QC Manager Job at CESO, INC. (Akron)

QC Manager

We are a food manufacturer and distributor, and are currently looking for a QC M...

Location

Canada , Richmond

Salary:

6700.00 - 7200.00 CAD / Month

Azuma Foods Canada

Expiration Date

Until further notice

Requirements

Complete 2-year or 4-year degree in Food Science, Food Technology, or Science education with 6 credits courses relevant to food safety or equivalent
Minimum 5-year QC/QA in food industry with 3-year management experience
Minimum 3-year audit experience against one of GFSI schemes, preferably FSSC 22000
Experienced in establishing food safety management system against one of GFSI schemes
Excellent knowledge at food safety system
Experienced in leading food safety team
Excellent organizational and analytical skills and attention to detail
Excellent problem-solving skills
Excellent time management to handle multitask at fast pace working environment
Experience in setting department goals, managing department budget, and evaluating crews

Job Responsibility

Implement, maintain, and continue improve the food safety system
Conduct in house food safety training
Investigate non-conformities, review corrective action plan, and verify the implementation
Lead food safety team
Hire, train, supervise, and evaluate department staff
Set department goals and budget
Report any food safety issues to direct department supervisor or manager
Report any injuries to direct department supervisor or manager and first aid attendant

Fulltime

Quality Control Technician

The Quality Control Technician is responsible for performing inspections, testin...

Location

United States , Akron

Salary:

Not provided

OnQ

Expiration Date

Until further notice

Requirements

High School or equivalent work experience
1-3 years quality control experience
Previous Warehouse and shipping experience
Thorough knowledge of production techniques
Proficient in Microsoft Excel
Strong problem-solving skills and attention to detail
Effective written and verbal communication skills
Ability to work in a fast-paced environment and meet deadlines consistently
Willing to help in all areas on the production floor and other depts.
Work well within a team

Job Responsibility

Oversee established QC process and work directly with the QC Manager to drive continuous improvement by utilizing lean techniques
Maintain a production traceability program that will enable tracking of production by day and line
QC audit production for all first and last pieces of production while periodically inspecting 10% to 20% throughout the production process, inspecting up to 100% if requested
Identify and document non-conforming materials and provide assistance with rework
Prepare and post all QC documents to shared network
Work with QC Manager to help develop Corrective Action Responses (CARs) for any identified quality issues
Ensure recurring audits for shipping, receiving, and fulfillment activities are actioned while tracking quality control metrics for each
Work closely with graphics, engineering, shipping, receiving, fulfillment, and production departments to drive the QC process
Effectively communicate with all levels of management
Action OnQ QC processes as well as assist QC Manager help develop and implement new processes

Fulltime

Manager, Quality Systems (QMS)

As the Manager, Quality Systems, you will support the design, implementation, an...

Location

Canada , Vancouver

Salary:

94880.00 - 118600.00 CAD / Year

AbCellera Biologics

Expiration Date

Until further notice

Requirements

5+ years of experience managing quality systems in a GxP-regulated environment, with demonstrated application of global CMC/GMP requirements and relevant regulations and guidance
Bachelor’s degree in a relevant scientific or engineering discipline with 8+ years of industry experience in biotechnology, pharmaceuticals, or life sciences
Strong understanding and hands-on experience with quality management systems and continuous improvement principles, including their application to QC laboratory operations and regulated environments
Solid understanding of drug development processes from discovery through CMC development, with the ability to translate business and regulatory requirements into practical, compliant solutions
Experience supporting, configuring, or owning QC laboratory electronic systems (e.g., LIMS, LES, CDS) in a GMP-regulated environment, including system lifecycle management and change control
Proactive in identifying opportunities for improvement, with strong critical thinking and problem-solving skills

Job Responsibility

Establishing, supporting, maintaining, monitoring, and continuously improving the QC Quality Management System (QMS) framework and associated quality system processes in compliance with applicable global CMC/GMP requirements
Supporting the operation, administration, and lifecycle management of QC laboratory electronic systems (eSystems), ensuring they effectively support sample management, analysis, data acquisition, data review, and result reporting in compliance with global GMP, data integrity, and regulatory requirements
Contributing to the design, implementation, and evolution of the QC data architecture, identifying eSystem capabilities needed to support QC workflows, data integrity (ALCOA++), and phase-appropriate compliance
Serving as the Business Process Owner (BPO) for QC laboratory systems (e.g. LIMS, LES, CDS), overseeing system changes, enhancements, and upgrades throughout the system lifecycle
Overseeing and maintaining QC eSystems master data, including user roles, permissions, system configurations, and controlled data objects
Developing, reviewing, and maintaining GMP procedures, work instructions, controlled documentation, and training materials governing the compliant and effective use, administration, and data management of QC eSystems, including delivery of end-user training sessions
Providing QC eSystem support for investigations, deviations, and CAPAs, including data retrieval, audit trail review, and system impact assessments
Supporting qualification and computer system validation activities for QC systems (e.g., protocol and risk assessment review, validation deviations/exceptions, and lifecycle documentation)
Managing QC eSystem licensing, user access, vendor relationships, and budgeting/forecasting for QC digital infrastructure
Collaborating cross-functionally with QC, Quality Systems, IT, Engineering, Validation, and external vendors to ensure QC eSystems are fit-for-purpose, compliant, and aligned with laboratory and business processes

What we offer

Equity
Annual bonus dependent on team and company performance
6% (non-match) RRSP contribution
CAD $1,500 annual Active Lifestyle Allowance
Annual vacation
Professional development opportunities
Comprehensive health benefits
Scientific and technical mentorship
Teams and social groups to build community and connections

Fulltime

Quality Control Manager

CMS Corporation is currently seeking a Quality Control Manager (QCM) to oversee ...

Location

United States , Tamuning

Salary:

Not provided

CMS Corporation

Expiration Date

Until further notice

Requirements

Minimum of five (5) years of combined experience as a Superintendent, QC Manager, Project Manager, Construction Manager, or Project Engineer on similar contracts
Minimum of two (2) years direct experience as a QC Manager
Completed the Construction Quality Management (CQM) for Contractors course within the past 5 years or must obtain within 90 days of award
Must be capable of reviewing construction drawings and interpreting critical path schedules
Must be familiar with EM 385-1-1 Appendix Q requirements and able to oversee construction involving activities such as excavation, confined space entry, fall protection, electrical work, cranes, and rigging
Must be on-site when work relevant to their area of oversight is being performed
Bachelor’s degree from an accredited institution in Engineering, Construction Management, Architecture, Engineering Technology, or a related field
CQM certification required (current or within 90 days of contract award)
Completion of OSHA 30-Hour and 40-Hour Contract Safety Awareness Courses (within 60 days)
Strong working knowledge of EM 385-1-1 and associated regulations

Job Responsibility

Maintain safety on-site in coordination with project safety personnel
Participate in key project meetings including preconstruction, coordination, and progress meetings
Lead and document the Three-Phase Quality Control process
Schedule and manage Preparatory and Initial Phase meetings and report on outcomes
Coordinate with the Superintendent to stop non-conforming work and log deficiencies
Submit daily QC reports with photo documentation
Coordinate submittal reviews and maintain submittal registers
Track and review testing activities and maintain logs and reports
Maintain daily updates to as-built drawings and ensure proper documentation of changes
Ensure all materials and work are in compliance with contract requirements

What we offer

Health, Vision, and Dental Insurance
AFLAC
401(k) with company match
Paid Time Off
Life Insurance
Paid Holidays

Fulltime

New

Quality Control Supervisor

We are looking for a dedicated Quality Control Supervisor to join our Radiopharm...

Location

United Kingdom , Guildford

Salary:

Not provided

Alliance Medical Ltd

Expiration Date

Until further notice

Requirements

Educated to degree level in a relevant scientific discipline
Appropriate industrial experience in QC testing of pharmaceuticals
Experience in radiopharmacy is highly desirable
Previous experience in QC testing of radiopharmaceuticals within a GMP‑compliant environment
Experience in the operation, maintenance, and validation of QC equipment (HPLC, GC, rTLC, Gamma spectrometry, Traditional wet chemistry techniques)
Understanding of completing maintenance activities within a GMP‑regulated facility
Experience working in a radiation‑controlled environment is desirable
Proficient in Microsoft Windows, Word, Excel, PowerPoint, and Project
Excellent written and verbal communication skills
Strong interpersonal skills

Job Responsibility

Oversee day-to-day QC activities for all radiopharmaceutical products
Maintain full competency in QC analysis and participate in routine testing
Manage raw materials including testing and release
Oversee environmental monitoring and media fills
Communicate any equipment, facility, or process issues to management
Share best practice across the UK radiopharmacy network
Undertake training to perform frontline fault diagnosis
Support QC Manager and OEM engineers during maintenance, testing, and validation
Support routine calibration of all QC equipment
Liaise with QC Managers to ensure adequate resources meet operational demands

Fulltime

Quality Control Manager

The Quality Control Technician is responsible for performing inspections, testin...

Location

United States , Akron

Salary:

Not provided

OnQ

Expiration Date

Until further notice

Requirements

5+ years of proven QC experience in the manufacturing sector
College degree or equivalent work experience - Relevant educational background, preferably in the field of manufacturing
Experienced in physical warehouse activities as it pertains to the manufacturing of products.
Understanding of common product warehousing, inventory and shipping practices.
Experience with managing contract manufacturers including purchasing, receiving, packing and shipping activities.
Working knowledge of QA and QC practices common to product manufacturing.
Knowledge of manufacturing methods particular to Printed materials, plastics, woodworking and machined and fabricated metal processes.
Proficient in Microsoft Excel.
Strong problem-solving skills and attention to detail.
Effective written and verbal communication skills.

Job Responsibility

Manage the QC process and drive continuous improvement by utilizing lean techniques.
Develop and maintain a production traceability program that will enable tracking of production by day and line.
QC audit production for all first and last pieces of production while periodically inspecting goods throughout the process.
Prepare and post all QC documents to shared network.
Implement and maintain Corrective Action Response (CAR) for any identified quality issues.
Oversee the schedule of recurring audits for shipping, receiving and fulfillment activities and create quality control metrics for each department.
Work closely with graphics, engineering, shipping, receiving, fulfillment and production departments to drive the QC process.
Effectively communicate with all levels of management
Action OnQ QC processes as well as develop and implement new processes.
Assist with the development and implementation of high priority programs as needed.

Fulltime

New

Senior QC Systems Officer

We are recruiting for a Senior QC Systems Officer to join a leading pharmaceutic...

Location

United Kingdom , Wrexham

Salary:

Not provided

SRG

Expiration Date

Until further notice

Requirements

A degree or similar qualification in Chemistry or a relevant scientific field
Proven experience in a GMP Quality Control (QC) laboratory setting
Excellent technical knowledge relating to laboratory equipment, and QC instrumentation such as HPLC
Experience in Instrument & equipment qualification, change management & troubleshooting
Strong computer skills & knowledge of QC Pharmaceutical Automated Systems & Automated Systems Validation

Job Responsibility

Provide technical expertise & support for QC equipment & Instrumentation
Manage the qualification, procurement, implementation & validation of new equipment
Manage GMP QC computer systems such as HPLC software, ensuring compliance with quality & data integrity regulations
Lead equipment related deviation investigations

Fulltime

Quality Control Manager/specialist (pol) - Dod Installation

POL Quality Control Managers/Quality Control Specialists. Position Summary: Resp...

Location

Salary:

Not provided

CMS Corporation

Expiration Date

Until further notice

Requirements

Five (5) years of DoD POL construction-related management experience within the last five (5) years (commercial or military experience does not apply)
Three (3) consecutive years of on-site experience as a POL Quality Control Specialist within the last five (5) years
Associate’s degree in Construction Management or Engineering, or a High School Diploma/GED with equivalent field experience
Certificate of completion from a USACE or NAVFAC QC Management course (current, not older than 4 years)
Ability to meet eligibility requirements for access to U.S. Government facilities (security clearance not required)
OSHA 30-Hour Training Certificate (not older than 5 years)
Confined Space Competent Person Certificate
Current CPR & AED Certificate
Ability to represent the company verbally, in writing, and in person
Ability to make decisions and take responsibility for results

Job Responsibility

Responsible for overall management of the QC program and acting in all QC matters for the contractor
Coordinate, implement, oversee, and document the quality control program on DoD POL projects
Identify, analyze, and develop improvements in productivity and client service as they relate to the quality management system

QC Manager

CESO, INC.

Location:
United States , Akron ▼
Charlotte
Cleveland
Dayton
Minneapolis
Nashville
Rogers

Category:
IT - Administration

Contract Type:
Not provided

Salary:

Job Description:

Job Responsibility:

Requirements:

Nice to have:

Additional Information:

Job Posted:
February 17, 2026

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CESO, INC.

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Job Posted:February 17, 2026

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