11 Quality Control Specialists jobs in Syracuse
Bridge Inspection - Quality Control Engineer
Posted 3 days ago
Job Viewed
Job Description
Prudent Engineering is in need of a Bridge Inspection - Quality Control Engineer to join our growing Bridge Inspection Team. This is a full-time position based in our Albany, Syracuse, or Rochester, New York offices.
Job Summary:
The Bridge Inspection QC Engineer is responsible for ensuring the accuracy, completeness, and compliance of bridge inspection reports and data, adhering to all applicable federal, state, and local regulations, codes, and standards.
What you'll be able to do:
- Conduct thorough reviews of bridge inspection reports, element level data, load ratings, and other related documentation for completeness, accuracy, consistency, and adherence to established procedures, standards, and specifications.
- Verify the accuracy and integrity of field data, including element condition ratings, measurements, and photographs. Ensure proper documentation of deficiencies and recommendations for maintenance or repair.
- Ensure all inspection activities and documentation comply with relevant federal, state, and local regulations, including NBIS requirements and NYSDOT policies.
- Provide technical guidance and support to bridge inspection teams regarding inspection procedures, data collection techniques, and report preparation.
- Develop and deliver training programs for bridge inspectors to enhance their skills and knowledge.
- Maintain accurate records of QC reviews, track deficiencies, and monitor corrective actions. Generate reports on QC activities and findings.
- Effectively communicate with bridge inspection teams, NYSDOT personnel, and other stakeholders regarding QC findings and recommendations.
- Utilize and maintain proficiency in relevant bridge inspection software and databases.
- Currently registered as a Professional Engineer (PE) in New York State or have the ability to transfer an out-of-state PE registration.
- At least five years of bridge experience in design, construction, inspection, or other bridge related work.
- Completed NHI Course - Safety Inspection of In-Service Bridges.
- NHI Bridge Inspection Training and other relevant certifications (e.g., fracture critical inspection) are preferred.
- Thorough understanding of bridge inspection principles, techniques, and procedures.
- Familiarity with AASHTO LRFD Bridge Design Specifications, NYSDOT Bridge Inspection Manual, and NBIS requirements.
- Strong analytical, problem-solving, quality control and management skills.
- Excellent written and verbal communication skills.
- Proficiency in using bridge inspection software and databases. Ability to work independently and as part of a team.
- Valid New York driver's license and ability to travel.
- A base salary of $65 to $90 per hour. *
- Medical, dental, and vision insurance.
- 401K with company match.
- PTO and paid holidays.
- Unlimited opportunities to advance your career.
Prudent Engineering is an Equal Opportunity Employer.
*Actual compensation may vary based on work experience, location, market conditions, education/training, certifications, and other credentials, as well as applicable knowledge and skills.
About the Firm:
Our mission: Transforming infrastructure for the next generation with passion and kindness.
We provide quality, cost-effective engineering services to state and local governments and private-sector clients across New York State and Pennsylvania. Our project portfolio features experience in bridge, highway, and structural design; condition and safety inspection; civil and site engineering support; construction inspection and administration; survey and mapping; and hydrographic services.
Quality Assurance Engineer
Posted 16 days ago
Job Viewed
Job Description
Location: Skaneateles, NY 13135
Duration: 12 Months Contract
Pay range: $28/hr. on W2
Job Summary:
- This position is responsible for areas of the Quality System. Identify and assess regulatory and quality risk in activities and processes according to regulatory agency rules and guidelines and Client quality practices.
Essential Functions:
- This position manages the project investigations and day-to-day task assignments within the Corrective and Preventive Action (CAPA) program within their assigned site. The position also has responsibility to work closely with various managers at the facility to monitor, manage and maintain metrics for the CAPA program in their specific area. Additionally, this position is responsible for standardizing the CAPA program across different Client sites in the Front Line Care (FLC) division.
- Specific responsibilities may include, but are not limited to:
- Ensures efficient processing of nonconformance management for the Quality Management System in Trackwise.
- Maintain Quality Metrics for Client/CAPA timeliness and makes recommendations for improvement.
- Leads and facilitate discussions with CAPA owners to drive completion of investigations, root-cause analysis, impact analysis, and closure of events.
- Write, review, analyze and revise written Standard Operating Procedures (SOPs) and submit procedural changes as needed to meet Corporate, Divisional, Plant, Regulatory Requirements, etc.
- Identifies areas for process/quality improvements and supports those efforts.
- Owns and manages several project investigation records at one time.
- Analyze trends to monitor the effectiveness of the CAPA process and drive remediation for improvement
- Follows Good Documentation Practices (GDP) and ensures compliant documentation related to area of responsibility.
Qualifications, Knowledge, And Skills Required:
- Must have computer proficiency with solid experience in Microsoft Word, Excel, Trackwise, SAP, and other systems.
- Ability to work effectively as part of a cross functional team.
- Ability to relate and work well with people.
- Excellent organizational, presentation, and verbal/written communication skills.
- Attention to detail.
- Ability to multi-task and work well under pressure.
- Expertise in interpreting regulations and familiarity with GDP and GMP
- Experience with working in an environment subject to compliance with 21 CFR Parts 7, 11, 803, 806, 810, 820 strong preferred.
- Associate or BS in business, science, or engineering required
- 1-2 years' experience in Quality with a medical device/pharma or other regulated industry.
- Working knowledge of other medical device regulatory requirements (US, Canada and Europe) highly desirable.
- The physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of the job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.
- While performing the duties of this job, the employee:
- Must be able to sit for most of the work day.
- Ability to stand or walk for long periods as well.
- Must have good hand to eye coordination and dexterity
Physical Requirements:
- Dynamic Lifting capability: Must have the ability to lift 40 pounds at a time.
- Work environment characteristics described here are representative of those that must be met by an employee to successfully perform the essential functions of the job.
- Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.
This is a manufacturing environment regulated by the FDA and many other work rules to prevent damage to the product we manufacture. Some of those work rules include but are not limited to:
- Wearing a static protective smock at all times while in the work area
- Wearing a ground wrist strap and plugging that wrist strap into the working table.
- Working in close proximity to other employees.
- Working in an environment that is temperature and humidity controlled.
Quality Assurance Engineer
Posted 22 days ago
Job Viewed
Job Description
Chipton Ross is seeking a Quality Assurance Engineer for a contract opportunity in Skaneateles, NY.
JOB SUMMARY:
We are seeking a Systems or Quality Engineer to be responsible for integrating design procedures, templates, and guidance documents within our client's ISO 13485 compliant Quality Management System (QMS). The successful candidate will have a working knowledge of FDA/ISO regulations, specifically ISO 13485 (7.3) and 21 CFR 820.30, and the application of Good Documentation Practices. Demonstrate ability in writing quality system procedures. The ideal candidate will have a demonstrated ability to communicate with a wide range of stakeholders, including Quality, Systems/Risk, Project Management, Regulatory Affairs, Marketing, and others.
BASIC QUALIFICATIONS (REQUIRED SKILLS/EXPERIENCE):
1. Medical Device experience
2. Knowledge of ISO 13483 and 21 CFR 820.30
3. Experience writing Standard operating procedures (SOP's)
4. Strong writing and communication skills
5. Knowledge of Agile Product Lifecycle Management Tool preferred
6. Knowledge of SAP Tool preferred
POSITION RESPONSIBILITIES:
o Complete SOP gap assessments for process integration focused on the Front Line Care division.
o Participate in 'deep dive' reviews of selected procedures with Subject Matter Experts (SMEs). Ensure that process details driven by prior corrective actions are reviewed and maintained as appropriate.
o Write/update, review, analyze, and revise Standard Operating Procedures (SOPs), work instructions, forms, templates.
o Drive reviews/approvals of SOPs with cross functional Subject Matter Experts (SME's).
o Monitor actions for proper SOP implementation.
o Report periodic integration status to stakeholders.
o Work with different functional groups and produce appropriate documentation in support of SOP integration.
o Strong verbal and written communication skills, documentation practices, be self-motivated and possess strong interpersonal skills.
o Excellent problem-solving skills and attention to detail.
REQUIRED EDUCATION:
Relevant Bachelor's Degree required
WORK HOURS:
First Shift, Full Time
Quality Assurance Engineer II
Posted 22 days ago
Job Viewed
Job Description
We are seeking a Systems or Quality Engineer to be responsible for integrating design procedures, templates, and guidance documents within our ISO 13485 compliant Quality Management System (QMS). The successful candidate will have a working knowledge of FDA/ISO regulations, specifically ISO 13485 (7.3) and 21 CFR 820.30, and the application of Good Documentation Practices. Demonstrate ability in writing quality system procedures. The ideal candidate will have a demonstrated ability to communicate with a wide range of stakeholders, including Quality, Systems/Risk, Project Management, Regulatory Affairs, Marketing, and others.
Responsibilities:
- Complete SOP gap assessments for process integration focused on the Front-Line Care division.
- Participate in 'deep dive' reviews of selected procedures with Subject Matter Experts (SMEs). Ensure that process details driven by prior corrective actions are reviewed and maintained as appropriate.
- Write/update, review, analyse, and revise Standard Operating Procedures (SOPs), work instructions, forms, templates.
- Drive reviews/approvals of SOPs with cross functional Subject Matter Experts (SME's).
- Monitor actions for proper SOP implementation.
- Report periodic integration status to stakeholders.
- Work with different functional groups and produce appropriate documentation in support of SOP integration.
- Strong verbal and written communication skills, documentation practices, be self-motivated and possess strong interpersonal skills.
- Excellent problem-solving skills and attention to detail.
- Is a bachelor's degree Required? YES.
- How many years of recent experience does this person need to have? 2-4.
- Medical Device experience.
- Knowledge of ISO 13483 and 21 CFR 820.30.
- Experience writing Standard operating procedures (SOP's).
- Strong writing and communication skills.
- Knowledge of Agile Product Lifecycle Management Tool.
- Knowledge of SAP Tool.
Quality Assurance Engineer I- CTQ
Posted 16 days ago
Job Viewed
Job Description
SUMMARY:
This position is responsible for areas of the Quality System. Identify and assess regulatory and quality risk in activities and processes according to regulatory agency rules and guidelines and *** quality practices.
ESSENTIAL FUNCTIONS:
This position manages the project investigations and day-to-day task assignments within the Corrective and Preventive Action (CAPA) program within their assigned site. The position also has responsibility to work closely with various managers at the facility to monitor, manage and maintain metrics for the CAPA program in their specific area. Additionally, this position is responsible for standardizing the CAPA program across different *** sites in the Front Line Care (FLC) division. Specific responsibilities may include, but are not limited to:
- Ensures efficient processing of nonconformance management for the Quality Management System in Trackwise.
- Maintain Quality Metrics for Client/CAPA timeliness and makes recommendations for improvement.
- Leads and facilitate discussions with CAPA owners to drive completion of investigations, root-cause analysis, impact analysis, and closure of events.
- Write, review, analyze and revise written Standard Operating Procedures (SOPs) and submit procedural changes as needed to meet Corporate, Divisional, Plant, Regulatory Requirements, etc.
- Identifies areas for process/quality improvements and supports those efforts.
- Owns and manages several project investigation records at one time.
- nalyze trends to monitor the effectiveness of the CAPA process and drive remediation for improvement
- Follows Good Documentation Practices (GDP) and ensures compliant documentation related to area of responsibility.
- Must have computer proficiency with solid experience in Microsoft Word, Excel, Trackwise, SAP, and other systems.
- bility to work effectively as part of a cross functional team.
- bility to relate and work well with people.
- Excellent organizational, presentation, and verbal/written communication skills.
- ttention to detail.
- bility to multi-task and work well under pressure.
- Expertise in interpreting regulations and familiarity with GDP and GMP
- Experience with working in an environment subject to compliance with 21 CFR Parts 7, 11, 803, 806, 810, 820 strong preferred.
- ssociate or BS in business, science, or engineering required
- 1-2 years' experience in Quality with a medical device/pharma or other regulated industry.
- Working knowledge of other medical device regulatory requirements (US, Canada and Europe) highly desirable.
While performing the duties of this job, the employee:
- Must be able to sit for most of the work day.
- bility to stand or walk for long periods as well.
- Must have good hand to eye coordination and dexterity
- Physical Requirements: Dynamic Lifting capability: Must have the ability to lift 40 pounds at a time.
This is a manufacturing environment regulated by the FDA and many other work rules to prevent damage to the product we manufacture. Some of those work rules include but are not limited to:
- Wearing a static protective smock at all times while in the work are
- Wearing a ground wrist strap and plugging that wrist strap into the working table.
- Working in close proximity to other employees.
- Working in an environment that is temperature and humidity controlled.
Cascade Maverik: Quality Assurance Associate
Posted today
Job Viewed
Job Description
Audit manufacturing processes, lab testing processes and health & safety requirements Perform visual inspection of each product checking parts and assemblies to ensure that each product meets all standards of presentation and quality in a timely fash Quality Assurance, Assurance, Continuous Improvement, Production Associate, Associate, Quality, Business Services
Senior Software Quality Assurance Engineer
Posted today
Job Viewed
Job Description
Senior Software Quality Assurance Engineer Minimum Years of Experience Required : 6+ Years Salary range : $125,000 - $150,000 Work Authorization : Candidates must be a Permanent Resident or have existing work authorization in the United States to be considered. We are unable to sponsor work visas for this position. About the Role : We are seeking a Senior Software Quality Assurance Engineer to ensure the quality and reliability of our software products, with a specific focus on testing features and systems that incorporate AI / ML models. You will be responsible for designing and executing comprehensive test plans, developing automated tests, and identifying and tracking defects, including those related to AI model performance or integration issues. This role requires a meticulous approach, a strong commitment to quality, and an understanding of the unique testing challenges presented by AI. Key Responsibilities : Develop and execute comprehensive test plans and test cases (manual and automated) for software features, including those that rely on AI / ML models. Design, develop, and maintain automated testing frameworks and scripts using appropriate tools (e.g., Selenium, Pytest, etc.). Identify, record, document thoroughly, and track bugs, including investigating potential issues related to AI model behavior or data. Collaborate closely with software developers, product managers, and ML engineers to understand the functionality and expected behavior of AI-powered features and ensure testability. Develop strategies for testing the integration of AI models within the software system. Contribute to the continuous improvement of our QA processes and methodologies, particularly for testing AI components. Perform regression testing and performance testing as needed. Advocate for quality throughout the software development lifecycle. Contribute to the design of testable software features. Qualifications : Minimum 6 years of experience in software quality assurance. Strong knowledge of SQA methodologies, tools, and processes. Experience in writing clear, concise, and comprehensive test plans and test cases. Hands-on experience with automated testing tools and frameworks. Experience with testing backend APIs and frontend applications. Familiarity with SQL and testing database interactions. Understanding of the software development lifecycle and agile methodologies. Experience or strong interest in testing applications that incorporate machine learning models or AI features is highly desirable. Excellent attention to detail and problem-solving skills. Benefits : 401(k) with company match Professional Development Opportunities Flexible Work Arrangements Comprehensive Health, Dental, and Vision Insurance Generous Paid Time Off and Holidays Create a job alert for this search Senior Quality Assurance Engineer • Syracuse, New York, United States #J-18808-Ljbffr
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Quality Assurance Associate-DIRECT HIRE!
Posted 10 days ago
Job Viewed
Job Description
**Salary:**
+ $21/hr (depending on experience)
**Shift:**
+ 1 st Shift: 6am-430pm (M-TH or T-F)
**Benefits:**
+ Health, Vision, Dental, and Life insurance
+ 401(k) matching
+ Employee assistance program
+ Flexible spending account
+ Paid time off
+ Parental leave
+ Referral program
+ Tuition reimbursement
**Responsibilities** :
+ Perform in-house line audits of pharmaceutical filling and packaging operations; review manufacturing activities and documentation for compliance with SOPs
+ Perform line clearances, in-process, and end-item inspections
+ Review and apply specifications for acceptance of in-coming packaging components, raw materials, and finished products
+ Generate, review, and issue batch production records
+ Release materials & components for use in production
+ Organize and issue printed materials to production
+ Monitor & interpret charts and gauges
+ Log book review, issuance, and archival. Successful candidates will be highly motivated, self-starters with knowledge of contemporary cGMP practices and procedures. Good written and oral communication is essential.
+ Technical writing is a plus.
**Qualifications** :
+ Associate's degree in science, or equivalent is required. Bachelor's degree in science, or equivalent is preferred.
+ 1-4+ years' experience in Quality Assurance or Manufacturing, preferably in an FDA regulated environment.
+ Working knowledge of cGMPs is preferred.
+ Knowledge and skill in using micrometers, calipers, and light inspection unit is required. Must be able to effectively manage time and work with minimal supervision is preferred, training will be provided onsite.
Apply now for immediate consideration for these QA Auditor roles in Syracuse, NY. We look forward to connecting with you!
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**APPLY TODAY** with your updated resume and **TEXT "Start" to ( ** for more information and next steps!
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USA - Quality Assurance Engineer I- CTQ
Posted 22 days ago
Job Viewed
Job Description
Onsite Hybrid
SUMMARY:
This position is responsible for areas of the Quality System. Identify and assess regulatory and quality risk in activities and processes according to regulatory agency rules and guidelines and Baxter quality practices.
ESSENTIAL FUNCTIONS:
This position manages the project investigations and day-to-day task assignments within the Corrective and Preventive Action (CAPA) program within their assigned site. The position also has responsibility to work closely with various managers at the facility to monitor, manage and maintain metrics for the CAPA program in their specific area. Additionally, this position is responsible for standardizing the CAPA program across different Baxter sites in the Front Line Care (FLC) division. Specific responsibilities may include, but are not limited to:
• Ensures efficient processing of nonconformance management for the Quality Management System in Trackwise.
• Maintain Quality Metrics for Client/CAPA timeliness and makes recommendations for improvement.
• Leads and facilitate discussions with CAPA owners to drive completion of investigations, root-cause analysis, impact analysis, and closure of events.
• Write, review, analyze and revise written Standard Operating Procedures (SOPs) and submit procedural changes as needed to meet Corporate, Divisional, Plant, Regulatory Requirements, etc.
• Identifies areas for process/quality improvements and supports those efforts.
• Owns and manages several project investigation records at one time.
• Analyze trends to monitor the effectiveness of the CAPA process and drive remediation for improvement
• Follows Good Documentation Practices (GDP) and ensures compliant documentation related to area of responsibility.
QUALIFICATIONS, KNOWLEDGE, AND SKILLS REQUIRED
• Must have computer proficiency with solid experience in Microsoft Word, Excel, Trackwise, SAP, and other systems.
• Ability to work effectively as part of a cross functional team.
• Ability to relate and work well with people.
• Excellent organizational, presentation, and verbal/written communication skills.
• Attention to detail.
• Ability to multi-task and work well under pressure.
• Expertise in interpreting regulations and familiarity with GDP and GMP
• Experience with working in an environment subject to compliance with 21 CFR Parts 7, 11, 803, 806, 810, 820 strong preferred.
EDUCATION/EXPERIENCE REQUIRED
• Associate or BS in business, science, or engineering required
• 1-2 years' experience in Quality with a medical device/pharma or other regulated industry.
Working knowledge of other medical device regulatory requirements (US, Canada and Europe) highly desirable.
The physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of the job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.
While performing the duties of this job, the employee:
• Must be able to sit for most of the work day.
• Ability to stand or walk for long periods as well.
• Must have good hand to eye coordination and dexterity
• Physical Requirements: Dynamic Lifting capability: Must have the ability to lift 40 pounds at a time.
Work environment characteristics described here are representative of those that must be met by an employee to successfully perform the essential functions of the job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.
This is a manufacturing environment regulated by the FDA and many other work rules to prevent damage to the product we manufacture. Some of those work rules include but are not limited to:
• Wearing a static protective smock at all times while in the work area
• Wearing a ground wrist strap and plugging that wrist strap into the working table.
• Working in close proximity to other employees.
• Working in an environment that is temperature and humidity controlled.
EEO:
"Mindlance is an Equal Opportunity Employer and does not discriminate in employment on the basis of - Minority/Gender/Disability/Religion/LGBTQI/Age/Veterans."