validation specialist

Validation & Engineering Group

<div><p><b><i>Validation &amp; Engineering Group, Inc. </i></b>(V&amp;EG) is a leading services supplier who provides solutions for the Pharmaceutical, Biotechnology, Chemical, Food, and Medical Devices industries in the following areas: Laboratory, Compliance, Computer, Engineering, Project Management, Validation, and other services.</p>
<p>We are seeking a talented, dedicated individual committed to work under the highest ethics standards for the following position:</p>
<ul><li><b>Validation Specialist for Packaging Equipment</b></li>
</ul>
<p>Qualifications:</p>
<ul><li>Bachelor's Degree in Science or Engineering.</li>
<li>Minimum of 3 years of experience in direct pharmaceutical, medical device or biotechnology industries.</li>
<li>Experience in direct process / manufacturing areas.</li>
<li>Must be fully bilingual (English / Spanish) with excellent oral skills.</li>
<li>Must be proficient using MS Windows and Microsoft Office applications.</li>
<li>Strong knowledge in cGxP and regulatory guidance as well as understanding of how they are applied to regulatory compliance.</li>
<li><b>Experience in Design Documentation (URS, DS), IQ, OQ, PQ protocols development and execution, deviations and reports generation.</b></li>
<li><b>SDLC, Risk Assessment, Data Integrity, Factory Acceptance Test (FAT) &amp; Site Acceptance Test (SAT).</b></li>
<li>Strong knowledge in:
<ul><li><b>Material cleaning systems</b></li>
<li><b>Collaborative robots</b></li>
<li><b>EFD for lubrication process</b></li>
<li><b>Cognex vision system for inspection</b></li>
<li><b>Automated Box Erector</b></li>
<li><b>Zebra printers and label applicators</b></li>
<li><b>Cognex Vision system for labels inspection</b></li>
<li><b>Semi-Automatic Case Former and sealer</b></li>
<li><b>Checkweigher</b></li>
<li><b>Automated Palletizer (Collaborative robots)</b></li>
<li><b>Stretch Wrapper</b></li>
</ul></li><li>Technical Writing skills and investigations processes.</li>
<li>Available to work extended hours, possibility of weekends and holidays.</li></ul></div>

LL01-250714 Validation Specialist for Packaging Equipment

Julphar

<div>
 At Julphar, we are on a journey of culture transformation &amp; our mission is to provide a better quality of life for the entire family by delivering best in class solutions and real value with compassion and professionalism.
 <br/>
 <br/>
 Our core values: Respect, Collaboration, innovation, Integrity and Compassion - Combined with a focus on diversity, inclusion, and equal opportunities - are key drivers in our aim to make a positive impact on the lives of the patients we serve, enable Talents , create a healthy work environment, and accomplish our goals through world-class research and with the compassion and commitment of our employees.
 <br/>
 <br/>
 <strong>
  Main Responsibilities
  <br/>
  <br/>
 </strong>
 <ul>
  <li>
   Prepare, review, and oversee process and cleaning validation documentation and execution activities for Sterile Facilities, including Liquid Injectables, Lyophilized products, and Sterile Powder Filling.
  </li>
  <li>
   Conduct process validation for various dosage forms such as Oral Solid Dosage (Tablets, Capsules, PPS), Oral Liquids (Syrups, Suspensions, Oral Drops), and Semi-Solids (Ointments, Creams, Suppositories).
  </li>
  <li>
   Manage process validation activities for API biological drug substances and sterile products.
  </li>
  <li>
   Demonstrate familiarity with filter validation requirements in sterile areas.
  </li>
  <li>
   Design and execute Aseptic Process Simulation (APS) studies, including preparation of related protocols and reports.
  </li>
  <li>
   Lead the visual inspection qualification process.
  </li>
  <li>
   Manage shipping validation activities for cold chain products.
  </li>
  <li>
   Oversee cleaning validation activities, including dirty equipment hold-time studies.
  </li>
  <li>
   Review and support Change Controls, CAPAs, and Deviations associated with qualification and validation activities.
  </li>
  <li>
   Act as Quality General in EQMS to complete actions related to qualification and validation.
  </li>
  <li>
   Monitor and verify CAPA effectiveness related to validation activities.
   <br/>
   <br/>
  </li>
 </ul>
 <strong>
  Core Competencies
  <br/>
  <br/>
 </strong>
 <ul>
  <li>
   Strong results orientation with a high level of accountability and ownership.
  </li>
  <li>
   Ability to prioritize, multitask, and perform effectively under pressure to meet deadlines.
  </li>
  <li>
   Excellent communication, interpersonal, and collaboration skills.
  </li>
  <li>
   Highly disciplined, organized, and self-motivated to learn and implement new practices.
  </li>
  <li>
   Proven technical expertise in qualification and validation within sterile and biotech facilities.
  </li>
  <li>
   Strong implementation skills with adaptability to changing business requirements.
  </li>
  <li>
   Ability to work effectively in cross-functional environments, collaborating with internal and external stakeholders.
  </li>
  <li>
   Strong capability to communicate technical, scientific, and regulatory information clearly&mdash;both verbally and in writing.
   <br/>
   <br/>
  </li>
 </ul>
 <strong>
  Qualification &amp; Functional Knowledge
  <br/>
  <br/>
 </strong>
 <ul>
  <li>
   Education: Bachelor&rsquo;s degree in Pharmacy or Science.
  </li>
  <li>
   Experience: Minimum 3&ndash;5 years of relevant experience in qualification and validation within the pharmaceutical/biotech industry.
  </li>
  <li>
   Hands-on experience with regulatory audits (SFDA, WHO, EU, USFDA).
  </li>
  <li>
   Strong working knowledge of QMS systems such as Agile, Veeva Vault, TrackWise, and AmpleLogic.
  </li>
  <li>
   Excellent computer proficiency and command of English (written and spoken).
  </li>
  <li>
   Demonstrated problem-solving and team coordination skills.
  </li>
  <li>
   Solid understanding of cGMP principles and Risk Assessment methodologies.
   <br/>
   <br/>
  </li>
 </ul>
 We value people from different backgrounds. Could this be your story? Apply today or visit www.Julphar.net to read more about us and the journey of Julphar
</div>


Specialist - Product Lifecycle

Waayslive solution

<p>5 years Experience Responsibilities: Define business rules, KPIs, and validation checks for Stock &amp; Retail datasets.<br/>Validate Silver and Gold datasets to ensure accuracy and alignment with business requirements.<br/>Collaborate with engineering teams to embed validation logic into ETL/ELT pipelines.<br/>Required Skills<br/>Strong SQL and data validation experience.<br/>Exposure to data profiling, quality assurance, and KPI definition.</p><p>Job Type: Full-time</p><p>Pay: Up to &#8377;1,700,000.00 per year</p><p>Work Location: Remote</p>

DA Analyst

<div><p><b>Validation &amp; Engineering Group, Inc. (V&amp;EG)</b> is a leading technical services provider specializing in high-quality Commissioning &amp; Qualification, Validation, Compliance, Quality Assurance, and Engineering services for the Biotechnology, Pharmaceutical, Advanced Therapies, Medical Device, and Chemical (API) industries.</p>
<p>We are seeking a talented, dedicated individual committed to working under the highest ethical standards for the following position:</p>
<p></p><ul><li><b>Packaging Validation Engineer</b></li>
</ul>
<p><b>Position Overview:</b><br>
We are seeking a Validation Engineer with strong experience in pharmaceutical packaging systems and GMP manufacturing environments. The selected candidate will focus on the qualification of packaging equipment and processes, ensuring compliance with regulatory requirements and company standards. This role will support validation, packaging engineering, and continuous improvement initiatives to maintain and enhance product quality and operational efficiency.</p>
<p></p><p><b>Responsibilities:</b></p>
<ul><li><b>Lead and execute equipment and process qualification activities (IQ/OQ/PQ) for primary and secondary packaging systems, including serialization/aggregation systems.</b></li>
<li>Prepare and execute validation protocols and reports, ensuring adherence to cGMP, FDA, and EU regulatory expectations.</li>
<li>Support packaging validation life-cycle documentation, including URS, FRS, DS, FAT, SAT, risk assessments, and traceability matrices.</li>
<li>Participate in deviations, CAPAs, and change control processes related to packaging systems and associated utilities.</li>
<li>Collaborate with Production, Engineering, and Quality to troubleshoot equipment and process issues during qualification and routine operations.</li>
<li>Support technology transfer activities and new product introductions related to packaging operations.</li>
<li>Coordinate multiple project tasks from inception to completion, applying sound project management and documentation practices.</li>
<li>Ensure compliance with GMPs, Good Engineering Practices (GEP), and company standards and procedures.</li>
</ul>
<p></p><p><b>Requirements / Skills:</b></p>
<ul><li>Bachelor of Science degree in Engineering (Mechanical, Packaging, Chemical, or related discipline) or in Natural Sciences.</li>
<li><b>5+ years of experience in pharmaceutical, medical device, or biotech environments, with a focus on equipment qualification and packaging systems.</b></li>
<li>Solid knowledge of primary and secondary packaging equipment and materials (vials, syringes, bottles, labels, cartons, etc.).</li>
<li>Strong understanding of validation principles, including IQ/OQ/PQ, risk assessments, and validation life-cycle documentation.</li>
<li>Experience developing and executing technical documents (URS, FRS, DS, FAT/SAT, protocols, and reports).</li>
<li>Familiarity with serialization and aggregation systems (Optel) preferred.</li>
<li>Excellent analytical, organizational, and technical writing skills.</li>
<li>Strong communication skills (written and verbal) with ability to interface effectively with cross-functional teams and clients.</li></ul></div>

ATL01-111025_ Packaging Validation Engineer_PA

Commonwealth Bank of Australia

<div><p><b>Organization:
</b></p><p>At CommBank, we never lose sight of the role we play in other people&rsquo;s financial wellbeing. Our focus is to help people and businesses move forward to progress. To make the right financial decisions and achieve their dreams, targets, and aspirations. Regardless of where you work within our organisation, your initiative, talent, ideas, and energy all contribute to the impact that we can make with our work. Together we can achieve great things.
</p><p></p><p><b>Job Title: </b>Data Scientist, AI &amp; General Model Validation
</p><p></p><p><b>Location: </b>Bangalore
</p><p></p><p><b>Business &amp; Team:
</b></p><p>Model Risk &amp; Validation team plays a critical role in safeguarding the integrity of data-driven decisions across the Group. We provide second-line assurance through rigorous oversight and challenge, ensuring every model meets internal and regulatory standards. Join us and be part of a team that&rsquo;s shaping the future of risk, technology, and AI across the bank.
</p><p>At CBA, our Model Risk &amp; Validation team plays a critical role in safeguarding the integrity of data-driven decisions across the Group.
</p><p></p><p><b>Impact &amp; contribution:
</b></p><p>As a key member of our <b>Model Risk &amp; Validation </b>team, you&rsquo;ll drive robust validation processes, deploy cutting-edge analytics tools, and embed robust risk management practices across our model ecosystem. You&rsquo;ll work with a high-performing quantitative team, collaborating to uphold the integrity of our model risk framework while influencing the Group&rsquo;s broader AI and transformation strategies
</p><p></p><p><b>Roles &amp; Responsibilities:
</b></p><ul><li><p>Model Validation &ndash; Apply your problem solving and critical thinking skills to assess model performance, compliance, and risks.
</p></li><li><p>AI Evaluation Pipelines &ndash; Code in python or equivalent programming languages to establish evaluation pipelines for AI/Gen-AI models in a CI/CD environment.
</p></li><li><p>Stakeholder Engagement &ndash; Establish strong professional relationships with model developers, business units, to ensure transparency and alignment.
</p></li><li><p>Continuous Improvement &ndash; Develop and integrate AI-driven tools to enhance model development/validation quality and speed.
</p></li></ul><p></p><p><b>Essential Skills:
</b></p><ul><li><p>6 to 9 years of experience working with predictive modelling, Gen-AI, and/or software engineering.
</p></li><li><p>Strong programming skills and experience with tools like Python, R, SQL, Spark, TensorFlow, and Py Torch; familiarity with version control (GitHub).
</p></li><li><p>Ability to solve technical problems and execute validation tasks independently.
</p></li><li><p>Excellent communication skills, with the ability to translate complex technical concepts for diverse audiences.
</p></li><li><p>Any experience with Gen-AI techniques like RAG, prompt engineering, and/or orchestration tools (e.g., Lang Chain, LangGraph) would be highly preferred.
</p></li><li><p>Experience with platforms like AWS SageMaker, AWS Bedrock, or H2O.ai is a plus.
</p></li></ul><p></p><p><b>Education Qualification : </b>Bachelor&rsquo;s degree or Master&rsquo;s degree in Engineering in Computer Science/Information Technology.
</p><p></p><div><div><div><div><div><div><div><p>If you're already part of the Commonwealth Bank Group (including Bankwest, x15ventures), you'll need to apply through Sidekick to submit a valid application. We&rsquo;re keen to support you with the next step in your career.
</p><p></p><p>We're aware of some accessibility issues on this site, particularly for screen reader users. We want to make finding your dream job as easy as possible, so if you require additional support please contact HR Direct on 1800 989 696.
</p></div></div></div></div></div></div></div><p></p>Advertising End Date: 20/11/2025</div>

Data Scientist

Teva Pharmaceuticals

<div><div><div><div><p>Apply now &raquo;</p>
</div></div><div><div><div><div><div><p>Quality Control Analyst II
</p></div></div></div></div><div></div><div><div><div><div><b>Date: </b>Nov 7, 2025
</div></div></div></div><div><div><div><div><b>Location:
</b>Chennai, India, 600113
</div></div></div></div><div><div><div><div><b>Company: </b>Teva Pharmaceuticals
</div></div></div></div><div><div><div><div><b>Job Id: </b>64271
</div></div></div></div><div><div><div><div><div><div><div><div><b>Who we are</b></div>
</div><div>Together, we&rsquo;re on a mission to make good health more affordable and accessible, to help millions around the world enjoy healthier lives. It&rsquo;s a mission that bonds our people across nearly 60 countries and a rich, diverse variety of nationalities and backgrounds. Working here means working with the world&rsquo;s leading manufacturer of generic medicines, and the proud producer of many of the products on the World Health Organization&rsquo;s Essential Medicines List. Today, at least 200 million people around the world take one of our medicines every single day. An amazing number, but we&rsquo;re always looking for new ways to continue making a difference, and new people to make a difference with.</div></div><div><div><div><b>
How you&rsquo;ll spend your day</b></div>
</div><div><ul><li>Detailed description of MAIN tasks and responsibilities:</li><li>Performing Stability analysis, Method transfer, Method Validation and review of analytical documents.</li><li>Preparation and review of Method Transfer Protocols (MTP), Method transfer report (MTR), Method of analysis (MTH), Standard Testing Procedure, Test Data Sheet (TDS) for Stability Analysis, Method transfer and Method Validation, Stability Summary Reports and any document related to stability analysis, method transfer and method validation in compliance with current guidelines. Review and maintenance of all logbooks of the department</li><li>Preparation of departmental SOP&rsquo;s in compliance with current guidelines. Review of departmental SOP&rsquo;s, training of analysts and other technical staff and review validation of data transfer, data management using computer systems.</li><li>Preparation and review of validation protocols in compliance with current guidelines.</li><li>Calibration and validation of all instruments / equipments.</li><li>Entry of stability sample results in LIMS &amp; SAP.</li><li>Handling of LSCMS software</li><li>Initiation of Quality Forms in Track wise Harmony, documents in Glorya EDMS and CAPA in Trackwise Harmony.</li></ul></div></div><div><div><div><b>
Your experience and qualifications</b></div>
</div><div><ul><li>M. Pharmacy</li><li>10 years and 7 months of experience</li></ul></div></div><div><div><div><b>
Teva&rsquo;s Equal Employment Opportunity Commitment</b></div>
</div><div>Teva Pharmaceuticals is committed to equal opportunity in employment. It is Teva's global policy that equal employment opportunity be provided without regard to age, race, creed, color, religion, sex, disability, pregnancy, medical condition, sexual orientation, gender identity or expression, ancestry, veteran status, national or ethnic origin or any other legally recognized status entitled to protection under applicable laws. We are committed to a diverse and inclusive workplace for all. If you are contacted for a job opportunity, please advise us of any accommodations needed to support you throughout the recruitment and selection process. All accommodation information provided will be treated as confidential and used only for the purpose of providing an accessible candidate experience.</div></div></div>
</div></div></div></div></div><p></p><div><p>Apply now &raquo;</p></div></div></div><div></div>

Quality Control Analyst II

Search 6896+ Validation specialist jobs near you this November. New roles added regularly across leading industries. Apply today.

6896 validation specialist jobs NEAR_ME

LL01-250714 Validation Specialist for Packaging Equipment

LL01-250714 Validation Specialist for Packaging Equipment

Specialist - Product Lifecycle

DA Analyst

ATL01-111025_ Packaging Validation Engineer_PA

Data Scientist

Quality Control Analyst II