ERBE Product Specialist

We are NOW Hiring! Ultra Vision is looking for a Full-Time Clinical Application to join our Medical Laboratories Line. ✅ Brief Job Description: - Trains and supports customers’ technicians, scientists, and physicians on the safe, approved use of Ultra Vision’s medical devices, including on-site and remote clinical support, equipment and software upgrades, standardized site-visit reporting, and device-deficiency reporting and root-cause follow-up, all in line with SOPs and medical device regulations. ✅ Requirements: -Science, vet, and Pharmacy graduates. -Resident in Cairo or Giza. -Minimum 2 years of experience in (Laboratory Devices field) -Strong learning agility. -Analytical thinking skills, attention to detail, problem solver. -Very good English, good computer skills, and good communication skills are basic. 📩 Interested candidates are invited to send their CV to: hr@uvfit.net 📌 Subject: Application-1026 Join our team and build your career with ULTRA VISION. Show more

Bachelor's degree ( Pharmacy, Vet, Science, or any related field) 1-3 years of sales experience in the Gyna Excellent communication and presentation skills. Proficiency in Microsoft Office Suite (Word, Excel, PowerPoint). Ability to travel as required. Strong problem-solving skills and attention to detail. A valid driver's license./ Preferable Own Car Show more

Hello, Greetings from ZettaMine!!! Freelancing Opportunity: We are hiring a POD Lead – Scientific Computing Expert (Life Sciences PhD) for a short-term Frontier AI Research, Computational Biology & Scientific Evaluation project across the following locations. Eligible Locations: 🇧🇩 Bangladesh | 🇧🇷 Brazil | 🇨🇴 Colombia | 🇪🇬 Egypt | 🇬🇭 Ghana | Indonesia | 🇳🇬 Nigeria | 🇹🇷 Turkey Role: POD Lead – Scientific Computing Expert (Life Sciences PhD) Educational Eligibility: PhD, postdoctoral experience, or equivalent research experience in Life Sciences, Medicine, or a closely related discipline, with strong computational and scientific programming expertise. Mode: Remote Start: Immediate Mandatory Eligibility Criteria Technical Qualification: PhD, postdoctoral, or equivalent research experience in Life Sciences, Medicine, or a closely related field, with demonstrated computational and scientific programming expertise. Strong scientific programming skills, particularly in Python. Previous experience working as a POD Lead in similar projects, leading and mentoring technical trainers. Expertise in at least one area, such as Bioinformatics, Computational Genomics, Systems Biology, Computational Neuroscience, Biostatistics, Computational Drug Discovery, Structural Biology, Protein Engineering, or Computational Microbiology. Ability to independently validate scientific reasoning, research methodologies, computational workflows, and analytical outputs. Experience reviewing scientific datasets, analysis pipelines, reference solutions, computational environments, and automated tests. Strong understanding of scientific accuracy, statistical methods, reproducibility, data validation, and computational evaluation. Ability to identify incorrect assumptions, analytical errors, unreliable results, and weaknesses in automated grading systems. Strong analytical and problem-solving skills, with the ability to provide clear, actionable technical feedback. Experience mentoring trainers, reviewing deliverables, maintaining quality standards, and ensuring timely project delivery. Preferred Qualifications: Familiarity with bioinformatics tools such as Samtools, BCFtools, GATK, BWA, STAR, Salmon, DESeq2, edgeR, Seurat, Scanpy, or Biopython. Familiarity with scientific workflow tools such as Nextflow, Snakemake, Docker, Conda, Git, and high-performance computing (HPC) environments. Knowledge of computational drug discovery and structural biology tools such as RDKit, OpenMM, GROMACS, AutoDock Vina, or PyMOL. Familiarity with medical imaging, clinical research, biostatistics, or biomedical data analysis tools. Experience designing scientific benchmarks, research challenges, or computational evaluation tasks. Prior experience in AI training, AI evaluation, or scientific research projects is an added advantage. Availability Minimum 40 hours per week. Availability to work at least 8 hours per day. Minimum 4 hours of overlap with PST business hours. Immediate availability for a 3-week contract assignment. What You’ll Work On Lead and mentor a pod of approximately 5–10 technical trainers developing realistic, terminal-based scientific tasks for a frontier AI training and evaluation initiative. Design challenging, multi-step scientific workflows across computational biology, bioinformatics, medicine, and life sciences. Review scientific tasks end to end, including problem statements, biological and clinical datasets, reference files, computational pipelines, environments, reference solutions, and automated tests. Ensure tasks reflect authentic scientific research and clinical analysis workflows that require meaningful computational reasoning. Validate scientific methods, statistical assumptions, calculations, code, intermediate outputs, and final results for accuracy and reproducibility. Verify that computational pipelines use appropriate tools, reference databases, genome builds, annotation versions, and software dependencies. Evaluate outputs such as variant calls, differential gene expression, cluster assignments, protein structure metrics, survival estimates, model performance, medical image segmentation, and pharmacokinetic parameters. Review automated graders to ensure they assess scientific correctness and analytical quality rather than merely checking output formatting. Ensure tasks are reproducible and executable in controlled computational environments, with appropriate testing and validation procedures. Identify flawed scientific assumptions, incorrect calculations, unreliable tests, hard-coded outputs, and other evaluation weaknesses. Ensure datasets are appropriately licensed, public or synthetic, and de-identified, with no protected health information or unauthorized restricted-access data. Screen tasks for biosafety and dual-use concerns and escalate potentially harmful biological content when necessary. Provide actionable written feedback, track revisions, and ensure quality issues are resolved before task approval. Onboard trainers, allocate tasks, monitor productivity, resolve technical blockers, and maintain consistent delivery standards. Maintain documentation covering task guidelines, recurring issues, quality expectations, and best practices. Offer Details Employment Type: Contractor assignment (no medical or paid leave). Contract Duration: 3 weeks. Expected Start: Immediate / next available project start. Working Hours: Minimum 40 hours per week, with at least 4 hours of overlap with PST. Interested Candidates: Please share your updated CV and LinkedIn profile at md.afreen@zettamine.com and complete the registration and assessment process using the links above. Thanks & Regards, Saranya M (Afreen) ZettaMine Show more

Position Purpose: Oversee the development, implementation, and operation of medical management information systems and/or new technology solutions to meet Corporate, Health Plan, and Specialty business unit needs. Key Details: This is a remote Director, Clinical Systems Operations (Pharmacy) opportunity supporting Eastern or Central business hours. The team will consist of 11 individuals, including 4 direct reports. This role will lead Clinical Systems for the Pharmacy team, coordinating 50+ clinical program and initiative workflows across various business rules and overseeing 10,000+ programmed communications to members, providers, and pharmacies, with an annual volume of more than 8 million. Responsibilities include managing the systems that support direct clinical interactions with members and other clinical program activities; providing business rules for clinical data informatics to identify populations and medication-related problems by linking eligibility, medical, and pharmacy claims data across large data sets; and managing program triage to pharmacists and technicians based on program type, language, and state board of pharmacy licensure rules. The role will oversee system documentation and enhancements, business cases and business requirements, regulatory programming and reporting requirements, software defects, new feature implementation, vendor activities, system integrations, and User Acceptance Testing (UAT), while partnering closely with IT to support system and program needs. Desired experience includes prior direct ownership and management of clinical applications, as well as clinical systems operations leadership, pharmacy or managed care operations, regulatory compliance and reporting, vendor management, healthcare technology platform management, workflow and process optimization, and cross-functional leadership. Oversee the development and functionality of clinical systems and programs to improve efficiency and effectiveness, including system design and requirements gathering Provide direction and guidance to various business functions to ensure systems meet business expectations and alignment with standard solutions and processes Evaluate systems and programs performance, recommend improvement opportunities and implement changes Oversee the implementations of new clinical systems and upgrades and modifications of existing clinical systems Oversee the investigation and resolutions of issues of all clinical systems Able to travel up to 30% of the time Education/Experience: Bachelor's degree in Nursing, Computer Science, Business Administration, MIS or clinical related field or equivalent experience. 7+ years of applications, project management, or implementation experience. Previous management experience including responsibilities for hiring, training, assigning work and managing performance of staff. Prior ownership of clinical applications and clinical systems operations leadership, highly preferred. Pay Range: $134,600.00 - $249,000.00 per year At Centene, we connect people to the care they need to live healthier lives — and the work you do here makes that impact real every day. You’ll take on meaningful challenges that directly support individuals, families, and communities, building your skills while making healthcare more accessible and effective. It’s work with a purpose you can see, backed by a team committed to improving lives well beyond the workday. Centene offers a comprehensive benefits package including: competitive pay, health insurance, 401K and stock purchase plans, tuition reimbursement, paid time off plus holidays, and a flexible approach to work with remote, hybrid, field or office work schedules. Actual pay will be adjusted based on an individual's skills, experience, education, and other job-related factors permitted by law, including full-time or part-time status. Total compensation may also include additional forms of incentives. Benefits may be subject to program eligibility. Centene is an equal opportunity employer that is committed to diversity, and values the ways in which we are different. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, veteran status, or other characteristic protected by applicable law. Qualified applicants with arrest or conviction records will be considered in accordance with the LA County Ordinance and the California Fair Chance Act Show more