TECHNICAL WRITER
Recruiter
Candidate Source Ltd
Listed on
20th November 2018
Location
Nottingham
Salary/Rate
£33000 - £35000
Type
Permanent
Start Date
ASAP
This job has now expired please search on the home page to find live IT Jobs.
TECHNICAL WRITER - ENGINEERING / PHARMACEUTICAL SECTOR- £33000 - £35000 + BONUS - BASED NOTTINGHAMThis fast-growing, profitable and progressive company is one of the world’s leading suppliers of laboratory equipment for use in the pharmaceutical industry. They hold an enviable position within a niche market. Success is based on high quality, flexibility, responsiveness, technological innovation and excellent staff.
To continue their success, they wish to add the position of Technical Writer to their small, but highly effective team.
Your primary role will involve creating and maintaining instruction manuals, technical and validation documents to enable the launch of new products and support existing products in the market. You will also be required to create and deliver training material.
Specifically, you’ll be responsible for:
- Working with the teams across the business to gain in-depth understanding of the products and documentation requirements and ensuring conformity to the relevant Pharmacopeia.
- Managing documents and updates
- Creating instruction manuals suitable for both English speaking and English not as a first language audiences
- Developing online help guides
- Completing Product Change documentation and ensuring required actions are completed
- Creation of required certificates e.g. calibration, CE, EMC
- Creating validation documentation (DQ, IQ, OQ, PQ) and managing change control
- Reviewing and updating Assembly Work Instructions, FAT checklists etc
- Creating training material and presenting this to customers, distributors and agents, and staff
- Authoring technical articles and white papers suitable for press release
- Reviewing current documents and developing/modifying clear standards for documentation within the company.
To be successful, you must have the following qualities and experience:
- Background and qualifications in engineering (e.g. BEng)
- Experience in the pharmaceutical or similarly regulated industry is preferable.
- Working knowledge of GMP/GLP best practice
- Experience of creating validation documents
- Ability to turn complex terminology into simple and visual means
- Excellent English literacy to generate high standard documents
- Meticulous with high attention to detail
- Strong organisational skills with the ability to meet challenging deadlines whilst remaining calm under pressure.
- Highly computer literate with good knowledge or Microsoft Office
- Strong problem-solving skills
- Knowledge of ISO 9001 would be an advantage.
Candidate Source Ltd is an advertising agency and the details sent in your application will be passed to a third party responsible for processing the application. This will include holding and sharing your personal data and our legal basis for this is legitimate interest subject to your declared interest in a job. Our privacy policy can be found on our website and we can be contacted to inform you of the third partys details should you wish.
