THE OPPORTUNITY

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 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. Our benefits include an Onsite Café, 1/2 mile Walking Trail, Basketball and Tennis Courts; access to Medical, Dental, Vision, Life Insurance, 401K with a 6% match and an annual bonus; and accrued PTO, wellness days and floating holidays.

Reporting to the Supervisor or Sr. Lead, you will work onsite on the 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.

• Shift: Day
• Hours: 8-5pm
• Follow M-F schedule
• Job level will be determined based on years of relevant experience to our processes and equipment

Responsibilities :

• Become trained on basic processes and equipment and serves as a hands-on resource in Production.
• Conduct all assigned activities in a safe and cGMP compliant manner.
• Clean, prepare, and sterilize production equipment and disinfect production rooms.
• Assembly, set-up, and disassembly of production equipment.
• Execute process steps according to defined SOPs and BPRs.
• Document activities following cGMPs.
• Handle biologically and chemically hazardous good.
• Interface with process automation systems and electronic business systems (e.g, PAS, BAS, PLCs, LIMS, SAP, LiveLink.)
• Involved in Qualification and Validation activities.
• Involved in completion of root cause investigations and CAPA implementation.

Qualifications:

• High school diploma/GED required, with training and education from biotechnology coursework being a plus;
• 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.
• Basic knowledge of cGMP requirements preferred
• Experience completing SOPs and documenting work
• 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.

LI-Onsite

OUR BENEFITS

CSL Seqirus employees that work at least 30 hours per week are eligible for benefits effective day 1. We are committed to the wellbeing of our employees and their loved ones. CSL Seqirus offers resources and benefits, from health care to financial protection, so you can focus on doing work that matters. Our benefits are designed to support the needs of our employees at every stage of their life. Whether you are considering starting a family, need help paying for emergency back up care or summer camp, looking for mental health resources, planning for your financial future, or supporting your favorite charity with a matching contribution, CSL Seqirus has many benefits to help achieve your goals.
Please take the time to review our benefits site to see what’s available to you as a CSL Seqirus employee.

• Become trained on basic processes and equipment and serves as a hands-on resource in Production.
• Conduct all assigned activities in a safe and cGMP compliant manner.
• Clean, prepare, and sterilize production equipment and disinfect production rooms.
• Assembly, set-up, and disassembly of production equipment.
• Execute process steps according to defined SOPs and BPRs.
• Document activities following cGMPs.
• Handle biologically and chemically hazardous good.
• Interface with process automation systems and electronic business systems (e.g, PAS, BAS, PLCs, LIMS, SAP, LiveLink.)
• Involved in Qualification and Validation activities.
• Involved in completion of root cause investigations and CAPA implementation