QC Lab Technician – First Shift (GMP/FDA)

Actalent

Boca Raton (FL)

In loco

USD 48.000 - 52.000

Tempo pieno

7 giorni fa
Candidati tra i primi

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Vantaggi offerti da questo lavoro

401k Benefits Paid time off

Descrizione del lavoro

Actalent in Boca Raton, FL is seeking a detail-oriented Laboratory Technician to support quality control, GMP compliant testing, inspections, and documentation within a regulated manufacturing environment.

The role emphasizes routine product and laboratory testing, review of batch records, sample management, and contributions to quality investigations and continuous improvement initiatives with strong written and verbal communication.

Competenze

  • Experience in quality control, GMP, laboratory procedures, and quality assurance.
  • Familiarity with GMP, FDA regulations, and quality systems.
  • Strong organizational skills and attention to detail.
  • Good analytical and problem-solving abilities.
  • Strong written and verbal communication skills.
  • Ability to accurately follow written procedures and maintain detailed documentation.

Mansioni

  • Perform routine product and laboratory testing in accordance with established procedures.
  • Conduct quality inspections and document results accurately.
  • Review batch records and other quality documentation for completeness and compliance.
  • Manage, track, and maintain product and laboratory samples.
  • Assist with quality investigations, deviations, and documentation as needed.
  • Maintain accurate records in accordance with GMP and FDA requirements.
  • Support quality systems and continuous improvement initiatives.
  • Identify and communicate potential quality issues to appropriate team members.

Conoscenze

Quality control
GMP
Laboratory procedures
Quality assurance
Organizational skills
Analytical thinking
Communication skills
Procedural documentation

Formazione

Associate degree in Biology, Chemistry, or related field

Descrizione del lavoro

Actalent in Boca Raton, FL is seeking a detail-oriented Laboratory Technician to support quality control, GMP compliant testing, inspections, and documentation within a regulated manufacturing environment.

The role emphasizes routine product and laboratory testing, review of batch records, sample management, and contributions to quality investigations and continuous improvement initiatives with strong written and verbal communication.

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