Top 7 Quality assurance specialist Jobs in Dover, De

Quality Specialist
CSL Plasma —Dover, DE
- Full-time
- Customer service
- HIPAA
- Mid-level
Temporary Quality Assurance Specialist
HEALTHPLANONE, LLC —Dover, DE
- Full-time
- Spanish
- Microsoft Outlook
- Writing skills
- Health insurance
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- Computer Science
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- $23.90 - $35.85 an hour
- Full-time
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- 3 years
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Quality Assurance Specialist - Pharmaceuticals
WuXi AppTec —Middletown, DE
- 5 years
- Engineering
- Experience equivalent to degree accepted

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Quality Specialist

CSL Plasma -
Dover, DE

Apply Now

Job Details

Full-time

Qualifications

High school diploma or GED

Full Job Description

Entity: CSL Plasma

Job Category: Quality

Job Family: Plasma Center

Job Type: Full Time

Location: Dover, Delaware, United States

Employer Reference: R-280582

Job Description

The Opportunity

This position provides immediate support to the Assistant Manager of Quality in monitoring plasma center processes to ensure overall compliance with CSL Operating Procedures, as well as all applicable local, state, federal requirements. This role will ensure compliance to training needs, SOPs, processes and other regulatory or company directives are adhered in order to support the operations and quality requirements for business operations.

Reporting compliance status data to operational quality management
Collaborate with center management in the development and implementation of continuous improvement plans
Collaborate with Assistant Manager of Quality (AMQ), to be able to represent the center during internal and external audits, responds to questions, and may stop operations, including shipments to address quality concerns
Responsible for coordinating and managing training activities, policies and processes at the center level.

You will report to the Assistant Manager Quality

The Role

Perform final QA review and release for all shipment and associated documents, to ensure shipment meets customer specifications.
Ensure center records QA review to ensure thoroughness, accuracy and timeliness of required information. Initiate investigation and ensure documentation of regulatory deficiencies. Determine the need for corrective action, ensure appropriate documentation and determine effectiveness of the action.
Perform center records QA review to ensure thoroughness, accuracy and timeliness of required information. Initiate investigation and ensure documentation of regulatory deficiencies. Determine the need for corrective action, ensure appropriate documentation and determine effectiveness of the action.
Maintain and review Plasma center personnel training documents to ensure documents comply with CSL procedures, SOP’s, CLIA/COLA and other applicable requirements.
Maintain the Learning Management System to ensure data integrity, report generation and data analysis to comply with company and regulatory standards.
Initiates schedule, coordinate and monitor the delivery of all training, such as new hire, annual and any retraining to meet center or other training and regulatory requirements. Ensure the most current version of training materials at the center is being used
Collaborates with center management when viewing the Quality Management System to identify, coordinate and deliver retraining for the purpose of correcting or improving operational or quality issues.
Conduct periodic process assessments to ensure compliance of CSL written procedures. Initiate investigation to ensure documentation of deficiencies and development of corrective action plans, as necessary in partnership with management.
Identifying and communicate non-conformities to CSL’s SOP’s. In the absence of the AQM, may conduct monthly quality team meeting to inform, promote, assess and identify opportunities for continuous process improvement in quality, safety, and training for implementation.
Promote Safety, Health and Environment Policies & Procedure. Ensure safety training and safety practices are implemented and followed within the center.
Conducts and may lead internal audits to monitor facility compliance with CSL procedures and policies, cGMP, OHSA, FDA, and other regulations, as applicable, and develop center responses for deficiencies. In the absence of the AQM, host external audits conducted by the regulatory agencies and customers.
Responsible to initiate, investigate and close Trackwise reports in a timely manner. Confirm through follow-up, to ensure appropriate corrective action was initiated, implemented, and effective.
Maintain clean efficient work environment. Comply with all Health Safety and Environmental (HSE) and Occupational Safety and Health Administration (OSHA) policies and procedures. Conduct routine internal procedure and documentation audits, as applicable.
Follow all Standard Operating Procedures (SOPs), company policies and procedures.
Comply with all local, state and federal regulations and laws to include, but not limited to: ADA, Civil Rights, EEOC, FDA, GHA, HIPAA, and OSHA.
Maintain confidentiality of all personnel, donor and center information. Understand policies and procedures associated with hyperimmune programs at the center, if applicable.
Assist Plasma center staff in completing other special projects or assignments, as requested.
Perform other job-related duties, as assigned.dd 4-6 key responsibilities of the job

Your skills and experience

Education

High school diploma or equivalent required. Associate or Bachelor’s degree in business administration or biological sciences preferred.

Experience

Minimum 1-year leadership experience or equivalent of one-year experience in a regulated environment.
Strong customer service skills
Strong critical reasoning, decision-making and problem solving skills to analyze situations
Organizational skills and attention to details to handle multiple tasks, short deadlines, frequent interruptions, and shifting priorities in support of changing company objectives
Understand Quality Systems and/or regulated training requirements

Working Conditions

(physical & mental requirements)

Occasionally required to work with the public when they are dissatisfied
80% of the time standing and walking and 20% of the time sitting
Reach, bend, kneel and have high level of manual dexterity
See and speak with customers and observe equipment operation
Occasionally be required to lift and carry 25 lbs.
Exposure to hot and cold temperatures, sudden temperature changes, working with freezers and various odors

#VHP

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

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quality assurance specialist jobs in dover, de

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Job Description

About CSL Plasma

Our Benefits

You Belong at CSL

Equal Opportunity Employer

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