pharmaceutical process engineer

Bechtel

<div><p><b>Requisition ID: 289281</b></p><ul><li><b>
Relocation Authorized: National - Family</b></li><li><b>
Telework Type: Part-Time Telework</b></li><li><b>
Work Location: Chandler, AZ, Houston, TX</b></li></ul><p></p><div><div><div><h2 class="jobSectionHeader"><b><br>
Extraordinary teams building inspiring projects:</b></h2></div><div><p>
Since 1898, we have helped customers complete more than 25,000 projects in 160 countries on all seven continents that have created jobs, grown economies, improved the resiliency of the world's infrastructure, increased access to energy, resources, and vital services, and made the world a safer, cleaner place.</p><p>
Differentiated by the quality of our people and our relentless drive to deliver the most successful outcomes, we align our capabilities to our customers' objectives to create a lasting positive impact. We serve the Infrastructure; Nuclear, Security &amp; Environmental; Energy; Mining &amp; Metals, and the Manufacturing and Technology markets. Our services span from initial planning and investment, through start-up and operations.</p><p>
Core to Bechtel is our Vision, Values and Commitments. They are what we believe, what customers can expect, and how we deliver. Learn more about our extraordinary teams building inspiring projects in our Impact Report.</p></div></div><div><div><h2 class="jobSectionHeader"><b>
Job Summary:</b></h2></div><div><p>
Bechtel is seeking a highly skilled and experienced <b>Senior Process Engineer</b> to join its <b>Manufacturing and Technology Global Business Unit (M&amp;T GBU)</b> Engineering Team. This role is pivotal in delivering technical excellence across strategic initiatives, estimates, studies, and project execution phases.<br>
This role should have experience in either the semiconductor or pharmaceutical industries leading process design and optimization efforts, ensuring compliance with industry standards, and supporting project execution. The ideal candidate will bring deep domain expertise in one or both sectors and demonstrate the ability to manage complex engineering challenges in a collaborative environment.<br>
<i>&quot;This position is designated as part-time telework per our global telework policy and will require at least three days of in-person attendance per week at the assigned office or project. Weekly in-person schedules will be determined by the individual and their supervisor, in consultation with functional or project leadership&rdquo;</i> #LI-MJ1</p><p>
</p></div></div><div><div><h2 class="jobSectionHeader"><b>Major Responsibilities:</b></h2></div><div><ul><li>
Lead process engineering tasks for semiconductor or pharmaceutical projects from initial design through startup and turnover.</li><li>
Oversee and specify Process utility systems for Semiconductor (bulk/specialty gases, UPW, wastewater) and pharma (WFI, PW, clean steam, process gases).</li><li>
Develop and review PFDs, P&amp;IDs, equipment datasheets, and control philosophies.</li><li>
Ensure designs meet industry related codes and standards.</li><li>
Conduct chemical compatibility assessments and safety/environmental reviews for hazardous materials.</li><li>
Collaborate with cross-functional engineering teams.</li><li>
Interface with clients, vendors, and construction teams for technical alignment and project execution.</li><li>
Support commissioning, startup, and troubleshooting of utility and process systems.</li><li>
Mentor junior engineers and drive continuous improvement initiatives.</li></ul></div></div><div><div><h2 class="jobSectionHeader"><b>
Education and Experience Requirements:</b></h2></div><div><ul><li>
Requires bachelor's degree (or international equivalent) and 10-13 years of relevant experience or 14-17 years of relevant work experience in either semiconductor or pharmaceutical industries.</li><li>
Experience in sterile manufacturing, biologics, or high-potency API facilities.</li><li>
Experience with fab expansions, greenfield projects, or retrofit designs.</li><li>
Professional certifications (e.g., ISPE, Six Sigma, PMP) or PE License are a plus.</li></ul></div></div><div><div><h2 class="jobSectionHeader"><b>
Required Knowledge and Skills:</b></h2></div><div><ul><li>
Strong grasp of process engineering principles and practices relevant to both semiconductor fabrication and pharmaceutical manufacturing.</li><li>
Demonstrated leadership in large EPC projects and greenfield design/construction, with experience in multidisciplinary team coordination and project management.</li><li>
Strong communication skills for technical presentations, stakeholder engagement, and client-facing roles in both pharma and semiconductor sectors.</li><li>
Comprehensive understanding of chemical safety, HAZOP, risk assessments, hazardous material handling, and environmental permitting/compliance.</li><li>
Advocate for innovation and continuous improvement, with proficiency in Microsoft tools and the ability to operate effectively in dynamic, ambiguous project environments.</li><li>
Skilled in process simulation and engineering design software, including AutoCAD, Bluebeam, Pipe-Flo, Aspen Plus, and Excel.</li><li>
Extensive experience in design, engineering, and construction of semiconductor facilities, with deep knowledge of chemical and gas systems, UPW, wastewater treatment, and abatement technologies.</li><li>
Technical expertise in pharmaceutical operations, including GMP regulations (FDA 21 CFR Part 210/211, EU GMP Annex 1), clean utility systems, hygienic design, and contamination control strategies.</li><li>
Proficient with major industry regulations and standards such as SEMI (semiconductor), GMP, ASME BPE, ISPE Baseline Guides, ASTM E2500 (pharma), and compliance requirements from EPA, DOT, and OSHA.</li><li>
Hands-on experience with validation, CQV documentation, and automation/data integrity standards (GAMP 5, 21 CFR Part 11) in pharmaceutical projects.</li></ul></div></div><div><div><h2 class="jobSectionHeader"><b>
Total Rewards/Benefits:</b></h2></div><div><p>
For decades, Bechtel has worked to inspire the next generation of employees and beyond! Because our teams face some of the world's toughest challenges, we offer robust benefits to ensure our people thrive. Whether it is advancing careers, delivering programs to enhance our culture, or providing time to recharge, Bechtel has the benefits to build a legacy of sustainable growth. Learn more at Bechtel Total Rewards</p></div></div><div><div><h2 class="jobSectionHeader"><b>
Diverse teams build the extraordinary:</b></h2></div><div><p>
As a global company, Bechtel has long been home to a vibrant multitude of nationalities, cultures, ethnicities, and life experiences. This diversity has made us a more trusted partner, more effective problem solvers and innovators, and a more attractive destination for leading talent.</p><p>
We are committed to being a company where every colleague feels that they belong-where colleagues feel part of &quot;One Team,&quot; respected and rewarded for what they bring, supported in pursuing their goals, invested in our values and purpose, and treated equitably.</p></div></div></div><p></p><p><b><i><br>
Bechtel is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity and expression, age, national origin, disability, citizenship status (except as authorized by law), protected veteran status, genetic information, and any other characteristic protected by federal, state or local law. Applicants with a disability, who require a reasonable accommodation for any part of the application or hiring process, may e-mail their request to </i></b><b>acesstmt@bechtel.com</b></p></div>

Senior Process Engineer

Fluid Tech System

<p>ChatGPT Log in You said: Please write a job description for mechnical design Engineer for mahashakti pharmamach vatva location ChatGPT said: Here&rsquo;s a professional job description for a Mechanical Design Engineer position at Mahashakti Pharmamach, Vatva: Job Title: Mechanical Design Engineer Location: Vatva, Ahmedabad, Gujarat Company: Mahashakti Pharmamach Pvt. Ltd. Industry: Pharmaceutical Machinery Manufacturing About the Company: Mahashakti Pharmamach is a leading manufacturer of pharmaceutical machinery, specializing in high-quality, precision-engineered equipment for tablet, capsule, and packaging lines. With a commitment to innovation, performance, and reliability, we deliver world-class engineering solutions to the pharmaceutical industry. Job Summary: We are seeking a talented and motivated Mechanical Design Engineer to join our design and development team at our Vatva facility. The ideal candidate will be responsible for designing, developing, and improving pharmaceutical machinery components and systems, ensuring functionality, manufacturability, and cost-effectiveness. Key Responsibilities: Design and develop mechanical components and assemblies for pharmaceutical machinery using CAD software (SolidWorks / AutoCAD / Creo, etc.) Prepare detailed engineering drawings, BOMs, and 3D models as per project requirements. Work closely with the production, purchase, and quality teams to ensure design feasibility and manufacturability. Modify and improve existing machine designs to enhance performance and efficiency. Participate in prototype development, testing, and validation. Ensure designs comply with GMP, safety, and regulatory standards applicable to the pharma machinery industry. Prepare and maintain design documentation and revision control. Collaborate with clients and internal teams to understand technical requirements and propose effective solutions. Required Skills &amp; Qualifications: Education: Diploma / B.E. / B.Tech in Mechanical Engineering or related field. Experience: 2&ndash;5 years of experience in mechanical design (preferably in pharmaceutical / packaging / process machinery industry). Software Skills: Proficiency in 3D and 2D design tools (SolidWorks, AutoCAD, Creo, or equivalent). Strong understanding of mechanical systems, sheet metal design, fabrication, and assembly processes. Good knowledge of materials, tolerances, and GD&amp;T. Strong problem-solving, analytical, and communication skills. Ability to work independently and in a team environment. Preferred Qualifications (Optional): Experience in design of tablet press, capsule filling, or blister packing machines. Knowledge of pneumatics, hydraulics, and automation integration. Familiarity with ISO and GMP documentation standards. Salary: Commensurate with experience and industry standards. Work Location: Mahashakti Pharmamach Pvt. Ltd. GIDC Vatva, Ahmedabad, Gujarat How to Apply: Interested candidates can send their updated resume to [company email address] with the subject line &ldquo;Application for Mechanical Design Engineer &ndash; Vatva&rdquo;. Would you like me to make it more formal for a job portal posting (like Naukri/LinkedIn) or simpler and shorter for an internal company hiring flyer? You said: Jd for planning Engineer ChatGPT said: Here&rsquo;s a professional Job Description (JD) for a Planning Engineer position at Mahashakti Pharmamach, Vatva: Job Title: Planning Engineer Location: Vatva, Ahmedabad, Gujarat Company: Mahashakti Pharmamach Pvt. Ltd. Industry: Pharmaceutical Machinery Manufacturing About the Company: Mahashakti Pharmamach Pvt. Ltd. is a reputed manufacturer of high-performance pharmaceutical machinery and process equipment. We are committed to delivering precision-engineered, efficient, and reliable machines that meet global quality standards. Job Summary: We are looking for a Planning Engineer to coordinate and control production planning and scheduling activities. The ideal candidate will ensure timely delivery of projects, optimal resource utilization, and smooth workflow across departments from design to dispatch. Key Responsibilities: Prepare and maintain detailed production plans and schedules for manufacturing pharmaceutical machinery. Coordinate with design, procurement, production, and quality teams to ensure project timelines are met. Monitor project progress, identify bottlenecks, and take corrective actions to avoid delays. Develop and maintain project tracking reports and dashboards. Plan and allocate resources (manpower, materials, machines) effectively to meet delivery schedules. Prepare and review daily/weekly/monthly production reports. Support management in capacity planning, workload analysis, and process optimization. Communicate with suppliers and vendors to ensure timely availability of materials. Ensure adherence to project deadlines, quality standards, and company policies. Required Skills &amp; Qualifications: Education: Diploma / B.E. / B.Tech in Mechanical / Production / Industrial Engineering or equivalent. Experience: 2&ndash;5 years of experience in production or planning (preferably in pharmaceutical machinery or related manufacturing industry).</p><p>Job Type: Full-time</p><p>Pay: &#8377;12,031.54 - &#8377;30,000.00 per month</p><p>Benefits:</p><ul><li>Provident Fund</li></ul><p>Work Location: In person</p>

Planning Engineer

Fresenius Medical Care

<div></div><div><div><p>Supplier Quality Engineer II, Fresenius USA Manufacturing, Inc., a Fresenius Medical Care N.A. company, Lexington, MA (Remote)
</p><p></p><p><b>Job Duties:</b></p><p>
Responsible for assuring End-to-End quality and sustainability with allocated supply base, validating, and releasing components, and supporting the definition and implementation of supplier quality functional excellence initiatives. Specific duties include:</p><p></p><ul><li>
Interfacing directly with suppliers to follow up on quality and performance issues, managing Supplier Corrective Action Requests.</li><li>
Performing on-site and remote supplier quality audits for new suppliers, participating in supplier approval process.</li><li>
Documenting and following up on audit results and required actions to be addressed by the supplier.</li><li>
Tracking, analyzing and reporting on supplier performance metrics to stakeholders within quality, logistics and manufacturing management using the appropriate software tools.</li><li>
Performing problem analysis, process and machine capability studies as required, and determining and proposing statistical process controls for appropriate supplier&rsquo;s processes.</li><li>
Collaborating with stakeholders to define deliverables meeting user needs and acceptance criteria.</li><li>
Ensuring documentation is aligned with corporate standards including FMEA, DFMEA, Manufacturing Process Characterization / PFMEA, product life cycles.</li><li>
Performing gap analysis of Design Control Quality System, determined changes required to close gaps, and implement changes.</li><li>
Preparing Supplier Corrective Action Reports (SCARs) and Supplier Nonconformance Reports (SNCs), interfacing with both internal customers and the supply base to ensure effective actions are taken to reach closure.</li><li>
Execute Supplied Part Approval Process including providing supplier with required deliverables, then reviewing and approving these deliverables.</li><li>
Review and update Supplier Quality SOPs using Quality tools and principles.</li></ul><p></p><p><b>
Requirements</b><b>:</b></p><p>
Position requires either a Bachelor&rsquo;s degree (or an equivalent foreign degree) in Industrial Engineering, Pharmaceutical Engineering, Pharmacy or a related life sciences field and 5 years of experience as a Quality Engineer working in the medical device or pharmaceutical sector or alternatively, a Master&rsquo;s degree(or an equivalent foreign degree) in Industrial Engineering, Pharmaceutical Engineering, Pharmacy or a related life science field and 3 years of experience as a Quality Engineer working in the medical device or pharmaceutical sector. Must also have had 3 years of experience (which can have been gained concurrently with either of the primary experience requirements above) working with the following:</p><ul><li>
Performing on-site and remote supplier quality audits and participating in the supplier selection and approval process;</li><li>
Tracking, analyzing, and reporting supplier performance metrics to internal stakeholders within quality, logistics, and manufacturing management using the appropriate software tools;</li><li>
Maintaining Risk Management files including Hazard analysis, Design FMEA, Use FMEA and Process FMEA for assigned product families;</li><li>
Utilizing Root Cause Analysis concepts to investigate issues and implement Corrective and Preventive actions including effectiveness checks.</li><li>
Performing Design of Experiments (DoE) using Minitab and analyzing various process parameters with the use of statistical tools (SPC) such as Gage R &amp; R, Gage linearity and Bias study, interaction plot, process capability study to optimize the blending and compression process.</li></ul><p></p><p>
This position requires approximately 10% domestic and international travel.</p><p></p><p>
This is a telecommuting position working from home. May reside anywhere in the United States.</p><p></p><p>
Salary is $163,030 - $171,181 per year for a 40-hour work week.</p></div><p></p><p><b>
EOE, disability/veterans</b></p></div>

Supplier Quality Engineer II

<p>Dear Team,</p><p>We are seeking a talented and motivated Mechanical Design Engineer to join our design and development team at our Vatva facility. The ideal candidate will be responsible for designing, developing, and improving pharmaceutical machinery components and systems, ensuring functionality, manufacturability, and cost-effectiveness.</p><p>ChatGPT</p><p>Log in<br/>You said:<br/>Please write a job description for mechnical design Engineer for mahashakti pharmamach vatva location<br/>ChatGPT said:<br/>Here&rsquo;s a professional job description for a Mechanical Design Engineer position at Mahashakti Pharmamach, Vatva:</p><p>Job Title: Mechanical Design Engineer<br/>Location: Vatva, Ahmedabad, Gujarat<br/>Company: Mahashakti Pharmamach Pvt. Ltd.<br/>Industry: Pharmaceutical Machinery Manufacturing</p><p>About the Company:<br/>Mahashakti Pharmamach is a leading manufacturer of pharmaceutical machinery, specializing in high-quality, precision-engineered equipment for tablet, capsule, and packaging lines. With a commitment to innovation, performance, and reliability, we deliver world-class engineering solutions to the pharmaceutical industry.</p><p>Job Summary:<br/>We are seeking a talented and motivated Mechanical Design Engineer to join our design and development team at our Vatva facility. The ideal candidate will be responsible for designing, developing, and improving pharmaceutical machinery components and systems, ensuring functionality, manufacturability, and cost-effectiveness.</p><p>Key Responsibilities:<br/>Design and develop mechanical components and assemblies for pharmaceutical machinery using CAD software (SolidWorks / AutoCAD / Creo, etc.)</p><p>Prepare detailed engineering drawings, BOMs, and 3D models as per project requirements.</p><p>Work closely with the production, purchase, and quality teams to ensure design feasibility and manufacturability.</p><p>Modify and improve existing machine designs to enhance performance and efficiency.</p><p>Participate in prototype development, testing, and validation.</p><p>Ensure designs comply with GMP, safety, and regulatory standards applicable to the pharma machinery industry.</p><p>Prepare and maintain design documentation and revision control.</p><p>Collaborate with clients and internal teams to understand technical requirements and propose effective solutions.</p><p>Job Type: Full-time</p><p>Pay: &#8377;12,226.04 - &#8377;30,000.00 per month</p><p>Benefits:</p><ul><li>Provident Fund</li></ul><p>Work Location: In person</p>

Mechanical Design Engineer

CECO Environmental Corporation

<div>
 <strong>
  Job Summary
  <br/>
  <br/>
 </strong>
 CECO Environmental is a global leader in providing sustainable solutions for industrial air, water, and energy transition. Since 1966, we&rsquo;ve been addressing the world&rsquo;s most pressing environmental challenges. Our mission is to protect people, the environment, and industrial equipment, making a tangible impact across industries like renewable energy, semiconductor manufacturing, power generation, and water treatment. As a purpose-driven company, we foster a culture of innovation, collaboration, and integrity, ensuring that every project we undertake creates lasting positive change. At CECO, you&rsquo;ll be part of a growing, dynamic team committed to a cleaner, safer, and more sustainable future.
 <br/>
 <br/>
 As part of the CECO Environmental family of brands,
 <strong>
  Peerless Separation &amp; Filtration
 </strong>
 plays a critical role in delivering specialized water solutions that protect both people and the environment. By joining our team, you&rsquo;ll contribute to our shared mission of protecting global industrial operations and shaping the future of environmental stewardship.
 <br/>
 <br/>
 <strong>
  Your Responsibilities Will Be
  <br/>
  <br/>
 </strong>
 <ul>
  <li>
   Conduct process simulations using software like Aspen Plus, ProMax, or HYSYS to model and optimize oil &amp; gas and/or water treatment
  </li>
  <li>
   Develop and maintain process flow diagrams (PFDs), piping and instrumentation diagrams (P&amp;IDs), and other engineering documents.
  </li>
  <li>
   Perform hydraulic and heat balance calculations to ensure equipment sizing and process operability.
  </li>
  <li>
   Experience of PSV, control valve sizing, equipment sizing, good understanding of pumps, instruments etc
  </li>
  <li>
   Provide technical support to operations teams during troubleshooting, commissioning, and debottlenecking
  </li>
  <li>
   Identify and implement process improvement opportunities to enhance efficiency, safety, and reliability.
  </li>
  <li>
   Stay current with evolving industry standards and regulations for oil &amp; gas and/or water
  </li>
  <li>
   Collaborate with cross-functional teams (e.g., design, procurement, operations) to ensure project success.
  </li>
  <li>
   Communicate technical information clearly and concisely to both technical and non-technical audiences.
   <br/>
   <br/>
  </li>
 </ul>
 <strong>
  Required Qualifications
  <br/>
  <br/>
 </strong>
 <ul>
  <li>
   Bachelor&rsquo;s degree in chemical
  </li>
  <li>
   Minimum 6-10 years of experience in process engineering, preferably in the oil &amp; gas and/or water treatment
  </li>
  <li>
   Strong proficiency in process simulation software like Aspen Plus, ProMax, or
  </li>
  <li>
   Experience with PFD, P&amp;ID, and other engineering documentation
  </li>
  <li>
   Excellent understanding of mass and heat transfer and fluid
  </li>
  <li>
   Proven ability to work independently and manage multiple projects
  </li>
  <li>
   Strong problem-solving and analytical
  </li>
  <li>
   Knowledge of all International Standards like Shell DP, API, ASME
  </li>
  <li>
   Excellent communication and interpersonal
  </li>
  <li>
   Ability to work effectively in a team environment
   <br/>
   <br/>
  </li>
 </ul>
 <strong>
  We Offer
  <br/>
  <br/>
 </strong>
 At CECO, we are committed to a culture where every employee is valued and respected for their unique experiences and perspectives. We believe a diverse and inclusive work environment contributes to the rich exchange of ideas and diversity of thoughts, that inspires innovation and brings the best solutions to our customers.
 <br/>
 <br/>
 <strong>
  About Us
  <br/>
  <br/>
 </strong>
 CECO&rsquo;s Commitment to Our People
 <br/>
 <br/>
 At CECO, our people are at the center of everything we do. Whether you&rsquo;re a professional looking for a career change, an undergraduate student exploring opportunities, or a recent graduate with an advanced degree, you&rsquo;ll find your chance to make a difference with CECO.
 <br/>
 <br/>
 <strong>
  About Ceco
  <br/>
  <br/>
 </strong>
 CECO Environmental is a leading environmentally focused, diversified industrial company whose solutions protect people, the environment, and industrial equipment across the globe, serving a broad landscape of industrial air, industrial water and energy transition markets.
 <br/>
 <br/>
 We serve these markets and our global customers through our key business segments: Engineered Systems and Industrial Process Solutions. Learn more about CECO by visiting About Us .
</div>


Sr. Process Engineer

Argenta

<div><p><i>At Argenta, we&rsquo;re more than a company &mdash; we&rsquo;re a global team, dedicated to healthier animals. We believe that when their lives are made better, we're all the better for it.</i></p><p></p><p><br>
Founded in 2006, we support companies big and small to develop and manufacture health products for pets and livestock. Our trusted, innovative solutions and services cover every stage of the process, from molecule to market.</p><p></p><p><br>
We&rsquo;re in a unique position. We are the world&rsquo;s only combined contract research and contract development and manufacturing organization (CRO/CDMO) dedicated to animal health.</p>
<p>
Our uniqueness means:</p><p></p><p><br>
We are ambitious, growing and building a &lsquo;one team&rsquo; culture, guided by our values.</p>
<ul>
<li><ul><li><i>We are team players;</i></li>
<li><i>We are doers;</i></li>
<li><i>We are customer-centric;</i></li>
<li><i>We are innovators</i>.</li>
</ul>
</li></ul><p>We value diversity, as a global company, we get the richness of working with different people in different places whether it be location, stages of their career, their development, their role. We believe that when everyone works together and puts their best &ldquo;paw&rdquo; forward we will make the lives of the animals we care for, better.</p><p></p><p><br>
With bases in New Zealand, the US, the UK and Europe, our 900+ colleagues are driven by our partnership approach and purpose: Healthy Animals. Let&rsquo;s Make It Happen, Together.</p><p></p><p><br>
TEAM PLAYERS who want to DO great work and find INNOVATIVE ways to make animals lives better through our CUSTOMER CENTRIC efforts should apply.</p><p></p><p><br>
Argenta is currently looking to fill the role of <b><i>Senior Engineer at our Shawnee, KS location</i></b>. This position is an established, technically competent professional who develops and implements manufacturing process solutions. Leads projects and is often called upon by peers for guidance. Directs projects or discipline teams. Meets customer needs in support of Business goals. Coaches and teaches junior members of the department. This position will also provide direct engineering support for OSD Production &amp; Process Equipment in support of Manufacturing through the application of engineering-based principles and disciplines. Will work closely with personnel within Engineering, Maintenance, Production, Quality &amp; Technical Service Groups to understand current production processes/issues, initiate and support process improvements and improve maintenance procedures in support of system reliability.</p><p></p><p><b><br>
Key Accountabilities:</b></p>
<ul>
<li>Makes independent decisions within defined areas of responsibility. Serves as a consultant to management within a specified areas/discipline. Advance technical project proposals to senior management, following through successful completion. Influences commitment of resources at divisional / departmental level.</li>
<li>Continuously improve and support existing production equipment to support the efficient operation of the Argenta production facility.</li>
<li>Manage capital projects, develop and track budgets.</li>
<li>Interface with internal and external resources to facilitate the transfer of process knowledge to the manufacturing environment.</li>
<li>Ensure that all Engineering activities within the area of responsibility adhere to all applicable engineering standards, codes, cGMP&rsquo;s, FDA and EU guidelines, safety and environmental procedures.</li>
<li>Reviews and approves standard operating procedures describing validation principles and activities.</li>
<li>Participate with completing risk analyses for qualifications and validations with participation of Quality, Production and MEU.</li>
<li>Actively participates during all phases of equipment life cycle by supporting the development of specifications, design and installation of equipment, systems, facilities, and utilities, and processes to ensure compliance to cGMP requirements.</li>
<li>Provides guidance and technical information to others, supporting and/or execution of IQ/SAT</li>
<li>Actively participates in Engineering, functional testing in OQ, and coordination and testing during PQ, PV, and CV activities.</li>
<li>Other duties as assigned by the supervisor.</li></ul><br>
<p></p>
<p><b>
Competencies:</b></p>
<ul>
<li>Bachelor&rsquo;s degree in Engineering.</li>
<li>Strong knowledge of pharmaceutical regulations and cGMP standards (FDA, EMA, EU).</li>
<li>Solid understanding of pharmaceutical manufacturing principles, with specific expertise in Oral Solid Dosage (OSD) facility and process design&mdash;including formulation, blending, granulation, compression, coating, and packaging operations.</li>
<li>Demonstrated experience providing subject matter expertise in OSD technologies, supporting regulatory strategy, technology transfer, and commercialization readiness.</li>
<li>Proven ability to collaborate with clients and cross-functional project teams to ensure OSD solutions meet regulatory and operational requirements.</li>
<li>Experience with advanced OSD technologies such as continuous manufacturing, Process Analytical Technology (PAT), and high-potency containment systems.</li>
<li>Comprehensive knowledge of current pharmaceutical technologies, installation practices, and problem-solving methodologies to effectively direct technical teams.</li>
<li>Strong working knowledge of pharmaceutical manufacturing equipment, unit operations, and processing, with expertise in Oral Solid Dosage (OSD) products&mdash;including mixing, blending, granulation, milling, tablet compression, and piece-forming technologies.</li>
<li>Proven experience in the practical application of engineering principles within a pharmaceutical manufacturing environment.</li>
<li>Solid understanding of GMP regulations as interpreted by the FDA, EU, and CVM, along with familiarity with OSHA health and safety and EPA environmental requirements.</li>
<li>Demonstrated ability in creative problem solving, as well as tactical and strategic decision-making.</li>
<li>Excellent written, verbal, and organizational skills, with the ability to collaborate effectively across internal teams and with external partners.</li>
<li>Strong understanding of factory processes, process engineering fundamentals, and process safety requirements.</li>
<li>Proficiency in computer systems and software tools relevant to engineering and manufacturing operations.</li></ul></div>

Senior Engineer

Abdi Ibrahim Pharmaceuticals

<div>
 <p>
  <strong>
   Abdi &Idot;brahim
  </strong>
  , founded in 1912, has the largest product portfolio in the sector and is the largest employer in the Turkish pharmaceutical industry with 5.500 employees. Abdi &Idot;brahim has been the leader of Turkey&rsquo;s pharmaceutical industry since 2002 with its powerful vision.
 </p>
 <p>
  <br/>
 </p>
 <p>
  Today, Abdi &Idot;brahim operates in 17 countries outside T&uuml;rkiye, exports to more than 70 countries ranging from Canada to European Union member states, from North Africa to Asia. As a corporate citizen working towards creating a better world and a better future, adhering to its mission in the sector and to the requirements of societal priorities, Abdi &Idot;brahim focuses on sustainability in all its business processes.
 </p>
 <p>
  <br/>
 </p>
 <p>
  Its vision for 2025 - apart from maintaining its status as a wholly local company - is to become "one of the top 100 pharmaceutical companies in the world.
 </p>
 <p>
  <br/>
 </p>
 <p>
  We are looking for an
  <strong>
   "Pharmaceutical Development Manager"
  </strong>
  to join our R&amp;D Center located in Esenyurt.
 </p>
 <p>
  <br/>
 </p>
 <p>
  <br/>
 </p>
 <p>
  <strong>
   Job Description
  </strong>
 </p>
 <p>
  <br/>
 </p>
 <p>
  &bull; Strategically plan, execute, and manage pharmaceutical product development processes and technology transfers.
 </p>
 <p>
  &bull; Lead project teams, manage resources, and ensure effective time management,
 </p>
 <p>
  &bull; Contribute to R&amp;D strategies through new product and process development activities,
 </p>
 <p>
  &bull; Manage documentation and validation processes in compliance with regulatory guidelines (EMA, FDA, etc.),
 </p>
 <p>
  &bull; Collaborate closely with Production, Quality, Regulatory Affairs, and Licensing departments,
 </p>
 <p>
  &bull; Demonstrate leadership that fosters team development, motivation, and collaboration.
 </p>
 <p>
  <br/>
 </p>
 <p>
  <strong>
   Qualifications
  </strong>
 </p>
 <p>
  <br/>
 </p>
 <p>
  &bull; Bachelor&rsquo;s, Master&rsquo;s and/or Doctorate degree in Chemistry, Chemical Engineering, Pharmacy, or related fields,
 </p>
 <p>
  &bull; Minimum of 15 years of experience in pharmaceutical development within pharmaceutical companies,
 </p>
 <p>
  &bull; Preferably managerial experience in pharmaceutical development or a closely related area,
 </p>
 <p>
  &bull; Strong knowledge of current publications, guidelines, and global regulatory processes,
 </p>
 <p>
  &bull; Excellent command of written and spoken English,
 </p>
 <p>
  &bull; Preferably experienced in working with multicultural teams,
 </p>
 <p>
  &bull; Strong communication skills, proactive mindset, and well-developed leadership competencies.
 </p>
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Pharmaceutical Development Manager

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