Manager, QC Systems Job at AbCellera Biologics (Vancouver)

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Specialist QC, QC Systems (Deviations)

This job specification outlines the general responsibilities associated with the...

Location

Ireland , Dun Laoghaire

Salary:

67993.20 - 91990.80 EUR / Year

Amgen

Expiration Date

Until further notice

Requirements

Hold a third level qualification in science related discipline
Have minimum 6 years’ experience in Biotechnology/ Pharmaceutical setting
Possess key competencies to include Planning and Organisation, Communication, Teamwork, Flexibility and Adaptability
Excellent Technical Writing skills
Proficient in Root Cause Analysis
Detailed knowledge of the QC function and is operationally savvy
Proven Experience of handling GMP investigations within a Quality System
Demonstrated Leadership attributes: Delivers Results

Job Responsibility

Champion for Investigations in Quality Control
Owns and Manages Investigations for QC through DQMS
Authors and reviews investigation reports
Participates routinely in the investigation triage process
Ensures investigations are kept up to date and compliant with procedures
Ensure investigations result in robust CAPA to prevent recurrence
Seeks out opportunity to improve the process and management of Investigations
Error Management Champion, SME for error management and error reduction in QC
Lead improvement initiatives as required e.g. Predict, Prevent, Improve (PPI)
Strong focus on RFT and Lean

Fulltime

Specialist, QC Systems

As the Specialist, QC Systems, you will support the design, implementation, and ...

Location

Canada , Vancouver

Salary:

76000.00 - 95000.00 CAD / Year

AbCellera Biologics

Expiration Date

Until further notice

Requirements

3+ 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 5+ 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

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
Supporting 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)
Supporting 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
Strong sense of community and connections through work, clubs, and socials

Fulltime

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

Site QA / QC Manager

Are you ready to take the helm as a Site QA/QC Manager in the dynamic world of s...

Location

Mozambique , Afungi

Salary:

Not provided

Airswift Sweden

Expiration Date

Until further notice

Requirements

Bachelor’s degree in Engineering, Quality Assurance, or a related field
Relevant QA/QC certifications (e.g., ISO 9001 Lead Auditor) preferred
Minimum of 5 years of experience in QA/QC management within the oil and gas industry, particularly in subsea projects
Proven experience in managing quality assurance for subsea installation projects
Familiarity with Floating Production Storage and Offloading (FPSO) systems and their associated quality requirements
Strong knowledge of umbilical systems and their installation processes
Exceptional analytical skills with a keen eye for detail to identify potential quality issues
Excellent verbal and written communication abilities to interact effectively with various stakeholders

Job Responsibility

Oversee all QA/QC activities on-site, ensuring that all work complies with project specifications and standards
Conduct regular inspections and audits of materials, processes, and installations to verify adherence to quality standards
Maintain comprehensive records of inspections, tests, and non-conformance reports, ensuring transparency and traceability
Work closely with project managers, engineers, and subcontractors to foster a culture of quality and continuous improvement
Identify potential quality issues early and implement corrective actions to mitigate risks
Provide guidance and training to site personnel on quality control processes and standards

Fulltime

QC Project Manager

We are seeking a Quality Control (QC) Project Manager to support medical facilit...

Location

United States , Grand Forks Air Force Base

Salary:

Not provided

Bodwé Professional Services

Expiration Date

Until further notice

Requirements

Minimum 4 years of project management experience OR 2 years of medical project management experience
Strong working knowledge of the Military Health System and Defense Health Agency
Familiarity with DHA Facilities Enterprise, Defense Health Networks (DHNs), and service-level facility planning organizations
Working knowledge of DoD medical space planning and design criteria, including SEPS
Proficiency in Microsoft Office Suite: Word, Excel, PowerPoint, Access, SharePoint, and Outlook
Experience with construction administration, documentation, and QA/QC processes
Strong understanding of industry standards for medical facility planning and design
Excellent written and verbal communication skills, with the ability to interact at a senior/executive level
Must have or be able to obtain and maintain a Real ID or Passport in order to undergo commercial airfare travel
Must have or be able to obtain and maintain a valid driver's license

Job Responsibility

Provide on-site project management support for SRM/O&M projects within MTFs
Conduct field surveys, requirements analysis, and stakeholder coordination
Prepare and deliver weekly status reports and project updates
Facilitate design reviews, prioritize work, and support relocation efforts
Coordinate outages and participate in project meetings with stakeholders
Perform continuous on-site surveillance of construction activities
Inspect contractor quality control processes and ensure compliance with contract requirements
Monitor testing requirements and maintain detailed project documentation
Maintain weekly progress photos and construction records
Review contractor submittals, shop drawings, and samples

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

Qc equipment qualification engineer (microbiology / lab systems)

You will join our Life Sciences team in Singapore, supporting qualification and ...

Location

Singapore , Singapore

Salary:

Not provided

Amaris Consulting

Expiration Date

Until further notice

Requirements

Experience in pharmaceutical lab environments (QC / QA / Production), minimum 4 years
Experience in equipment qualification and validation
Academic background in Science, Biology, Microbiology, or related field
English proficiency

Job Responsibility

Drive and support QC equipment qualification activities in line with defined project timelines
Lead qualification lifecycle documentation and execution, including: URS, ERES, HLRA, Vendor & in-house IQ/OQ, PQ and Qualification Reports (QR)
Manage change control processes related to equipment qualification
Investigate and resolve qualification-related deviations and discrepancies
Collaborate with cross-functional stakeholders to ensure compliance and alignment
Ensure timely execution, review, and closure of qualification protocols
Support CAPEX-related activities within QC lab environments
Maintain compliance with HSE (Health, Safety, Environment) guidelines
Identify risks, propose mitigation plans, and participate in risk assessments
Contribute to continuous improvement initiatives in lab operations

What we offer

An international community bringing together 110+ different nationalities
An environment where trust has a central place: 70% of our key leaders started their careers at the first level of responsibilities
A robust training system with our internal Academy and 250+ available modules
A vibrant workplace that frequently gathers for internal events (afterworks, team buildings, etc.)

Fulltime

IT Project Manager - ELN Platforms (Electronic Lab Notebook) & Scientific Data Systems

The IT Project Manager – ELN, Scientific Data Platforms & Manufacturing Systems ...

Location

India , Hyderabad

Salary:

Not provided

NTT DATA

Expiration Date

Until further notice

Requirements

10-15+ years in IT delivery with program-level ownership
8+ years delivering ELN or scientific data platforms in regulated environments
5+ years of MES implementation or integration experience (e.g., batch execution, eBR)
5-8 years of GxP validation (CSV/CSA) ownership across lab and/or manufacturing systems
5+ years driving adoption across scientific and/or manufacturing organizations
5+ years integrating ELN with LIMS/CDS/SDMS AND/OR MES with lab systems
Proven decision-making authority (not support roles)
Notice Period: 30 Days

Job Responsibility

Lead full lifecycle: strategy → design → configuration → integration → validation → deployment → adoption → optimization
Own delivery across lab systems and manufacturing platforms (MES)
Align scientific data strategy with manufacturing execution and batch data flows
Deliver against measurable outcomes: Adoption, Data quality, Compliance, Cycle time
Translate experimental workflows (R&D, QC) and manufacturing processes into structured digital systems
Standardize experiment design (ELN) and batch records & execution workflows (MES)
Ensure traceability from development → production
Own CSV/CSA validation strategy across ELN, MES, integrated lab/manufacturing systems
Ensure compliance with GxP, 21 CFR Part 11, ALCOA+ principles
Accountable for audit readiness and validation documentation completeness

Fulltime

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Manager, QC Systems

Job Description

Job Responsibility

Requirements

What we offer

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