Site QA / QC Manager Job at Airswift Sweden (Afungi)

Construction Field Engineer (Interface Engineer- Instrument)

Job summary/Role description: Reports to the Site Manager. Field Engineering is ...

Location

United Arab Emirates , Ruwais

Salary:

Not provided

Met T&S

Expiration Date

Until further notice

Requirements

Bachelor’s Degree in Engineering
No experience is required – Fresh Graduates
Completed National Service (without exception)
Excellent communication skills in English
Willingness to work at site (Ruwais)
Fluent English
Excellent analytical skills
Excellent communications and interpersonal skills
Strong interpersonal, team-oriented skills, self-motivation and direction, with strong bias toward timely performance and problem resolution
Attention to detail, strong communications and interpersonal skills

Job Responsibility

Reports to the Site Manager
Field Engineering is the logical continuation of engineering activities carried out at Home Office
Responsible for the checking and the correct management of the Project documentation, of the amendments and/or additions to the same
Cooperates with the Site Manager and the Construction Manager in verifying the feasibility of the construction schedule on the ground of the actual availability at Site of technical documentation and materials
Ensures any addition or change to the technical documents according to Field requirements and he is responsible for reviewing of site technical queries, including field sketches and modifications to any project engineering drawings, as required
Executes, in coordination with Contractor Home Office, any modifications and additions to Project documents, providing for final “as-built” revision of the same
To ensure the recording, filing, reproduction, proper distribution and control of Plant Construction documents
Provide assistance to Construction Management/Supervision Group for Project system definitions and turnover/hand over documentation at Project completion phase
To ensure inspection, as required to support the QA-QC group
Review, as required, construction method statements

What we offer

Single Status
Accommodation on Site
Local Transportation on Site

Fulltime

Director of Quality

Mantell Associates is partnered exclusively with a globally operating CDMO to re...

Location

United States , Massachusetts

Salary:

Not provided

Mantell Associates

Expiration Date

Until further notice

Requirements

Significant quality leadership experience within a CDMO, pharmaceutical or biotechnology manufacturing environment – CDMO experience strongly preferred
Proven experience leading site-level quality operations at scale, ideally within a large, complex GMP manufacturing facility
Hands-on experience across both biologics/mAb and small molecule modalities
Deep knowledge of FDA GMP regulations (21 CFR Parts 210/211/600) and relevant ICH guidelines
Demonstrated experience managing FDA inspections with a strong track record of successful outcomes
Proven QC oversight experience, with a solid understanding of analytical operations and laboratory compliance
Strong client-facing skills with the ability to build credibility and trust at a senior level
Exceptional leadership and people management skills, with experience developing large, diverse quality teams
Strategic thinker with the operational presence to engage credibly at all levels of a large manufacturing site
Bachelor’s degree or above in a relevant life sciences discipline

Job Responsibility

Own and drive the site QMS, ensuring all systems, processes and documentation are robust, inspection-ready and aligned with global quality standards
Lead site GMP compliance across biologics/mAb and small molecule manufacturing operations, ensuring adherence to FDA regulations and ICH guidelines
Oversee the site CAPA programme, deviation management and change control processes, ensuring issues are investigated thoroughly and resolved effectively
Drive a proactive, right-first-time quality culture across all site functions, from manufacturing and QC through to supply chain and engineering
Provide strategic and operational oversight of the site QC function, ensuring analytical testing, raw data review and results reporting meet the highest standards of accuracy and compliance
Partner with QC leadership to ensure laboratory operations are fully compliant, inspection-ready and continuously improving
Oversee out-of-specification (OOS) and out-of-trend (OOT) investigations, ensuring robust root cause analysis and appropriate corrective actions
Serve as the site quality authority for all regulatory matters, leading preparation for and management of FDA inspections and any other relevant agency interactions
Provide quality oversight and input into regulatory submissions, ensuring site-level documentation and data packages meet agency expectations
Monitor the evolving regulatory landscape and proactively update site quality systems and practices to maintain compliance

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

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

GIS Intern

The GIS Intern will support projects to manage our maps and mechanisms for track...

Location

United States , Cleveland

Salary:

19.82 - 21.85 USD / Hour

Engage Cleveland

Expiration Date

Until further notice

Requirements

Candidate must be enrolled in school or must have graduated within 24 months from the date of application
Declared Majors: Geography/GIS, Environmental Sciences, Information Technology Systems, Engineering, Engineering Technology, Planning, or a related field of study
Any of the following degree program levels may qualify: Bachelor’s degree (Junior/Senior), Master’s degree, Doctoral degree
Candidate must be able to commit to a fixed-term assignment of 12 months with an option to extend at NEORSD’s discretion
Candidate must be able to work 40 hours per week (Monday-Friday) during normal business hours
ArcGIS experience is preferred
Candidate must possess a valid driver’s license with a driving record in accordance with the District’s acceptable guidelines

Job Responsibility

Analyze and update impervious area (IA) dataset to support the Regional Stormwater Management Program
Perform data analysis, QA-QC and updates in accordance with billing procedures/guidelines
Performs data research to support QA-QC task including County Parcel Auditor sites and Billing Agent systems
Develop products (maps, data, and reports) to document progress on QZ-QC tasks
Coordinate with the Community Discharge Permit Program Specialist to process OUPS tickets, including mapping locations, creating polygons, updating attributes, managing documentation, and distributing drawings through Outlook or ShareFile
Ensure timely completion of tickets within two business days
Create and update web maps, application, scripts, and datasets to support District data collection and maintenance needs
Follow procedures to archive completed project datasets from ArcGIS online and document as needed
Provide metadata creation and updates as requested

What we offer

Health Insurance Coverage
Various Retirement Planning Options (Ohio Public Employee Retirement System and Deferred Compensation Plans)
Flexible Spending Accounts
Employee Assistance Program
Free Parking at our facilities
Corporate Discounts
Active Health & Wellness Program that promotes a life/work balance

Fulltime

New

Project Manager

Location

Malaysia , Kuala Lumpur

Salary:

13000.00 - 15000.00 RM / Month

Randstad

Expiration Date

June 14, 2026

Requirements

Bachelor’s Degree in Civil Engineering, Architecture, Construction Management, or a related field
Minimum of 8 years in property development, specifically handling projects from end-end
Proficiency in MS Project, AutoCAD, and financial modeling for development
Exceptional negotiation tactics, a solutions-oriented mindset, and the ability to manage diverse stakeholder interests under pressure

Job Responsibility

Conduct feasibility studies and due diligence for potential land acquisitions
Manage the appointment of consultants (Architects, Engineers, Surveyors) and lead the design development phase
Navigate the local authority submission process to secure all necessary planning permissions and building approvals
Oversee the tendering process, including pre-qualification of contractors and evaluation of bids
Negotiate contracts and ensure all legal and insurance requirements are met before mobilization
Liaise with the Quantity Surveyor to finalize the Bill of Quantities (BQ) and project budgets
Act as the primary point of contact between the developer, site teams, and external stakeholders
Monitor site progress against the Master Program, identifying potential bottlenecks before they impact the critical path
Ensure rigorous Quality Assurance (QA) and Quality Control (QC) standards are upheld on-site
Manage project cash flows, approve progress claims, and control variations to prevent budget overruns

Fulltime

New

Corporate Quality Manager

Your mission Contribution to the Continuous Improvement of the Corporate Midas ...

Location

China , Shanghai

Salary:

Not provided

Life Science Talent

Expiration Date

Until further notice

Requirements

Graduation in Science e.g. Chemistry, Pharmacy, Biotechnology is also preferred
Minimum 5 years of working experiences in the Pharmaceutical Industry
Minimum 3 years in Quality Management aspects (e. g. Auditing, Project Management, Production, Validation, QA, QC etc.), auditing experience is preferred
Excellent knowledge of national and international pharmaceutical guidelines (e. g. EU GMP Parts, WHO-Guidelines, ICH-Guidelines, US FDA, cGxP guidelines etc.)
Business/Technical fluent English skills
Experience in working in cross-functional project teams
High social competences, good team worker
Flexibility and ability to work in fast developing environment
Effective Time Management skills

Job Responsibility

Contribution to the Continuous Improvement of the Corporate Midas Pharmaceutical Quality System
Management of international GxP and Regulatory standards during sourcing, development, procurement, manufacturing and supply chain of Drug Substances (IM, API) and Medicinal products (FDF)
Participation and Coordination of Corporate Quality Management activities
QM Compliance Process Responsibilities
e.g. Document management, Change control, Deviation, Complaint, CAPA, Trainings
Communication with the manufacturing and development partner and reviewing, advising and compiling of GxP and regulatory relevant documents
Product Life Cycle Management
Registration, Coordination, Evaluation and follow-up of Changes, Non-conformities which appear in the framework of internal as well as external established processes
Securing the high Midas compliance level with regard to international cGMP regulations (e.g. EU, US, AUS)
Cooperation in inter-divisional, Midas Pharma group-wide and / or cross-company projects

Fulltime

Quality Manager

Are you an experienced Quality professional looking for a hands-on role where yo...

Location

United Kingdom , Bishop's Stortford

Salary:

36000.00 - 45000.00 GBP / Year

SRG

Expiration Date

Until further notice

Requirements

Proven experience of quality assurance gained in food, beverage or consumer goods manufacturing
A hands-on, self-starter who can manage multiple, changing priorities and problem solve independently
Excellent communications skills, able to maintain relationships with clients and suppliers alike
Willing to travel to UK manufacturing sites
Competence with basic analytical and laboratory equipment.

Job Responsibility

Leading QC testing, approval & remote sign‑off of production samples
Investigating issues, conducting root cause analysis & driving corrective actions
Owning relationships with technical clients, including support for ongoing production
Maintaining accurate, compliant documentation & overseeing risk management
Supporting continuous improvement, safeguarding and technical troubleshooting
Reviewing & approving analytical & micro results as part of positive release
Building & managing relationships with external manufacturing partners
Auditing, onboarding & supporting new suppliers, including early‑stage production runs
Applying compliance knowledge while enabling innovation within category legislation
Managing approvals for new products, including sensory and analytical assessments

What we offer

bonus
private healthcare

Fulltime

Site QA / QC Manager

Airswift Sweden

Location:
Mozambique , Afungi

Category:
Energy

Contract Type:
Not provided

Salary:

Job Description:

Job Responsibility:

Requirements:

Additional Information:

Job Posted:
January 15, 2026

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