Quality Control Associate Position Overview
This is an excellent opportunity for individuals who are looking to join a leading multinational in the Pharmaceutical industry.
The successful candidate will be responsible for planning and performing analyses with great efficiency and accuracy, as well as reporting, evaluating, and approving analytical data.
* Plan and perform multiple complex routine/non-routine methods and procedures and a large variety of assays.
* Report, evaluate, back-up/archive, trend and approve analytical data.
Key Responsibilities
The Quality Control Associate will be responsible for:
* Troubleshoot, solve problems, and communicate with stakeholders.
* Initiate and/or implement changes in controlled documents.
* Participate in audits, initiatives, and projects that may be departmental or organizational in scope.
Requirements
The successful candidate will possess:
* A Bachelor's degree in a Science related field is required.
* 3+ years of biopharmaceutical QC experience or related quality control or GMP laboratory experience in the pharmaceutical or medical device industry.
* Strong background in Chemistry and Analytical testing is required.
Preferred Qualifications
* Experience with regulatory compliance in cGMP manufacturing and testing of pharmaceutical products.
* Experience with analytical techniques such as Compendial testing would also be advantageous.
What We Offer
This position offers a chance to work with a leading multinational in the Pharmaceutical industry. The company values its employees and provides opportunities for growth and development.