Dunboyne, Ireland | Posted on 04/25/2025
* Industry Pharma/Biotech/Clinical Research
* Work Experience 1-3 years
* City Dunboyne
* State/Province Meath
* Country Ireland
Job Description
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 over 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 employment contract, providing exposure to top pharmaceutical client sites in a diverse, multicultural work setting.
Employee Value Proposition
Employees are the “heartbeat” of PSC Biotech. We provide unparalleled career development through in-house training and mentorship, along with continuous guidance to facilitate career progression. We aim to create high-performing teams that exceed client expectations regarding quality, stay within budget, and meet deadlines.
Overview:
An exciting opportunity has arisen for a Manufacturing Biotech Associate. The Manufacturing BioTech Associate will work in a self-directed shift team to successfully deliver batch operations, identify and resolve issues to ensure the site can deliver for our patients, fostering a culture that supports Quality, EHS, Learning, and Continuous Improvement.
Requirements
What you will do:
* Contribute your energy, knowledge, and innovation to the production of biologic drug substances on your designated shift. Responsibilities include preparation, operation, and monitoring of equipment, use of business systems, and tasks such as cleaning, validation, and in-process testing.
* Progress automated recipes using paperless technology to generate drug substances through inoculation and cell culturing activities, leading to filtration and purification.
* Set up single-use equipment between runs, conduct production according to GMP and EHS standards, and drive process optimization and improvement using standard work and lean techniques.
* Focus on delivering to patients by maintaining a culture of safety, ensuring right-first-time execution, and engaging in the development of self and peers.
Work Experience Required:
* A science qualification in a technical, engineering, or science-based discipline or equivalent.
* 0 to 3 years’ experience in biotechnology and/or pharmaceutical manufacturing or equivalent.
* Experience in a highly regulated pharmaceutical manufacturing environment.
* Good understanding of biologic drug substance production is an advantage.
* Ability to work as part of a shift team and independently in a constructive manner.
* Logical thinking and proactive approach under pressure.
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