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. We serve 350 clients across more than 23 countries worldwide. Our services include cloud-based software solutions for Quality Management and Regulatory Inspections, pharmaceuticals contract manufacturing professionals, and metrology services.
Take your Career to a new Level
PSC Biotech disrupts the conventional consultancy model by offering a unique Employee Value Proposition (EVP) that includes the opportunity to work with talented professionals in the Pharma/Biotech industry. We provide permanent contracts of employment, offering exposure to top pharmaceutical client sites in diverse cultural settings.
Employee Value Proposition
Employees are the heartbeat of PSC Biotech. We support career development through in-house training, mentorship, and ongoing guidance to facilitate growth. We aim to create high-performing teams that exceed client expectations in quality, stay within budget, and meet deadlines.
Overview
We have a fantastic opportunity for an Analytical Scientist R&D at our Dunboyne facility. The role involves collaboration with the Enabling Technology and Engineering groups to leverage Process Automation and Process Analytical Technology (PAT). The Microbiology Lab Operations team will work closely with Operations to understand facility needs and adapt resources accordingly.
This is a shift-based role (4 days on / 4 days off, 7-day rolling shift from 7am to 7pm)
Responsibilities
* Drive laboratory operations, including equipment qualification (PQ), documentation, SOP review, and contributing to lab and process setup.
* Review and lead trending and reporting of laboratory data to support batch release and analyze end-of-quarter and year reports.
* Maintain and manage laboratory stock and order consumables as needed.
* Participate in and lead departmental and cross-functional meetings.
* Support internal and external audits, ensuring inspection readiness.
* Promote site safety and a culture of continuous improvement.
* Support GMP activities, troubleshooting, and execution of in-process and drug substance analysis studies.
* Collaborate on introducing innovative solutions and participate in lean lab initiatives.
* Organize testing schedules and ensure adherence to deadlines.
* Foster team effectiveness and promote success through own actions and training.
* Support changing business needs, including occasional out-of-hours testing.
Skills & Qualifications
* Degree in Biological Sciences, Engineering, or related field; MSc preferred.
* Minimum 3 years of relevant industry experience.
* Ability to work effectively both independently and as part of a team.
* Knowledge of biologics drug substance manufacturing and microbiological testing techniques.
* Proactive, logical thinking, and effective communication skills.
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