Quality Lead II Job at Airswift Sweden (Midland)

Director of Quality and Regulatory Affairs

The Director of Quality and Regulatory Affairs leads the global QA/RA function a...

Location

United States , Burlington

Salary:

170000.00 - 180000.00 USD / Year

Myomo

Expiration Date

Until further notice

Requirements

Bachelor’s degree in a scientific, technical, or related discipline
advanced degree preferred
8-10+ years of progressive experience in Quality Assurance and Regulatory Affairs within the medical device industry, including significant management experience
5+ years of experience with Class I and/or Class II medical devices
Experience operating within FDA-regulated cGMP environments, including regulatory submissions and agency interactions
Strong knowledge of FDA 21 CFR Part 820/QMSR, ISO 13485, EU MDR, ISO 14971, and Design Controls
Experience managing Quality Management Systems (QMS) for medical devices
Experience supporting global regulatory activities (e.g., EU, Canada, APAC preferred)
Demonstrated experience leading QA/RA teams, including talent development and performance management
RAC certification or equivalent is preferred

Job Responsibility

Lead the global QA/RA function and is responsible for execution of the company’s quality and regulatory strategy
Ensure compliance with applicable global regulations and standards (including FDA and ISO requirements) and oversees quality systems across the product lifecycle
Partner cross-functionally to support product development, regulatory submissions, and ongoing compliance activities, while driving continuous improvement in quality processes
Contribute to the development and lead execution of the Quality strategy
Lead departmental planning and budgeting, optimizing resources and operational efficiency
Direct QA/RA staff, including organizational design, talent development and performance management
Develop and continuously improve quality programs, policies, and processes
Ensure Quality Management System (QMS) processes are established, implemented, and maintained
Lead regulatory activities and compliance interactions, serving as the primary liaison with regulatory authorities
Oversee development and execution of global regulatory strategies for product submissions and lifecycle management

Fulltime

Quality Lead

Location

Brunei

Salary:

Not provided

Bureau Veritas Certification CZ, s.r.o.

Expiration Date

Until further notice

Requirements

HND/HNC in Mechanical Engineering or relevant discipline
IRCA Lead Auditor certified
CSWIP 3.1 + CSWIP/PCN Level 2 in Radiographic Interpretation
BGAS Grade 2 / NACE Level 2 Coating Inspector
Two additional NDT Level II qualifications (or “have had”)
Minimum 12 years QA/QC experience, including 6 years in a lead or senior role (10/5 for Bruneian development)

Job Responsibility

Lead the QA/QC function and oversee all quality personnel
Approve Quality Plans, ITPs, Surveillance Plans, and QA procedures
Lead audits, surveillance, and quality investigations
Ensure all inspection activities comply with QA/QC requirements and ISO 9001 / ISO 17020
Manage NCRs, corrective actions, and continuous improvement initiatives
Provide technical assurance for inspection reports and deliverables

Lead Quality Inspector

Reporting to the Quality Supervisor, you will be responsible for performing visu...

Location

United States , Houston

Salary:

65000.00 - 70000.00 USD / Year

Celeros Flow Technology

Expiration Date

Until further notice

Requirements

NACE Level II Coatings required
Supervisory experience required
Experienced in use of precision inspection equipment (ex., mics, callipers. Etc) to measure dimensional details as listed on drawings
Knowledge in reading & interpret blueprints, including GD&T
Experience in using and programming of Articulated ARMs is required
Knowledge of manufacturing processes and techniques, test equipment and procedures, and assembly applications
Use of hand and power tools
Strong computer skills including MS Office Suite skills, including Word, Excel, and Outlook
Experience with SAP (Required)
Ability to work in a team-oriented environment that is fast-paced and demanding

Job Responsibility

Performing visual, mechanical inspection of purchased or manufactured parts, in process or finished, to determine if the parts conform to specifications, drawings, designated codes and standards
Using precision measuring and testing equipment, including calipers, height gage, micrometre’s, surface plate, Articulated ARM, Optical Comparator to perform mechanical inspections
Preparing a Non-Conformance Report (NCR) for any part that does not meet specified requirements and processing it per established procedures
Document nonconformances in SAP- NCR module where needed and complete the transactions in SAP
Review and verification of materials received from vendors
Witnessing internal testing procedures to verify accuracy of results
Interpreting and executing an Inspection and Test Plan (ITP)
Interfacing with third-party inspectors to verify completion of required customer requests
Handling other assigned work-related functions as deemed necessary and appropriate by your immediate supervisor
Provide on-the-job training and guidance to Level I inspection personnel

What we offer

Health Insurance (effective on start date)
Dental/Vision (effective on start date)
Flexible Spending Accounts/Health Savings Accounts
Life Insurance/Disability/Accident/Critical Illness
401(k) Savings Plan with generous company match
Tuition Reimbursement
Paid time off/Generous Holiday Schedule

Fulltime

Quality Assurance Engineer II

Join our Business Operations team as a Quality Assurance Engineer II, where you'...

Location

United States , Lincoln, NE or Omaha, NE

Salary:

80000.00 - 110000.00 USD / Year

EdTech Jobs

Expiration Date

Until further notice

Requirements

2+ years of software testing experience
Experience in fast-paced environments with changing deadlines
Solid experience designing and executing tests across the stack (front-end UI validation to API testing)
Proficiency with key languages (e.g. Python, Typescript)
Experience with modern automation frameworks (e.g. Playwright, Selenium)
Naturally curious problem solver
Effective team player within a global team
Leading with empathy and clear communication

Job Responsibility

Champion quality and prevention in every scrum ceremony
Own quality strategy and testing
Create comprehensive test plans
Use data to drive high-quality projects
Lead initiatives that level up the quality mindset across the entire squad
Automate processes aligning with development speed
Make informed decisions on what, how, and when to automate

What we offer

Flexible vacation time
Company-wide holidays and timeout (meeting-free) days
Remote work options
Open, honest culture with trust and autonomy
Tons of resources and opportunities for professional development
Tech stack and hardware provided
Employee Assistance Program
Employee resource groups
Fitness partner Peerfit
Medical insurance with vision, dental, fertility healthcare and family forming benefits

Fulltime

New

Immunology Tech I

At Boston Children’s Hospital, the quality of our care – and our inclusive hospi...

Location

United States , Boston

Salary:

18.34 - 25.90 USD / Hour

Boston Children's Hospital

Expiration Date

Until further notice

Requirements

Performs skin testing and pulmonary function testing for outpatient clinic patients
Instructs patients in the use of study medications, diaries, and study procedures
Explains to patients and parents allergy environmental control measures
Guides patients through the Allergy Immunology Program
Monitors quality control of clinical procedures and/or assessments
Assists with clinical research studies
Conducts preliminary telephone interviews to explain procedures and eligibility requirements
Schedules study patients after obtaining pertinent demographic data and assists with study patient visits
Works together with all program staff to ensure highest quality service
Communicates issues to Tech II, Lead Technician and/or Practice Administrator

Job Responsibility

Performs skin testing and pulmonary function testing for outpatient clinic patients
Instructs patients in the use of study medications, diaries, and study procedures
Explains to patients and parents allergy environmental control measures
Guides patients through the Allergy Immunology Program
Monitors quality control of clinical procedures and/or assessments
Assists with clinical research studies
Conducts preliminary telephone interviews
Schedules study patients
Works together with all program staff
Communicates issues to Tech II, Lead Technician and/or Practice Administrator

What we offer

flexible schedules
affordable health, vision and dental insurance
child care and student loan subsidies
generous levels of time off
403(b) Retirement Savings plan
Pension
Tuition and certain License and Certification Reimbursement
cell phone plan discounts
discounted rates on T-passes

Fulltime

Data Analyst Quality Assurance Lead

The Data Analyst/Quality Assurance Lead performs data collection and analysis fo...

Location

United States , Las Vegas

Salary:

95000.00 - 105000.00 USD / Year

Arcata Associates, Inc

Expiration Date

Until further notice

Requirements

Bachelor's Degree in a Quality Assurance, Technical discipline, Business Administration, Management or related discipline
At least four years of related experience
In lieu of a bachelor's degree, a combination of formal education and technical experience is acceptable
Experience with quality methodology, analytical concepts and applications are preferred
American Society of Quality (ASQ) Auditor Certification preferred
must be obtained within the 6-month probationary period if selected candidate does not possess certification
Excellent interpersonal skills and proven ability to communicate effectively in both oral and written form
Highly skilled in the use of a PC and PC-based business applications software such as Microsoft Office, specifically Word, PowerPoint and Excel
Strong planning, organization, data analysis, data management and problem-solving skills are required
Demonstrated skill, knowledge, and technical competence in the reading and interpretation of schematics, plans, manufacturer's manuals, Government procedural documents, management reports, and other similar documents

Job Responsibility

Creates and distributes Quality Metrics (i.e. report cards) to be used in tracking Annex 2 trends for major departments
Acts as the Critical Spares Program Administrator, coordinating and compiling departmental inputs on behalf of the Critical Spares Program
Provides oversight to the QA staff assigned to the Business Operations department as directed by the DM/QA Supervisor
Provides oversight of the Technical Order Distribution Office (TODO) duties performed by the QA department for Technical Orders (TOs), Time Compliance Technical Orders (TCTOs), and Computer Program Identification Numbers (CPINs)
Provide oversight of the ETool Program in conjunction with the IT department and the QA Lead TODO
Continually review the processes governing all aspects of the J-Tech II Annex 2 Quality Management System providing recommendations to management on opportunities to improve the current business model
Reviews the applicable sections of the J-Tech II contract, contract modifications, and external related documents to ensure new requirements are identified and included in the Quality Management System
Performs inspections of equipment, systems, and services required of the QA Department
Performs audits required of the J-Tech contract and perform JT4 Corporate Management audits as assigned
Maintains audit/inspection documentation and records IAW with JT4/Annex 2 practices

What we offer

Medical, Dental, Vision, and much more

Fulltime

911 Dispatch Supervisor

Individuals in this position supervise and direct subordinate staff. Tasks inclu...

Location

United States , Frisco

Salary:

87436.00 - 104923.00 USD / Year

Summit County, CO

Expiration Date

Until further notice

Requirements

High school graduate or equivalent
Minimum three (3) years of 911 dispatching experience
two years of relevant supervisory experience preferred
Working knowledge of law enforcement, fire, and EMS procedures and practices
thorough knowledge of computer systems and their application to Public Safety Communications
EMD, CPR, NIMS, CBI certifications
Successful completion of APCO Supervisory course within the first year of employment
Meets or exceeds all requirements for subordinate levels (Dispatcher I, Dispatcher II, Dispatch Lead)
Knowledge of basic supervisory and employee management principles
Ability to think analytically and apply sound judgement, solve problems, make effective decisions, and act with integrity

Job Responsibility

Supervise and direct subordinate staff
Assign and delegate work projects
Schedule employees to ensure proper staffing levels
Ensure standards of service are maintained in accordance with national standards and the mission and vision of the Summit County 911 Center
Responsible for performance management, including: work performance, coaching, mentoring, and implementing corrective action
Perform the duties of a 911 dispatcher as required
General supervision of assigned employees and daily oversight of dispatchers on the supervisor’s shift
Participate in hiring and training dispatchers
Make disciplinary decisions and initiate disciplinary actions
evaluate performance of dispatchers

Fulltime

Manager II Quality Assurance Solutions

As the Manager II, Quality Assurance - Solutions, you will lead all aspects of D...

Location

United States , Cleveland

Salary:

136000.00 - 170000.00 USD / Year

Baxter

Expiration Date

Until further notice

Requirements

Bachelor’s degree in Microbiology, Biology, Chemistry, or Engineering, or equivalent experience, required
5+ years of Engineering/Manufacturing/Quality experience required, with 3-5 years of leadership experience
FDA regulated manufacturing experience preferred
Six Sigma Green Belt Certification or industry-standard equivalent preferred
Project Management skills and experience are preferred
Experience and skills in Lean Manufacturing are preferred

Job Responsibility

Lead quality oversight for the Devices areas
Develop, assign, and implement systems, procedures, and policies to ensure compliance with ISO Standards, cGMP's, FDA regulations, and company policies
Conduct audits and implement changes to specifications, SOPs, and forms for regulatory compliance and process improvement
Ensure product compliance through established inspection criteria and procedures
Coordinate inspection activities throughout the production cycle
Analyze statistical data and product specifications to determine and improve quality standards
Prepare and submit reports to Managers and other Departments or Agencies as required
Communicate quality philosophy to key personnel
Actively participate in quality management teams within the organization
Manage and support area associates, encouraging a teamwork environment

What we offer

Support for Parents
Continuing Education/ Professional Development
Employee Heath & Well-Being Benefits
Paid Time Off
2 Days a Year to Volunteer
Medical and dental coverage that start on day one
Insurance coverage for basic life, accident, short-term and long-term disability, and business travel accident insurance
Employee Stock Purchase Plan (ESPP)
401(k) Retirement Savings Plan (RSP)
Flexible Spending Accounts

Fulltime

Quality Lead II

Airswift Sweden

Location:
United States , Midland

Category:
Energy

Contract Type:
Not provided

Salary:

Job Description:

Job Responsibility:

Requirements:

Nice to have:

Additional Information:

Job Posted:
January 06, 2026

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