Industry Pharma/Biotech/Clinical Research Work Experience 4-5 years City Dublin State/Province Dublin Country Ireland Job DescriptionAbout PSC Biotech Who we are?
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 points 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 through 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.
Job Summary: An exciting opportunity has opened in the Manufacturing Support team for a Technical Writer.In this role, you will be responsible for owning and managing change controls critical to site development and managing the operational documentation updates as required by each project.This role is primarily based on-site.Primary Responsibilities:Develop/Update and maintain Operations procedures in accordance with site and corporate requirements.
Serve as a document owner.
Assist in generation of training materials and may assist in providing training on scientific or technical aspects of the process.
Liaise with Manufacturing/Inspection/Engineering regarding documentation changes in an effective and timely manner.Develop protocols for execution in Manufacturing & Inspection in support of change controls, non-conformances & troubleshooting investigations with support from relevant SMEs.Involvement in projects as part of continuous process improvement and/or troubleshooting.Ownership and management of change controls as required.Issuance and updates of paper batch records in line with production schedule.Liaise with Quality Assurance to ensure that GMP standards are maintained in line with current OS.Partner with Operations lead/appropriate SME to ensure updates are correct and aligned with project deliverables/timelines.Perform document trending upon project completion to identify key issues/mistakes in document processing.Support data verification of Operations owned protocols reports and risk assessments.Support the production support team in reducing document turnaround times.Use specified software packages and standard procedures, responsible for compiling and maintaining all relevant documentation including SOPs.Provide technical and clerical support to the manufacturing, inspection & engineering teams in the preparation of documentation, collation of data and tracking of SOPs.Ensure Non-conformances are triaged within the established goal and serve as a deviation owner for minor deviations.Own corrective/preventative actions and effectiveness verification.Support execution of C&Q, characterisation, functional testing protocols as required by project. NOTE: This may require flexible working hours.RequirementsKnowledge/Skills: Strong Project Management and organizational skills, including ability to follow assignments through to completion.Excellent verbal and written communication skills: Strong Technical writing skills for GMP documentation (e.g., investigations, procedures, change controls) and good Presentation skills.Escalate issues professionally and in a timely manner.Ensures compliance within the regulatory environment.Demonstrated ability to work independently and deliver right first-time results under minimal direction.Experience participating in and leading cross-functional teams.Experience in managing multiple, competing priorities in a fast-paced environment.Bachelor's degree in a Science or Engineering discipline.3+ years of experience in Chemistry/Microbiology/Engineering/Validation gained within a biotech, pharma or health care organization.Experience with regulatory compliance in cGMP manufacturing and testing of pharmaceutical products is an advantage.
#J-18808-Ljbffr