QC and Training Manager Job at JUJUR (São Paulo)

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

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 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 Assurance Manager

This role shall reports to Site Quality Head.

Location

Singapore , Tuas

Salary:

Not provided

Amgen

Expiration Date

Until further notice

Requirements

Doctorate degree
Master’s degree and 2 years of directly related experience
Bachelor’s degree and 4 years of directly related experience
Diploma and 8 years of directly related experience
8+ years of experience in the pharmaceutical industry
Training experience in GMP environment preferred
Proven leadership in cross-functional project management and strategic planning
Strong communication, influencing, and stakeholder management skills
Familiarity with compliance frameworks (EMA, HSA, FDA) and GMP standards

Job Responsibility

Act as site SME and business process owner for training and Learning Management System and represent Singapore site in the Learning and Performance global network
Lead and mentor staff in Team
Support SME and Functional Area Managers as clients of training process, provide infrastructure for training material development and effective deployment and monitoring
Plan, coordinate, implement and monitor GMP training programs and initiatives
Assist in investigations and CAPAs by identifying human performance factors and improvement opportunities
Provide Training impact and assignment requirements to SOP revisions and Change Controls
Represent Training program in internal and external inspections representing areas of responsibility. Ensure training records are accurate and readily available during inspections
Ensure training related metrics and KPIs are monitored and analyzed for site management review and corporate management reviews
Manage New Hire Orientation training and scheduling
Support Quality Systems activities

What we offer

Vast opportunities to learn and move up and across our global organization
Diverse and inclusive community of belonging, where teammates are empowered to bring ideas to the table and act
Generous Total Rewards Plan comprising health, finance and wealth, work/life balance, and career benefits

Manager Quality Assurance Excellence and Innovation

This role shall reports to Site Quality Head. ASM Quality Strategic Planning & G...

Location

Singapore , Tuas

Salary:

Not provided

Amgen

Expiration Date

Until further notice

Requirements

Doctorate degree
Master’s degree and 2 years of directly related experience
Bachelor’s degree and 4 years of directly related experience
Diploma and 8 years of directly related experience
8+ years of experience in the pharmaceutical industry
Training experience in GMP environment preferred
Proven leadership in cross-functional project management and strategic planning
Strong communication, influencing, and stakeholder management skills
Familiarity with compliance frameworks (EMA, HSA, FDA) and GMP standards

Job Responsibility

Act as site SME and business process owner for training and Learning Management System and represent Singapore site in the Learning and Performance global network
Lead and mentor staff in Team
Support SME and Functional Area Managers as clients of training process, provide infrastructure for training material development and effective deployment and monitoring
Plan, coordinate, implement and monitor GMP training programs and initiatives
Assist in investigations and CAPAs by identifying human performance factors and improvement opportunities
Provide Training impact and assignment requirements to SOP revisions and Change Controls
Represent Training program in internal and external inspections representing areas of responsibility
Ensure training records are accurate and readily available during inspections
Ensure training related metrics and KPIs are monitored and analyzed for site management review and corporate management reviews
Manage New Hire Orientation training and scheduling

What we offer

Vast opportunities to learn and move up and across our global organization
Diverse and inclusive community of belonging, where teammates are empowered to bring ideas to the table and act
Generous Total Rewards Plan comprising health, finance and wealth, work/life balance, and career benefits

Qc and Safety Trainer

This position shall have overall responsibility for the environmental services t...

Location

United States , Bethesda

Salary:

41600.00 - 62400.00 USD / Year

CBRE Government & Defense Services

Expiration Date

Until further notice

Requirements

Experience in Microsoft Office
Minimum two years’ experience with training
Strong written and oral communication skills
Customer Service Skills

Job Responsibility

Administer quality control management program as it relates to environmental service operations
Responsible for overall quality assurance program
Maintain records of inspections and certifications
Prepare monthly reports depicting findings of quality inspections
Periodically review the quality control program to ensure compliance
Examine processes for preventative and corrective maintenance
make suggestions based on findings
Perform inspections and re-inspections to ensure problems have been resolved
Research safety and quality topics online
May prepare incident and accident reports

What we offer

medical
well-being
financial planning
short-term incentives

Fulltime

Senior Manager, Quality Control Systems Templating

Lead the team responsible for creation and management of master data templates f...

Location

India , Hyderabad

Salary:

Not provided

Amgen

Expiration Date

Until further notice

Requirements

Master’s degree with 12-16 years of Pharma and Biotech commercial or clinical manufacturing Quality Control experience
Minimum of 5-7 years experience directly managing people and/or leadership experience leading teams, projects, programs, or directing the allocation of resources
Strong project management skills and experience supervising professionals in a Quality organization working with cross functional and global stakeholders across multiple time zones
Working knowledge of cGMP regulations, practices, and trends pertaining to Quality Control
Experience with various laboratory computer systems, equipment/instrumentation, and applications
Excellent written and verbal communication skills, ability to work in a team environment and build relationships with partners
Track record of building and maintaining a high performing team
Strong leadership and negotiation skills with a demonstrated ability to influence others
Demonstrated innovative thinking and ability to transform work organizations
Demonstrated ability to navigate through ambiguity and provide structured problem solving

Job Responsibility

Oversight of the AIN-based QC Systems team in support of QC system master data creation, management and qualification
Collaboration with the global business process owner(s) to resolve issues encountered by the team
Management of request prioritization in alignment with QC network needs
Maintaining alignment between sites on use of QC systems and driving further standardization of testing documentation
Collaboration with other global and site-based QC teams to achieve QC network goals
Support staff training, career development and performance management of team across all three shifts
Responsible for ensuring compliance with safety guidelines, cGMPs and other applicable regulatory requirements
Champion process improvements to increase efficiency and productivity
Assign workload appropriately and strategically based on required interactions with sites in the QC network across multiple timezones
Evaluate master data requests and categorize based on complexity

What we offer

Reasonable accommodation for individuals with disabilities

Fulltime

Qc laboratory apprentice

QC Laboratory Apprenticeship Program 2026. The QC Apprentice will serve as an in...

Location

Ireland , Cork

Salary:

Not provided

BioMarin Pharmaceutical

Expiration Date

Until further notice

Requirements

Pass (Grade O6 or better) in 5 leaving certificate subjects, including Mathematics and one science subject
250 CAO points
OR Successful Level 6 Laboratory Technician Apprentices
Candidates with a Level 6 in a related discipline
Current employee with relevant experience and qualifications
Mature student

Job Responsibility

Management and delivery of samples from production to QC
Carrying out environmental monitoring and water sampling activities
Assisting laboratory analytical personnel, supporting housekeeping activities and consumable stock management
Participating in all training and completion of training records
Ensuring QC documentation and laboratory records are up to date and of an appropriate standard
Assisting in laboratory investigations
Identifying opportunities for improvement within the QC and associated environments
Evaluate results against defined acceptance criteria
Maintain the laboratory in an inspection-ready state

What we offer

Achieve a nationally recognized qualification while working
Get paid a competitive salary whilst working towards a qualification
Learn from experienced mentors in a world-class biopharma environment
Build valuable skills and career prospects in a growing industry
Be part of a supportive, inclusive, and professional team

Fulltime

QC and Training Manager

JUJUR

Location:
Brazil , São Paulo

Category:
-

Contract Type:
Not provided

Salary:

Job Responsibility:

Requirements:

Additional Information:

Job Posted:
January 15, 2026

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Location:Brazil , São Paulo

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