Manager Quality Trauma Surgery Program (RN) / Department Of Surgery
Quality assurance manager job in Bridgeport, CT
Control # 4300600021
Work where every moment matters.
Every day, over 40,000 Hartford HealthCare colleagues come to work with one thing in common: Pride in what we do, knowing every moment matters here. We invite you to become part of Connecticut's most comprehensive healthcare network.
St. Vincent's Medical Center in Bridgeport has more than 3,200 employees. It includes a 473-bed community teaching hospital, a 76-bed inpatient psychiatric facility in Westport, a large multispecialty provider group, and special needs services for adults and children. St. Vincent's is the first hospital in Fairfield County to be integrated into the Hartford HealthCare network and is the system's second-largest hospital.
Job Summary
The Manager Quality Trauma Surgery Program provides leadership and operational support for the St. Vincent's Medical Center (SVMC) Trauma Program's (TP) development, implementation, and assessment to ensure an organized, effective, and efficient quality-focused, approach to providing high-quality trauma care. This position provides multiple services to include the coordination of TP initiatives between Trauma Program leaders, faculty, and HHC facilities, which includes clinical, educational, and research initiative collaboration and information sharing as relevant.
This position's continuum of involvement spans departmental, inter-hospital, system, community, state, and national interventions. In addition, this role involves frequent interaction and collaboration with a variety of stakeholders across the HHC System and non-HHC facilities at a variety of professional and clinical levels with an emphasis on high-quality customer service.
This position reports to Director of Clinical Operations, Inpatient Surgery with a substantial dyad of accountability to the Trauma Program Medical Director.
Essential Functions/Responsibilities
1. Promotes and operationalizes the goals and objectives of the trauma program to achieve its strategic vision for an integrated system. Establishes collaborative partnerships with all relevant parties characterized by vision, leadership and communication. Oversee and manages Trauma Quality Performance Team consisting of a Performance Improvement Nurse, Trauma Registrars, and Injury Prevention Coordinator. Acts as a departmental representative/collaborator with all Injury Prevention Center initiatives.
2. Champions and leads quality performance improvement/evaluation and patient safety efforts that ensure compliance with hospital/department rules and regulations, policies and procedures. Collaborates with other Quality and Safety colleagues/programs to inform planning at the SVMC hospital and System level. Coordinates and manages standing TP meetings, M&Ms, and multi-disciplinary M&M and PIP meetings.
3. Provides leadership in the design and implementation of a systematic process for monitoring, evaluating and improving the quality and effectiveness of trauma patient care. Identifies quality of care issues and brings to closure to ensure quality patient care. Ensures process includes data abstraction and verification, query design, statistical analysis, trending and reporting, to develop data sets into useful information to develop strategies for achieving improved outcomes.
4. Collaborate with and/or supervises appropriate personnel to implement, maintain and administer quality trauma databases and files according to QA protocols, HIPPA standards and legal/risk management laws. Reviews and communicates data to appropriate staff members, regulatory agencies and the national trauma registry to ensure accurate risk-adjusted benchmarking.
5. Develops and implements outcome standards, credentialing standards, policies and procedures and clinical and system process pathways in collaboration with system participants. Provides required feedback to team members in quality improvement committees, health care teams and work group meetings. Works collaboratively with managers, educators, staff and affiliated institutions to coordinate quality improvement and development efforts system wide.
6. Delivers continuous quality improvement development initiatives for providers and staff to forward the mission of the department. Collaborates, develops and supports risk prevention and peer review policy.
7. Identifies and participates in areas for allied health and community education and prevention programs. Participates and collaborates with the Injury Prevention Coordinator.
8. Facilitate problem solving throughout the continuum of care with focus on cost awareness and concern for cost position in system activities. Participates in Root Cause Analysis (RCA) as relevant/appropriate.
9. Participate in legislative and professional forums related to trauma/surgery care in order to influence public policy and advocate for the needs of patients. Coordinates and collaborates on educational activities in a high-performance culture that emphasizes empowerment, quality, effectiveness and standards to achieve the mission of the healthcare system.
Qualifications
Licensure, Certification, Registration
· Registered Nurse, Licensed in Connecticut. APRNs and PAs Licensed in CT also applicable
Education
· BS in Nursing required.
· Healthcare Quality and Safety related advanced training or Certificate(s) preferred.
· Master's degree in nursing or related field, or evidence of pursuing on a continuing basis with degree completion within 2 years of job acceptance preferred.
Experience
· Minimum Five (5) years of clinical experience in required areas such trauma care, emergency care, critical care and surgery.
· Trauma Experience or prior/current TPM experience.
· Experience in managing a healthcare related quality and safety program that includes quality management, peer review and program development.
· Minimum of 2 years documented experience leading and building a multi-disciplinary performance improvement team and program with demonstrated successful outcomes preferred.
· Evidence of past Scientific Journal Peer-Reviewed Publication preferred.
Language Skills
· Ability to read, write and speak English.
Knowledge, Skills and Ability Requirements
· Must possess knowledge of professional theory, practices, and regulations.
· Strong interpersonal and communication skills.
· Ability to work collaboratively with multidisciplinary team members, hospital staff, physicians and patients.
· Ability to manage staff and change.
· Strong critical thinking, problem solving and decision-making skills
· Information management, analysis and presentation skills.
· Strong ability to demonstrate cultural sensitivity in all interactions with patients/families and co-workers.
· Must be able to work independently as well as collaboratively.
· Must have a strong aptitude for detail.
· Must be computer literate and be proficient in keyboarding, spreadsheets, word processing, and databases.
· Documentation of continued professional growth.
We take great care of careers.
With locations around the state, Hartford HealthCare offers exciting opportunities for career development and growth. Here, you are part of an organization on the cutting edge - helping to bring new technologies, breakthrough treatments and community education to countless men, women and children. We know that a thriving organization starts with thriving employees-- we provide a competitive benefits program designed to ensure work/life balance. Every moment matters. And this is your moment.
Manager Quality Trauma Surgery Program (RN) / Department Of Surgery
Quality assurance manager job in Bridgeport, CT
Control # 430#######
Work where every moment matters.
Every day, over 40,000 Hartford HealthCare colleagues come to work with one thing in common: Pride in what we do, knowing every moment matters here. We invite you to become part of Connecticut's most comprehensive healthcare network.
St. Vincent's Medical Center in Bridgeport has more than 3,200 employees. It includes a 473-bed community teaching hospital, a 76-bed inpatient psychiatric facility in Westport, a large multispecialty provider group, and special needs services for adults and children. St. Vincent's is the first hospital in Fairfield County to be integrated into the Hartford HealthCare network and is the system's second-largest hospital.
Job Summary
The Manager Quality Trauma Surgery Program provides leadership and operational support for the St. Vincent's Medical Center (SVMC) Trauma Program's (TP) development, implementation, and assessment to ensure an organized, effective, and efficient quality-focused, approach to providing high-quality trauma care. This position provides multiple services to include the coordination of TP initiatives between Trauma Program leaders, faculty, and HHC facilities, which includes clinical, educational, and research initiative collaboration and information sharing as relevant.
This position's continuum of involvement spans departmental, inter-hospital, system, community, state, and national interventions. In addition, this role involves frequent interaction and collaboration with a variety of stakeholders across the HHC System and non-HHC facilities at a variety of professional and clinical levels with an emphasis on high-quality customer service.
This position reports to Director of Clinical Operations, Inpatient Surgery with a substantial dyad of accountability to the Trauma Program Medical Director.
Essential Functions/Responsibilities
1. Promotes and operationalizes the goals and objectives of the trauma program to achieve its strategic vision for an integrated system. Establishes collaborative partnerships with all relevant parties characterized by vision, leadership and communication. Oversee and manages Trauma Quality Performance Team consisting of a Performance Improvement Nurse, Trauma Registrars, and Injury Prevention Coordinator. Acts as a departmental representative/collaborator with all Injury Prevention Center initiatives.
2. Champions and leads quality performance improvement/evaluation and patient safety efforts that ensure compliance with hospital/department rules and regulations, policies and procedures. Collaborates with other Quality and Safety colleagues/programs to inform planning at the SVMC hospital and System level. Coordinates and manages standing TP meetings, M&Ms, and multi-disciplinary M&M and PIP meetings.
3. Provides leadership in the design and implementation of a systematic process for monitoring, evaluating and improving the quality and effectiveness of trauma patient care. Identifies quality of care issues and brings to closure to ensure quality patient care. Ensures process includes data abstraction and verification, query design, statistical analysis, trending and reporting, to develop data sets into useful information to develop strategies for achieving improved outcomes.
4. Collaborate with and/or supervises appropriate personnel to implement, maintain and administer quality trauma databases and files according to QA protocols, HIPPA standards and legal/risk management laws. Reviews and communicates data to appropriate staff members, regulatory agencies and the national trauma registry to ensure accurate risk-adjusted benchmarking.
5. Develops and implements outcome standards, credentialing standards, policies and procedures and clinical and system process pathways in collaboration with system participants. Provides required feedback to team members in quality improvement committees, health care teams and work group meetings. Works collaboratively with managers, educators, staff and affiliated institutions to coordinate quality improvement and development efforts system wide.
6. Delivers continuous quality improvement development initiatives for providers and staff to forward the mission of the department. Collaborates, develops and supports risk prevention and peer review policy.
7. Identifies and participates in areas for allied health and community education and prevention programs. Participates and collaborates with the Injury Prevention Coordinator.
8. Facilitate problem solving throughout the continuum of care with focus on cost awareness and concern for cost position in system activities. Participates in Root Cause Analysis (RCA) as relevant/appropriate.
9. Participate in legislative and professional forums related to trauma/surgery care in order to influence public policy and advocate for the needs of patients. Coordinates and collaborates on educational activities in a high-performance culture that emphasizes empowerment, quality, effectiveness and standards to achieve the mission of the healthcare system.
Qualifications
Licensure, Certification, Registration
· Registered Nurse, Licensed in Connecticut. APRNs and PAs Licensed in CT also applicable
Education
· BS in Nursing required.
· Healthcare Quality and Safety related advanced training or Certificate(s) preferred.
· Master's degree in nursing or related field, or evidence of pursuing on a continuing basis with degree completion within 2 years of job acceptance preferred.
Experience
· Minimum Five (5) years of clinical experience in required areas such trauma care, emergency care, critical care and surgery.
· Trauma Experience or prior/current TPM experience.
· Experience in managing a healthcare related quality and safety program that includes quality management, peer review and program development.
· Minimum of 2 years documented experience leading and building a multi-disciplinary performance improvement team and program with demonstrated successful outcomes preferred.
· Evidence of past Scientific Journal Peer-Reviewed Publication preferred.
Language Skills
· Ability to read, write and speak English.
Knowledge, Skills and Ability Requirements
· Must possess knowledge of professional theory, practices, and regulations.
· Strong interpersonal and communication skills.
· Ability to work collaboratively with multidisciplinary team members, hospital staff, physicians and patients.
· Ability to manage staff and change.
· Strong critical thinking, problem solving and decision-making skills
· Information management, analysis and presentation skills.
· Strong ability to demonstrate cultural sensitivity in all interactions with patients/families and co-workers.
· Must be able to work independently as well as collaboratively.
· Must have a strong aptitude for detail.
· Must be computer literate and be proficient in keyboarding, spreadsheets, word processing, and databases.
· Documentation of continued professional growth.
We take great care of careers.
With locations around the state, Hartford HealthCare offers exciting opportunities for career development and growth. Here, you are part of an organization on the cutting edge - helping to bring new technologies, breakthrough treatments and community education to countless men, women and children. We know that a thriving organization starts with thriving employees-- we provide a competitive benefits program designed to ensure work/life balance. Every moment matters. And this is your moment.
Oracle Financial Functional Test Lead
Quality assurance manager job in Stamford, CT
JOB DETAILS:
Role: Oracle Financial Functional Test Lead
Skills: Oracle Financials, Oracle Functional, SOX Controls, FAH, Oracle QA Testing, Regulatory Reporting, QA and Testing Processes
Experience: 10+years
We at Coforge are seeking an Oracle Financial Functional Test Lead. The ideal candidate will have extensive experience in Oracle Financials, FAH, Oracle Functional, SOX Controls, Oracle QA Testing, Regulatory Reporting
The skills needed are-
Experience working on Oracle Financials functional
- Understand of risk and sox controls, experience FAH, and Regulatory Reporting experience.
Experience withing BFS will be helpful as well.
-Experience in QA and testing processes
- Excellent communication skills
QA Manager
Quality assurance manager job in Danbury, CT
360 IT Professionals is a Software Development Company based in Fremont, California that offers complete technology services in Mobile development, Web development, Cloud computing and IT staffing. Merging Information Technology skills in all its services and operations, the company caters to its globally positioned clients by providing dynamic feasible IT solutions. 360 IT Professionals work along with its clients to deliver high-performance results, based exclusively on the one of a kind requirement.
Our services are vast and we produce software and web products. We specialize in Mobile development, i.e. iPhone and Android apps. We use Objective C and Swift programming languages to create native applications for iPhone, whereas we use Android Code to develop native applications for Android devices. To create applications that work on cross-platforms, we use a number of frameworks such as Titanium, PhoneGap and JQuery mobile.
Furthermore, we build web products and offer services such as web designing, layouts, responsive designing, graphic designing, web application development using frameworks based on model view controller architecture and content management system. Our services also extend to the domain of Cloud Computing, where we provide Salesforce CRM to effectively manage one's business and ease out all the operations by giving an easy platform. Apart from this, we also provide IT Staffing services that can help your organization to a great extent as you can hire highly skilled personnel's through us.
We make sure that we deliver performance driven products that are optimally developed as per your organization's needs. Take a shot at us for your IT requirements and experience a radical change.
Job Description
Responsibilities:
· Provide necessary definition, development and deployment of software quality assurance strategy and roadmap.
· Develop and maintain current and comprehensive test plans for Navigators applications.
· Act as Subject Matter Expert on the technical aspects, and tools related to testing end to end processes.
· Lead and develop the execution of manual and automation test cases and scripts.
· Lead and perform various types of testing including functional, regression, performance, user acceptance, etc.
· Identify, document and track quality issues through to completion.
· Responsible for maintaining up-to-date test plans.
· Supervise quality assurance team who may be both internal and external resources and who may be geographically dispersed to ensure the delivery of the QA department goals and objectives
· Works with project managers to develop project schedules and resource allocation models for QA related projects and other activities such as software deployment in production environments.
· Responsible embedding for QA as part of the SDLC
· Meet target deployment schedules.
· Measure and evaluate product and QA team performance; recommend improvements.
· Identify risks and manage contingencies.
· Gather and communicate testing results.
· Work with Internal Audit to test and evaluate the design and operating effectiveness of internal controls.
Requirements:
· Bachelor's Degree or equivalent experience
· 7+ years of software testing experience
· 4+ years of team leadership
· Thorough understanding of formalized QA process and concepts
· Proven track record of delivering projects on time and within budget
· Experience with Software Development Life Cycle (SDLC)
· Strong analytical and problem solving abilities
·
Additional Information
Thanks & Regards
Vikas Kumar
vikas.kumar(@)360itpro.com
QA Manager (LS)
Quality assurance manager job in Stratford, CT
At ALS, we encourage you to dream big.
When you join us, you'll be part of a global team harnessing the power of scientific testing and data-driven insights to build a healthier future.
QA Manager Imagine your future with us! At ALS, we encourage you to dream big. When you join ALS, you join a purpose and values-driven team that empowers you to innovate, create, and thrive. Our global team turns up each day with passion and commitment to do amazing things, always challenging our thinking to find ways to solve some of the world's most complex problems for a safer, healthier world.
About the role:
The primary purpose of this position is to actively support the laboratory's Quality Management System in accordance with management's commitment to quality, and the organization's Mission Statement.
About you:
• Collaborate with laboratory management to ensure that the Quality Assurance and Quality Control program is applied effectively;
• Coordinate and monitor quality system implementation throughout the facility;
• Initiate Quality System updates as required to maintain compliance with corporate quality program and regulatory requirements.
• Ensure compliance with local and corporate quality assurance policies, as well as those of the laboratory's accrediting authorities;
• Manage laboratory accreditation applications and renewals;
• Coordinate, perform, and review internal audits of the laboratory quality program;
• Coordinate regulatory, client, and third party quality assessments;
• Coordinate statistical process control, corrective action responses;
• Coordinate document and record control;
• Coordinate the annual certification and/or calibration of laboratory support equipment;
• Coordinate development, review, and revisions of Standard Operating Procedures;
• Approve documents for use in the laboratory as a designated signatory;
• Communicate Quality Management System updates to the laboratory, and monitor Quality Management System implementation throughout the facility;
• Develop and implement on-going employee training programs related to the Quality Management System;
• Train new hires in Ethics and QA policies;
• Other duties as assigned.
Required Qualifications:
• Minimum of a Bachelor's degree in Science preferably in Chemistry or any other physical science;
• Five years' experience in environmental laboratory;
• Two years' experience in quality system management;
• Experience with Quality System standards, including NELAC, ISO17025, U.S. Department of Defense Quality System Manual;
• Proficiency in MSOffice applications, including MSWord, MSExcel, and MSAccess;
• Must be able to travel when required.
Physical Demands:
• Able to sit for 80% of an 8-hour day.
• Able to speak and hear clearly while communicating with co-workers and managers;
• Dexterity in hands and fingers to operate equipment and handle glassware;
• Must have average vision and able to see to read reports and operate equipment;
• Hearing and speech to communicate in person and over the telephone;
Working at ALS:
Our people are our most valuable asset and drive our success at ALS. We are a diverse community of dedicated professionals united by our passion to make a difference in the world. We reward excellence and uphold our values in our work and how we treat each other. At ALS, you'll be supported to expand your skills and develop new ones so you can reach your full potential. We invest in our people with a range of programs and provide opportunities across the company, giving our people scope to grow diverse careers and develop as leaders. We want everyone to have a safe, flexible and rewarding career that makes a positive impact on our people, the planet and the communities where we work.
Our benefits include:
• Structured wage increases
• Comprehensive benefit package (including medical, dental, and vision coverage, life and disability insurance, retirement plan with company match, employee assistance and wellness programs, access to company perks)
• Additional vacation days for years of service
• Business support for education or training after 9 months with the company
• Learning & development opportunities (unlimited access to e-learnings and more)
About ALS:
ALS is a global leader in scientific testing, providing comprehensive testing solutions to clients in more than 60 countries across a wide range of industries, including environment, food and beverage, mining, personal care, pharmaceutical, healthcare and equipment reliability. Using state-of-the-art technologies and innovative methodologies, our dedicated international teams deliver the highest-quality testing services and personalized solutions supported by local expertise. We help our clients leverage the power of data-driven insights for a safer and healthier world.
Everyone matters:
ALS is proud to be an equal opportunity employer committed to achieving and maintaining a workforce which reflects and affirms the diversity of our society
ALS is a VEVRAA Federal Contractor.
EOE AA Minority, Female, Veteran, Individuals with Disabilities
Click Here to view the EEO is the Law poster
Click Here to view the FMLA Law poster
Click Here to view the EPPA Law Poster
Click Here to view the Pay Transparency Provision
Click Here to view company E-Verify Participation Poster
ALS also welcomes applications from people with all levels of ability. Accommodation is available on request for candidates taking part in all aspects of the selection process.
Working at ALS
The ALS team is a diverse and dedicated community united by our passion to make a difference in the world.
Our values are important to us, and shape how we work, how we treat each other and how we recognise excellence.
At ALS, you'll be supported to develop new skills and reach your full potential. We invest in our people with programs and opportunities that help you build a diverse career with us.
We want everyone to have a safe, flexible and rewarding career that makes a positive impact on our people, the planet and our communities.
Everyone Matters
ALS is proud to be an equal opportunity employer and is committed to fostering an inclusive work environment where the strengths and perspectives of each employee are both recognised and valued.
Qualified candidates will be considered without regard to race, colour, religion, national origin, military or veteran status, gender, age, disabilities, sexual orientation, gender identity, pregnancy and pregnancy-related conditions, genetic information and any other characteristics protected by the law. We invite resumes from all interested parties, including women, members of minority groups, and persons living with disabilities.
ALS also welcomes applications from people with all levels of ability. Accommodation is available on request for candidates taking part in all aspects of the selection process.
Eligibility
To be eligible to work at ALS you must be a Citizen or Permanent Resident of the country you are applying for, or either hold or be able to obtain, a valid working visa.
How to apply
Please apply on-line and provide a cover letter and CV that best demonstrate your motivation and ability to meet the requirements of this role.
Auto-ApplyQuality Manager
Quality assurance manager job in Wallingford, CT
WHO WE ARE We are a leading supplier of methacrylate chemistry. As a global company with around 2,900 employees, we are represented on four continents. We serve a global market with our MERACRYL methacrylates and PMMA molding compounds under the PLEXIGLAS brand (in the Americas registered under the trademark ACRYLITE ), which we manufacture in our worldwide production network. Our products supply growth markets including the automotive, construction, and medical technology industries.
Röhm is committed to operating with social responsibility, and sustainability forms an integral part of our business strategy. We view our employees as our strength, and we value diversity and inclusion. If you thrive in an environment where individual contributions are both visible and recognized, Röhm may be right for you.
WHAT THE ROLE DELIVERS
Ensure excellent quality practices and products at the Wallingford site.
Oversee the development, implementation, and control of quality standards and processes to ensure product quality consistently exceeds customer expectation.
Cultivate a culture of quality excellence and actively drive continuous improvement efforts.
Responsible for the Quality Management System (QMS), providing leadership, direction, and training to ensure all QMS elements are met.
Responsible for budgeting and managing Quality-related costs.
Scope includes oversight of relevant unit measures such as number of plants, locations, and units/pounds.
Directly supervise approximately 1 staff member and 6 hourly employees.
Make decisions on Quality process definitions, best practices, and standardization guidelines.
Suggest quality culture enhancements, seeking management team approval.
Develop an environment that fosters continuous improvement.
Determine the acceptable quality of incoming raw material and finished product.
WHAT YOU WILL DO
Ensure that the quality requirements of our customers, company and regulatory agencies are fully understood and achieved.
Oversee the development, implementation, control, and distribution of all Quality practices, universally applied standards, methodologies, and metrics at the site.
Develop and implement ISO9001/Responsible Care 14001 Business Management System and related activities for the site.
Manages direct and indirect personnel
Act as the primary Roehm liaison with the Union for all matters concerning the potential deviations from the contract. Provide guidance to the Plant Manager on Union grievances and contractual related issues and opportunities
Manage and maintain Quality related tools and equipment at the plant. Ensure equipment is set up to Roehm Quality specifications, ensuring a routine schedule is established for preventive maintenance, and staff are trained and competent in these activities.
Drive continuous improvement initiatives at the site by identifying key quality issues and implementing necessary programs or changes.
Develop and oversee quality Key Performance Indicators (KPIs) for the plant, and set objectives.
Acts as the plant liaison to the Commercial Group and customers concerning quality matters and Customer Quality Notification resolution.
Review and address quality complaints, ensuring appropriate corrective actions are taken, and championing root cause analysis.
Implement procedures from the Global QM System and ensure compliance with external certification bodies.
Other duties as assigned.
Contacts (Nature of Engagement):
Communicates with personnel at all levels, internally and externally in relation to quality matters.
The incumbent interfaces with all site management functions (production, safety, maintenance and engineering).
Works collaboratively, and engages with key stakeholders to establish compliance with quality strategy.
Develops and maintains strong relationships with internal and external stakeholders to achieve organization's quality targets.
Salary range $126,600- $158,300 per year, plus eligible for bonus. The posted salary range reflects the national average for this role. Final compensation may vary based on location, experience, and qualifications. This role is eligible for an annual performance bonus in addition to base salary.
Benefits Summary: Full-Time positions are eligible for a comprehensive benefits package including medical, dental, and vision insurance; 401(k) with company match, discretionary company contribution, paid time off and holidays, and wellness programs.
WHAT WE ARE SEEKING
Bachelor's Degree in Quality Management, Industrial Engineering, Manufacturing Engineering, or a related discipline.
5 or more years of experience in Quality Management and continuous improvement. Experience and knowledge of injection molding preferred.
Experience in the chemical, plastics, pharmaceutical, or manufacturing fields desired.
Quality certification(s) preferred.
Adept at root cause analysis and implementing corrective and preventive actions.
Strong analytical skills and manufacturing process knowledge.
Working knowledge of ISO 9001 Quality Management Systems.
One-up and one-back style lot traceability experience.
Certification such as Six Sigma, Lean Manufacturing, or Quality Management systems preferred.
Experience with internal audits.
Excellent human relations and communication skills.
Experience working in a union-represented environment.
Knowledge of SAP, Microsoft Office, Statistical Process Control, Minitab, PowerBI, Tableau, or similar software.
Understanding of 2D drawings.
PHYSICAL DEMANDS & WORKING CONDITIONS
Hazardous Exposures-limited exposure to hazardous materials and loud noise
Physical Lifting Requirements and frequency:
light (up to 20 pounds)
Other Physical Requirements and frequency (regular, up to 3 hrs/day):
Climbing Stairs
Walking
Standing
Stooping/Kneeling
Pulling/Pushing
Auto-ApplyManufacturing Quality Manager
Quality assurance manager job in Shelton, CT
Job Description
Dependable. Enthusiastic. Driven to succeed. Bring your manufacturing skills to a role that has direct impact on delivering cutting edge technology to our global customer base.
Family-owned for over 75 years, Precision Resource is a leading global supplier of precision metal components and assemblies using a fineblank production method. We provide solutions to quality, cost and production challenges for market-leading customers in industries such as automotive, heavy duty, medical, electronics, cutlery and defense.
Precision Resource offers:
Benefits package including health, dental, life and vision insurance
401(k) with match and profit sharing
Annual bonus based on division profitability
Vacation and flexible paid holidays
Wellness and Employee Assistance Programs
Tuition reimbursement and paid training
Work with an established team of long-term employees
Our Connecticut division, located in Shelton, seeks a Quality Manager.
Summary
The Quality Manager has overall responsibility for managing the Quality department in order to establish advanced quality and reliability engineering to enhance product quality, reliability and acceptance.
Essential Duties and Responsibilities
Set, direct & support priorities of the Quality team (development of accountabilities for each team member)
Review/re-set objectives in conjunction with on-time performance evaluations
Develop, implement and improve departmental metrics
Drive continual improvement process within the Quality department
Develop a continuous learning process for all staff (proper measurement techniques, identifications fit/function - critical characteristics, standardization of acceptance criteria)
Ensure NCR's (Nonconformance Reporting), inspection, SPC, Gauge Maintenance, Cost of Quality, internal audits, etc. are accurate and completed in a timely manner
Lead/support problem resolution and responsiveness of all customer quality related issues
Customer liaison
Attend supplier conferences
Review all 8D reports and corrective actions implemented
Actively participate in APQP, FMEA and quote review meetings
Ensure Division maintains IATF 16949 certification
Improve and maintain accurate Quality procedures and manuals
Qualifications, Education, Experience
BS in Engineering or highly technical training equal to a 4-year program or 4-10 years of manufacturing experience in the metal working industry
5- 10 years of supervisory experience within a manufacturing environment
Experience with formal documentation systems and methods particularly ISO9001 and IATF 16949
Experience in the automotive industry preferred.
Precision Resource is an equal opportunity employer, M/F/D/V. To learn more, visit **********************************
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Quality Assurance Manager
Quality assurance manager job in Cold Spring Harbor, NY
Job Description
We're working with a well-established, leading manufacturer of personal care and household cleaning items that is searching for a Quality Manager. This person will ensure compliance with FDA OTC drug and cosmetic regulations, GMP standards, and internal quality requirements. The QA Manager will drive a culture of quality, maintain inspection readiness, and lead continuous improvement initiatives. This role will report to the Director of Quality Systems.
Location
: Long Island, NY
Job Responsibilities:
Develop, implement, and maintain the Quality Management System covering document control, CAPA, deviation management, audits, and supplier qualification.
• Ensure compliance with FDA OTC regulations.
• Review and approve GMP documentation including master batch records, production records, testing protocols, and validation documents.
• Lead investigations, root cause analysis, and corrective/preventive actions.
• Prepare for and manage internal, supplier, and external (FDA or customer) audits.
• Support new product introductions ensuring compliance with quality and regulatory requirements.
• Oversee supplier quality performance, raw material specifications, and incoming inspection processes.
• Collaborate cross-functionally with manufacturing, R&D, packaging, and regulatory teams to ensure product quality at every stage.
• Maintain calibration and maintenance programs for testing and inspection equipment.
• Lead, train, and develop the QA team, fostering a proactive quality culture.
Required Skills/Qualifications:
Bachelor's degree in Microbiology, Chemistry, Life Sciences, Engineering, or related discipline required.
5+ years of progressive experience in Quality Assurance or Quality Systems within FDA-regulated industries.
2+ years of leadership experience managing quality teams and laboratories in a cGMP-compliant manufacturing environment, ideally within OTC or personal care products.
Strong knowledge of FDA OTC regulations, GMP, and quality systems management.
Excellent communication, leadership, and problem-solving skills.
Familiarity with root cause analysis, CAPA management, and continuous improvement tools.
ASQ or equivalent quality certification is a plus.
Effective communicator.
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Quality Control Manager
Quality assurance manager job in New Haven, CT
The Quality Control Manager is responsible for ensuring the manufacture and timely release of a high-quality product that meets or exceeds all specifications and complies with FDA and other regulatory agencies. The role is fully integrated with the business objectives, focusing on developing and implementing methods to test and monitor product quality in all phases of manufacture, from the receipt of raw materials to the release of finished products. The manager will lead, coach, and provide direction to QA and QC professionals to optimize the department's performance, teamwork, and effectiveness.
Responsibilities
* Direct and manage activities and workflow in the QC and QA functions on both strategic and day-to-day levels.
* Lead, coach, and provide direction to QC and QA personnel, assessing strengths and providing training or developmental opportunities as needed.
* Ensure adherence to Quality procedures and compliance with all specifications and regulations, implementing new quality systems or measures as necessary.
* Collaborate with customers to provide necessary documentation and responses as requested.
* Participate in the review and evaluation of new vendors.
* Analyze, troubleshoot, and propose solutions to technical problems.
* Authorize the release of final products.
* Work collaboratively with Production Operations management to gauge production requirements and priorities to optimize workflow.
* Collaborate with technical staff on various projects, including R&D and compliance.
* Lead internal and external audit activities, coordinating audit schedules and agendas with outside parties, and function as the primary company representative during audits.
* Work with the Compliance Manager to lead corrective and preventative action activities for audit responses.
* Work collaboratively with department managers to ensure appropriate sanitation procedures are implemented and followed.
* Support company mission and values, promoting adherence to all safety, cGMP, and company policies.
* Perform other responsibilities as assigned.
Essential Skills
* Minimum 5 years of successful management experience in a QC/QA role within the pharmaceutical or related consumer product industry.
* Demonstrated leadership and managerial skills.
* Strong analytical skills with demonstrated ability to solve problems.
* Solid comprehension of FDA regulations, cGMP, and Quality procedures.
Additional Skills & Qualifications
* Proficiency in quality control and assurance, GMP, laboratory procedures, chemistry, biology, and inspection.
* Experience in leadership development.
Work Environment
The role involves working in a regulated environment, ensuring compliance with FDA and other regulatory standards. The position requires collaboration with various departments, including production operations, technical staff, and compliance management. The work includes leading audit activities and working closely with customers and vendors. The environment is fast-paced, focused on optimizing workflow and ensuring high-quality product output while promoting safety and adherence to company policies.
Job Type & Location
This is a Permanent position based out of New Haven, CT.
Pay and Benefits
The pay range for this position is $110000.00 - $115000.00/yr.
Tower Laboratories, Ltd. is a privately held company founded in 1979 and specializes in the development and manufacture of effervescent products. Headquartered in Centerbrook, CT, we also have manufacturing facilities in Clinton, CT and Montague, MI.
Under the direction and leadership of Owner/President Norman Needleman, we are a company that looks to build partnerships with customers and suppliers. We strive for an environment where employees are valued, quality is job one, and continuous improvement is a constant focus. We also look to support the communities in which we work and live, carrying out our business in an environmentally and socially responsible manner.
We are the country's leading supplier of store brand effervescent products (denture cleansers, antacid/pain relief, cold relief). We also produce a number of effervescent products for contract customers consisting of prescription and over the counter (OTC) drugs, dietary supplements, medical devices, personal care products and specialty applications.
Over the years, Tower Laboratories has developed core competencies and proprietary knowledge that allows us to develop and produce quality, stable effervescent products in a cost-efficient manner. This knowledge and related intellectual property offers a competitive advantage for both Tower Laboratories and our customers.
All of our manufacturing facilities are cGMP compliant, and we offer product development expertise (from concept through commercialization) for any application involving effervescence as a delivery system.
Workplace Type
This is a fully onsite position in New Haven,CT.
Application Deadline
This position is anticipated to close on Dec 12, 2025.
About Actalent
Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.
The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.
If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing due to a disability, please email actalentaccommodation@actalentservices.com for other accommodation options.
QA Automation Testing Manager
Quality assurance manager job in Stamford, CT
Must Have Technical/Functional Skills We're seeking a QA Automation Testing Manager (SDET) with 10+ years leading multiteam QA programs, to drive engineering-quality practices across complex banking platforms and integrations. You will architect automation frameworks, embed quality into CI/CD, and lead a team of SDETs/QA engineers to deliver reliable, compliant releases at speed. Experience in BFSI systems (core banking, payments, digital channels) and hands-on coding for test automation is essential.
Job description
* Automation Architecture & Delivery
* Design, implement, and scale UI/API/DB automation frameworks (Selenium java/UFT, RestAssured/Postman, Cucumber/BDD, TestNG/JUnit).
* Integrate automated suites into CI/CD (Azure DevOps/Jenkins/GitLab) with quality gates, parallelization, test impact analysis, and artifact publishing.
* Establish coding standards for test harnesses, mocks, data builders, and service virtualization; enforce code reviews and static analysis for test code.
Domain‑Focused Testing (Banking)
* Translate banking use cases (core deposits/loans, ACH/wires, card/payments, digital banking) into robust automated scenarios and data validations.
* Partner with product owners and vendor teams (e.g., Fiserv, internal platforms) to triage defects, validate patches/hotfixes, and maintain regression beds.
Program Leadership & Governance
* Lead a squad of SDETs/QA engineers-capacity planning, mentoring, and upskilling on advanced automation topics.
* Orchestrate defect triage, root‑cause analysis, and risk‑based test planning; own release readiness (go/no‑go) and rollback validation.
* Drive shift‑left practices (contract testing, API first, early data checks) and shift‑right observability (synthetic monitoring, production validation dashboards).
* Compliance & Security
* Ensure test evidence meets BFSI regulatory/audit needs (SOX); automate traceability from user stories to test results and logs.
Required Qualifications
* 10-12+ years in software testing/quality engineering, with 5+ years leading SDET/automation teams.
* Strong hands‑on coding in Java/C# (or equivalent) for test automation (frameworks, utilities, custom drivers).
* Proven delivery of CI/CD‑integrated automation at scale; expert in test design for microservices, REST APIs, and event‑driven systems.
* BFSI domain experience-core banking or payments-and vendor/platform collaboration (e.g., Fiserv) for patch/regression cycles.
* Solid grasp of SQL and data validation; familiarity with logs/metrics (Splunk/Sumo/Grafana) for test diagnostics.
Preferred Skills
* Experience with OSAT‑style regression accelerators or similar enterprise frameworks; comfortable with shift‑left/shift‑right test strategies.
* Performance testing (JMeter/LoadRunner)
* ISTQB (Advanced), Agile/SAFe, or cloud certifications (Azure/AWS).
Generic Managerial Skills, If any
* Tools & Stack (Illustrative)
* Automation: Selenium, Cypress, Playwright, RestAssured, Postman, Cucumber/BDD, Appium (mobile)
* CI/CD & SCM: Azure DevOps, Jenkins, GitLab, GitHub Actions; Git
* Test Management : Azure Test Plans, ALM/Octane, Zephyr/Xray
* Data/DB: SQL Server, Oracle, PostgreSQL; TDM/masking tools
* Observability: Splunk/Sumo, Grafana/Prometheus; quality dashboards
Education
Bachelor's in computer science/engineering or related field (advanced degree a plus).
TCS Employee Benefits Summary:
* Discretionary Annual Incentive.
* Comprehensive Medical Coverage: Medical & Health, Dental & Vision, Disability Planning & Insurance, Pet Insurance Plans.
* Family Support: Maternal & Parental Leaves.
* Insurance Options: Auto & Home Insurance, Identity Theft Protection.
* Convenience & Professional Growth: Commuter Benefits & Certification & Training Reimbursement.
* Time Off: Vacation, Time Off, Sick Leave & Holidays.
* Legal & Financial Assistance: Legal Assistance, 401K Plan, Performance Bonus, College Fund, Student Loan Refinancing.
Salary Range : $100,000-$120,000 a year
QA Manager
Quality assurance manager job in Deer Park, NY
Open Scientific provides contract staffing and direct hire recruitment services for the scientific, engineering, laboratory and manufacturing sectors.
Job Description
An ever growing company is looking for an experienced QA Manager. The ideal candidate has at least 5 years of management experience in the pharmaceutical/nutraceutical/food industry.
Pay: $70,000 to $80,000
Responsibilities & Duties:
Responsible for all quality systems for label manufacturer of clinical trials and investigational
drug products.
Responsible for a staff of 22 individuals, including 3 Managers and 2 supervisors.
Develop, write, revise and approve all SOPs.
Solely responsible for customer audits, including audit responses.
Instituted company-wide calibration program, effectiveness training, mock recalls, AQL
statistical sampling plans, line clearance methods and specifications for components.
Developed code system for customer complaints, investigations, utilized in trending analysis.
Developed training matrices for all employees.
Responsible for cGMP and SOP training programs.
Write and execute validation protocols - Installation Qualification (IQ), Operational
Qualification (OQ) and Performance Qualification on various equipment
Complete customer Quality Agreements, Technical Agreements and questionnaires.
Revised and enhanced preventative maintenance program, ensuring overall compliance.
Maintain Material Safety Data Sheet (MSDS) manuals, facility pest control and emergency
lighting programs.
Additional Information
All your information will be kept confidential according to EEO guidelines.
Supplier Quality Development Mgr
Quality assurance manager job in Rocky Hill, CT
At Henkel, you'll be part of an organization that's shaping the future through innovation, sustainability and collaboration. With our trusted brands like Persil, 'all, Loctite, Snuggle, and Schwarzkopf and our cutting-edge technologies, you'll have countless opportunities to explore new paths and grow.
This position is with our Adhesive Technologies business unit - where we empower our people to transform industries and provide our customers with a competitive advantage through adhesives, sealants and functional coatings.
Dare to learn new skills, advance in your career and make an impact at Henkel.
What you´ll do
* Lead and Execute Comprehensive Supplier Quality Audits (System - ISO 9001/IATF 16949, Process - VDA 6.3, and Product).
* Drive Supplier Quality Development Programs by conducting root cause analysis and improvement plans of systemic supplier weaknesses.
* Own End-to-End Supplier Issue Resolution Processes (Supplier Complaints and Customer Complaints caused by Suppliers) by leading cross-functional sessions for complaints resolution, especially in Critical and High Potential cases.
* Drive cost recovery initiatives from suppliers by leveraging root cause analysis outcomes, contractual terms, and cross-functional alignment with Legal and Procurement teams.
* Review and approve supplier qualification packages, ensuring compliance with Henkel's product-specific requirements and adhesive material validation protocols.
What makes you a good fit
* Proven expertise in supplier quality auditing (ISO 9001, IATF 16949, VDA 6.3), root cause analysis (8D, A3, FRPS), supplier development and qualification, cross-functional leadership, and digital/lean transformation-supported by strong analytical, communication, and negotiation skills.
* Qualification: Bachelor's degree in engineering, Chemistry, or a related field (master's or relevant certifications are a plus).
* 7+ years of experience in Supplier Quality or Quality Engineering, ideally in the chemical or manufacturing industry.
* Health Insurance: affordable plans for medical, dental, vision and wellbeing starting on day 1
* Work-Life Balance: Paid time off including sick, vacation, holiday and volunteer time, flexible & hybrid work policies (depending on role), and vacation buy / sell program
* Financial: 401k matching, employee share plan with voluntary investment and Henkel matching shares, annual performance bonus, service awards and student loan reimbursement
* Family Support: 12-week gender neutral parental leave (up to 20 weeks for parents giving birth), fertility support, adoption & surrogacy reimbursement, discounted child and elderly care, and scholarships
* Career Growth: diverse national and international growth opportunities, access to thousands of skills development courses, and tuition reimbursement
The salary for this role is $95,000.00 - $110,000.00. This is the range that we in good faith anticipate relying on when setting wages for this position. We may ultimately pay more or less than the posted range and this range. This salary range may also be modified in the future.
Henkel does not accept unsolicited resumes from search firms or employment agencies. Unsolicited referrals and resumes are considered Henkel property and therefore, Henkel will not pay a fee for any placement resulting from the receipt of an unsolicited referral.
Henkel is an equal opportunity employer. We evaluate qualified applicants without regard to race, color, religion, sex, age, national origin, disability, veteran status, genetic information, and other legally protected categories.
JOB ID: 25080459
Job Locations: United States, CT, Rocky Hill, CT
Contact information for application-related questions: *****************************
Please do not use this email address for sending your application or CV. To apply, please click on the "Apply for this role" button below. Applications sent via e-mail will not be accepted.
Application Deadline: As long as the vacancy is listed on our Career Site, we are happy to receive your application
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How is work at Henkel
About Henkel
Building on a strong legacy of almost 150 years, we are leading the way to reimagine and improve life every day. Today and for generations to come. Through our innovative and sustainable brands and technologies, across our teams around the world.
Henkel holds leading positions in both industrial and consumer businesses: Our portfolio includes well-known hair care products, laundry detergents, fabric softeners as well as adhesives, sealants, and functional coatings.
Easy ApplyQuality Control Manager - Pharmaceuticals
Quality assurance manager job in Central Islip, NY
Job Brief:
Required Citizenship / Work Permit / Visa Status:
US Citizen / Green Card Holder /H1B
Must Haves:
The candidate must have a Bachelor's in Pharmaceuticals or in a relevant field of study.
The candidate must have at least 9 years of experience in Quality Control (QC) function of a pharmaceutical organization.
The candidate must have at least 2-3 years of supervisory/managerial experience.
Responsibilities:
1. Key Accountabilities
Accountability Cluster
Major Activities / Tasks
I. Plan the quality control routine operations and stability studies in order to ensure timely completion of stability studies and smooth functioning of release activity
· Monitor the commitment dates for release of RM, PM, FP & water analysis and process/cleaning validation section by conducting performance dialogues and handshake
· Review the plans prepared and monitor timely execution of activities in all the shifts to avoid delays
· Review the monthly planner and production plans to ensure timely availability of required resources and ensure no sample is overdue
II. Monitor the execution of all routine quality control operation and stability studies to ensure timely delivery and meet regulatory requirements and cGMP, GLP guidelines
· Monitor routine/stability operations closely and ensure that all necessary SOPs are followed by the team
· Provide technical guidance related to troubleshooting in chromatography, experimentation design etc. to minimize non-conformances
· Monitor timely implementation of new updates in specifications and QCPs to meet compliance
· Perform online review of reports generated to ensure zero data integrity issues in Lab
· Monitor sample charging and sample pull-out as per schedule
· Monitor reserved samples storage and destruction as per schedule and perform UD release
· Monitor the stability chamber daily for excursions and other related issues
III. Drive the investigation of the batch for non-conformance and ensure its closure within the timelines defined in SOPs to facilitate smooth operations
· Evaluate root cause analysis in case of OOS, OOT, incidences and rejection and propose CAPAs
· Investigate the stability chamber excursions and propose CAPAs
· Ensure that all non-conformances are routed through proper channel and are investigated as per SOP
· Communicate with respective QC/QA heads for compliance and ensure timely closure of CAPAs by tracking in SmartSolve
IV. Monitor completion of stability studies as per protocol/schedule to avoid delays in product launch
· Perform analysis for stability samples without any errors as per schedule
· Ensure timely completion of ANDA samples testing and submission of data by verifying it with ANDA schedule
· Plan the routine/stability activities by coordinating with ADL/R&D about dates of product dossier filing
· Resolve analytical and product related issues by escalating to ADL, R&D and transfer unit
V. Provide technical guidance to the team w.r.t batch release and stability studies and evaluate their performance to ensure team development and improved lab efficiency
· Identify the training needs of employees based on the updates in the pharmacopeial guidelines
· Monitor the training imparted on laboratory techniques, quality control procedures and principles of cGMP & GLP
· Monitor the productivity of all the teams in the section by reviewing %SLA and %NC rates
· Ensure the completion of training and qualification of analyst by taking feedback and timely reviewing his work
Skills Required:
The candidate must have at least 9 years of experience in Quality Control (QC) function of a pharmaceutical organization.
The candidate must have at least 2-3 years of supervisory/managerial experience.
QA Specialist
Quality assurance manager job in Shirley, NY
Nature and Scope Ensures quality system compliance with GMPs, procedures and documentation within the company and in keeping with the internal audit program. Interacts with all levels of the organization and maintains on-going dialogue with management.
Essential Duties and Responsibilities
Nothing in this job description restricts management's right to assign or reassign duties and responsibilities to this job at any time.
* Under supervision, assist with documentation for the closure of investigations.
* Assist in gathering data for reports, metrics, Annual Product reviews, Quarterly reports and external requests.
* Scheduling departmental meetings, maintaining meeting minutes and attendance.
* Maintain departmental records and files (both electronic and manual).
* Participate in cross-functional project teams as required.
* Support, coordinate, and assist with regulatory agency audit tasks as required in support of regulatory agency inspections.
* Support and maintain quality programs, policies, processes, procedures and controls ensuring compliance with current Good Manufacturing Practices (cGMP).
* Keep training curriculum current.
* Ensure all work is performed and documented in accordance with existing company policies and procedures.
* Perform any other tasks/duties as assigned by management.
Education Requirements and Qualifications
To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. The requirements listed below are representative of the knowledge, skill and/or ability required.
* High School or GED diploma required. Associate's degree or equivalent years of experience preferred.
* Experience working in a Quality role within a cGMP manufacturing environment required.
* Knowledge and understanding of quality assurance principles, controls and interactions between Quality Systems; FDA guidance, ICH, PIC/S, etc.
* Strong attention to detail, adherence to SOPs.
* Ability to work effectively in a collaborative environment.
* Ability to effectively work under dynamic constraints, with success in managing multiple activities concurrently and producing outstanding results.
* Strong organizational, interpersonal and communication skills (oral and written). Written skills must be audit-level appropriate for non-routine or complex issues.
* PC Skills Required (MS Word, Excel).
* Ability to work overtime as needed.
Physical Environment and Requirements
* Physically able to wear cleanroom/protective gowning and equipment, including but not limited to gowning, goggles, face shields, and protective gloves. PPE is essential for the health and safety of employees.
Expected Salary Range:
$70,100 - $85,000
The salary range, displayed is the minimum and maximum annual salary range of compensation for the role that the employer in good faith believes to be accurate at the time of the posting of an advertisement for the role. Actual compensation for the role will be based on a number of different factors including but not limited to the candidate's qualifications, education, knowledge, skills and experience.
American Regent also offers a competitive total rewards package which includes healthcare, life insurance, profit sharing, paid time off, matching 401k as well as a wide range of other benefits.
American Regent celebrates diversity and we are committed to creating an inclusive environment for all employees. We are an Equal Opportunity Employer and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability status, or protected veteran status.
Applicants have rights under Federal Employment Laws.
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* Employee Polygraph Protection Act: *********************************************************
Alert: We're aware of individuals impersonating our staff to target job seekers. Please note:
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* Our recruiting process includes multiple in person and/or video interviews and assessments.
* If you are unsure about the legitimacy of a message, contact John Rossini at *************************** before responding.
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Auto-ApplyQA Specialist
Quality assurance manager job in Melville, NY
Certified Group partners with customers to deliver innovative scientific solutions and expertise - So The World Can Trust In What It Consumes. As a leading provider of laboratory testing, regulatory consulting, and certification & audit services, Certified Group includes Food Safety Net Services (FSNS), FSNS Certification & Audit, Certified Laboratories, EAS Consulting Group, and Labstat International Inc. Certified Group provides analytical testing and regulatory guidance services in the food & beverage, dietary supplements & NHP, cosmetics, OTC, personal care, tobacco, nicotine, cannabis, and hemp industries.
We are seeking a highly skilled Quality Assurance Specialist to join our team!
In this key role you will work on ensuring compliance with FDA regulations within our industry. The ideal candidate will have extensive experience in managing electronic Quality Management Systems (eQMS), particularly in areas such as Corrective and Preventive Actions (CAPA), Customer Complaints, Out of Specification (OOS) investigations, and conducting Internal Audits. The Quality Assurance Specialist will play a pivotal role in maintaining and improving our quality management processes to uphold the highest standards of product quality and regulatory compliance.
Responsibilities:
* Assist in the implementation, maintenance, and continuous improvement of the electronic Quality Management System (eQMS) to ensure compliance with FDA regulations.
* Lead and coordinate Corrective and Preventive Action (CAPA) processes, including investigation, root cause analysis, implementation of corrective actions, and effectiveness checks.
* Handle Customer Complaints and Out of Specification (OOS) investigations, ensuring timely resolution and documentation according to regulatory requirements.
* Conduct thorough Internal Audits to assess compliance with established quality procedures, identify areas for improvement, and develop corrective actions as needed.
* Collaborate with cross-functional teams to provide quality assurance guidance and support throughout all stages of operation.
* Develop and maintain quality-related documentation, including Standard Operating Procedures (SOPs), work instructions, and quality records, equipment maintenance records in accordance with FDA regulations.
* Verify that all laboratory instruments and equipment are calibrated and maintained according to established schedules and regulatory standards to ensure accuracy and compliance. Assist in the preparation and hosting of regulatory agency inspections and audits, as well as follow-up activities to address any findings or observations.
* Stay abreast of regulatory requirements and industry best practices related to quality assurance and quality management systems and proactively implement necessary changes to ensure compliance.
Requirements:
* Bachelor's degree in a scientific or technical field, such as Chemistry, Biology, Engineering, or related discipline.
* 3-5 years of experience in a quality assurance role within an FDA regulated industry, preferably in pharmaceuticals, medical devices, or biotechnology.
* Strong understanding of FDA regulations and guidelines, including cGMP, 21 CFR Part 11, and ICH guidelines.
* Proven experience in managing electronic Quality Management Systems (eQMS), such as Qualtrax, Intact, or similar platforms.
* Proficiency in conducting investigations, root cause analysis, and implementing corrective actions for CAPA, Customer Complaints, and OOS events.
* Experience in conducting Internal Audits and familiarity with audit processes and methodologies.
* Excellent communication skills, with the ability to effectively collaborate with cross-functional teams and communicate quality requirements to stakeholders at all levels of the organization.
* Strong attention to detail and analytical skills, with the ability to analyze complex data sets and identify trends or areas for improvement.
* Ability to work independently, prioritize tasks, and manage multiple projects simultaneously in a fast-paced environment.
BENEFITS:
* Progressive 401k Retirement Savings Plan
* Employer Paid Short- Term and Long-Term Disability, and Life Insurance
* Group Medical
* Tuition Reimbursement
* Flexible Spending Accounts
* Dental
* Paid Holidays and Time Off
* Many positions which qualify for the company bonus program
Certified Group values diversity in its workforce. The company is firmly committed to a policy of Equal Opportunity and will administer its policies in a manner that treats each employee and applicant for employment on the basis of merit. Certified Group will take affirmative action to seek out qualified applicants without regard to race, color, religion, sex, national origin, age, handicap, or veteran status.
Facilities & Construction - Quality Control & Operations Manager
Quality assurance manager job in Fairfield, CT
The Quality Control & Operations Manager (QCOM) is responsible for managing and performing the daily QC responsibilities of specific assigned projects to ensure the projects are constructed in accordance with the established University standards. The role includes direct oversight and review of the entire documentation and physical inspection phase of the workflow process and working with other in-house personnel (e.g., Project Managers, Capital Projects Director, etc.) and external personnel to produce and document quality projects. The incumbent reports directly to the Executive Director of Capital Projects.
In addition to the above, the position will require to be the facilities liaison between off-campus entities & University Construction & Facilities Department director(s).
Principal Duties & Responsibilities
The QCOM must be on the project site at all times during physical work activities.
The QCOM will be an individual within an on-site work organization who will be responsible for overall project QC management and have the authority to act in all QC matters. The QCOM will aid in the continued development, implementation, and administration of the university-specific QC Plan for projects in the construction phase.
Ensure all project personnel, including CMs/ GCs/ subcontractors, understand and comply with the University QC requirements.
Certify that all submittals are in compliance with contract requirements.
Develop the Preparatory QA/QC Meeting agendas, facilitate the Preparatory Meetings, and participate in the Initial, Follow-up, and Final Inspections.
Conducts preparatory, initial, and follow-up meetings to establish an understanding of the standards of Construction desired for each definable feature of work. Verifies and documents that all materials received for the project are in conformance with approved submittals and contract specifications. Verifies all onsite materials are handled and stored properly for use on the project
Review plans and specifications to ensure requirements are met for each scope of work within assigned Projects.
Complete necessary inspection reports and documentation.Records daily quality control observations on all construction activities in daily inspection logs and takes photos of the progress.
Inspect and evaluate the adequacy of work performed by contractors; Identify non-conformities, analyze root causes, and inform stakeholders of required corrective measures.
Coordinate University QC activities with GC/ CMs.
Maintain daily project reports/ logs for assigned Projects.
Manage and monitor required University owned material & systems testing and verify proper testing process of CM owned scope.
Conduct pre-final/final inspections; establish punch list; and ensure all deficiencies are corrected.
Conduct and/or attend QC meetings.
Verify that the assembling and submittals required by the Contractor(s) for project closeout documents include O&M manuals, as-builts, warranties, and other relevant project-specific information/ data per University standards.
Prepare documentation for each definable feature of work in their area of responsibility; Distribute written inspection/test results to appropriate project personnel/stakeholders.
Ability to organize tasks and work efficiently
Assist the Executive Director of Capital Projects with project management related tasks in the construction phase as assigned;
Schedule monitoring
Financial monitoring
Closeout phase administration
Development & administering of scope required for Existing Facility Assessments
Other duties as assigned.
Knowledge, Skills, Abilities & Other Attributes
Bachelor's Degree from an accredited college or university program in one of the following disciplines: Engineering, Architecture, Construction Management, Engineering Technology, Building Construction, or Building Science; related field or equivalent combination of education and experience may be substituted for this requirement.
Must have 5+ years of relevant construction experience as a quality control manager or have worked in the construction field for a CM/GC firm for medium ($10 million or more) construction projects.
Must have a good understanding of applicable construction laws for local, state, and federal regulatory requirements.
Ability to communicate with clients in written and oral formats, solve problems, and have attention to detail with proper paperwork.
Ability to prioritize and organize own work to meet agreed-upon deadlines.
Works with others to achieve team goals.
Thorough knowledge and understanding of construction means and methods.
Unusual Working Conditions
Able to navigate through active construction sites and adhere to all site safety requirements necessary to accomplish inspections as required for the role.
May require evening and weekend hours.
Quality Assurance Coordinator
Quality assurance manager job in Stamford, CT
*This role is geared toward an entry level candidate (i.e. recent college graduate who possesses 1-3 years of professional work experience)
About Harvest Hill:
Harvest Hill Beverage Company is one of the nation's largest independent branded beverage producers, delivering consistent annual revenue growth, with sales of over $1 billion. The company was formed in June 2014 with the acquisition of Juicy Juice and further expanded with 3 subsequent acquisitions which were consolidated into one company in May 2017. Our portfolio of iconic brands includes Juicy Juice , SunnyD , Veryfine , Fruit2O , Little HUG , Daily's Cocktails , and Nutrament . We manufacture, market, and distribute across multi-channels including Grocery, Mass Merchandisers, Warehouse Clubs, Convenience, Foodservice, and Liquor Distributors.
Harvest Hill is headquartered in Stamford, CT with a nationwide network of manufacturing and distribution facilities, employing over 1,000 employees in the United States. For more information visit harvesthill.com.
Position Summary:
The QA Coordinator posts files to appropriate internal/external sites and ensures corresponding databases are maintained and up to date. Creates, maintains and ensures all internal HHBC finished product quality documentation is current, accurate and project timelines for the QA team are maintained. The QA Coordinator creates updates & sustains Customer Portal and program documentation; carries out follow-up activities with customers and generates finished product standards as necessary. Directly assist in customer, consumer and field complaint support activities.
Primary Position Responsibilities:
• Maintain and update internal/external databases (TraceGains/Repositrak/Others) with customer documentation through active engagement in customer portal processes. Generate monthly reports defining completeness, gaps and goals.
• Preserve the Harvest Hill customer list identifying products and manufacturing locations with a routine engagement of the gap assessment and resolution activities.
• Efficiently coordinate the tracking of consumer, customer and field complaints with weekly reports.
• Issue ongoing consumer investigation requests and maintain logs with timeline completion rates. Follow-up with sites on investigations. Support QA Mgr in trends and Complaint rates by categories.
• Assists QA Mgr in developing concise feedback on status of field CAPA's and associated timelines.
• Supports retrieval of technical details in the development of external and internal technical specifications for finished goods. Meanwhile adhering to HH, FDA, State and Local Regulations and Co-Manufacturing Alliance agreements.
• Update and sustain Customer Portal with appropriate program documentation. Ensure through management engagement that customers receive the correct and accurate information. (no more no less). Foster meetings and communication with sales, customer service and QA to ensure accuracy.
• Illustrate QA meetings as assigned, document activities and initiate follow-up.
• Manage the receipt of new products, trial samples, consumer complaints that are delivered to the CT office. Track and photo packages received, identify location to store and act on disposal as required. Reach out to Sr Director or QA Mgr for direction.
• Generate quarterly project timelines for the QA department corporate team.
• Analyze & support QA Mgr in recommended next steps as it relates to handling and transportation deficiencies of finished goods.
• AX acumen for the HHBC QA team. Within the first 180 days, train on AX, develop tutorials and train all members of our CT staff.
• Review all co manufacturer requests for destruction of surplus, expired or defunct finished goods.
• As a back-up to cross-functional QA team, learn documentation OOSR, ATS, shelf-life update process.
• Support Co-Man and DC Trace exercises which occur a few times a year.
• Support product manual upkeep with direct supervision by Head of FSQA.
• Additional duties that may be assigned.
Position Qualifications:
• Candidate should possess a BS/BA degree in science, project management or related field and a minimum preferred of two years of professional career experience.
• Proven experience of working with databases, include inputting and extracting data.
• Excellent attention to detail with organizational and planning skills.
• Ability to self-manage, prioritize and work under pressure to tight deadlines.
• Ability to communicate effectively with colleagues, participants and external stakeholders.
• Ability to work effectively as part of a team.
• Undertake any training and professional development as and when required.
• Proficient in Microsoft Office, particularly Access, Word and Excel. Systems experience may include: Microsoft Access, TRACEGAINS, Sharepoint and Red Zone.
Auto-ApplyCustomer Service and Quality Assurance Coordinator - Japanese
Quality assurance manager job in Islandia, NY
▶︎ Job Details: • Job Title: Customer Service and Quality Assurance Coordinator • Working Location: Long Island City, NY 11101 • Working Style: On-site • Employment Type: Full-time, Non-exempt • Salary: DOE (approximately $20 - 25 per hr) • Language: English (Business level), Japanese (Business level)
▶︎ Position Overview:
We are seeking a proactive and detail-oriented professional to take ownership of key responsibilities directly reporting to senior management. This role will be pivotal in enhancing our customer satisfaction, addressing claims, and maintaining effective communication with clients and partners.
▶︎ What will you do:
• Client and Supplier Communication: Serve as the main liaison between the company and clients, suppliers, or business partners during the inspection and quality control process.
• Claims Management and Issue Resolution: Act as the primary point of contact for claims received from overseas customers.
• Negotiation and Relationship Building: Act as the primary point of contact for claims received from overseas customers.
• Negotiation and Relationship Building: Collaborating with the estimator, negotiate effectively with partners and suppliers to address and resolve concerns while maintaining positive working.
• Quality Assurance Support: Collaborate with the operations team to inspect and review incoming goods, ensuring compliance with quality standards.
• Customer Service and Feedback Management: Follow up with customers' post-delivery to ensure satisfaction and address any concerns or returns.
▶︎ Required Qualifications & Skills:
• 2 years of customer service experience preferred.
• Exceptional communication and interpersonal skills with an ethical mindset.
• Detail-oriented with excellent problem-solving abilities.
• Ability to work collaboratively with internal teams and external partners.
• Experience in a flexible work environment is a plus.
• English and Japanese language skills at a business level.
• Strong organization and self-motivation skills.
• Ability to communicate effectively and work in a team.
• Understanding of collaboration in a fast-paced environment.
• Proficiency in using computers and technology for inventory and communication purposes.
▶︎ Preferred Qualifications:
• Understanding of supply chain logistics, including common obstacles and practical solutions (not required but a plus).
▶︎ Work Environment:
• Full-time, on-site position: Work performed in an office environment, requiring the ability to operate standard office equipment and keyboards, with verbal communication.
Auto-ApplyManufacturing Quality Manager
Quality assurance manager job in Shelton, CT
Dependable. Enthusiastic. Driven to succeed. Bring your manufacturing skills to a role that has direct impact on delivering cutting edge technology to our global customer base.
Family-owned for over 75 years, Precision Resource is a leading global supplier of precision metal components and assemblies using a fineblank production method. We provide solutions to quality, cost and production challenges for market-leading customers in industries such as automotive, heavy duty, medical, electronics, cutlery and defense.
Precision Resource offers:
Benefits package including health, dental, life and vision insurance
401(k) with match and profit sharing
Annual bonus based on division profitability
Vacation and flexible paid holidays
Wellness and Employee Assistance Programs
Tuition reimbursement and paid training
Work with an established team of long-term employees
Our Connecticut division, located in Shelton, seeks a Quality Manager.
Summary
The Quality Manager has overall responsibility for managing the Quality department in order to establish advanced quality and reliability engineering to enhance product quality, reliability and acceptance.
Essential Duties and Responsibilities
Set, direct & support priorities of the Quality team (development of accountabilities for each team member)
Review/re-set objectives in conjunction with on-time performance evaluations
Develop, implement and improve departmental metrics
Drive continual improvement process within the Quality department
Develop a continuous learning process for all staff (proper measurement techniques, identifications fit/function - critical characteristics, standardization of acceptance criteria)
Ensure NCR's (Nonconformance Reporting), inspection, SPC, Gauge Maintenance, Cost of Quality, internal audits, etc. are accurate and completed in a timely manner
Lead/support problem resolution and responsiveness of all customer quality related issues
Customer liaison
Attend supplier conferences
Review all 8D reports and corrective actions implemented
Actively participate in APQP, FMEA and quote review meetings
Ensure Division maintains IATF 16949 certification
Improve and maintain accurate Quality procedures and manuals
Qualifications, Education, Experience
BS in Engineering or highly technical training equal to a 4-year program or 4-10 years of manufacturing experience in the metal working industry
5- 10 years of supervisory experience within a manufacturing environment
Experience with formal documentation systems and methods particularly ISO9001 and IATF 16949
Experience in the automotive industry preferred.
Precision Resource is an equal opportunity employer, M/F/D/V. To learn more, visit **********************************
Auto-ApplySupplier Quality Development Mgr
Quality assurance manager job in Rocky Hill, CT
**_About_** **_this_** **_position_** At Henkel, you'll be part of an organization that's shaping the future through innovation, sustainability and collaboration. With our trusted brands like Persil , 'all , Loctite , Snuggle , and Schwarzkopf and our cutting-edge technologies, you'll have countless opportunities to explore new paths and grow.
This position is with our Adhesive Technologies business unit - where we empower our people to transform industries and provide our customers with a competitive advantage through adhesives, sealants and functional coatings.
Dare to learn new skills, advance in your career and make an impact at Henkel.
**What you´ll do**
+ Lead and Execute Comprehensive Supplier Quality Audits (System - ISO 9001/IATF 16949, Process - VDA 6.3, and Product).
+ Drive Supplier Quality Development Programs by conducting root cause analysis and improvement plans of systemic supplier weaknesses.
+ Own End-to-End Supplier Issue Resolution Processes (Supplier Complaints and Customer Complaints caused by Suppliers) by leading cross-functional sessions for complaints resolution, especially in Critical and High Potential cases.
+ Drive cost recovery initiatives from suppliers by leveraging root cause analysis outcomes, contractual terms, and cross-functional alignment with Legal and Procurement teams.
+ Review and approve supplier qualification packages, ensuring compliance with Henkel's product-specific requirements and adhesive material validation protocols.
**What makes you a good fit**
+ Proven expertise in supplier quality auditing (ISO 9001, IATF 16949, VDA 6.3), root cause analysis (8D, A3, FRPS), supplier development and qualification, cross-functional leadership, and digital/lean transformation-supported by strong analytical, communication, and negotiation skills.
+ Qualification: Bachelor's degree in engineering, Chemistry, or a related field (master's or relevant certifications are a plus).
+ 7+ years of experience in Supplier Quality or Quality Engineering, ideally in the chemical or manufacturing industry.
+ Health Insurance:affordable plans for medical, dental, vision and wellbeing starting on day 1
+ Work-Life Balance: Paid time off including sick, vacation, holiday and volunteer time, flexible & hybrid work policies (depending on role), and vacation buy / sell program
+ Financial: 401k matching, employee share plan with voluntary investment and Henkel matching shares, annual performance bonus, service awards and student loan reimbursement
+ Family Support: 12-week gender neutral parental leave (up to 20 weeks for parents giving birth), fertility support, adoption & surrogacy reimbursement, discounted child and elderly care, and scholarships
+ Career Growth:diverse national and international growth opportunities, access to thousands of skills development courses, and tuition reimbursement
The salary for this role is $95,000.00 - $110,000.00. This is the range that we in good faith anticipate relying on when setting wages for this position. We may ultimately pay more or less than the posted range and this range. This salary range may also be modified in the future.
Henkel does not accept unsolicited resumes from search firms or employment agencies. Unsolicited referrals and resumes are considered Henkel property and therefore, Henkel will not pay a fee for any placement resulting from the receipt of an unsolicited referral.
Henkel is an equal opportunity employer. We evaluate qualified applicants without regard to race, color, religion, sex, age, national origin, disability, veteran status, genetic information, and other legally protected categories.
**JOB ID:** 25080459
**Job Locations:** United States, CT, Rocky Hill, CT
**Contact information for application-related questions:** *****************************
Please do not use this email address for sending your application or CV. To apply, please click on the "Apply for this role" button below. Applications sent via e-mail will not be accepted.
**Application Deadline:** As long as the vacancy is listed on our Career Site, we are happy to receive your application
**Job-Center:** If you have an application already, you can create or log in to your accounthere (******************************************************************************************************************************************************** to check the status of your application. In case of new account creation, please use your email address that you applied with.
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