Manufacturing Associate (Downstream) – Day

CSL•Holly Springs, NC

2d•Onsite

About The Position

Seqirus is a world leader in influenza vaccine production, operating a state-of-the-art manufacturing facility in Holly Springs, NC. The company is an integrated global entity, collaborating internationally to protect communities from seasonal influenza and global pandemic threats. Joining Seqirus means contributing to making a difference in people's lives through a culture of possibility, creativity, and purpose. This Manufacturing Associate (Downstream) role is a shop floor position within manufacturing operations, reporting to a Supervisor or Sr. Lead. The associate will be trained to provide the technical skill-sets required to safely, compliantly, efficiently, and cost-effectively manufacture high-quality biologicals. CSL Seqirus is part of CSL, one of the largest influenza vaccine providers globally, contributing significantly to influenza prevention and pandemic preparedness with facilities in the U.S., U.K., and Australia, utilizing various technologies to offer a broad portfolio of differentiated influenza vaccines.

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