Pharma Technical Writer - Small Molecule (Hybrid)

Covalen; Cork; Hybrid; EUR 42,000 - 62,000; Full time

Benefits offered by this job

Hybrid working model

Extensive training & development

Internal career progression

Employee assistance programme

Hive medical cash plan

PRSA Scheme

Employee engagement initiatives

Bike to work scheme

Job summary

Covalen in Ireland is seeking a Technical Writer for Small Molecule operations to support pharmaceutical manufacturing documentation and compliance. You will own document revision, routing, and batch records, and contribute to environmental monitoring and training documentation, working within a hybrid model.

The role requires a strong technical writing background, experience in pharma production, and the ability to collaborate with engineering, QA, EHS and chemistry teams to deliver

Qualifications

• Relevant Science/Engineering degree or operational experience.
• Experience in pharma production operations or projects.
• Proven technical writing skills for creating documents.
• Strong planning and organizational abilities.
• Ability to work in a hybrid environment.

Responsibilities

• Own document revision and routing on document management system and drive on time approval
• Design, update sampling plans related to environmental monitoring
• Design, update and improve facility/process procedures and business processes.
• Design, update and improve Manufacturing and Cleaning Batch Records.
• Design, generate and update Operations Area Logbooks
• Design, generate and update Training Documentation
• Design, update and improve EH&S systems and documentation.
• Design and generate Protocols across a number of departments
• Design update/improve other documentations associated with the small molecule business
• Work with Technical groups in developing key technical documents to facilitate the start of a new facilitating and the introduction of the new products
• Support a dynamic Small Molecule manufacturing environment.
• Develop/learn key understanding of core manufacturing principles.
• Involvement in New Product Introductions.
• Deliver in innovative Continuous Manufacturing Areas.
• Support multiple manufacturing functions (Eng, Chemistry, QA, EHS)

Skills

Science/Engineering degree

Pharma manufacturing experience

Technical writing

Documentation control

Teamwork

Education

3rd level qualification in Science/Engineering

Job description

Covalen in Ireland is seeking a Technical Writer for Small Molecule operations to support pharmaceutical manufacturing documentation and compliance. You will own document revision, routing, and batch records, and contribute to environmental monitoring and training documentation, working within a hybrid model.

The role requires a strong technical writing background, experience in pharma production, and the ability to collaborate with engineering, QA, EHS and chemistry teams to deliver