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Dermorepubliq Corporation

Quality Control Analyst

Early Applicant
  • a month ago
  • Be among the first 50 applicants

Job Description

KEY QUALIFICATIONS
  • Bachelor's degree in Chemistry, Biochemistry, or a related field. Advanced degree (MSc or PhD) preferred.
Minimum of 2-3 years of experience in a quality control laboratory, preferably within the cosmetic or pharmaceutical industry.
  • Proficiency in analytical techniques such as HPLC, GC, UV-Vis spectroscopy, FTIR, and titration.
Strong understanding of GLP, GMP, and regulatory requirements for cosmetic products.
  • Excellent attention to detail and organizational skills.
Strong problem-solving abilities and the ability to work independently or as part of a team.
  • Effective communication skills, both written and verbal.
Proficiency in using laboratory information management systems (LIMS) and other relevant software.
  • Working Conditions:
Laboratory environment with regular exposure to chemicals and reagents.
  • Use of personal protective equipment (PPE) is required.
May require occasional lifting of laboratory equipment and supplies.

  • DUTIES AND RESPONSIBILITIES
Perform routine and non-routine chemical analyses of raw materials, in-process samples, and finished cosmetic products using standard laboratory equipment and techniques.
  • Develop, validate, and implement analytical methods for testing cosmetic products, ensuring accuracy, precision, and compliance with industry standards.
Conduct stability studies to evaluate the shelf life and performance of cosmetic products under various conditions.
  • Maintain and calibrate laboratory instruments, ensuring they are in good working condition and providing accurate results.
Prepare and standardize chemical reagents, solutions, and reference materials used in analytical testing.
  • Document and interpret analytical data, preparing detailed reports and presenting findings to the Quality Control Manager.
Assist in the investigation of product quality issues, identifying root causes and recommending corrective actions.
  • Ensure compliance with Good Laboratory Practices (GLP), Good Manufacturing Practices (GMP), and relevant regulatory guidelines (e.g., FDA, EU regulations).
Participate in internal and external audits, providing necessary documentation and support to demonstrate compliance with quality standards.
  • Collaborate with cross-functional teams, including R&D, production, and regulatory affairs, to support product development and improvement initiatives.
Stay current with industry trends, advancements in analytical techniques, and regulatory changes affecting cosmetic products.

Job Types: Full-time, Permanent

Schedule:
  • 8 hour shift
Day shift
Shift system

More Info

Industry:Other

Function:cosmetic industry

Job Type:Permanent Job

Skills Required

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Date Posted: 24/10/2024

Job ID: 97738081

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