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$91k–$118k/yr
Full-time
bachelor degree
Posted 41d ago
~40 hrs/week
Responsibilities
Provides quality oversight for all departments within the assigned packaging value stream to ensure product quality and adherence to CSL standards. Manages quality operations including investigations, CAPAs, change controls, and the development of department personnel.
Requirements
Requires a bachelor's degree in a scientific or technical field and at least five years of industry experience. Candidates should have experience managing teams and possess significant technical expertise in change management and cGMP guidelines.
Full job description
Job Purpose: Quality oversight of the activities for all departments within the assigned Value Stream. This includes operational quality oversight for the area and for the processes, to assure appropriate quality of the products manufactured within the value stream.
Responsibilities:
Overseeing adherence to any applicable CSL standards and procedures, via review and approval of related records, support and approval of quality risk assessments, non-conformances, investigations, CAPAs, and change controls, and monitoring and continuous improvement of quality performance metrics. • Oversees all Quality related activities that support within the Value Stream to support the process. • Partner with all teams within the value stream regarding product quality aspects. • Responsible for support and oversight of manufacturing shop floor quality, shop floor hygiene / sterility assurance. • Agency audit participation including assisting in the presentation of quality investigations and decisions to health authorities, leading tours, or acting as backroom support or as a host. • Maintains a current status for departmental GMP training requirements and provides oversight to onboarding training to department personnel. • Accountable to manage all batch documentation review per unit operations and issue batch disposition recommendation within deviation investigations. • Partners with the team to support/review/approval of trends, product technical complaints, investigations, corrective & preventative actions, and change control. • Leads the respective teams to facilitate new ways of working to develop the desired culture within relevant quality areas. • Foster a culture of continuous improvement through employee selection, training and mentoring while focusing on operational efficiency and the elimination of “non-value added” activities. • Responsible for the management and execution of performance management process. Development of department personnel for Quality Assurance Operations including talent management process. • Places a high priority on developing others through coaching, feedback and developmental goals. • Responsible for representing Quality Assurance Operations on local and global projects and serving on steering committees as required. Collaborates and acts as liaison globally with other CSL sites regarding investigation resolution • Complies with requirements from CSL Behring’s Safety Program, including Health and Safety mandates and OSHA requirements. • Reinforces safe working practices with team and champions the safety culture within the site team. • Manage and direct the personnel headcount and assist with departmental budget planning. • Maintain a status for departmental training requirements and provide training to department personnel. • Responsible for ensuring all deviation events are properly classified, investigated, and given correct final disposition. Responsible for ensuring proper Root Cause Analysis tools are used for investigations resulting in robust corrective and preventive actions. Responsible for review/approval of all high/substantial risk investigations. Oversee environmental investigations that are relative to routine monitoring and/or product monitoring. Responsible for contact with other CSL sites and Global communication regarding investigations and/or changes.
Drive continuous improvement initiatives and provide quality oversight of change management activities. • Assists in hosting regulatory agency inspections, as required by Quality Assurance Management.
Qualifications:
Education
Undergraduate degree in relevant discipline (or equivalent) B.A. or B.S. degree preferably in scientific or technical field (e.g., chemistry, biology, physics, engineering, computer science, technical writing) or experience and training equivalent to such a degree.
Experience
Five (5) years industry experience. 1 or more years’ experience managing teams directly or in a networked accountability
2-3 years' experience supervising two or more staff members preferred. Specific experience in Quality/Change management role preferred. (Proved demonstration to perform min role may also be considered.)
Demonstrated ability to influence decisions, drive continuous improvement, increase value of systems to the business and create an environment of continuous inspection readiness and right-first-time execution.
Knowledge of cGMPs and regulatory agency guidelines preferred.
Demonstration competency of verbal and written communication.
The expected base salary range for this position at hiring is $91,000 - $118,000. Please note this salary range reflects the minimum and maximum base pay that CSL expects to pay for this position at the listed location as of the time of this posting. Individual base salary for a successful candidate is determined by qualifications, skill level, experience, competencies and other relevant factors. In addition to base salary, total compensation for this role may also include incentive compensation and equity.
Different qualifications or responsibilities may apply based on local legal and/or educational requirements. Refer to local job documentation where applicable.
About CSL Behring
CSL Behring is a global biotherapeutics leader driven by our promise to save lives. Focused on serving patients’ needs by using the latest technologies, we discover, develop and deliver innovative therapies for people living with conditions in the immunology, hematology, cardiovascular and metabolic, respiratory, and transplant therapeutic areas. We use three strategic scientific platforms of plasma fractionation, recombinant protein technology, and cell and gene therapy to support continued innovation and continually refine ways in which products can address unmet medical needs and help patients lead full lives.
CSL Behring operates one of the world’s largest plasma collection networks, CSL Plasma. Our parent company, CSL, headquartered in Melbourne, Australia, employs 32,000 people, and delivers its lifesaving therapies to people in more than 100 countries.
At CSL, Inclusion and Belonging is at the core of our mission and who we are. It fuels our innovation day in and day out. By celebrating our differences and creating a culture of curiosity and empathy, we are able to better understand and connect with our patients and donors, foster strong relationships with our stakeholders, and sustain a diverse workforce that will move our company and industry into the future.
CSL is an Equal Opportunity Employer. If you are an individual with a disability and need a reasonable accommodation for any part of the application process, please visit https://www.csl.com/accessibility-statement.
CSL is a leading global biopharma company with a dynamic portfolio of lifesaving medicines, including those that treat haemophilia and immune deficiencies, vaccines to prevent influenza, and therapies in iron deficiency, dialysis and nephrology. Since our start in 1916, we have been driven by our promise to save lives using the latest technologies.
Today, CSL – including our businesses, CSL Behring, CSL Seqirus, and CSL Vifor – provides lifesaving products to patients in more than 100 countries and employs 29,000+ people. Our unique combination of commercial strength, R&D focus and operational excellence enables us to identify, develop and deliver innovations so our patients can live life to the fullest.
See our community guidelines: https://bit.ly/3Bs17Ra
Offices: 655 Elizabeth St, Melbourne, Victoria 3000, AU · 1020 1st Ave, King of Prussia, PA 19406, US
Complex biologicalsvaccinesplasma and plasma derived therapeuticsbiotechnologyand biopharmaHealth DiagnosticsHealth CareBiotechnologyMedical
Based on 3912 listings with disclosed salaries, most manufacturing jobs in Illinois pay between $68k–$153k per year. Individual offers vary with seniority, company size, and specialization.
How many Manufacturing jobs are open in Illinois right now?
There are currently 11,439 open manufacturing positions in Illinois listed on Clera. New openings are added daily as companies post roles.
Which companies are hiring for Manufacturing roles in Illinois?
Companies currently hiring include Caterpillar Inc., Allergan, RJW Logistics Group, Northrop Grumman, Kraft Heinz, among others. Browse the listings above to see every active employer.
Are there remote or hybrid Manufacturing jobs in Illinois?
Yes — 1065 of the 11439 open manufacturing positions offer remote or hybrid work (257 remote, 808 hybrid).
How do I apply for Manufacturing jobs in Illinois?
Each listing links directly to the employer's application page. Apply early — fresh listings get the most recruiter attention in the first two weeks.