
Quality Project Manager
Westborough, MAJobSeen 1 day agoSeen in employer's feed 1 day ago
Most applications go out cold — see where you stand first. No sign-up to start.
Watch jobs like this. New roles like this one near Westborough, MA, by email.
Don't just apply. Show up ready.
Olive works from this exact posting.
At a glance
Olive lists jobs from US employers, including remote roles you can work from the United States.
Requirements
Credentials this posting asks for.
Job overview
The Associate Quality Control Manager works with Operations, Quality, and Engineering to improve quality performance and ensure compliance with quality standards. The role performs inspections and tests on assemblies, components, and products throughout production, and supports process improvements, failure analysis, nonconformance and corrective-action activities, and audits. It is intended to build professional quality-control experience for a higher-level quality role.
Skills & qualifications
Skills
Qualifications
Benefits
Full job description
Summary:
The Associate Quality Control Manager will work with Operations, Quality and Engineering to continuously improve quality performance while ensuring compliance to quality standards. This role performs a variety of quality control inspections/tests on assemblies, components and product at various stages of the production process to ensure compliance with quality and reliability standards. This position is intended for an individual to acquire Professional Quality Control experience that can be leveraged in a higher level Quality role.
Essential Duties and Responsibilities:
-
Perform dimensional and visual acceptance inspection of raw material, in-process and completed Electro-Mechanical Assemblies to drawings, specifications, work instructions and routing sheets.
-
Make recommendations for improving processes, technical documents, equipment and/or train operators.
-
Conduct any required special testing, failure analysis, validations, etc.
-
Troubleshoot returned merchandise from customers (RMAs).
-
Documentation : develop and maintain all appropriate and required Level documents, i.e., checklist, work instructions, logs, etc.
-
Inspection : Perform inspection of sub-assemblies, raw material, periodic in-process checks, and final inspections, using internal drawings, schematics and quality inspections tools.
-
Non-conformance : Initiate and process nonconforming material documentation and related activities associated with non-conforming material and/or product with Process and Quality Engineers.
-
Corrective Action : Assist with the process of documentation and related activities associated with internal and external corrective action, preventative actions.
-
Audits: Support internal and external (registrar and customer) audits as required..
-
Maintain a safe and clean work environment.
Qualifications
Job Knowledge, Skills & Abilities:
-
Some experience with Geometric Dimensioning and Tolerancing (GD&T). Desired.
-
Self-motivated, analytical, good time management, detail oriented and thorough.
-
Ability to work well with other people. Strong communication skills in speaking and writing.
-
Excellent organizational, verbal, facilitation, listening, and written communication skills.
-
Strong analytical skills and problem solving.
-
Able to use the Microsoft Office Suite, specifically Word, Outlook, Excel and Power Point
-
Experience assisting with process validations (IQ/OQ/PQ) is a plus.
Experience/Education:
-
Bachelor's degree.
-
10 years working in an electronic manufacturing environment especially in a contract manufacturing.
-
10 years of previous quality experience.
-
Mil-STD 883 Experience is a plus
-
AS9102 or First Article Inspection experience is a plus.
Due to ITAR and / or CUI compliance, this position requires candidates to be a U.S. Citizen.
Benefits Offered: Comprehensive benefit package including medical, dental and vision coverage; company-paid basic life/AD&D insurance, short-term and long-term disability insurance; voluntary supplemental insurances, flexible spending accounts and employee assistance program (EAP). Sick Leave, Vacation Time, and company-paid Holidays are also provided as paid time off. NEOTech also provides a 401(k) Retirement Savings Plan option with a company match.
NEOTech is an Equal Opportunity/Affirmative Action employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex including sexual orientation and gender identity, national origin, disability, protected Veteran status, or any other characteristic protected by applicable federal, state, or local law.
NEOTech has a long-standing commitment to maintaining a safe, quality-oriented and productive work environment. We also want all employees to perform their duties safely and efficiently, in a manner that protects their interests and those of their co-workers. We recognize that alcohol and drug abuse pose a threat to the health and safety of NEOTech employees and to the security of the Company’s equipment and facilities. For these reasons, NEOTech is committed to the elimination of drug and alcohol use and abuse in the workplace. Candidates being considered for hire must pass a pre-employment background check and drug test which include screening for illegal drugs and marijuana.
Similar jobs, posted recently
Open roles like this one, listed in the last 30 days.
Manager - Corporate ComplianceCVS Health · Woonsocket, RI (Hybrid) · $66–146K/yrPosted 1w agoPosted 1w ago
Manager, Project ManagementPanera Bread · Newton, MA (Hybrid) · $92–110K/yrPosted 4 days agoPosted 4 days ago
Program Manager - Terminal Modernization (Onsite)RTX Corporation · marlborough, MA · $108–205K/yrPosted 5 days agoPosted 5 days agoQuality Management Nurse ConsultantCVS Health · Remote · US · $61–130K/yrPosted 4 days agoPosted 4 days ago
Manager, Marketing Ops, Content Quality ReviewCVS Health · Hartford, CT (Hybrid) · $66–159K/yrPosted 3 days agoPosted 3 days ago
You've read the whole posting — now see how you match it.