Quality assurance engineer Work, Jobs in Clitheroe, Lan (with Salaries)

Quality Engineer
Kindeva Drug Delivery Careers —Clitheroe
- Full-time
- Microsoft Word
- Computer literacy
- Continuous improvement
- Free parking
- Health & wellbeing programme
Quick apply
Special Process Quality Engineer
Safran —Burnley
- Full-time
- Engineering
- English
- Databases
- Flexitime
- Employee assistance programme
Quality Assurance Engineer
Safran —Burnley
- Full-time
- Engineering
- Hotel
- Continuous improvement
- Flexitime
- Employee assistance programme
Automation Quality Assurance Engineer
Key Group —Preston
- Full-time
Quality engineer/manager
ServiceCal —Heywood
- Full-time
QA Engineer
Zellis —Manchester
- Master's degree
- Analysis skills
- Agile
- Annual leave
Quality Engineer
TT Electronics plc —Rochdale
- Full-time
- Engineering
- Continuous improvement
- No degree
- Annual leave
- Employee assistance programme
12d
Quality Engineer
Costain —Wigan
- Full-time
- Quality control
- Contracts
- Construction experience
ACTEMIUM Design - Quality Manager
VINCI Energies —Chorley
- Continuous improvement
- Team management
- Quality control
Quality Engineer
Dauch —Halifax
- Engineering
- Analysis skills
- Continuous improvement
ACTEMIUM Design - Quality Manager
Actemium UK —Chorley
- Hybrid work
- Continuous improvement
- Team management
- Quality control
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quality assurance engineer jobs near clitheroe, lan

Quality Engineer

Kindeva Drug Delivery Careers -
Clitheroe

Quick apply

Job details

Full-time

Benefits

Free parking
Health & wellbeing programme
Cycle to work scheme
Free flu jabs
Company pension
Employee assistance programme
Private medical insurance
Flexible schedule
Referral programme
Sick pay
On-site parking

Qualifications

Microsoft Word
Technical project or programme management experience
Non-conformance investigation
Computer literacy
Quality management change control procedures
Lean
Quality management
ISO 9001
Minitab
Six Sigma
Continuous improvement
Manufacturing
Project management experience
Communication skills
FDA regulations
Time management

Full job description

Kindeva Drug Delivery

Our Work Matters:
At Kindeva we make products that save lives, ensuring better health and well-being for patients around the world.

The Impact You Will Make:
This role is joining our dynamic team in Manufacturing Technology (Process & Manufacturing Engineering) where you will be supporting the production and assembly of complex precision components for pulmonary/inhalation drug delivery devices.

In this role you will support/lead the projects & investigations at Kindeva, across the full production lifecycle of MDI valves and cans, from raw material production through to finished product.

Investigation & Project scope may cover across process, production, chemical, quality, project, systems and sourcing.

Key Responsibilities include, but are not limited to:

Leading product quality investigations, including troubleshooting product and process defects and implementing effective corrective actions.
Validation of new and existing products and processes.
Continuous Improvement is the foundation of the company so identifying opportunities and executing projects to reduce costs and improve quality are a significant part of the role.
Progressing and prioritising multiple projects or investigations of varying sizes simultaneously, communicating with project stakeholders and the wider business.
Application of data analysis and continuous improvement tools such as Minitab and LSS.
Applying technical expertise for assigned products and processes, including troubleshooting, and managing improvements.
Developing documentation such as SOP's, validation protocols, reports and change controls.
Compliance with industry regulations.
Maintain the sites excellent safety record by actively engaging in a safety-first approach.

Skills & Experience:

2+ years’ experience working in a manufacturing industry or similar role.
Educated to degree level or equivalent in a Manufacturing, Chemical Engineering, Pharmaceutical Engineering, or related field.
Experience of any of the following - GMP working environment, Quality Assurance, Validation, Project management, ISO 9001 and working within a QMS.
Knowledge of lean manufacturing principles, Six Sigma, or other continuous improvement methodologies is a plus.
Good understanding of the pharmaceutical industry standards and regulatory requirements (cGMP, FDA, EMA) is an advantage.
Experience in managing projects & investigations at the same time.
Computer literate, familiar with Microsoft Word and Excel

Key Capabilities:

Good organisational, interpersonal, and time management skills.
Enthusiastic, flexible, conscientious and proactive in approach.
Take a positive approach to own training and development.
Good decision-making and problem-solving skills.
Strong verbal and numerical aptitude skills.
Good communication skills.
Strong team player with the ability to work independently.

What we Offer:

Attractive compensation package.
Company pension scheme (up to 10% employer contribution).
25 days holiday per year (plus bank holidays) plus service days after 5 years.
Private Medical Insurance.
Company sick pay.
Employee Assistance Program with 24/7 confidential helpline support for employee and immediate family.
Life assurance of four times life cover salary.
Flexible working hours.
Wellness programmes.
Employee recognition program.
Employee development.
Free on-site parking.
Discount and cashback at many retailers.
Cycle to work scheme.
Flu vaccinations.
Employee referral scheme.

Additional Information:
Working Hours: 37.5hrs per week (Onsite)

Location: Up Brooks, Clitheroe

All applicants must be eligible to work in the UK.

We believe our people make the difference at Kindeva, we look for skilled, passionate, and driven professionals to come and work with us to help us excel in manufacturing technologies and processes, which bring lifesaving products to patients worldwide.

#LI-AC1

Kindeva does not accept unsolicited assistance from headhunters or recruitment firms for any of our job openings. Any resumes or candidate profiles submitted to Kindeva employees—regardless of format—without a valid, signed agreement and an approved job order from an authorized signatory in Talent Acquisition will be considered the sole property of Kindeva. No fees will be paid in the event that a candidate is hired as a result of an unsolicited resume or referral.

Kindeva is an Equal Opportunity Employer

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