Supervisor, Quality Control Position Available In [Unknown county], South Carolina

Supervisor, Quality Control
Employer
CSL
Location
Union, SC
Start date
May 2, 2025
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Company

Job Details Responsibilities:

1 Supervises and trains the Quality Inspectors to ensure inspection and testing is executed efficiently and in compliance with CSL procedures and industry regulations. Maintains department schedule to support operational needs. Maintains and manages the stock of supplies within budget.2 Evaluates current test methods for improvement opportunities. Develops new test methods for compliance withupdates to regulations, standards and changes in equipment.3 Assists with validations and qualifications, DOE’s and other activities that determine the systematic suitability of aproduct.4 Monitors and regularly supervises the group to ensure process and procedural adherence. Responsible for annualperformance reviews.5 Processes product complaint investigations to include tracking, evaluation/investigation, probable/root causedetermination and documenting of correction/corrective action assessment.6 Evaluates and assists with deviations and the initiation of Rick / Impact Assessments and required escalationsfor related CAPAs.7 Conducts data analysis and utilizes reporting tools with ability to present data and results in a comprehensive,detailed, and organized fashion.8 Generates daily, weekly, and monthly trending reports as required.9 Provide input to the risk management process for updates to documentation and any pFMEAs.10 Participates or supports as necessary in Key Customer Audits to ensure highest level of total customer satisfaction and may be required to travel to Key Customer facilities.11 Escalates complaints/product performance issues to Management as required.12 Participates and supports process, policy improvements, and guidance for enhancement projects such as Leanprojects, supporting action items, and the revision of Standard Operating Procedures (SOP’s) and work instructions(WI).13

Supervisory Responsibilities:

Carries out supervisory responsibilities in accordance with the organization’s policies and applicable laws. Responsibilities include interviewing, hiring, training and developing employees; planning,assigning and directing work; appraising performance; rewarding and disciplining employees; addressing complaintsand resolving problems.14 Perform job-related duties as assigned.

JOB SPECIFICATIONSEducation
Bachelor Degree in a relevant scientific discipline (Biology, Chemistry, etc.) preferred Experience
Three (3)+ year’s supervisory and/or demonstrated leadership experience in Quality Control and
sampling in a FDA regulated industry
Knowledge of test methods, method validation, Good Documentation Practices
Strong understanding of cGMPs and procedure/process knowledge
Must be skilled and competent with Microsoft Office, computer knowledge or experience with document control software and enterprise resource planning software
Strong organizational skills and attention to details to handle multiple tasks, short deadlines, frequent interruptions and shifting priorities in support of changing company objectives Strong leadership, written and verbal communication, interpersonal and presentation skills to drive
results. May be required to lead teams without the benefit of a direct reporting relationship
Establish solid working relationships to interface with and support leadership, third parties and other
positions and circumstances within the organization
Excellent customer service orientation with flexibility and adaptability to respond quickly to changes
as required by the business operations
Maintain a professional demeanor and handle confidential information with discretion Additional Comments
N/A Working Conditions (physical & mental requirements)
Sit; use hands to finger, handle, or feel objects, tools, or controls
Stand; walk; reach with hands and arms; and stoop, kneel, crouch, or crawl
Shares information with internal contacts with common desire to reach a solution
Understands complex problems to collaborate and explore alternative solutions
Ability to make decisions which have moderate impact on immediate work unit
Ability to compose letters, outlines, memorandum and basic reports and/or to orally communicate technical information
Ability to compute, analyze and interpret numerical data for reporting purposes
Occasionally exposed to hazardous chemicals
Occasionally required to wear personal protective equipment
Exposure to moving mechanical parts, vibration and/or moderate noise levels
Ability to life or carry up to 30 lbs.
Work in fast paced environment with frequent interruptions

Note:

All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, disability, veteran status, national origin or other legally protected classifications Our Benefits CSL offers the following benefits for this full-time position: Options for health care benefits, including choices of plans for medical, dental, and vision, prescription drug coverage; Company-provided basic life insurance and Short- and Long-Term Disability; the option to participate in CSL’s 401(k) Savings Program; Paid Time Off (PTO) for use in connection with vacations, illness, and other personal business; and paid observed holidays as designated by the Company. For more information on CSL Plasma benefits visit cslbenefits/cslp. About CSLPlasma CSL Plasma is one of the world’s largest collectors of human plasma. Our work helps to ensure that people with rare and serious diseases are able to live normal, healthy lives. We are committed to our work because lives depend on us. Learn more about CSL Plasma. We want CSL to reflect the world around us As a global organization with employees in 35+ countries, CSL embraces inclusion and belonging. Learn more about Inclusion & Belonging at CSL. Do work that matters at CSL Plasma!
Company CSL is a global biotechnology company with a dynamic portfolio of lifesaving medicines, including those that treat hemophilia and immune deficiencies, vaccines to prevent influenza, and therapies in iron deficiency 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 three businesses, CSL Behring, CSL Seqirus and CSL Vifor – provides lifesaving products to patients in more than 100 countries and employs 32,000 people. Areas of Expertise We focus and demonstrate global leadership in three distinct areas—rare and serious diseases; influenza vaccines; and iron deficiency and nephrology. Rare & Serious Diseases 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. Vaccines 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. CSL Seqirus utilizes egg, cell and adjuvant technologies to offer a broad portfolio of differentiated influenza vaccines in more than 20 countries. Iron Deficiency & Nephrology With our iron deficiency and iron deficiency anemia expertise in heart failure, kidney disease, gastroenterology or inflammatory bowel disease, patient blood management and women’s health, we help patients affected by these conditions to live better, healthier lives. Company info
Phone
610-878-4000
Location
1020 First Avenue
King of Prussia
Pennsylvania
19406
United States