Manufacturing Bioprocess Associate-Drug Substance
- Industry: Pharma/Biotech/Clinical Research
- Work Experience: 1-3 years
- City: Meath
- State/Province: Meath
- Country: Ireland
Job Description
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, 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.
Employee Value Proposition
Employees are the 'heartbeat' of PSC Biotech. We provide unparalleled empowering career development through Learning & Development, in-house training, and mentorship to facilitate career progression. We believe in creating high-performing teams that can exceed our client's expectations regarding quality of all scalable and business unit deliverables, staying under budget, and ensuring timelines for our deliverables are being met.
Overview:
An amazing opportunity has arisen for a Manufacturing Bioprocess Associate to provide operational support for manufacturing operations of the Late Stage and Launch Pipeline products at our new state-of-the-art single-use biotechnology facility in Ireland. This role will involve supporting manufacturing operations on a shift rotation basis.
Reports to: Drug Substance Process Operations Manager
Requirements
Role Functions:
- The Manufacturing Bioprocess Associate will support end-to-end production operations for both Fed Batch and Continuous Manufacturing.
- Shift role 24/7 (Onsite)
- Support on-floor manufacturing of pipeline products on a shift rotation.
- Operate equipment according to electronic batch records, sampling plans, and standard operating procedures.
- Work as part of a multi-disciplined, diverse, and dedicated process team where flexibility and teamwork are essential.
- Support weekend or out-of-hours work on select timeframes to support manufacturing activities.
- Conduct all work activities with strict adherence to the safety and compliance culture on site.
- Support the authoring of electronic batch records, sampling plans, work instructions, and standard operating procedures.
Skills and Education Required:
- 2+ years experience in a GMP Manufacturing environment.
- Ability to work independently and within a cross-functional team.
- Familiarity with contamination control and batch release requirements.
- Familiarity with Emerson DeltaV, Pas X, and the use of Automation in a manufacturing process.
- Experience with various Single-Use technologies in a manufacturing environment.
Preferred Experience and Skills:
- Understanding of Upstream and Downstream Unit Operations for mAb manufacturing.
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