Cogent Resources

QC Officer

North Sydney, 2060, Sydney, New South Wales

Manufacturing, Transport & Logistics / Other

Full time

Posted 15/04/2025
Closed 29/04/2025

Join Our Team as a Quality Control Officer in Pharmaceutical Manufacturing!

We are working with a leading employer in the pharmaceutical industry that specializes in manufacturing consumable health products. They are seeking a Quality Control Officer to play a crucial role in ensuring the quality of raw materials, in-process samples, and finished goods. If you're looking to make a meaningful impact in a dynamic and innovative company, this opportunity could be the perfect fit for you!

Why This Role is Exciting:

  • Variety Every Day: As a contract manufacturer for the pharmaceutical industry, you'll experience a wide range of challenges and responsibilities, ensuring that no two days are the same.

  • Critical Impact: Your work will directly affect the timeliness and success of the business, providing the compliance data that is vital to industry standards and regulations.

  • Collaborative Environment: Be part of a forward-thinking team that values continuous improvement and strives to maintain the highest standards of quality and compliance.

Key Responsibilities:

  • Quality Control Testing: Perform testing and analysis on raw materials, in-process samples, and finished products according to rigorous procedures and specifications.

  • Regulatory Compliance: Ensure compliance with FDA guidelines, cGMP, and company SOPs to meet industry standards.

  • Data Review & Approval: Review, approve, and ensure the accuracy and completeness of analytical data and test reports.

  • Audit Participation: Actively participate in both internal and external audits and inspections, ensuring the laboratory adheres to the highest compliance standards.

  • Continuous Improvement: Contribute to refining quality systems and processes within the lab to help the company stay ahead of industry standards.

What We’re Looking For:

  • Educational Background: Bachelor’s degree in Chemistry, Biochemistry, Pharmaceutical Sciences, or a related field (Master's degree is a plus!).

  • Relevant Experience: 2-3 years of experience in a pharmaceutical laboratory environment, particularly in quality control and analytical testing.

  • Technical Expertise: Proficiency with analytical techniques like HPLC, GC, UV-Vis, FTIR, and wet chemistry methods.

  • Problem-Solving Skills: Strong ability to troubleshoot technical issues in the lab and find effective solutions.

  • Attention to Detail: A meticulous approach to ensuring the accuracy of experimental data, documentation, and test results.

If you're looking for a role that will challenge and inspire you, apply now and join a team that values your expertise and dedication to quality and compliance!

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