facilitate the implementation of the Quality Strategy and support governance processes, identifying opportunities for improved process efficiencies and implementing changes.

Skills

Communication skills

Attention to detail

Self-motivated

SAP/LIMS/Veeva knowledge

Education

Bachelor’s Degree or equivalent experience

Job description

Job title

Quality Assurance Compliance Associate

Location

Fort Worth, TX (Onsite)

Duration

12 months

Job Description

• Providing tactical site support to ensure compliance with current Good Manufacturing Practices (cGMP), Health Authority, Alcon Quality Manual, and International Organization for Standardization (ISO) standards
• Independently review and coordinate labeling artwork changes driven by the global lifecycle management, package engineering, and supplier quality teams
• Collaborate with cross-functional teams to drive problem-solving and innovation through scientific principles
• Apply specialized knowledge to make significant decisions and perform tasks to achieve objectives in Quality Assurance Compliance and contribute to the organization's overall compliance
• Facilitate the implementation of the Quality Strategy and support governance processes, identifying opportunities for improved process efficiencies and implementing changes

General Job Description (other responsibilities may be assigned):

Bachelor’s Degree (or equivalent years of related experience)

Desired Competencies

• Excellent communication skills, in both verbal and written form
• Highly attentive to details and comfortable speaking up
• Self-driven and action oriented
• Knowledge of manufacturing applications (e.g. SAP, LIMS, Veeva)