Details:
- Salary: £30,000 - 35,000 - Annum
- Location: South East Berkshire Woose Hill
- Date: 4 days ago
Description:
We are looking to recruit an experienced Process Technician to support the development, optimisation, control and validation of manufacturing processes within UK Manufacturing.
The role will also involve supporting process qualification activities, coordinating manufacturing trials, contributing to staff training and promoting the continuous improvement of production processes and associated quality practices.
This position will be based within the Site Engineering Department at our Intersurgical UK medical device manufacturing facility.
The successful candidate will be able to:
Support the development, optimisation and improvement of manufacturing processes.
Support process qualification and validation activities, including Installation Qualification (IQ), Operational Qualification (OQ) and Performance Qualification (PQ).
Assist with validation and qualification projects to ensure manufacturing processes meet the required quality standards.
Carry out periodic verification of the validated state of equipment and processes, as required.
Identify opportunities for continuous improvement in production processes and quality practices.
Work collaboratively with cross-functional teams to resolve process-related issues and achieve project objectives.
Essential Experience/Qualifications
Experience working collaboratively with cross-functional teams to support production and quality objectives.
Experience working with controlled documentation, including work instructions, procedures and quality records.
Good problem-solving skills, with the ability to identify issues and support the implementation of effective solutions.
Desirable Experience/Qualifications
A relevant qualification or degree in Engineering, Manufacturing or a related discipline.
Experience supporting process validation and qualification activities, including IQ, OQ and PQ.
Knowledge and understanding of relevant quality management systems, such as ISO 13485.
Experience preparing and reviewing technical documentation, including validation and qualification protocols, reports and standard operating procedures.
Key Skills
Excellent verbal and written communication skills
Able to build good working relationships
Able to work well under pressure and meet deadlines
Able to multitask and prioritise workload
Able to work independently as well as within a team
Able to work effectively across a number of interrelated departments
Self-motivated
Keen and willing to learn
Have a can-do attitude with an enthusiastic approach to work
I.T. Literate – Microsoft Office
Methodical, organised and structured approach to work
Excellent attention to detail
Able to gather, evaluate, critically interpret and communicate information
Strong analytical and problem solving skills
Able to work in a safe manner complying with Health and Safety Legislation
Able to function in a highly regulatory environment with a focus on compliance
Flexibility to work additional hours if required to support the business needs
Hours of Work
40 hours per week
Monday to Friday
Equal Opportunities
We are committed to creating a diverse and inclusive workplace for all. We are an Equal Opportunities Employer and welcome applications from all individuals, regardless of age; disability; gender; gender reassignment; marital or civil partnership status; pregnancy and maternity; race; religion or belief; sexual orientation, or any other characteristic protected by law. We believe that diversity enriches our workplace and enhances our ability to deliver exceptional results. We assess all applications based on skills, qualifications, and experience, ensuring a fair and equitable recruitment process.
**No Agencies please