Microbiologist jobs in Wilmington, DE - 246 jobs

We are seeking a highly motivated QC Microbiologist who is interested in joining our fast-paced, dynamic QC environment to perform microbiological sampling in support of Facility Utilities Monitoring and Environmental Monitoring Program in support of the GMP manufacturing facility of a cell therapy product including sampling of raw material and release testing. Duties & Responsibilities • Sampling Lead - Utililities, gases, EM and Raw Materials • Submit micro identifications to CRO • Responsible for daily scheduling of junior analyst sampling schedule • Manage variable sample influx by potentially adjusting daily schedule • Communicate expected sample test times and results with QC Lab Assistants • Participate in aseptic processing in a clean room environment • Performs environmental monitoring sampling of plant utilities and production clean zones using particle counters, contact plates and microbial air samplers • Perform protocol driven studies for bioburden, endotoxin, , EM, Raw Materials -ID, etc • Report testing results via Laboratory Inventory Management System (LIMS) • Generating data to support site manufacturing and/or complaint investigations and resolving project-related questions • Performs routine and non-routine microbiological testing such as water bioburden and media growth promotion; Gram staining and microbial identifications • Performs enumeration and characterization of microorganisms recovered from samples • Perform growth promotion • Identifies bacteria and susceptibilities, molds, yeast, parasites, and other related organisms • Perform Microbiological test methods for cell therapy product, raw material and release testing Minimum Requirements • B.S. in Biology/Microbiology, or related sciences with 3-5 years of related experience. • Previous working experience in a QC laboratory GMP manufacturing facility highly desirable • Strong time management and organization skills are required • Knowledge of regulatory requirements and standards (FDA, EU, ICH, ISO, USP) a plus • Aseptic technique or cleanroom experience desired • The ability to work off-shift hours, based on business needs, is required • Able to work independently with minimum supervision • Good accurate and clear documentation skills is required Qualifications Minimum Requirements • B.S. in Biology/Microbiology, or related sciences with 3-5 years of related experience. • Previous working experience in a QC laboratory GMP manufacturing facility highly desirable • Strong time management and organization skills are required • Knowledge of regulatory requirements and standards (FDA, EU, ICH, ISO, USP) a plus • Aseptic technique or cleanroom experience desired • The ability to work off-shift hours, based on business needs, is required • Able to work independently with minimum supervision • Good accurate and clear documentation skills is required Additional Information All your information will be kept confidential according to EEO guidelines.

Integrated Resources, Inc is a premier staffing firm recognized as one of the tri-states most well-respected professional specialty firms. IRI has built its reputation on excellent service and integrity since its inception in 1996. Our mission centers on delivering only the best quality talent, the first time and every time. We provide quality resources in four specialty areas: Information Technology (IT), Clinical Research, Rehabilitation Therapy and Nursing. Following is the position details: Title: Microbiologist - Permanent Position Location: West Chester, PA. Job Description: We are seeking a highly motivated QC Microbiologist who is interested in joining our fast-paced, dynamic QC environment to perform microbiological sampling in support of Facility Utilities Monitoring and Environmental Monitoring Program in support of the GMP manufacturing facility of a cell therapy product including sampling of raw material and release testing. Duties & Responsibilities · Sampling Lead - Utililities, gases, EM and Raw Materials · Submit micro identifications to CRO · Responsible for daily scheduling of junior analyst sampling schedule · Manage variable sample influx by potentially adjusting daily schedule · Communicate expected sample test times and results with QC Lab Assistants · Participate in aseptic processing in a clean room environment · Performs environmental monitoring sampling of plant utilities and production clean zones using particle counters, contact plates and microbial air samplers · Perform protocol driven studies for bioburden, endotoxin, , EM, Raw Materials -ID, etc · Report testing results via Laboratory Inventory Management System (LIMS) · Generating data to support site manufacturing and/or complaint investigations and resolving project-related questions · Performs routine and non-routine microbiological testing such as water bioburden and media growth promotion; Gram staining and microbial identifications · Performs enumeration and characterization of microorganisms recovered from samples · Perform growth promotion · Identifies bacteria and susceptibilities, molds, yeast, parasites, and other related organisms · Perform Microbiological test methods for cell therapy product, raw material and release testing Minimum Requirements · B.S. in Biology/Microbiology, or related sciences with 3-5 years of related experience. · Previous working experience in a QC laboratory GMP manufacturing facility highly desirable · Strong time management and organization skills are required · Knowledge of regulatory requirements and standards (FDA, EU, ICH, ISO, USP) a plus · Aseptic technique or cleanroom experience desired · The ability to work off-shift hours, based on business needs, is required · Able to work independently with minimum supervision · Good accurate and clear documentation skills is required Qualifications BS/MS in biology or microbiology Additional Information Feel free to forward my email to your friends/colleagues who might be available. We do offer referral bonus Thank you for your time and consideration. I look forward to hearing from you! Regards, Neha Thakur Life Sciences Recruiter Integrated Resources, Inc. IT Life Sciences Allied Healthcare CRO Certified MBE |GSA - Schedule 66 I GSA - Schedule 621I (Direct) 732-844-8735 www.irionline.com Gold Seal JCAHO Certified ™ for Health Care Staffing “INC 5000's FASTEST GROWING, PRIVATELY HELD COMPANIES” (8th Year in a Row)

At Johnson & Johnson, we believe health is everything. Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at ******************* Job Function: Discovery & Pre-Clinical/Clinical Development Job Sub Function: Biotherapeutics R&D Job Category: Scientific/Technology All Job Posting Locations: Malvern, Pennsylvania, United States of America Job Description: About Innovative Medicine Our expertise in Innovative Medicine is informed and inspired by patients, whose insights fuel our science-based advancements. Visionaries like you work on teams that save lives by developing the medicines of tomorrow. Join us in developing treatments, finding cures, and pioneering the path from lab to life while championing patients every step of the way. Learn more at *******************/innovative-medicine We are searching for the best talent for a Scientist, Laboratory Automation to be in Malvern, PA. Purpose: The Biotherapeutics Development & Supply (BTDS) organization is responsible for the development, clinical supply, marketed product support, and life cycle management of Biotherapeutics. Within BTDS, the Analytical Development (AD) group supports method development and validation, as well as product development, release, and stability analytics via automated workflows. The Laboratory Automation & Robotics team is recruiting for a Scientist, Laboratory Automation to collaborate in migrating analytical assays from manual processes to end-to-end fully automated workflows. In this role you will collaborate with Method Development, Assay Automation, Integrations, Orchestration, Information Technology, Data Science, and Operations to increase sample testing volume while reducing time-to-result, hands-on time, repetitive strain, and assay variability. The primary scientific areas of focus will be therapeutic antibodies and cell and gene therapies - automating analytical workflows such as antigen binding, cell-based bioassays, chromatography, flow cytometry, mass spectrometry, and molecular biology. You will be responsible for: Collaborating within a cross-functional team to design, develop, and deploy end-to-end laboratory automation. Creating, optimizing, maintaining, and continuously improving high-throughput workflows using liquid-handling robots and integrated automation workcells. Expanding the scope of existing automation by introducing new functionalities. Evaluating novel devices/instruments/technologies for the enhancement of laboratory processes. Troubleshooting laboratory automation by liaising with internal subject matter experts and external vendors to perform root cause analysis based on detailed scientific and technical investigations. Sharing knowledge and documenting best practices within the automation team, and supporting and training end-users to independently complete automated workflows. Partnering with Information Technology and Data Science teams to automate data flows to ensure data integrity through capture in appropriate electronic systems and high-throughput processing via review by exception. Qualifications / Requirements: Education: A minimum of a B.S. in Biology, Chemistry, Computer Science, Engineering, Physics, or a related field is requited. An advanced degree is preferred. Required: A minimum of 3 years of laboratory automation experience. Experience operating, maintaining, developing, and optimizing in one or both of the following domains: (1) Liquid-handling robots from Hamilton, Tecan, Beckman Coulter, Dynamic Devices, Agilent, PerkinElmer, etc. and/or (2) Integrated automation workcells using scheduling software such as Biosero Green Button Go, HighRes Biosolutions Cellario, or Thermo Scientific Momentum. Experience implementing automated laboratory workflows within the biotechnology or pharmaceutical industries. Experience migrating biological or biochemical assays/methods onto automated systems. Ability to gather, understand, and assign priorities to user requirements for complicated laboratory workflows, and to translate them into robust automated solutions. Strong organizational, time management, and interpersonal skills (both written and oral), and a commitment in close collaboration with scientists, vendors, and end users across seniority levels. Preferred: Experience working in a regulated environment (e.g. CLIA, GLP, GMP, GxP). Experience with programming languages such as C#, Python, and Visual Basic. Experience with analytical assay/method development. Experience with automated sample management systems from Azenta, Askion, and/or Hamilton. Experience with instrument API calls. Experience with 3D printing and rapid prototyping. Johnson & Johnson is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, age, national origin, disability, protected veteran status or other characteristics protected by federal, state or local law. We actively seek qualified candidates who are protected veterans and individuals with disabilities as defined under VEVRAA and Section 503 of the Rehabilitation Act. Johnson & Johnson is committed to providing an interview process that is inclusive of our applicants' needs. If you are an individual with a disability and would like to request an accommodation, external applicants please contact us via *******************/contact-us/careers, internal employees contact AskGS to be directed to your accommodation resource. #LI-Hybrid Required Skills: Preferred Skills:

The Research Technologist (part-time, 20 hours/week) position is a research role in the Nemours Biobank and Molecular Analysis Program that primarily supports the Lung Health Cohort (LHC) study funded by the National Institutes of Health. This individual will manage receipt and storage of biospecimens from the (LHC) American Lung Association Airways Clinical Research Center network (ALA-ACRC) sites and other ALA-ACRC studies as required. Also manages shipment of biospecimens to investigators from the biobank. Maintains both handwritten and computerized records of specimens received and shipped. Prepares reports including budgets, and other regulatory documents. Ability to multi-task is essential. Experience with computer databases preferred. Qualifications: Associate Degree is required; Bachelor's degree preferred 2 years significant laboratory experience preferred Responsibilities include: 1. Receives biospecimens from the LHC collection sites into the ALA-ACRC biorepository housed at Nemours Biobank and Molecular Analysis Program (BMAP), which includes tracking incoming shipments, accepting shipments, cataloging shipment biospecimens, completing paperwork and computer entry related to acquisition. 2. Prepares biospecimens for shipment from the ALA-ACRC biorepository to ACRC investigators under an approved protocol. Communicates with and tracks shipments to the recipient site. Catalogues biospecimens shipped, completing paperwork and computer entry related to shipment. 3. Prepares reports of biospecimens received and shipped as requested. 4. Prepares budgets, material transfer agreements, and other regulatory documents, and coordinates shared email in baskets. 4. Develops SOPs with assistance of BMAP Program Manager, Laboratory Manager, and ALA-ACRC Nemours investigators. 5. Order necessary supplies as requested by BMAP Program Manager, Laboratory Manager, and ALA-ACRC Nemours investigators.

The Research Technologist (part-time, 20 hours/week) position is a research role in the Nemours Biobank and Molecular Analysis Program that primarily supports the Lung Health Cohort (LHC) study funded by the National Institutes of Health. This individual will manage receipt and storage of biospecimens from the (LHC) American Lung Association Airways Clinical Research Center network (ALA-ACRC) sites and other ALA-ACRC studies as required. Also manages shipment of biospecimens to investigators from the biobank. Maintains both handwritten and computerized records of specimens received and shipped. Prepares reports including budgets, and other regulatory documents. Ability to multi-task is essential. Experience with computer databases preferred. Qualifications: * Associate Degree is required; Bachelor's degree preferred * 2 years significant laboratory experience preferred Responsibilities include: 1. Receives biospecimens from the LHC collection sites into the ALA-ACRC biorepository housed at Nemours Biobank and Molecular Analysis Program (BMAP), which includes tracking incoming shipments, accepting shipments, cataloging shipment biospecimens, completing paperwork and computer entry related to acquisition. 2. Prepares biospecimens for shipment from the ALA-ACRC biorepository to ACRC investigators under an approved protocol. Communicates with and tracks shipments to the recipient site. Catalogues biospecimens shipped, completing paperwork and computer entry related to shipment. 3. Prepares reports of biospecimens received and shipped as requested. 4. Prepares budgets, material transfer agreements, and other regulatory documents, and coordinates shared email in baskets. 4. Develops SOPs with assistance of BMAP Program Manager, Laboratory Manager, and ALA-ACRC Nemours investigators. 5. Order necessary supplies as requested by BMAP Program Manager, Laboratory Manager, and ALA-ACRC Nemours investigators.

The Research Technologist (part-time, 20 hours/week) position is a research role in the Nemours Biobank and Molecular Analysis Program that primarily supports the Lung Health Cohort (LHC) study funded by the National Institutes of Health. This individual will manage receipt and storage of biospecimens from the (LHC) American Lung Association Airways Clinical Research Center network (ALA-ACRC) sites and other ALA-ACRC studies as required. Also manages shipment of biospecimens to investigators from the biobank. Maintains both handwritten and computerized records of specimens received and shipped. Prepares reports including budgets, and other regulatory documents. Ability to multi-task is essential. Experience with computer databases preferred. Qualifications: Associate Degree is required; Bachelor's degree preferred 2 years significant laboratory experience preferred Responsibilities include: 1. Receives biospecimens from the LHC collection sites into the ALA-ACRC biorepository housed at Nemours Biobank and Molecular Analysis Program (BMAP), which includes tracking incoming shipments, accepting shipments, cataloging shipment biospecimens, completing paperwork and computer entry related to acquisition. 2. Prepares biospecimens for shipment from the ALA-ACRC biorepository to ACRC investigators under an approved protocol. Communicates with and tracks shipments to the recipient site. Catalogues biospecimens shipped, completing paperwork and computer entry related to shipment. 3. Prepares reports of biospecimens received and shipped as requested. 4. Prepares budgets, material transfer agreements, and other regulatory documents, and coordinates shared email in baskets. 4. Develops SOPs with assistance of BMAP Program Manager, Laboratory Manager, and ALA-ACRC Nemours investigators. 5. Order necessary supplies as requested by BMAP Program Manager, Laboratory Manager, and ALA-ACRC Nemours investigators.

For 75 years, Charles River employees have worked together to assist in the discovery, development and safe manufacture of new drug therapies. When you join our family, you will have a significant impact on the health and well-being of people across the globe. Whether your background is in life sciences, finance, IT, sales or another area, your skills will play an important role in the work we perform. In return, we'll help you build a career that you can feel passionate about. **Job Summary** We are seeking an experienced Research Study Technician II to join our Insourcing Solutions team, located in Philadelphia, PA. As the Research Study Technician II you will facilitate the goals of drug discovery projects through hands-on conduct of in vivo experiments in rodents. Additional responsibilities include: + Reviews and complies with all policies, guidelines and operating procedures pertaining to the animal care and research program. + May coordinate (or assist) or manage schedules of other team members; resolves schedule conflicts + Assemble, set up, operate and maintain any necessary experimental equipment to conduct in-vivo studies. + Conduct laboratory procedures in compliance with established protocols/plans and with regulatory and laboratory requirements. + Document experimental data in technical notebooks or approved electronic files including activities undertaken, existing conditions, observed results and variation from expected data patterns. + Record, prepare, and analyze data for inclusion in project reports. + Able to perform the following techniques in rodents: + PO, IV, SQ, IP, IM, and IN dosing and/or inoculation techniques + Blood collection from multiple vessels or cardiac, and perfusions + Tumor measurements, body weights, IBD and EAE scoring, behavioral monitoring, etc + Rodent telemetry and physiological recordings + Necropsy, tissue and fluid collections + Rodent euthanasia using CO2, anesthesia, and/or approved physical methods. + Experience in generating/supporting/conducting patient derived mouse models will be an added advantage + Support study set-up, take downs, ex-vivo assays + Aseptic tissue culture experience with human cancer cell lines + Interact with other personnel within the department, multiple research groups, to develop a network of resources to facilitate completion of assignments. + Perform animal care and husbandry as needed, including receipt, stocking, and maintenance of research supplies. **Job Qualifications** To qualify for this role candidates must have one of the following combinations of education/experience: + B.S./B.A. degree in Biological Sciences or related field, or Associate's degree in veterinary technology or equivalent college level program and 4 years of previous laboratory animal research experience, using the skills listed above. OR + High School Diploma and at least 6 years of previous laboratory animal research experience, with 3 years using skills listed above. Certification/Licensure: AALAS certification preferred but not required. The pay range for this position is $37.50 to $39.00 USD per hour. Please note that salaries vary within the range based on factors including, but not limited to, experience, skills, education, certifications, and location. **About Insourcing Solutions** Charles River Insourcing Solutions℠ can streamline research by delivering operational and cost efficiencies through the strategic insourcing of GMP, GLP and non-GLP research services from discovery through safety assessment. Insourcing Solutions℠ provides you with the ability to maintain control of your facility and expertise while leveraging available space. **About Charles River** Charles River is an early-stage contract research organization (CRO). We have built upon our foundation of laboratory animal medicine and science to develop a diverse portfolio of discovery and safety assessment services, both Good Laboratory Practice (GLP) and non-GLP, to support clients from target identification through preclinical development. Charles River also provides a suite of products and services to support our clients' clinical laboratory testing needs and manufacturing activities. Utilizing this broad portfolio of products and services enables our clients to create a more flexible drug development model, which reduces their costs, enhances their productivity and effectiveness to increase speed to market. With over 20,000 employees within 110 facilities in over 20 countries around the globe, we are strategically positioned to coordinate worldwide resources and apply multidisciplinary perspectives in resolving our client's unique challenges. Our client base includes global pharmaceutical companies, biotechnology companies, government agencies and hospitals and academic institutions around the world. At Charles River, we are passionate about our role in improving the quality of people's lives. Our mission, our excellent science and our strong sense of purpose guide us in all that we do, and we approach each day with the knowledge that our work helps to improve the health and well-being of many across the globe. We have proudly worked on 80% of the drugs approved by the U.S. Food and Drug Administration (FDA) in the past five years. We're committed to providing benefits that elevate your quality of life. Based on your position these may include: bonus/incentives based on performance, 401K, paid time off, stock purchase program, Health and wellness coverage, employee and family wellbeing support programs, and work life balance flexibility. **Equal Employment Opportunity** Charles River is an equal opportunity employer and is committed to providing equal employment opportunities for all qualified applicants and employees without regard to race, color, sex, religion, national origin, ancestry, age, mental or physical disability, family status, pregnancy, military or veteran status, or any other characteristic protected by federal, state, or local laws. It is unlawful in some states (including Massachusetts) to require or administer a lie detector test as a condition of employment or continued employment. An employer who violates this law shall be subject to criminal penalties and civil liability. If you are interested in applying to Charles River Laboratories and need special assistance or an accommodation due to a disability to complete any forms or to otherwise participate in the resume submission process, please contact a member of our Human Resources team by sending an e-mail message to crrecruitment_**********. This contact is for accommodation requests for individuals with disabilities only and cannot be used to inquire about the status of applications. For more information, please visit *************** 231144

Laboratory of Dr. Paul Wise, PhD MONELL CHEMICAL SENSES CENTER The Monell Chemical Senses Center is a world-renowned non-profit research institute, and a global leader dedicated to advancing knowledge about the senses of taste, smell, and related senses and translating its discoveries into real-world advances in policy, practice, and behavior. Monell is located in the heart of the vibrant educational and life sciences hub of Philadelphia. The Wise lab is seeking a Research Technician The scientist in this role will work with a dynamic project team to execute psychophysical/sensory experiments toward understanding sensory mechanisms underlying beverage preference. Specific responsibilities include maintaining stocks and purchasing research supplies, recruiting and scheduling human research participants, preparing samples for tasting, executing psychophysical tests following specified protocols, record keeping/data entry, and communicating results to the project team. Skills and Experience Required: B.A. or B.S. in Behavioral or Biological Science, Chemistry, Food Science, or related field Ability to strictly implement research protocols and maintain records Ability to instruct research participants to ensure accurate data collection Strong organizational skills and attention to detail Strong communication and interpersonal skills Evidence of being a good team player Demonstrated passion, enthusiasm, and flexibility Familiarity with MS Office software, including Word and Excel Application Instructions Please apply through our Career Center by following the link below. ************************************************************************************************************************ Id=19000101_000001&job Id=956960&lang=en_US&source=CC2 Equal Employment Opportunity Statement Monell provides equal employment opportunities to all employees and applicants for employment and prohibits discrimination and harassment of any type without regard to race, color, religion, age, sex, national origin, disability status, genetics, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state or local laws. This policy applies to all terms and conditions of employment, including recruiting, hiring, placement, promotion, termination, layoff, recall, transfer, leaves of absence, compensation, and training.

Could you be our next Research Operations Assistant-LIMR at Lankenau Medical Center? Why work as a Research Operations Assistant with Main Line Health? * Make an Impact! The Research Operations Assistant is responsible for the preparation and submission (electronic and hard copy) of grant applications, progress reports, and manuscripts. The Assistant is responsible for the preparation of posters, and general correspondence for investigators, clinicians and other research personnel. The role also assists with the development of LIMR's marketing communications materials and updating LIMR's website and social media content. * Develop and Grow your Career! Invest in furthering your education through seeking certifications or advanced degrees by taking advantage of our Tuition Reimbursement! This position is eligible for up to $6,000 per year based upon your Full or Part-time status. * Join the Team! Like our patients, the Main Line Health Family encompasses a wide range of backgrounds and abilities. Just as each of our patients requires a personalized care plan, each of our employees, physicians, and volunteers, bring distinctive talents to Main Line Health. Regardless of our unique design, we all share a purpose: providing superior service and care. * Position-Specific Benefits include: You are eligible for up to 120 hours of paid time off per year based on your Full or Part-time status. We also offer a number of employee discounts to various activities, services, and vendors... And employee parking is always free! Position: Research Operations Assistant Shift: Monday-Friday 8 am-4:30 pm- this role is 100% onsite. Experience: A minimum of three years of grant editorial, marketing, and public relations experience preferred. Education:: Bachelor's degree in journalism, Communications or similar field preferred. Ability to read, write, speak, understand and communicate in English sufficiently to perform job duties. Additional Information * Requisition ID: 79240 * Employee Status: Regular * Schedule: Full-time * Shift: Day Job * Pay Range: $26.53 - $41.11 * Job Grade: 209

Job Title: Supervisor, Microbiology Job Type: Full-time About Us: As a developer, manufacturer, and supplier of essential medicines, Hikma Pharmaceuticals USA Inc. and its affiliates' purpose is to put better health within reach, every day for millions of patients around the world. We are a trusted, reliable partner and dependable source of over 760 high-quality generic, specialty and branded pharmaceutical products that hospitals, physicians and pharmacists need to treat their patients across North America, the Middle East, North Africa and Europe. Through our global footprint of 30+ manufacturing plants, 8+ R&D centers, and 9,000+ empowered employees, we are committed to making high-quality medicines accessible to the people who need them. Description: We are committed to building a diverse and inclusive team and encourage applications from candidates of all backgrounds. We are seeking a talented and motivated Supervisor, Microbiology. In this role, you will be responsible for the supervision of microbiologists performing pharmaceutical microbiological procedures and the accuracy of test results and raw data generated. The qualified candidate must possess a strong background in sterility testing using isolator technology, sterility testing validation, Biological Indicator studies, water system sampling and testing, bioburden testing, Bacterial Endotoxin Testing (BET), bioburden and BET validation testing, microbial identifications, disinfectant studies, Antimicrobial Effectiveness Testing (AET) and AET validation, growth promotion testing of media/diluents, preparation of cryopreserved microbial cultures, and media/diluent preparation. The qualified candidate must have experience interacting with the FDA and other regulatory/audit groups. This position will be responsible for resolving technical/equipment problems, implementing corrective/preventive actions, writing/ revising standard operating procedures, forms, protocols, test methods and change controls, and providing guidance to less senior staff. Key Responsibilities: * Control the workflow of the microbiology laboratory by supervising, planning, organizing, and directing the activities of the group to support production, stability program, technical services, and R&D. Ensure adequate supplies and equipment are available for testing and maintain expenses at or below budget. Analyze workflow, prepare metrics, and make recommendations to improve productivity and efficiency of group and generate cost savings. * Enforce policies and procedures by monitoring the testing techniques and accuracy of all records and documentation that is done in the lab to ensure compliance. Ensure that team members are properly trained and proficient before allowing them to perform any tasks. Review laboratory records for accuracy, completeness, compliance, and conformance to specifications. Approve laboratory records and ensure initiation of laboratory events and investigations as required. Ensure compliance in the group and keep the department ready for both internal and external audits. * Oversee instrument/equipment maintenance and calibration programs. Troubleshoot and resolve instrument/equipment problems. Ensure maintenance and calibrations are done in accordance with required schedule. Develop proposals for new laboratory systems and equipment. Execute validation studies, prepare summary reports, and change controls. Stay current on laboratory instruments and methods. Ensure completion of all protocols, validations, and summary reports in a timely manner. * Prepare and/or revise SOPs to ensure compliance with regulations and current practices. Keep current on regulations and industry best practices pertaining to the group and update SOPs to improve compliance. Prepare and execute change controls as needed to support changes to the program. * Make appropriate staffing recommendations, support laboratory cross-training efforts, evaluate team member performance, perform appraisals, and ensure team members have development plans. * Resolve deviations. Investigate and/or work closely with investigators to determine root cause of deviations. Prepare all necessary reports in a timely manner to meet compliance requirements and business needs. * Interact with FDA and other regulatory/audit groups. Working knowledge of FDA regulations and application of GLPs and GMPs Qualifications: We value the skills and experiences candidates bring to the table. While we have listed some qualifications below, we encourage candidates to apply even if they do not meet all of them: * Must have a BS and 7 years of pharmaceutical microbiology experience or a MS and 5 years of pharmaceutical microbiology experience. Must have 3-5 years of supervisory experience. * Excellent organizational and project management skills and ability to handle multiple projects. * Excellent writing and computer skills and ability to present data in a logical manner. * Excellent interpersonal, communication, influencing, negotiation skills. * Understanding of scientific strategies and ability to invent new methods or new avenues of investigation. * Demonstrated effectiveness in task completion, decision making, and problem solving. * Working knowledge of FDA regulations, application of GLPs and GMPs. Experience interacting with personnel from regulatory agencies Preferred Qualifications: * Pharmaceutical Microbiology experience with injectable/aseptic manufacturing preferred. Compensation: Base Salary: $66,600 to $133,0750 annually. The compensation for this position will be determined during the interview process and will vary based on multiple factors, including, but not limited to, work location, prior experience and job-related knowledge, relevant skills and expertise, current business needs, and market factors. The Talent Acquisition team can provide more details about the specific salary range for the job location during the hiring process. What We Offer*: * Annual performance bonus, commission, and share potential * Auto enrollment in a Hikma-sponsored 401(k) program at a pre-tax contribution rate of 3% of eligible pay. Hikma will match 100% of the first 6% of eligible pay that you contribute * A generous paid time off (PTO) bank starting with 20 days (prorated based on hire date). Additional days granted upon reaching work milestone anniversaries * 3 personal days (prorated based on hire date) * 11 company paid holidays * Comprehensive benefits including health, dental, vision, mental health, disability, life insurance, prescription drug coverage, and a variety of voluntary benefits * Employee discount program * Wellbeing rewards program * Safety and Quality is a top organizational priority * Career advancement and growth opportunities * Tuition reimbursement * Paid maternity and parental leave * Eligibility requirements apply to some benefits and depend on the job classification, role, and length of employment. Benefits are subject to change as well as specific plan or program terms. Recruiters: Please note that Hikma has a set roster of approved recruiters for specific roles agreed to in advance and does not accept unsolicited resumes or calls from third-party recruiters or employment agencies regarding open positions. In the absence of a signed agreement and approval from Hikma's Human Resources department to submit resumes for a specific position, Hikma will not approve, nor will be under an obligation to make, any payment to such non-approved third-parties in the event a candidate they refer is hired by Hikma. Equal Opportunity Employer: Hikma Pharmaceuticals USA Inc. is an Equal Opportunity Employer. Employment decisions are made without regard to race, color, religion, national or ethnic origin, sex, sexual orientation, gender identity or expression, age, disability, protected veteran status, or other characteristics protected by law. Location: Cherry Hill, NJ, US, 08003 Nearest Major Market: Philadelphia

LanceSoft is a nationally certified Minority Business Enterprise (MBE) that has established itself as a pioneer in providing highly scalable, cost-effective workforce solutions to a diverse set of customers across various industries in the United States. Headquartered in Virginia, LanceSoft currently operates out of several locations in the US and Canada. Title: Research Associate Location: West Chester, PA Duration: 12 Months Job Description: OVERALL RESPONSIBILITIES: The Research Associate - Biomaterials R&D will work in a laboratory environment performing research and development activities on in collaboration with scientists and engineers in support of R&D or product development projects for the DePuy Synthes Biomaterials organization. POSITION DUTIES & RESPONSIBILITIES: The individual will be actively involved in laboratory work related to physical, biological, or chemical testing of prototype medical devices, or drug-device combination products. The individual will work in a team environment, and will use standard chemical or biological laboratory methods and electronic instruments to generate data in collaboration with other researchers. The individual will help design experiments, write protocols, execute experiments, document data appropriately, and communicate results to the research team. The individual will contribute to the efficient operation of laboratories, including maintaining inventories of materials and supplies, and monitoring function of lab instruments, and will provide other project or product support as needed in order to support Synthes' business demands. The individual will know and follow all laws and policies that apply to one's job, and maintain the highest levels of professionalism, ethics and compliance at all times. They will diligently participate in our compliance program-related activities as denoted by your supervisor or our Chief Compliance Officer. This position requires work in a Biosafety Level 2 lab. PROFESSIONAL EXPERIENCE REQUIREMENTS: Experience conducting laboratory experiments is required. Experience with standard biology and chemistry methods and computerized instruments is preferred Ability to multitask and meet deadlines in a fast-paced environment. Must be highly motivated, well organized, team oriented, analytical and flexible. Skilled in Microsoft PowerPoint, Word, Excel, and standard experimental analysis software. EDUCATIONAL REQUIREMENTS: Bachelors degree in chemistry, biology, materials science, or related discipline BS with 3 years of experience or MS with 1 year of experience preferred. OTHER REQUIREMENTS: This position requires less than 5% travel. Additional Information Regards, Anuj Mehta ************

APPLICATION INSTRUCTIONS: * CURRENT PENN STATE EMPLOYEE (faculty, staff, technical service, or student), please login to Workday to complete the internal application process. Please do not apply here, apply internally through Workday. * CURRENT PENN STATE STUDENT (not employed previously at the university) and seeking employment with Penn State, please login to Workday to complete the student application process. Please do not apply here, apply internally through Workday. * If you are NOT a current employee or student, please click "Apply" and complete the application process for external applicants. JOB DESCRIPTION AND POSITION REQUIREMENTS: The Laboratory of Marina Feric in the Department of Biochemistry and Molecular Biology and Center for Eukaryotic Gene Regulation at the Pennsylvania State University is seeking a Research Technologist - Life Sciences (Advanced Professional)/ Lab Manager. The Feric lab takes an interdisciplinary approach to uncover the biomolecular driving forces underlying the organization of the cell in the context of human health and age-related diseases. This position will be responsible for coordinating the ordering, maintaining appropriate inventory, storage, and maintenance of supplies, lab ware, and instruments essential to the operation of the lab; Develop, design and conduct one or more small or moderately complex research projects or experiments in line with plan, reviews progress and evaluates results; Train users in equipment operation and research techniques, explain and demonstrate technology and equipment capabilities, operations limitations and outcomes; Author/co-author on papers, proposals, presentations and reports; Participate in formulating research methods and suggesting options for improving quality and recommending solutions; identify problems and related technical issues leading to long-term solutions by identifying technical approaches for problem solving; Mentor and supervise assigned trainees in the development of technical scientific skills; and May be responsible for operation of a specialized research area or laboratory. Preferred experience includes protein purification, cell culture, and genetic engineering in addition to basic molecular/cell biology techniques. Ideal candidates will have experience training undergraduates, graduates, and postdocs as well as strong communication, organizational, and problem-solving skills. Candidates must be able to work independently and as part of a team. This position typically requires a Bachelor's degree or higher (Master's degree preferred) plus 7 years related experience or an equivalent combination of education and experience. This is a limited term position funded for one year from date of hire with excellent possibility of refunding. Our lab is committed to advancing diversity and inclusion efforts at Penn State and we encourage individuals who identify as members of groups historically underrepresented in STEM to apply. This position will require successful completion of standard background checks. The Pennsylvania State University is committed to and accountable for advancing diversity, equity, and inclusion in all of its forms. We embrace individual uniqueness, foster a culture of inclusive excellence that supports both broad and specific diversity initiatives, leverage the educational and institutional benefits of diversity, and engage all individuals to help them thrive. We value inclusive excellence as a core strength and an essential element of our public service mission. The salary range for this position, including all possible grades is: $42,100.00 - $61,000.00 Salary Structure - additional information on Penn State's job and salary structure. CAMPUS SECURITY CRIME STATISTICS: Pursuant to the Jeanne Clery Disclosure of Campus Security Policy and Campus Crime Statistics Act and the Pennsylvania Act of 1988, Penn State publishes a combined Annual Security and Annual Fire Safety Report (ASR). The ASR includes crime statistics and institutional policies concerning campus security, such as those concerning alcohol and drug use, crime prevention, the reporting of crimes, sexual assault, and other matters. The ASR is available for review here. Employment with the University will require successful completion of background check(s) in accordance with University policies. EEO IS THE LAW Penn State is an equal opportunity, affirmative action employer, and is committed to providing employment opportunities to all qualified applicants without regard to race, color, religion, age, sex, sexual orientation, gender identity, national origin, disability or protected veteran status. If you are unable to use our online application process due to an impairment or disability, please contact ************. Federal Contractors Labor Law Poster PA State Labor Law Poster Affirmative Action Penn State Policies Copyright Information Hotlines University Park, PA

Laboratory of Dr. Paul Wise, PhD MONELL CHEMICAL SENSES CENTER The Monell Chemical Senses Center is a world-renowned non-profit research institute, and a global leader dedicated to advancing knowledge about the senses of taste, smell, and related senses and translating its discoveries into real-world advances in policy, practice, and behavior. Monell is located in the heart of the vibrant educational and life sciences hub of Philadelphia. The Wise lab is seeking a Research Technician The scientist in this role will work with a dynamic project team to execute psychophysical/sensory experiments toward understanding sensory mechanisms underlying beverage preference. Specific responsibilities include maintaining stocks and purchasing research supplies, recruiting and scheduling human research participants, preparing samples for tasting, executing psychophysical tests following specified protocols, record keeping/data entry, and communicating results to the project team. Skills and Experience Required: B.A. or B.S. in Behavioral or Biological Science, Chemistry, Food Science, or related field Ability to strictly implement research protocols and maintain records Ability to instruct research participants to ensure accurate data collection Strong organizational skills and attention to detail Strong communication and interpersonal skills Evidence of being a good team player Demonstrated passion, enthusiasm, and flexibility Familiarity with MS Office software, including Word and Excel Application Instructions Please apply through our Career Center by following the link below. ************************************************************************************************************************ Id=19000101_000001&job Id=956960&lang=en_US&source=CC2 Equal Employment Opportunity Statement Monell provides equal employment opportunities to all employees and applicants for employment and prohibits discrimination and harassment of any type without regard to race, color, religion, age, sex, national origin, disability status, genetics, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state or local laws. This policy applies to all terms and conditions of employment, including recruiting, hiring, placement, promotion, termination, layoff, recall, transfer, leaves of absence, compensation, and training.

The research tech assists in experiments as part of a team of bio-medical researchers. They will also record experimental results and collaborate effectively with other team members. 1 Performs a variety of basic, analytical and technical laboratory experiments, analysis and other duties as required in the study, following established methods and procedures. 2. Assist with data collection. (e.g. manage, service and operate research devices; record observations). 3. Prepare internal reports related to research or lab operations 4. Assist in general maintenance of the laboratory. Additional responsibilities and requirements: Use training in developing and applying Large Language Models and Machine Learning models to contribute to drug discovery approaches related to an NIH-sponsored research project in the lab focused on identifying/developing G protein-coupled receptor-targeting drugs for use in treating obstructive lung diseases. Demonstrated expertise, or prior job experience focused on employing AI tools, is required. Research experience in basic biology or biochemistry is preferred but not required; a candidate with training or experience in biological science but with good AI competencies will be considered. Expected to learn new techniques to accomplish the research project. Education Requirements: Bachelor's Required. Work Shift Workday Day (United States of America) Worker Sub Type Regular Primary Location Address 1020 Locust Street, Philadelphia, Pennsylvania, United States of America Nationally ranked, Jefferson, which is principally located in the greater Philadelphia region, Lehigh Valley and Northeastern Pennsylvania and southern New Jersey, is reimagining health care and higher education to create unparalleled value. Jefferson is more than 65,000 people strong, dedicated to providing the highest-quality, compassionate clinical care for patients; making our communities healthier and stronger; preparing tomorrow's professional leaders for 21st-century careers; and creating new knowledge through basic/programmatic, clinical and applied research. Thomas Jefferson University, home of Sidney Kimmel Medical College, Jefferson College of Nursing, and the Kanbar College of Design, Engineering and Commerce, dates back to 1824 and today comprises 10 colleges and three schools offering 200+ undergraduate and graduate programs to more than 8,300 students. Jefferson Health, nationally ranked as one of the top 15 not-for-profit health care systems in the country and the largest provider in the Philadelphia and Lehigh Valley areas, serves patients through millions of encounters each year at 32 hospitals campuses and more than 700 outpatient and urgent care locations throughout the region. Jefferson Health Plans is a not-for-profit managed health care organization providing a broad range of health coverage options in Pennsylvania and New Jersey for more than 35 years. Jefferson is committed to providing equal educa tional and employment opportunities for all persons without regard to age, race, color, religion, creed, sexual orientation, gender, gender identity, marital status, pregnancy, national origin, ancestry, citizenship, military status, veteran status, handicap or disability or any other protected group or status. Benefits At Jefferson, we offer a comprehensive total rewards package designed to support the health and well-being of our colleagues and their families. It includes a wide range of benefits including competitive pay, health and retirement benefits, life and disability insurance, paid time off, educational benefits, financial and mental health resources and much more. Our diverse benefits offerings ensure you have the coverage and access to services you need to thrive both personally and professionally.

NBME is seeking a highly skilled and innovative Research Technologist to support the development of early-stage prototypes and experimental tools used in assessment research. In this role, you will work closely with NBME's Construct and Research teams to design and implement rapid prototypes that explore new assessment formats and user interactions. Much of this work is "greenfield," allowing you to independently build functional research tools using Shiny, low-code/no-code technologies, and modern engineering frameworks such as Angular and AWS. You will also collaborate with product engineering teams to adapt and extend existing production systems for later-stage efficacy studies, ensuring research findings can transition smoothly into product development. This is an ideal opportunity for a self-directed engineer who enjoys problem-solving, learning new technologies, and working at the intersection of research and innovation. This role has been designated as primarily remote, meaning it requires little to no onsite attendance. While this role can be designated as remote, you are offered the flexibility to select if you prefer to work primarily remotely, hybrid, or onsite. We're open to considering candidates within 50 miles of our office location in Philadelphia, PA. At NBME, we continue to innovate and improve how we fulfill the evolving needs of the healthcare community. This commitment starts and ends with the people at NBME. By recruiting and empowering talented individuals from various disciplines and backgrounds, which includes professionals with diverse life experiences, abilities, and perspectives, NBME can take a well-informed, robust approach to advancing medical education and assessment for years to come. RESPONSIBILITIES Collaborate closely with research teams to understand study goals, gather requirements, and design functional prototypes that support early-stage assessment innovation. Independently develop rapid prototypes using tools such as Shiny, survey platforms, low/no-code environments, and modern front-end frameworks. Modify and extend existing production systems (Angular, AWS) to support efficacy studies, experimental groupings, and customized research conditions. Conduct testing, validation, and iteration of prototypes to ensure they meet research objectives and usability expectations. Contribute to product development workflows through hands-on coding, technical exploration, and quality assurance support. Evaluate emerging prototyping tools and technologies, recommending those that align with research needs and accelerate innovation. Collaborate with cross-functional teams to ensure continuity between research prototypes and production software. Communicate progress and technical considerations clearly to research, engineering, and product stakeholders. QUALIFICATIONS Skills and Abilities Proficiency in multiple programming languages and frameworks, including strong front-end development skills (Angular 2+, TypeScript, JavaScript, HTML, CSS). Experience with rapid prototyping using low-code/no-code tools, Shiny (or willingness to learn), AI-assisted development tools, and related platforms. Strong understanding of algorithms, data structures, system design, and software architecture. Ability to work independently with limited direction, making sound technical decisions in ambiguous or exploratory environments. Excellent problem-solving skills with the ability to pivot quickly and manage multiple concurrent research efforts. Strong collaboration and communication skills, with the ability to work effectively with academic researchers and product engineering teams. Commitment to continuous learning and staying current with emerging technologies and prototyping approaches. Experience 8+ years of professional software development experience spanning the full SDLC. Experience building prototypes, experimental interfaces, or research-oriented software strongly preferred. Experience with AWS services such as Lambda, S3, DynamoDB, SQL, Node.js, and CDK is a plus. Familiarity with source code control concepts and UI/UX design principles. Experience with R is a plus Education Bachelor's degree in computer science or a related technical field ; equivalent experience will be considered. About NBME NBME is a not-for-profit organization that specializes in the creation of assessments and learning tools for physicians and health professionals. Our mission is to advance assessment of these professionals to achieve optimal care for all, supporting the development of a highly effective, diverse and compassionate health care workforce. Founded in 1915, NBME develops and manages the United States Medical Licensing Examination with the Federation of State Medical Boards. We offer a comprehensive portfolio of assessment products for every stage of the medical school journey and provide assessment services to various health profession organizations. We are dedicated to advancing innovative assessment approaches through research, collaboration and contributions to the medical education and assessment communities. In 2024, we expanded our assessment capabilities to include simulation through the acquisition of MedVR Education. Learn more on NBME's website. NBME's Community Collaborations and Contributions NBME believes that a key path to meeting our mission is collaborating with and supporting our communities. Our Community Collaborations and Contributions programs provide resources and recognition to medical educators and researchers advancing the field of assessment throughout their careers. In addition, we invest in fee assistance, scholarships and pathway programs to aid learners and help support increased representation in health care. Headquartered in Philadelphia, NBME also gives to local organizations that advance health equity and access and positively impact social determinants of health. Compensation we are offering for this position is at $110,560 - 149,256/year. Please note that the offered rate for this position typically aligns with the minimum to midrange of this grade, but it can vary based on the successful candidate's qualifications and experience, department budget, and an internal equity review. The NBME offers competitive salaries, excellent benefits, and a rewarding work environment. Excellent Benefits include: Healthcare, Dental, Prescription, and Vision plans; 401(k) w/match, Tuition Reimbursement Plan, Commuter Benefit: Public Transit or Parking options. Remote Friendly Workplace. NBME is an Equal Opportunity Employer. We will consider all qualified applicants for employment without regard to race; color; sex; gender identity; sexual orientation; religious practices and observances; national origin; pregnancy, childbirth, or related medical conditions; status as a protected veteran or spouse/family member of a protected veteran; or disability.

NBME is seeking a highly skilled and innovative Research Technologist to support the development of early-stage prototypes and experimental tools used in assessment research. In this role, you will work closely with NBME's Construct and Research teams to design and implement rapid prototypes that explore new assessment formats and user interactions. Much of this work is "greenfield," allowing you to independently build functional research tools using Shiny, low-code/no-code technologies, and modern engineering frameworks such as Angular and AWS. You will also collaborate with product engineering teams to adapt and extend existing production systems for later-stage efficacy studies, ensuring research findings can transition smoothly into product development. This is an ideal opportunity for a self-directed engineer who enjoys problem-solving, learning new technologies, and working at the intersection of research and innovation. This role has been designated as primarily remote, meaning it requires little to no onsite attendance. While this role can be designated as remote, you are offered the flexibility to select if you prefer to work primarily remotely, hybrid, or onsite. We're open to considering candidates within 50 miles of our office location in Philadelphia, PA. At NBME, we continue to innovate and improve how we fulfill the evolving needs of the healthcare community. This commitment starts and ends with the people at NBME. By recruiting and empowering talented individuals from various disciplines and backgrounds, which includes professionals with diverse life experiences, abilities, and perspectives, NBME can take a well-informed, robust approach to advancing medical education and assessment for years to come. RESPONSIBILITIES * Collaborate closely with research teams to understand study goals, gather requirements, and design functional prototypes that support early-stage assessment innovation. * Independently develop rapid prototypes using tools such as Shiny, survey platforms, low/no-code environments, and modern front-end frameworks. * Modify and extend existing production systems (Angular, AWS) to support efficacy studies, experimental groupings, and customized research conditions. * Conduct testing, validation, and iteration of prototypes to ensure they meet research objectives and usability expectations. * Contribute to product development workflows through hands-on coding, technical exploration, and quality assurance support. * Evaluate emerging prototyping tools and technologies, recommending those that align with research needs and accelerate innovation. * Collaborate with cross-functional teams to ensure continuity between research prototypes and production software. * Communicate progress and technical considerations clearly to research, engineering, and product stakeholders. QUALIFICATIONS Skills and Abilities * Proficiency in multiple programming languages and frameworks, including strong front-end development skills (Angular 2+, TypeScript, JavaScript, HTML, CSS). * Experience with rapid prototyping using low-code/no-code tools, Shiny (or willingness to learn), AI-assisted development tools, and related platforms. * Strong understanding of algorithms, data structures, system design, and software architecture. * Ability to work independently with limited direction, making sound technical decisions in ambiguous or exploratory environments. * Excellent problem-solving skills with the ability to pivot quickly and manage multiple concurrent research efforts. * Strong collaboration and communication skills, with the ability to work effectively with academic researchers and product engineering teams. * Commitment to continuous learning and staying current with emerging technologies and prototyping approaches. Experience * 8+ years of professional software development experience spanning the full SDLC. * Experience building prototypes, experimental interfaces, or research-oriented software strongly preferred. * Experience with AWS services such as Lambda, S3, DynamoDB, SQL, Node.js, and CDK is a plus. * Familiarity with source code control concepts and UI/UX design principles. * Experience with R is a plus Education * Bachelor's degree in computer science or a related technical field required; equivalent experience will be considered. About NBME NBME is a not-for-profit organization that specializes in the creation of assessments and learning tools for physicians and health professionals. Our mission is to advance assessment of these professionals to achieve optimal care for all, supporting the development of a highly effective, diverse and compassionate health care workforce. Founded in 1915, NBME develops and manages the United States Medical Licensing Examination with the Federation of State Medical Boards. We offer a comprehensive portfolio of assessment products for every stage of the medical school journey and provide assessment services to various health profession organizations. We are dedicated to advancing innovative assessment approaches through research, collaboration and contributions to the medical education and assessment communities. In 2024, we expanded our assessment capabilities to include simulation through the acquisition of MedVR Education. Learn more on NBME's website. NBME's Community Collaborations and Contributions NBME believes that a key path to meeting our mission is collaborating with and supporting our communities. Our Community Collaborations and Contributions programs provide resources and recognition to medical educators and researchers advancing the field of assessment throughout their careers. In addition, we invest in fee assistance, scholarships and pathway programs to aid learners and help support increased representation in health care. Headquartered in Philadelphia, NBME also gives to local organizations that advance health equity and access and positively impact social determinants of health. Compensation we are offering for this position is at $110,560 - 149,256/year. Please note that the offered rate for this position typically aligns with the minimum to midrange of this grade, but it can vary based on the successful candidate's qualifications and experience, department budget, and an internal equity review. The NBME offers competitive salaries, excellent benefits, and a rewarding work environment. Excellent Benefits include: Healthcare, Dental, Prescription, and Vision plans; 401(k) w/match, Tuition Reimbursement Plan, Commuter Benefit: Public Transit or Parking options. Remote Friendly Workplace. NBME is an Equal Opportunity Employer. We will consider all qualified applicants for employment without regard to race; color; sex; gender identity; sexual orientation; religious practices and observances; national origin; pregnancy, childbirth, or related medical conditions; status as a protected veteran or spouse/family member of a protected veteran; or disability.

*Please note that while we welcome applications, we do not have any current openings on our teams for these roles. We will update this space as new opportunities become available.* INTEGRAL MOLECULAR, Inc., is a Philadelphia biotech company specializing in the discovery and characterization of therapeutic antibodies using cutting-edge technology platforms that are enabling the discovery of novel therapeutics against intractable targets. We are a close-knit, small company composed of smart, curious scientists that takes an active interest in nurturing and developing all our team members. Our company is in an exciting growth phase where we are launching new products and reaching new markets. To support our growth, we seek a Research Technician to join our Membrane Proteome Array research team. Opportunities: Opportunity to develop laboratory molecular biology skills Opportunity for scientific development leading to professional advancement Responsibilities: Setup and execute routine laboratory experiments Perform DNA isolation and associated quality control assays Maintain plasmid library using high throughput techniques Perform tasks using aseptic techniques including working within a biological safety cabinet Organize large data sets within an Excel spreadsheet Required Qualifications: 6 months - 2 years hands-on laboratory experience Associate or Bachelor's degree in Biology, Chemistry, medical technology or related field Demonstrated ability to adhere to standard operating protocols and learn quickly Ability to work in a team-based environment with a collaborative and proactive attitude Excellent communication skills Attention to detail Other Qualifications (desired but not necessary): Experience with molecular biology techniques such as (PCR, E. coli transformation, Sanger sequencing and analysis) Experience performing quality control assays Previous general work experience Please note: We are only accepting local candidates who live within the greater Philadelphia metro area and can commute to our offices daily for this position. Integral Molecular is an Equal Opportunity Employer.

Research Asst III25003501Description Temple University's School of Medicine is searching for a Research Assistant!Salary Range: $26. 98/hr. A variety of important factors are reviewed by HR when considering salary, including job duties, the applicant's education and experience, all relevant internal equity considerations, department budget, and funding source. Become a part of the Temple family and you will have access to the following:Full medical, dental, vision coverage Paid time off9 Federally Observed Paid Holidays3 Personal DaysTuition remission - eligible employees and their dependents can obtain a degree TUITION FREEA generous retirement plan and so much more!Position Summary:Conducting in vivo operant self-administration studies in rats to assess effects of glutamate release inhibitors and transport activators on methamphetamine (METH) self-administration. This includes conducting surgeries to implant catheters into the jugular vein of rats and conducting behavioral experiments to assess effects on METH intake, reinforcing strength, extinction, and relapse-like behaviors. Job Details:* This is a grant funded position Required Education and Experience:* Bachelor's Degree degree emphasis on neuroscience, biology, and clinical psychology and possesses some directly related experience. An equivalent combination of education and experience may be considered. Required Skills and Abilities:* Experience with drug abuse liability assessments and surgical procedures* Experience with the behavioral assays including locomotor, self-administration, conditioned place preference, forced swim assay, elevated plus maze assay* Experience with cellular techniques especially qPCR to test mRNA levels of different neurochemical markers in the glutamate and cytokine systems. Essential Duties:* Analyzing rat self-administration data includes METH intake, reinforcing efficacy, and relapse-like behaviors. * Analyzing rat self-administration data using Microsoft Excel and GraphPad Prism. This includes statistical analysis using ANOVA and post-hoc tests such as Dunnett's and Tukey's analysis. It also includes preparation of graphs for publication purposes using Prism and PowerPoint. * Interpretating rat self-administration results involving the effects of glutamatergic drugs on METH self-administration behaviors. * Preparing manuscripts for publication including writing up Methods and Results sections for manuscripts. Temple University is committed to a policy of equal opportunity for all in every aspect of its operations, including employment, service, and educational programs. The University has pledged not to discriminate on the basis of age, color, disability, marital status, national origin or ethnic origin, race, religion, sex (including pregnancy), sexual orientation, gender identity, genetic information or veteran status. Compliance Statement: In the performance of their functions as detailed in the position description employees have an obligation to avoid ethical, legal, financial and other conflicts of interest to ensure that their actions and outside activities do not conflict with their primary employment responsibilities at the institution. Employees are also expected to understand and be in compliance with applicable laws, University and employment policies and regulations, including NCAA regulations for areas and departments which their essential functions cause them to interact. Temple University's Annual Security and Fire Safety Report contains statistics, policies, and procedures related to campus safety. Go here to review: *************** temple. edu/reports-logs/annual-security-report You may request a copy of the report by calling Temple University's Department of Public Safety at ************. Primary Location: Pennsylvania-Philadelphia-Health Sciences Campus (HSC)-Medical Education and Research BuildingWork Locations: Medical Education and Research Building Schedule: Part-time Job Posting: Jan 8, 2026, 7:39:21 PM

The University of Pennsylvania, the largest private employer in Philadelphia, is a world-renowned leader in education, research, and innovation. This historic, Ivy League school consistently ranks among the top 10 universities in the annual U.S. News & World Report survey. Penn has 12 highly-regarded schools that provide opportunities for undergraduate, graduate and continuing education, all influenced by Penn's distinctive interdisciplinary approach to scholarship and learning. As an employer Penn has been ranked nationally on many occasions with the most recent award from Forbes who named Penn one of America's Best Large Employers in 2023. Penn offers a unique working environment within the city of Philadelphia. The University is situated on a beautiful urban campus, with easy access to a range of educational, cultural, and recreational activities. With its historical significance and landmarks, lively cultural offerings, and wide variety of atmospheres, Philadelphia is the perfect place to call home for work and play. The University offers a competitive benefits package that includes excellent healthcare and tuition benefits for employees and their families, generous retirement benefits, a wide variety of professional development opportunities, supportive work and family benefits, a wealth of health and wellness programs and resources, and much more. Posted Job Title Research Technician C Job Profile Title Technician, Research Laboratory C Summary A research technician position is available in the Folkert lab in the Department of Surgery at the University of Pennsylvania. We are seeking a highly motivated individual to work in collaboration with the Principal Investigator, students, residents and/or graduate students to study the immune response to peritoneal surface malignancies, including appendix cancer, colon cancer, and peritoneal mesothelioma. A successful candidate would be detail-oriented, highly organized, and able to work independently after appropriate training and supervision in basic lab techniques and safety. Prior wet lab experience is advantageous, although additional training will be provided. This position will be an excellent opportunity to gain experience performing basic and translational research using patient-derived specimens, offer opportunities for publication, and the chance to work in a collaborative, multidisciplinary setting. · The successful candidate will perform a broad range of routine laboratory tests and procedures to support medical and scientific research. Performs experiments and basic cell biology and immunology techniques, including cell culture, RNA extraction, cDNA synthesis, RT-qPCR, flow cytometry and histology. Collects specimens from the operating room and processes them for downstream assays including cell culture, RNA extraction, sequencing and flow cytometry. Performs mouse experiments including tumor transplants, tumor volume measurements and drug treatments. Assists senior researchers with experiments and provides laboratory support through preparation of media and reagents, equipment upkeep, supply ordering, inventory, and overall lab organization. Job Responsibilities o Conduct experiments and enter findings into computer o Analyze the results of tests or experiments to ensure conformity to specifications, and generating preliminary figures from data generated towards eventual inclusion in a manuscript o Processing samples, including collecting samples from the operating room and processing for downstream applications. Preparation and shipping of samples when needed. o Collect blood or tissue samples from patients. o Maintaining a detailed log/database of collected specimens. o Maintain and passage cell cultures o Optimize novel in vitro culture systems, including slice culture and organoid models o Perform murine tumor transplants, tumor volume measurements and drug treatments o Maintaining a detailed log/database of collected specimens. o Provide scientific and technical guidance for ongoing projects o Maintain organized laboratory records and ensure compliance with safety protocols o Maintain inventory of lab supplies, order supplies, oversee general laboratory maintenance and safety compliance, Collection and processing of human blood and tumor specimens and maintaining a database of collected specimens, Collecting and analyzing data through biological assays and microscopy, including cell culture assays, flow cytometry and RT-qPCR, Perform routine animal studies, including tumor and tissue harvests and preparations as well as drug treatments, Other duties and responsibilities as assigned. o Other duties and responsibilities as assigned o He/she will collaborate closely with other lab members and the Principal Investigator on projects. Qualifications Bachelor of Science and 0 to 1 years of experience or equivalent combination of education and experience is required. This position is contingent upon grant funding. Job Description A research technician position is available in the Folkert lab in the Department of Surgery at the University of Pennsylvania. We are seeking a highly motivated individual to work in collaboration with the Principal Investigator, students, residents and/or graduate students to study the immune response to peritoneal surface malignancies, including appendix cancer, colon cancer, and peritoneal mesothelioma. A successful candidate would be detail-oriented, highly organized, and able to work independently after appropriate training and supervision in basic lab techniques and safety. Prior wet lab experience is advantageous, although additional training will be provided. This position will be an excellent opportunity to gain experience performing basic and translational research using patient-derived specimens, offer opportunities for publication, and the chance to work in a collaborative, multidisciplinary setting. · The successful candidate will perform a broad range of routine laboratory tests and procedures to support medical and scientific research. Performs experiments and basic cell biology and immunology techniques, including cell culture, RNA extraction, cDNA synthesis, RT-qPCR, flow cytometry and histology. Collects specimens from the operating room and processes them for downstream assays including cell culture, RNA extraction, sequencing and flow cytometry. Performs mouse experiments including tumor transplants, tumor volume measurements and drug treatments. Assists senior researchers with experiments and provides laboratory support through preparation of media and reagents, equipment upkeep, supply ordering, inventory, and overall lab organization. Job Responsibilities o Conduct experiments and enter findings into computer o Analyze the results of tests or experiments to ensure conformity to specifications, and generating preliminary figures from data generated towards eventual inclusion in a manuscript o Processing samples, including collecting samples from the operating room and processing for downstream applications. Preparation and shipping of samples when needed. o Collect blood or tissue samples from patients. o Maintaining a detailed log/database of collected specimens. o Maintain and passage cell cultures o Optimize novel in vitro culture systems, including slice culture and organoid models o Perform murine tumor transplants, tumor volume measurements and drug treatments o Maintaining a detailed log/database of collected specimens. o Provide scientific and technical guidance for ongoing projects o Maintain organized laboratory records and ensure compliance with safety protocols o Maintain inventory of lab supplies, order supplies, oversee general laboratory maintenance and safety compliance, Collection and processing of human blood and tumor specimens and maintaining a database of collected specimens, Collecting and analyzing data through biological assays and microscopy, including cell culture assays, flow cytometry and RT-qPCR, Perform routine animal studies, including tumor and tissue harvests and preparations as well as drug treatments, Other duties and responsibilities as assigned. o Other duties and responsibilities as assigned o He/she will collaborate closely with other lab members and the Principal Investigator on projects. Qualifications + Bachelor of Science and 0 to 1 years of experience or equivalent combination of education and experience is required. This position is contingent upon grant funding. Job Location - City, State Philadelphia, Pennsylvania Department / School Perelman School of Medicine Pay Range $19.23 - $19.23 Hourly Rate Salary offers are made based on the candidate's qualifications, experience, skills, and education as they directly relate to the requirements of the position, and in alignment with salary ranges based on external market data for the job's level. Internal organization and peer data at Penn are also considered. Equal Opportunity Statement The University of Pennsylvania is an equal opportunity employer. Candidates are considered for employment without regard to race, color, sex, sexual orientation, religion, creed, national origin (including shared ancestry or ethnic characteristics) , citizenship status, age, disability, veteran status or any class protected under applicable federal, state or local law . Special Requirements Background checks may be required after a conditional job offer is made. Consideration of the background check will be tailored to the requirements of the job. University Benefits + Health, Life, and Flexible Spending Accounts : Penn offers comprehensive medical, prescription, behavioral health, dental, vision, and life insurance benefits to protect you and your family's health and welfare. You can also use flexible spending accounts to pay for eligible health care and dependent care expenses with pre-tax dollars. + Tuition : Take advantage of Penn's exceptional tuition benefits . You, your spouse, and your dependent children can get tuition assistance here at Penn. Your dependent children are also eligible for tuition assistance at other institutions. + Retirement: Penn offers generous retirement plans to help you save for your future. Penn's Basic, Matching, and Supplemental retirement plans allow you to save for retirement on a pre-tax or Roth basis. Choose from a wide variety of investment options through TIAA and Vanguard. + Time Away from Work: Penn provides you with a substantial amount of time away from work during the course of the year. This allows you to relax, take vacations, attend to personal affairs, recover from illness or injury, spend time with family-whatever your personal needs may be. + Long-Term Care Insurance: In partnership with Genworth Financial, Penn offers faculty and staff (and your eligible family members) long-term care insurance to help you cover some of the costs of long-term care services received at home, in the community or in a nursing facility. If you apply when you're newly hired, you won't have to provide proof of good health or be subject to underwriting requirements. Eligible family members must always provide proof of good health and are subject to underwriting. + Wellness and Work-life Resources : Penn is committed to supporting our faculty and staff as they balance the competing demands of work and personal life. That's why we offer a wide variety of programs and resources to help you care for your health, your family, and your work-life balance. + Professional and Personal Development: Penn provides an array of resources to help you advance yourself personally and professionally. + University Resources: As a member of the Penn community, you have access to a wide range of University resources as well as cultural and recreational activities. Take advantage of the University's libraries and athletic facilities, or visit our arboretum and art galleries. There's always something going on at Penn, whether it's a new exhibit at the Penn Museum, the latest music or theater presentation at the Annenberg Center, or the Penn Relays at Franklin Field to name just a few examples. As a member of the Penn community, you're right in the middle of the excitement-and you and your family can enjoy many of these activities for free. + Discounts and Special Services : From arts and entertainment to transportation and mortgages, you'll find great deals for University faculty and staff. Not only do Penn arts and cultural centers and museums offer free and discounted admission and memberships to faculty and staff. You can also enjoy substantial savings on other goods and services such as new cars from Ford and General Motors, cellular phone service plans, movie tickets, and admission to theme parks. + Flexible Work Hours: Flexible work options offer creative approaches for completing work while promoting balance between work and personal commitments. These approaches involve use of non-traditional work hours, locations, and/or job structures. + Penn Home Ownership Services: Penn offers a forgivable loan for eligible employees interested in buying a home or currently residing in West Philadelphia, which can be used for closing costs or home improvements. + Adoption Assistance: Penn will reimburse eligible employees on qualified expenses in connection with the legal adoption of an eligible child, such as travel or court fees, for up to two adoptions in your household. To learn more, please visit: ******************************************** The University of Pennsylvania's special character is reflected in the wide variety of backgrounds, experiences, and perspectives of the Penn community. We seek talented faculty and staff who will constitute a vibrant community and help create an educational and working environment that best supports the University's commitment to excellence in teaching, research, and scholarship. The University of Pennsylvania is an equal opportunity employer. Candidates are considered for employment without regard to race, color, sex, sexual orientation, religion, creed, national origin (including shared ancestry or ethnic characteristics), citizenship status, age, disability, veteran status, or any class protected under applicable federal, state or local law.