validation specialist

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, have 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.
 
 
 
 
 
 Minapharm Group of Pharmaceutical Companies employ a collective workforce with more than 1400 individuals &amp; continues to expand their workforce with Talented Human Capital.
 
 
 
 
 
 
 
 
 Our Core Values:
 
 
 
 
 <ul>
 <li>
 Diversity &amp; Respect
 </li>
 <li>
 Integrity &amp; Accountability
 </li>
 <li>
 Collaboration
 </li>
 <li>
 Leadership &amp; Empowerment
 </li>
 <li>
 Innovation &amp; Continuous Learning
 </li>
 </ul>
 
 
 
 
 
 
 Job Mission:
 
 
 
 
 Validation Section Head will lead validation activities related to introduction of new products, technical transfer, validation of processes (including process performance qualification, validation of sterilization processes &amp; aseptic process simulation) and gowning qualification.
 
 
 
 
 
 
 
 Duties &amp; Responsibilities:
 
 
 
 <ol>
 <li>
 Prepares process validation (including process performance qualification, validation of sterilization processes &amp; aseptic process simulation), cleaning validation &amp; gowning qualification procedures, master plans and protocols.
 </li>
 <li>
 Prepare annual plans for process validation (including process performance qualification, validation of sterilization processes &amp; aseptic process simulation), cleaning validation &amp; gowning qualification with coordination with different departments (eg: strategic operations, supply chain, production, engineering, QC &hellip; etc).
 </li>
 <li>
 Issue purchase requests for all department requirements required to execute process and cleaning validation activities and ensure their availability on time.
 </li>
 <li>
 Coordinate with different departments (eg: production, engineering, QC &hellip; etc) the execution of process validation (including process performance qualification, validation of sterilization processes &amp; aseptic process simulation), cleaning validation &amp; gowning qualification protocols as per approved annual plans.
 </li>
 <li>
 Handles any deviations or changes related to process validation (including process performance qualification, validation of sterilization processes &amp; aseptic process simulation), cleaning validation &amp; gowning qualification.
 </li>
 <li>
 Periodically evaluate status of qualification and validation of process validation (including process performance qualification, validation of sterilization processes &amp; aseptic process simulation), cleaning validation &amp; gowning qualification and prepares periodic reports.
 </li>
 <li>
 Participate in different multidisciplinary teams and relevant activities as required.
 </li>
 <li>
 Lead, coach &amp; develop subordinates.
 </li>
 <li>
 Perform other relevant tasks as required.
 </li>
 </ol>
 
 
 
 
 
 
 Qualifications(Educational Background &amp; Work Experience) :
 
 
 
 <ul>
 <li>
 BSc in Pharmaceutical sciences or Sciences .
 </li>
 <li>
 9 - 12 years in pharmaceutical industry including extensive experience in process validation / cleaning validation activities in sterile manufacturing.
 </li>
 </ul>
 
 
 
 
 
 Training:
 
 
 <ul>
 <li>
 WHO &amp; EU GMP process validation and cleaning validation guidelines.
 </li>
 <li>
 Sterilization techniques and validation of sterilization processes.
 </li>
 <li>
 Aseptic processing &amp; aseptic process simulation.
 </li>
 <li>
 Production technologies.
 </li>
 </ul>
 
 
 
 
 
 Knowledge:
 
 
 <ul>
 <li>
 EDA, WHO, ICH, PIC/S &amp; EU guidelines and/or regulations related to validation.
 </li>
 </ul>
 
 
</div>

QA Validation Section Head, Process & Cleaning

Julphar

<div></div><div><div><div><div><div>Detailed Job Description:
<ul>
<li>Lead MS&amp;T activities supporting commercial manufacturing, technology transfer, and site readiness.</li>
<li>Act as the technical bridge between R&amp;D, Technology Transfer, Production, Quality, and Engineering.</li>
<li>Prepare, review, approve, archive, retrieve, and distribute validation documents.</li>
<li>Ensure compliance with GMP documentation and data integrity requirements.</li>
<li>Maintain validation master plans and validation schedules.</li>
<li>Ensure robust scientific understanding and control of manufacturing processes across the product lifecycle.</li>
<li>Support in writing the URS (user requirement specifications) for Project activities, ensuring all assets has URSs before entering the Purchasing Cycle</li>
<li>Follow-up with procurement and CAPEX manager</li>
<li>Support in preparation the technical evaluation of quotations from different vendors</li>
<li>Co-ordinate with procurement, MS&amp;T, QA in RAK site for any similar equipment procurement</li>
<li>Lead and execute the validation lifecycle using the V‑Model approach (URS, FAT, SAT, IQ, OQ, PQ, re‑qualification).</li>
<li>Ensure all critical utilities (PW, WFI, HVAC, compressed gases, nitrogen) remain in a validated state.</li>
<li>Ensure cleanroom qualification activities comply with ISO‑14644 requirements.</li>
<li>Review and approve validation protocols, reports, and risk assessments.</li>
<li>Lead or support investigations related to process deviations, OOS, OOT, and atypical results.</li>
<li>Perform root cause analysis using scientific and statistical tools.</li>
<li>Propose technically sound CAPAs and process improvements.</li>
<li>Support batch disposition decisions from a technical perspective.</li>
<li>Partner in FAT, SAT, DQ, IQ, OQ, PQ for equipment, CSV, systems (Water, utilities, HVAC, electricity, Thermal mapping).</li>
<li>Lead process validation activities for new and existing products.</li>
<li>Execute and oversee cleaning validation, sterilization validation, and transport validation.</li>
<li>Lead aseptic process simulation (media fills) and gowning qualification programs.</li>
<li>Support visual inspection qualification activities where applicable.</li></ul> 


Core Competency:
<ul>
<li>In terms of competency, you are highly result-oriented with an intense sense of accountability &amp; ownership.</li>
<li>High compliance adherence, having strong diligence, initiative-taking, and flexibility.</li>
<li>Excellent communication, interpersonal, and collaboration skills.</li>
<li>Must be able to manage tasks, plan workload effectively, prioritize, and easily adapt to changing situations.</li>
<li>Contribute to EHS activities, audits, and continual improvement initiatives.</li></ul> 


Qualification/Functional Knowledge:
<ul>
<li>Bachelor&rsquo;s degree in pharmacy, Chemical Engineering, Mechanical Engineering, Electrical Engineering, Industrial Engineering, or related scientific discipline 
(master&rsquo;s degree in pharmacy / engineering is an advantage)</li>
<li>Minimum 6&ndash;10 years of experience in pharmaceutical manufacturing within GMP‑regulated environments, with extensive hands‑on experience in qualification and validation activities</li>
<li>Strong and practical knowledge of:</li>
<li>cGMP, SFDA, WHO, EU GMP, and ICH guidelines</li>
<li>Qualification and validation lifecycle using the V‑Model approach</li>
<li>GMP documentation practices and regulatory inspection expectations</li>
<li>Proven experience in validation of:
<div><ul><li>Manufacturing equipment and production lines</li></ul>
<ul><li>Critical utilities (PW, WFI, HVAC, compressed gases, nitrogen)</li></ul>
<ul><li>Cleanrooms in compliance with ISO 14644</li></ul>
<ul><li>Sterile and non‑sterile manufacturing facilities</li></ul>
</div></li><li>Hands‑on experience in:
<div><ul><li>Installation Qualification (IQ), Operational Qualification (OQ), Performance Qualification (PQ)</li></ul>
<ul><li>Re‑qualification and periodic review programs</li></ul>
<ul><li>FAT and SAT execution and documentation</li></ul>
</div></li><li>Strong experience in:
<div><ul><li>Process validation, cleaning validation, sterilization validation, and aseptic process simulation (media fills)</li></ul>
<ul><li>Gowning qualification, visual inspection qualification, and transport validation</li></ul>
</div></li><li>Practical knowledge of calibration systems, including rationale, acceptance criteria, frequency setting, and outsourced calibration management</li>
<li>Solid experience in Computerized System Validation (CSV):</li>
<li>Validation of manufacturing, utilities, QC, and validation systems</li>
<li>Compliance with 21 CFR Part 11 and data integrity (ALCOA+) principles</li>
<li>Strong experience in EQMS activities, including:</li>
<li>Change Control impact assessments</li>
<li>Deviation investigations and root cause analysis</li>
<li>CAPA development and effectiveness checks</li>
<li>Audit support and regulatory inspection readiness</li>
<li>Experience acting as validation SME during internal, customer, and regulatory audits, including SFDA inspections</li>
<li>Strong leadership and team‑coordination skills with experience assigning and reviewing work of validation engineers and SMEs</li>
<li>Excellent analytical, problem‑solving, and risk‑assessment skills</li>
<li>Proficiency in MS Office and electronic QMS / validation management system</li></ul></div></div></div></div></div>

Lead-MSAT (Validation)

Hikma

<div><div><div><div><div><div><div>Description:
Location: Saudi Arabia, Riyadh

Job Type: [Full-time]

Hashtag: #LI-NA1 


About Us:

For over 45 years, Hikma Pharmaceuticals has been putting better health within reach, every day, by creating high-quality medicines and making them accessible to those who need them. We are helping to shape a healthier world that enriches all our communities, and our global team of 9,500+ empowered employees are central to this mission. 


As a trusted and reliable partner of over 800 high-quality generics, specialty and branded pharmaceutical products, we are driven to improve access to medicine. Through our 29 manufacturing plants, 9 R&amp;D centers across the MENA, North America and Europe, our footprint allows us to play a critical role in serving patients. 


Description: 


We are looking for a talented Validation Engineer to join us. At Hikma you&rsquo;ll be supported by a culture of progress and belonging where people are encouraged to develop, wellbeing is prioritised and our inclusive approach values contributions from all. We&rsquo;re seeking candidates who embody our values: Innovative, driven to keep learning; Caring, genuinely compassionate in their work; and Collaborative, eager to solve problems together. 


If you want to be part of a team that cares about impact, this is the place for you. 


Key Responsibilities:
<div>
<ul><li>Prepare all documents needed in validation (protocols, sampling plan, reports&hellip;etc.).</li></ul>
<ul><li>Reviewing, approving, and evaluating all documents generated in the validation department (SOPs, protocols, reports&hellip;etc.).</li></ul>
<ul><li>Monitor and execute the PV activities and collect the required samples.</li></ul>
<ul><li>Follow up on the approval of all PV documents.</li></ul>
<ul><li>Updating and reviewing process history.</li></ul>
<ul><li>Follow up plans and tasks on a daily basis.</li></ul>
<ul><li>Coordinating, planning, and advising with related departments for process activities.</li></ul>
<ul><li>Performing other duties related to the job as assigned by the direct supervisor/Manager.</li></ul>
<ul><li>Superb communication and interpersonal skills for coordinating between the various departments and staff of the company as well as the validation.</li></ul>
<ul><li>Knowledge of the various state and federal pharmaceutical validation laws and legislations that are enforced from time to time.</li></ul>
<ul><li>Must be well organized with good oral and written skills besides giving attention to details.</li></ul>
<ul><li>Verifying equipment, machines, instruments, and systems to be qualified.</li></ul>
<ul><li>Ensuring compliance with cGMPs for all related equipment, machines, instruments, and systems.</li></ul>
<ul><li>Calibration technician works with a variety of machinery, including analytic and electronic measuring devices.</li></ul></div> 


Qualifications:

We are looking for candidates whose experience and skills align closely with the qualifications outlined below: 


Education: Bachelor's degree in engineering or pharmacist or relevant fields.

Experience: At least 0-3 years of experience in related fields

Skills and Competencies:
<ul>
<li>Good skill AutoCAD program is highly required</li>
<li>English fluency and reporting skills are highly required</li>
<li>Strong Numerical Skills</li>
<li>Analytical Thinking</li>
<li>Computer Skills</li>
<li>Initiative and Drive for Results</li>
<li>Collaboration and Teamwork</li>
<li>Change &amp; Innovation</li>
<li>Communication &amp; English fluency</li>
</ul>
Learn more about Hikma in KSA hikma-ksa-factsheet-aug-2025-en.pdf 

</div></div></div></div><div><div><div><div>Location:
Riyadh, SA, 11564</div></div></div></div></div></div></div>

Engineer, Validation

Thndr

<div>
 
 About The Team/Role
 
 
 
 We&rsquo;re looking for an Operations Generalist to support our Operations team in managing the end-to-end lifecycle of user agreements and signature validation.
 
 
 This role will focus on reviewing user-submitted agreements and signatures, validating them against internal Standard Operating Procedures (SOPs), managing approval and rejection decisions, and executing the operational steps required post-review.
 
 
 This is a detail-oriented operational role that plays a critical part in maintaining documentation accuracy and process integrity.
 
 
 
 What You&rsquo;ll Do
 
 
 
 <ul>
 <li>
 Review user agreements and validate signatures against internal (Standard Operating Procedures) SOPs.
 </li>
 <li>
 Execute post-approval and post-rejection operational steps
 </li>
 <li>
 Maintain and manage tracking sheets related to agreement status and signature validation
 </li>
 <li>
 Coordinate with relevant teams to ensure a seamless user experience
 </li>
 <li>
 Monitor and maintain the overall health of the signature process and escalate inconsistencies
 
 
 </li>
 </ul>
 
 What You&rsquo;ll Need
 
 
 
 <ul>
 <li>
 Strong attention to detail
 </li>
 <li>
 High level of ownership and accountability
 </li>
 <li>
 Clear written communication skills
 </li>
 <li>
 Efficiency and consistency
 </li>
 <li>
 Uncompromising integrity and strong dedication to professionalism
 </li>
 <li>
 Ability to meet given targets
 </li>
 <li>
 Adhere to company policies, data privacy regulations, and confidentiality standards while handling sensitive information
 
 
 </li>
 </ul>
 
 Nice to Have
 
 
 
 <ul>
 <li>
 Knowledge of Know Your Customer (KYC) and User Agreement Processes: Familiarity with KYC procedures, including reviewing user agreements, signatures, and onboarding documentation, is a plus.
 </li>
 <li>
 Experience with Cloud Platforms or Remote Tools: Familiarity with cloud-based tools (e.g., Google Drive, Dropbox) and remote collaboration tools (e.g., Slack, Trello)
 </li>
 <li>
 Adaptability: Willingness and ability to quickly learn new software or tools as required by the organization.
 </li>
 <li>
 Communication Skills: Strong verbal and written communication skills to interact with team members and respond to queries effectively.
 </li>
 <li>
 Familiarity with Data Validation Tools: Experience with tools or processes for validating and cleaning data.
 
 
 </li>
 </ul>
 
 
 Who Are We?
 
 
 
 
 
 Thndr
 
 was founded with the dream to democratize access to investing through smart tech and human design, which is just a fancy way of saying giving anyone with a smartphone easy access to preserve and grow their wealth. At the same time, we&rsquo;re promoting local investment products to propel the economies that we serve
 
 
 History has shown that investing is the single greatest way to build long-term wealth&mdash;but before
 
 Thndr
 
 , only a very small percentage of people had access to investing due to:
 
 
 <ul>
 <li>
 High barriers to entry - In the form of minimum account balances, brick-and-mortar onboarding, and low financial literacy.
 </li>
 <li>
 Irrelevant experience - Catered towards traders and financial experts, therefore alienating the majority of the population.
 </li>
 <li>
 Fragmented offering&mdash;Investment products are not gathered in a single outlet.
 
 
 </li>
 </ul>
 On our short journey we&rsquo;ve validated that there is a need for our solution, as illustrated by these key figures:
 
 
 <ul>
 <li>
 3 million app downloads
 </li>
 <li>
 $8.8bn in annualized traded value
 </li>
 <li>
 #1 platform in terms of traded value
 </li>
 <li>
 84% of our users are investing for the first time
 </li>
 <li>
 65% of our users come from outside of capital cities and have previously had limited access to financial institutions
 
 
 </li>
 </ul>
 Building on our success with
 
 Thndr
 
 , we are continuing to change culture and break down barriers by launching
 
 Rumble
 
 , the first-of-its-kind subscription-based investment recommendations platform.
 
 
 
 Rumble
 
 was born with the vision to empower everyday individuals to build wealth confidently and intelligently through access to timely and in-depth advice from the industry&rsquo;s top experts.
 
 
 You can consider
 
 Rumble
 
 your new financial advisor. Going beyond traditional investment advice, offering long- and short-term investment recommendations and financial content through engaging articles and videos that can guide users on their financial journey and maximize their returns.
 
 
 We&rsquo;re proud of how far we&rsquo;ve come and the size of our impact in just a few years - but we&rsquo;re just getting started and are excited for what&rsquo;s to come.
 
 
 It&rsquo;ll take a lot of passion, bold risks, and hard work to fulfill our mission of democratizing investing in MENA and giving everyone an equal opportunity to generate and grow their wealth.
 
 
 At Thndr, we&rsquo;re looking for people invigorated by our mission, not just those who simply check off all the boxes. We&rsquo;re looking for people that are hungry to become agents of change and that understand the huge responsibility associated with dealing with people&rsquo;s money.
 
 
 Join us if you&rsquo;re ready to be one of the first to build the premier trading platform in the MENA region. Apply now and help shape the future of trading!
 
 
</div>

Operations Generalist

Rhombus Power Inc.

<div>
 Rhombus Power, Inc. delivers AI-powered predictive intelligence in real time for defense and national security organizations worldwide. Our mission-built products&mdash; Ambient AI and Guardian&mdash; are transforming strategic, operational, and tactical decision-making. By empowering the shift from reactive analysis to proactive, predictive intelligence and decision support, Rhombus Power is providing foresight and freedom of action when it matters most.
 
 
 Come join our cross-disciplinary and world-class team that is delivering game-changing solutions to transform global security.
 
 
 Learn more about Rhombus Power, Inc. and watch a demonstration of Guardian, our AI Platform here:
 
 
 https://www.youtube.com/watch?v=3PxY6su1Q-Q
 
 
 https://www.youtube.com/@rhombuspower8558/videos
 
 
 https://www.youtube.com/watch?v=Iby5WVNfQiI
 
 
 See the following articles to learn more about what we do:
 
 
 https://www.rhombuspower.com/news-and-media
 
 
 
 About the Role: This is a contractor role. Candidates need to be located in the D.C. region, and have the ability to come onsite.
 
 
 
 As an Associate Data Analyst, you will play a critical role in verifying and improving the quality of event data that fuels our predictive intelligence systems. You'll review event records extracted from global news sources&mdash;checking the accuracy of event classifications, actor identification, geographic tagging, and temporal coding against original source material.
 
 
 
 This Position Is Perfect For Individuals Who Are
 
 
 
 <ul>
 <li>
 Highly detail-oriented with strong reading comprehension
 </li>
 <li>
 Knowledgeable about and interested in global current events and geopolitics
 </li>
 <li>
 Able to navigate and interpret news articles from diverse international sources
 </li>
 <li>
 Excited to apply their analytical skills to real-world defense applications and gain experience working with machine learning and artificial intelligence.
 </li>
 <li>
 Have prior experience serving in a data labeling role maintaining high accuracy under demanding timelines.
 
 
 </li>
 </ul>
 
 Key Responsibilities
 
 
 
 <ul>
 <li>
 Review event records against original news sources to verify accuracy of event type, actors involved, location, and date.
 </li>
 <li>
 Identify and flag coding errors, misattributions, or inconsistencies in event data.
 </li>
 <li>
 Apply sound judgment on ambiguous cases; document reasoning to maintain validation consistency.
 </li>
 <li>
 Proactively communicate with project leadership on progress, challenges, and workflow improvements, including quality assurance.
 </li>
 <li>
 Help refine validation standards and contribute to process improvements where possible.
 </li>
 <li>
 Develop deeper expertise in event data structures and gain familiarity with how validated datasets improve machine learning model performance.
 </li>
 <li>
 Maintain and uphold data security standards.
 
 
 </li>
 </ul>
 
 Qualifications
 
 
 
 <ul>
 <li>
 An undergraduate degree, completed or in-progress.
 </li>
 <li>
 Strong knowledge of international affairs, geopolitics, or current events&mdash;regional expertise (South Asia, East Asia, Middle East, etc.) is a plus.
 </li>
 <li>
 Excellent English reading comprehension; additional language proficiency is highly valued.
 </li>
 <li>
 Strong command of Microsoft Suite and Google tools such as Excel, Word, Sheets, etc. and well-versed in file management&mdash;we want those who are highly organized.
 </li>
 <li>
 Detail oriented with experience reviewing data for errors or inconsistencies and making corrections to maintain quality and accuracy.
 </li>
 <li>
 Proven analytical and logical reasoning skills&mdash;able to manage multiple datasets and tasks with precision and consistency.
 </li>
 <li>
 Self-starter with a bias for action, strong attention to detail, and ability to maintain accuracy and productivity under tight deadlines.
 
 
 </li>
 </ul>
 
 About Rhombus
 
 
 
 Rhombus Power Inc. (Rhombus) is a startup located in the heart of Silicon Valley at Stanford Research Park in Palo Alto. We use cutting-edge cross-disciplinary approaches to solve pressing Big Data and Sensing problems in security, energy, and healthcare. Our advisory board includes two Nobel Laureates and a Draper Prize winner.
 
 
 Rhombus compensates, motivates, and develops employees, who are trusted, empowered, and involved. Employees have clear roles and expectations &ndash; and their roles are flexible enough to move at the speed of innovation in order to meet and exceed client expectations. We have a unique culture of global purpose, rooted in the innovation and progress of Silicon Valley.
 
 
 Rhombus knows that diversity is a condition for success. We are committed to hiring and retaining a diverse workforce. We are proud to be an Equal Opportunity/Affirmative Action Employer.
</div>

Associate Data Analyst, Washington D.C.

Arizona Arthritis and Rheumatology

<div>Description:

Our providers work together to keep patients healthy and are recognized for excellence in medicine and for being pioneers in new treatments, ably supported by our Research department.
We are an equal employment opportunity employer and will consider all qualified applicants without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status or disability.
Our vision is to provide the best Rheumatology care, anywhere and, to balance sustainable operation with the highest possible level of patient care.
We are a seeking an ambitious, friendly, positive, and compassionate Clinical Research Systems Quality Specialist to join our team.
Under minimal supervision, the System Quality Specialist (SQS) owns and improves the quality, integrity, and compliance readiness of clinical research electronic systems (e.g., CTMS, eSource/EDC, eRegulatory, M365, and related reporting tools). The SQS defines data quality standards and controls, manages system change control and quality validation/testing, monitors system performance using dashboards and metrics, and maintains audit-ready documentation (SOPs, training records, configuration and validation evidence). The SQS partners with cross-functional stakeholders to implement study builds and amendments, communicate system updates, ensure appropriate access controls, and drive corrective/preventive actions to prevent recurring system and data quality issues.
RESPONSIBILITIES<ul><li>
Establish and maintain system quality management practices for clinical research platforms (e.g., CTMS, eSource/EDC, eRegulatory, M365), including documentation standards, validation evidence, and release readiness criteria</li><li>
Ensure architecture and data inputs for systems below continuously meet or exceed minimum quality standards</li><li>
Clinical Conductor CTMS</li><li>
Advarra eSource +EDC</li><li>
Veeva SiteVault eReg</li><li>
Monday Work Management</li><li>
SharePoint Pages &amp; Training Workflows</li><li>
Power Query/BI Dashboards</li><li>
in the CTMS system for both protocol and financial compliance</li><li>
Review, finalize and approve esource and CTMs builds for all new studies and amendments</li><li>
Ensure all systems are updated when amendments occur and announce changes to stakeholders</li><li>
Perform routine quality inspections of system data inputs for compliance with internal policy, standard operating procedures, ICH-GCP Standards, local and FDA regulations</li><li>
Ensure all system quality controls are in place prior to release (e.g., procedural instructions, conditional/required fields, data constraints, standardized build templates, and controlled vocabularies) to reduce downstream queries and protocol deviations</li><li>
Perform root cause analysis for recurring system/data quality issues; lead remediation plans to prevent reoccurrence (process, training, configuration, or automation changes)</li><li>
Maintain dashboards/metrics (e.g., query rates, missing/late data, build defect rates, timeliness KPIs) and drive corrective/preventive actions</li></ul>
Learn more about AARA on our website at http://azarthritis.com
Requirements:

QUALIFICATIONS<ul><li>
Bachelor&rsquo;s Degree or equivalent</li><li>
2 years clinical research coordinator experience</li><li>
Rheumatology Experience Preferred</li><li>
Must be able to sit for long periods of time</li><li>
Demonstrated experience applying quality controls to electronic clinical research systems to ensure accurate, complete, and timely data</li><li>
Expensive working knowledge of relevant electronic systems, including eSource, CTMS, eReg, and Microsoft 365</li><li>
Strong understanding of good clinical practice, FDA regulations, &amp; data integrity principles (e.g., ALCOA/C+) with an ability to translate them into system configuration, workflows, and user guidance</li><li>
Proficiency building and interpreting operational quality metrics and dashboards</li></ul></div>

Clinical Research Systems Quality Specialist

Lime Software Logics (SMC-PVT) Limited

Job Title: Data Scraper/ AutomationJob Type: Full-TimeJob Timings: 7 PM to 4 AM (Mon to Fri)Job Location: Business Center, Main Shahra-e-Faisal, Near Nursery, KarachiSalary Range: 60K to 100KJob Overview: We are looking for a skilled Lead Scraper / Automation Specialist to design and manage automated workflows for bulk lead collection across multiple online sources. This role focuses on building reliable scraping and automation systems, ensuring data accuracy, and delivering clean, segmented lead databases ready for outbound campaigns and CRM integration. The ideal candidate is highly technical, detail-oriented, and comfortable working independently on large-scale data extraction tasks.Key Responsibilities:<ul><li>Develop and run automated scraping workflows to collect leads in bulk from websites, directories, LinkedIn, and other online platforms.</li><li>Build custom scripts and automation tools to extract emails, phone numbers, and business contact information at scale.</li><li>Ensure data quality and validation at scale to deliver actionable lead lists.</li><li>Segment leads based on industry, location, company size, role, or other criteria for targeted outreach.</li><li>Maintain structured lead databases ready for integration into CRMs and outreach tools.</li><li>Continuously optimize automation workflows for speed, accuracy, and reliability.</li></ul>Requirements:<ul><li>Proven experience in automated bulk lead scraping and data extraction.</li><li>Hands-on experience with Python, Selenium, BeautifulSoup, Phantombuster, or similar automation tools.</li><li>Strong ability to extract emails, phone numbers, and contact info from multiple sources at scale.</li><li>Experience with data validation, cleaning, and enrichment for large datasets.</li><li>Self-driven and capable of working independently with minimal supervision.</li><li>Strong problem-solving skills and attention to detail in automation workflows.</li></ul>Nice to Have:<ul><li>Ability to also collect social media profiles for enriched lead data.</li><li>Familiarity with API integrations to automate syncing scraped leads to CRMs.</li><li>Previous experience supporting B2B and B2C outbound campaigns at scale.</li></ul>Pay: Rs60,000.00 - Rs100,000.00 per monthApplication Question(s):<ul><li>Are you able to manage the night shift ?</li><li>Your current salary?</li><li>Do you have experience of Python, Selenium, BeautifulSoup, Phantombuster, or similar automation tools.</li></ul>Work Location: In person

Data Scraper/ Automation

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