QA Specialist III (Batch Release)

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.

As the QA Specialist you will be reporting to the Manager, Quality and will be responsible for batch release, investigating documents, reviewing complaints and handling the process.

Experience with SAP and Veeva is very helpful for this position. If you are looking to move into a team with growth opportunity, this would be an ideal role for you.

You will be you will work onsite at our CSL Seqirus in Holly Springs, NC location Monday-Friday during primary business hours.

Benefits Include flexible hours M-F, Onsite Café, Medical, Dental, Vision, Life Insurance, 401K, and PTO available from your first day of hire.

Responsibilities :

Responsible for release process, specifically : Release of incoming raw materials, manufactured buffers, and intermediatesEnsure that all aspects of drug product / substance comply with the requirements of the Seqirus Quality policies and meet all relevant cGMP regulatory requirements.

Support batch release team through completion of LRPs and other release tasks

• Responsible for Product Complaints, specifically : Investigate product complaints as an investigation owner and as a Quality Assurance ApproverHolly Springs SME and Single Point of Contact (SPOC) for global complaint processes and initiatives
• SME for Quality Management Systems for Change Controls, Deviations, Product Complaints and Change Notifications
• Lead recall process activities.
• Support the Holly Springs stability program, Annual Product Quality Review (APQR).
• Responsible for author, review and approval of documents (SOPs, protocols / reports, Specifications, work instructions) within the Electronic Document Management System (EDMS)

Qualifications :

• University degree in a relevant scientific discipline (Pharmacy, Chemistry, Biology, Biochemistry)
• 5+ years' GMP experience in pharmaceutical / biotech or other regulated industry
• Experience with SAP
• Proven examples of investigational experience
• Knowledge of current Good Manufacturing Practices (cGMP) principles
• Knowledge of FDA and EMA requirements

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 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.