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.
Overview:
The Quality Assurance Specialist within Our Company is required to
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Work a 4 shift pattern role
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Technical knowledge of sterile manufacturing processes
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Perform timely reviews of batch documentation / investigations / reports highlighting and assist in the resolution of concerns commensurate with the risk
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Respond quickly to unplanned events, technical issues
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Operational experience of quality systems in a dynamic manufacturing environment eg SAP, Trackwise, MES
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Full understanding of relevant quality and compliance regulations knowledge of requirements for cGMP, US and EU regulatory requirements
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Conduct, report and display of Quality right first time, audit readiness metrics weekly to ensure continuous audit readiness and cGMP compliance
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Support the spot check/walk-through process of the production lines
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Involved in customer complaint investigation if required
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Work well cross functionally and be an active team member
Responsibilities:
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Provide Quality support to IPT production teams to ensure cGMP standards are maintained.
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Understanding of sterile manufacturing operations is preferred.
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Ability to learn and utilize computerized systems for daily performance of tasks.
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Ability to prioritize, manage multiple tasks, and meet deadlines.
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Perform timely reviews on batch documentation ( EBR’s ) / line clearances/ assist in the resolution of concerns commensurate with the risk. Liaise with other Department representatives to promote improvements in GMP and Quality standards
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Comply with our current Manufacturing Division, Quality and EHS Management System requirements, as relevant to commercial operations.
Reporting Structure:Reports to Quality Manager
Qualification , Education and Skills
Skills and Knowledge
Typical Minimum Education
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Bachelor’s Degree or higher preferred in a Science discipline
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Typical Minimum Experience
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1-2 years experience in a Quality Role at pharmaceutical manufacturing facility preferably aseptic manufacturing
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Experience in SAP, MES, Trackwise desirable
Technical
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Working knowledge of regulatory/code requirements to Irish, European and International Codes, Standards and Practices
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Knowledge of cGMP and GDP essential Report, standards, policy writing skills required
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Competent in the use of MES and SAP
The position is onsite and remote or hybrid is not applicable for this role,
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This is a shift position – 4 cycle - 12 hours per shift e.g
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Week 1- long week: Monday – Tuesday Days, Friday, Sat, Sun nights
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Week 2- short week: Wed and Thurs Days,
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Week 3:Long week: Monday – Tuesday nights, Friday, Sat and Sun Days
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Week 4: short week: Wednesday and Thurs Nights
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For the job shift experience, working in a quality function or in an aseptic environment is beneficial
