Job Summary:
We are seeking a highly qualified individual to fill a Quality Control position in our Pharmaceutical company. This is an 18-month contract with hybrid working options, requiring on-site attendance for at least 3 days a week.
Key Responsibilities:
* Manage the batch disposition process to ensure timely release of products
* Maintain compliance with site practices and regulatory requirements
* Support major investigations and resolve product deviations prior to batch release
* Participate in cross-functional teams as Quality/Qualified Person representative
* Provide additional QP support for quality-related issues
* Participate in internal committees and provide audit support
* Maintain up-to-date knowledge of pharmaceutical legislation and industry practice
Requirements:
* Advanced degree preferred
* At least 8 years of cGMP experience with relevant work experience as Qualified Person named on the Manufacturer's/Importer's Authorization
* Proven leadership skills equivalent to 2+ years of management responsibility
* Post Graduate Qualification required (MSc or equivalent)
* Biologics manufacturing experience highly desirable
* Experience in Sterile Manufacturing and/or Clinical Trials Regulations highly desirable