statistical programmer

RHO Inc

<div><p>Join us in redefining what it means to work for a CRO.
</p><p>When you work at Rho, it&rsquo;s more than just a job&mdash;you become part of the Rho Factor. We&rsquo;re a proud bunch of science nerds who love tackling big challenges together. We&rsquo;re not your typical CRO, and we&rsquo;re not trying to be. Here, curiosity is encouraged, fresh approaches are welcome, and collaboration is at the heart of everything we do.</p><p>
Whether you&rsquo;re a data wizard, analytical genius, project mastermind, or any other role, you&rsquo;ll fit right into the equation of the Rho Factor. Expect plenty of geeky jokes, eccentric personalities, spontaneous brainstorms, and a supportive community where people genuinely care about their work&mdash;and each other.</p><p>
You&rsquo;ll have the opportunity to experience a thriving company with real stability - financial, workforce, and corporate, which has created a safe environment to innovate and develop over a long and rewarding career.
</p><p><b>Why Rho?</b></p><ul>
<li>The foundation of our organization was built on Biometrics, and it continues to be a thriving focal point for our business with strong employee tenure and stability.</li>
<li>We are large enough for strong stability, but small enough for you to have strong visibility and exposure to grow your career!</li>
<li>Support and collaboration is everywhere &ndash; from the top down. You have plenty of artillery to be successful here</li>
<li>It&rsquo;s fun and vibrant &ndash; our culture is unbeatable</li>
<li>Lastly, we do great work and our studies are properly staffed, that makes for very happy people!</li>
</ul><p>As a Senior Statistical Programmer, you&rsquo;ll have the opportunity to design and write program specifications for CDISC conversions, revise programs for corrections, independently create agency-accepted eSubmission deliverables, review statistical analysis plans and study documents and provide feedback to Biostatistics. You&rsquo;ll be able to consult with sponsors, internal and external project leads, and other programmers and lead the programming team on multiple studies.</p><p>
Our Statistical Programmers will tell you, joining Rho has been one of their best career moves in terms of contentment, financial rewards and career growth, which is why we have such stability in the group!</p><p>
What you will be doing:</p><ul>
<li>Lead and participate in the development and validation of high quality CDISC datasets based on the implementation guides and consultations with sponsors, project leads, systems analysts, other programmers, and end users</li>
<li>Use your expertise in data standards and regulatory requirements to lead discussions with clients about appropriate approaches to database design</li>
<li>Use study protocol, CRF, Data Transfer Agreements from vendors, data sources, CDISC CT, TAUGS, and CDISC implementation guides to independently author SDTM specifications from scratch; use Pinnacle 21 to run data conformance and create define.xml for SDTM and ADaM submissions</li>
<li>Act as the CDISC subject matter expert</li>
<li>Convert designs and specifications into computer code and analyze code to find causes of errors and revise programs</li>
<li>Write and maintain documentation of changes to computer code, programs, and specifications</li>
<li>Review user and technical documentation written by others to confirm consistency with program operations</li>
<li>Offer expertise relevant to statistical programming and CDASH data collection for study start up, execution, and close out: review protocols, draft CRFs; prepare and review validation plans, review vendor DTAs, etc</li>
<li>Modify and maintain software programs written by others</li>
<li>Provide mentorship and training to peers and more junior programmers in areas of expertise</li>
<li>Ensure effective, accurate and timely communication of key issues and progress to the team and Sr. Management</li>
<li>Perform functional lead activities on assigned projects while maintaining scope and budget oversight</li>
<li>May provide guidance and input to the budgets and business submissions of proposals</li><br>
</ul><br>
<br>
<b>Requirements</b><br>
<ul><li>
BA/BS in computer science, statistics, or related field along with at least 6 years performing statistical programming in the SAS language within the CRO/Pharmaceutical industry</li><li>
Extensive experience and understanding in SDTM model including transforming raw data files while adhering to CDISC standards from end to end (raw data to eSub); advanced understanding of SDTM model and experience with; both specification, programming, and conformance of SDTM CDISC; strong CDISC skills with an emphasis on SDTM End to End submissions experience</li><li>
ADaM model and experience with both specification, programming, and conformance of ADaM CDISC is a plus</li><li>
SAS/Base knowledge with an emphasis on data step programming; competency modifying pre-existing SAS code, as well as writing SAS code from specs.</li><li>
Clinical trials including knowledge of applicable clinical research regulatory requirements; i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines</li><li>
Data/submission conformance tools (such as P21), creation of define.xml, SDSP, and study data reviewer&rsquo;s guides</li><li>
Strong Communicator: Demonstrate written, verbal and presentation skills to help showcase the successes of your work and Rho&rsquo;s.</li><li>
Committed to Quality: Every job at Rho requires an attention to detail, a deep understanding of our high-quality scientific standards, and an ability to care about every outcome.</li><li>
High-Character: Contribute to our collaborative culture with honesty and integrity. At Rho, we value a strong team spirit highlighted by loyalty, accountability, and mutual trust. We work smart together, we work hard together, and we laugh together. We take responsibility for our actions, forgive honest mistakes and respect one another.</li><li>
Critical Thinker: Rho values thinking. Draw on your native ingenuity, sharpened and enhanced by our intellect, training, and experience. We evaluate situations and opportunities objectively and incisively; we then craft novel, practical solutions.</li><li>
Agile and Adaptable: Rho values the ability to change quickly. We eagerly anticipate, respond to, and take advantage of changes in our environment. We embrace risk but manage it by planning, accepting, and learning from both failures and successes. The opportunity to adapt and evolve energizes us.</li></ul><br>
<b>
Benefits</b><p><br>
A few more things to know about us:</p><p><br>
</p><p>Benefits: Rho provides a comprehensive benefits package for all benefit-eligible employees, which includes medical, vision, dental, HSA, FSA, EAP, life &amp; disability insurance and 401(k). All employees are eligible for paid time off, holidays, parental leave and bereavement leave.
</p><p>Flexibility: We encourage a work-life balance that allows employees to bring their best selves to work while being passionate about their lives outside work.
</p><p>As required by pay transparency laws in some states, Rho provides the range of starting compensation (annual salary or hourly rate) it reasonably expects to pay for a given role. Actual compensation is influenced by a wide array of factors including but not limited to role responsibilities and location as well as candidate skill set and level of experience. The range of starting pay for this role is $110,000-135,000 per year</p><p></p><p>
EOE. Veterans/Disabled</p></div>

Senior Statistical Programmer

Biogen

<div><div><p><b>Job Title: Director, Statistical Programming
</b></p></div><p></p><div><p><b>About This Role:
</b><br>
As the Director of Statistical Programming within the Analytics and Data Sciences (ADS) team, you will lead the global statistical programming department, driving strategy and execution across all stages of drug development. You will manage resources to ensure study, program, and therapeutic area milestones are met, collaborating with various departments to align strategies and uphold quality standards. Your role is pivotal in developing operational strategies for statistical programming, fostering partnerships with external vendors, and enhancing internal processes. By implementing best practices and innovation in data standards and statistical reporting, you will significantly contribute to the success of our drug programs and the advancement of our development sciences. As a senior leader, you will empower your team through coaching and advocacy, facilitating a culture of excellence and continuous improvement.
</p></div><div><p><b>What </b><b>You&rsquo;ll </b><b>Do:
</b></p></div><div><ul><li><p>Develop and implement operational and sourcing strategies for statistical programming and data standards.
</p></li></ul></div><div><ul><li><p>Lead the management of statistical programming vendor relationships and strategic partnerships.
</p></li></ul></div><div><ul><li><p>Ensure timely execution of statistical programming and electronic submission activities across all drug programs.
</p></li></ul></div><div><ul><li><p>Identify opportunities for technical and process improvements and drive implementation.
</p></li></ul></div><div><ul><li><p>Develop and oversee programming standards, conventions, and efficient procedures.
</p></li></ul></div><div><ul><li><p>Provide leadership in talent acquisition, retention, and development within the department.
</p></li></ul></div><div><ul><li><p>Collaborate with cross-functional teams to align strategies and ensure optimal data delivery and analysis.
</p></li></ul></div><div><ul><li><p>Manage resources and budgets effectively to meet program goals.
</p></li></ul></div><div><ul><li><p>Stay updated on regulatory requirements and trends to ensure compliance.
</p></li></ul></div><div><ul><li><p>Promote a culture of innovation and continuous improvement within the team.
</p></li></ul></div><p></p><div><p><b>Who You Are:
</b></p><p>You are a visionary leader with a strategic mindset and a passion for driving excellence in statistical programming. Your strong collaboration skills enable you to build effective partnerships and influence without authority. You possess a deep understanding of regulatory requirements and a commitment to maintaining high-quality standards. Your ability to manage complex projects and navigate cross-functional initiatives makes you an asset to any team. You thrive in a dynamic environment where you can inspire and develop others to achieve their full potential.
</p></div><p></p><div><p><b>Required Skills:
</b></p></div><div><ul><li><p>Bachelor&rsquo;s degree required ; Masters or PhD in Statistics or Mathematics preferred.
</p></li></ul></div><div><ul><li><p>12+ years of relevant work experience in data management and analysis.
</p></li></ul></div><div><ul><li><p>12+ years of SAS Base programming experience, with 7+ years using SAS STAT, GRAPH, and MACRO.
</p></li></ul></div><div><ul><li><p>12+ years of relevant industry experience and clinical trial experience.
</p></li></ul></div><div><ul><li><p>7+ years of clinical database experience.
</p></li></ul></div><div><ul><li><p>7+ years in a supervisory role.
</p></li></ul></div><div><ul><li><p>Extensive knowledge of regulatory requirements and drug submission guidelines.
</p></li></ul></div><div><ul><li><p>Strong management and leadership skills with the ability to lead cross-functional teams.
</p></li></ul></div><div><ul><li><p>Proven ability to manage multiple priorities and drive process improvements.
</p></li></ul></div><div><ul><li><p>Excellent written and oral communication skills.
</p></li></ul></div><p></p><div><p><b>Preferred Skills:
</b></p></div><div><ul><li><p>Experience with strategic change management within a large cross-functional initiative.
</p></li></ul></div><div><ul><li><p>Strong skills in compelling communication, driving execution, and cultivating networks.<br>
</p></li></ul></div><p></p><br>
Job Level: Management<br>
<p><br>
<b>Additional Information
</b></p><p></p>The base compensation range for this role is: $198,000.00-$272,000.00<br>
<p><br>
Base salary offered is determined through an analytical approach utilizing a combination of factors including, but not limited to, relevant skills &amp; experience, job location, and internal equity.<br>
</p><br>
<p>Regular employees are eligible to receive both short term and long-term incentives, including cash bonus and equity incentive opportunities, designed to reward recent achievements and recognize your future potential based on individual, business unit and company performance.<br>
</p><br>
<p>In addition to compensation, Biogen offers a full and highly competitive range of benefits designed to support our employees&rsquo; and their families <i>physical, financial, emotional, </i>and <i>social well-being </i>; including, but not limited to:
</p><ul><li>Medical, Dental, Vision, &amp; Life insurances
</li><li>Fitness &amp; Wellness programs including a fitness reimbursement
</li><li>Short- and Long-Term Disability insurance
</li><li>A minimum of 15 days of paid vacation and an additional end-of-year shutdown time off (Dec 26-Dec 31)
</li><li>Up to 12 company paid holidays + 3 paid days off for Personal Significance
</li><li>80 hours of sick time per calendar year
</li><li>Paid Maternity and Parental Leave benefit
</li><li>401(k) program participation with company matched contributions
</li><li>Employee stock purchase plan
</li><li>Tuition reimbursement of up to $10,000 per calendar year
</li>Employee Resource Groups participation<br>
<li>
</li></ul><br>
<p><b>Why Biogen?
</b></p><p>We are a global team with a commitment to excellence, and a pioneering spirit. As a mid-sized biotechnology company, we provide the stability and resources of a well-established business while fostering an environment where individual contributions make a significant impact. Our team encompasses some of the most talented and passionate achievers who have unparalleled opportunities for learning, growth, and expanding their skills. Above all, we work together to deliver life-changing medicines, with every role playing a vital part in our mission. Caring Deeply. Achieving Excellence. Changing Lives.<br>
</p><br>
<p>At Biogen, we are committed to building on our culture of inclusion and belonging that reflects the communities where we operate and the patients we serve. We know that diverse backgrounds, cultures, and perspectives make us a stronger and more innovative company, and we are focused on building teams where every employee feels empowered and inspired. Read on to learn more about our Biogen.<br>
</p><br>
<p>All qualified applicants will receive consideration for employment without regard to sex, gender identity or expression, sexual orientation, marital status, race, color, national origin, ancestry, ethnicity, religion, age, veteran status, disability, genetic information or any other basis protected by federal, state or local law. Biogen is an E-Verify Employer in the United States.</p></div><p></p>

Director, Statistical Programming

Jazz Pharmaceuticals

<div><div><h2 class="jobSectionHeader"><b>Job Details</b></h2>
</div><div><div><div><div>Req ID:</div><div>
R011229</div></div>
<div><div>Locations:</div><div>
Palo Alto, CA; Philadelphia, PA - [<b>Remote/Home-Based</b>]</div></div>
<div><div>Category:</div><div>
Research &amp; Development</div></div></div><div><br>
</div><p></p><div><p><b>If you are a current Jazz employee please apply via the Internal Career site.</b></p>
<p>
Jazz Pharmaceuticals is a global biopharma company whose purpose is to innovate to transform the lives of patients and their families. We are dedicated to developing life-changing medicines for people with serious diseases &mdash; often with limited or no therapeutic options. We have a diverse portfolio of marketed medicines, including leading therapies for sleep disorders and epilepsy, and a growing portfolio of cancer treatments. Our patient-focused and science-driven approach powers pioneering research and development advancements across our robust pipeline of innovative therapeutics in oncology and neuroscience. Jazz is headquartered in Dublin, Ireland with research and development laboratories, manufacturing facilities and employees in multiple countries committed to serving patients worldwide. Please visit www.jazzpharmaceuticals.com for more information.</p>
<div><p><b>Brief Description:</b></p><p>
The Senior Principal Statistician, Biostatistics will be a lead statistician on individual studies, across related studies, and for integrated summaries and will design and report Phase I to IV clinical studies and regulatory filings under the supervision of a more senior statistician. This role is responsible for all statistical aspects of study design, study analysis and validation, and study documentation. The Senior Principal Statistician will provide timely and scientifically sound statistical expertise to clinical development projects and develop and execute statistical strategy, design, and analyses for clinical trials. This position will work collaboratively with clinical development, pharmacology, pharmacovigilance, clinical drug supply, project management, regulatory affairs, medical writing, clinical data management, and clinical operations. The Senior Principal Statistician will manage work done by statistics and programming external vendors.</p><p><b>
Essential Functions</b></p><ul><li>
Participate in department and cross-functional meetings to optimize clinical study designs, endpoints, and analysis strategies in protocols.</li><li>
Collaborate with cross-functional team members to meet study any recurring report timelines.</li><li>
Support the development and implementation of study protocols.</li><li>
Review and provide input to data capture systems and participate in their validation.</li><li>
Develop statistical programs as necessary to simulate clinical trial design operating characteristics, perform analysis, prepare data displays, verify data accuracy and validity of analyses performed by statistical programming.</li><li>
Write statistical analysis plans, review statistical analysis plans written by other statisticians, perform and oversee data analysis and validation, and interpret analyses.</li><li>
Prepare for and attend meetings with regulatory agencies.</li><li>
Work with biostatistics compound/therapeutic area lead, peer management, and employees to develop, implement, and maintain department standards and practices.</li><li>
Review timelines and analysis plans for CRO work to ensure timeliness and quality deliveries.</li></ul><ul><li>
Review and validate CRO deliverables.</li><li>
Act as the statistical subject matter expert with medical writers and other colleagues in the production of clinical reports, integrated summaries, and other documents.</li><li>
Respond to statistical questions from regulatory agencies.</li></ul><p><b>
Required Knowledge, Skills, and Abilities
</b></p><ul><li>Knowledge of clinical trial design and analysis, including experience with complex statistical methods and models, including statistical principles and methodology and principles of statistical inference, including hypothesis testing and deriving estimates, parametric and non-parametric models and techniques, principles of sample size calculations for comparing two arms, principles of design of experiments in introducing conditions designed to affect an outcome of interest, and phase II-IV clinical trial data analysis.</li><li>
Experience in using SAS and R; knowledge of other statistical applications and programming languages a plus.</li><li>
Knowledge of applicable regulatory requirements and guidelines, e.g., ICH Guidelines and drug development regulatory requirements as they relate to statistics, including statistical contributions to marketing applications and CDISC standards.</li><li>
Able to work in a fast-paced, flexible, team-oriented environment.</li><li>
Possess excellent interpersonal and communication skills (written and verbal).</li><li>
Strong attention to detail with a view to bring studies to a quality conclusion.</li><li>
Flexible, positive, creative thinker, good communicator.</li><li>
Work without close supervision. Well-developed time management skills are important.</li></ul><p><b>
Required/Preferred Education and Licenses</b></p><ul><li>
MS or MPH in statistics, mathematics, or a related discipline with a statistical focus and &gt; 4 years of experience in pharmaceutical or biotechnology industry.</li><li>
PhD in statistics, mathematics, or a related discipline with a statistical focus and &gt; 2 years of experience in the pharmaceutical or biotechnology industry.</li><li>
Knowledge of drug development regulations pertinent to statistical analysis.</li><li>
Knowledge of the oncology or hematology therapeutic area is preferred</li><li>
Bayesian and adaptive design experience is preferred.</li><li>
Proficient SAS &amp; R programming skills, solid understanding of CDISC models and standards.</li><li>
Excellent writing and communication skills, demonstrated leadership abilities and excellent interpersonal skills.</li></ul><p>
 #LI-Remote</p></div>
<p><i>Jazz Pharmaceuticals is an equal opportunity/affirmative action employer and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, disability status, protected veteran status, or any characteristic protected by law.</i></p>
<p><b>FOR US BASED CANDIDATES ONLY</b></p><p>
Jazz Pharmaceuticals, Inc. is committed to fair and equitable compensation practices and we strive to provide employees with total compensation packages that are market competitive. For this role, the full and complete base pay range is: $156,000.00 - $234,000.00</p><p>
Individual compensation paid within this range will depend on many factors, including qualifications, skills, relevant experience, job knowledge, and other pertinent factors. The goal is to ensure fair and competitive compensation aligned with the candidate's expertise and contributions, within the established pay framework and our Total Compensation philosophy. Internal equity considerations will also influence individual base pay decisions. This range will be reviewed on a regular basis.</p><p>
At Jazz, your base pay is only one part of your total compensation package. The successful candidate may also be eligible for a discretionary annual cash bonus or incentive compensation (depending on the role), in accordance with the terms of the Company's Global Cash Bonus Plan or Incentive Compensation Plan, as well as discretionary equity grants in accordance with Jazz's Long Term Equity Incentive Plan.</p><p>
The successful candidate will also be eligible to participate in various benefits offerings, including, but not limited to, medical, dental and vision insurance, 401k retirement savings plan, and flexible paid vacation. For more information on our Benefits offerings : https://careers.jazzpharma.com/benefits.html.</p></div></div></div><p></p>

Senior Principal Statistician

M4 CONTRACTING S.A.R.L

<p><b>AV Programmer / Engineer &ndash; Construction Company</b></p><p><b>Job Summary</b></p><p>We are seeking a skilled AV Programmer / Engineer to design, program, configure, commission, and support Audio Visual (AV) systems for commercial, residential, hospitality, and mixed-use construction projects. The role involves integration of AV technologies with ELV systems, troubleshooting onsite issues, and ensuring successful project delivery according to client specifications and industry standards.</p><p><b>Key Responsibilities</b></p><ul><li>Design and develop AV system control logic and programming.</li><li>Configure and commission AV systems including:</li><li>Video conferencing systems</li><li>Digital signage</li><li>Background music systems</li><li>Meeting room AV solutions</li><li>Home automation and smart systems</li><li>Program and troubleshoot platforms such as:</li><li>Crestron</li><li>Extron</li><li>AMX</li><li>Q-SYS</li><li>Biamp</li><li>Prepare technical submittals, schematics, cable schedules, and as-built documentation.</li><li>Coordinate with consultants, contractors, and clients during project execution.</li><li>Conduct FAT/SAT testing and system commissioning.</li><li>Diagnose and resolve hardware/software integration issues onsite.</li><li>Ensure compliance with project specifications, safety standards, and local regulations.</li><li>Provide end-user training and technical support after project handover.</li><li>Collaborate with ELV, ICT, and MEP teams during installation and integration phases.</li><li>Support estimation and BOQ preparation when required.</li></ul><p><b>Required Qualifications</b></p><ul><li>Bachelor&rsquo;s degree or Diploma in:</li><li>Electronics Engineering</li><li>Electrical Engineering</li><li>Computer Engineering</li><li>Audio Visual Technology</li><li>3&ndash;7 years of experience in AV integration or AV programming within construction or system integration companies.</li><li>Strong knowledge of:</li><li>TCP/IP networking</li><li>AV over IP</li><li>DSP configuration</li><li>HDMI distribution</li><li>Control systems</li><li>Structured cabling</li><li>Experience with AutoCAD and technical documentation.</li><li>Familiarity with international AV standards and best practices.</li><li>Ability to read and interpret IFC drawings and schematics.</li></ul><p><b>Preferred Skills</b></p><ul><li>Certification in:</li><li>Crestron</li><li>Extron</li><li>Q-SYS</li><li>Dante</li><li>Knowledge of:</li><li>Video wall systems</li><li>IPTV</li><li>Unified communications</li><li>Smart home systems</li><li>BMS integration</li><li>Strong troubleshooting and problem-solving skills.</li><li>Good communication and client coordination abilities.</li></ul><p><b>Software &amp; Tools</b></p><ul><li>AutoCAD</li><li>Visio</li><li>Revit (preferred)</li><li>DSP software tools</li><li>AV programming platforms</li><li>Microsoft Office Suite</li></ul><p>Pay: AED6,000.00 - AED8,000.00 per month</p><p>Work Location: In person</p>

AV Programmer / Engineer

Hyve Solutions

<div>
 <strong>
  @HYVE Solutions,
 </strong>
 missions to help customers, business partners, and employees achieve success through shared goals, strategies, resources and technology solutions.
 <br/>
 <br/>
 nformation Systems Engineer: Performs IT functions such as design, analysis, evaluation, testing, debugging and implementation of applications programs supporting the company infrastructure business processes and operations and/or network-based (cloud) product systems. Analyzes, installs, acquires, modifies and supports operating systems, database or utilities software. Plans, conducts and directs the analysis of business problems with automated systems solutions. Analyzes, designs, acquires and implements projects for LAN and/or WAN systems. Plans, designs, acquires and implements telecommunications voice/wire systems. At higher job levels, may contribute to the development, testing, evaluation or design of system or infrastructure architecture used throughout the IT solution set. Survey Tip: Use this job family if company does not identify their information systems jobs by functional designations, such as Programmer/Analyst (6451-6456), Systems Programmer (6441-6446), Business Systems Analyst (6461-6466), Network Engineer (6471-6476) and Telecommunications Engineer (6431-6436). May be working in conjunction with Professional Services and outsourcing functions. May include web-enabled solutions.
 <br/>
 <br/>
 <strong>
  @ HYVE Solutions
 </strong>
 , we believe employees are our greatest asset and we empower them to make a difference in our business. Diversity and inclusion make us all better. Qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, sexual orientation, gender identity, disability or protected veteran status.
</div>


Systems Admin

American Trim

<div><p><b>Job Summary:</b></p>
<p>
The Laser Programmer will focus on developing, optimizing, and maintaining laser-based manufacturing processes including cutting, welding, drilling, engraving, and surface treatment. The Laser Programmer will play a critical role in improving production efficiency, product quality, and equipment reliability, while ensuring compliance with laser safety standards.</p>
<p><b>
Job Responsibilities:</b></p>
<ul>
<li>Develop, write, and maintain laser cutting programs using CAM software (TruTops and FastSuite) to support production operations. Responsibilities include creating efficient and accurate tool paths, nesting layouts, and cut sequences for a range of materials and part geometries.</li>
<li>Develop, test, and optimize laser manufacturing processes (cutting, welding, marking, etc.) by establishing and refining parameters for various metals, alloys, and polymers to ensure quality, consistency, and throughput.</li>
<li>Collaborate with process engineers, design engineers, and production teams to integrate laser systems into manufacturing workflows.</li>
<li>Optimize process parameters (beam power, speed, focus, assist gases, etc.) to meet quality, efficiency, and cost objectives.</li>
<li>Conduct feasibility studies and proof-of-concept trials for new products and materials.</li>
<li>Troubleshoot laser equipment and processes to minimize downtime and ensure stable, repeatable performance.</li>
<li>Work with equipment vendors and suppliers to evaluate and install new laser systems.</li>
<li>Develop standard operating procedures (SOPs), work instructions, and training materials for operators and technicians.</li>
<li>Ensure compliance with ANSI Z136 laser safety standards and company EHS policies.</li>
<li>Provide technical support for maintenance, calibration, and upgrades of laser systems.</li>
<li>Drive continuous improvement initiatives, including cycle time reduction, scrap reduction, and yield improvement.</li></ul><p></p><h4 class="jobSectionHeader"><b><br>
Experience</b></h4>
Required<ul><li>
3 year(s): Minimum three (3) years of experience with industrial laser processing (cutting, welding, marking, drilling, or additive manufacturing). A combination of educational and direct work experience may be considered.
</li></ul><h4 class="jobSectionHeader"><b>Education</b></h4>
Preferred<ul><li>
High School or better</li><li>
GED or better</li></ul><p>
Equal Opportunity Employer<br>
This employer is required to notify all applicants of their rights pursuant to federal employment laws. For further information, please review the Know Your Rights (https://www.eeoc.gov/poster) notice from the Department of Labor.</p></div>

Laser Programmer

Viet Robotics & Automation Systems

<p>PLC Programmer (Siemens / Allen-Bradley) &ndash; Industrial Automation Engineer</p><p>Build the Future of Industrial Automation With Us</p><p>We are looking for a skilled <b>PLC Programmer (Siemens / Allen-Bradley)</b> to join our growing automation engineering team. If you enjoy designing, programming, and optimizing industrial control systems that power real-world production lines, this role is for you.</p><p>You will work on cutting-edge automation projects involving PLCs, SCADA systems, robotics integration, and industrial control systems across manufacturing and process industries.</p><p>This is a hands-on engineering role where your work directly impacts efficiency, productivity, and innovation in industrial operations.</p><p>Key Responsibilities</p><ul><li>Program, configure, and troubleshoot PLC systems (Siemens S7 / TIA Portal, Allen-Bradley RSLogix / Studio 5000)</li><li>Develop and maintain HMI and SCADA systems</li><li>Support commissioning of automation systems on-site and remotely</li><li>Perform system integration with sensors, drives, and industrial equipment</li><li>Diagnose and resolve automation and control system issues</li><li>Collaborate with electrical and mechanical engineering teams</li><li>Support preventive maintenance and system optimization</li></ul><p>Requirements</p><ul><li>Experience in PLC programming (Siemens and/or Allen-Bradley)</li><li>Knowledge of industrial automation systems and protocols (Modbus, Profibus, Ethernet/IP)</li><li>Ability to read electrical schematics and control diagrams</li><li>Experience in HMI/SCADA development</li><li>Strong problem-solving and troubleshooting skills</li><li>Willingness to travel for site commissioning (if required)</li><li>Degree or diploma in Electrical, Electronics, Mechatronics, or related field (preferred, not mandatory if experienced)</li></ul><p>What We Offer</p><ul><li>Competitive salary based on experience</li><li>Opportunity to work on international-standard automation projects</li><li>Career growth into Senior Engineer / Project Engineer roles</li><li>Hands-on training with advanced automation technologies</li><li>Supportive engineering team environment</li><li>Overtime compensation (if applicable)</li></ul><p>About the Company</p><p>We are an industrial automation engineering company specializing in PLC systems, SCADA integration, and smart manufacturing solutions. Our mission is to help industries improve productivity, safety, and efficiency through advanced automation technologies.</p><p>Why Join Us</p><ul><li>Work on real industrial automation systems (not just simulations)</li><li>Exposure to international clients and projects</li><li>Strong technical learning environment</li><li>Opportunity to grow in a fast-expanding automation sector</li></ul><p>Apply Now</p><p>If you are passionate about industrial automation and PLC programming, we would love to hear from you. Submit your CV and relevant project experience today.</p><p>Pay: QAR5,000.00 - QAR8,000.00 per month</p><p>Work Location: In person</p>

PLC Programmer (Siemens / Allen-Bradley)

Search 350+ Statistical programmer jobs near you this June. New roles added regularly across leading industries. Apply today.