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Location
In office (Brisbane)
Seniority
Senior · 5+ years exp
Visa
Sponsors visas in United States; no register of this country names it
Employment
Contractor

Confirmed on the employer's own hiring board on Nov 14, 2026. First seen by Alion on Nov 13, 2026. Planet Pharma scores B on the Alion truth index.

Overview
Company
Impact
Profile match
Planet Pharma is a life sciences recruitment and staffing firm headquartered in Deerfield, Illinois, that places contract and permanent professionals with pharmaceutical, biotechnology, medical device and contract research organizations. Founded in 2012, it offers contract and direct hire staffing, strategic resourcing, executive search, functional service provider models and global workforce solutions, with offices in Deerfield, Chicago and Raleigh and placements in the United States, Europe and Asia. Planet Pharma recruits for clients research scientists and associates, clinical trial managers, quality engineers, compliance specialists, medical writers and production supervisors.

Duties & Responsibilities:

  • Develop and maintain expert knowledge of quality control procedures, processes, and test methods.
  • Conduct thorough inspections of products or services to ensure they meet established quality standards including, but not limited to, laser systems, handpieces, and accessories.
  • Perform various testing and analysis procedures, such as dimensional checks, material testing, laser power measurements and laser system and handpiece functional testing.
  • Collect and analyze quality data to identify trends, patterns, and areas for improvement.
  • Prepare and maintain detailed records of quality inspection results.
  • Collaborate with production and engineering teams to identify and implement process improvements that enhance product quality.
  • Provide recommendations for adjustments to manufacturing processes or procedures.
  • Create and update quality documentation, including inspection procedures, checklists, and reports.
  • Ensure that all quality-related documentation complies with regulatory standards.
  • Investigate and determine the root causes of quality issues or defects.
  • Develop and implement corrective and preventive actions to address identified issues.
  • Communicate issues and defects to peers in manufacturing and engineering.
  • Escalate issues to management as appropriate.
  • Provide training to production and quality control staff on quality standards, procedures, and best practices.
  • Ensure compliance with industry regulations, quality standards, and company policies.
  • Stay informed about changes in regulations and standards affecting the industry.
  • Verify quality control processes are performed per procedure and communicate discrepancies in procedures and processes to quality engineering and quality management.
  • Other duties as needed or required.

Qualifications

Minimum Requirements & Qualifications:

  • High school diploma or equivalent
  • 5+ years of experience in medical device quality control, manufacturing, or related field.
  • Working knowledge of quality management systems and methodologies.
  • Proficiency in using various quality measurement tools and equipment.
  • Excellent analytical and problem-solving skills.
  • Effective communication and interpersonal skills.
  • Attention to detail and a commitment to maintaining high-quality standards.
  • Familiarity with industry-specific regulations and standards.
  • Computer proficiency required in Word, Excel, and FileMaker Pro.
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