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manufacturing engineer

TechnipFMC

<div>
 TechnipFMC is committed to driving real change in the energy industry. Our ambition is to build a sustainable future through relentless innovation and global collaboration &ndash; and we want you to be part of it. You&rsquo;ll be joining a culture that values curiosity, expertise, and ideas as well as equal opportunities, inclusion, and authenticity. Bring your unique energy to our team of more than 21,000 people worldwide, and discover a rewarding, fulfilling, and varied career that you can take in anywhere you want to go.
 
 
 
 Job Purpose
 
 
 
 Review and interpret customer/industrial specifications
 
 
 
 Job Description
 
 
 
 <ul>
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 Understand and interpret customer/industrial specifications
 </li>
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 Be involved with design engineering team at design review stage
 </li>
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 Be involved on Quality issues and looking at RCAs
 </li>
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 Participate in department discussions relating to technical issues and lessons learnt
 </li>
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 Shows commitment to QHSE through participation in safety and quality initiatives
 </li>
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 Understand the workflow for the control of machining documentation and issuance of machining procedures fora project
 </li>
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 Understanding of new Machining Procedures
 </li>
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 Be involved in new processes
 </li>
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 Awareness of DFX
 </li>
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 Involve in audits (Adherence to codes &amp; specs)
 </li>
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 Support tenders and product engineering quotation activities
 </li>
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 Ensure timely and accurate release of production &amp; manufacturing packages
 </li>
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 Attend daily meeting on Notification Review Board (NRB), Obeya etc improve throughput and manufacturing costs
 
 
 </li>
 </ul>
 
 You Are Meant For This Job If
 
 
 
 Bachelor&rsquo;s degree in Mechanical / Manufacturing Engineering or equivalent
 
 
 
 Skills
 
 
 
 Analysis and Problem Solving
 
 
 Communication
 
 
 Leadership Competencies
 
 
 Act with Agility
 
 
 Adopt a Growth Mindset
 
 
 
 
 Being a global leader in the energy industry requires an inclusive and diverse environment. TechnipFMC promotes diversity, equity, and inclusion by ensuring equal opportunities to all ages, races, ethnicities, religions, sexual orientations, gender expressions, disabilities, or all other pluralities. We celebrate who you are and what you bring. Every voice matters and we encourage you to add to our culture.
 
 
 
 
 
 TechnipFMC respects the rights and dignity of those it works with and promotes adherence to internationally recognized human rights principles for those in its value chain.
 
 
</div>

Manufacturing Engineer - Machining Intern (Tamheer)

GE Vernova

<div><div><div>The ECT Rotor Method Engineer is an early‑career role designed to provide hands‑on exposure to rotor manufacturing and repair methods within a structured learning environment. The role focuses on supporting method engineering activities under the guidance of senior Method Engineers, with emphasis on understanding manufacturing processes, standard work, and shop floor execution. 
 
This position is part of a defined early‑career planning program, where selected engineers will rotate through key method engineering activities over a one‑year period while supporting ongoing rotor operations.<h1 class="jobSectionHeader">
Job Description</h1>
What you&rsquo;ll do:
Manufacturing Method Support<ul><li>
Support senior Method Engineers in developing, updating, and maintaining standard manufacturing and repair methods for rotor components.</li><li>
Assist in preparing method sheets, work instructions, and standard plans in accordance with approved engineering and quality requirements.</li><li>
Learn how to interpret engineering drawings, repair instructions, and process specifications for shop floor application.</li></ul>
Shop Floor &amp; Operations Support<ul><li>
Provide day‑to‑day technical support to rotor operations under supervision.</li><li>
Observe and support machining and repair activities (e.g., turning, VTL, horizontal lathe) to understand process flow and constraints.</li><li>
Verify method execution on the shop floor and escalate deviations or concerns to senior engineers.</li></ul>
New Product Introduction (NPI) Exposure<ul><li>
Assist with NPI‑related activities, including:<ul><li>
Process documentation</li><li>
Method updates</li><li>
Fixture and tooling reviews</li></ul></li><li>
Participate in process trials and validations under guidance.</li></ul>
Quality &amp; Continuous Improvement<ul><li>
Support investigations related to Non‑Conformance Reports (NCRs) by gathering data and participating in discussions.</li><li>
Participate in Kaizens, PSRs, and basic Root Cause Analysis (RCA) activities as part of learning and process improvement.</li><li>
Identify improvement opportunities related to safety, quality, cost, and cycle time, with recommendations reviewed by senior engineers.</li></ul>
Digital &amp; Lean Manufacturing Tools<ul><li>
Learn and support the use of digital manufacturing and production tools used within the rotor area.</li><li>
Support lean production line activities and standard work documentation updates.</li></ul>
Learning &amp; Compliance<ul><li>
Follow all EHS, quality, and manufacturing procedures.</li><li>
Actively participate in technical training, method reviews, and mentoring sessions.</li><li>
Maintain accurate documentation and records as assigned.</li></ul><div></div>
Level of Responsibility &amp; Autonomy<ul><li>
Operates under close supervision of Lead Method Engineer and PB Method Engineer.</li><li>
Executes clearly defined and reviewed tasks using established procedures.</li><li>
Limited autonomy; technical decisions and method changes require approval from senior engineers.</li><li>
Escalates technical, quality, or safety concerns promptly.</li></ul>
What you&rsquo;ll bring:<ul><li>
Bachelor&rsquo;s degree in Mechanical Engineering or other Engineering disciplines.</li><li>
Maximum 2 years of experience in Manufacturing and /or Repair Environment.
</li><li>Basic understanding of manufacturing processes and engineering drawings</li><li>
Willingness to work in a shop‑floor manufacturing environment</li></ul>
What will make you stand out:<ul><li>
Strong interest in manufacturing and industrial processes</li><li>
Good verbal and written communication skills</li><li>
Ability to learn quickly and follow standard processes</li><li>
Team‑oriented mindset with openness to feedback</li><li>
Basic proficiency in Microsoft Office tools (Excel, Word)</li><li>
Exposure to Lean Manufacturing or continuous improvement concepts is a plus</li></ul><h1 class="jobSectionHeader">
Additional Information</h1><div><div><div><div><div><div><div>
Relocation Assistance Provided: No</div></div></div></div></div></div></div></div></div></div>

Early Career Training - Rotor Method Engineer

Stellar Hunters

<div>We are seeking a collaborative, technically proficient, and user-focused Pharmaceutical Engineer to design, develop, and optimize drug substance and drug product manufacturing processes that enable safe, efficient, and reproducible production of pharmaceutical therapies. The successful candidate will work closely with research, formulation, analytical, manufacturing, quality, and supply chain teams to translate lab-scale work into robust, GMP-ready manufacturing workflows. This role requires strong chemical and pharmaceutical engineering fundamentals, hands-on experience with process development and scale-up, and a pragmatic approach to process characterization, control, and technology transfer.<h3 class="jobSectionHeader">
Key Responsibilities - Pharmaceutical Engineering</h3><ul><li>
Design, develop, and optimize unit operations and integrated processes for small-molecule and/or biologic drug substance and drug product manufacturing to meet quality, yield, and scalability objectives.</li><li>
Plan and execute bench- and pilot-scale experiments to characterize critical process parameters, establish robust operating ranges, and define scale-up strategies using DOE and statistical analysis.</li><li>
Develop and maintain process flow diagrams, batch records, SOPs, validation protocols, and technical transfer documentation to support GMP manufacturing and technology transfers.</li><li>
Implement in-process monitoring strategies and support analytical method development to inform process control, release criteria, and troubleshooting activities.</li><li>
Collaborate with formulation, analytical, and manufacturing teams to select and evaluate equipment (reactors, mixers, granulators, dryers, sterilization systems, filling/finish equipment) and ancillary systems for process integration and scale-up.</li><li>
Lead technology transfer activities, including preparing transfer packages, training operators, and supporting startup and qualification at pilot and commercial sites.</li><li>
Partner with quality and regulatory teams to ensure processes, validation activities, and documentation meet cGMP expectations and support regulatory submissions as needed.</li><li>
Mentor and collaborate with scientists, engineers, operators, and external partners to transfer knowledge, share best practices, and drive continuous process improvement and technology adoption.</li><li>
Support process economics, capacity planning, and resource optimization to align process designs with business goals and manufacturing constraints.</li><li>
Engage with vendors and equipment suppliers to evaluate technologies, define integration approaches, and ensure vendor deliverables meet functional and regulatory requirements.</li></ul><h4 class="jobSectionHeader">
Required Qualifications - Skills &amp; Experience</h4><ul><li>
Bachelor&rsquo;s degree in Chemical Engineering, Pharmaceutical Engineering, Chemical Biology, or a related discipline; equivalent practical experience will be considered.</li><li>
3+ years of hands-on experience in pharmaceutical process development, scale-up, or manufacturing support for drug substance or drug product operations.</li><li>
Practical experience with unit operations relevant to pharmaceutical manufacturing (reaction, crystallization, filtration, drying, milling, granulation, coating, aseptic processing) and process control strategies.</li><li>
Experience designing and interpreting DOE studies, process characterization, and statistical analysis to define critical process parameters and acceptance criteria.</li><li>
Familiarity with analytical methods used for release and in-process testing (HPLC, dissolution, particle size, moisture analysis, assay/purity) and ability to collaborate with analytical groups to implement appropriate controls.</li><li>
Working knowledge of regulatory and quality systems relevant to pharmaceutical manufacturing, including cGMP principles, validation practices, and change control workflows.</li><li>
Strong problem-solving and troubleshooting skills across chemical, mechanical, and process control domains.</li><li>
Excellent written and verbal communication skills; able to produce clear technical documentation and present findings to cross-functional stakeholders.</li></ul><h4 class="jobSectionHeader">
Preferred Qualifications - Domain &amp; Tools</h4><ul><li>
Experience with pilot-scale and GMP manufacturing environments, including technology transfers and operator training.</li><li>
Familiarity with process analytical technology (PAT), inline/online monitoring, and automation/control systems (SCADA/DCS) for process control and continuous manufacturing approaches.</li><li>
Knowledge of formulation science, aseptic processing, lyophilization, and containment strategies for potent compounds is a plus.</li><li>
Experience with single-use systems, scale-down models, process modeling tools, and continuous or intensified processing technologies.</li><li>
Advanced degree (MS/PhD) in a relevant field or relevant certifications in pharmaceutical engineering, quality, or regulatory affairs is a plus.</li></ul><h5 class="jobSectionHeader">
Work Environment &amp; Compensation</h5><ul><li>
Full-time role within a collaborative, cross-functional product and manufacturing organization; onsite or hybrid presence is expected depending on project needs and facility requirements.</li><li>
Competitive salary and benefits package commensurate with experience, including health coverage, retirement plan options, paid time off, and professional development support.</li><li>
Opportunities for training, certifications, and career progression in an inclusive, mission-driven organization committed to scientific excellence.</li><li>
We are committed to diversity, equity, and inclusion and foster a respectful work environment that supports work-life balance and employee well-being.</li></ul></div>

Pharmaceutical Engineer

<div>We are seeking a collaborative, technically adept, and user-focused Biochemical/bioprocess Engineer to develop, optimize, and scale bioprocesses that enable safe, efficient, and reproducible production of biological products. The successful candidate will partner with research, analytical, manufacturing, quality, and supply chain teams to translate lab-scale processes into robust, GMP-ready manufacturing workflows. This role requires strong biochemical engineering fundamentals, hands-on experience with upstream/downstream process development, and a pragmatic approach to process characterization, control, and transfer.<h3 class="jobSectionHeader">
Key Responsibilities - Biochemical / Bioprocess Engineering</h3><ul><li>
Design, develop, and optimize upstream and downstream bioprocesses (microbial, mammalian, or cell-free systems as applicable) to meet product quality, yield, and scalability objectives.</li><li>
Plan and execute bench- and pilot-scale experiments to characterize critical process parameters and establish robust operating ranges using DOE and statistical analysis.</li><li>
Develop and maintain process flow diagrams, batch records, SOPs, and technical transfer documentation to support GMP manufacturing and technology transfers.</li><li>
Implement and refine analytical assays and in-process monitoring strategies to inform process control, release criteria, and troubleshooting activities.</li><li>
Collaborate with upstream and downstream teams to select and evaluate unit operations (bioreactors, filtration, chromatography, centrifugation, etc.) and ancillary systems for process integration and scale-up.</li><li>
Lead&gt;</li><li>
Partner with quality and regulatory teams to ensure processes and documentation meet cGMP expectations and support regulatory submissions as needed.</li><li>
Mentor and collaborate with scientists, operators, and external partners to transfer knowledge, share best practices, and drive continuous process improvement and technology adoption.</li><li>
Support process economics, capacity planning, and resource optimization to align process designs with business goals and manufacturing constraints.</li><li>
Engage with vendors and equipment suppliers to evaluate technologies, define integration approaches, and ensure vendor deliverables meet functional and regulatory requirements.</li></ul><h4 class="jobSectionHeader">
Required Qualifications - Skills &amp; Experience</h4><ul><li>
Bachelor&rsquo;s degree in Chemical Engineering, Biochemical Engineering, Chemical Biology, or a related discipline; equivalent practical experience will be considered.</li><li>
3+ years of hands-on experience in bioprocess development, scale-up, or manufacturing support for biologics, cell therapies, enzymes, or other biologically-derived products.</li><li>
Practical experience with upstream (cell culture, fermentation) and downstream (clarification, filtration, chromatography) unit operations and process control strategies.</li><li>
Experience designing and interpreting DOE studies, process characterization, and statistical analysis to define critical process parameters and acceptance criteria.</li><li>
Familiarity with bioprocess analytical methods (HPLC, ELISA, qPCR, particle analysis, impurity profiling) and ability to collaborate with analytical groups to develop in-process and release assays.</li><li>
Working knowledge of regulatory and quality systems relevant to biologics manufacturing, including cGMP principles, documentation practices, and change control workflows.</li><li>
Strong problem-solving and troubleshooting skills across biological, mechanical, and process control domains.</li><li>
Excellent written and verbal communication skills; able to produce clear technical documentation and present findings to cross-functional stakeholders.</li></ul><h4 class="jobSectionHeader">
Preferred Qualifications - Domain &amp; Tools</h4><ul><li>
Experience with pilot-scale and GMP manufacturing environments, including technology transfers and operator training.</li><li>
Familiarity with single-use systems, scale-down models, and bioreactor control systems (SCADA/DCS) and automation for process control.</li><li>
Knowledge of downstream purification technologies, process modeling tools, and continuous processing approaches.</li><li>
Experience with process analytical technology (PAT), real-time analytics, and advanced in-line monitoring strategies.</li><li>
Advanced degree (MS/PhD) in a relevant field, or relevant certifications in bioprocess engineering, quality, or regulatory affairs is a plus.</li></ul><h5 class="jobSectionHeader">
Work Environment &amp; Compensation</h5><ul><li>
Full-time role within a collaborative, cross-functional product and manufacturing organization; onsite or hybrid presence is expected depending on project needs and facility requirements.</li><li>
Competitive salary and benefits package commensurate with experience, including health coverage, retirement plan options, paid time off, and professional development support.</li><li>
Opportunities for training, certifications, and career progression in an inclusive, mission-driven organization committed to scientific excellence.</li><li>
We are committed to diversity, equity, and inclusion and foster a respectful work environment that supports work-life balance and employee well-being.</li></ul></div>

Biochemical/Bioprocess Engineer

Central Ventilation Systems W.L.L. (Doha

a. Management of all production activities including; material management, operations, day to day management of production activities.b. Generating Daily Production reports to accurately show jobs in progress, and scheduled jobs.c. Ensure material is produced and delivered as per the committed timelines.d. Work with Operations Manager to set production targets, and provide regular updates on any variances.e. Ensure all production processes are executed as per customer specifications.f. Handling production workers &ndash; day shift and night shift organization and allocations of workers subject to work load.g. Development of production staff skills to improve production rates, quality, and efficiency.h. Coordination with stores and logistics to ensure adequate material supply to execute jobs in hand.i. Managing machine maintenance schedules to ensure periodic maintenance, avoid downtime, and upkeep of machines and tools.j. Enforce and Implement ISO 9001 procedures and requirements. Maintain and update all ISO related records.k. Update daily production plans.l. Delivery Coordination.m. Set up Production quality protocols.n. Coordinate material consumption/usage with Operations Manager.o. Setup and enforce welding procedures and protocols.p. Identify process improvement requirements by identifying, design and implementation of Jigs and Fixtures.Job Types: Full-time, PermanentPay: From ﷼3,500.00 per monthApplication Question(s):<ul><li>Your current Location</li><li>Notice Period</li><li>Reason for change</li><li>Last drawn salary (mention currency if not in SAR)</li></ul>Experience:<ul><li>Manufacturing Duct Dampers Grilles Diffusers: 3 years (Preferred)</li><li>Autocad and CAD MEP: 3 years (Preferred)</li></ul>

Production Engineer - Duct Dampers Grills Diffusers Louvers

Schweitzer Engineering Laboratories

<div>Schweitzer Engineering Laboratories provides complete power system protection, control, monitoring, automation, security and integration for utilities and industries worldwide. We are looking for Project Engineer &ndash; Project Manager to provide technical support to customers. A successful candidate must have knowledge and experience of power system with full life-cycle project management of multiple large multi-discipline projects from proposal conception to commissioning and close-out, effectively track and stabilize projects, implement solutions for obstacles and anticipate customer needs, and related SEL products to complete complex assignments. 
This is your chance to build your career with a global leader and innovator in the power protection industry. 
As a Project Engineer &ndash; Project Manager, a typical day might include the following:<ul><li>
Possesses, understands and applies knowledge and experience of power system with full life-cycle project management of multiple large multi-discipline projects from proposal conception to commissioning and close-out, effectively track and stabilize projects, implement solutions for obstacles and anticipate customer needs, and related SEL products to complete complex assignments.</li><li>
Lead in training and assisting customers with the creation, design configuration, validation, installation, commissioning and operation of automation and/or protection systems.</li><li>
Lead in assigning, completing and implementing work within agreed upon scope, schedule and budget to a high level of quality and safety.</li><li>
Assist in the identification, preparation and presentation of successful proposals for SEL equipment, services, and systems.</li><li>
Mentor and develop professional staff. May supervise as necessary.</li><li>
Model, teach, and apply SEL Values, Principles of Operations, and World Class Manufacturing Principles.</li><li>
Understand. Create. Simplify.</li><li>
Other duties as assigned.</li></ul>
This job might be for you if you have:<ul><li>
B.S. In Electrical Engineering or relevant discipline.</li><li>
5+ years relevant application experience with electric power systems, industry practices, and project management practices and philosophies.</li><li>
Demonstrated knowledge of electric power system protection and control, integration and/or automation and communications applications.</li><li>
Demonstrated proven knowledge of electric power system design, studies, information and communication technology and protective relay applications.</li><li>
Willing to travel both domestically and internationally a minimum of 25% based on focus area.</li><li>
Strong writing, documentation, and speaking skills.</li><li>
Ability to learn new skills and assume new responsibilities.</li><li>
Ability to work cooperatively in a team environment.</li><li>
Background check results are satisfactory to SEL.</li><li>
Negative drug test result(s).</li></ul> 
Preferred Qualifications<ul><li>
Professional Engineer License or equivalent certification.</li><li>
Electrical utility, industrial plant, consulting engineering, or system integrator experience.</li><li>
Project management experience.</li><li>
Working knowledge of Vision or other project management tracking software.</li></ul>
Location 
Saudi Arabia &ndash; Khobar
Why SEL? 
Competitive pay. Superior benefits. Inspiring work.
We provide and take care of our employees with outstanding benefits, competitive pay, challenging work, and a rewarding career.<ul><li>
Top tier medical, prescription, dental, vision, life, and disability insurance.</li><li>
Varied leave plans like annual leaves, sick leaves, parental leaves etc. to maintain a healthy life balance.</li><li>
Yearly flight tickets to home country for expat employees and their family members based on their eligibility.</li><li>
Developmental programs like tuition assistance, internships, skill development courses and engineering development programs (EDP).</li><li>
Wellbeing benefits like free and confidential Employee Assistance Program (EAP) and reimbursable yearly gym membership.</li><li>
International Travel Medical and Security Assistance to assist our traveling employees and accompanying family members worldwide.</li></ul>
Pay Range Data 
We base our starting pay offer on location and job-related factors such as candidate experience, training, knowledge, and skills.
Communication with Applicants 
We communicate with all applicants. If you do not receive a response about your application, please check your SPAM filter or reach out to us at careers@selinc.com.
SEL is an Equal Opportunity Employer: Vets/Disabled.</div>

Project Engineer II - Project Manager

Halloul Naft

The Role
 To ensure the reliability, availability, and performance of all plant equipment and utilities through effective preventive and corrective maintenance programs. The Maintenance Engineer plays a key role in maintaining safe, efficient, and continuous operation of the production facility. Key Responsibilities • Develop, implement, and supervise preventive and predictive maintenance schedules. • Lead troubleshooting and root cause analysis (RCA) for equipment breakdowns. • Maintain detailed maintenance logs, history cards, and asset tracking systems. • Oversee corrective activities to minimize downtime and optimize spare part usage. • Manage mechanical, electrical, and instrumentation systems reliability. • Coordinate with OEMs and vendors for support, spare parts, and service contracts. • Participate in equipment installation, commissioning, and modifications. • Supervise and coach the Planner, Technicians and Forklift Driver as needed. • Assign daily maintenance tasks and monitor completion reports. • Report maintenance KPIs to the Production Manager. • Maintain safety compliance for all maintenance activities
 
Requirements
 <ul>
<li>Bachelor’s degree in Mechanical Engineering, Electrical Engineering, Mechatronics, or related technical field. • Minimum 5 years of maintenance experience in an industrial or chemical production environment. • Proven experience in developing and implementing preventive and predictive maintenance programs. • Strong hands-on experience in troubleshooting industrial equipment and conducting root cause analysis (RCA). • Solid knowledge of mechanical, electrical, and instrumentation systems in a production facility. • Experience with CMMS systems, maintenance logs, asset tracking, and documentation control. • Ability to manage equipment reliability and minimize downtime in continuous production operations. • Experience coordinating with OEMs, contractors, and spare parts suppliers. • Practical experience in equipment installation, commissioning, and plant modifications. • Fluent English (spoken and written). • NativeArabic • Strong command of technical English.</li>
</ul>
About the company
 Halloul Naft is a Saudi Arabian company specializing in the production and supply of chemical reagents used for the transportation of crude oil and petroleum products across the Gulf region. The company operates its own manufacturing facility in Saudi Arabia and is actively expanding its presence in the United States.

Maintenance Engineer – Chemical Production

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