Quality coordinator Work, Jobs in Crawley, Wsx (with Salaries)

Quality Coordinator
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- Full-time
- Analysis skills
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- Computer skills
4d
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Jonas Software —Woking
- Full-time
- Organisational skills
- Communication skills
- Time management
5d

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Quality Coordinator

Thermo Fisher Scientific -
Horsham

Apply Now

Job details

Full-time
4 days ago

Qualifications

Non-conformance investigation
Stakeholder collaboration
Quality management change control procedures
Internal department liaison
Quality management
Microsoft Office Suite
Analysis skills
Continuous improvement
Risk management
Computer skills
Document control software
Multidisciplinary collaboration
Training & development
Root cause analysis
Communication skills
Internal quality assurance

Full job description

Work Schedule

Standard (Mon-Fri)

Environmental Conditions

Office

Job Description

As part of the Thermo Fisher Scientific team, you’ll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life every single day to enable our customers to make the world healthier, cleaner and safer. We provide our global teams with the resources needed to achieve individual career goals while helping to take science a step beyond by developing solutions for some of the world’s toughest challenges, like protecting the environment, making sure our food is safe or helping find cures for cancer.

DESCRIPTION:
As a Quality Coordinator, you will play a critical role in our operational quality team, ensuring any issues are investigated and solutions implemented to prevent recurrences. Your work will impact on production and delivery of our products, to meet client expectations.

Conduct root cause analysis and write formal investigation
Collaborate with other areas (both internally and externally) as required to deliver comprehensive investigations
Raise appropriate Corrective and Preventive Actions (CAPAs) to correspond with investigation outcomes and prevent recurrence
Ensure timely completion of all TrackWise investigations / actions
Complete other tasks using the electronic Quality Management System (e.g. change controls etc)
When required raise deviations (QRs) in a timely manner
Update processes within the electronic Documentation System (eDMS)
Conduct risk assessments to identify potential issues and implement any required actions to reduce risk
Develop and deliver training, provide coaching and support
Assist in the introduction and implementation of new processes as required
Support regulatory inspections, client and internal audits to ensure compliance
Implement Practical Process Improvement (PPI) methods to update processes
Provide general support to all operational areas, ensuring a Quality culture
Undertake any other adhoc duties as required

REQUIREMENTS:

Degree level preferred, experience in pharmaceutical, medical device or regulated industry preferred
Additional certifications in Quality Systems or GMP preferred
Experience with quality systems and documentation including batch records, SOPs, deviations, CAPA
Proficiency in quality management and software systems (TrackWise, SAP, etc.)
Strong analytical and problem-solving skills for quality investigations and root cause analysis
Excellent written and verbal communication skills
Ability to work independently and collaborate effectively with cross-functional teams
Proficient computer skills including Microsoft Office applications
Strong attention to detail and commitment to accuracy
Ability to prioritize and adapt in a changing environment
Experience with continuous improvement methodologies preferred

Apply Now

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