Qc Analyst . job from PSC Biotech Ltd in Cork, County Cork, Ireland

About PSC Biotech Ltd

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 Description:

QC Analyst - Bioassay

Job Description

Performs advanced tests and analyses to assure that products align with established specifications.

Carries out complex calculations and documents test results.

This is a volume driven position that that directly touches product.

Compiles and analyzes data on reoccurring product defects to determine root cause. Documents analysis results.

Analyzes raw material inspection logs for consistent failures.

Notifies purchasing and quality departments about suppliers that have provided inferior products.

Studies work processes, measurements and performance metrics to identify improvement areas.

Recommends new or modified procedures based on findings.

Collaborates with customers, suppliers and associates to define and improve quality standards and expectations.

Participates on process improvement teams. Monitors and scrutinizes internal and external complaints and compiles data to be used in reports.

Performs analyses in order to achieve compliance with specifications using a wide variety of chemical, biological and physical standard procedures

Key Responsibilities:

• Attending daily meetings, working on own initiative.

• Testing and reviewing daily

• Training new analysts

• Always aim to meet site metrics

• Promoting 6S within the laboratories

Requirements
Qualifications

Education:

A minimum of a bachelor’s degree in a science related discipline and 3 years of experience in a pharma company.

Experience and Skills:

• Cell culture experience necessary

• Cell bioassay and Process impurity testing experience required such as DNA, ELISA and HCP.

• Proficient in Lab report writing.

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Job Types: Full-time, Permanent

Salary: €20.00-€39.00 per hour

Schedule:

• Monday to Friday