Job Description
About PSC Biotech
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 to 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 with constant guidance to facilitate career progression. We believe in creating high-performing teams that can exceed our clients’ expectations regarding the quality of all scalable and business unit deliverables, staying under budget and ensuring timelines for our deliverables are being met.
Overview:
The role will support the technical aspects of engineering/maintenance activities and will include CMMS change management, report generation, CMMS data management, document collection, technical writing, and data processing. Hybrid working options - 3 days onsite. This may change depending on business requirements, so the candidate needs to be available to come on-site.
Requirements
Responsibilities:
* Management and implementation of CMMS change requests.
* Generate reports and metrics on maintenance systems management KPIs for multiple departments.
* Assist with equipment record management.
* Uploading spare parts and Bill of Material.
* Assist and comply with change control procedures.
* Complete accuracy reviews of the equipment records and maintenance plans.
* Collect information and write SOPs, route for review and approval via the Documentation Management System.
* Write training documents/manuals with input from equipment owners, engineers, and vendors.
* Schedule and organise review meetings.
* Liaise with Engineering Document Management and assist with the maintenance of this system.
* Perform other tasks as assigned by supervisor.
Skills:
* Self-motivated with high attention to detail.
* Strong communication, organizational, and analytical skills.
* Strong understanding of standard software applications: MS Word, Excel, Access, and SharePoint.
* Experience with using SAP or similar software.
* Administration work in engineering/laboratory or manufacturing office.
* Technical writing skills.
* Knowledge of GMP requirements in an engineering environment.
* Experience with reporting on maintenance management systems.
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