Technical Writer
A 12-month contract Technical Writer role in Cork supporting a Biologics Centre of Excellence: drafting and maintaining SOPs, protocols, and work instructions, migrating documents into Veeva Quality Documents, and producing training materials. Requires a science/engineering background, strong technical writing skills, and Veeva/Compliance Wire expertise.
- Compensation
- Not disclosed
- Location
- Cork, Ireland
- Work setup
- Not specified
- Seniority
- Not specified
- Employment
- Contract
- Experience
- Not specified
- Category
- Technical writing
- Posted
Skills
Must have
- Third level qualification in a Science or Engineering discipline, and/or extensive proven experience in technical document writing
- Strong technical writing expertise
- Training coordination experience
- Subject Matter Expert knowledge of Veeva Quality Documents & Compliance Wire
- Draft, review, and approve BPDs, SOPs, technical protocols & reports, forms, and work instructions
- Apply data integrity and ALCOA principles with compliance best practices
- Excellent verbal and written communication skills
- Outstanding organisational skills, initiative, self-motivation, and ability to work independently
Nice to have
- Experience managing documentation transitions into Veeva Quality Documents and initiating Change Requests
- Experience developing training programs, guides, and e-learning modules
Full description
About PSC Biotech Who are we?
PSC Biotech is a leading Biotech Consultancy firm founded
in 1996, headquartered in Pomona, California, USA, with Global operations in
Ireland, India, Singapore, Australia and the US, serving 350 clients in more
than 23 countries worldwide. We provide cloud-based software solutions for
Quality Management and Regulatory Inspections, pharmaceuticals contract
manufacturing professionals, and metrology services to our clients.
‘Take your Career to a new Level’
PSC Biotech disrupts the conventional consultancy model
by aligning our EVP as one of the unique selling point which includes the
opportunity to work with the most talented cohort of like-minded professionals
operating in the Pharma/ Biotech Industry. We offer a permanent contract of
employment giving exposure of working in Top Pharmaceutical client sites in a
diverse-cultural work setting.
Employee Value Proposition
Employees are the “heartbeat” of PSC Biotech, we provide
unparalleled empowering career development though Learning & Development
in-house training mentorship through constant guidance to facilitate career
progression. We believe in creating high performing teams that can exceed our
client’s expectations with regards to quality of all scalable and business unit
deliverables, staying under budget and ensuring timelines for our deliverables
are being met.
Summary
- The Biologics Centre of Excellence Technical Writer
supports Biologics CoE operations through effective document management and
training administration. This role requires strong technical writing expertise
with training coordination, thereby ensuring regulatory compliance, inspection
readiness, and support personnel cross-training. The role requires demonstrated
skills for initiative, self-motivation, outstanding organisational skills, and
a proven ability to work independently.
- 12 Month of Contract with possibility of an extension
Requirements
Key Responsibilities
- Lead, develop, and drive the ongoing enhancement of the
documentation management strategy
- Produce high-quality, accurate documentation by applying
data integrity and ALCOA principles, adhering to compliance best practices, andensuring all materials are appropriate for their intended audience