Site director Work, Jobs in Cardiff, Wls (with Salaries)

Senior Director / Site Quality Head - Canada
Teva —Whitchurch
- Master's degree
- Bachelor's degree
- Continuous improvement
- Employee stock purchase plan
- Employee assistance programme
7d
Site Director
Dunster Beach Holidays —Dunster
- £45,000 - £55,000 a year
- Full-time
- Hospitality
- Management
- Supervising experience
- Annual leave
Quick apply
8d
Programme Director
Safran —Cwmbran
- Full-time
- Engineering
- Leadership
- Communication skills
- Employee assistance programme
Operations Director
Integrated Division —Weston-super-Mare
- Full-time
- Continuous improvement
- Manufacturing
- Leadership
- Free parking
- Employee assistance programme
1d
Full Time Transport Manager
United Worldwide Logistics Ltd —Bridgend
- £42,000 - £45,000 a year
- Full-time
- In-person
- Free parking
- Sick pay
Quick apply
DC Site Manager, EMEA
Vantage Data Centers UK Management Company Ltd —Newport
- Customer service
- Engineering
- Bachelor's degree
- Annual leave
Quick apply
Director, Global Sourcing
Revvity —Cardiff
- Master's degree
- Bachelor's degree
- Team management
Senior Finance Executive - Head of Finance, Finance Director, CFO
Huboo Tech Ltd —Bristol
- £75,000 - £110,000 a year
- Full-time
- Accounting
- Financial services
- In-person
Quick apply
10d
Business Development Manager
Wilmington plc —Cardiff
- £42,000 - £45,000 a year
- Full-time
- Hybrid work
- CRM software
- Business development
- Organisational skills
- Annual leave
- Employee discount
1d
Project Manager (Land & New Business)
Hafod —Cardiff
- £42,000 - £52,500 a year
- Full-time
- Hybrid work
- Project management
- Organisational skills
- Construction experience
13d
Marine Operations Director
Caudal Energy —Cardiff
- Full-time
- Hybrid work
- Engineering
- Maintenance
- Contracts
Quick apply
Funeral Home Assistant
Ivor Thomas Funerals —Cardiff
- £13.55 an hour
- Full-time
- Customer service
- English
- Maths
Quick apply
Senior Assistant (Executive Assistant), Leadership Support Centre, Central Business Services
Deloitte —Cardiff
- Hybrid work
- Microsoft Powerpoint
- Microsoft Outlook
- Conflict management
VacancyTitle: Resident Services Associate
Grainger plc —Cardiff
- Full-time
- Remote
- Customer service
- Annual leave
Hospital Director
Elysium Healthcare —Abertillery
- Full-time
- Business development
- Team management
- Leadership
- Free parking
- Annual leave
Quick apply
6d
Land Manager
Taylor Wimpey —Cardiff
- Annual leave
- Employee discount
7d
Associate Director- Environmental Impact Assessment
AECOM —Cardiff
- Full-time
- Hybrid work
- Master's degree
- Travel
- Mentoring
Product Manager - Atamis
Banyan Software —Cardiff
- Writing skills
- Product management
- Software development
Quick apply
Account Manager
Wilmington plc —Cardiff
- £34,000 - £40,000 a year
- Full-time
- Hybrid work
- Customer service
- Organisational skills
- In-person
- Annual leave
- Employee discount
1d
Senior Commercial Manager
Arcadis —Cardiff
- Microsoft Excel
- Data analysis skills
- Mentoring

I want to receive the latest job alerts for site director in cardiff, wls

By signing in to your account, you agree to SimplyHired's Terms of Service and consent to our Cookie and Privacy Policy.

Senior Director / Site Quality Head - Canada

Teva -
Whitchurch

Apply Now

Job details

7 days ago

Benefits

Employee stock purchase plan
Employee assistance programme
Employee discount
Life insurance

Qualifications

Biology
Non-conformance investigation
Stakeholder collaboration
Stakeholder liaison
Internal quality management system auditing
Quality control within general manufacturing industry
Master's degree
Quality assurance
Bachelor's degree
Continuous improvement
Continuous improvement cycles oversight
Partnership building
Quality control
Manufacturing
Quality management system (QMS) implementation
Leadership
Internal quality assurance
Corporate regulatory compliance oversight
Internal audits
FDA regulations
Product lifecycle management

Full job description

We Are Teva

We’re Teva, a leading innovative biopharmaceutical company, enabled by a world-class generics business. Whether it’s innovating in the fields of neuroscience and immunology or delivering high-quality medicine worldwide, we’re dedicated to addressing patients’ needs now and in the future. Here, you will be part of a high-performing, inclusive culture that values fresh thinking and collaboration. You'll have the room to grow, the flexibility to balance life with work, and the opportunity to better health worldwide, together.

Our Team, Your Impact

The Site Quality Head provides strategic and operational leadership for all Quality functions across Manufacturing, Packaging, Importation, and Laboratory Operations. This role is accountable for fostering a strong quality culture, ensuring compliance with regulatory requirements, and maintaining the highest standards of product quality and patient safety.

Key responsibilities include oversight of quality systems and processes, including but not limited to:

Development, implementation, and execution of quality procedures and standards
Establishment Licensing compliance
Quality on the Floor activities, audits, and batch disposition/release
Management of laboratory investigations, deviations, complaints, and nonconformances
CAPA development, implementation, and effectiveness monitoring
Quality metrics, trending, and performance reporting
Validation program compliance
Oversight of equipment, facilities, and utility systems to ensure adherence to established quality requirements

The role is responsible for leading the development, standardization, implementation, monitoring, and continuous improvement of Quality Systems, compliance programs, industry best practices, and corporate quality initiatives. The successful candidate will drive proactive quality and compliance improvements while strengthening a culture of operational excellence and Good Manufacturing Practice (GMP) compliance.

This position also serves as the Senior Person In Charge (SPIC) for Controlled Drug Substances and Narcotics.

How You’ll Spend Your Day

Lead the site's Quality organization, including Quality Assurance, Quality Control, Microbiology, Quality Systems, and Quality Compliance.
Ensure a robust and continuously improving Quality Management System (QMS) is maintained.
Ensure products are manufactured, released, and distributed in compliance with cGMP requirements and approved regulatory specifications.
Serve as the highest-ranking quality authority on site with independent decision-making responsibility regarding product quality and potential market actions.
Assess, manage, and mitigate quality risks to ensure products are safe, effective, and compliant before reaching patients.
Partner with business leaders to ensure a reliable and compliant supply of products.
Develop, implement, and continuously improve the Site Quality Program in collaboration with the Site General Manager and Corporate Quality leadership.
Oversee the collection, analysis, and communication of quality data and performance metrics to site leadership, Corporate Quality, and key internal and external stakeholders.
Direct Quality Control laboratory operations, including analytical method transfers, testing, and approval or rejection of raw materials, packaging components, in-process materials, and finished products.
Champion a sustainable culture of quality by promoting accountability, open communication, continuous improvement, and employee engagement.
Build and maintain strong partnerships with the site leadership team and cross-functional stakeholders.
Act as a strategic business partner to Supply Chain, Project Management, R&D, Manufacturing Sciences & Technology (MS&T), and Commercial teams to achieve business objectives and project milestones.Provide leadership and expert support during internal audits, customer inspections, and regulatory inspections.
Ensure Quality KPIs meet established targets and that CAPA commitments are implemented on time, with effectiveness verified through ongoing monitoring.
Develop, manage, and oversee the annual Quality Operations budget while optimizing resources and organizational effectiveness.
Provide quality oversight for two pharmaceutical manufacturing sites located in the United States.
Travel approximately 5% within the United States.

Your Skills and Experience

Canadian university degree, or a degree recognized as equivalent by a Canadian university, in Chemistry, Chemical Engineering, Biology, Pharmacy, or a closely related life sciences discipline. Preferred: Master's degree or equivalent advanced degree in Chemistry, Biology, Pharmacy, or a related scientific field.
Minimum of 10 years of progressive pharmaceutical manufacturing quality leadership experience.
Extensive knowledge of cGMP requirements and expectations from major global regulatory authorities, including Health Canada, the U.S. FDA, and the European Medicines Agency (EMA).
Strong understanding of pharmaceutical manufacturing, packaging, technology transfer, quality systems, and regulatory compliance requirements.
Comprehensive knowledge of Health Canada, FDA, EU, and ICH regulations and guidelines, as well as Chemistry, Manufacturing, and Controls (CMC) content for regulatory submissions.
Deep understanding of pharmaceutical production processes, product lifecycle management, equipment qualification, validation programs, and manufacturing technologies.
Demonstrated experience leading and preparing for regulatory inspections, including GMP and pre-approval inspections conducted by the FDA and Health Canada.
Proven expertise in Quality Systems management and continuous improvement initiatives.
Strong leadership track record with experience building, developing, coaching, and inspiring large, high-performing teams.
Excellent communication, stakeholder management, and strategic leadership capabilities.

How We’ll Take Care of You

At Teva Canada we provide a rewarding and collaborative work experience, with career growth and development opportunities for employees, in a safe and caring environment! Beyond base pay, Teva also offers a comprehensive suite of wellness and benefits programs tailored to role and employment type, that continue to rank among the best in our industry! Our competitive offerings are designed to provide flexibility, security, and meaningful choices, empowering employees to thrive both personally and professionally throughout their journey with us. As part of our commitment to well-being, employees may have access to:

Teva Canada’s choices Benefit Plan including Health, Dental, Disability, Life Insurance
Employee Assistance Program & Virtual Health Programs
Retirement Savings Programs
Employee Stock Purchase Plan (ESPP)
Time for yourself or those you care about, through paid time for Vacation, Wellness days, Care/Sick days, Teva Days and Volunteer Days
Education Assistance Program
Recognition programs such as Employee Service Awards
Employee Discounts
And much more!

More exciting details on the specific total rewards offerings to be provided at the offer stage depending on the position and employment type hiring for. This position will fill a current vacancy and Teva Canada may use an artificial intelligence (AI) system to assist with the initial screening and evaluation of job applications by analyzing for relevant skills, professional experience, and education, that best match the posted job qualifications. It is important to note that all final decisions in this process are made by a member of the hiring team.

Already Working @Teva?

Make sure to apply through our internal career site on Twist—your one-stop shop for career development

Teva’s Equal Employment Opportunity Commitment

Teva Pharmaceuticals is committed to equal opportunity in employment. It is Teva's global policy that equal employment opportunity be provided without regard to age, race, creed, color, religion, sex, disability, pregnancy, medical condition, sexual orientation, gender identity or expression, ancestry, veteran status, national or ethnic origin or any other legally recognized status entitled to protection under applicable laws. We are committed to a diverse and inclusive workplace for all. If you are contacted for a job opportunity, please advise us of any accommodations needed to support you throughout the recruitment and selection process. All accommodation information provided will be treated as confidential and used only for the purpose of providing an accessible candidate experience.

Apply Now

Refine Your Search

site director jobs in cardiff, wls

Senior Director / Site Quality Head - Canada

Site Director

Programme Director

Operations Director

Full Time Transport Manager

DC Site Manager, EMEA

Director, Global Sourcing

Senior Finance Executive - Head of Finance, Finance Director, CFO

Business Development Manager

Project Manager (Land & New Business)

Marine Operations Director

Funeral Home Assistant

Senior Assistant (Executive Assistant), Leadership Support Centre, Central Business Services

VacancyTitle: Resident Services Associate

Hospital Director

Land Manager

Associate Director- Environmental Impact Assessment

Product Manager - Atamis

Account Manager

Senior Commercial Manager

I want to receive the latest job alerts for site director in cardiff, wls

Related Searches

Explore jobs in more locations

We Are Teva

Our Team, Your Impact

How You’ll Spend Your Day

Your Skills and Experience

How We’ll Take Care of You

Already Working @Teva?

Teva’s Equal Employment Opportunity Commitment

Jobseeker tools

Employer Tools

Browse

Stay Connected