Research technician jobs in Camden, NJ

QC Environmental Monitoring Expert Duration: 06 months Fully Onsite First Shift: Monday-Friday with evening and weekend shifts (9am to 3pm core hours) with evening and weekend shifts as needed (Potential scheduling flexibility with management approval). (OT) may be required. There will be a 2-week training period Job Description: Perform Environmental Monitoring in GMP Classified areas including viable air, non-viable air, surface sampling, and settling plate analysis. Prepare Environmental Monitoring samples for analysis Participate in laboratory investigations associated with Environmental Monitoring Enter data in appropriate GMP systems (LIMS/LES, Veeva, SAP/ERP) Complete necessary SOP and Hands-On training associated with Environmental Monitoring Requirements Must be experienced in Environmental monitoring in GMP area (minimum of 3-5 years experience) Education: Minimum of a BS in biology/microbiology or related science field

*New Rates* Join us in shaping the future of healthcare as an allied health professional at Redeemer Health. We offer a dynamic environment equipped with state-of-the-art facilities and a culture that prioritizes safety. With our workforce spanning southeastern Pennsylvania and New Jersey, we celebrate diversity and inclusivity. We're committed to your long-term success, providing competitive benefits, as well as resources like educational assistance and a unique onboarding program that sets you up for long-termsuccess while introducing you to our mission and celebrated service orientation. Join us, and let's make a difference together. SUMMARY OF JOB: Operates/monitors all types of Cath Lab equipment under the supervision of the Cath Lab physician and/or Clinical Unit Coordinator. Assists the physician and nursing personnel during Diagnostic & Interventional catheterization procedures. Provides various types of patient care in the Cardiovascular Lab under the direct supervision of a registered nurse or physician. There are times, based upon unusual work volume (increase or decrease), emergencies, or severe weather conditions, when it will become necessary for you to accept and perform a work assignment or assist with tasks which are outside of your regular duties or cross-trained assignment in which you possess the basic knowledge and skill to perform the assignment safely. CONNECTING TO MISSION: All individuals, within the scope of their position, are responsible for performing their job in light of the Mission & Values of the Health System. Regardless of position, every job contributes to the challenge of providing health care. There is an on-going responsibility for ensuring that the values of Respect, Compassion, Justice, Hospitality, Holistic Approach, Stewardship and Collaboration are present in all interactions with patients, residents, families and one another in the services we provide. RECRUITMENT REQUIREMENTS: Graduate of an American Registry of Radiologic Technologists (ARRT) accredited school of Radiology or Cardiovascular Technology. ARRT or CVT/RCIS Certification preferred. 6 months of Diagnostic Radiology or Interventional Radiology/Catheterization procedure experience. Will consider graduates of CVT programs with extensive clinical rotations. Successful completion of basic EKG Arrhythmia course or equivalent training & experience. Current BLS certification. ACLS certification preferred. Ability to work various shifts and/or on-call hours when required. LICENSE AND REGULATORY REQUIREMENTS: Current Pennsylvania AART or CVT/RCIS registration preferred. CPR and ACLS certifications EQUAL OPPORTUNITY: Redeemer Health is an equal opportunity employer. We prohibit discrimination in employment due to race, color, gender, religion, creed, national origin, age, sex, sexual orientation, gender identity or expression, disability veteran status or any other protected classification required by law.

The Epidemiologist Research Associate is responsible for all infectious disease surveillance, investigations and interventions utilizing state-of-the-art public health principles, and methodologies of the science of epidemiology. Work shall be performed under the professional and programmatic oversight of the Delaware County Health Department Administration using relevant national standards of excellence; designated epidemiology and analytical tools and standards; and Delaware County Health Department policies, procedures and regulations. The position provides a 24/7/365 expert, consultative service for the scientific disciplines of epidemiology, medicine, public health and disease prevention and control within the County. The position may supervise professional, technical and clerical subordinates. Incumbents shall conduct assessments of public health hazards; carry out epidemiological investigations; communicate/consult with regional and local health officials; and attend professional meetings throughout the United States as guided by Delaware County Health Department Administration. The Epidemiology Research Associate reports to the Delaware County Health Department Epidemiologist. Essential Duties * Responsible for disease outbreak investigations, managing and analyzing population-based data to identify risk factors and health needs, and analyzing service-based data to provide program evaluations * Routinely analyze births, deaths, and disease data, and provide epidemiological interpretation * Conduct disease cluster analysis by examining population-based data, preparing statistics, providing epidemiological interpretation of statistics, and writing reports * Lead design, planning, analysis, and reporting of information and health intelligence based on large population-based data sets * Assist in the evaluation of interventions or programs' effectiveness * Research public health issues and prepare health reports and issue briefs * Assist other staff members gain knowledge of basic epidemiology tools and techniques * Participate in coordinated response activities during public health emergencies through the department's emergency management and incident command system * Provide technical assistance for users of surveillance systems and/or other databases * Member of health needs assessment Core Committee * Work shall be performed under the professional and programmatic oversight of the Delaware County Health Department, Epidemiology Division * The ERA provides expert consultative service for the scientific disciplines of epidemiology, medicine, public health and disease prevention and control within the County * The position may supervise professional, technical, and clerical subordinates * Incumbents shall conduct assessments of public health hazards; carry out epidemiological investigations; communicate/consult with regional and local health officials; and attend professional meetings * Perform other duties, tasks and special projects, as required. Qualifications * Master's degree in public health with concentration in epidemiology and/or biostatistics * 3-5 years of field experience in detecting, controlling, or reporting illness and diseases preferred * Skills in data analysis based on large data sets, questionnaires, and interviews * Strong skills in oral and written communication, which includes preparation of reports, training education to public health partners and the general public, preparing written manuscripts for peer-reviewed journals and other publications * Expertise with statistical software SAS, STATA, SPSS, Epi-Info, etc. * Familiarity with complex surveys and statistical analysis, e.g., CDC NHANES * Demonstrated experience effectively leading and directing staff and/or volunteers * Valid driver's license and ability to pass a background check * Ability to interact appropriately and effectively with a wide range of persons * Ability to maintain and handle confidential information * Ability to follow protocol, procedures, and established guidelines * Ability to be flexible and adapt to changing circumstances and needs * A strong work ethic and ability to manage a demanding and changing workload * Strong relationship-building skills Preferred Skills, Knowledge & Experience * Strong critical thinking and problem-solving abilities to identify, analyze, and address complex epidemiological issues. * Commitment to maintaining high ethical standards in research, including adherence to ethical guidelines and regulations governing human subjects research. * Ability to adapt to changing research environments and methodologies, and to

Research Technician - Alhadeff Lab 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 Alhadeff lab at the Monell Chemical Senses Center in Philadelphia, Pennsylvania, USA, is seeking a full-time Research Technician to help with ongoing research on gut-brain signaling and how it contributes to the neural control of feeding behavior. The position involves assisting with lab organization and management as well as performing primary neuroscience research using rodent models. The Research Technician will be trained by PhD-level staff in basic neuroscience research techniques, including behavioral assays, imaging, optogenetics, chemogenetics, histology, colony care, breeding and management techniques, and basic wet-lab and organizational skills. Flexibility with scheduled hours is necessary. Although we are open to applicants with all types of career goals, this position is an especially good opportunity for those who are considering applying to graduate school in Neuroscience, Biology, or a related field in the future. We particularly encourage candidates from diverse and/or underrepresented backgrounds to apply. Please visit ******************* for more information on the ongoing research projects that this position will support. Key Responsibilities: Learning and performing basic neuroscience techniques in rodent models, including behavioral assays, imaging, optogenetics, chemogenetics, and/or histology Learning and performing surgical techniques Working with other lab members on collaborative research projects Analyzing data, writing experimental reports and data summaries,and presenting research findings to others in the lab Assisting with lab organization, cleaning, ordering, and management Qualifications: Minimum requirements for the position: BA/BS in Biology or related sciences is preferred Experience with rodent models is preferred Excellent organizational and interpersonal skills are essential. Ideal candidates should be detail-oriented and able to work independently Location: Monell Chemical Senses Center, Philadelphia, Pennsylvania Reports To: Amber Alhadeff, PhD. Application Instructions Please apply through our Career Center by following the link below. ************************************************************************************************************************ Id=19000101_000001&job Id=955388&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.

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 ************

The Monell Chemical Senses Center provides post-baccalaureate students with opportunities for hands-on lab research and other professional activities. Enrollment in any post-baccalaureate program Ability to commute to Monell (3500 Market Street, Philadelphia, 19104)

The Biobank and Molecular Analysis Program (BMAP) at Nemours Children's Health is seeking a full-time Clinical Research Technologist to perform a primary specimen processing and shipping role in the CAP accredited program. This individual will work under the supervision of senior laboratory staff and performs some assignments independently as discussed and approved by senior lab staff. This individual will conduct routine specimen processing, data entry, and shipping, focusing on projects in support of Hematology/Oncology studies, including blood fractionation, mononuclear cell extraction, and tissue culture. Additional responsibilities include assisting in processing clinical trial specimens, monitoring reagents and supplies, as well as assisting senior laboratory staff in the processing of core facility specimens and specialized instrumentation. Maintains both handwritten and computerized records of work performed. Assists in implementation of new laboratory protocols and processes, and maintenance of lab equipment. Performs basic safety functions in the lab, including testing of equipment. Performs basic data analysis; prepares tables/charts/graphs and assists in organizing data. Participates at research laboratory meetings. Qualifications: * Bachelor's degree in Biological Science or related degree required * A minimum of 1-3 years working in a biomedical clinical or research laboratory Primary Responsibilities: * Responsible for processing and shipping of various biological specimens (blood and body fluid, tissue, bone marrow, etc) and utilizing databases for specimen tracking, following laboratory protocols and SOP's. * Assists in maintaining the laboratory environment, reagents, equipment, and function, at a level consistent with CAP guidelines. * Function independently as assigned and assists in resolving issues in coordination with senior lab staff/PI. * Carry out simple laboratory tests/cultures and research experiments. * Gather measurements and records data under close supervision. * Support research operations by cleaning and maintaining equipment. Understand and demonstrates safe use and operation of lab equipment. * Understands and is knowledgeable of Nemours safety policies, procedures and performs basic safety functions. * Engage in and actively follows the five Nemours Associate Core Competencies - Cultural Stewardship; Relationship Management; Commitment to Improvement and Quality; Effective Communication and Champions Change. * Complete annual Nemours mandatory training as assigned.

The Biobank and Molecular Analysis Program (BMAP) at Nemours Children's Health is seeking a full-time Clinical Research Technologist to perform a primary specimen processing and shipping role in the CAP accredited program. This individual will work under the supervision of senior laboratory staff and performs some assignments independently as discussed and approved by senior lab staff. This individual will conduct routine specimen processing, data entry, and shipping, focusing on projects in support of Hematology/Oncology studies, including blood fractionation, mononuclear cell extraction, and tissue culture. Additional responsibilities include assisting in processing clinical trial specimens, monitoring reagents and supplies, as well as assisting senior laboratory staff in the processing of core facility specimens and specialized instrumentation. Maintains both handwritten and computerized records of work performed. Assists in implementation of new laboratory protocols and processes, and maintenance of lab equipment. Performs basic safety functions in the lab, including testing of equipment. Performs basic data analysis; prepares tables/charts/graphs and assists in organizing data. Participates at research laboratory meetings. Qualifications: Bachelor's degree in Biological Science or related degree required A minimum of 1-3 years working in a biomedical clinical or research laboratory Primary Responsibilities: Responsible for processing and shipping of various biological specimens (blood and body fluid, tissue, bone marrow, etc) and utilizing databases for specimen tracking, following laboratory protocols and SOP's. Assists in maintaining the laboratory environment, reagents, equipment, and function, at a level consistent with CAP guidelines. Function independently as assigned and assists in resolving issues in coordination with senior lab staff/PI. Carry out simple laboratory tests/cultures and research experiments. Gather measurements and records data under close supervision. Support research operations by cleaning and maintaining equipment. Understand and demonstrates safe use and operation of lab equipment. Understands and is knowledgeable of Nemours safety policies, procedures and performs basic safety functions. Engage in and actively follows the five Nemours Associate Core Competencies - Cultural Stewardship; Relationship Management; Commitment to Improvement and Quality; Effective Communication and Champions Change. Complete annual Nemours mandatory training as assigned. About Us Nemours Children's Health is an internationally recognized children's health system. With more than 1.7 million patient encounters annually, we provide medical care in five states through two freestanding state-of-the-art children's hospitals - Nemours Children's Hospital, Delaware and Nemours Children's Hospital, Florida. Our pediatric network includes 80 primary-urgent-and specialty care practices and more than 40 hospitalists serving 19 affiliated hospitals. We generate annual revenues of more than $1.7 billion derived from patient services, contributions from the Alfred I. DuPont Trust, as well as other income. As one of the nation's premier pediatric health systems, we're on a journey to discover better ways of approaching children's health. Putting as much focus on prevention as cures and working hand in hand with the community to make every child's world a place to thrive. It's a journey that extends beyond our nationally recognized clinical treatment to an entire integrated spectrum of research, advocacy, education, and prevention, leading to the healthiest generations of children ever. Inclusion and belonging guide our growth and strategy. We are looking for individuals who are passionate about, and committed to, leading efforts to provide culturally relevant care, reducing health disparities, and helping build an inclusive and supportive environment. All of our associates are expected to ensure that these philosophies are embedded in their day-to-day work with colleagues, patients and families. To learn more about Nemours Children's and how we go well beyond medicine, visit us at *************** .

The Biobank and Molecular Analysis Program (BMAP) at Nemours Children's Health is seeking a full-time Clinical Research Technologist to perform a primary specimen processing and shipping role in the CAP accredited program. This individual will work under the supervision of senior laboratory staff and performs some assignments independently as discussed and approved by senior lab staff. This individual will conduct routine specimen processing, data entry, and shipping, focusing on projects in support of Hematology/Oncology studies, including blood fractionation, mononuclear cell extraction, and tissue culture. Additional responsibilities include assisting in processing clinical trial specimens, monitoring reagents and supplies, as well as assisting senior laboratory staff in the processing of core facility specimens and specialized instrumentation. Maintains both handwritten and computerized records of work performed. Assists in implementation of new laboratory protocols and processes, and maintenance of lab equipment. Performs basic safety functions in the lab, including testing of equipment. Performs basic data analysis; prepares tables/charts/graphs and assists in organizing data. Participates at research laboratory meetings. Qualifications: Bachelor's degree in Biological Science or related degree required A minimum of 1-3 years working in a biomedical clinical or research laboratory Primary Responsibilities: Responsible for processing and shipping of various biological specimens (blood and body fluid, tissue, bone marrow, etc) and utilizing databases for specimen tracking, following laboratory protocols and SOP's. Assists in maintaining the laboratory environment, reagents, equipment, and function, at a level consistent with CAP guidelines. Function independently as assigned and assists in resolving issues in coordination with senior lab staff/PI. Carry out simple laboratory tests/cultures and research experiments. Gather measurements and records data under close supervision. Support research operations by cleaning and maintaining equipment. Understand and demonstrates safe use and operation of lab equipment. Understands and is knowledgeable of Nemours safety policies, procedures and performs basic safety functions. Engage in and actively follows the five Nemours Associate Core Competencies - Cultural Stewardship; Relationship Management; Commitment to Improvement and Quality; Effective Communication and Champions Change. Complete annual Nemours mandatory training as assigned.

through the following https://www.paycomonline.net/v4/ats/web.php/jobs/ViewJobDetails?job=32012&clientkey=703E6F23E139A9E15CD4746A9D25637D&jpt=1b79bf1ead1b4f21088d5e********** The mission of the Health Federation of Philadelphia is to improve access to and quality of health care services for under served and vulnerable individuals and families. Since 1983, The Health Federation has served as a network of the community health centers in Southeastern Pennsylvania, providing a forum for the region's federally qualified health centers and the Philadelphia Department of Public Health to collaborate and mobilize resources for their shared goals of improving the health of the population by expanding access to high quality care. Job Description JOB SUMMARY Who we are: The mission of the Philadelphia Department of Public Health (PDPH) is to protect and promote the health of all Philadelphians and to provide a safety net for the most vulnerable. Within PDPH, the Division of Chronic Disease and Injury Prevention (aka “Get Healthy Philly”), works to change policies, systems, and environments to make healthy living an easy choice for residents. The goals of our programs are to reduce obesity, smoking, and other known risk factors for chronic diseases. We are also expanding our injury prevention work, with a focus on reducing gun violence. The Division is especially concerned about documenting, understanding, and working to reduce disparities in health. The Public Health Data Lab at Get Healthy Philly conducts innovative research and analysis that directly informs city policy and guides public health decisions. We provide the evidence base to answer questions like: Why do some neighborhoods have higher rates of cancer mortality than others? Will restrictions on the sale of certain tobacco products reduce the rate of teen vaping in Philadelphia? What policies or programs have worked to reduce gun violence in other communities, and could they work in Philadelphia? Our values : Get Healthy Philly's work is guided by our commitment to all people's health and humanity. We believe: · All people have the right to live to their fullest potential. · All communities have the right to create environments that allow them to grow and thrive. · Public health policy must be based on collaboration and true community partnerships. · Genuine public health progress must be based on the recognition that knowledge comes in many forms and many places in our society. · Success and progress will only come when we treat people, communities, partners, and staff with care and respect. Join us! We are seeking a skilled and dynamic Research Associate with experience conducting research and using evidence for decision-making. Candidates should have experience with designing and analyzing rigorous quantitative and qualitative research and have strong communication and technical writing skills. The Associate will plan, manage and implement data analytic activities related to the work of the Get Healthy Philly team. This will include collecting, cleaning, and managing data; performing statistical analysis; and summarizing results for scientific, policy-oriented, and public audiences. The Associate will use appropriate data sources to monitor trends, patterns, and changes in risk factors and health outcomes. Factors of interest include the health behaviors of individuals, the demographic characteristics of populations, the policy environment, and the built environment. While academic journal publications are encouraged, the primary purpose of our work is to inform and advise policymakers and the public. JOB SPECIFICATIONS Responsibilities/Duties · Reviews and synthesizes existing literature on topics related to chronic conditions and injury prevention · Develops and fields data collection efforts, including surveys · Manages, cleans, analyzes, and interprets data · Performs regular data matches between health-related data sources · Guides research projects through Institutional Review Board approval · Collaborates with academic, medical, and policy partners · With a team, develops new research and data analysis tasks based on the Division's needs · Contributes to research and data products including reports, data briefs, charts, presentations, and manuscripts · Works collaboratively with other Associates and Analysts to develop the analysis skills of the entire team · Contributes to program evaluation planning · Contributes to writing grants · Contributes to manuscript development for peer-reviewed journals · Participates in division meeting Qualifications Qualifications · A master's degree or PhD in epidemiology, public policy, demography, economics, data science, statistics, or a related field. · Two to five years of experience in public health or social science research. · Demonstrated experience in data analysis with statistical software such as R, Stata, or SAS. OR · Any equivalent combination of education and experience determined to be acceptable by the Department of Public Health which has included a bachelor's degree as an educational minimum. Desired skills · Knowledge of and experience with epidemiological or social science research methods, including study design, methodology, and preparation of scientific reports · Ability to analyze data, write project proposals, and write technical reports · Ability to summarize findings for a variety of audiences, e.g. scientists, policy makers, and the public · Interest in using data skills in an applied setting to advance health policy goals · Strong analytic abilities with statistical software (e.g., R, Stata, SAS, etc.) · Experience with interactive data visualization and/or mapping software a plus · Excellent oral and written communication skills · Experience working with sensitive health information · Able to work as a team, prioritize and handle multiple tasks and deadlines, and work independently Work Environment Standard office setting with extended periods at work station and periodic use of office equipment. Position Type and Work Schedule Full time position, typical hours are Monday through Friday 8:30 am to 5:00 pm. Flex office schedule options available with supervisor approval. Travel Frequent local travel between sites to attend meetings. May occasionally travel outside the city. Physical Demands Limited physical demands. Associate will work primarily in an office setting. Salary and Benefits Our employees are our most valuable resource, so we offer a competitive and comprehensive benefits package, which can include: · Medical with vision benefits · Dental insurance · Flexible spending accounts · Life, AD&D and long-term care insurance · Short- and long-term disability insurance · 403(b) Retirement Plan, with a company contribution · Paid time off including vacation, sick, personal and holiday · Employee Assistance Program Eligibility and participation are handled consistent with the plan documents and HFP policy. TO APPLY To apply, please submit: 1) A resume or CV 2) A cover letter that includes: a. Your experience with statistical software such as R, SAS or Stata, b. Your experience in or with Philadelphia, if any, and c. Your past or proposed contributions to diversity, equity, and inclusion. 3) A writing sample (optional) Additional Information All applicants must apply to the position through the following link. Also, please upload a resume and cover letter when applying. https://www.paycomonline.net/v4/ats/web.php/jobs/ViewJobDetails?job=32012&clientkey=703E6F23E139A9E15CD4746A9D25637D&jpt=1b79bf1ead1b4f21088d5e**********

Enjoy what you do while contributing to a company that makes a difference in people's lives. Shady Grove Fertility, one of the premier fertility centers in the United States, continually seeks experienced, compassionate, and dynamic team players who are committed to delivering exceptional patient care to join our growing practice. The work we do building families offers stimulation, challenge, and personal reward. If you're an Embryologist looking for a new opportunity to work in a fast-paced, professional environment where your talent contributes to changing people's lives, then we want to talk to you. This position requires collaborating with physicians and other medical providers by providing expert care and service for fertility treatments. Sign on Bonus of 10K! We currently have an opening for a full-time Embryologist to work in our fast paced, high volume, Embryology Lab located in our Chesterbrook, PA office. Working Monday - Friday 7:30 AM to 4:00 PM with rotating weekends, holiday rotation. Approximately 1 weekend/month How You'll Contribute: We always do whatever it takes, even if it isn't specifically our “job.” In general, the Embryologist is responsible for: Identification, assessment and culture of oocytes; sperm preparation and insemination of oocytes (conventional insemination and ICSI) Assessment and selection embryos for transfer; embryo vitrification, warming and storage Oocyte vitrification, warming and storage Preparation and care of gametes/embryos throughout the laboratory process: IVF, ICSI, VIT, ET, Warming and Embryo Biopsy Vitrification and warming of embryos at varying stages of development Assessing fertilization and zygote quality following insemination Familiarity with data entry into an EMR Familiarity with MESA, PESA, TESA and TESE collection Experience with regulatory guidelines and inspections (e.g. CLIA, FDA, TJC, CAP) What You'll Bring: Minimum 5 years experience in Embryology. Must have a Bachelor's degree or higher in a relevant laboratory science. Must demonstrate the ability to function effectively without direct supervision, and to perform laboratory services in accordance with the Laboratory Philosophy and Operating Standards. Proven ability to access, input, and retrieve information from a computer. Knowledge of office procedures and office machines (i.e. computer, fax, copier, etc.). Ability to work as part of a multidisciplinary team. Ability to work in a high standard, stressful environment. Ability to communicate accurately and concisely. Ability to develop interpersonal working relationships with colleagues Must be authorized to work in the U.S.A. More important than the best skills, however, is the right person. Employees who embrace our mission, vision, and core values are highly successful. What We Offer: We are proud to provide a comprehensive and competitive benefits package tailored to support the needs of our team members across all employment types: Full-Time Employees (30+ hours/week): Medical, dental, and vision insurance, 401(k) with company match, tuition assistance, performance-based bonus opportunities, generous paid time off, and paid holidays Part-Time Employees: 401(k) with company match and performance-based bonus opportunities Per Diem Employees: 401(k) with company match At Shady Grove Fertility, we promote and develop individual strengths in order to help staff grow personally and professionally. Our core values guide us daily to work hard and enjoy what we do. We're committed to growing our practice and are always looking to promote from within. This is an ideal time to join our team! How To Get Started: To have your resume reviewed by someone on our Talent Acquisition team, click on the “Apply” button. Or if you happen to know of someone who might be interested in this position, please feel free to share the job description by clicking on an option under “Share This Job” at the top of the screen.

We are on the prowl for a Lab Technician to join our Mount Olive, New Jersey team at Symbiotic Research, a Tentamus North America company! If you are deeply passionate about science and enthusiastic about broadening your expertise, we invite you to apply today and become a vital part of our mission. How you will contribute as a vital part of our team: The Laboratory Technician will contribute to a world class laboratory by performing various laboratory duties under the direction of scientific staff which may include: Performing sample extraction, workup and pipetting. Adhere to all laboratory safety practices and follow applicable GLP regulations and government guidelines to conduct studies. Document all work performed following GDP principles. Communicate clearly with laboratory staff and scientists. Rely on SOPs and/or methods to perform the functions of the job. Prepare routine solutions; upkeep with laboratory cleanliness, organize all lab supplies to be easily accessible for all and provide laboratory maintenance. Maintain and calibrate the laboratory instruments as assigned. Support laboratory staff as needed. Position & Schedule Full-Time, 40 hours per week, Monday - Friday 8:30AM - 5:00PM or 9:00AM - 5:30PM with a 30-minute lunch break. Qualifications Our ideal candidate will be authorized to work in the United States indefinitely without restriction or sponsorship; have a BS in Biology preferred or related science field or experience working in a scientific laboratory setting; and an ability to work both independently and within a team. Other items include: Has knowledge of the use, maintenance, and/or calibration of most GLP equipment. Knowledge of laboratory operations. Must be able to work in a flexible environment, perform a variety of tasks and prioritize work. Ability to work under minimum supervision. Ability to implement scientific procedures and processes involved with residue, environmental fate and metabolism studies. Exhibit excellent oral and strong written communication skills. Self-sufficient in planning and executing daily responsibilities and the ability to tend to experimental details and attention to detail. Good computer skills and being adept with standard software (e.g. Windows, Excel, Word). Must be able to read, understand, and follow SOPs, policies and regulations, and provide general laboratory support. Required to frequently stand, walk, and sit. The employee must occasionally lift and/or move up to 40 pounds. What's in it for you? $16 per hour and a comprehensive and low-cost benefit plans (medical, dental, vision, disability, life insurance, HSA) Ample PTO and a matching 401k About Tentamus: Labs for Life . We are a global network of full-service accredited analytical laboratories providing crucial quality and safety analysis for clients locally, nationally, and beyond using proven methods of chemistry and microbiology. Many of the products you use and consume daily rely on Tentamus labs. With 20 labs in North America and growing (100 globally), we celebrate having talented diverse scientific and service-oriented professionals. Learn More: Tentamus Website | Symbiotic Research Website

At ALS, we encourage you to dream big. When you join us, you'll be part of a global team harnessing the power of scientific testing and data-driven insights to build a healthier future. Microbiology Analyst Imagine your future with us! At ALS, we encourage you to dream big. When you join ALS, you join a purpose and values-driven team that empowers you to innovate, create, and thrive. Our global team turns up each day with passion and commitment to do amazing things, always challenging our thinking to find ways to solve some of the world's most complex problems for a safer, healthier world. General Accountability: The primary purpose of this position is to perform microbiology analyses on drinking water, waste water and biosolids according to method specification and client requirements. Specific Responsibilities: Analyze drinking water, wastewater and sludge/solid samples for microbiological parameters such as coliform, E. coli, fecal coliforms, and standard plate count. Perform all quality control requirements associated with the microbiology methods and maintain appropriate records. Prioritize work by creating schedules to complete daily assignments and data review and reporting promptly. Interpret and author SOPs, perform reagent formulation, record bench level observations, and keep records in bound and electronic notebooks. Be responsive and responsible for meeting method holding times and incubation cycle times by pulling and interpreting media within method prescribed parameters. Meets production levels on a daily and weekly basis in order to meet client deadlines. Able to work independently with little supervision. Make timely notifications for public water compliance on regulated drinking water samples. Able to work in a team with co-workers and participate in schedule rotations as needed to meet microbiology department needs. Assist in maintaining a clean audit ready laboratory at all times Ensure compliance with assigned SOP's, QA manual and HSE policies. Recognize and maintain safe working conditions. Follow PPE policies. Handle hazardous material appropriately and safely. Maintain a clean, orderly work environment. Perform other duties as assigned and directed. About you Required Knowledge, Skills & Abilities: Experience in document control, the use of SOP's, reagent formulation, and bench level observation and recordkeeping in bound and electronic notebooks. An understanding of basic quality assurance parameters specifically measure of precision and accuracy is preferred. Experience in the analysis of environmental samples for microbiological and wet chemistry parameters using EPA methodologies. Able to work independently with little supervision as well as the ability to work as a team, be a team player and support fellow co-workers. Produces quality, error free work. Attitude and cooperation - has an upbeat and positive attitude, offers ideas and solutions to correct problem areas Seeks assistance when needed before a situation gets “out of hand” Professional appearance and conduct to both ALS staff and clients. Diligent work ethic. Adaptable and able to change an approach or method quickly to fit different situations Communicates information well to co-workers / team members to include all those involved in the decision-making process. Motivated and fast paced personality. Multi-tasked, organized, detail oriented, and possess excellent problem solving capabilities; will have good time management capabilities. Must be dependable and reliable. Able to learn new software/computer systems for inventory management. Ability to work overtime when needed. Required Qualifications: A Bachelor of Science in Biology or a related field Previous laboratory experience is preferred. Computer skills, Microsoft programs. Physical Demands: The ability to stand, bend and sit for 100% of shift. Able to speak and hear clearly while communicating with staff, management and clients. Able to lift 50+ lbs. on a consistent basis (may use a dolly for situations requiring heaving loads). Dexterity in hands and fingers to operate computers and instrumentation. Average vision and able to see to read reports and operate instrumentation. Hearing and speech to communicate in person and over the telephone. Able to perform repetitive motion actions. Ability to work overtime when needed. We would like to thank everyone for their interest in ALS Environmental but only candidates selected for an interview will be contacted. “ALS Group is proud to be an equal opportunity employer committed to achieving and maintaining a workforce which reflects and affirms the diversity of our society” EOE AA M/F/Vet/Disability Click Here to view the EEO is the Law poster Working at ALS The ALS team is a diverse and dedicated community united by our passion to make a difference in the world. Our values are important to us, and shape how we work, how we treat each other and how we recognise excellence. At ALS, you'll be supported to develop new skills and reach your full potential. We invest in our people with programs and opportunities that help you build a diverse career with us. We want everyone to have a safe, flexible and rewarding career that makes a positive impact on our people, the planet and our communities. Everyone Matters ALS is proud to be an equal opportunity employer and is committed to fostering an inclusive work environment where the strengths and perspectives of each employee are both recognised and valued. Qualified candidates will be considered without regard to race, colour, religion, national origin, military or veteran status, gender, age, disabilities, sexual orientation, gender identity, pregnancy and pregnancy-related conditions, genetic information and any other characteristics protected by the law. We invite resumes from all interested parties, including women, members of minority groups, and persons living with disabilities. ALS also welcomes applications from people with all levels of ability. Accommodation is available on request for candidates taking part in all aspects of the selection process. Eligibility To be eligible to work at ALS you must be a Citizen or Permanent Resident of the country you are applying for, or either hold or be able to obtain, a valid working visa. How to apply Please apply on-line and provide a cover letter and CV that best demonstrate your motivation and ability to meet the requirements of this role.

The Biobank and Molecular Analysis Program (BMAP) at Nemours Children's Health is seeking a full-time Clinical Research Technologist to perform a primary specimen processing and shipping role in the CAP accredited program. This individual will work under the supervision of senior laboratory staff and performs some assignments independently as discussed and approved by senior lab staff. This individual will conduct routine specimen processing, data entry, and shipping, focusing on projects in support of Hematology/Oncology studies, including blood fractionation, mononuclear cell extraction, and tissue culture. Additional responsibilities include assisting in processing clinical trial specimens, monitoring reagents and supplies, as well as assisting senior laboratory staff in the processing of core facility specimens and specialized instrumentation. Maintains both handwritten and computerized records of work performed. Assists in implementation of new laboratory protocols and processes, and maintenance of lab equipment. Performs basic safety functions in the lab, including testing of equipment. Performs basic data analysis; prepares tables/charts/graphs and assists in organizing data. Participates at research laboratory meetings. Qualifications: Bachelor's degree in Biological Science or related degree required A minimum of 1-3 years working in a biomedical clinical or research laboratory Primary Responsibilities: Responsible for processing and shipping of various biological specimens (blood and body fluid, tissue, bone marrow, etc) and utilizing databases for specimen tracking, following laboratory protocols and SOP's. Assists in maintaining the laboratory environment, reagents, equipment, and function, at a level consistent with CAP guidelines. Function independently as assigned and assists in resolving issues in coordination with senior lab staff/PI. Carry out simple laboratory tests/cultures and research experiments. Gather measurements and records data under close supervision. Support research operations by cleaning and maintaining equipment. Understand and demonstrates safe use and operation of lab equipment. Understands and is knowledgeable of Nemours safety policies, procedures and performs basic safety functions. Engage in and actively follows the five Nemours Associate Core Competencies - Cultural Stewardship; Relationship Management; Commitment to Improvement and Quality; Effective Communication and Champions Change. Complete annual Nemours mandatory training as assigned.

Artech is the 10th Largest IT Staffing Company in the US, according to Staffing Industry Analysts' 2012 annual report. Artech provides technical expertise to fill gaps in clients' immediate skill-sets availability, deliver emerging technology skill-sets, refresh existing skill base, allow for flexibility in project planning and execution phases, and provide budgeting/financial flexibility by offering contingent labor as a variable cost. Job Description As a member of Janssen Developability Group, you will be working with a team responsible for developability assessments and pre-clinical formulation development, aiding the identification of small molecule clinical candidates. You will be responsible for generating data under the guidance and supervision of a senior scientist, while maintaining accurate and well-organized laboratory records, worksheets and notebooks. Ideal candidate will be able to multi-task while working in a fast-paced and team-oriented environment. Technical qualifications: 1. Hands-on expertise with analytical techniques used for the solution characterization of small molecules, such as chromatography (HPLC and uPLC, ideally with Empower data acquisition software) is a must have. 2. Experience with solid-state characterization of small molecules such as, thermal analysis, X-ray diffraction, particle size measurements and light microscopy is highly desired. 3. Good understanding of biopharmaceutical principles and hands-on expertise with pre-clinical formulation development and preparation is desired. 4. Experience in the design of pre-formulation, forced degradation studies, and peptide formulations is preferred. Qualifications 1. BS in Chemistry, Pharmaceutical Sciences, chemistry or other closely related field preferred with 3+ years of experience in Biotech or Pharmaceutical industry. 2. Candidates with equivalent educational and professional backgrounds will also be considered. Additional Information Best Regards, Anuj Mehta ************

The Monell Chemical Senses Center was founded in 1968 as the world's first nonprofit scientific institute devoted exclusively to basic research on the chemical senses: taste, smell, and chemosensory irritation. Research at Monell contributes to a wide range of scientific and practical knowledge. With more than fifty Ph.D.-level scientists, the Center is making major progress toward understanding how the chemical senses function and their importance in everyday life. The Center is located in the University City area of Philadelphia. The Dalton Lab is looking for a new Research Technician. Training will be provided and specific tasks will be tailored to the lab's current needs and your abilities. For more information please visit ********************************* for more lab-specific details. Principal Responsibilities: Include recruiting and testing subjects Stimuli preparation Ordering supplies Management and organization of data General lab maintenance. Qualifications: BA/BS in Psychology or related field (biology) is required. Occasional evening hours are required for subject testing. Prior experience working with human subjects is preferred. Proficiency in R coding

The candidate should have a BS/MS in biological sciences with research experience in cellular immunology and/or cell biology including significant hands-on experience performing cell culture and following proper aseptic technique. The successful candidate will be able to apply different research techniques in the work including immune cell isolation, immune cell culture, ELISA, MSD, and luminex assays. Experience with assays using purified immune cells, T-cell culture, and hybridoma generation would be ideal. The candidate should have a good understanding of immunology and/or cell biology, be able work independently, have strong quantitative skills, and be familiar with basic data analysis software and data interpretation. Good organizational skills, experimental documentation, and a proven ability to work collaboratively in a fast paced, highly matrixed, interactive environment is essential. Additional Information

Artech Information Systems is the #12 Largest IT Staffing Company in the U.S. and an employer of choice for over 7,000 consultants. We recruit world-class talent for IT, engineering, and other professional jobs at 70+ Fortune and Global 500 companies coast-to-coast across the U.S., India, and China. We are one of the fastest-growing companies in the US and we welcome you to search the thousands of jobs in our cutting-edge GEM system for employment opportunities that fit your qualifications. At the forefront of the staffing industry, Artech is a minority and women-owned business enterprise (MWBE) committed to maximizing global workforce solutions on behalf of its clients. Artech's deep heritage, proven expertise and insightful market intelligence has secured long-term partnerships with Fortune 500 and government clients seeking world-class professional resources. Job Description BS with 3-6 years experience or an MS with 1-3 years experience. Works in a research environment in support of new or modified discoveries as it relates to Janssen R&D. The individual will be actively involved in laboratory work related to the sampling of chemicals, raw materials, and-or blood and tissues for the determination of pharmacokinetic properties of therapeutics coming from various research targets through in vivo experimentation. The individual will be adept at establishing and writing protocols and interacting with Therapeutic Teams to design the most appropriate experiments. ESSENTIAL FUNCTIONS include but not limited to:- Interact with vivarium staff to coordinate in vivo study execution and sample acquisition.- Manage processing and characterization of samples obtained from in vivo studies.- Execute soluble protein isolation and analysis via bead-based multiplex platform.- Mammalian cell culture and aseptic technique.- Ability to manage workload, coordinate in vivo studies and prioritize tasks.- Demonstration of oral, written and interpersonal skills including the ability to document and effectively communicate interpretation of data and results validation of assays. • Janssen is looking for a motivated individual to join our Spring House-based team and contribute experimentally to programs targeting inflammatory bowel disease. The candidate should have a BS with 3-6 years of experience, a MS with 1-3 years of experience or a PhD in biological sciences, with substantial training in immunology, pharmacology and/or cellular biology. Hands-on experience with diverse cell-based assays for therapeutic screening is necessary, particularly analysis of cell responses using ELISA and FACS. Hands-on experience with cell culture (cell lines and primary cells) is absolutely required. Experience with human or mouse whole blood assays and blood handling skills is preferred. Direct experience with biochemical techniques, such as protein quantification and western blot analysis, are preferred. The candidate should also have strong quantitative skills and data analysis capabilities. Good organizational skills, flexibility and a proven ability to work collaboratively in a fast paced, highly matrixed, interactive environment is of the essence. • The candidate should have a BS/MS/PhD in biological sciences with substantial training in cell biology, and/or immunology. The individual will be actively involved in laboratory work requiring strong skills in cell culture, transfection, RT-PCR, Western blot, Luminex, and FACS. The individual should have good organizational skills and the ability to manage his/her workload and prioritize tasks. As a self-starter, this candidate should be detailed-orientated and a quick learner. Essential functions include the demonstration of oral, written and interpersonal skills including the ability to document and effectively communicate interpretation of data and results. Proven ability to work well in a quick paced, highly matrixed, interactive environment is vital. Qualifications BS Additional Information For more information, Please contact Best Regards, Akriti Gupta ************** Morristown, NJ 07960

The candidate should have a BS/MS in biological sciences with research experience in cellular immunology and/or cell biology including significant hands-on experience performing cell culture and following proper aseptic technique. The successful candidate will be able to apply different research techniques in the work including immune cell isolation, immune cell culture, ELISA, MSD, and luminex assays. Experience with assays using purified immune cells, T-cell culture, and hybridoma generation would be ideal. The candidate should have a good understanding of immunology and/or cell biology, be able work independently, have strong quantitative skills, and be familiar with basic data analysis software and data interpretation. Good organizational skills, experimental documentation, and a proven ability to work collaboratively in a fast paced, highly matrixed, interactive environment is essential. Additional Information