Associate , Manufacturing Manufacturing Operations Manufacturing Operations Multi Discipline CSL Seqirus
Listed on 2026-09-28
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Manufacturing / Production
Pharmaceutical Manufacturing, Manufacturing & Industrial Operations, Production Associate / Production Line, Production QC/QA
Do you want to work with a company that tackles fascinating problems and find solutions to complex challenges? Seqirus has an exciting opportunity to join our expanding team in Holly Springs, NC. With an advanced manufacturing facility and 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 on the front line 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.
The incumbent will be a shop floor employee in the manufacturing organization. The incumbent will provide (be trained in) the technical skill-sets necessary to manufacture high-quality biologicals safely in a compliant, efficient, and cost-effective manner.
- Shift: Nights
- Hours:
6PM – 6AM - Follows 2-2-3 schedule
- Becomes trained on basic processes and equipment and serves as a hands-on resource in Production
- Conducts all assigned activities in a safe and cGMP compliant manner.
- Tasks will include, but are not limited to:
Cleaning, preparing, and sterilizing production equipment
- Cleaning and disinfecting production rooms
- Assembly, set-up, and disassembly of production equipment
- Executing process steps according to defined SOPs and BPRs
- Documenting activities in accordance with cGMPs
- Handling biologically and chemically hazardous goods
- Interfacing with process automation systems and electronic business systems (e.g, PAS, BAS, PLCs, LIMS, SAP, Live Link)
- Supporting Qualification and Validation activities
- Identifying and communicating process issues
- Supports team effort in the effective and timely completion of root cause investigations and CAPA
- Supports a high-performance teamwork environment and demonstrate Seqirus Values and Behaviors
- High school diploma/GED or associate’s degree with 1+ years’ transferrable skills OR bachelor’s degree with 0+ years’ experience OR equivalent; experience in pharmaceutical, biotechnology, and/or sterile production environments preferred
- Basic knowledge of cGMP requirements preferred
- Experience executing SOPs and documenting work preferred
- Basic mechanical aptitude or knowledge of electronic / mechanical equipment preferred
Different qualifications or responsibilities may apply based on local legal and/or educational requirements. Refer to local job documentation where applicable.
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