Laboratory Document Controller

Recruiter
EasyWeb Group
Location
Wokingham
Salary
£30,000 to £35,000 per annum
Posted
26 Mar 2019
Closes
23 Apr 2019
Ref
00327177
Contact
Candidate Services
Contract Type
Permanent
Hours
Flexible
Laboratory Document Controller

Intersurgical is a thriving innovative medical manufacturing company and a world leader in providing plastic disposable products for the respiratory care business.

Position: Laboratory Document Controller
Location: Wokingham, Berkshire
Job type: Full Time, Permanent
Hours: 40 hours per week, Monday to Friday
Salary: £30,000 to £35,000 per annum

Closing date for applications: 25th April, 2019

About the role:

A new opportunity has arisen for a hardworking and enthusiastic Laboratory Document Controller to join our thriving UK medical manufacturing company to work within our expanding Technical Department.

We are looking to recruit someone who will be responsible for reviewing all the documentation produced by the Technical Laboratory to ensure that it complies with the company Quality Management System and regulatory requirements. …

The ideal candidate will be able to function effectively within the Technical Department and across a number of other interrelated departments, dealing with a variety of tasks whilst having the ability to work both independently and as part of a team. An excellent eye for detail, ability to process and cross-examine technical information and good data analysis skills are required.

This is a great opportunity for an enthusiastic and dedicated individual seeking to work as part of a product development laboratory within a thriving UK medical manufacturing company.

About you:

- Qualification or degree in a science or related subject
- Experience with technical documentation writing / reviewing
- Good communication
- Able to multitask and prioritise workload
- Able to work in a team and on own initiative
- Able to function effectively across a number of interrelated departments
- Self-motivated and willing to learn
- Methodical, organised and structured approach to work
- Attention to detail
- Able to gather, evaluate, critically interpret and communicate information

Desirable Experience / Qualifications:

Experience working within a GLP laboratory, working to the requirements of (or equivalent of) the following:

- ISO / IEC 17025 General Requirements for the Competence of Testing and Calibration Laboratories.
- CFR21 Part 58 Good Laboratory Practice for Non-Clinical Laboratory Studies.

You may have experience of the following: Laboratory Document Controller, Document Controller, Technical Document Writer, Laboratory Assistant, Lab Assistant, Laboratory Technician, Lab Technician, Technical Author, Document Specialist, Compliance, Regulation, Regulatory, etc.

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