Quality Specialist Job Description
We are seeking a highly motivated individual to join our Supplier Quality team as a Quality Specialist on a six-month contract.
The successful candidate will conduct quality-related activities, preparing compliant documents and records, reviewing and approving quality records, product labels, and product specification documents.
This role will also support the implementation of projects within our global Supplier Quality Organisation.
Responsibilities:
1. Contributes to and ensures timely achievement of overall project goals and tasks. Independently manages daily work schedule to perform assigned duties that support project goals.
2. Ensures compliance to global policies and procedures through creation of compliant records and documentation.
3. Focuses on accuracy and attention to detail to ensure records generated and reviewed are accurate.
4. Reviews multiple data sources and records at the same time to identify gaps and follow leads to investigate solutions. Provides gap analysis, data sets, and justifications in support of change. Utilizes global and local networks to execute changes.
5. Ensures assigned projects and tasks are performed to meet the quality requirements of customers, internal quality systems, internal & external auditors, and other external agencies.
6. Records and analyzes metrics and trends for key supplier quality processes.
Requirements:
* Bachelor's Degree in Life Science, Pharmaceutical Science, Quality, or a closely related discipline OR relevant combination of education and experience.
* 1-2 years experience working in Quality or a related field in a commercial cGMP healthcare facility. Less experience may be acceptable with an advanced degree.
Key Skills:
* Experience with Microsoft Word and Excel is essential, along with a keen eye for detail.
* Takes initiative and follows through with others to ensure tasks get completed on time.
* Able to work independently, with colleagues, and with minimal management oversight.