Quality Assurance Specialist
Posted 2 days ago by LanceSoft UK
Negotiable
Undetermined
Onsite
Slough, England, United Kingdom
Summary: The QA Specialist III role involves setting up and implementing new Document Management Systems (DMS) and quality records globally, with a focus on project updates and stakeholder alignment. The position requires monitoring internal quality records and supporting investigations as needed, while fostering a strong quality culture within the organization. The role is based in Slough and is a 5-month contract position. Candidates should have significant experience in the pharmaceutical or CDMO industry, particularly in quality assurance roles.
Key Responsibilities:
- Setting up and assisting in the implementation of new DMS and quality records global systems.
- Providing regular updates on project realization to line manager and/or Senior leadership team.
- Monitoring internal quality records to ensure timely completion.
- Performing and supporting deviation or investigation activities.
- Taking personal responsibility for fostering a strong quality culture.
- Performing all business-related activities as reasonably requested by management.
Key Skills:
- B.Sc or equivalent experience in Life Science or QA discipline.
- Minimum 5 years’ experience in pharmaceutical or CDMO industry in QA relevant roles.
- Extended experience in PQS systems, deviations, and investigations.
- Advanced level of expertise in quality assurance practices.
Salary (Rate): undetermined
City: Slough
Country: United Kingdom
Working Arrangements: on-site
IR35 Status: undetermined
Seniority Level: undetermined
Industry: Other
Job Title: QA Specialist III
Location: Slough (Onsite)
Duration: 5 months contract
Job Description
Setting up and assisting in the implementation of new DMS and quality records global systems, including clean-up activities, preparation work, validation and qualification support, enrolment in the online training program, and alignment with stakeholders to ensure a robust system implementation. Provide regular updates on the project realization to line manager and/or Senior leadership team where required. Monitoring internal quality records to ensure timely completion, where applicable. Perform and support deviation or investigation where applicable Performing all business related activities as reasonably requested and instructed by the line manager or senior management team. Taking personal responsibility for fostering a strong quality culture.
Qualifications Required:
B.Sc or equivalent experience
Field of Study: Life Science or QA discipline
Work Experience Area: Minimum 5 years’ experience in pharmaceutical or CDMO industry in QA relevant roles, Level: Advanced - 5-10 years Area: Extended experience in PQS systems, deviation, investigations, Level: Advanced - 5-10 years