Top 16 Quality manager Jobs in Nixa, Mo

Assistant Manager of Quality
CSL Plasma —Springfield, MO
- Full-time
- 5 years
- Mid-level
- Clinic
Quality Manager - Springfield Remanufacturing Corp
SRC Holdings Corp. —Springfield, MO
- Management
- 5 years
- Engineering
- Paid holidays
- Health insurance
Quick Apply
Director of Corporate Quality
DIGITAL MONITORING PRODUCTS —Springfield, MO
- Full-time
- Engineering
- Analysis skills
- Manufacturing
- Paid holidays
- Disability insurance
Quality Assurance Manager, MT
LinkOne Ingredient Solutions —Springfield, MO
- $70,000 - $82,000 a year
- Weekends as needed
- Microsoft Excel
- Up to 50% travel
- 5 years
Quick Apply
Manufacturing Quality Supervisor
Central States Industrial —Springfield, MO
- $29 - $34 an hour
- Full-time
- Mid-level
- US work authorization
- Leadership
- Health insurance
- Paid time off
Supervisor, Quality Control
Curia —Springfield, MO
- Online Application
- Background check
- 5 years
- Pass drug screening
- Paid training
- Paid holidays
2d
Contractor Quality Assurance/Control Supervisor - Landfill Construction/Cap Construction
Ayuda Companies —United States
- $90,000 - $120,000 a year
- Full-time
- Background check
- Construction site
- Pass drug screening
- Disability insurance
- Health insurance
Quick Apply
Nationwide QC Lead - Fiber Deployment
Advantage Tech —United States
- $42.87 - $51.63 an hour
- Full-time
- Construction site
- Travel
- Senior level
Quick Apply
Project Manager - Air Quality
SWCA Environmental Consultants —United States
- $102,047.40 - $134,152.20 a year
- Online Application
- Remote
- 7 years
- Bachelor of Science
- Engineering
- Profit sharing
- Health insurance

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Assistant Manager of Quality

CSL Plasma -
Springfield, MO

Apply Now

Job Details

Full-time

Qualifications

Supervising experience
Bachelor's degree
Legal compliance
Manufacturing company experience
Quality assurance experience within healthcare

Full Job Description

Entity: CSL Plasma

Job Category: Quality

Job Family: Plasma Center

Job Type: Full Time

Location: Springfield, Missouri, United States

Employer Reference: R-282554

Job Description

Responsibilities:• Ensure center is “inspection ready” at all times by managing adherence to Standard Operating Procedures (SOPs), compliance policies and the quality system, utilizing sound Quality principles, self-inspection learnings, non-conformity discovery and appropriate remediation. Prepare regular reports to center, area and corporate quality management as to the state of quality and systems at the center.• Manage site Quality Control program including but not limited to calibrations management, monitoring of compliance to defined processes e.g. sampling, competency checks, Key Performance Indicators (KPIs), trending and analysis of KPIs, root cause and failure mode impact assessment and change management.• Lead and develop direct reports ensuring they are competently skilled to perform their QA roles. Lead by example; consistently motivate staff through education to high levels of competency that drive success in a dynamic and regulated environment. Upon proper review with center and quality management, recruit, hire, conduct performance reviews and enact corrective actions, up to and including termination.• Participate with management to develop programs and methods to streamline center processes resulting in improved customer/donor service, product yields and financial results while maintaining compliance and quality.• Receive and provide feedback to staff on observations leading to improved adherence to GMP standards. Report concerns or deficiencies to area personnel and/or area management immediately. Make recommendations for remedial actions to resolve audit observations and other non-compliance issues of deficiencies.• Lead and function as the key quality representative for site supplier, customer and regulatory audits. Lead center review of findings, coordination of remediation (CAPA), if needed and successful closure of timely audits. Utilize quality tools and applications to facilitate understanding of issues and documentation.• Maintain clean efficient work environment and ensure sufficient operating supplies and availability of forms, as needed. Comply with all Health Safety and Environmental (HSE) and Occupational Safety and Health Administration (OSHA) policies and procedures. Conduct routine audits of internal procedures and documentation, as necessary. Promote safety in all actions.• Adhere to all HR policies and practices through fair and equitable treatment of all employees. Communicate effectively with HR to ensure HR compliance and ensure center management is doing the same.• Comply with all federal, state and local regulatory and company policies and procedures.• Responsible for notification to the ADOQ for any event that negatively affects the safety, quality, identity, purity or potency of the product that results in pausing or disruption of business. If necessary, notification must be elevated to any of the following, Regional Director, Associate Director of QA, Divisional Director or Director of Quality Systems and Assurance.• Maintain confidentiality of all personnel, donor and center information. Understand policies and procedures associated with hyper immune programs at the center if applicable.• Lead investigations into deviations to determine root cause, correction/preventative actions and effectiveness checks. Monitor CAPA’s and effectiveness checks to ensure issues are resolved.Qualifications:• Bachelor degree in scientific discipline/life sciences or related discipline• 5+ years' experience related to quality and regulatory/ Plasma industry experience• Demonstrated leadership/supervisory experience• Knowledge of government and industry regulationsDifferent qualifications or responsibilities may apply based on local legal and/or educational requirements. Refer to local job documentation where applicable.

About CSL Plasma

CSL Plasma operates one of the world's largest and most sophisticated plasma donation networks, with nearly 330 donation centers in the U.S. and Europe. CSL Plasma is a subsidiary of CSL, a global biopharma company. Plasma collected at CSL Plasma facilities is used by CSL for the sole purpose of manufacturing lifesaving plasma-derived therapies for people in more than 100 countries. The parent company, CSL (ASX:CSL; USOTC:CSLLY), headquartered in Melbourne, Australia, employs 29,000+ people. For more information about CSL Plasma visit, https://www.cslplasma.com/.

Our Benefits

For more information on CSL Plasma benefits visit https://cslbenefits.com/cslp.

You Belong at CSL

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.

To learn more visit https://www.csl.com/careers/inclusion-and-belonging

Equal Opportunity Employer

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.

Apply Now

Refine Your Search

quality manager jobs in nixa, mo

Assistant Manager of Quality

Quality Manager - Springfield Remanufacturing Corp

Director of Corporate Quality

Quality Assurance Manager, MT

Manufacturing Quality Supervisor

Supervisor, Quality Control

Contractor Quality Assurance/Control Supervisor - Landfill Construction/Cap Construction

Nationwide QC Lead - Fiber Deployment

Project Manager - Air Quality

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Job Description

About CSL Plasma

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Equal Opportunity Employer

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