Manager, Quality & Safety Salary at Labels Inc BETA

Job Description: Participate in the New Product Development (NPI) and design changes, Design History File (DHF) and Device Master Record (DMR) reviews meetings and fully understand the design control process and Quality Engineering. Utilize technical training and compliance experience to ensure that company design control projects comply with internal design control procedures in accordance with FDA and ISO requirements. ESSENTIAL JOB RESPONSIBILITIES AND DUTIES INCLUDE: Responsible for overall Design Quality process to ensure that company design control projects comply with internal design control procedures in accordance with FDA, ISO and other applicable requirements. Act as a subject matter expert on design control process and risk management process. Lead Risk Management activities from Product Concept through Commercialization. Provide guidance to internal and external stakeholders and ensure that design control requirements are being met in an effective manner in order to achiev

Vendor Quality Management Manager Key Duties and Responsibilities: Monitors metrics and dashboards for emerging trends for vendors in assigned GMP/GDP area(s). Ensures adequate management and mitigation of risk arising from vendors Supports processes and procedures to report on, manage, and mitigate vendor risk to acceptable levels. Leads and/or participates in process and system improvement efforts as a vendor quality SME. Provides onsite front and/or back room inspection support as assigned Provides insight on vendor risk and its potential impact in quality and business forums Must Have: Strong knowledge of regulatory requirements in GMP/GDP areas Demonstrated experience with key performance indicators and quality metrics for vendors Expertise in risk assessment as it pertains to third parties / suppliers Strong interpersonal skills to explain difficult information and work to build alignment Demonstrated ability to communicate effectively, both orally and in writing Mathematical acu

The Quality Manager position, based in Bedford, MA, will be responsible for: Supporting quality engineering requirements for new product development activities ISO certification and ongoing maintenance of the Quality Management System Driving a cultu Manager, Quality Engineer, Product Development, Management, Quality, Manufacturing, Technology

Vendor Quality Management Manager Key Duties and Responsibilities: Monitors metrics and dashboards for emerging trends for vendors in assigned GMP/GDP area(s). Ensures adequate management and mitigation of risk arising from vendors Supports processes and procedures to report on, manage, and mitigate vendor risk to acceptable levels. Leads and/or participates in process and system improvement efforts as a vendor quality SME. Provides onsite front and/or back room inspection support as assigned Provides insight on vendor risk and its potential impact in quality and business forums Must Have: Strong knowledge of regulatory requirements in GMP/GDP areas Demonstrated experience with key performance indicators and quality metrics for vendors Expertise in risk assessment as it pertains to third parties / suppliers Strong interpersonal skills to explain difficult information and work to build alignment Demonstrated ability to communicate effectively, both orally and in writing Mathematical acu

The Vendor Quality Management Manager proactively assesses vendor risk in GMP/GDP areas and translates this assessment into insights, recommendations, and actions that allow the company to demonstrate appropriate and tailored oversight of our third parties. The role contributes to advancement of processes, tools, and systems that are fit-for-purpose across GMP/GDP areas and vendor types. The ideal candidate MUST have experience working in pharmaceutical quality, Veeva (QMS), supervisor background and has been through inspection process (compliance). Key Duties and Responsibilities: Monitors metrics and dashboards for emerging trends for vendors in assigned GMP/GDP area(s). Ensures adequate management and mitigation of risk arising from vendors Supports processes and procedures to report on, manage, and mitigate vendor risk to acceptable levels. Leads and/or participates in process and system improvement efforts as a vendor quality SME. Provides onsite front and/or back room inspection

Technology & Industry Leaders (Electronics - Automotive) Career Advancements About Our Client My client stands out as a pioneering force in the power electronics industry, known for its cutting-edge and innovative solutions. The company's commitment to high power density and efficiency has positioned it as a leader in the market. They have a global presence, providing reliable power components, modules, and systems to a diverse range of industries, including data centers and telecommunications. Its emphasis on quality management systems ensures products adhere to the highest standards, fostering trust among clients and partners. With a focus on continuous improvement and a reputation for technological excellence, my client remains at the forefront of advancing power electronics worldwide. Job Description Quality Manager key responsibilities: Oversee the RMA (Return Merchandise Authorization) process, including customer requests, return evaluations, and authorization issuance. Serve as

Now Hiring: Quality Engineer – RMA Program Manager (Electronics Manufacturing) Job Type: Permanent (direct to company) Location: *On-site* - Andover, MA We seek a highly technical, customer-focused Quality Engineer to oversee and enhance our client's Return Merchandise Authorization (RMA) program. In this role, you’ll be the primary point of contact for customer-returned products, driving timely processing, failure analysis, and root cause investigation—all while ensuring high standards of product quality and customer satisfaction. Key Responsibilities: Review and process customer RMA requests, determine eligibility, and generate RMA numbers based on company policies. Manage the full RMA lifecycle: product returns, tracking, resolution, and communication with customers. Serve as a technical liaison between customers, engineering, and manufacturing teams to evaluate return issues. Guide engineers in failure analysis and helps prepare technical reports for customer-facing issues. Publish

GDP Operational QA Quality Manager Minimum qualifications: Bachelor’s degree in a scientific or allied health field (or equivalent degree) and 5+ years of relevant work experience, or relevant comparable background. Preferred Qualifications: Bachelor's in a scientific or allied health field and relevant GDP & GMP work experience, or relevant comparable background. 5+ years’ experience serving in a Quality role. Clear understanding to ensure operations do not compromise the quality of products and can demonstrate compliance with GDP. Influencing skills in areas with no direct reporting authority. Strong interpersonal and communication skills. Auditing skills, appropriate qualifications in auditing an advantage. Proficiency in using Microsoft Office applications required (MS Word, MS Excel, MS PowerPoint)