Quality manager Work, Jobs in Coatbridge, Nlk (with Salaries)

Manager, Quality Assurance
LGC Biosearch Technologies —Bellshill
- Full-time
- Analysis skills
- Bachelor's degree
- Continuous improvement
- Employee assistance programme
- Employee discount
Quick apply
19h
Quality Manager
Albert Bartlett —Airdrie
- Full-time
- Data analysis skills
- Analysis skills
- Quality control
- Free parking
- Employee assistance programme
Quick apply
Manufacturing Shift Lead Quality
Finsbury Food Group —Coatbridge
- Full-time
- Microsoft Word
- Bakery
- Continuous improvement
- Employee assistance programme
- Employee discount
Quick apply
Manager, Quality Assurance
Planet DDS —Glasgow
- Computer Science
- Engineering
- Bachelor's degree
- Annual leave
- Referral programme
Quality Manager
Aggreko —Dumbarton
- Full-time
- Continuous improvement
- Team management
- Quality control
- Employee assistance programme
Quality Assurance Manager ( Cambuslang Part time)
Dominos —Cambuslang
- Part-time
- Management
- Continuous improvement
- Quality control
Quality Manager
Livingston Precision Engineering Ltd —Livingston
- Full-time
- In-person
- Free parking
Quick apply
Electrician Supervisor / Quality Control Manager
Greener Energy Group Ltd —Paisley
- Full-time
- Management
- Supervising experience
- Continuous improvement
- Annual leave
Quick apply
Production Manager – Tent Manufacturing Facility
The Beal Group —Glasgow
- £37,000 - £45,000 a year
- Full-time
- Continuous improvement
- Team management
- Quality control
Quick apply
Head of Quality, Safeguarding and Improvement
Aberlour Child Care Trust —Stirling
- £57,495 - £61,746 a year
- Annual leave
3d
Production Manager
ABP UK —Glasgow
- Full-time
- English
- Maths
- Continuous improvement
- Free parking
- Employee assistance programme
Quick apply
BMS Project Manager - Scotland Regions
Learnd —Bellshill
- Full-time
- Hybrid work
- PMP
- Writing skills
- Analysis skills
- Employee assistance programme
Quick apply
QA Manager
Bell Building Projects Ltd —Glasgow
- Full-time
- Continuous improvement
- Quality control
- Construction experience
12d
Senior Production Manager - Backshift
ABP UK —Glasgow
- Full-time
- English
- Maths
- Continuous improvement
Quick apply
Production Team Leader- Chilled- Dayshift
Albert Bartlett —Airdrie
- Day shift
- Supervising experience
- Quality control
- Training & development
- Free parking
Quick apply
Governance & Compliance Manager
Morris & Spottiswood —Glasgow
- Hybrid work
- Continuous improvement
- Quality control
- Contracts
9d
Project Manager
Morris and Spottiswood —Glasgow
- Full-time
- Management
- Quality control
- Construction experience
Quick apply
20h
Production Team Leader - Backshift
Albert Bartlett —Airdrie
- £14.26 an hour
- Overtime
- Continuous improvement
- Quality control
- Training & development
- Free parking
Quick apply
Project Manager
Bell Building Projects Ltd —Glasgow
- Full-time
- Management
- Microsoft Office
- First Aid Certification
Project Manager – External Fire Remediation
Bell Building Projects Ltd —Glasgow
- Full-time
- Management
- Business development
- No degree
- Annual leave

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Manager, Quality Assurance

LGC Biosearch Technologies -
Bellshill

Quick apply

Job details

Full-time
19 hours ago

Benefits

Employee assistance programme
Employee discount

Qualifications

Document control
Non-conformance investigation
8D methodology
Quality management change control procedures
Internal quality management system auditing
ERP software
Compliance audits
Analysis skills
Quality assurance
Bachelor's degree
Continuous improvement
Continuous improvement cycles oversight
Team management
Quality control
Organisational skills
Document control software
Supplier quality management
Supply chain quality assurance
Root cause analysis
Quality management system (QMS) implementation
Leadership
Communication skills
Internal quality assurance
ISO 13485
FDA regulations

Full job description

Company Description

With manufacturing sites across the US, UK, Germany and Denmark, LGC Biosearch Technologies has plans to continue growing. We deliver mission critical genomics to our diverse customer base in molecular diagnostics, pharma/biotech and agrigenomics. Our integrated portfolio of products, services and expertise supports our purpose of Science for a Safer World and we have embodied our mission by working with customers to enable research into life-altering treatment for disease and illness worldwide. We are currently seeking candidates who are up for the challenge of operating in a high-growth, purpose-driven organisation.

Job Description

The Manager, Quality Assurance, is crucial in leading our dedicated QA team and ensuring every product achieves high standards, customer satisfaction, and regulatory standards. This role is unique by providing an opportunity to operate in a dynamic environment where your contributions have a direct impact on our success and reputation.

To perform this job successfully, an individual must be able to capably perform each of the following essential duties:

Oversee, manage, coordinate, lead, and prioritize quality assurance (QA) activities to guarantee adherence to ISO 9001, customer, regulatory, and quality management system (QMS) standards.
Lead and develop the QA team by defining priorities and arranging daily tasks. Deliver mentoring, training, and performance evaluation. Promote a culture of quality, ownership, conformity, and ongoing progress.
Coordinate product inspection, batch release, and disposition activities to guarantee products meet established quality, customer, and regulatory standards.
Coordinate quality system processes such as document control, record management, CAPA’s, deviations, non-conformances, change control, supplier quality, management review, and audits, acting as the site’s Management Representative.
Direct the establishment, execution, and continual advancement of the QMS by following quality performance statistics and reviewing quality data trends. Coordinate CAPA effectiveness and support quality aims. Explore ways to improve conformity and operational results.
Direct internal, customer, supplier, and regulatory audit processes, acting as the chief contact for auditors, regulatory authorities, customers, and suppliers; manage audit responses, regulatory inspections, and ensure the swift closure of audit findings, CAPA’s, deviations, and non-conformances.
Review and approve quality documentation, specifications, protocols, validation packages, technical reports, and quality records to guarantee alignment with internal and external requirements.
Monitor, examine, and share quality performance metrics and crucial compliance indicators, providing regular updates and recommendations via management review processes.
Lead continuous advancement projects by reviewing quality metrics, risk analyses, audit findings, customer insights, and operational performance patterns.
Work closely with Operations, Quality Control, Supply Chain, customers, suppliers, and regulatory bodies to advance business goals, ensure quality standards, and maintain regulatory adherence.
Provide leadership and subject matter expertise on quality systems, regulatory requirements, auditing, and industry guidelines, maintaining knowledge of ISO 9001, ISO 13485, and applicable FDA regulations.
Perform other duties as required to support quality, compliance, operational, and business objectives.

Qualifications

ESSENTIAL KNOWLEDGE AND QUALIFICATIONS:

Bachelor’s degree in chemistry, biochemistry, biological sciences, life sciences, or a related discipline or equivalent combination of applicable education and relevant work experience.
Proven experience in managing QMS processes, including CAPA’s, audits, deviations, non-conformances, change control, and document control.
Previous experience managing people, with the capability to guide, nurture, and inspire teams.
Prior business partnering experience collaborating with leaders to find opportunities for improving performance, efficiency, and employee engagement.
Strong knowledge of quality management systems and applicable standards such as ISO 9001 and/or ISO 13485.
Experience handling or aiding internal, customer, supplier, and regulatory audits.
Practical understanding of root cause analysis and continuous improvement methods (e.g., 5 Why, 8D, A3).
Strong analytical, problem-solving, communication, and organizational skills, with the ability to prioritise various tasks and deliver quality outcomes.
Proficient in Microsoft Office applications and the use of quality metrics and trend analysis to support decision-making.

Desired expertise and qualifications:

Experience in ISO 9001 and/or ISO 13485 settings, familiarity with FDA Quality System Regulations (21 CFR Part 820) and internal audit techniques; Lead Auditor certification is an advantage.
Strong knowledge of quality tools and methods, such as root cause analysis, corrective action procedures, training delivery, and organizational change management.
Experience with electronic Quality Management Systems (eQMS), document management platforms, and ERP systems, with familiarity in EtQ and IFS preferred.

Additional Information

Our values

PASSION
CURIOSITY
INTEGRITY
BRILLIANCE
RESPECT

Benefits

25 days holidays
Life assurance & health allowance
Discounts with local and national retailers
Free 24/7 Employee Assistance Programme
Recognition schemes and monetary awards

At LGC, we foster a culture of inclusion and collaboration. We believe that diverse perspectives lead to better outcomes and encourage applicants from all backgrounds to apply. We are an equal opportunity employer and offer reasonable accommodations to individuals with disabilities. If you require any adjustments throughout the recruitment process, please let us know.

Join us in this outstanding opportunity to be part of a company that is leading advancements in the industry!

All your information will be kept confidential according to EEO guidelines.

#lgcij

Quick apply

Refine Your Search

quality manager jobs in coatbridge, nlk

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