validation specialist

Julphar

At Julphar, we are on a journey of culture transformation & 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. 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. Key Responsibilities <ul><li>Lead the preparation and execution oversight of process validation and cleaning validation activities for oral solid dosage forms including tablets, capsules, and granules.</li><li>Responsible for process validation of manufacturing steps like granulation (wet/dry), blending, compression, encapsulation, coating, and packaging.</li><li>Responsible for designing and executing cleaning validation activities for oral solid dosage manufacturing using a risk-based approach aligned with current regulatory guidelines, including FDA, EMA, WHO, ICH Q9(R1), and PDA TR 29 & 49. Ensure scientifically justified acceptance limits based on PDE/HBEL, MACO calculations, and visual cleanliness studies. Address multiproduct equipment cleaning strategies, define clean and dirty hold times supported by microbiological and analytical data, and maintain the Cleaning Validation Master Plan (CVMP) to ensure compliance with global regulatory expectations and readiness for inspections.</li><li>Execute hold time studies for bulk materials, intermediates, and equipment cleaning (clean and dirty hold times), ensuring alignment with current GMP and industry standards.</li><li>Support continued process verification (CPV) by reviewing trend data, in-process controls, and product performance metrics to ensure lifecycle process robustness.</li><li>Lead packaging process validation for oral dosage forms including blister packing, bottle filling, and carton packaging to ensure accuracy, label compliance, and product integrity during storage and transport.</li><li>Design and implement transport validation protocols to assess product stability under simulated and real-world shipping conditions (temperature, vibration, humidity).</li><li>Responsible for providing the support for qualification and validation of equipment used in oral solids manufacturing including granulators, mixers, tablet presses, capsule filling machines, coaters, and blenders.</li><li>Conduct risk assessments to manage cross-contamination, shared equipment use, and cleaning effectiveness, aligned with EU, WHO, and FDA guidelines.</li><li>Manage and investigate incidents, deviations, OOS, and complaints related to validation activities. Ensure closure through effective CAPA implementation and change control.</li><li>Act as Quality representative in EQMS systems for validation-related activities and monitor CAPA effectiveness. </li></ul>Core Competency <ul><li>In terms of competency, you are highly result oriented with strong sense of accountability & ownership.</li><li>Ability to prioritize, multi-task and work effectively under pressure to meet deadlines.</li><li>Good communication, interpersonal and collaboration skills.</li><li>Highly disciplined and must be organized, self-motivated to learn new learnings and implement them at workplace</li><li>Technical expertise required for the Qualification and Validation in Sterile and Biotech plants.</li><li>Good implantation skills and easily adapt to changing situations.</li><li>Must be able to work in a cross-functional environment interacting with other internal and external departments</li><li>Must be able to communicate technical, scientific, and regulatory information, both written and verbally. </li></ul>Qualification/Functional Knowledge <ul><li>Bachelor's or master's degree in pharmacy, Chemistry, Biotechnology, or related field.</li><li>8-10 years of experience in pharmaceutical validation with a focus on solid oral dosage forms.</li><li>Proven expertise in process, cleaning, packaging, transport validation, and hold time studies.</li><li>Sound knowledge of EU GMP, FDA, WHO, ICH Q8-Q10, Annex 15, PICS, and GAMP 5.</li><li>Strong command of QRM principles, data integrity, PDE/MACO calculations, and QMS documentation.</li><li>Experience with regulatory inspections (USFDA, MHRA, EU, TGA, ANVISA) preferred.</li><li>Excellent leadership, communication, documentation, and cross-functional coordination </li></ul>We value people from different backgrounds. Could this be your story? Apply today or visit to read more about us and the journey of Julphar<img src="https://www.jobg8.com/Tracking.aspx?xFcAYD4BOV%2fup%2fGaapIK0DBK8bkHUBOqw" width="0" height="0" />

Process Lead Product Life Cycle Oral Solids

Minapharm Pharmaceuticals

<div>
 
 
 
 
 About Minapharm:
 
 
 
 
 
 Minapharm Pharmaceuticals is a leading pharmaceutical company in Egypt and the Middle East and the largest end-to-end manufacturer of biological therapies in MEA with over 20 years of experience in cellular and bioprocess engineering. Headquartered in Cairo, Minapharm commercializes over 100 life-saving and life-enhancing products ranging from small molecules to complex bioengineered proteins and viral vectors, with an impressive immunotherapy pipeline. Together with its wholly-owned Berlin-based subsidiary, ProBioGen AG - a world-leading CDMO, Minapharm has established an integrated business model making it the only gene-to-market company in the region. Consolidating its international platform of intelligent biopharmaceutical technologies with the longstanding process development and manufacturing expertise in the MEA, Minapharm, together with ProBioGen, has incorporated MiGenTra GmbH headquartered in Berlin and manufacturing in Cairo, to enhance the accessibility to critical healthcare transforming medicines through product development and commercialization of Biosimilar mABs, Cell, and Gene Therapies and vaccines, at affordable prices in Egypt, and MEA.
 
 
 
 
 
 
 
 
 Our Values:
 
 
 
 
 
 &middot; Diversity &amp; Respect
 
 
 &middot; Integrity &amp; Accountability
 
 
 &middot; Collaboration
 
 
 &middot; Leadership &amp; Empowerment
 
 
 &middot; Innovation &amp; Continuous Learning
 
 
 
 
 
 
 
 
 Job Summary:
 
 
 
 
 
 Coordinate, implement and report process validation inside production departments to verify the continuous capability of production processes to comply with local authorities, WHO, EU regulations and fulfill cGMP guidelines.
 
 
 
 
 
 
 
 
 Duties &amp; responsibilities:
 
 
 
 
 <ol>
 <li>
 Follow up the monthly plan and communicate with production departments to perform the required validation tasks.
 </li>
 <li>
 Create formulas and recipes on ERP.
 </li>
 <li>
 Prepare validation protocol
 </li>
 <li>
 Witness the different processes of manufacturing, withdraw samples and send it to quality control department to analyze the samples.
 </li>
 <li>
 Withdraw cleaning validation samples from production machines to ensure their compliance with cGMP.
 </li>
 <li>
 Issue validation report with outcomes of the validation and statistical process analysis.
 </li>
 <li>
 Share in qualification activities, thermal validation, mapping and CSV
 </li>
 <li>
 Prepare relevant SOPs, procedures.
 </li>
 <li>
 Batch record review to ensure compliance with cGMP.
 </li>
 <li>
 Deviation reporting &amp; set CAPAs
 </li>
 <li>
 Create &amp; Review qualification reports.
 </li>
 <li>
 Carry out any additional job-related tasks that are assigned.
 </li>
 </ol>
 
 
 
 
 
 
 
 Qualifications:
 
 
 
 
 <ul>
 <li>
 6-9 years of relevant experience in pharmaceutical industry.
 </li>
 <li>
 B.SC of pharmacy or engineering
 </li>
 </ul>
 
 
 Acquired trainings in:
 
 
 <ul>
 <li>
 cGMP
 </li>
 <li>
 Sterile &amp; aseptic techniques
 </li>
 <li>
 Six Sigma.
 </li>
 <li>
 QRM.
 </li>
 </ul>
 
 
 Must have knowledge:
 
 
 <ul>
 <li>
 Intermediate Knowledge of the general rules of good manufacturing practice,
 </li>
 <li>
 Intermediate Knowledge of Six Sigma.
 </li>
 <li>
 Background on solid &amp; sterile manufacturing techniques.
 </li>
 <li>
 Awareness of TQM.
 </li>
 </ul>
 
 
</div>

Process Validation & Qualification expert

NielsenIQ

<div><div><div>The Reference Data Specialist is responsible for instructions of client deliverables, coding and data input validation focusing on specific industry/category or set of categories (e.g. Beverages, Food, Health and Beauty Products). As a Reference Data Specialist at NielsenIQ, you create and deliver client outputs in a correct and timely manner.<ul><li>
Responsible for instructions of client deliverables, coding and data input validation focusing on specific industry/category or set of categories.</li><li>
Does cross coding and item-related quality checks on a daily basis.</li><li>
May act as a back-up to other coders when needed;</li><li>
Keep track/document special instructions related to category assignment.</li><li>
Plan and execute a complex daily personal workload and support to meet departmental and company schedules.</li><li>
Ensure accuracy throughout the process, from validation before database setup to managing samples, and identify areas for improvement.</li><li>
Answer external questions and act as a liaison with everyone from clients to stakeholders; To be able to identify, investigate and coordinate the resolution of data, process, or product related queries.</li><li>
Willing to be trained to be a category expert.</li></ul></div></div><div><div><h2 class="jobSectionHeader">
Qualifications</h2></div><div><ul><li>
Fresh graduate or with 1 year experience in data and operational areas are welcome</li><li>
FMCG background or experience as an encoder is a plus.</li><li>
Able to work as part of a team in a multicultural environment</li><li>
Passionate in data. A high degree of accuracy, proactivity, good analytical skill and logical thinking.</li><li>
High level of accountability and willingness to take ownership.</li><li>
Eager to learn and willingness to grow.</li><li>
Proactively, willing to voice out and share opinion.</li></ul></div></div><div><div><h2 class="jobSectionHeader">
Additional Information</h2></div><div></div><div>
Our Benefits<ul><li>
Flexible working environment</li><li>
Volunteer time off</li><li>
LinkedIn Learning</li><li>
Employee-Assistance-Program (EAP)</li></ul>

About NIQ
NIQ is the world&rsquo;s leading consumer intelligence company, delivering the most complete understanding of consumer buying behavior and revealing new pathways to growth. In 2023, NIQ combined with GfK, bringing together the two industry leaders with unparalleled global reach. With a holistic retail read and the most comprehensive consumer insights&mdash;delivered with advanced analytics through state-of-the-art platforms&mdash;NIQ delivers the Full View&trade;. NIQ is an Advent International portfolio company with operations in 100+ markets, covering more than 90% of the world&rsquo;s population.
For more information, visit NIQ.com
Want to keep up with our latest updates? 


Our commitment to Diversity, Equity, and Inclusion
At NIQ, we are steadfast in our commitment to fostering an inclusive workplace that mirrors the rich diversity of the communities and markets we serve. We believe that embracing a wide range of perspectives drives innovation and excellence. All employment decisions at NIQ are made without regard to race, color, religion, sex (including pregnancy, sexual orientation, or gender identity), national origin, age, disability, genetic information, marital status, veteran status, or any other characteristic protected by applicable laws. We invite individuals who share our dedication to inclusivity and equity to join us in making a meaningful impact. To learn more about our ongoing efforts in diversity and inclusion, please visit the https://nielseniq.com/global/en/news-center/diversity-inclusion</div></div></div>

Reference Data Specialist

Jamjoom Pharma

<div><h3 class="jobSectionHeader">Join Jamjoom Pharma as a Junior Validation Manager &ndash; Quality Department</h3>
Are you a detail-oriented professional with a passion for quality assurance in the pharmaceutical industry?
Jamjoom Pharma is looking for a dedicated Junior Validation Manager to strengthen our Quality team. In this role, you&rsquo;ll play a vital part in ensuring product integrity, regulatory compliance, and operational excellence. Your expertise will help shape validation strategies that support smarter decisions, enhance performance, and drive sustainable growth across our manufacturing operations.
 Key Responsibilities<ul><li>
Prepare and execute Process Validation Protocols and Reports for new and existing products (Prospective, Concurrent, Retrospective).</li><li>
Develop and implement Cleaning Validation Protocols that meet global standards.</li><li>
Oversee all Process and Cleaning Validation activities, ensuring full compliance with cGMP and regulatory guidelines.</li><li>
Collect, review, and verify complete documentation for validation processes.</li><li>
Prepare Process Validation files for export markets, including CTD and eCTD formats.</li><li>
Lead Performance Qualification (PQ) for machines, utilities, and production equipment.</li><li>
Participate in Computerized System Validation (CSV) activities to support data integrity and system compliance.</li><li>
Collaborate cross-functionally with QA, Production, Engineering, and RA teams to drive validation strategy.</li></ul>
 What We&rsquo;re Looking For<ul><li>
Proven experience in pharmaceutical validation.</li><li>
Strong knowledge of regulatory frameworks (ICH, WHO, FDA, EMA, GMP, and other international validation guidelines).</li><li>
Detail-oriented, organized, and proactive leadership style.</li><li>
Excellent documentation and communication skills.</li></ul>
 Qualifications &amp; Experience<ul><li>
Bachelor&rsquo;s degree in pharmacy (mandatory).</li><li>
Minimum of 10 years of hands-on experience in Validation and Qualification within the pharmaceutical industry.</li><li>
Proven experience in preparing CTD/eCTD dossiers for international markets.</li><li>
Practical knowledge in process validation, cleaning validation, equipment qualification (IQ/OQ/PQ), and CSV.</li><li>
Strong analytical and documentation skills.</li></ul></div>

Junior Validation Manager

Capgemini Engineering

<div>At Capgemini Engineering, the world leader in engineering services, we bring together a global team of engineers, scientists, and architects to help the world&rsquo;s most innovative companies unleash their potential. From autonomous cars to life-saving robots, our digital and software technology experts think outside the box as they provide unique R&amp;D and engineering services across all industries. Join us for a career full of opportunities. Where you can make a difference. Where no two days are the same.
<div><div><div><h2 class="jobSectionHeader">Job Description
</h2></div><div>Functional Validation Engineer
Location: Bangalore
Experience: 4&ndash;9 years
Notice Period: Immediate to 30 days
Choosing Capgemini means choosing a place where you&rsquo;ll be empowered to shape your career, supported by a collaborative global community, and inspired to reimagine what&rsquo;s possible. Join us in helping leading organizations unlock the value of technology and drive scalable, sustainable growth.
Your Role
As a Functional Validation Engineer, you will be responsible for validating complex systems and subsystems in the signalling and locomotive domain. You&rsquo;ll work closely with engineering and QA teams to ensure functionality, reliability, and compliance with industry standards.
In this role, you will:
<ul><li>Perform functional validation activities using NI Test Stand and Wireshark.
</li><li>Validate signalling systems and locomotive components to ensure operational integrity.
</li><li>Develop and execute test cases based on system requirements and specifications.
</li><li>Analyze test results and troubleshoot issues to support system improvements.
</li><li>Collaborate with cross-functional teams to enhance validation coverage and efficiency.
</li><li>Document validation processes and contribute to internal knowledge-sharing initiatives.
</li></ul></div></div><div><div><h2 class="jobSectionHeader">Job Description - Grade Specific
</h2></div><div>Your Profile
<ul><li>4&ndash;9 years of experience in functional validation or system testing.
</li><li>Hands-on experience with NI Test Stand and Wireshark.
</li><li>Exposure to signalling and locomotive domain technologies.
</li><li>Strong analytical and problem-solving skills.
</li><li>Effective communication and collaboration abilities.
</li><li>Bachelor&rsquo;s degree in Engineering, Computer Science, or a related field.
</li></ul>What You&rsquo;ll Love About Working Here
<ul><li>Flexible work arrangements and supportive policies for work-life balance.
</li><li>Inclusive culture that fosters innovation and collaboration.
</li><li>Access to continuous learning and certifications in emerging technologies.
</li></ul></div></div></div>Capgemini is a global business and technology transformation partner, helping organizations to accelerate their dual transition to a digital and sustainable world, while creating tangible impact for enterprises and society. It is a responsible and diverse group of 340,000 team members in more than 50 countries. With its strong over 55-year heritage, Capgemini is trusted by its clients to unlock the value of technology to address the entire breadth of their business needs. It delivers end-to-end services and solutions leveraging strengths from strategy and design to engineering, all fueled by its market leading capabilities in AI, generative AI, cloud and data, combined with its deep industry expertise and partner ecosystem.</div>

Functional Validation

TMP Worldwide Advertising and Communications LLC for HCL_C3I

Do you have previous lab experience? Are you familiar with blood testing and Validation testing? If so, we have a great opportunity for you!Basic Purpose: Validation Testing is a process that provides objective evidence that a new or modified laboratory test is accurately validated, and it ensures the results are transmitted back to client&rsquo;s interface successfully. Validation demonstrates that on a test patient that it performs accurately and reliably that includes reference ranges, units of measurements, source, and all pertaining to that individual test codes while ensuring that the results are trustworthy for patient diagnosis and treatment.The Connectivity Validation Testing analyst will provide first level technical support for Quest Diagnostics external and internal clients and all other clients to perform validation testing in various LIS - Lab Systems.The Validation Testing analyst will review and complete validation testing requests through a ticket process in the SNOW application.The analyst is accountable for meeting individual and team Key Performing Indicators as well as handling high-severity requests within established timeframes.Validation Requirements:o Ability to Thrive in a High-Demand Environment.o You must be able to work efficiently and manage tasks under pressure in a fast-paced, high-demand work environment.o Results Entry Experience Preferred.o A background in entering results or related technical skills is preferred.o Self-Starter with Problem-Solving Skills.o Must demonstrate the ability to think creatively and independently with minimal need for micromanagement.o We must consistently meet the team requirement of closing a minimum of 125 tickets per month.o Strong Organizational Skills.o Must possess excellent organizational skills to manage multiple tasks and priorities effectively.o Effective Communication Skills.o Must have strong verbal and written communication skills, with the ability to collaborate effectively with colleagues, clients, sales representatives, management, and Tier 2 support.Responsibilities/Accountabilitieso Review and complete validation of testing requests with &lt; 3 days and 5 days TAT.o Ensure all validation activities adhere to established security policies, compliance standards, and support procedures.o Collaborate with cross-functional teams to coordinate and execute referral testing to meet team&rsquo;s goals.o Maintain clear and consistent communication by updating tickets and daily documentation.o Identify and escalate issues or risks encountered during the validation process, especially on Hospital, VIP clients that are priority.Qualifications / Educationo Understanding of PHI/PII and commitment to maintaining confidentiality and data security.o Excellent analytical, problem-solving, customer service, and communication skills (both written and verbal).o 2&ndash;3 years of strong customer service and technical support experience, with proven ability to resolve issues efficiently.o Associate degree (AA) in a computer-related field (desired but not required)o Strong ability to troubleshoot complex problems and deliver efficient, effective solutions under minimal supervision.o Entering results for test codes.o 1&ndash;2 years of experience in a laboratory setting.Special requirements.o Ability to work Overtime when required.o Consistently complete all assigned tickets with minimal supervision.o Strong critical thinking skills applied to resolve issues efficiently.Pay Range Minimum: $40,000 per year (or $19.23 per hour)Pay Range Maximum: $45,000 per year (or $21.63 per hour)HCL is an equal opportunity employer, committed to providing equal employment opportunities to all applicants and employees regardless of race, religion, sex, color, age, national origin, pregnancy, sexual orientation, physical disability or genetic information, military or veteran status, or any other protected classification, in accordance with federal, state, and/or local law. Should any applicant have concerns about discrimination in the hiring process, they should provide a detailed report of those concerns to secure@hcltech.com for investigation.A candidate&rsquo;s pay within the range will depend on their skills, experience, education, and other factors permitted by law. This role may also be eligible for performance-based bonuses subject to company policies. In addition, this role is eligible for the following benefits subject to company policies: medical, dental, vision, pharmacy, life, accidental death &amp; dismemberment, and disability insurance; employee assistance program; 401(k) retirement plan; 10 days of paid time off per year (some positions are eligible for need-based leave with no designated number of leave days per year); and 10 paid holidays per year.Job Type: Full-timeBenefits:<ul><li>401(k)</li><li>401(k) matching</li><li>Dental insurance</li><li>Employee assistance program</li><li>Employee discount</li><li>Flexible spending account</li><li>Health insurance</li><li>Health savings account</li><li>Life insurance</li><li>Paid time off</li><li>Professional development assistance</li><li>Referral program</li><li>Relocation assistance</li><li>Retirement plan</li><li>Tuition reimbursement</li><li>Vision insurance</li></ul>Job Type: Full-timeBenefits:<ul><li>401(k)</li><li>401(k) matching</li><li>Dental insurance</li><li>Employee discount</li><li>Flexible spending account</li><li>Health insurance</li><li>Paid time off</li><li>Retirement plan</li><li>Tuition reimbursement</li><li>Vision insurance</li></ul>Application Question(s):<ul><li>How many years of Validation testing experience do you have?</li><li>Do you have 1&ndash;2 years of experience in a laboratory setting?</li><li>Are you familiar with the SNOW application/system?</li></ul>Education:<ul><li>Associate (Required)</li></ul>Work Location: Hybrid remote in Addison, TX 75001Job Type: Full-timePay: $40,000.00 - $45,000.00 per yearBenefits:<ul><li>401(k)</li><li>Dental insurance</li><li>Health insurance</li><li>Life insurance</li><li>Paid time off</li><li>Tuition reimbursement</li><li>Vision insurance</li></ul>Work Location: In person

Lab testing Analyst Needed!!

Simtra BioPharma Solutions

<div>Simtra BioPharma Solutions (Simtra) is a world-class Contract Development Manufacturing Organization, partnering with pharmaceutical and biotech companies to bring their sterile injectable products to market. With facilities in Bloomington, Indiana, US and Halle/Westfalen, Germany, we offer a wide range of delivery systems including pre-filled syringes, liquid/lyophilized vials, diluents for reconstitution, powder-filled vials and sterile crystallization.

Our product types include biologics and small molecules, cytotoxics, highly potent compounds, diluents for reconstitution and vaccines &ndash; which are all directly injected into patients worldwide. As such, there is a strong emphasis on quality and continuous improvement at Simtra. We hold ourselves to the highest quality and regulatory standards.

While our primary focus is cGMP manufacturing, we offer many support services including formulation and development, lyophilization optimization, global regulatory support and secondary packaging. Our teams are driven to help clients scale, innovate and bring life-changing medicines to patients worldwide. 


Why join Team Simtra? Because we:

Make it HAPPEN &ndash; We bring a growth mindset to every opportunity, developing new skillsets and exceeding our expectations and those of our customers.

Make it TOGETHER &ndash; We work as one, respecting each voice and tapping into our unique strengths across teams&mdash;so we can solve problems in new ways.

Make it RIGHT &ndash; We hold ourselves to a high standard of excellence, fulfilling our commitments to the customer, their patients, and our team members.

Make it COUNT &ndash; We take pride in our day-to-day work, knowing the impact we make &ndash; taking on challenges big and small to improve patient health. 


This role:

he Validation (CQV) Engineer II is a key member of the Engineering team. The candidate must have a working knowledge of the overall requirements dictated by worldwide regulatory agencies with respect to commissioning, qualification, and validation (CQV) process. This position works directly with the Engineering department and other functional areas and is considered the lead validation resource. The Validation Engineer II understands industry best practices and maintains a state of audit readiness always. This position reports to the Director of Engineering and is 100% onsite at the Bloomington, Indiana facility. 


The responsibilities:
<ul>
<li>Develop documentation for CQV activities (URS, Trace Matrix, IQOQ Protocols etc)</li>
<li>Write and execute protocols (field verification)</li>
<li>Develop summary reports and analyze results to ensure compliance with cGMP and regulatory requirements</li>
<li>Track validation activities and accurately report out on progress and anticipated timelines</li>
<li>Manage change controls and assess for validation impacts</li>
<li>Continuously interact with all levels of management ensuring effective, ongoing communications across teams and stakeholders</li>
<li>Anticipate potential conflict situations and manages to a successful outcome</li>
<li>Assist Project Manager to ensure identification and communication of projects risks, development of risk plan, and leads team in the proactive management of risk response strategies</li>
<li>Assist Project Managers to create/maintain project schedules and track team deliverables for project completion</li>
<li>Participates in Internal/Client/Corporate/Regulatory Agency audits</li></ul> 


Required qualifications:
<ul><li>BS degree in an Engineering or Science discipline</li>
<li>2+ years experience in commissioning, qualification, and validation in a regulated industry</li>
<li>Familiarity with ISPE Baseline Guide 5</li>
<li>Experience managing multiple projects in different stages at the same time</li>
<li>Strong technical writing skills</li>
<li>Advanced proficiency in Microsoft Office Suite</li>
<li>Preferred experience in:
<ul><li>Facilities and equipment startup</li>
<li>Fill equipment (Pre-filled Syringe filler, vial filler, Lyos)</li>
<li>Walk-downs and troubleshooting</li>
<li>Utilities (WFI, Clean Steam, HVAC)</li>
<li>Building automation</li>
<li>Pharmaceutical manufacturing processes</li>
<li>Computer system validation</li></ul></li> 
</ul>
Physical / safety requirements:
<ul>
<li>Ability to stand or sit for extended periods of time</li>
<li>Duties may require overtime work, including nights and weekends</li>
<li>Must be able to gown qualify for Grade A/B/C/D areas</li></ul> 


In return, you'll be eligible for [1]:
<ul>
<li>Day One Benefits
<ul><li>Medical &amp; Dental Coverage</li>
<li>Flexible Spending Accounts</li>
<li>Life and AD&amp;D Insurance</li>
<li>Supplemental Life Insurance
<ul><li>Spouse Life Insurance</li>
<li>Child Life Insurance</li>
</ul></li><li>Short and Long-Term Disability Insurance</li>
<li>401(k) Retirement Savings Plan with Company Match</li>
<li>Time Off Program
<ul><li>Paid Holidays</li>
<li>Paid Time Off</li>
<li>Paid Parental Leave and more</li>
</ul></li><li>Adoption Reimbursement Program</li>
<li>Education Assistance Program</li>
<li>Employee Assistance Program</li>
<li>Community and Volunteer Service Program</li>
</ul></li><li>Additional Benefits
<ul><li>Voluntary Insurance Benefits
<ul><li>Vision Coverage</li>
<li>Accident</li>
<li>Critical Illness</li>
<li>Hospital Indemnity Insurance</li>
<li>Identity Theft Protection</li>
<li>Legal and more</li>
</ul></li><li>Onsite Campus Amenities
<ul><li>Workout Facility</li>
<li>Cafeteria</li>
<li>Credit Union</li>
</ul>
</li></ul></li></ul>[1] Current benefit offerings are in effect through 12/31/25

Disclaimer

This job description is intended to provide the minimum knowledge, skills and abilities necessary to perform the job. It may not be inclusive of all the duties and responsibilities of the job. Simtra reserves the right to make modifications based on business requirements. 


Equal Employment Opportunity

Simtra is proud to be an equal opportunity employer. Simtra evaluates qualified applicants without regard to race, color, religion, gender, national origin, age, sexual orientation, gender identity or expression, protected veteran status, disability/handicap status or any other legally protected characteristic. 


Data Privacy

To learn more about Simtra's approach to data privacy, please review the Simtra Recruitment Platform Global Privacy Policy: https://simtra.com/privacy-policy/</div>

Validation (CQV) Engineer II

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