Quality Assurance Specialist

Keystone Industries; Gibbstown (NJ); On-site; USD 80,000 - 100,000; Full time

Benefits offered by this job

Weekly Pay

Comprehensive Health Coverage

401(k) Retirement Plan

Paid Time Off & Holidays

Employee Assistance Program

Career Development Opportunities

Job summary

Keystone Industries in Gibbstown, NJ is seeking a Quality Assurance Specialist to ensure products meet GMP, ISO 13485 and regulatory requirements. You will coordinate QA activities, lead internal audits, and support CAPA and change management.

The role emphasizes documentation, training, and supplier qualification, with opportunities to influence quality systems and participate in management reviews.

Qualifications

• Minimum 5 years of Quality Assurance and ISO Quality System experience.
• FDA cGMP knowledge for medical devices; ISO 13485 experience is required.
• Strong analytical and problem-solving skills with documentation focus.

Responsibilities

• Lead QA activities for new projects across divisions and coordinate regulatory compliance.
• Perform batch record reviews and manage CAPA, deviations, and change control.
• Maintain and improve Quality Management System elements and generate management reports.
• Assist with risk assessments, supplier qualification, and internal audits.

Skills

Quality Assurance

Regulatory knowledge

Auditing

Documentation

Leadership

Education

Bachelor’s degree in a technical field

Tools

MasterControl

Job description

Company Overview

We are passionate about our employees. We strive to create an environment that is stimulating and motivating and a culture that fosters mutual respect, teamwork, and career development. Come join the Keystone team so we can build your career together!

Job Details

In addition to competitive starting salaries, we offer a wide variety of competitive benefits, perks and programs that provide our employees the resources to pursue their goals, both at work and in their personal lives.

Please visit our website at www.keystoneind.com to learn more about Keystone Industries and career opportunities.

Position Details

• Title: Quality Assurance Specialist
• Schedule: 8:30 am - 5:00 pm M-F, with some flexibility.
• Location: Gibbstown, NJ (08027)
• Salary/Pay Range (based on experience and qualifications): $80,000 - $100,000 annually, based on experience and qualifications.

Position Overview

The Quality Assurance Specialist ensures products and processes adhere to relevant industry standards, regulations, and specifications by coordinating and supporting activities of the QA Team related to Keystone’s Quality Management System as identified below:

Essential Job Functions

• Provide general guidance, and/or training to members of the team on Annual Product Reviews (APRs), Internal Audits, Change Management, Complaint Management, CAPA, deviation and Batch Card approval.
• When assigned, serve as the lead QA liaison for new project initiatives across new divisions, leading all related QA activities.
• Ensure all record requirements for project planning, design control, purchasing activities, customer complaints and other feedback, etc. are met.
• Define/clarify cGMP and ISO standard requirements and help coordinate Keystone's efforts for meeting them. Coordinate/revise/assist with the GMP/GDP training program and ISO Awareness program as needed.
• Oversee the Supplier Quality Management System. Work with other department members to qualify suppliers and perform continuous evaluation. Issue and manage supplier corrective action requests. Lead external (supplier) audits and complete associated reports.
• Maintain assigned quality system elements, including but not limited to the Internal Audit system, APRs, Customer Complaint Handling, Deviations, Non-Conformances, and CAPA systems. Participate in the completion, review and approval of the documents associated with these systems.
• Generate reports to update management on GMP Compliance status.
• Perform batch record reviews, ensure follow-up and resolution of any issues, and confirm that all documentation is completed and maintained accurately.
• Assist with quality system documentation including but not limited to writing, revising and proof-reading Quality System Procedures, Keystone's Quality Manual, department or task instructions, SOP's, checklists, forms, etc.
• Prepare and maintain product technical documents, validation documents, change managements and other technical and quality system documents and records as necessary.
• Assist with Management Reviews of the Quality System. Review and summarize trend analysis data as requested such as customer complaints, product and system non-conformances, returns and credit data, CAR/PARs, etc. Prepare or assist with Management Review Reports, Annual product Review Report, data presentation and ensure appropriate meeting minutes are recorded, and follow-up activities are performed and documented.
• Advise with project planning, design control and risk assessment responsibilities as necessary. Assist with risk analysis and product Post Market Surveillance activities as required.
• Help to update device tech files to meet new regulatory requirements.
• Assist with cleaning and process validation activities as needed.
• Inform Management of problems found within the quality system and updates on improvements or necessary corrective actions.
• Participate in external regulatory, customer and ISO Notified Body audits. Act as SME for QMS related activities. Help coordinate/document resulting corrective action closeout activities.
• Create, revise, and manage contractual quality agreements and standards with external partners.
• Support company goals/objectives and plans for meeting set goals.
• Handle customer communication as necessary.
• Complete special assignments and prepare reports/project summaries, as required.
• Perform additional duties/tasks as needed or requested by management.

Qualifications

• Minimum 5 years of Quality Assurance and ISO Quality System experience. Relevant experience may be leveraged.
• Strong analysis and problem-solving skills, including, but not limited to, the ability to review and analyze Manufacturing, Quality Control, and validation data.
• Demonstrated FDA cGMP knowledge for medical devices. Pharmaceutical knowledge a plus.
• Understanding of current ISO 13485 and supporting ISO standard requirements.
• Demonstrated knowledge of system auditing techniques and requirements.
• Demonstrated knowledge of FDA’s complaint handling requirements.
• Demonstrated knowledge of Clinical and Biological Evaluation standards/requirements.
• Leadership/mentoring skills.
• Strong decision-making skills.
• Ability to successfully prioritize and track multiple concurrent/complex projects with minimal guidance.
• Exceptional interpersonal skills-ability to interface and communicate/collaborate at all levels internally and externally.
• Excellent writing skills.
• Exceptional project management and organizational skills.
• Excellent time-management skills and deadline driven.
• High attention to detail.
• Proficiency in Microsoft Office applications (Outlook, Excel, Word, PowerPoint).

Desired Skills

• MasterControl a plus.

Education/Certifications

• Bachelor’s degree in a technical field (chemistry, biology, biochemistry, or similar); will consider non-degreed relevant work experience in quality, regulatory, or related field.
• ISO Quality System Training.
• Internal Auditor Training.

Safety

• Comply with all safety regulations; maintains a safe work environment at all times.
• Adhere to always wearing the proper PPE/Safety equipment.
• Understand and comply with all written safety, health, and environmental procedures.
• Attend all required scheduled Health, Safety and Environmental training sessions.
• Participate in required Health, Safety and Environmental initiatives and programs.
• Perform required administrative functions related to Health, Safety and Environmental functions such as completing forms, checklists, and log sheets.

Physical Demands and Work Environment

• Physical Demands: Employee is required to walk; stand; sit; use hands and fingers to manipulate objects, tools, or controls; reach with hands and arms to operate a computer and other office equipment, and occasionally lift/move up to 25 lbs. Minimal need to balance, stoop, bend, kneel or climb.
• Work Environment: This position is located in an office setting, within a manufacturing facility. Noise intensity level: quiet to low. Employees may occasionally need to enter manufacturing or lab areas, including cleanroom environments, which may include exposure to moderate noise, moving equipment, and hazardous contaminants. When entering these areas, employees must adhere to all applicable safety protocols, including Personal Protective Equipment (PPE) and/or gowning requirements. Occasional travel may be required for audits, inspections, site visits, customer meetings or events, and industry conferences.

Benefits And Perks

• Weekly Pay
• Comprehensive Health Coverage - Medical, Dental & Vision Plans
• Flexible Spending Accounts (FSA) - Medical & Dependent Care or Health Savings Account (HSA) Options
• Company-Paid Life Insurance + Additional Voluntary Options
• 401(k) Retirement Plan with 3% Employer Contribution (after 1 year)
• Fitness Benefits - Onsite Gym (Headquarters) or Membership Reimbursement (other sites)
• Paid Time Off & Holidays to support work-life balance
• Employee Assistance Program (EAP) for confidential support
• Financial Wellness Resources
• Employee Discounts & Perks (Eagles games, concert tickets, etc.)
• Company Social Events & Team Activities
• Career Development Opportunities & Internal Growth