Quality Specialist 1
at Q Solutions
Livingston, Scotland, United Kingdom -
Start Date | Expiry Date | Salary | Posted On | Experience | Skills | Telecommute | Sponsor Visa |
---|---|---|---|---|---|---|---|
Immediate | 02 Dec, 2024 | Not Specified | 04 Sep, 2024 | 1 year(s) or above | Documentation Practices,Microsoft Outlook,Presentation Skills,Medical Technology,Excel | No | No |
Required Visa Status:
Citizen | GC |
US Citizen | Student Visa |
H1B | CPT |
OPT | H4 Spouse of H1B |
GC Green Card |
Employment Type:
Full Time | Part Time |
Permanent | Independent - 1099 |
Contract – W2 | C2H Independent |
C2H W2 | Contract – Corp 2 Corp |
Contract to Hire – Corp 2 Corp |
Description:
JOIN OUR TEAM AS A LAB QUALITY SPECIALIST
Are you passionate about maintaining high standards in laboratory quality? Do you thrive in a dynamic environment where your skills can make a real impact? If so, we have the perfect opportunity for you.
QUALIFICATIONS
- Education: Bachelor’s Degree in medical technology or equivalent.
- Experience: At least 1 year in a regulated laboratory environment.
- Knowledge: Strong understanding of laboratory quality systems, procedures, and good documentation practices.
- Skills: Proficient in Microsoft Outlook, Word, and Excel. Excellent organizational, interpersonal, communication, and presentation skills.
- Multitasking: Ability to handle multiple tasks simultaneously.
Responsibilities:
- Quality Management Support: Provide essential support to our Quality Management System.
- Documentation Review: Ensure lab documentation is accurate and compliant with regulations and SOPs.
- Audit Preparation: Assist in client audits by responding to inquiries and reviewing documentation to ensure readiness.
- Educational Programs: Support and deliver quality educational programs, including workshops, presentations, and training sessions.
- Project Coordination: Coordinate and schedule quality projects with minimal assistance.
- Staff Meetings: Participate in staff meetings, discussing findings and recommendations for non-compliance issues.
- Process Evaluation: Identify process gaps, recommend actions, and communicate analyses to management.
- Mentorship: Mentor junior staff and support the onboarding of new hires.
- Continuous Education: Engage in self-study and attend training sessions to stay updated.
- Safety and Compliance: Uphold safety, quality, and 6S requirements, and comply with all regulatory requirements.
REQUIREMENT SUMMARY
Min:1.0Max:6.0 year(s)
Pharmaceuticals
Pharma / Biotech / Healthcare / Medical / R&D
Clinical Pharmacy
Graduate
Medical technology or equivalent
Proficient
1
Livingston, United Kingdom