QA Analyst I – Onsite Fort Worth | Regulatory & Quality

WaveCrest Staffing Group

Fort Worth (TX)

On-site

USD 60,000 - 75,000

Full time

8 days ago

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Benefits offered by this job

Medical
Dental
Holiday
PTO 401K matching

Job summary

Alcon in Fort Worth, TX seeks a detail-oriented Quality Assurance Analyst I to support regulatory compliance and quality assurance in a manufacturing setting. The role requires collaboration with cross-functional teams to ensure cGMP adherence and alignment with ISO standards.

Responsibilities include reviewing labeling changes, driving process improvements, and supporting governance and compliance initiatives.

Qualifications

  • Bachelor's degree or equivalent years of related experience.
  • Excellent written and verbal communication skills.
  • Strong attention to detail, problem-solving, and organizational skills.
  • Self-motivated, proactive, and comfortable raising quality concerns.
  • Familiarity with manufacturing applications such as SAP, LIMS, or Veeva is preferred.
  • Knowledge of cGMP and quality assurance processes is a plus.

Responsibilities

  • Ensure compliance with cGMP, health authority requirements, Alcon Quality Manual, and applicable ISO standards.
  • Review and coordinate labeling artwork changes with cross-functional teams.
  • Collaborate with internal teams to resolve quality issues and drive process improvements.
  • Support quality strategy implementation, governance processes, and compliance initiatives.
  • Identify opportunities to improve operational efficiency and maintain quality standards.

Skills

Excellent written and verbal comms
Attention to detail
Problem-solving
Organizational skills
Self-motivated and proactive

Education

Bachelor's degree or equivalent years of related experience

Tools

SAP
LIMS
Veeva

Job description

Alcon in Fort Worth, TX seeks a detail-oriented Quality Assurance Analyst I to support regulatory compliance and quality assurance in a manufacturing setting. The role requires collaboration with cross-functional teams to ensure cGMP adherence and alignment with ISO standards.

Responsibilities include reviewing labeling changes, driving process improvements, and supporting governance and compliance initiatives.

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