assurance specialist

PharmEng Technology

<div>
 
 About The Job Quality Assurance Specialist
 
 
 
 
 Quality Assurance Specialist
 
 
 
 
 Washington, DC
 
 
 
 
 Contract
 
 
 
 
 Job Description
 
 
 
 Experience: 2-3 years in Quality Assurance (QA) or a strong background in process/manufacturing
 
 
 Industry: Pharmaceutical, GMP environment
 
 
 
 Responsibilities
 
 
 
 Manage documentation processes to ensure compliance with Good Manufacturing Practices (GMP)
 
 
 Handle Corrective and Preventive Actions (CAPA), change control, and deviation management
 
 
 Develop and maintain controlled environments and ensure compliance with industry standards
 
 
 Support the client in managing and streamlining documentation to enhance efficiency and compliance
 
 
 Work towards reducing on-site quality documentation by 80%Collaborate with cross-functional teams to ensure consistent quality standards
 
 
 
 Skills and Qualifications:
 
 2-3 years of experience in Quality Assurance or a strong background in process/manufacturing within the pharmaceutical industry
 
 
 Expertise in documentation management, CAPA, change control, deviations, and complianceStrong understanding of GMP regulations and standards
 
 
 Excellent attention to detail and problem-solving skills
 
 
 Ability to work effectively in a controlled environment
 
 
 Strong communication and interpersonal skills
 
 
 
 Key Objectives
 
 
 
 Reduce 80% of on-site quality documentation
 
 
 Streamline processes to enhance efficiency and compliance
 
 
 Support Client in documentation management
</div>

Quality Assurance Specialist

Addison Group

<div>
 
 
 Title:
 
 QA (Quality Assurance) Specialist
 
 
 
 Location:
 
 Hybrid in Itasca, Illinois
 
 
 
 Compensation:
 
 $70,000
 
 
 
 
 
 Our client is seeking a Quality Assurance Specialist to join their team! The QA Specialist will be responsible for monitoring Quality Assurance standards and ensuring all industry specific protocols and procedures are compliant and properly carried out.
 
 
 
 
 
 
 Responsibilities:
 
 
 
 &middot; Evaluate/approve new products as warranted
 
 
 &middot; Participate in the development of new products and reformulations of existing products
 
 
 &middot; Establish product monitoring programs for assigned categories
 
 
 &middot; Monitor products for assigned categories for compliance
 
 
 &middot; Prepare and participate in competitive product reviews
 
 
 &middot; Write/maintain/update product specifications
 
 
 &middot; Capture Brand Standard Intelligence via Product Monitoring protocol and competitive shopping evaluations
 
 
 &middot; Gather/track/update/store information per established guidelines
 
 
 &middot; Manage withdrawal/recall situations to gather information needed by the Regulatory team
 
 
 &middot; Apply superior knowledge during product investigations and problem-solving circumstances, following up to closure
 
 
 &middot; Provide technical expertise and product knowledge to internal and external customers
 
 
 &middot; Provide back-up to Senior QA Specialists
 
 
 &middot; Evaluate/approve new supplier facilities
 
 
 &middot; Manage vendors related to assigned categories
 
 
 &middot; All other duties as assigned
 
 
 
 
 
 
 
 
 
 
 
 
 
 This position is eligible for Medical, Dental, Vision, 401(k).
 
 
 
</div>

STARS Behavioral Health Group

<div><h1 class="jobSectionHeader">Partner with us in making a positive change!</h1>
Join a team where your work truly matters. We're proud to have been certified as a Great Place to Work for 8 years by our own employees. We invite you to partner with us in our mission to improve mental healthcare.
Job Title:
Quality Assurance Specialist
Division/Program:
Olive View Crisis residential Treatment - Central Star
Starting Compensation:
23.00-25.00 USD Per Hour
Working Location:
Sylmar, CA
Working Hours/Shift:
Sunday-Thursday 8am-4:30pm
Why Join Our Team?<ul><li>
Competitive Compensation: Offering a salary that matches your skills and experience.</li><li>
Generous Time Off: Enjoy ample vacation and holiday pay.</li><li>
Comprehensive Benefits Package:</li><li><ul><li>
Employer-paid medical, dental, and vision coverage.</li><li>
Additional voluntary benefits to support your lifestyle.</li></ul></li><li>
Professional Growth Opportunities:</li><li><ul><li>
On-the-job training with access to paid CEU opportunities.</li><li>
Career development programs designed to help you grow.</li><li>
Supervision for BBS hours for AMFT, ACSW, and APCC professionals (where applicable).</li></ul></li></ul>
Employee Recognition &amp; Rewards: A culture that celebrates and rewards your hard work and dedication<div><div><div>
What you bring to SBHG (qualifications):<ul><li>
Bachelor&rsquo;s degree in Quality Improvement/Quality Assurance, human services, psychology, or related social science field, or LVN license.
</li><li>Two (2) years of experience in the mental health field or a QA position required, preferably in in-patient setting.</li><li>
Two (2) years of experience in QA/TQM preferred.
</li><li>One (1) year experience in LACDMH clinical documentation preferred.</li><li>
Must possess a valid CA driver's license and maintain a driving record that meets the company driver eligibility policy.</li></ul>
How you will make a difference:
The Quality Assurance Specialist is responsible for the aiding the QA Manager in the execution of the quality assurance program policies and procedures for the Crisis Residential Treatment facilities. The position is responsible for auditing documentation to reconcile with billing and oversees documentation of services by staff to assure conformity with Medi-Cal, Los Angeles County DMH, other outside agencies, and internal standards and policies. The Quality Assurance Specialist manages all charts with deficiencies by processing them to the appropriate department for correction. The position is also responsible for ensuring the discharged chart is closed in the correct order and completed. Position aids the QA Manager in the oversight of the Continuous Quality Assurance program, medical records and records all CQI data. Assists in the coordination and development of CQI presentations and information gathering to execute presentations as needed. Activities performed can be time sensitive with expectations of frequent reporting of progress along with thorough oversight for accuracy. Regular interaction with all staff members, physicians, and outside agencies is expected. This position has responsibility for gathering and analyzing agency data and assisting in the agency&rsquo;s quality control, quality assurance, and quality improvement efforts. In addition, the Quality Assurance Specialist&rsquo;s duties will include but are not limited to ensuring that the chart documentation is maintained, data collection into the L.A. County data collection sites is maintained and other quality improvement tasks as assigned.
Division/Program Overview:
<ul><li>16-bed facilities</li><li>
Designed for adults with mental health challenges or a recent crisis who need intensive treatment.</li><li>
24/7 programs as an alternative to urgent care or hospitalization.</li><li>
Individuals can live on-site in a homelike setting for a short term while they receive counseling and learn basic living and interpersonal skills.</li><li>
Able to receive physical and psychological evaluation, mental health, and case management services, in addition to assistance locating permanent housing.</li></ul></div></div></div>
Learn more about SBHG at: https://www.starsinc.com/stars-inc/
For Additional Information:
samlopez@starsinc.com
In accordance with California law, the grade for this position is 24.84 - 39.74. Placement within the grade is determined based on experience, internal equity, and other factors permitted by law.</div>

DeepHealth

<div>
 
 Job Description
 
 
 
 
 Job Title: Quality Assurance Specialist - US&Acirc;
 
 
 
 
 Reports to: Head of Quality &amp; Regulatory
 
 
 
 
 FLSA Status: Exempt
 
 
 
 
 Job Summary
 
 
 
 The Quality Assurance Principal is responsible for supporting DeepHealth products and product development, along with the Quality Management System throughout the organization. The Quality Assurance Principal will be responsible for collaborating cross-functionally to support and guide product development. The Quality Assurance Principal will work cross-functionally and within the team to support the Quality processes, such as QMS training, complaint and CAPA management.&Acirc;
 
 
 
 Essential Duties And Responsibilities
 
 
 
 As the Quality Assurance Principal, this position will:&Acirc;
 
 
 <ul>
 <li>
 Actively engage cross-functionally within the organization, such as with the Engineering, Clinical and Marketing teams, to develop new products within the Product Lifecycle Management (PLM) and New Product Introduction (NPI) processes.&Acirc;
 </li>
 <li>
 Act as the Quality lead for design changes to existing DeepHealth products, including non-medical devices, to ensure compliance with the applicable standards and guidances.&Acirc;
 </li>
 <li>
 Guide junior Quality Assurance team members to ensure consistent implementation of Quality processes, including design control and risk management.&Acirc;
 </li>
 <li>
 Take ownership of product specific Quality Management System processes, such as CAPAs and complaint management, across the organization to ensure compliance and drive efficiency.
 </li>
 <li>
 Work cross-functionally to integrate products as a result of corporate and/or product acquisitions.&Acirc;
 </li>
 <li>
 Work as a team member with the Quality Assurance team to ensure compliance to US and OUS standards and regulations.&Acirc;
 </li>
 <li>
 Participate in the development of junior staff, as requested&Acirc;
 </li>
 <li>
 Collect/monitor quality metrics in support of Management Review&Acirc;
 
 
 </li>
 </ul>
 
 PLEASE NOTE: This is not an exhaustive list of all duties, responsibilities and requirements of the position described above. Other functions may be assigned and management retains the right to add or change duties at any time.
 
 
 
 
 Minimum Qualifications, Education And Experience
 
 
 
 <ul>
 <li>
 Bachelor's degree in relevant field (or equivalent experience, i.e. Associate's degree with 5 years of experience).&Acirc;
 </li>
 <li>
 Minimum of -10 working in a regulated industry (FDA and Software as a Medical Device preferred).&Acirc;
 </li>
 <li>
 Strong knowledge of FDA Quality System Regulations, including but not limited to, 21 CFR 11, and 21 CFR 820.&Acirc;
 </li>
 <li>
 Knowledge of EU Medical Device Regulation (MDR), ISO13485, ISO 14971, and IEC 62304 preferred.&Acirc;
 </li>
 <li>
 Knowledge and understanding of pre- and post- market clinical studies, including but not limited to, 21 CFR 812, 21 CFR 50, and 21 CFR 56, preferred but not required.&Acirc;
 </li>
 <li>
 Participation in regulatory audits a plus&Acirc;
 </li>
 <li>
 Excellent written and oral communication skills&Acirc;
 
 
 </li>
 </ul>
 
 Physical Demands
 
 
 
 This position often requires sitting, standing, walking, bending, twisting, reaching with hands and arms, using hands and fingers, handling, or feeling, speaking, listening, and high-level cognitive thinking. Also, must be able to lift up to 10 pounds occasionally. The position requires the ability to travel (~10% of time), drive a vehicle, and utilize other forms of transportation.&Acirc;
 
 
 
 Working Environment
 
 
 
 Remote. This position requires domestic / international travel up to 15%.
 
 
 
 ACCOMMODATIONS
 
 
 
 Reasonable accommodations may be made to enable people with disabilities to perform the essential functions of the job.
 
 
 
 Pay Range
 
 
 
 USD $98,000.00 - USD $120,000.00 /Yr.
</div>

Serenity C & C, Inc.

We are seeking a Quality Assurance (QA) Specialist with experience in the mental health field to ensure our organization meets compliance standards, improves service delivery, and maintains the highest level of care for our clients. The ideal candidate will have a strong background in quality control, compliance, and regulatory requirements within mental health services.Key Responsibilities:<ul><li>Monitor and evaluate the quality of mental health services provided.</li><li>Ensure compliance with state, federal, and accreditation regulations (e.g., HIPAA, Joint Commission).</li><li>Develop and implement quality improvement plans to enhance service delivery.</li><li>Conduct audits and risk assessments to identify areas for improvement.</li><li>Train staff on best practices, policies, and compliance requirements.</li><li>Analyze data and report findings to leadership for continuous improvement.</li><li>Investigate and resolve client complaints related to service quality.</li></ul>Qualifications:<ul><li>Bachelor&rsquo;s or Master&rsquo;s degree in psychology, social work, healthcare administration, or a related field.</li><li>Experience in quality assurance, compliance, or auditing within the mental health field.</li><li>Knowledge of mental health regulations, Medicaid/Medicare policies, and accreditation standards.</li><li>Strong analytical, communication, and problem-solving skills.</li></ul>Pay: From $45,000.00 per yearBenefits:<ul><li>401(k)</li><li>401(k) matching</li><li>Dental insurance</li><li>Health insurance</li><li>Life insurance</li><li>Paid time off</li><li>Tuition reimbursement</li></ul>Work Location: In person

bastion technologies

<div>The Quality Assurance Specialist will support the space program in the MSFC Safety Mission Assurance Booster Resident Office at Kennedy Space Center in Merritt Island, FL. 
RESPONSIBILITIES:<ul><li>
Provide support on all quality areas to include Quality Plans, Surveillance Plans, Inspection Instructions, First Article Inspections, and Nonconformance resolutions.</li><li>
Provide technical reviews for assurance of quality requirements compliance during hardware production and manufacturing processes.</li><li>
Perform process surveillance using witnessing/monitoring techniques and verify test result/documentation of raw materials, components, and sub-assemblies per approved inspection documents/specification requirements.</li><li>
Maintain current, company and customer training and certifications to maintain a quality inspection stamp and meet stamp warranty expectations.</li><li>
Work with company and customer personnel to resolve inspection questions and communicate technical issues to project engineers to ensure compliance with final product specification requirements.</li><li>
Perform accurate mechanical, physical, and visual inspections, monitor and/or perform nondestructive test/evaluation, perform process surveillance using witnessing/monitoring techniques and verify test result/documentation of raw materials, components, and sub-assemblies per approved inspection documents/specification requirements.</li><li>
Knowledge of higher-level quality assurance (ISO/AS) system requirement documents and can interpret and apply QA system level requirements while performing all quality assurance duties.</li><li>
May be required to initiate corrective action reports, document/report inspection results and monitor corrective actions implementation for effectiveness.</li><li>
Maintain current, company and customer training and certifications. Specifically, SMA STEP 1 and NDE Level II certifications.</li><li>
Work as part of an integrated team with Bastion Technologies and NASA SMA personnel to resolve surveillance and examination result questions and communicate technical issues to project engineers to ensure compliance.</li>
Other duties as assigned. 
<li>
</li></ul> 
REQUIRED:
This position has been posted at multiple levels (must meet minimum level indicated). Depending on the candidate's experience, requirements, and business needs, we reserve the right to consider candidates at any level for which this position has been advertised. 
<ul><li>
This position requires US Citizenship due to the sensitivity of customer related information.</li><li>
Must have a High School or equivalent .</li><li>
Must have 10+ years of recent and related work experience.</li><li>
Possess the ability to read blueprints, technical charts, and specification sheets.</li><li>
Possess the ability to prepare written documentation of inspection results using company/customer forms or software.</li><li>
Must be knowledgeable in AS9100 and ISO 9001 Quality System Requirements.</li><li>
Candidates should be comfortable with adapting to changing environments (work assignments, customers) quickly in support of the mission.</li><li>
Candidate must be willing to perform Inspection/Witness of Vendors hardware, as well as perform General QA Inspection and surveillance as normal day-to-day operations.</li></ul> 
DESIRED:<ul><li>
The ideal candidate will have a familiarity with NASA Quality Systems and procedures.</li><li>
Knowledge of KSC/VAB and/or Launch Vehicle manufacturing and/or aerospace related experience.</li><li>
Multiple of the following certifications: Ultrasonic Testing (UT), Penetrant Testing (PT) Magnetic Particle Testing (MT), Radiographic Testing (RT) and Eddy Current Testing (ET) minimum Level I desired.
</li><li>Previous experience working with aerospace flight critical hardware in an ESD/FOD sensitive environments, witnessing critical quality assurance and assembly operations of various components and complex assemblies.</li><li>
Mechanical Inspector with experience utilizing calipers, micrometers, optical measurement devices and other shop tools.
</li><li>Experience in creating written reports for inspections/S&amp;MA surveillance assignments.</li></ul> 
WORK LOCATION:
<ul><li>This position is located onsite; some travel may be required.</li><li>
Schedules are subject to change based on the requirements of the position and/or customer needs.</li><li>
This position will require periodic shift work and (paid) overtime.</li></ul> 
BACKGROUND INVESTIGATIONS REQUIRED:
All Bastion employees must be able to pass a national agency check and some positions require clearance and will require an extensive background verification/check process. 
DRUG AND ALCOHOL SCREENING REQUIRED:
All Bastion employees must be able to pass a pre-employment drug screen and are required to participate in periodic random drug and alcohol screenings. 
STANDARD BASTION REQUIREMENTS:<ul><li>
Must have experience with Microsoft Office Suite, Word, Excel, PowerPoint, TEAMS and SHAREPOINT.</li><li>
All of Bastion's employees must be team players with strong work ethics and must be culture oriented.</li><li>
Able to communicate effectively, verbally and in written form, with internal and external customers.</li><li>
Able to follow company programs, processes, procedures, practices, requirements, goals, and objectives.</li><li>
Must be organized with good time management skills and must be able to work outside normal schedule and adjust schedule to meet peak periods and surge requirements.</li><li>
Generally, an office environment, but can involve inside or outside work depending on the task.</li><li>
Work may involve sitting or standing for extended periods (90% of the time) and may require lifting and carrying up to 25 lbs. (5% of the time).</li><li>
Regular attendance in accordance with an established work schedule is critical.</li></ul> 
BASTION BENEFITS:
Bastion offers a wide range of benefits for their full-time employees; medical, prescription, dental, vision, AD&amp;D, disability benefits, life insurance, retirement 401k, vacation, sick pay, holidays, flexible work schedules (when available), along with many other options. We also support career advancement through professional training and development. 
ABOUT BASTION:
Bastion offers career opportunities with competitive benefits, exciting possibilities for advancement, and an exceptional work environment; the well-being of our employees is a priority, and our flexibility allows our employees a great work life balance. Our culture is based on strong business ethics, integrity, and professionalism. Our team members are known for their initiative and high-quality work. When it comes to our employees, we value, respect, and help them grow in their careers. 
WORKPLACE EXCELLENCE:
At Bastion, we are passionate about our people and our safety culture. Individual thoughts, opinions, and perspectives bring value and help us develop solutions for challenging problems, they make us more inventive, and more resilient. 
All qualified applicants will receive consideration for employment without regard to race, color, sex, sexual orientation, gender identity, religion, national origin, disability, veteran status, or other legally protected status. 
Bastion participates in e-Verify. 
#MidSeniorLevel 
#LI-Onsite 
BT-26056</div>

PROOF

<div>Location: Detroit, MI Full-Time IN PERSON 5 days/week

About Us 
We're Proof, a high growth company in the legal tech industry founded in 2017. Our best-in-class legal services platform is trusted by over 3,000 law firms across the U.S. and serves countless pro se parties. Our core offerings, Service of Process and E-Filing, are designed to make legal services more accessible, efficient, and transparent. We are on track to double our business again this year and are looking for dedicated, detail-oriented professionals to join our team as we continue to scale.

If you are passionate about transforming the legal industry and believe in making legal services more affordable and accessible to all, we invite you to join our mission-driven team.
<h3 class="jobSectionHeader">
Position Overview</h3>

We are seeking a Quality Assurance Specialist with a legal or paralegal background to support our team in the creation, editing, and preparation of affidavits of service and nonservice for law firms and pro se parties. This role is essential to ensuring legal compliance and the highest level of accuracy in our service of process and e-filing operations.

The ideal candidate will bring expertise in legal documentation, a keen attention to detail, and a thorough understanding of legal language, ensuring our affidavits are precise, compliant, and delivered on time. This is an excellent opportunity for individuals with legal assistant, paralegal, or law firm experience who thrive in fast-paced environments.
<h3 class="jobSectionHeader">
Key Responsibilities</h3>
<ul><li>Prepare and Edit Legal Affidavits: Draft, review, and edit service of process affidavits for accuracy, completeness, and legal compliance. Ensure all affidavits meet state and federal guidelines.</li>
<li>Quality Assurance: Conduct meticulous reviews of legal documents to ensure accuracy in spelling, grammar, and content.</li>
<li>Compliance Oversight: Ensure all documents are fully compliant with legal standards, including state-specific filing requirements and procedural guidelines.</li>
<li>E-Filing: Prepare and finalize certain affidavits for electronic filing, ensuring proper formatting and accuracy.</li>
<li>Collaboration: Work closely with legal teams, process servers, and other departments to maintain efficient workflows and meet deadlines.</li>
<li>Adaptability: Stay current with evolving legal procedures and process changes, adapting quickly to new technologies and methods.</li>
</ul><h3 class="jobSectionHeader">Qualifications</h3>
<ul><li>Legal/Paralegal Expertise: Prior experience working as a paralegal, legal assistant, or in a similar legal environment.</li>
<li>Document Drafting &amp; Review: Strong background in preparing, editing, and reviewing legal documents such as affidavits, legal briefs, or similar materials.</li>
<li>Compliance Knowledge: Familiarity with state and federal legal guidelines related to service of process and e-filing.</li>
<li>Attention to Detail: Exceptional editing and proofreading skills with a focus on accuracy and legal precision.</li>
<li>Organized &amp; Responsible: Demonstrated ability to manage multiple tasks with a high degree of organization and responsibility.</li>
<li>Professional Demeanor: Consistently professional, courteous, and responsive in all communications.</li>
<li>Critical Thinking: Ability to problem-solve and proactively address issues before escalation.</li>
<li>Education: Bachelor's degree or paralegal certification is preferred but not required.</li>
<li>Must be able to come into the downtown Detroit office 5 days per week.</li>
</ul><h3 class="jobSectionHeader">Compensation &amp; Benefits</h3>
<ul><li>Hourly Pay: $21 - $23 per hour, plus overtime, based on experience and location</li>
<li>Bonus Plan: Eligible to participate in the company bonus plan</li>
<li>Comprehensive Benefits: Medical, dental, vision, disability insurance, and 401(k) available</li>
<li>Flexible time off (paid planned and sick time, and paid holidays)</li>
<li>Workplace Equipment: Necessary equipment provided</li>
</ul>
E-Verify

This company participates in E-Verify, for more information view the Participation and Right to Work Posters. 
 
#LI-DNP</div>

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