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Manufacturing Biotech Associate, Dunboyne
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Client:
Location:
Dunboyne, Ireland
Job Category:
Other
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EU work permit required:
Yes
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Job Reference:
bc8f7982c6eb
Job Views:
2
Posted:
27.04.2025
Expiry Date:
11.06.2025
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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 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, providing exposure to 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 in-house training, mentorship, and continuous guidance to facilitate career progression. We aim to create high-performing teams that exceed our clients’ expectations regarding quality, staying within budget, and meeting deadlines.
Overview:
A fantastic and exciting opportunity has arisen for a Manufacturing Biotech Associate. The Manufacturing BioTech Associate will work in a self-directed shift team to deliver batch operations successfully, identify and resolve issues to ensure the site can deliver for our patients, in 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 substance on your designated shift team. Responsibilities include preparation, operation, and monitoring of equipment, use of business systems, and tasks such as cleaning, validation, and in-process testing.
* Progress an automated recipe using paperless technology to generate drug substance through inoculation and cell culturing activities, leading to filtration and purification of the product.
* Set up single-use equipment between runs, carry out the production process according to world-class GMP and EHS standards, and drive process optimization and improvement using standard work and lean techniques.
* Focus on delivering to the patient by maintaining a culture of safety, emphasizing right-first-time principles, and engaging in the development of yourself and peers.
Work Experience Required:
* A science qualification in a technical, engineering, or science-based discipline, or equivalent.
* 0 to 3 years’ experience in the biotechnology and/or pharmaceutical industry, or equivalent.
* Experience in a highly regulated pharmaceutical manufacturing environment.
* Good understanding of biologic drug substance production; experience is an advantage.
* Ability to work as part of a shift team and independently in a constructive manner.
* Ability to think logically and be proactive under pressure.
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