Technical Documentation Specialist
- Recruiter
- Confidential
- Location
- Newquay
- Salary
- Competitive
- Posted
- 18 Jun 2021
- Closes
- 28 Jun 2021
- Sectors
- Travel & Tourism
- Contract Type
- Permanent
- Hours
- Full Time
Find what drives you on a team with a more than 70-year history of discovery, determination, and innovation. As a global leader in high-tech filtration, separation, and purification, Pall Corporation thrives on helping our customers protect people. Our products serve a wide range of markets, so if your interests lie along the spectrum of Life Sciences to Industrial, you'll find a rewarding role here. For the exponentially curious, Pall is a place you can thrive and amplify your impact on the world.
Pall is proud to work alongside a community of nine fellow Danaher Life Sciences companies. Together, we're pioneering the future of science and medicine, developing products that enable researchers in the fight to save lives.
We are recruiting for a phenomenal opportunity as a Technical Documentation Specialist based at our site in Newquay.
Summary purpose of the position:
Collate, distribute & control the technical documentation generated by the Product Engineering team. Use technical data gathering by searching the network of legacy & active project folders for relevant and associated information required by project teams. Supply technical data input into spreadsheets, project plans, change control projects & weekly team meetings. Maintain and improve documentation quality, consistency to ensure standard practise is maintained by all team members. Work with cross functional teams, take actions & conform to sign off procedures for medical change control. Control technical documentation for engineering projects linked value streams whilst ensuring all documentation is within the guidelines of an ISO13485 and ISO9001 compliant Quality Management System.
Main Duties -
Internal audits of risk assessments & change control technical documentation to ensure standard work is utilised by the all teams.
Collating, indexing & archiving of all change control documentation on the projects.
Ensuring standard work is applied across all project controlled by PE
Supporting problem solving process (PSP) to optimally close performance gaps by getting to the true root cause and implementing effective, balanced countermeasures
Active participation in the continuous improvement projects which will include proactive leadership during Kaizen and Shin kaizen events, Participation in Gemba Walks.
Chip in to Reliability improvement programs including best CAPA practices;
Control of all Product Artwork & Label Changes, including all required change control
Raising of purchase Req's linked to projects controlled by the PE
Control budget spreadsheets for PE team, including, Travel Expenses, Non-Bom purchases, Mould Tooling repairs, Engineering trials & Materials
Maintaining the system for engineering-controlled materials & products under evaluation
Maintaining spreadsheets for quotation received for repairs & project specific materials
Position proficiencies:
Knowledge & Key Skills:
Good interpersonal skills, ability to work with a cross functional team
Ability to read and assess technical documentation and specifications
Technical writing skills to generate technical reports and instructions
Ability to prioritise, handle and complete projects with limited direction, on time/in full.
Good understanding and Experience with the technical change control validation techniques for FDA Regulated manufacturing
Experience with working in an ISO13485 and ISO9001 compliant Quality Management System
Demonstrate the ability to work on unusually complex technical problems and provide solutions which are highly innovative and ingenious
Driven candidate who acts with a sense of urgency to achieve business goals
Crucial Experience:
Several years' experience in Life Science oriented industrial company or similarly regulated industry.
Desirable Qualifications/Education:
Degree or proven experience in a technical field
Very good knowledge of MS Office / SAP or similar
Excellent written and spoken English
Project Management skills
At Danaher, we are dedicated to building and sustaining a truly diverse and inclusive culture. These are not just words on a page-Diversity and Inclusion is a top priority for the company, and it ties deeply to each of our core values. Danaher Corporation and all Danaher Companies are equal opportunity employers that evaluate applicants without regard to race, color, national origin, religion, sex, age, marital status, disability, veteran status, sexual orientation, gender identity, or other characteristics protected by law.
We will ensure that individuals with disabilities are provided reasonable accommodation to participate in the job application or interview process, to perform essential job functions, and to receive other benefits and privileges of employment. Please contact us to request accommodation.
When you join us, you'll also be joining Danaher's global organization, where 69,000 people wake up every day determined to help our customers win. As an associate, you'll try new things, work hard, and advance your skills with guidance from dedicated leaders, all with the support of powerful Danaher Business System tools and the stability of a tested organization.
Danaher is committed to a diverse and inclusive culture where everyone feels they belong and all voices are heard. We believe in our associates and the unique perspectives they bring to every challenge, which is why we'll empower you to push the boundaries of what's possible.
If you've ever wondered what's within you, there's no better time to find out.
When you join us, you'll also be joining Danaher's global organization, where 69,000 people wake up every day determined to help our customers win. As an associate, you'll try new things, work hard, and advance your skills with guidance from dedicated leaders, all with the support of powerful tools and the stability of a tested organization.
At Danaher, we value diversity and the existence of similarities and differences, both visible and not, found in our workforce, workplace and throughout the markets we serve. Our associates, customers and shareholders contribute unique and different perspectives as a result of these diverse attributes.
If you've ever wondered what's within you, there's no better time to find out
Pall is proud to work alongside a community of nine fellow Danaher Life Sciences companies. Together, we're pioneering the future of science and medicine, developing products that enable researchers in the fight to save lives.
We are recruiting for a phenomenal opportunity as a Technical Documentation Specialist based at our site in Newquay.
Summary purpose of the position:
Collate, distribute & control the technical documentation generated by the Product Engineering team. Use technical data gathering by searching the network of legacy & active project folders for relevant and associated information required by project teams. Supply technical data input into spreadsheets, project plans, change control projects & weekly team meetings. Maintain and improve documentation quality, consistency to ensure standard practise is maintained by all team members. Work with cross functional teams, take actions & conform to sign off procedures for medical change control. Control technical documentation for engineering projects linked value streams whilst ensuring all documentation is within the guidelines of an ISO13485 and ISO9001 compliant Quality Management System.
Main Duties -
Internal audits of risk assessments & change control technical documentation to ensure standard work is utilised by the all teams.
Collating, indexing & archiving of all change control documentation on the projects.
Ensuring standard work is applied across all project controlled by PE
Supporting problem solving process (PSP) to optimally close performance gaps by getting to the true root cause and implementing effective, balanced countermeasures
Active participation in the continuous improvement projects which will include proactive leadership during Kaizen and Shin kaizen events, Participation in Gemba Walks.
Chip in to Reliability improvement programs including best CAPA practices;
Control of all Product Artwork & Label Changes, including all required change control
Raising of purchase Req's linked to projects controlled by the PE
Control budget spreadsheets for PE team, including, Travel Expenses, Non-Bom purchases, Mould Tooling repairs, Engineering trials & Materials
Maintaining the system for engineering-controlled materials & products under evaluation
Maintaining spreadsheets for quotation received for repairs & project specific materials
Position proficiencies:
Knowledge & Key Skills:
Good interpersonal skills, ability to work with a cross functional team
Ability to read and assess technical documentation and specifications
Technical writing skills to generate technical reports and instructions
Ability to prioritise, handle and complete projects with limited direction, on time/in full.
Good understanding and Experience with the technical change control validation techniques for FDA Regulated manufacturing
Experience with working in an ISO13485 and ISO9001 compliant Quality Management System
Demonstrate the ability to work on unusually complex technical problems and provide solutions which are highly innovative and ingenious
Driven candidate who acts with a sense of urgency to achieve business goals
Crucial Experience:
Several years' experience in Life Science oriented industrial company or similarly regulated industry.
Desirable Qualifications/Education:
Degree or proven experience in a technical field
Very good knowledge of MS Office / SAP or similar
Excellent written and spoken English
Project Management skills
At Danaher, we are dedicated to building and sustaining a truly diverse and inclusive culture. These are not just words on a page-Diversity and Inclusion is a top priority for the company, and it ties deeply to each of our core values. Danaher Corporation and all Danaher Companies are equal opportunity employers that evaluate applicants without regard to race, color, national origin, religion, sex, age, marital status, disability, veteran status, sexual orientation, gender identity, or other characteristics protected by law.
We will ensure that individuals with disabilities are provided reasonable accommodation to participate in the job application or interview process, to perform essential job functions, and to receive other benefits and privileges of employment. Please contact us to request accommodation.
When you join us, you'll also be joining Danaher's global organization, where 69,000 people wake up every day determined to help our customers win. As an associate, you'll try new things, work hard, and advance your skills with guidance from dedicated leaders, all with the support of powerful Danaher Business System tools and the stability of a tested organization.
Danaher is committed to a diverse and inclusive culture where everyone feels they belong and all voices are heard. We believe in our associates and the unique perspectives they bring to every challenge, which is why we'll empower you to push the boundaries of what's possible.
If you've ever wondered what's within you, there's no better time to find out.
When you join us, you'll also be joining Danaher's global organization, where 69,000 people wake up every day determined to help our customers win. As an associate, you'll try new things, work hard, and advance your skills with guidance from dedicated leaders, all with the support of powerful tools and the stability of a tested organization.
At Danaher, we value diversity and the existence of similarities and differences, both visible and not, found in our workforce, workplace and throughout the markets we serve. Our associates, customers and shareholders contribute unique and different perspectives as a result of these diverse attributes.
If you've ever wondered what's within you, there's no better time to find out