Job Description
A Quality Assurance Specialist is required to support a leading pharmaceutical company on their manufacturing site, this is an hourly rate 12 month contract with great opportunity for further work.
Main Responsibilities:
* Reviews routine manufacturing and engineering documentation including batch manufacturing records
* Supports customer complaint investigations
* Authors, reviews, and approves Standard Operating Procedures (SOPs)
* Identifies and manages deviations and Corrective Action and Preventative Actions (CAPAs)
* Facilitates internal audits and walkthroughs
Qualification and Experience:
* 3+ years of industry experience across pharmaceutical or medical device
* Proven knowledge of working within Good Manufacturing Practices (GMP) environment
* Proven experience working in a manufacturing environment
* Must have experience with batch records and tablet manufacturing
Description:
The ideal candidate will possess excellent analytical and problem-solving skills, with the ability to work effectively in a team environment. They will be responsible for ensuring the quality of products and processes, identifying and mitigating potential risks, and contributing to the development of SOPs and other quality-related documents.
Key Skills:
* Strong understanding of GMP regulations and industry standards
* Excellent communication and interpersonal skills
* Ability to analyze and resolve complex problems
* Experience with batch record management and tablet manufacturing
About Our Client:
We are a leading pharmaceutical company dedicated to delivering high-quality products and services. Our team is committed to excellence and is passionate about making a positive impact on people's lives.