Associate I/II/III, Manufacturing

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 the 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 an 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, you will be onsite working in our Holly Springs facility as a manufacturing associate within manufacturing operations. You will provide (train in) the technical skills sets necessary to manufacture high-quality biologicals safely in a compliant, efficient, and cost-effective manner.

• Shift: Days
• Hours: 6AM – 6PM
• Follows 2-2-3 schedule

Responsibilities:

Becomes trained in basic processes and AVI equipment while serving as a hands-on resource in Production.

Conducts all assigned activities in a safe and cGMP compliant manner. Passing a vision test is required for associate role. Tasks will include, but are not limited to:

• Manual inspection of syringes/AVI processing
• Assembly, set-up, and disassembly of production equipment
• Executing process steps according to defined SOPs and BPRs
• Documenting activities in accordance with cGMPs
• Interfacing with process automation systems and electronic business

systems (e.g, PAS, BAS, PLCs, SAP)

• Supporting Qualification and Validation activities as needed
• Identifying and communicating process issues
• Supports a high-performance teamwork environment and demonstrate Seqirus Values and Behaviors

Education:

• High school diploma/GED required, preferably coupled with Biotechnology coursework; bachelor’s degree in science or engineering preferred

Experience:

• 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.