As a quality assurance consultant, you will contribute to safeguarding the integrity of our pharmaceutical products and processes. You'll tackle the challenge of maintaining the highest standards of quality control, working closely with cross-functional teams to ensure compliance and excellence. Your expertise in GMP environments, coupled with a proactive approach, will be pivotal in upholding our commitment to delivering safe and effective treatments. We value your problem-solving skills, attention to detail, and ability to thrive in a dynamic setting.
Responsibilities:
- Oversight: maintain strict control over incoming goods, materials, and equipment, ensuring alignment with our quality standards.
- Collaboration: work alongside QC and manufacturing teams to manage the equipment lifecycle and material quality.
- Quality systems: review and approve QMS records and documents, playing a key role in upholding our quality assurance framework.
- Point of contact: serve as the go-to quality assurance consultant for system implementations within the QC Cell Tech Operation.
- Vendor relations: engage in supply chain management, including material and vendor qualifications, to ensure the integrity of our products.