PSC Biotech
Job title:
Administrative Digital Lab Record
Company
PSC Biotech
Job description
About 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 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.
Job Title: Administrative Digital Lab Record
The position reports to the DLR Project Lead.
The position offers the opportunity to work with a team of professionals responsible for the introduction of Digital Laboratory Records to our modern analytical laboratories using the most up to date technology and quality assurance procedures. The laboratory operates under Lean principles and employees the use of a wide variety of analytical techniques.
Requirements
What you will do:
- Complete activities for the project plan for DLR implementation with agreed upon deliverables – such as LabX and Empower interface with GLIMS.
- Review and approval of plan, protocols, and completion reports.
- Work to client standards for project deliverables.
- Work in SAP updates for the Analytical department.
- Update of site procedures and standards.
- Liaising with vendors in relation to hardware and software.
- Be part of a dynamic team responsible for DLR requirements all across all the laboratories.
Requirements
What skills you will need:
- Applications are invited from candidates who have a degree in Science (Chemistry, Physics or related Life Science) and/or relevant experience.
- Have knowledge of GMP standards
- Have knowledge Laboratory safety standards.
- Must have good communication skills, both written and verbal.
- Strong documentation skills are required.
- Must be motivated, focused and technically strong.
- To maintain accurate records in compliance with GMP expectations
- To understand and internalise procedures relevant to GMP operations.
- Communication – written, oral.
- Team and interpersonal skills
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Expected salary
Location
Tipperary
Job date
Tue, 02 Jan 2024 23:51:33 GMT
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