What are the responsibilities and job description for the Qc specialist position at CSL?
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 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 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.
You will report to the Manager, QC and will be a member of the QC team in Holly Springs Influenza Vaccine manufacturing facility You will support both onsite and off-site testing.
The QC function provides critical testing on raw materials, environment, utilities, in-process controls, and drug product / drug substance.
The information provided by QC ensure manufacturing controls are effective and patient safety is maintained. You will work onsite at our CSL Seqirus in Holly Springs, NC location Monday-Friday during primary business hours.
Benefits Include Outdoor Amenities, Onsite Café, Medical, Dental, Vision, Life Insurance, 401K with a 6% match, and PTO available from your first day of hire.
You will have responsibilities including providing technical expertise related to the process, equipment, and business systems that drive strategic improvements in the services provided to our customers.
You will provide front-line support as relates to technical quality, and system issues related to their specific department (Chemistry, Microbiology, Environmental Monitoring, Biochemistry, Virology, Compliance, and Logistics).
Qualifications :
Bachelor degree in a relevant scientific discipline (Biology, Microbiology, Chemistry, etc.)
3 years' experience in pharmaceutical / biotech mfg. operations, QC technical role or equivalent.
Experience writing and investigating Deviations is required for this position
Basic knowledge of cGMP and FDA requirements.
Experience with Laboratory Systems and Investigation / Deviation / CAPA writing.
Demonstrated technical writing skills.
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.
About CSL Seqirus
CSL Seqirus is part of CSL Limited (ASX : CSL). As one of the largest influenza vaccine providers in the world, CSL Seqirus is a major contributor to the prevention of influenza globally and a transcontinental partner in pandemic preparedness.
Learn more about CSL Seqirus .
We want CSL Seqirus to reflect the world around us
As a global organization with employees in 35 countries, CSL embraces diversity and inclusion. Learn more about Diversity & Inclusion at CSL Seqirus.
Do work that matters at CSL Seqirus!
Watch our 'On the Front Line' video to learn more about CSL Seqirus
Last updated : 2024-10-06
