Technical Author

Employment Solutions Ltd; England; On-site; GBP 40,000 - 45,000; Full time

Job summary

A leading company in healthcare and pharmaceuticals is seeking a Technical Author to join their team in Heywood. The ideal candidate will have a degree and valuable experience in validation protocols and CE/UKCA compliance. Responsibilities include producing high-quality technical documentation, collaborating with cross-functional teams, and ensuring adherence to legal standards. The role offers a competitive salary between £40,000 and £45,000, along with benefits such as performance-based bonuses and 24 holiday days plus bank holidays.

Benefits

Company sick pay

Shopping and leisure discounts

Simply Health cashback plan

Credit Union membership

Death in service cover

Nursery voucher salary sacrifice scheme

Qualifications

• Experience in writing high-quality validation and compliance documentation.
• Familiarity with validation documentation templates.
• Experience collaborating in cross-departmental teams.

Responsibilities

• Produce high-quality validation, compliance, and technical documentation.
• Prepare essential validation documentation and operator manuals.
• Develop Standard Test Protocols and procedure manuals.
• Collaborate with Compliance Engineer and other departments.
• Monitor and report on regulations affecting products.

Skills

Experience with validation protocols

Knowledge of medical and pharmaceutical validation

Understanding of CE and UKCA compliance

Ability to produce technical documentation

Education

Degree or equivalent compliance experience

Job description

Are you an experienced Technical Author looking to join a leading company in the healthcare and pharmaceutical sectors? This company, a pioneer in manufacturing clean air and containment equipment, is seeking a dedicated Technical Author to contribute to their innovative team in Heywood. This is an exceptional opportunity to be part of a dynamic organization that values precision, collaboration, and continuous improvement.

The ideal candidate should have a degree or equivalent compliance experience in a similar industry, with desirable knowledge of medical and pharmaceutical validation. The role requires experience in validation protocols, risk assessments, and operator manuals, alongside an understanding of CE and UKCA compliance and related directives.

Key Responsibilities

• Produce high-quality validation, compliance, and technical documentation to support the design and manufacture of the company's products.
• Prepare essential validation documentation including Requirements Traceability Matrices, Design Qualifications, Factory Acceptance Tests, Installation and Operation Qualifications, Operator Manuals, and Risk Assessment and Method Statements.
• Develop Standard Test Protocols and procedure manuals, ensuring adherence to applicable protocols, guidelines, and legal standards.
• Collaborate closely with the Compliance Engineer and other departments such as Production, Customer Care, Sales, and After Market to ensure comprehensive documentation.
• Monitor and report on new regulations and standards and their impacts on the company's products.

Compensation & Benefits

The Technical Author role offers a competitive salary of £40,000-£45,000, an annual performance-based bonus, and 24 days' holiday plus bank holidays.

Additional benefits include:

• Company sick pay
• Shopping and leisure discounts
• A Simply Health cashback plan
• Credit Union membership
• Death in service cover
• A nursery voucher salary sacrifice scheme

How to Apply

If you are ready to take the next step in your career as a Technical Author, do not miss out on this remarkable opportunity. Apply today by clicking 'Apply', emailing a CV to the company, or contacting the recruiter.

Take the leap and become a valued member of this company as a Technical Author.