QC Analyst in Analytical Testing
3 weeks ago
Dunboyne, Ireland | Posted on 12/06/2024
- Industry: Pharma/Biotech/Clinical Research
- Work Experience: 1-3 years
- City: Dunboyne
- State/Province: Meath
- Country: Ireland
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 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, and constant guidance to facilitate career progression. We believe in creating high-performing teams that can exceed our client’s expectations regarding the quality of all scalable and business unit deliverables, staying under budget, and ensuring timelines for our deliverables are being met.
An amazing opportunity has arisen for a QC Analyst in Analytical Testing in our new state-of-the-art single-use multiproduct Biotech facility. In our start-up site, the role will be responsible for Quality Control testing and all associated laboratory activities related to Biochemistry and Analytical Methods.
What you will do:
Bring energy, knowledge, innovation, and influence to carry out the following:
- Perform a variety of routine analytical techniques and associated documentation, including but not limited to Capillary Electrophoresis, UPLC, HPLC, GC, and Wet Chemistry methods in compliance with GMP requirements.
- Support activities including general lab readiness, audit readiness, laboratory equipment qualification, and analytical method technical transfer, verification, and validation.
- Drive the development of technical skills through coaching and motivate a high-performing culture across the team. Foster a continuous improvement environment and bring strong problem-solving and troubleshooting capabilities.
- Consistently deliver on specific area Key Performance Indicators. Operate to the highest standards of Safety, Quality, and Compliance. Demonstrate a commitment to learning and personal development that supports Quality, EHS, L&D, and continuous improvement.
What skills you will need:
In order to excel in this role, you will more than likely have:
- 1-3 years’ experience in the biotechnology and/or pharmaceutical industry, particularly in relation to Capillary Electrophoresis, UPLC, HPLC, or GC testing.
- Preferably Lean Six Sigma experience.
- Ability to think logically and be proactive under pressure.
- Ability to work as part of a team and on your own initiative in a constructive manner.
- Flexible and self-motivated.
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