Job Overview:
We are seeking a highly skilled Senior Quality Control Associate to join our team. This is an excellent opportunity for a talented professional to work in a leading multinational organization.
Main Responsibilities:
* Conduct analytical testing of various products and materials with great efficiency and accuracy.
* Develop, implement and optimize complex routine and non-routine methods and procedures.
* Evaluate, report and approve analytical data to ensure compliance with regulatory standards.
* Troubleshoot and solve problems related to quality control in a timely and effective manner.
* Participate in audits, initiatives and projects that impact the department or organization.
* Review protocols and perform assay validation and equipment qualification/verification.
* Introduce new techniques to the laboratory, including method transfers, reports, validations and protocols.
* Contribute to regulatory filings as required.
* Evaluate lab practices for compliance on a continuous basis.
* Approve lab results.
* Interact with external resources as necessary.
Requirements:
* Bachelor's degree in a Science-related field.
* 4+ years of biopharmaceutical QC experience or related quality control or GMP laboratory experience in the pharmaceutical or medical device industry.
* Experience with regulatory compliance in cGMP manufacturing and testing of pharmaceutical products.