Job Description About PSC Biotech Who are we?
PSC Biotech is a leading Biotech Consultancy firm founded in ****, 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.
Overview: A fantastic opportunity has arisen for a Validation Specialist.
The successful candidate will take a lead on utilising the latest innovations in technology.
The role is based at the Drug Substance and Drug Product Facility in Co.
Louth which is a new facility build working to obtain qualification and continued product development.
The site is the first facility in the network focused on manufacturing a live virus vaccine.
Requirements Responsibilities: Support the site validation activities across a number of workstreams.
Develop and maintain the site Validation Master Plan.
Drive development of site cleaning strategy and implement/maintain cleaning and sanitisation protocols and procedures for pharmaceutical equipment, ensuring compliance with regulatory guidelines.
Perform risk assessments to determine the criticality of cleaning processes and set acceptance criteria.
Oversee cleaning validation studies, ensuring proper execution, data collection, and documentation.
Collaborate with production and maintenance teams to establish cleaning procedures and cleaning validation requirements.
Draft, review and approve cleaning validation documentation, reports, and deviation investigations.
Conduct periodic reviews of cleaning validation programs to ensure their ongoing effectiveness.
Support equipment qualification post Operational Qualification (OQ) through to Process Performance Qualification (PPQ) and subsequent revalidation.
Support global regulatory submissions, internal audits and external inspections/audits as needed.
Facilitate problem solving risk assessment projects/meetings.
Making problems visible and strive for continuous improvement.
Lead and support various organizational initiatives as needed (examples include safety, financial forecasting, work standardization, etc).
Keep up to date with scientific and technical developments.
Maintain continuous focus on quality and safety compliance and unflinching focus on the customer.
Skills Required: 3-5 years direct experience with a pharmaceutical or biotechnology company with a working knowledge of current regulatory requirements and current Good Manufacturing Practices.
Bachelor's degree (or higher) in Biological Sciences/Chemical Engineering/Biological Engineering/Chemistry etc.
Prior experience in Cleaning Validation, Temperature Mapping activities, and qualification of Parts Washers and/or Autoclaves.
Experience with upstream cell culture and/or downstream formulation/fill finish processes.
Experience with technology transfer, regulatory filing, and commercial drug substance/drug product manufacturing of biologics.
Prior experience in drug substance/drug product, process performance qualification and validation, site readiness and authoring regulatory CTD sections.
Requirements 3-5 years direct experience with a pharmaceutical or biotechnology company with a working knowledge of current regulatory requirements and current Good Manufacturing Practices.
Bachelor's degree (or higher) in Biological Sciences/Chemical Engineering/Biological Engineering/Chemistry etc.