Manufacturing Associate (Downstream) – Day

CSL Plasma•Holly Springs, NC

18h•Onsite

About The Position

Seqirus has an exciting opportunity to join our expanding team in Holly Springs, NC. With a state-of-the-art manufacturing facility and an expertise in influenza science, we are one of the world leaders in the production of the influenza vaccine. We operate as one integrated global company, drawing together expert staff from different countries to collaborate. Together, we're working to protect communities from seasonal influenza and global pandemic threats. When you join Seqirus, you join a team dedicated to making a difference in people's lives. It's a feeling of possibility, creativity, and purpose that inspires us every day. Reporting to the Supervisor or Sr. Lead, you will be a shop floor employee in manufacturing operations. You will provide (train in) the technical skill-sets necessary to manufacture high quality biologicals safely in a compliant, efficient, and cost-effective manner.

Requirements

High school diploma/GED required
Minimum of 1 year of transferrable skills and experience OR equivalent education, coursework or hands-on training in biomanufacturing related areas
experience in pharmaceutical, biotechnology, or sterile production environments.

Nice To Haves

training and education from biotechnology coursework being a plus
Basic knowledge of cGMP requirements preferred
Experience with downstream purification operations and filtration, chromatography, or similar unit operations is an advantage
Experience completing SOPs and documenting work
Basic mechanical aptitude or knowledge of electronic / mechanical equipment preferred.

Responsibilities

Become trained on basic processes and equipment and serve as a hands-on resource in Production.
Conduct all assigned activities in a safe and cGMP compliant manner.
Cleaning, preparing, and sterilizing production equipment.
Clean and disinfect production rooms.
Assembly, set-up, and disassembly of production equipment.
Complete process steps according to defined SOPs and BPRs.
Document activities following cGMPs.
Handle biologically and chemically hazardous goods.
Work with process automation systems and electronic business systems (e.g, PAS, BAS, PLCs, LIMS, SAP, LiveLink.)
Involved in Qualification and Validation activities.
Identify process issues.
Involved in completion of root cause investigations and CAPA.
Work within a collaborative teamwork environment