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QA/QC Engineer

Date Posted: February 23, 2024

Job Description

We are currently seeking a detail-oriented QA/QC Engineer to join our quality team within the pharmaceutical industry. In this critical role, you will be responsible for ensuring that all products and processes meet established quality standards and regulatory requirements. Your expertise in quality assurance and control will be instrumental in identifying areas for improvement, implementing corrective actions, and maintaining the highest quality standards in our manufacturing processes.

Key Responsibilities

  • Develop, implement, and maintain quality assurance protocols and methods for processing materials into partially finished or finished products.
  • Design and execute QA/QC testing procedures to ensure products meet quality and efficiency standards.
  • Conduct thorough inspections and analyses of quality control processes, make recommendations for improvements, and monitor implementation success.
  • Collaborate with cross-functional teams, including R&D, manufacturing, and engineering, to address quality issues and ensure compliance with regulatory standards.
  • Manage the documentation necessary for quality assurance processes and compliance with regulatory standards.
  • Analyze data to identify trends, investigate quality issues, and implement strategic quality improvements.
  • Conduct audits of processes and quality systems for compliance with internal standards and regulatory requirements.
  • Train and guide team members on quality control and assurance practices.

Required Qualifications and Skills

  • Bachelor’s degree in Chemistry, Biology, Pharmaceutical Sciences, Engineering, or a related field.
  • Minimum of 3 years of experience in a QA/QC role within the pharmaceutical or related regulated industry.
  • In-depth knowledge of quality assurance methodologies, quality control processes, and regulatory requirements applicable to the pharmaceutical industry.
  • Strong analytical and problem-solving skills, with a keen attention to detail.
  • Proficient in statistical analysis and familiar with statistical software.
  • Excellent communication and interpersonal skills, with the ability to work effectively in a team environment and interact with all levels of the organization.
  • Proven ability to manage multiple projects simultaneously and meet deadlines.
  • Familiarity with GMP, FDA, and other regulatory guidelines.

If you are keen to grow your career with this job, apply with us and send us your resume now. All shortlisted candidates will be contacted shortly.

Reference no.: 122-4948-2918-NW

Registration no.: 968446516E

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