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UPMC Presbyterian is hiring a full-time Laboratory Support Technician, Medical Laboratory Technician, or Medical Laboratory Scientist to support the Microbiology Lab! We are looking for individuals who are interested in working evening hours, 3 p.m. to 11:30 p.m., with rotating weekends and holidays. In this role, you will join a highly innovative lab with a large, diverse team that allows you to make a direct impact on life-changing medicine. This lab provides high-volume service to multiple hospitals within the UPMC system and is the core laboratory for the Urban area! Applicants will be placed into the appropriate job title and salary based on their individual experience and education. The Medical Lab Technician salary starts at $23.44 an hour. The Medical Lab Scientist level salary starts at $28.90 an hour. MLS/MLT roles are eligible for a generous sign-on bonus for those who qualify! Responsibilities: • Answers phone inquiries., • Investigates specimen status and report disposition., • Directs callers to additional resources as needed, • Receives, sorts, prepares and delivers testing-ready specimens for analysis to work areas., • Demonstrates service orientation approach by conveying courtesy, respect, enthusiasm and a positive attitude in work situations., • Performs routine and basic instrument maintenance according to established protocols. Records temperatures if required., • Assists with restocking supplies to maintain an optimal inventory. Maintains clean and orderly storage spaces for room temperature, refrigerated, and frozen supplies., • Prepares and replenishes instrument reagents and consumables as needed., • Performs QA / QC procedures as assigned., • Assists with specimen/slide storage and retrieval., • Checks pending work lists. Investigates and resolves any unprocessed work., • Decontaminates work area, keeping a neat and clean working environment., • Keeps any glassware clean and dry, including tests for residue removal as needed., • Tests and cleans emergency eyewashes and showers as assigned., • Sorts laboratory waste as needed and ensures that proper disposal occurs., • Transports specimens off-site and delivers supplies where required., • Prepares specimens at workstations for testing. Includes building worklists, checking specimens for acceptability (clots, QNS), aliquoting specimens, loading/unloading specimens onto instruments., • Bachelor's of Science from an accredited college/university AND successful completion of an accredited Medical Technology program OR,, • Bachelor's of Science from an accredited college/university with a major in biological, chemical, physical, or clinical laboratory science AND ASCP or MLT categorical certification OR,, • Bachelor's of Science from an accredited college/university with a major in biological, chemical, physical, or clinical laboratory science AND at least two years of experience in a role equivalent to that of a Medical Laboratory Technician (MLT) in a clinical laboratory., • One year of experience in a hospital laboratory preferred., • Associate's Degree in a laboratory science (or eligible new graduate) with certification from an accredited institution as either a Medical Laboratory Technician (MLT) or as a Clinical Laboratory Assistant (CLA) OR,, • Bachelor's of Science from an accredited institution with a major in biological, chemical, physical, or clinical laboratory science AND 6 months of clinical laboratory experience OR,, • Equivalent education and experience as defined by CLIA '88 for individuals performing high complexity testing., • One year of experience in a hospital laboratory preferred., • High School diploma or equivalent, and at least 2 years of experience as a Specimen Processor (or equivalent) required in a clinical lab, OR, • Associate's Degree (with biology and chemistry courses) and at least 1year of experience as a Specimen Processor (or equivalent) in a clinical lab, OR, • Phlebotomy or Medical Assistant certification and 1 year of experience as a Specimen Processor (or equivalent) in a clinical lab, OR, • Successful completion of a 50-week U.S. military medical laboratory training course, OR, • Bachelor's of Science from an accredited institution with a major in biological or clinical laboratory science, OR, • Currently enrolled in a Medical Laboratory Scientist (MLS) or equivalent training program, with 3 years college credits required. Licensure, Certifications, and Clearances: • Medical Laboratory Assistant MLA (ASCP) or equivalent certification preferred., • Valid driver's license if one is departmentally required.

Position: Full-time Molecular Genomic Specialist I Location: Clinical Lab Building on UPMC Presbyterian's Oakland Campus Schedule: Monday - Friday, Daylight Hours (No Weekends or Holidays) The Molecular and Genomic Pathology Laboratory (MGP) is a dynamic state-of-the-art clinical laboratory that prides itself on providing the highest quality of patient care in the fields of inherited diseases, hematological malignancies, and solid tumors utilizing cutting edge molecular testing platforms and informatics approaches exemplified by next-generation sequencing. MGP offers its staff a challenging and rewarding career by offering a wide variety of job responsibilities as well as opportunities to identify and build upon individual strengths. MGP promotes lab-wide collaboration and teamwork where each staff member is valued for their unique skillset they can offer the team. Why Join Us? At MGP, we offer a dynamic and supportive environment where your expertise is valued. You’ll enjoy a rewarding career with opportunities to work on a diverse range of responsibilities while continually developing your skills. Our collaborative culture encourages teamwork, and each team member contributes their unique strengths to advance the mission of the lab. If you're ready to join a forward-thinking team dedicated to excellence in patient care, apply today to become part of the MGP Lab team! UPMC is currently offering a generous sign-on bonus of $15,000 for those who qualify! Responsibilities: • Independently perform clinical testing in accordance with established SOPs. Process all clinical, QC and PT specimens through clinical workflow., • Demonstrate high-level problem-solving skills and analytical abilities to successfully perform laboratory testing., • Accurately record relevant data and values in case folders and internal databases., • Process samples meticulously to avoid cross-contamination., • Meet established turn-around-time deadlines for clinical testing., • Maintain expertise in or knowledge of molecular biology techniques, including but not limited to: nucleic acid isolation, nucleic acid quantitation, PCR/RT-PCR/qPCR, Sanger sequencing, LOH, methylation analysis, MassARRAY MALDI-TOF, next-generation sequencing, etc., • Effectively communicate with other laboratory members including lab leadership. Maintain track of technical and professional development, including but not limited to attendance at seminars/webinars and participation in educational programs and activities., • Identify critical, abnormal and/or unacceptable results and follow-up according to established protocol., • Document all corrective action and follow-up with lead and/or supervisor., • Adhere to established laboratory and hospital policies and good clinical laboratory practice in areas of procedures, quality control, quality assurance and safety and compliance., • Operate, perform routine maintenance on, and calibrate all laboratory equipment as required., • Identify problems with instrumentation, methodology, specimens, and/or supplies and follow-up according to established protocols., • Maintain proficiency in appropriate Laboratory Information Management Systems (LIMS)., • Appropriately use automated and/or liquid handling machines for clinical testing., • Accurately and precisely analyze molecular assay results for final interpretation by medical staff., • BS degree, major in biological science field OR BS degree in chemical or physical science field with at least 1 year experience in clinical molecular laboratory AND 16 semester hours in chemistry (including at least 6 hours in inorganic chemistry), 16 semester hours in biology courses pertinent to the medical sciences, and 3 semester hours in mathematics., • Be able to pipet accurately and precisely., • Have scientific knowledge of molecular fundamentals and techniques, in order to understand the methodology of the assay and execute it properly both manually and using advanced instrumentation., • Possess high-level problem-solving skills for assay, instruments, controls, samples, and reagents/enzymes so they are able to notice, understand, and act upon performance trends of every step of every assay., • Understand basic molecular workflow principles and required proper precautions to ensure assay and specimen integrity., • Prior clinical lab experience and specifically NGS testing experience preferred. Licensure, Certifications, and Clearances: • Act 34 UPMC is an Equal Opportunity Employer/Disability/Veteran

Requires one of the following: Master's or doctorate in biology, 30 graduate biology credits, professional medical doctorate, (e.

About GNC Since 1935, GNC has been a global leader in health and wellness innovation, inspiring people to achieve their goals with a trusted and dynamic range of products. As #TeamGNC, we prioritize our consumers, constantly collaborating and developing new ideas to deliver cutting-edge solutions. Our team is passionate about driving change and turning aspirations into actions. We believe that good health is the greatest gift, and there's nothing more rewarding than helping others achieve it. Join us in empowering others to Live Well! What We’re Looking For: At GNC we embrace a “Live Well” philosophy, fostering a dynamic environment where innovation meets passion. Whether someone is an athlete or just starting to focus on their health, we want to deliver the cutting-edge products they deserve. We are looking for an individual who is excited and eager to play a pivotal role in driving excellence in the health and wellness industry. This position offers the opportunity to engage in a collaborative environment where you will make a personal impact every day. Role Overview The Scientific Affairs Specialist supports the scientific foundation of GNC’s nutritional products by ensuring accuracy, consistency, and relevance of scientific evidence used across product development, claims substantiation, and clinical research activities. This role is responsible for monitoring emerging scientific literature, maintaining organized scientific resources, and providing evidence-based support to internal teams. The position collaborates closely with Product Development, Regulatory, Marketing, and Clinical partners to ensure product decisions and communications are informed by current, credible scientific research and aligned with internal and external standards. What You’ll Do: This is a Full-Time Salary Position JOB RESPONSIBILITIES: • Maintain and manage GNC’s scientific library to support:, • Product formulation and design, • Claims substantiation, • Clinical research and trial initiatives, • Monitor PubMed and other scientific databases for relevant research related to:, • Dietary supplement ingredients, • Health outcomes and wellness-related topics, • Clinical and preclinical studies, • Support scientific review of product claims, marketing materials, and educational content, • Assist with clinical trial operations, including product randomization and labeling, product ordering, documentation management, and enrollment tracking, • Assist in the development of scientific substantiation dossiers for GNC brand products, • Monitor scientific, regulatory, and industry developments relevant to dietary supplements, • Collaborate with cross-functional teams to support alignment between scientific evidence, product strategy, and brand standards SUPERVISORY RESPONSIBILITIES: • This role has no direct supervisory responsibilities. Required Qualifications • Bachelor’s degree in a scientific discipline (e.g., Nutrition, Biology, Biochemistry, Pharmacology, or related field), • 3–5 years of experience in scientific affairs, research, or regulatory support, preferably within dietary supplements, food, pharmaceutical, or consumer health industries, • Demonstrated ability to evaluate, interpret, and summarize scientific literature, • Experience working with PubMed and other scientific research databases, • Strong written and verbal communication skills, • Proven ability to manage multiple priorities with attention to detail and deadlines Preferred Qualifications • Bachelor’s degree in relevant scientific field, required, • Master’s degree in a relevant scientific field is a plus, • Experience supporting clinical trials or human research, • Familiarity with dietary supplement regulations and claim substantiation requirements, • Experience collaborating with marketing or product development teams, • Strong interest in nutrition and evidence-based health solutions Key Attributes • Commitment to evidence-based decision making, • Emphasis on scientific accuracy and credibility, • Ongoing engagement with emerging research and industry developments, • Effective cross-functional collaboration, • Contribution to a portfolio of scientifically substantiated consumer products PHYSICAL ASPECTS/WORK ENVIRONMENT: • Hybrid work environment, 3 days in-person attendance (Pittsburgh, PA) in addition to ability to work remotely., • Regularly required to stand; walk; sit; use hands or fingers to handle or feel; reach with hands and arms; stoop, kneel, crouch, or crawl; and talk or hear, • Sedentary work. Exerting up to 10 pounds of force occasionally and/or negligible amount of force frequently or constantly to lift, carry, push, pull or otherwise move objects. Repetitive motion. Substantial movements (motions) of the wrists, hands, and/or fingers. The worker is required to have close visual acuity to perform an activity such as: preparing and analyzing data and figures; transcribing; viewing a computer terminal; extensive reading., • Work is performed in an office environment and requires the ability to operate standard office equipment and keyboards., • Specific vision abilities required by this job include long periods of computer screen usage, close vision, distance vision, color vision, peripheral vision, depth perception, and ability to adjust focus, • The noise level in the work environment is usually low/moderate, • This role supports the application of scientific research to consumer-facing products and communications. Success in this position requires analytical rigor, sound judgment, and the ability to communicate scientific concepts clearly to non-scientific audiences.

Job Type: Term (Fixed Term) Overview ___ is seeking technically excellent and mission-driven AI Security / Biosecurity Engineers to work across a number of our most critical and fast-paced AI security and biosecurity workstreams. RAND CAST works on pressing national security challenges related to emerging technologies. Our areas of focus include AI security, compute, biosecurity and bioresilience, and the intersection of AI and biotechnology. Emerging technologies, especially AI and biotechnology, have many promising beneficial and defensive applications. Given their dual-use nature, they also present a number of new security challenges. RAND CAST explores ambitious technical and policy approaches to solving these complex problems. We are a team of world-class technical and policy analysts, engineers, and scientists giving decision-makers the objective insights they need to navigate global emerging threats. Position Description We are looking for individuals who are driven by a bias for action; capable of developing and securing complex systems under high-stakes and fast-paced conditions; and can act as an owner, not just a contributor, with end-to-end ownership of critical, sensitive data infrastructure in a highly autonomous environment. We have a number of ongoing technical projects across our AI security and biosecurity teams. Candidates will discuss initial projects with program leads as part of the interview process. Qualifications Required: * Professional experience in software engineering with a focus on backend engineering and/or data engineering. * Demonstrated ability to build robust and technically complex systems with a security-first mindset. * Experience operating, monitoring, and deploying systems using modern cloud infrastructure. * Preference for working in a fast-paced, autonomous environment. * Excellent communication skills, both written and verbal, tailored to technical and non-technical audiences * Fluency with MS Office suite Preferred: * Advanced knowledge of integrating Large Language Models (LLMs) into workflows. * Background in biosecurity, dual-use technology, or AI security and misuse. * Ability to scope cross-functional projects with internal customers and own their execution. * Experience with distributed data processing platforms. Education Requirements PhD in Biological Sciences, Computational Biology, Biotechnology, Bioinformatics, Computer Science, Computer Engineering, Electrical Engineering, Cybersecurity, Information Security, Information Technology, Mathematics, Applied Mathematics, Physics, Applied Physics, Engineering Physics, Artificial Intelligence, Machine Learning, Engineering and Public Policy, Technology and Policy, National Security Policy, Policy Analysis, Political Science, International Relations, or similar is required. OR Master's degree in the fields listed above with 3+ years of professional experience, is required. OR Bachelor's degree in the fields listed above with at least 5+ years of professional experience, is required. Master's or PhD preferred. Term This position is structured as a three-year appointment with options to later extend the initial appointment and explore other opportunities for growth. Security Clearance Ability to obtain and maintain a U.S. government clearance is preferred. Location We are hiring for this position in San Francisco, CA; Washington, DC; Santa Monica, CA; Pittsburgh, PA; and Boston, MA. We offer a hybrid work arrangement, combining work from home and on-site options. Fully remote work will also be considered. Salary Range: $118,500 - $261,400 Technical Resident, Associate II = $118,500 - $171,900 Technical Resident, Specialist = $146,200 - $211,900 Visiting Technical Expert = $167,300 - $261,400 RAND considers a variety of factors when formulating an offer, including but not limited to, the specific role and associated responsibilities; a candidate's work experience, education/training, skills, expertise; and internal equity.The salary range includes base pay plus RAND's sabbatic pay (which provides additional compensation above base pay when vacation is taken). This position may be eligible for additional compensation. In addition, RAND provides strong benefits including health insurance coverage, life and disability insurance, savings plan, paid time-off and more. Equal Opportunity Employer

Job Type: Term (Fixed Term) Overview RAND's ___, part of the Global and Emerging Risks (GER) Division conducts cutting-edge research on transformative, high-impact technologies-including artificial intelligence and biotechnology-to shape policies that protect global security and advance the public good. Your work will address key questions related to global and emerging AI and biosecurity risks, understanding options for prevention and resilience, and examining their policy implications. You will communicate the results of your work to both technical and non-technical audiences through quick-turnaround policy briefs and detailed written research products. A recent example of one of our research products is the___report, which examined the current state of nucleic acid synthesis screening and offered recommendations for policymakers and industry leaders to further secure these technologies. RAND's reputation for excellence is built on our commitment to high-quality, rigorous analysis and objectivity. In this role, you will apply quantitative and qualitative skills to rigorously analyze AI and biosecurity problems of national and international importance. Qualifications All research positions at RAND require excellent analytic skills; the ability to communicate clearly and effectively, both orally and in writing; the ability to work effectively as a member of a multi-disciplinary team; and a strong commitment to RAND's core values of quality and objectivity. In addition, successful applicants will have: * Experience in nucleic acid synthesis, AI-enabled biodesign, dual-use research of concern, potential pandemic pathogens, personal protective equipment, bioterrorism, or pathogen agnostic biosurveillance preferred. * Demonstrated knowledge and ability to analyze or implement policies involving strategy, doctrine, operations, tactics, systems or organization. * Ability for quantitative analysis and modeling, including modeling of uncertainty. * Experience in government, intelligence community, or other relevant decision-making offices preferred, but not required. * Ability to present evidence of research experience, demonstrated through authorship of academic publications, conference presentations, or prior professional reports. Education & Experience Requirements RAND is hiring multiple AI & Biosecurity Research Residents at the Associate, Specialist, and Expert levels of experience. Minimum education and experience requirements at the Associate level include: A PhD in Statistics, Biostatistics, Biology, Physics, Chemistry, Geology, or other natural and physical sciences is required - OR - PhD or equivalent in Policy Analysis or any technical discipline, Health Services Management, Public Health, Epidemiology or Business, with demonstrable proficiency in formal methods of decision support analysis is required. OR A Master's degree in the fields listed above with at least 3 years of relevant professional experience, is required. OR A Bachelor's degree in the fields listed above with at least 5 years of relevant professional experience, is required. Security Clearance Ability to obtain and maintain a U.S. government clearance is preferred but not required. Location We are hiring for this position in San Francisco, CA; Washington, DC; Santa Monica, CA; Pittsburgh, PA; and Boston, MA. We offer a hybrid work arrangement, combining work from home and on-site options. Fully remote work will also be considered. Writing Sample A writing sample of 3 pages or more is required for this position. Applicants are encouraged to use recent pieces that have been published in academic or other journals, but may use master's theses or papers written for coursework, prior employment, or internships. Term This position is a 3-year term appointment with a possibility of renewal, alongside options for longer term employment. Salary Range: Biosecurity Resident, Associate = $126,400 - $183,300 Biosecurity Resident, Specialist = $145,600 - $227,600 Biosecurity Resident, Expert = $175,500 - $274,300 RAND considers a variety of factors when formulating an offer, including but not limited to, the specific role and associated responsibilities; a candidate's work experience, education/training, skills, expertise; and internal equity.Successful candidates will be offered employment in a specific title, as determined by the candidate's education and experience. The salary range includes base pay plus RAND's sabbatic pay (which provides additional compensation above base pay when vacation is taken). In addition, RAND provides strong benefits including health insurance coverage, life and disability insurance, savings plan, paid time-off and more. Equal Opportunity Employer

GAI Consultants, Inc. is seeking an experienced Senior Natural Resources/Biology Project Manager 1 to lead and manage complex natural resources impact assessment, permitting and regulatory compliance efforts for energy projects in California and the greater Southwest US region. Responsibilities span project lifecycle management-from siting/routing, CEQA/NEPA compliance and natural resources/waters impact permitting to agency coordination and construction support-while ensuring adherence to related regulatory requirements. The position combines the need for technical natural resources expertise with a passion for business development and the desire for leadership responsibilities. The ideal candidate has a proven track record of managing biological surveys, authoring habitat assessments and permit packages, and managing compliance monitoring for energy and transmission projects on time and within budget. #LI-JB1 Position Responsibilities: • Lead natural resource compliance strategy for energy projects across the full project lifecycle: routing/siting, environmental impact assessments, permitting and construction compliance., • Serve as the primary client contact and agency liaison: proactively engage and negotiate permitting pathways with USACE, USFWS, BLM, state wildlife agencies, and local jurisdictions; and maintain strong agency and client relationships that advance project approvals., • Prepare, submit, and track reports and related permit applications and agency consultations associated with local, state and federal regulations., • Identify potential project risks and negotiate complex permit conditions and mitigation strategies with agencies and stakeholders., • Manage technical and field teams (including subconsultants) related to biological studies, and the associated task/project budgets, schedules, and QA/QC processes to ensure timely and cost-effective project delivery., • Drive business development: identify opportunities, proposal strategy and writing, participate in interviews, and support account growth across energy infrastructure and energy markets., • Bachelor's degree in Biology, Environmental Science, Natural Resources, or a closely related discipline., • Minimum 10 years' experience in biological resources studies and environmental permitting for energy/transmission infrastructure projects, with proven expertise with environmental impacts analysis, siting/routing studies, CEQA/ NEPA documentation, and agency (BLM, USFWS, USACE) engagement involving federal and state Endangered Species Act, and state and federal jurisdictional waters assessments, permitting and mitigation strategy., • Strong project management skills with a successful track record of overseeing and delivering multiple complex natural resource based projects in various phases of development and geographic locations on time and on budget., • Excellent writing skills are required with proven ability to author, manage and review permit applications and technical reports supporting federal, state, and local regulatory documentation and permit application submissions., • Demonstrated success in business development, forecasting and client relationship management within an environmental consulting setting., • Excellent written and verbal communication skills with proven ability to present at public hearings, agency, and stakeholder meetings., • Strong organizational and analytical skills; ability to manage multiple priorities under tight deadlines., • Proven ability to work independently as well as collaboratively with multi-disciplinary teams both in office and remotely by leveraging interpersonal skills and emotional intelligence, attention to detail, and organizational skills., • Proficiency with Microsoft Office suite of programs (MS Word, Excel, PowerPoint, etc), • Ability to travel (up to 25%) to project sites, GAI office locations, business development events/conferences, stakeholder events, agency hearings, and client meetings as needed., • Master's Degree in Environmental Science, Biology, Natural Resources, or a closely related discipline., • Experience with energy projects on both public and private lands, and associated permitting and environmental review in the Southwestern US., • Strong knowledge of California and/or Southwest US flora and fauna, especially special-status species, • Well experienced with natural resources impact assessment, permitting, and compliance in California (CDFW, CESA, Section 401/1600 permitting.), • Established working relationships with USACE, USFWS, BLM, and state agencies., • This position is responsible for leading the successful delivery of scope, schedule, budget, and quality of environmental permitting and compliance tasks for energy projects., • Oversight and coordination of project task deliverables, which could include involvement with subconsultant partners., • Available to junior sta for guidance; Provides opportunities to junior sta for becoming familiar with task management and financials., • Recruiting and retaining sta., • Ability to develop and implement day-to-day routines for a team., • Delivers scope, schedule, budget, quality, safety, and profitability of all projects managed., • Develops and maintains successful client relationships on existing projects., • Ability to identify bid opportunities and coordinate and develop a proposed scope, schedule, and fee for submission in competitive bidding opportunities., • Strong verbal and written communication skills., • Ability to collaborate and communicate with and garner support from key stakeholders and staff., • Ability to read, analyze, and interpret general business periodicals, professional journals, technical reports and procedures, and governmental regulations., • Ability to write reports and other business correspondence. At GAI, exceptional people have an exceptional place to work, grow, lead, and achieve. Explore an array of opportunities in locations across the U.S. and join accomplished colleagues in tackling challenging projects for a range of markets. Enjoy comprehensive benefits and feel good about being part of a collaborative team that's committed to supporting the communities we serve. Join GAI and distinguish yourself in a company poised for unlimited growth. Benefits To Working at GAI Include: • Competitive salary -GAI is committed to paying market-based salaries, • Comprehensive benefits package including medical, vision, dental, company paid Long Term Disability, and Short-Term Disability (benefits start within 30 days of hire), • New paid Maternity/Paternity/Adoption program, • Generous Paid Time Off and 7 paid holidays, • 401k company match Equal Opportunity Employer/Protected Veterans/Individuals with Disabilities This employer is required to notify all applicants of their rights pursuant to federal employment laws. For further information, please review the ___ notice from the Department of Labor.

\na {\n text-decoration: none;\n color: #464feb;\n}\ntr th, tr td {\n border: 1px solid #e6e6e6;\n}\ntr th {\n background-color: #f5f5f5;\n}\n We’re hiring a Supervisor, Histology to support both UPMC St. Margaret and UPMC Passavant. \na {\n text-decoration: none;\n color: #464feb;\n}\ntr th, tr td {\n border: 1px solid #e6e6e6;\n}\ntr th {\n background-color: #f5f5f5;\n}\nThis role is based at UPMC St. Margaret as the home site and requires regular travel between both locations as needed. The position offers a consistent first‑shift, Monday–Friday schedule, with flexible start times between 5:00–7:00am depending on department needs. If you’re a collaborative, team‑oriented histology professional ready to step into a system‑level leadership role, we encourage you to apply. Responsibilities: \na {\n text-decoration: none;\n color: #464feb;\n}\ntr th, tr td {\n border: 1px solid #e6e6e6;\n}\ntr th {\n background-color: #f5f5f5;\n}\n • Recruit, hire, train, and evaluate laboratory staff while promoting fairness, professionalism, and service excellence., • Provide day‑to‑day leadership through coaching, scheduling, delegation, performance management, and disciplinary action as needed., • Ensure compliance with regulatory, licensing, CAP, UPMC, and laboratory policies while maintaining a safe work environment., • Oversee laboratory operations, productivity, workflow, and quality assurance initiatives; identify issues and implement improvements., • Serve as a liaison to pathologists, customers, and other departments, providing feedback and resolving concerns., • Provide technical guidance on complex testing and operational issues., • Maintain procedure manuals and remain current on developments in laboratory science and management., • Participate in committees, work groups, and professional development activities., • Successful completion of NAACLS accredited HT program, • OR Associate's degree OR 60 semester hours of academic credit from a regionally accredited college/ university with a combination of 12 semester hours of biology and chemistry, • OR Bachelor's degree with a combination of 30 semester hours of biology and chemistry., • 6 years of clinical laboratory experience post-training if certified as an Histotechnician or 5 years of clinical laboratory experience post-training if certified as a Histotechnologist. Licensure, Certifications, and Clearances: American Society Clinical Pathology Histotechnician (HT)or Histotechnologist (HTL) certification required. • American Society for Clinical Pathology, • Act 34 UPMC is an Equal Opportunity Employer/Disability/Veteran

UPMC Presbyterian is hiring a flexible full-time Laboratory Support Technician, Medical Laboratory Technician, or Medical Laboratory Scientist to support the Microbiology Lab! This position follows a Sunday through Wednesday schedule with evening hours and shift ranging from 8 to 10 hours per day and includes some holiday responsibilities. In this role, you will join a highly innovative lab with a large, diverse team that allows you to make a direct impact on life-changing medicine. This lab provides high-volume service to multiple hospitals within the UPMC system and is the core laboratory for the Urban area! Applicants will be placed into the appropriate job title and salary based on their individual experience and education. The Medical Lab Scientist level salary starts at $28.90 an hour. The Lab Support Technician salary starts at $19.80 an hour. MLS/MLT roles are eligible for a generous sign-on bonus for those who qualify! Responsibilities: • Follow established procedures for the collection (including phlebotomy, as required) and processing of specimens for analysis including the appropriateness and stability of the sample., • Perform qualitative and quantitative analytical procedures according to established protocols with precision and accuracy in a timely and efficient manner., • Recognize critical, abnormal and unacceptable test results and follow-up according to established protocols. Recognize factors that affect measurements and results and initiate the necessary corrective action according to established protocols. Identify problems with instrumentation, methodology, specimens, supplies, or results and take action as outlined in predetermined protocols., • Processes specimens for analysis. Enters accurate patient demographic information and laboratory test orders into the laboratory information system, while ascertaining adequacy of patient information and sample integrity., • Independently performs Moderately Complex or Waived tests (qualitative and quantitative). Performs High Complexity testing only with the oversight of a Medical Lab Scientist or with result review by a Supervisor or Manager., • Meets established testing protocols for precision and accuracy in a timely and efficient manner. Recognizes critical, abnormal and unacceptable test results and follows-up according to established protocols., • Performs and documents Quality Control according to established protocols. Informs supervisory personnel and/or pathologists of any unusual or problematic incidents., • Operate and maintain equipment within the scope of training utilizing defined schedules and written instructions to perform quality control checks, preventive maintenance, and calibration. Perform minor repairs. Use reagents and supplies cost-effectively; monitor and maintain an appropriate supply inventory., • Monitors and maintains supplies for functions the position is responsible for; uses materials and reagents cost-effectively., • Demonstrates dependability, reliability, and independent judgment. Recognizes priorities to accommodate department needs and acceptance of appropriate authority., • Follows all biohazard, chemical, and sharps safety guidelines. Maintains a safe work environment., • Honors confidentiality of patient information. Follows all compliance guidelines., • Bachelor's of Science from an accredited college/university AND successful completion of an accredited Medical Technology program OR,, • Bachelor's of Science from an accredited college/university with a major in biological, chemical, physical, or clinical laboratory science AND ASCP or MLT categorical certification OR,, • Bachelor's of Science from an accredited college/university with a major in biological, chemical, physical, or clinical laboratory science AND at least two years of experience in a role equivalent to that of a Medical Laboratory Technician (MLT) in a clinical laboratory., • One year of experience in a hospital laboratory preferred., • Associate's Degree in a laboratory science (or eligible new graduate) with certification from an accredited institution as either a Medical Laboratory Technician (MLT) or as a Clinical Laboratory Assistant (CLA) OR,, • Bachelor's of Science from an accredited institution with a major in biological, chemical, physical, or clinical laboratory science AND 6 months of clinical laboratory experience OR,, • Equivalent education and experience as defined by CLIA '88 for individuals performing high complexity testing., • One year of experience in a hospital laboratory preferred., • High School diploma or equivalent, and at least 2 years of experience as a Specimen Processor (or equivalent) required in a clinical lab, OR, • Associate's Degree (with biology and chemistry courses) and at least 1year of experience as a Specimen Processor (or equivalent) in a clinical lab, OR, • Phlebotomy or Medical Assistant certification and 1 year of experience as a Specimen Processor (or equivalent) in a clinical lab, OR, • Successful completion of a 50-week U.S. military medical laboratory training course, OR, • Bachelor's of Science from an accredited institution with a major in biological or clinical laboratory science, OR, • Currently enrolled in a Medical Laboratory Scientist (MLS) or equivalent training program, with 3 years college credits required. Licensure, Certifications, and Clearances: • Medical Laboratory Technician MLT(ASCP) or Clinical Laboratory Assistant (CLA) certification preferred., • Act 34 UPMC is an Equal Opportunity Employer/Disability/Veteran

Join UPMC’s Automated Testing Lab! UPMC Presbyterian is seeking a dedicated Medical Lab Technician, Medical Lab Scientist, or Lab Support Technician to join our Automated Testing Laboratory team located in the Clinical Lab Building in Oakland, just steps from UPMC Presbyterian Hospital. This is a full-time daylight shift position (7 a.m. – 3:30 p.m.) with rotating weekend and holiday responsibilities. If you’re passionate about precision, innovation, and making a difference in patient care through high-quality laboratory science, we invite you to bring your expertise to one of the region’s most advanced clinical lab environments. Applicants will be placed into the appropriate job title and salary based on their individual experience and education. The Medical Lab Technician's salary starts at $23.55/hour. The Laboratory Support Tech's salary starts at $19.80/hour. MLS/MLT roles are eligible for a generous sign-on bonus for those who qualify! Responsibilities: • Follow established procedures for the collection (including phlebotomy, as required) and processing of specimens for analysis including the appropriateness and stability of the sample., • Perform qualitative and quantitative analytical procedures according to established protocols with precision and accuracy in a timely and efficient manner., • Recognize critical, abnormal, and unacceptable test results and follow-up according to established protocols. Recognize factors that affect measurements and results and initiate the necessary corrective action according to established protocols., • Identify problems with instrumentation, methodology, specimens, supplies, or results and act as outlined in predetermined protocols., • Operate and maintain equipment within the scope of training utilizing defined schedules and written instructions to perform quality control checks, preventive maintenance, and calibration. Perform minor repairs. Use reagents and supplies cost-effectively; monitor and maintain an appropriate supply inventory., • Maintain in-depth knowledge of techniques, principles, and instruments, their interrelationships and physiological conditions affecting test results., • Conduct, direct, or assist with test development and methodology/equipment evaluation, selection, and implementation., • Performs High Complexity Testing (as defined by PA DOH) without direct supervision., • Assume responsibility for first-line supervision of the section/department temporarily as delegated., • Associate's degree in a laboratory science with certification (or eligible new graduate) from an accredited institution as a Medical Laboratory Technician (MLT), OR, • Bachelor of Science degree from an accredited institution with a major in biological, chemical, physical, or clinical laboratory science, with 6 months of clinical laboratory experience OR, • Equivalent education and experience as defined by CLIA '88 for individuals performing high complexity testing., • Bachelor of Science degree from an accredited college/university AND successful completion of an accredited Medical Lab Scientist program, OR, • Bachelor of Science degree from an accredited college/university with a major in biological, chemical, or clinical laboratory science AND ASCP or equivalent categorical or MLT certification, OR, • Bachelor of Science degree from an accredited college/university with a major in biological, chemical, physical, or clinical laboratory science AND at least two years' experience in a role equivalent to that of a Medical Laboratory Technician (MLT) in a clinical laboratory., • Prefer 1 year experience in a hospital laboratory., • High School diploma or equivalent, and at least 2 years experience as a Specimen Processor (or equivalent) required in a clinical lab, OR, • Associate degree (with biology and chemistry courses) and at least 1 year of experience as a Specimen Processor (or equivalent) in a clinical lab, OR, • Phlebotomy or Medical Assistant certification and 1 year of experience as a Specimen Processor (or equivalent) in a clinical lab, OR, • Successful completion of a 50 week U.S. military medical laboratory training course, OR, • B.S. degree from an accredited institution with a major in biological or clinical laboratory science OR, • Currently enrolled in a MLS (Medical Laboratory Scientist) or equivalent training program, with 3 years college credits required. Licensure, Certifications, and Clearances: • Medical Laboratory Scientist (MLS) (ASCP) or equivalent certification preferred., • Act 34 UPMC is an Equal Opportunity Employer/Disability/Veteran

Join Our Team at UPMC as a Histotechnician or Histotechnologist! UPMC is seeking a dedicated Histotechnician or Histotechnologist to join our dynamic Histology Lab team. This full-time position is perfect for someone passionate about contributing to life-changing medicine in a fast-paced, high-volume environment. Position Details: • Shift: Daylight shifts with variable start times between 3:00 a.m. and 7:00 a.m., Monday through Friday., • Applicants will be placed in the appropriate role (Histotechnician or Histotechnologist) and salary level based on experience and education. UPMC is currently offering a generous sign-on bonus for qualifying Histotechnicians and Histotechnologists! Responsibilities: • Understands CoPath related to Histology workflow., • Progresses towards working independently in an advanced staining area., • Performs QC checks at each phase of processing/ staining, • Processes and prepares surgical and autopsy tissue specimens for embedding, cutting, staining and coverslipping., • Embeds and cuts specialized tissue based on location including minute biopsy protocols., • Ensures all tissues are embedded and cut according to department-specific protocols with proper orientation and complete sections including no folds, chatter, artifacts, or floaters., • Accurately prepares slides for microtomy using the barcode label in order to maintain correct patient identification throughout the process., • Maintains instruments following quality control specifications and daily maintenance protocols., • Performs additional tasks such as filing, cleaning, stocking supplies. Histotechnician: * Successful completion of a NAACLS accredited HT program within the last 5 years OR an Associate's degree or at least 60 semester hours of academic credit from a regionally accredited college/university with a combination of 12 semester hours of biology and chemistry. • Successful completion of bachelor's degree from a regionally accredited college/university with a combination of 30 semester hours of biology and chemistry., • One year of clinical histology laboratory experience post training if not a graduate of accredited training program required. Licensure, Certifications, and Clearances: • American Society Clinical Pathology Histology Technician (HT) certification from ASCP is required within 18 months of hire., • Employees active in a Histotechnician position, on or before the effective date 1/1/2004, at a healthcare facility, are grandfathered regarding certification and will not need to obtain it unless they move into a different position that would require certification.

Job Locations US-PA-Pittsburgh (Moon Township) Category Ecological Services Type Full-Time As a Wetland Delineation Lead with Civil & Environmental Consultants, Inc. (CEC), you'll be part of a team to help clients navigate today's complex environmental regulatory landscape to achieve and maintain compliance with the Clean Water Act, Endangered Species Act, and related federal and state environmental regulations. Your primary responsibility will be leading wetland delineations in accordance with the USACE regional supplements for the Eastern Mountains and Piedmont, Midwest, and Northcentral and Northeast regions. This job is heavily field based. You will also assist with vegetation monitoring/assessment, threatened & endangered species surveys, fish and benthic macroinvertebrate sampling, and preparation of reports and permit applications. Endless perks are available to employees at CEC! Our office boasts a full-scale gym, cafe serving breakfast and lunch, and recreation rooms-creating the perfect balance of wellness and productivity. Throughout the year, employees enjoy ping pong, pool, cornhole, and pickleball tournaments as well as the annual summer picnic, themed happy hours, and fun team building activities including go-kart racing and curling! We also understand the importance of reaching beyond the office and giving back to the community-CEC employees volunteer for trail workdays to enhance local parks, maintain a CEC-designed pollinator garden for our office campus, and organize an annual charity golf tournament. At CEC Pittsburgh, we pride ourselves on fostering a culture of connection, collaboration, and growth within the office and in our community. Bachelor's degree in a natural sciences field (e.g., Ecology, Environmental Science, Environmental Studies, Biology, Ecology) • 3+ years of experience leading wetland delineations and other applied ecological field studies (fisheries, botany, invertebrates), • Ability to travel for out-of-town assignments (~50%), • Demonstrated ability to mentor new staff, • Completion of a 40-hour wetland delineation training course, • Familiarity with Section 401 and 404 Clean Water Act regulations and permitting We have support! We have a variety of Employee Resource Groups, including CEC Community - focused on giving back to the communities in which we work; CEC Ignite - focused on helping professionals early in their careers to develop their pathway; CEC iDEA - focused on inclusion, diversity, equality, and acceptance; and CEC Women - focused on creating internal and external opportunities for women to network and leverage professional experience! We care about our people! People and Culture are two of the five elements of our strategic plan. When you care about your people, they will want to grow a career with you - that is our goal. CEC offers you a small-firm work environment with large-firm opportunities. Not only will we help you develop professionally, but we will also provide an opportunity to become an owner of the firm and share in its success. CEC offers a matching 401(k); profit sharing; a performance bonus; company stock; medical, dental, and vision insurance; short and long-term disability; tuition assistance; professional development; and work-life balance. CEC is an equal opportunity employer. We do not discriminate in recruiting, hiring or promotion based on race, color, religion, sex (including sexual orientation, gender identity or expression, transgender status), national origin, age, disability, protected veteran status or any other basis or characteristic prohibited by applicable federal, state, or local law. THIRD PARTY RECRUITERS If CEC has not expressly requested recruiting services or contractually engaged with you for recruiting services on a specific position, any resumes or candidate profiles sent to CEC shall be considered unsolicited. Therefore, any such submissions will be considered property of CEC, with no associated fees due to your firm.

Biology Domains Covered Ecology and Evolutionary Biology, Genetics, Cell Biology, Biomedical Science, Microbiology, Molecular Biology, Biochemistry, Neuroscience, Miscellaneous Biology. Key Responsibilities - Author original biology questions that test deep conceptual understanding, not surface-

Clinical Biostatistics** - Statistical analysis planning across endpoint types (binary, continuous, time-to-event) - Multiplicity-adjusted hypothesis testing and sample size determination - Subgroup and heterogeneous treatment effect analyses with appropriate false discovery controls - Handling of e

You will create and evaluate Spanish/English prompts and responses, ensuring scientific precision while maintaining clear, natural Spanish phrasing consistent with academic conventions in the United States (Spanish-speaking), Spain, Chile, or Mexico, and alignment with English where needed. Minimum

We are seeking Biology tutors and teachers in Pittsburgh.

Ability to extract insights from noisy, high-dimensional data Reasoning & Scientific Thinking - Strong causal and mechanistic reasoning skills - Ability to generate testable hypotheses and evaluate competing explanations - Experience synthesizing evidence across experiments or datasets *

Job DescriptionWant to make a meaningful difference in peoples’ lives while earning a competitive salary? At Jushi Holdings Inc. ”) (CSE: JUSH) (OTCQX: JUSHF), we are shaping the future of the cannabis industry, the fastest growing jobs sector in the U.S. The Shift Supervisor will partner with the Dispensary Manager to lead the team. This role should lead by example by being the ultimate illustration of service, dedication, pace, and energy. The Shift Supervisor will also be primarily responsible for receiving deliveries, inputting inventory data, restocking product on the floor, and ensuring that all product remains in FIFO order. The Shift Supervisor should mentor, motivate, elevate, and inspire the team by keeping a positive and can-do attitude at all times.WHAT YOU WILL DO • Follow and uphold established policies for sales and customer service to ensure customer satisfaction, • Maintain in-depth knowledge of products and strains in the store, as well as industry-wide product knowledge and strive to train and share that knowledge with other members of the team, • Responsible for monitoring and maintaining inventory levels, ensuring an assortment of product, and communicating inventory action items with the Store Manager, • Assist Patient Care Specialists in the consultation of patients to ensure that the employee is empowered and informed on the right product choices by being knowledgeable about how different methods of cannabis consumption affect our patients differently, • Receive new deliveries in Inventory Room and ensure all manifests are accurate and compliant to map deliveries in MJ Freeway. Report any delivery discrepencies immediately to G/P & Inventory Manager to rectify., • Complete and appropriately delegate (if applicable) tasks assigned during a scheduled shift:, • Correct cash handling and discount application, • Verification of proper paperwork, documentation, and ID for patients, • Security measures and safety compliance, • Maintenance of an organized and clean store, • Support of open communication with the management team and other coworkers, • Reporting of team member issues or patient situations, • End of day daily update e-mails, • Opening and closing duties, • Work with the Management team to ensure retail store operations run smoothly, accurately, and in compliance with the applicable rules and regulations, including:, • Lead in the onboarding and training of new Patient Care Specialists in partnership with the Store Manager, • Able to complete all MOD cash and inventory functions for closing procedures, • Follow all Safety & Security procedures for opening and closingWHAT WE ARE LOOKING FOR, • High School diploma or General Education Development (GED) required, • Associate or Bachelor’s degree in any field preferred, • Experience or study emphasis in biology, medicine, horticulture, agriculture, business, management, or hospitality, • Minimum of 2 years combined dispensary, call center, retail, sales, hospitality, or customer service experience, • Excellent computer and technical skills, including experience with web browsers, retail POS systems, and credit card processing terminals., • High-level critical thinking, attention to detail, mathematical, language, and reasoning skills, • Must be comfortable adding, subtracting, multiplying and dividing fractions and decimals, and high-volume cash handlingPHYSICAL REQUIREMENTS, • Constantly perform desk-based computer tasks, • Frequently sitting and standing, • Occasionally stand/walk, reach/work above shoulders, grasp lightly/fine manipulation, grasp forcefully, use a telephone, sort/file paperwork or parts, lift/carry/push/pull objects that weigh up to 25 pounds, • Occasionally Twist/bend/stoop/squat, kneel/crawl, • Must be able to work a flexible schedule to include weekends and holidays, • Complete any needed assistance including oversight and coverage outside of, • the assigned region as required

Job Description Castle Biosciences Earns "Top Workplaces USA Award" for Phoenix, Pittsburgh, and Friendswood! Learn more at Castle Biosciences Inc. is growing, and we are looking to hire a full-time Clinical Services, Junior Specimen Processor working from our Pittsburgh, PA office location, with a start date of May 1, 2026. Why Castle Biosciences? Exceptional Benefits Package: • Excellent Annual Salary + 20% Bonus Potential, • 20 Accrued PTO Days Annually + 10 Paid Holidays, • 401K with 100% Company Match up to 6%, • 3 Health Care Plan Options + Company HSA Contribution, • Company Stock Grant Upon Hire A DAY IN THE LIFE OF A Junior Specimen Processor This role is primarily responsible for opening incoming specimen shipments received from various sources such as pathology laboratories, hospitals, and clinics, ensuring each specimen is accurately matched with the appropriate documentation. A significant portion of time is dedicated to sorting specimens based on test type and distributing them to the appropriate staff for processing, while also scanning records into the appropriate systems as needed. The position requires a strong focus on quality and accuracy, ensuring all work is complete and compliant with established procedures and departmental productivity standards. Additional responsibilities include ensuring timely delivery of specimens, performing specimen returns upon completion of testing, maintaining a clean and organized work area, and supporting supply chain integrity for both internal operations and external customer needs. The individual must follow all safety rules and defined practices, communicate any issues to supervisors as appropriate, and contribute positively to team efforts while adapting professionally to ongoing changes. REQUIRED QUALIFICATIONS • High school diploma or equivalent, and at least 1 year of experience in a laboratory or clinical setting preferred. PREFERRED QUALIFICATIONS • 1 year of experience in a laboratory or clinical setting preferred. *Please see the full job description at the end of the job ad. SCHEDULE • Monday-Friday, in office 5 days a week from 7:00 AM – 3:30 PM, working from the Pittsburgh, PA office location. READY TO JOIN OUR BIOTECH TEAM? We truly appreciate your time. If this feels like the right opportunity for you, we'd love for you to complete our mobile-friendly application. We're excited to learn more about you and look forward to connecting soon! Castle Biosciences Awards and Research Developments! WORK AUTHORIZATION All candidates must be legally authorized to work in the United States. Currently, Castle Biosciences does not sponsor H-1B visas, OPT, or employment-related visas. ABOUT CASTLE BIOSCIENCES INC. At Castle, it all comes down to people. After all, disease doesn't just happen - it happens to people. We believe that disease management and treatment decisions can be better informed through a person's unique biology, which is revealed through the scientific rigor of our innovative, laboratory-developed tests. We are committed to empowering healthcare providers and patients with the goal of improved outcomes. Every employee at Castle has an impact on patient care, and we work to ensure that everyone finds their work to be both challenging and rewarding. We behave with integrity and treat our colleagues with respect and kindness. Our culture fosters an environment of trust, transparency, and collaboration. We prioritize and encourage internal growth and professional development. Castle Biosciences is an equal opportunity employer as to all protected groups, including protected veterans and individuals with disabilities. If you have a disability and you believe you need a reasonable accommodation in order to search for a job opening or to submit an online application, please e-mail . This email was created exclusively to assist disabled job seekers whose disability prevents them from being able to apply online. Only messages left for this purpose will be returned. Messages left for other purposes, such as following up on an application or technical issues not related to a disability, will not receive a response. ** No third-party recruiters, please Job Posted by ApplicantPro

Job Description Castle Biosciences Earns "Top Workplaces USA Award" for Phoenix, Pittsburgh, and Friendswood! Learn more at Castle Biosciences Inc. is growing, and we are looking to hire a full-time Laboratory Team Lead, Technologist working from our Pittsburgh, PA laboratory location, with a start date of May 1, 2026. Why Castle Biosciences? Exceptional Benefits Package: • Excellent Annual Salary + 25% Bonus Potential, • 20 Accrued PTO Days Annually + 10 Paid Holidays, • 401K with 100% Company Match up to 6%, • 3 Health Care Plan Options + Company HSA Contribution, • Company Stock Grant Upon Hire A DAY IN THE LIFE OF A Lab, Team Lead, Technologist A typical day for the Team Lead involves coaching team members, troubleshooting issues, and resolving challenges while providing ongoing support to the team. The Team Lead collaborates closely with staff to coordinate scheduling and assignments, train and monitor testing activities, and facilitate clear communication across the team. This role primarily involves providing technical support and mentorship, assisting with testing procedures as needed, and monitoring daily workflow to ensure efficiency and quality. REQUIRED QUALIFICATIONS • Associate's degree (for direct supervision over Lab Testing Technicians) in a scientific discipline, • with 3-5 years of experience in clinical laboratory testing., • Technical Proficiency: Demonstrated expertise in clinical laboratory procedures and methodologies across multiple assays with proficiency in performing data analysis., • Collaboration: Proven ability to work effectively with others in a team-oriented environment. PREFERRED QUALIFICATIONS • Bachelor of Science preferred (for direct supervision over Molecular Technologists) in a scientific discipline or equivalent, • Preferred 2-4 years of experience in a High Complexity Testing. *Please see the full job description at the end of the job ad. SCHEDULE • Monday through Friday, from 8:00 am to 4:30 pm, working from our Pittsburgh, PA laboratory location., • Provide support outside scheduled hours as needed, and on weekends as necessary for troubleshooting issues, including reagents, equipment, environmental factors, building concerns, and patient sample testing. READY TO JOIN OUR BIOTECH TEAM? We truly appreciate your time. If this feels like the right opportunity for you, we'd love for you to complete our mobile-friendly application. We're excited to learn more about you and look forward to connecting soon! Castle Biosciences Awards and Research Developments! WORK AUTHORIZATION All candidates must be legally authorized to work in the United States. Currently, Castle Biosciences does not sponsor H-1B visas, OPT, or employment-related visas. ABOUT CASTLE BIOSCIENCES INC. At Castle, it all comes down to people. After all, disease doesn't just happen - it happens to people. We believe that disease management and treatment decisions can be better informed through a person's unique biology, which is revealed through the scientific rigor of our innovative, laboratory-developed tests. We are committed to empowering healthcare providers and patients with the goal of improved outcomes. Every employee at Castle has an impact on patient care, and we work to ensure that everyone finds their work to be both challenging and rewarding. We behave with integrity and treat our colleagues with respect and kindness. Our culture fosters an environment of trust, transparency, and collaboration. We prioritize and encourage internal growth and professional development. Castle Biosciences is an equal opportunity employer as to all protected groups, including protected veterans and individuals with disabilities. If you have a disability and you believe you need a reasonable accommodation in order to search for a job opening or to submit an online application, please e-mail . This email was created exclusively to assist disabled job seekers whose disability prevents them from being able to apply online. Only messages left for this purpose will be returned. Messages left for other purposes, such as following up on an application or technical issues not related to a disability, will not receive a response. ** No third-party recruiters, please Job Posted by ApplicantPro

Job DescriptionAbout Krystal Bio: At Krystal Biotech, we bring together the brightest and most eager minds to relentlessly pursue the discovery, development, manufacturing, and commercialization of genetic medicines to treat diseases with high unmet medical needs. Founded in 2016, Krystal is distinguished in three powerful ways: science and technology using our patented gene therapy platform, innovative manufacturing supported by our commercial scale facilities, and a unique commercialization model that focuses on the patient’s end-to-end experience. Krystal received U.S. FDA approval for the first and only redosable gene therapy treatment, VYJUVEK®, for the treatment of Dystrophic Epidermolysis Bullosa (DEB). Krystal continues to leverage our proprietary platform to rapidly advance a robust pipeline of investigational genetic medicines in respiratory, oncology, dermatology, and ophthalmology. Krystal is headquartered in Pittsburgh, PA, which is home to our two state-of-the-art CGMP manufacturing facilities with teams around the world and satellite offices in Switzerland, Germany, and Japan. We are a company built and run by people who care, are fearless in the face of a challenge, love the work they do, and practice the highest level of scientific integrity. As we grow, we are seeking team members that embody these values. Job Description Summary: Krystal Biotech, Inc. is seeking a highly motivated and experienced Quality Associate to support quality systems, GMP manufacturing processes and documentation practices at our headquarters in Pittsburgh's South Side. Primary Responsibilities: • Work with internal teams to obtain an understanding of the product and the documentation requirements., • Produce high-quality documentation that meets applicable standards and is appropriate for its intended use., • Develop expertise on FDA regulations and audit processes., • Initiate and update GMP manufacturing associated documentation, such as clearing procedures., • Provide oversight of daily QA functions which include review and approval of records generated by manufacturing and quality control documents., • Provide support for updates on standard operating procedures and associated forms., • Assist with QA efforts for site cGXP documentation related to the operation of gene therapy manufacturing., • Ensure compliance with regulatory agencies and oversee continuous improvement of company's QA and compliance functions.Requirements & Desired Competencies:, • Minimum of a Bachelor’s Degree (Biology or related Life Science) with 3+ years of relevant quality systems experience in the biotech or pharmaceutical industry., • Background that includes knowledge/experience in GMP, GLP, and GCP., • Experience with FDA audits is highly preferred., • Strong knowledge of GMP and ICH requirements., • Must be a self-starter and capable of working with minimal oversight., • Must be able to handle multiple roles and work in a fast paced and changing environment and know how to prioritize activities appropriately., • Excellent oral and written communication skills. Krystal Biotech, Inc. is an Equal Employment Opportunity and Affirmative Action Employers. Qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender perception or identity, national origin, age, marital status, protected veteran status, or disability status. Headhunters and recruitment agencies may not submit resumes/CVs through this Web site or directly to managers. Krystal Biotech, Inc. does not accept unsolicited headhunter and agency resumes. Krystal Biotech, Inc. will not pay fees to any third-party agency or company that does not have a signed agreement with Krystal Biotech, Inc. Powered by JazzHR fvll145mO7

Job DescriptionDescription: Introduction RETTEW is seeking an Environmental Scientist 2 to join our Natural Sciences Team within the Environmental and Geotechnology Practice. This role focuses on wetland delineation, permitting, and field investigations across the Tri-State region. If you enjoy hands-on fieldwork, technical writing, and collaborating with multidisciplinary teams, this position offers meaningful, diverse project experience. About RETTEW RETTEW is a 100% employee-owned engineering consulting firm providing multidisciplinary services across transportation, facilities and construction, environmental and geotechnology, energy, and land development. We are committed to technical excellence, strong client relationships, and developing our employees through hands-on project experience. Our employee-owners take pride in delivering high-quality solutions that strengthen the communities we serve. Work Environment Hybrid, structured schedule with flexibility to support work-life balance. Locations: Pittsburgh, PA; Morgantown, WV; or Akron-Canton, OH Safety & Compliance Requirements This position is designated as safety-sensitive and requires successful completion of all pre-employment screenings as a condition of employment. Responsibilities include operating company-owned vehicles and performing field-based work in active construction and utility environments. Continued compliance with RETTEW’s safety policies is required throughout employment. Position Summary The Environmental Scientist 2 supports wetland delineations, environmental investigations, and regulatory permitting efforts across Pennsylvania, Ohio, and West Virginia. This role partners closely with Team Leads and Project Managers to deliver high-quality technical documentation and field data that support responsible development and environmental stewardship. Responsibilities / Day-to-Day • Conduct stream and wetland delineations using the 1987 USACE Wetland Delineation Manual and applicable regional supplements, • Perform environmental field investigations and data collection, • Prepare detailed wetland delineation reports and technical documentation, • Assist with preparation of federal, state, and local environmental permit applications, including Clean Water Act Section 404 and 401 permits, • Coordinate with internal project teams to support multidisciplinary project delivery, • Communicate with clients and regulatory agencies as needed, • Support additional environmental tasks as assigned Qualifications Required • Bachelor’s degree in environmental science, ecology, biology, botany, or related field, • Minimum three years of wetland delineation experience using the 1987 USACE Wetland Delineation Manual and the Eastern Mountains and Piedmont, Northcentral Northeast, and Midwest Regional Supplements, • Ability to prepare clear, detailed delineation reports and technical documents, • Experience collecting field data using handheld GPS units, • Strong technical writing and communication skills, • Proficiency in Microsoft Office, • Ability to work outdoors in rugged terrain in all seasons, • Willingness to travel periodically, including overnight travel Preferred • Clean Water Act Section 404 and 401 permitting experience in Ohio and West Virginia, • Threatened and endangered species field survey experience What We Offer • Competitive salary range, based on experience, • Employee Stock Ownership Plan, ESOP, • Comprehensive benefits package including medical, dental, and vision, • 401(k) with company match, • Paid time off and paid holidays, • Hybrid work model with flexibility, • Opportunities for professional growth and expanded environmental expertise Equal Opportunity & Accommodations RETTEW is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, including pregnancy, sexual orientation, or gender identity, national origin, age, disability, veteran status, genetic information, or any other characteristic protected by applicable law. If you are an individual with a disability and require a reasonable accommodation to complete any part of the application process, please contact us at to request assistance. #LI-Hybrid Requirements: Requirements listed above

Job Description Patent Agent / Technical Specialist Location: Pittsburgh, PA Direct counsel is seeking a Patent Agent / Technical Specialist with 3+ years of patent prosecution experience to join a well-established national law firm. This role involves supporting the firm’s legal team on a wide variety of technical innovations, working with clients from start-ups to major corporations, and contributing to intellectual property strategy and patent portfolio management. Hybrid work options are available for qualified candidates. Responsibilities * Draft comprehensive and accurate patent applications to protect client inventions. * Manage patent prosecution processes, including responding to office actions and obtaining patent allowances. * Conduct prior art searches, assess patentability, and advise clients on patent strategy. * Review invention disclosures and support freedom-to-operate analyses and IP due diligence. * Develop strategies to address challenges in patent law, including subject matter eligibility issues. * Collaborate with clients to align IP strategies with business objectives. * Participate in team training and maintain high-quality work while meeting deadlines. Qualifications * 3+ years of hands-on experience drafting and prosecuting patent applications. * Bachelor’s or advanced degree in a life sciences discipline (molecular biology, biochemistry, microbiology, genetics, immunology, or related field). * Active registration with the United States Patent and Trademark Office (USPTO) in good standing. * Expertise in CRISPR, antibody therapeutics, cell and gene therapy, recombinant DNA, or bioinformatics is highly desirable. * Strong writing, organizational, and interpersonal skills. * Ability to work independently and collaboratively within a team-oriented environment. This position offers meaningful professional growth within a national law firm platform, providing exposure to sophisticated patent prosecution and IP strategy matters.

Job DescriptionResearch Associate / Sr. Research Associate, Preclinical/Product Development About Krystal Bio: At Krystal Biotech, we bring together the brightest and most eager minds to relentlessly pursue the discovery, development, manufacturing, and commercialization of genetic medicines to treat diseases with high unmet medical needs. Founded in 2016, Krystal is distinguished in three powerful ways: science and technology using our patented gene therapy platform, innovative manufacturing supported by our commercial scale facilities, and a unique commercialization model that focuses on the patient’s end-to-end experience. Krystal received U.S. FDA approval for the first and only redosable gene therapy treatment, VYJUVEK®, for the treatment of Dystrophic Epidermolysis Bullosa (DEB). Krystal continues to leverage our proprietary platform to rapidly advance a robust pipeline of investigational genetic medicines in respiratory, oncology, dermatology, and ophthalmology. Krystal is headquartered in Pittsburgh, PA, which is home to our two state-of-the-art CGMP manufacturing facilities with teams around the world and satellite offices in Switzerland, Germany, and Japan. We are a company built and run by people who care, are fearless in the face of a challenge, love the work they do, and practice the highest level of scientific integrity. As we grow, we are seeking team members that embody these values. Job Description Summary: The Product Development Team is seeking a highly motivated and innovative Research Associate / Senior Research Associate to join our multidisciplinary R&D team. The candidate will provide technical and scientific support in the development and testing of HSV-based gene therapy products and will participate in the design, development, and execution of experiments. To be successful, the candidate should demonstrate proficiency in fundamental molecular biology techniques and mammalian cell culture, show curiosity, initiative, and the ability to work well in a timeline-driven environment. Primary Responsibilities: • Design and execute studies to address fundamental question about our HSV-based gene therapy product candidates, • Adhere to scientifically-sound practices for experiment documentation, statistically driven data analysis, and interpretation of results, • Ensure that all safety guidelines are always followed strictly and maintain a clean and orderly environment, • Read the literature, find creative opportunities, and suggest alternative approaches to troubleshoot technical issues and plan next steps to meet deliverables., • Write documents such as standard operating procedures, technical memos, and reports, • Interact with cross-functional teams and effectively communicate scientific results, • Other duties as assignedRequirements and Desired Competencies:, • Bachelor's Degree (or Master's Degree) in life sciences with relevant laboratory experience, • Industry experience a plus, • Demonstrated experience with cloning, qPCR, aseptic cell culture techniques, virus production, ELISA, Western Blotting, and Immunostaining, • Hands-on experience working with rodent models a plus, • In depth understanding in one or more of the following areas is required: gene therapy, cell biology, molecular biology, immunology, and/or virology, • Experience with analytical method development and/or validation a plus, • High capability of multitasking in a fast-paced environment urL0WJWsJh

Job DescriptionBenefits: • 401(k), • Bonus based on performance, • Competitive salary, • Dental insurance, • Flexible schedule, • Health insurance, • Paid time off, • Profit sharing These positions will be responsible for providing industrial hygiene (IH)/environmental consulting services, including: • Indoor air quality assessment and other IH program design/implementation, • Fungal and microbial contamination investigations, • Human health risk assessments, • Service a wide range of clients, particularly within the insurance industry, • Provide expert witness testimony and litigation support services., • Assist our Director of Business Development in expanding the regional business for their respective offices.The ideal candidate will have:, • Advanced degree in Biology, Chemistry, Industrial Hygiene or Occupational Safety, as well as a Certified Industrial Hygienist (CIH) professional registration (or equivalent work experience), • Ten or more years relevant experience in environmental/IH consulting, health & safety, and/or insurance, • Strong written/verbal communications, presentation and interpersonal skills, • Prior business development experience, • Expertise in providing environmental/indoor air quality risk assessment and/or claim services in or to the insurance industry required.Founded in 1986, HETI is a full-service, nationwide environmental services company specializing in environmental and indoor air quality site assessment, site remediation, risk characterization, occupational health and safety services, and litigation/expert witness support. Through our network of offices throughout the U.S., we serve a variety of large and small businesses. We are an Equal Opportunity Employer and offer a competitive benefit package and a friendly, flexible work environment. Flexible work from home options available.

Job Description Company: Trileaf Corporation is a nationwide environmental, architecture, and engineering consulting firm that assists clients with environmental due diligence, regulatory compliance, and engineering and architectural design. From its headquarters in St. Louis, MO, and multiple branch offices throughout the U.S., Trileaf serves the wireless communications, commercial real estate and financial industries. Location: Pittsburgh, PA or Cleveland, OH (FULLY REMOTE) Job Summary: Trileaf is seeking a full-time, field Project Scientist with at 0-5 years of field experience conducting environmental due diligence work on commercial real estate and/or telecom projects, to include Phase I Environmental Site Assessments (Phase I ESAs) and Phase II ESAs. This position will be remote & based in the Ohio River Valley (ideally between Cleveland OH / Pittsburgh PA. Essential Job Functions: • Travel to project location, take detailed notes and photographs of site (3-4 days per week), • Conducting interviews, in person, via email, and phone, • Ordering & analyzing government database records, • Performing regulatory agency file reviews, • Reviewing historical data (including topographic maps, Sanborn fire insurance maps, city directories, and aerial photographs), • Drafting of a standardized report using information from these various sources, • Perform QA/QC to the satisfaction of both management and clients, • Completing requested revisions & submitting report within pre-established timelines, • Conducting field work to collect samples of potentially contaminated subsurface media (soil, groundwater, and soil vapor) and/or indoor air To be considered, the resume of the applicant must demonstrate the following qualifications/skills: • Attention to detail, • Strong work ethic, • Valid driver license, • Capable of field work, • Ability and willingness to travel (travel not expected to exceed 2-3 days at a time), • Good computer skills, • Independent worker, • Commitment to excellence, • Phase I Assessments, • 40-Hour HAZWOPER Certification, • Licensed Asbestos Inspector, • Management, • Mold assessment experience, • Phase II Environmental Site Assessments (ASTM E1903), • Property Condition Assessments (ASTM E2018), • Transaction Screen Assessments (ASTM E1528), • Record Search with Risk Assessments (SBA SOP 50 10 6) The listed salary range for this position is an expected range. The actual offer will be at the company's sole discretion and determined by relevant business considerations, including the final candidate's qualifications, years of experience, skillset, geographic location, and current market data. Trileaf Corporation is an equal opportunity employer that recognizes the value of diversity and inclusion in the workplace. We prohibit discrimination and harassment of any kind based on race, color, sex, age, religion, sexual orientation, national origin, disability, genetic information, pregnancy, or any other protected characteristic as outlined by federal, state, and local laws in jurisdictions where we operate.

Job Description Castle Biosciences Earns "Top Workplaces USA Award" for Phoenix, Pittsburgh, and Friendswood! Learn more at Castle Biosciences Inc. is growing, and we are looking to hire a full-time Quality Control Laboratory Testing Technician working from our Pittsburgh, PA laboratory location, with a start date of January 26, 2026. Why Castle Biosciences? Exceptional Benefits Package: • Excellent Annual Salary + 20% Bonus Potential, • 20 Accrued PTO Days Annually + 10 Paid Holidays, • 401K with 100% Company Match up to 6%, • 3 Health Care Plan Options + Company HSA Contribution, • Company Stock Grant Upon Hire A DAY IN THE LIFE OF A Quality Control Laboratory Testing Technician A typical day for the laboratory testing technician includes sample processing, performing quality control checks, and providing overall laboratory support. The technician works with equipment setup for staining and imaging, prepares reagents, manages specimens, and assists with inventory and quality management tasks. The majority of time in this role is spent on three main activities: equipment setup, monitoring, and maintenance; conducting inventory checks and stocking consumables; and managing slide specimens, including archiving, tracking, and proper storage. REQUIRED QUALIFICATIONS • At least an associate's degree in biological science (i.e., biology, chemistry, etc.), • Proven flexibility and dependable performance, • Laboratory work experience required PREFERRED QUALIFICATIONS • MLT (AA) recommended, not required, • Experience in a high complexity clinical laboratory setting preferred *Please see the full job description at the end of the job ad. SCHEDULE • Monday through Friday, 8:00 am to 4:30 pm, exempt position, working from our Pittsburgh, PA laboratory., • The role may require flexibility to meet operational needs. READY TO JOIN OUR BIOTECH TEAM? We truly appreciate your time. If this feels like the right opportunity for you, we'd love for you to complete our mobile-friendly application. We're excited to learn more about you and look forward to connecting soon! Castle Biosciences Awards and Research Developments! WORK AUTHORIZATION All candidates must be legally authorized to work in the United States. Currently, Castle Biosciences does not sponsor H-1B visas, OPT, or employment-related visas. ABOUT CASTLE BIOSCIENCES INC. At Castle, it all comes down to people. After all, disease doesn't just happen - it happens to people. We believe that disease management and treatment decisions can be better informed through a person's unique biology, which is revealed through the scientific rigor of our innovative, laboratory-developed tests. We are committed to empowering healthcare providers and patients with the goal of improved outcomes. Every employee at Castle has an impact on patient care, and we work to ensure that everyone finds their work to be both challenging and rewarding. We behave with integrity and treat our colleagues with respect and kindness. Our culture fosters an environment of trust, transparency, and collaboration. We prioritize and encourage internal growth and professional development. Castle Biosciences is an equal opportunity employer as to all protected groups, including protected veterans and individuals with disabilities. If you have a disability and you believe you need a reasonable accommodation in order to search for a job opening or to submit an online application, please e-mail . This email was created exclusively to assist disabled job seekers whose disability prevents them from being able to apply online. Only messages left for this purpose will be returned. Messages left for other purposes, such as following up on an application or technical issues not related to a disability, will not receive a response. ** No third-party recruiters, please Job Posted by ApplicantPro

Job Description About Peptilogics Peptilogics is a surgical therapeutics company dedicated to curing and preventing devastating medical device-related infections (MDRI). Our lead candidate, PLG0206, is a first-in-class drug that targets biofilm, a protective bacterial matrix that is the root cause of device infections across surgical categories, and has no approved cure to date. PLG0206 is currently being evaluated in a Phase 2/3 registration trial for the treatment of prosthetic joint infection (PJI), the first of multiple potential indications to treat and prevent MDRI. Job Title: Senior Director, Corporate Operations Location(s): Pittsburgh, PA or Remote Job Status: Full-Time Supervisor: Chief Operations Officer (COO) Position Overview The Senior Director, Corporate Operations will report to the COO and play a critical role in driving the execution of Peptilogics' operational and strategic priorities. This individual will partner with executive leadership to translate business goals into actionable plans, oversee cross-functional operations, and optimize systems and processes to support growth. The Senior Director will have broad exposure across the organization, with a focus on enabling execution, improving scalability, and contributing to key strategic initiatives. Essential Functions • Serve as a key operational leader, partnering with the COO and executive team to align strategy with execution, • Lead company-wide operational planning and ensure alignment with strategic goals, • Facilitate forecasts, budget development, resource allocation, vendor payments, and operational performance tracking with Finance, • Implement and improve systems, processes, and tools to drive operational scalability and excellence, • Implement and maintain the Quality Management System (QMS) and oversee SOP creation, updates, and audit readiness, • Ensure compliance across corporate operations, development activities, legal, insurance, and regulatory requirements; foster a culture of compliance, • Oversee management of non-owned physical facilities (labs, offices, external manufacturing sites), IT infrastructure, and enterprise software systems, • Work closely with the Development team to manage relationships with CROs, CMOs, and preclinical and clinical trial providers, • Lead sourcing, procurement, and logistics to support research, development, and external manufacturing operations, • Negotiate contracts and ensure cost-effective resource utilization across all operational activities, • Manage HCP contracting and compliance processes, • Serve as primary point of contact for legal service vendors and coordinate legal operational needs, • Identify operational risks, gaps, and bottlenecks, and proactively lead solutions, • Manage the Operations team including hiring, performance, coaching, and career development, • Drive operational KPIs and reporting, including preparation of materials for executive and board updates, • Support business development and partnership activities through operational due diligence and integration planning, • Support fundraising and investor relations by providing operational insights, data, and reporting, • Support cross-functional teams (R&D, Commercial, Project Management) in executing strategic initiatives, • Collaborate with the COO and Finance on long-range planning and scenario modeling, • Contribute to shaping company culture by supporting initiatives around collaboration, communication, and team building, • Bachelor's degree in a relevant field (e.g., life sciences, business, engineering); advanced degree (MBA, MS, PhD) preferred, • 10+ years of experience in biotech, pharmaceutical, or life sciences operations, • 3–5 years in a leadership or senior operations role, ideally in a high-growth or venture-backed environment, • Experience scaling operations in a startup or growth-stage company (preferred), • Prior operational involvement in fundraising, investor relations, or board reporting (preferred), • Strong project management and organizational skills, with the ability to manage complex, cross-functional initiatives, • Excellent financial and business acumen; experience with budgets, forecasts, and KPIs, • Proven ability to build, lead, and develop teams, • Deep understanding of operational compliance, including legal, regulatory, quality management (QMS), and audit readiness, • Proven ability to build, lead, and develop teams across diverse operational functions, • Exceptional interpersonal and collaboration skills, with the ability to influence at all levels, • Outstanding verbal and written communication skills, including executive-level reporting and presentations, • Excellent verbal and written communication skills, including executive-level reporting and presentations, • Ability to thrive in a dynamic, fast-paced environment with shifting priorities, • Ability to drive cross-functional alignment and collaboration across scientific, operational, and corporate teams, • Strategic thinking and ability to scale operations in a growth-stage environment or commercialization-ready biotech environment, • Experience with contract development, procurement, and resource optimization, • Familiarity with QMS implementation, SOP development, and compliance frameworks in a biotech/pharma setting, • Financial fluency to support investor relations, board reporting, and fundraising activities, • Familiarity with technology-driven R&D environments including computational biology, machine learning, • Change management and process improvement capabilities Peptilogics is proud to be an equal opportunity employer. We make hiring decisions based on qualifications, experience, and potential—without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, age, disability, veteran status, or any other protected status. We welcome candidates from all backgrounds to apply.

Job Description Castle Biosciences Earns "Top Workplaces USA Award" for Phoenix, Pittsburgh, and Friendswood! Learn more at Castle Biosciences Inc. is growing, and we are looking to hire a full-time IT, Application Support Analyst working from our Pittsburgh, PA office location, with a start date of April 20, 2026. Why Castle Biosciences? Exceptional Benefits Package: • Excellent Annual Salary + 20% Bonus Potential, • 20 Accrued PTO Days Annually + 10 Paid Holidays, • 401K with 100% Company Match up to 6%, • 3 Health Care Plan Options + Company HSA Contribution, • Company Stock Grant Upon Hire A DAY IN THE LIFE OF A IT, Application Support Analyst As an Application Support Analyst, you will be working within our IT department triaging and responding to internal stakeholders across multiple departments to provide support to our core business. You work on a small team, responsible for (but not limited to) serving as the first line of support for users, escalating and triaging level 1 issues as needed, and assisting users with production support by resolving data issues and addressing knowledge and process gaps. You will escalate higher level tickets to the appropriate IT teams, document root causes and actions taken to provide resolution, and manage ticket priorities to meet SLAs while communicating status updates and resolutions effectively with end users. You will also acquire, comb through, and monitor logs to perform root cause analysis. This role will spend the most time identifying and updating documentation for out-of-date processes, maintaining a self-help knowledge base, identifying and reproducing bugs for new work items, and creating and documenting ticket resolution processes for ongoing defects. REQUIRED QUALIFICATIONS • Bachelor's degree in information technology, Computer Science, Data Analytics, or Data Science, plus at least 1 year of relevant experience, or a minimum of 4 years of relevant work experience., • Basic SQL experience and understanding of relational database concepts, • Experience writing Knowledge Bases and End User Guides, • Excellent business communication and customer service skills, • Knowledge of databases, IT systems, and IT troubleshooting *Please see the full job description at the end of the job ad. SCHEDULE • Monday-Friday, full-time position with standard working hours, in office 5 days a week, working from the Pittsburgh, PA office location. READY TO JOIN OUR BIOTECH TEAM? We truly appreciate your time. If this feels like the right opportunity for you, we'd love for you to complete our mobile-friendly application. We're excited to learn more about you and look forward to connecting soon! Castle Biosciences Awards and Research Developments! WORK AUTHORIZATION All candidates must be legally authorized to work in the United States. Currently, Castle Biosciences does not sponsor H-1B visas, OPT, or employment-related visas. ABOUT CASTLE BIOSCIENCES INC. At Castle, it all comes down to people. After all, disease doesn't just happen - it happens to people. We believe that disease management and treatment decisions can be better informed through a person's unique biology, which is revealed through the scientific rigor of our innovative, laboratory-developed tests. We are committed to empowering healthcare providers and patients with the goal of improved outcomes. Every employee at Castle has an impact on patient care, and we work to ensure that everyone finds their work to be both challenging and rewarding. We behave with integrity and treat our colleagues with respect and kindness. Our culture fosters an environment of trust, transparency, and collaboration. We prioritize and encourage internal growth and professional development. Castle Biosciences is an equal opportunity employer as to all protected groups, including protected veterans and individuals with disabilities. If you have a disability and you believe you need a reasonable accommodation in order to search for a job opening or to submit an online application, please e-mail . This email was created exclusively to assist disabled job seekers whose disability prevents them from being able to apply online. Only messages left for this purpose will be returned. Messages left for other purposes, such as following up on an application or technical issues not related to a disability, will not receive a response. ** No third-party recruiters, please Job Posted by ApplicantPro

Job Description Castle Biosciences Earns "Top Workplaces USA Award" for Phoenix, Pittsburgh, and Friendswood! Learn more at Castle Biosciences Inc. is growing, and we are looking to hire a full-time Laboratory Team Lead working from our Pittsburgh, PA laboratory location, with a start date of March 1, 2026. Why Castle Biosciences? Exceptional Benefits Package: • Excellent Annual Salary + 25% Bonus Potential, • Schedule differential pay $4,000/year (Schedule-based pay only. Not applicable if schedule changes.), • 20 Accrued PTO Days Annually + 10 Paid Holidays, • 401K with 100% Company Match up to 6%, • 3 Health Care Plan Options + Company HSA Contribution, • Company Stock Grant Upon Hire A DAY IN THE LIFE OF A Lab, Team Lead A typical day for the Team Lead involves coaching team members, troubleshooting issues, and resolving challenges while providing ongoing support to the team. The Team Lead collaborates closely with staff to coordinate scheduling and assignments, train and monitor testing activities, and facilitate clear communication across the team. This role primarily involves providing technical support and mentorship, assisting with testing procedures as needed, and monitoring daily workflow to ensure efficiency and quality. REQUIRED QUALIFICATIONS • Associate's degree (for direct supervision over Lab Testing Technicians) in a scientific discipline, • with 3-5 years of experience in clinical laboratory testing., • Preferred 2-4 years of experience in a High Complexity Testing., • Technical Proficiency: Demonstrated expertise in clinical laboratory procedures and methodologies across multiple assays (at least two for PHX site) with proficiency in performing data analysis., • Collaboration: Proven ability to work effectively with others in a team-oriented environment. *Please see the full job description at the end of the job ad. SCHEDULE • Monday through Friday, from 12:30 pm to 9:00 pm, working from our Pittsburgh, PA laboratory location., • Provide support outside scheduled hours as needed, and on weekends as necessary for troubleshooting issues, including reagents, equipment, environmental factors, building concerns, and patient sample testing. READY TO JOIN OUR BIOTECH TEAM? We truly appreciate your time. If this feels like the right opportunity for you, we'd love for you to complete our mobile-friendly application. We're excited to learn more about you and look forward to connecting soon! Castle Biosciences Awards and Research Developments! WORK AUTHORIZATION All candidates must be legally authorized to work in the United States. Currently, Castle Biosciences does not sponsor H-1B visas, OPT, or employment-related visas. ABOUT CASTLE BIOSCIENCES INC. At Castle, it all comes down to people. After all, disease doesn't just happen - it happens to people. We believe that disease management and treatment decisions can be better informed through a person's unique biology, which is revealed through the scientific rigor of our innovative, laboratory-developed tests. We are committed to empowering healthcare providers and patients with the goal of improved outcomes. Every employee at Castle has an impact on patient care, and we work to ensure that everyone finds their work to be both challenging and rewarding. We behave with integrity and treat our colleagues with respect and kindness. Our culture fosters an environment of trust, transparency, and collaboration. We prioritize and encourage internal growth and professional development. Castle Biosciences is an equal opportunity employer as to all protected groups, including protected veterans and individuals with disabilities. If you have a disability and you believe you need a reasonable accommodation in order to search for a job opening or to submit an online application, please e-mail . This email was created exclusively to assist disabled job seekers whose disability prevents them from being able to apply online. Only messages left for this purpose will be returned. Messages left for other purposes, such as following up on an application or technical issues not related to a disability, will not receive a response. ** No third-party recruiters, please Job Posted by ApplicantPro

Job Description Clinical Laboratory Team Lead Location: Pittsburgh, PA Schedule: Monday–Friday | 12:30 PM – 9:00 PM Salary: $70,000 – $90,000 + $4,000 Shift Differential + Bonus Potential About the Role: A leading molecular diagnostics laboratory is seeking an experienced Clinical Laboratory Team Lead to oversee daily operations and support a team of laboratory professionals performing high-complexity testing. This role combines hands-on laboratory work, team leadership, quality oversight, and regulatory compliance within a fast-paced clinical laboratory environment. The Team Lead will act as a technical resource and liaison between laboratory staff and management, ensuring workflow efficiency, regulatory compliance, and high-quality diagnostic testing. This position is ideal for experienced Medical Technologists, Clinical Laboratory Scientists, or Lead Technologists looking to step into a leadership role. Key Responsibilities * Lead and support daily operations of a high-complexity clinical laboratory. * Supervise and mentor a team of 8–16 laboratory professionals. * Perform and review clinical laboratory testing and assay analysis. * Ensure compliance with CLIA, CAP, and laboratory quality standards. * Troubleshoot laboratory processes, equipment, and workflow while supporting quality improvement initiatives. Required Qualifications * Associate's degree in Biology, Molecular Biology, Biochemistry, Medical Laboratory Science, or related scientific discipline * 3–5+ years of clinical laboratory testing experience * Experience working in high complexity clinical laboratory environments * Experience with CLIA and CAP regulatory standards * Experience performing quality control analysis and assay troubleshooting * Experience using LIMS systems and laboratory data analysis tools Preferred Qualifications * Bachelor's degree in a scientific discipline * Experience as a Lead Medical Technologist, Senior Technologist, or Laboratory Lead * Experience preparing for CAP inspections * Experience mentoring or training laboratory staff * Experience with molecular diagnostics or proteomics testing * ASCP certification or equivalent Benefits • Stock Grant Program 401(k) with 100% employer match up to 6% (immediate vesting) * Health insurance starting Day 1 (employer covers majority of premiums) * Multiple health plan options available This company is an equal opportunity employer and values diversity in the workplace. All qualified applicants will receive consideration for employment without regard to protected characteristics.

Job Description Castle Biosciences Earns "Top Workplaces USA Award" for Phoenix, Pittsburgh, and Friendswood! Learn more at Castle Biosciences Inc. is growing, and we are looking to hire a full-time Laboratory Supervisor working from our Pittsburgh, PA laboratory location, with a start date of April 1, 2026. Why Castle Biosciences? Exceptional Benefits Package: • Excellent Annual Salary + 25% Bonus Potential, • This role is eligible for differential pay of $4,000/year subject to change based on schedule changes., • 20 Accrued PTO Days Annually + 10 Paid Holidays, • 401K with 100% Company Match up to 6%, • 3 Health Care Plan Options + Company HSA Contribution, • Company Stock Grant Upon Hire A DAY IN THE LIFE OF A Laboratory Supervisor This position supports the clinical laboratory's daily oversight by promoting efficient workflows, providing coaching, and addressing troubleshooting and issue resolution as they arise. The individual serves as a key communication link between laboratory staff and upper management while offering ongoing support to the laboratory team. The supervisor ensures all procedures are performed in accordance with established scientific methodologies and specialized analytical techniques, maintaining full compliance with applicable regulatory standards. Primary responsibilities include supervising day-to-day laboratory operations, ensuring adherence to quality management system policies and procedures, monitoring employee productivity, and providing guidance and coaching to support performance and operational excellence. REQUIRED QUALIFICATIONS • Minimum of a bachelor's degree in science related field, • Minimum of 3+ years in a clinical laboratory, with 1 (CAP) years' experience in high complexity molecular testing (CAP). *Please see the full job description at the end of the job ad. SCHEDULE • Monday through Friday, 12:30 pm to 9 pm, exempt position, working from the Pittsburgh, PA laboratory., • The role may require flexibility to meet operational needs. READY TO JOIN OUR BIOTECH TEAM? We truly appreciate your time. If this feels like the right opportunity for you, we'd love for you to complete our mobile-friendly application. We're excited to learn more about you and look forward to connecting soon! Castle Biosciences Awards and Research Developments! WORK AUTHORIZATION All candidates must be legally authorized to work in the United States. Currently, Castle Biosciences does not sponsor H-1B visas, OPT, or employment-related visas. ABOUT CASTLE BIOSCIENCES INC. At Castle, it all comes down to people. After all, disease doesn't just happen - it happens to people. We believe that disease management and treatment decisions can be better informed through a person's unique biology, which is revealed through the scientific rigor of our innovative, laboratory-developed tests. We are committed to empowering healthcare providers and patients with the goal of improved outcomes. Every employee at Castle has an impact on patient care, and we work to ensure that everyone finds their work to be both challenging and rewarding. We behave with integrity and treat our colleagues with respect and kindness. Our culture fosters an environment of trust, transparency, and collaboration. We prioritize and encourage internal growth and professional development. Castle Biosciences is an equal opportunity employer as to all protected groups, including protected veterans and individuals with disabilities. If you have a disability and you believe you need a reasonable accommodation in order to search for a job opening or to submit an online application, please e-mail . This email was created exclusively to assist disabled job seekers whose disability prevents them from being able to apply online. Only messages left for this purpose will be returned. Messages left for other purposes, such as following up on an application or technical issues not related to a disability, will not receive a response. ** No third-party recruiters, please Job Posted by ApplicantPro

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