Technical Writer

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

Technical Writer- Small Molecule At Covalen, we're not just a business process outsourcing (BPO) service provider - we're industry pioneers collaborating with organizations worldwide for over 25 years. From established sectors to cutting-edge industries, our tailored BPO solutions forge powerful partnerships, helping clients achieve their unique goals. We've built enduring relationships in Financial Services, Technology, and Utilities, working with some of the globe's largest and most forward-thinking companies.

Key Deliverables Supporting Pharmaceutical Manufacturing Operations and Technical groups to;

• 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)

Key Attributes

• Relevant Science/Engineering 3rd level qualification or operational experience
• Previous pharma production operations/ projects/process experience
• Strong sense of customer focus and teamwork
• Previously demonstrated flexibility and willingness to take on different job tasks
• Self motivated/ proactive approachCommitment to meet deadlines
• ‘Right first time’ attitude
• Demonstrated technical writing skills in the generation of documents
• Good planning and organisation skills essential

Benefits and Perks

• Hybrid-working model
• Extensive Training & Development.
• Internal career progression opportunities.
• Employee assistance programme (EAP).
• Hive medical cash plan.
• PRSA Scheme.
• Employee engagement initiatives
• Bike to work scheme.

What would you bring? As a valued team member, you'll play a crucial role in delivering customized BPO solutions, ensuring our clients achieve consistent high performance and meet their strategic objectives. Your expertise will contribute to our legacy of success in providing outsourced solutions for Fortune 500 companies.

Equal opportunity employer:

At Covalen, we champion diversity and equality, anchoring our workplace cultures and creative minds. We recognize the collective strength found in the diverse backgrounds, skills, and experiences of our team members. Our commitment to fostering an inclusive environment transcends gender, marital status, family status, age, disability, sexual orientation, race, religion, and membership in the Travelling community.