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

New

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

New

Director, Analytical Development and Quality Control

The Director, Analytical Development and Quality Control will oversee quality co...

Location

United States , Waltham

Salary:

175000.00 - 230000.00 USD / Year

Kailera Therapeutics

Expiration Date

Until further notice

Requirements

Bachelor’s degree and 10+ years of experience, or 8+ with advanced degree, in the pharmaceutical/biotech industry with experience in all phases of innovative drug development and commercial launch in accordance with global CMC regulatory filings (IND/NDA/MAA, etc.)
Strong expertise in analytical techniques HPLC/UPLC, LC–MS, SE-HPLC, and dissolution
Knowledge of drug development activities with respect to cGMP, quality systems, ICH guidelines, global regulatory requirements, and USP, EP, JP, and CHP requirements
Hands-on experience managing QC activities performed at CDMOs and third-party testing sites, with an emphasis on release and stability testing
Experience with stability-trending software
Proven experience supporting OOS/OOT investigations, deviations, CAPAs, and change controls
Strong track record of working with CROs/CMOs and managing external QC activities
Demonstrated leadership ability with experience mentoring and developing staff
Strong communication, cross-functional collaboration, and project-management skills
Innovative team-player with high energy for our dynamic company environment

Job Responsibility

Develop phase-appropriate QC strategies, procedures (SOPs), and workflows to support QC operations within the CMC team supporting clinical programs from early development through commercialization
Design, implement, and manage stability programs for drug substances and drug products, including protocol development, execution, trending, and reporting
Utilize stability trending and statistical analysis software (e.g., JMP, SLIMStat) to monitor product performance and predict shelf-life
Oversee QC activities at CDMOs and third-party testing sites, ensuring cGMP compliance, data integrity, and timely release and stability testing
Establish robust data management practices for QC, including electronic systems for data capture, trending, and archival, to support regulatory submissions
Ensure QC activities align with integrated development timelines and global regulatory expectations (ICH, USP, EP, JP)
Provide QC support for investigations (OOS/OOT), deviations, CAPAs, and change controls
Prepare for audits and inspections, representing QC to regulatory authorities
Collaborate cross-functionally with CMC, QA, and Regulatory teams to ensure accurate QC documentation (SOPs, CoAs, protocols, reports)
Strong, demonstrated ability to work effectively in teams and collaborate cross-functionally

What we offer

comprehensive health coverage
flexible time off
paid holidays
a year-end shutdown
monthly wellness stipend
generous 401(k) match
tuition reimbursement
commuter benefits
disability and life insurance
annual bonus opportunities

Fulltime

Director, Analytical Development and Quality Control

The Director, Analytical Development and Quality Control will oversee quality co...

Location

United States , Waltham, Massachusetts; San Diego, California

Salary:

175000.00 - 230000.00 USD / Year

Kailera Therapeutics

Expiration Date

Until further notice

Requirements

Bachelor’s degree and 10+ years of experience, or 8+ with advanced degree, in the pharmaceutical/biotech industry with experience in all phases of innovative drug development and commercial launch in accordance with global CMC regulatory filings (IND/NDA/MAA, etc.)
Strong expertise in analytical techniques HPLC/UPLC, LC–MS, SE-HPLC, and dissolution
Knowledge of drug development activities with respect to cGMP, quality systems, ICH guidelines, global regulatory requirements, and USP, EP, JP, and CHP requirements
Hands-on experience managing QC activities performed at CDMOs and third-party testing sites, with an emphasis on release and stability testing
Experience with stability-trending software
Proven experience supporting OOS/OOT investigations, deviations, CAPAs, and change controls
Strong track record of working with CROs/CMOs and managing external QC activities
Demonstrated leadership ability with experience mentoring and developing staff
Strong communication, cross-functional collaboration, and project-management skills
Innovative team-player with high energy for our dynamic company environment

Job Responsibility

Develop phase-appropriate QC strategies, procedures (SOPs), and workflows to support QC operations within the CMC team supporting clinical programs from early development through commercialization
Design, implement, and manage stability programs for drug substances and drug products, including protocol development, execution, trending, and reporting
Utilize stability trending and statistical analysis software (e.g., JMP, SLIMStat) to monitor product performance and predict shelf-life
Oversee QC activities at CDMOs and third-party testing sites, ensuring cGMP compliance, data integrity, and timely release and stability testing
Establish robust data management practices for QC, including electronic systems for data capture, trending, and archival, to support regulatory submissions
Ensure QC activities align with integrated development timelines and global regulatory expectations (ICH, USP, EP, JP)
Provide QC support for investigations (OOS/OOT), deviations, CAPAs, and change controls
Prepare for audits and inspections, representing QC to regulatory authorities
Collaborate cross-functionally with CMC, QA, and Regulatory teams to ensure accurate QC documentation (SOPs, CoAs, protocols, reports)
Strong, demonstrated ability to work effectively in teams and collaborate cross-functionally

What we offer

comprehensive health coverage
flexible time off
paid holidays
year-end shutdown
monthly wellness stipend
generous 401(k) match
tuition reimbursement
commuter benefits
disability and life insurance
annual bonus opportunities

Fulltime

Senior Site Development Civil Engineer

Bodwé is seeking a highly motivated Site Development Civil Engineer (CE III–IV) ...

Location

United States , Battle Creek

Salary:

Not provided

Bodwé Professional Services

Expiration Date

Until further notice

Requirements

Bachelor's degree in an ABET accredited Civil Engineering program
Minimum 6–10 years of relevant experience in site/civil engineering
At least 2 years in a project management or supervisory role
Professional Engineer (PE) license required
Proven experience managing multi-phase site development projects from planning through construction
Must possess the knowledge and expertise to teach, train, or mentor staff members on matters pertaining to civil engineering plans and specifications
Experience with site development projects
Must have Real ID or Passport in order to undergo commercial airfare travel
Must have valid driver's license
Proficiency in Microsoft Office suite, including Word, Excel, Outlook, Projects, and Teams

Job Responsibility

Serve as a Project Manager or Technical Lead on site development projects across tribal, federal, and municipal markets
Collaborate with the Site Development Practice Lead to develop scope, schedule, fee, and staffing plans
Maintain strong communication with clients, design teams, and internal partners throughout the project lifecycle
Supervise and mentor junior engineers and technical staff to support their growth and project contributions
Support practice-wide growth by contributing to strategic planning and practice group development
Lead or support the preparation of site plans, grading, stormwater management, utilities (sewer and water), access design, and erosion control plans
Perform or oversee engineering calculations, hydrologic modeling, stormwater reports, code compliance, and construction documentation
Provide technical QA and ensure design solutions meet regulatory, functional, and constructability standards
Provide oversight and feedback on QC processes during production and prior to milestone deliveries
Utilize AutoCAD Civil 3D and related tools to produce high-quality construction documents

Fulltime

New

Sr. Network Engineer

We are seeking a skilled Connectivity Engineer, LINE 3 FUCTION 1 to join our tea...

Location

United States , Annapolis Junction

Salary:

100000.00 - 200000.00 USD / Year

Applied Network Solutions

Expiration Date

Until further notice

Requirements

Twelve (12) years of experience in programs and contracts of similar scope, type and complexity are required
Bachelor's degree in engineering from an accredited college or university is required
Four (4) years of additional network engineering experience may be substituted for a bachelor's degree
An IAT level III baseline certification as defined by DoD 8570.01-M is required
An IAT II will be accepted (Security + CE, GSEC, or SSCP) if the candidate obtains an IAT level III (CISA, CISSP, CASP, GCIH, or GCED) within 1 year
TS/SCI Poly Required

Job Responsibility

Performs engineering services to enable all aspects of network management from network design through implementation, maintenance, sustainment of existing networks, and identification/correction of complex internetwork issues
Implements and sustains Wide area networks (WANs), Campus Area Networks (CANs), Data Center Networks/Interfaces (DCN/DCI), Network Security (NETSEC) and Tactical/Deployable Networking Systems
Analyzes design, specifications, and related documents
Implements communication system requirements to support the distributed functionality of a networked enterprise environment
Analyzes network characteristics (e.g. traffic connect time, transmission speeds, packet sizes and throughput), troubleshoots problems and recommends modification of network configurations
Resolve complex network problems, and operate network analyzers, WAN test equipment and network simulators
Perform site surveys, system installations, configuration management, maintenance, modernization, and sustainment of a global Enterprise Network
Perform Connectivity engineering services to pre and post deployment tests
Implement specific network solutions to support server requirements to include load-balancing, VPN’s, firewall contexts, and network address translation (NAT) where appropriate
Minimize network latency and maximize data throughput

What we offer

Family Medical, Dental (w/ adult orthodontia) and Vision coverage
Pet Discount Program
PTO (Paid Time Off)
Maternity/ Paternity Leave
Supplemental Military Leave Pay
11 Paid Holidays
401(k) plan with 6% Company Contribution
Generous Professional Development Program
100% Employer paid Short- and Long-Term Disability
100% Employer paid Life Insurance

Senior Quality Manager

Senior leadership role on a flagship hyperscale data centre build. Responsible f...

Location

Finland , Helsinki

Salary:

120000.00 - 130000.00 EUR / Year

Morson Talent

Expiration Date

Until further notice

Requirements

10+ years’ experience in Quality Management or QA/QC on large construction projects
Proven experience on hyperscale data centres or mission-critical environments
Strong understanding of MEP and CSA quality management
Track record of delivering high-quality, low-defect projects
Confident leader with experience managing and developing teams
Strong stakeholder management and communication skills
Degree in QA/QC, Engineering, Construction Management or equivalent experience
Able to operate at both strategic planning and site execution level
Comfortable working in fast-paced, high-pressure project environments
EU passport required, no sponsorship available

Job Responsibility

Lead the project quality team and manage performance and development
Develop, implement and maintain the Project Quality Plan
Establish all site-based QA and QC procedures, controls and systems
Audit quality performance continuously against agreed KPIs
Review technical specifications and develop Inspection and Test Plans
Train project teams and subcontractors on quality standards and expectations
Manage internal, external and client audits through to close-out
Chair weekly quality meetings with clients, subcontractors and suppliers
Publish clear and consistent quality metrics and reporting
Identify quality risks early and implement preventative controls

What we offer

Flights
single-occupancy accommodation
car hire if required

Fulltime

QA/QC Inspector

The QA/QC Inspector will be responsible for performing and documenting inspectio...

Location

United States , Denver

Salary:

Not provided

Apollo Mechanical Contractors

Expiration Date

Until further notice

Requirements

AWS CWI
Experience in ASME and AWS codes preferred
Ability to communicate clearly and effectively
Proficient with learning and applying technical concepts
Ability to multi-task
Willingness to learn and adapt quickly in a fast-paced environment
Display diplomacy and tact in collaborating with a wide variety of colleagues, customers and suppliers
Microsoft Office Suite (particularly Excel and Project)
Bachelor’s degree in construction management, business, engineering, or related field and/or equivalent job experience

Job Responsibility

Implement the QA/QC program on site
Perform various quality inspections i.e. Dimensional, Visual, welding, etc…
Coordinate quality inspections with all the site sub-contractors and vendors
Coordinate all nondestructive testing on site
Complete and coordinate the approval of the site QC technical submittals with the customer
Coordinate with the customers representative on all quality matters
Perform receiving inspections of equipment and material

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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