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About
Job Title: QA Associate
Job Type: 9 Month Contract
Hours of work: Mon - Fri
Industry: Pharmaceuticals
Location: Slough, England
Salary: £23.08
Job Details
Supervisory Organization: QA Operations
Reports to: Associate Director, QA
Job Profile: Grade 7
Primary Location: Slough
Role Purpose & Scope: (why does this job exist and what scope does it cover?)
* Manage GMP issues through QMS processes, site governance, and senior QA leadership to support site operations.
* Ensure quality standards meet customer and regulatory expectations, assessing compliance through GMP audits and documentation.
* Support continuous improvement initiatives alongside Senior QA leadership.
* Maintain compliance with Regulatory Authorities, Global Quality standards, and Customer expectations.
Responsibilities
* Review documentation generated during manufacturing, development, and laboratory processes.
* Advise on best practices for documentation and escalate issues as needed.
* Serve as a point of contact for Quality-related queries and escalate when necessary.
* Identify, report, and resolve non-conformances using GMP and quality procedures.
* Manage compliance issues via site QMS processes, including deviations and CAPAs.
* Participate in continuous improvement activities and PQS process enhancements.
* Mentor and coach staff in cGMP practices to ensure audit readiness.
Required Skills & Competencies
Skills:
* IT literacy (MS Office, database familiarity)
* Effective communication skills
* Risk-based decision making
* PQS experience
* Attention to detail and accurate data entry
* Workload prioritization and decision-making skills
* Ability to meet deadlines
* Organizational and planning skills
Competencies:
* Agility: willingness to learn and adapt
* Business Acumen: understanding of corporate strategy and impact
* Collaboration: teamwork and knowledge sharing
* Customer Focus: understanding and meeting customer needs
* Driving Results: goal orientation and quality maintenance
* Leadership: safety responsibility, accountability, and positive environment contribution
Qualifications
* Education: Bachelor of Science in Biology or related field
* Experience: Previous QA/GMP experience preferred but not essential
* Level: Advanced, 5-10 years
Other Requirements
* Knowledge of quality procedures and safety protocols
* Ability to identify and mitigate safety risks
Nice-to-have Skills
* Access, Scheduling
Work Experience
* QA, QA Test Automation
Languages
* English
Seniority Level
* Mid-Senior level
Employment Type
* Full-time
Job Function
* Quality Assurance
Industries
* Pharmaceuticals
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