QC Associate

• Industry Pharma/Biotech/Clinical Research
• Work Experience 4-5 years
• City Dublin
• State/Province Dublin
• Country Ireland

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.

Responsibilitiesinclude but are not limited to:

· Testingof in process, stability and finished product samples. eg HPLC, CE, SDS-PAGE,IEF analytical testing, characterization and sample and data management.

· Reviewand authorisation of Lab Data

· SupportAnalytical Technical Transfer activity testing reports and documentation.

· Documentreview/updates when required.

· EquipmentCalibration, Maintenance and Trouble Shooting.

· Trainingof QC Chemistry Laboratory colleagues.

· LaboratoryInvestigation support

· LaboratoryHousekeeping and maintaining GMP standards.

· Assistingin regulatory audits.

Thesuccessful candidate will:

· Holda third level qualification (Degree/Diploma) in Biochemistry, Chemistry,Biology Biotechnology, or similar Scientific Subject.

· Haveat least 5 years relevant experience in a pharmaceutical/healthcareenvironment.

· Bevery proficient in the use of Microsoft Word, Excel etc.

· Havestrong technical writing skills.

· Bedetail oriented, self-motivated with good troubleshooting and problem-solvingabilities.

· Bea self-starter and capable of working on own initiative.

· Proventrack record of meeting deadlines.

· Experiencewith analytical techniques such as HPLC, CE, SDS-PAGE, IEF testing would alsobe advantageous.