Postdoctoral Scholar Jobs in Montgomery, PA

The American Board of Internal Medicine (ABIM) is currently seeking a Measurement Scientist to join our Research & Innovations department. The Measurement Scientist will apply exceptional critical thinking and creative problem-solving skills to help ABIM develop the most advanced assessments in credentialing. Reporting to the Manager, Measurement Research, the Measurement Scientist has the following primary responsibilities: Apply creative problem-solving skills to solve practical problems in assessment. Design and implement innovative approaches to assessment. Develop a coherent research agenda to support valid interpretation and use of test scores. Collaborate with ABIM staff on original research and development projects. Communicate measurement concepts and analytic results to internal and external colleagues. Prepare manuscripts for publication and presentation at professional meetings. Provide psychometric analysis and consultation to improve internal operational testing activities. Perform operational activities to support ABIM exam programs. The ideal candidate has a doctorate in educational/psychological measurement, statistics, or a related field (actively pursuing a doctorate and close to completion will be considered). They should also have strong interpersonal skills and a solid foundation in the principles of psychometrics, including knowledge of test development, item response theory, and equating procedures. They must have demonstrated ability with research design and methodologies, and facility with R, SAS, SPSS, and other programming languages. Experience with the application of Generative AI and/or Natural Language Processing (NLP) in an assessment context is highly desirable. This role requires an on-site office presence at least two days per week. ABIM offices are located in the historic section of Philadelphia, 510 Walnut Street. Our technology and workplace operations teams provide for and support a seamless hybrid work environment for all ABIM employees. * * * At the American Board of Internal Medicine (ABIM), our team of unique and talented professionals, and the inspiring work they do, are essential to meeting the needs and expectations of ABIM's diverse community of physicians. ABIM is like no other workplace, and we are proud of it. We are committed to recognizing the importance of our people by investing in their lives through ongoing learning opportunities and exceptional total compensation & benefit offerings. We look forward to learning more about your interest in joining our team. Cover letter preferred but not required. EOE

Resolian is a Contract Research Organization (CRO) specializing in Drug Metabolism/ Pharmacokinetic (DMPK) and bioanalytical services for both small and large molecules. Resolian is growing and due to our growth, we are adding Scientists to our Bioanalytical, LC-MS team. Solid experience in a few of the area's listed below is needed to succeed in this role: Protein quantitation (must have) Immunoaffinity procedures LCMS (must have) Bioanalysis (must have) Small molecule and/ or large molecule Oligonucleotides Protein peptides- quantitative experience GxP including GOP & GCP Method development & sample analysis using LCMS Responsibilities: · Prepare reagents, standards, and control samples · Analyze samples using various techniques specific to department · Perform complex method development with limited supervision · Perform method validation or qualification · Operate analytical equipment · Lead troubleshooting activities; assays and equipment · Maintain analytical equipment · Review, evaluate, and interpret data results · Draft and present posters/presentations · Train and mentor lower level Scientists · Collaborate with clients and vendors · Ensure lab area is clean and inspection ready at all times · Remove lab waste · Record tasks in accordance with Good Documentation Practices (GDP) · Understand and apply regulatory requirements; GLP, GCP, 21CFR Part 11 · Follow applicable SOPs and procedural documents · Other tasks as assigned Qualifications & Education: BA/BS or higher with 5 years experience working LCMS at a CRO or pharma/ life sciences company PhD in relevant field with two years experience working in LCMS at a CRO or pharma/ life sciences company Experience in protein quantitation Experience immunoaffinity procedures Familiarity with high resolution mass spec is a plus Knowledge and understanding of regulatory requirements; GLP, GCP, 21CFR Part 11, GDP, GMP Able to independently perform complex lab work Able to work in a regulated environment Able to work effectively and contribute within a team Able to work with computer systems Able to document clearly Knowledge of and experience in a regulatory environment Team building experience More information about the LC-MS group: ************************************************ More information about Resolian: ****************

Compensation & Additional Details: Fully onsite in Malvern, PA 10 PTO Days + 6 Sick Days 12 month extending contract Compensation: $29-$32/hr exact rate is based on several factors, including skills, experience, and education. Benefit packages for this role will start on the 31st day of employment and include medical, dental, and vision insurance, as well as HSA, FSA, and DCFSA account options, and 401k retirement account access with employer matching. Employees in this role are also entitled to paid sick leave and/or other paid time off as provided by applicable law. Minimum Qualifications: -Bachelor's degree in scientific field, preferably Biotech -Minimum 1 year of experience working in a lab environment, preferably GMP -Minimum 1-2 years of experience working within cell culture (not just academia) -Minimum 1 year of experience working with Aseptic techniques -cGPMP, GMP, GDP (Good documentation practice) -Strong attention to detail -Extremely motivated individual -Cell Banking experience (preferred) Day-to-Day: One of our large pharmaceutical clients is looking to hire an Associate Scientist of Cell Banking to perform Cell Banking for the Cell Culture processes and/or bio-analytical testing within the API Large Molecule Process Development group in Malvern PA. The candidate's primary responsibilities will include but are not limited to the production, testing, inventory, and supply of Master, Working, and development Cell Banks for clinical, and commercial production as well as analytical testing for J&J biopharmaceutical and cell therapy products. Responsibilities will include: -Support Cell banking organization by performing Cell banking for Cell Culture processes and analytical testing. -Execute production, testing, and release of Master, Working, development, and analytical cell Banks and ensures the timely supply to customers. -Work in a team environment as well as contributing individually to meet project timeline and objectives. -Participate in Cell culture and cryopreservation of cells using aseptic techniques under GMP Compliant conditions. -Execute all activities per established procedures and protocols -Interface with internal and external customers to ship cell banks and supply critical information as per their requirements. -Collaborate cross-functionally to represent Cell Banking department. -Author, review, and approve technical documents, SOPs, and batch records.

Drexel University College of Medicine (DUCOM), Department of Microbiology and Immunology, invites applications for a postdoctoral fellow to join Dr. Hangjun Ke lab and the Malaria team at Drexel. Dr. Ke's laboratory focuses on the molecular biology of malaria parasites (Plasmodium spp.) and investigates parasite bioenergetics, organellar functions, and host-parasite interactions, with the goal of identifying essential pathways/proteins for the development of novel antimalarial therapeutics. The future postdoctoral fellow will have opportunities to work with other malaria labs within the department. A strong emphasis is placed on career development, participation in national/international conferences, communication skills, grant and manuscript writing skills, and leadership development. The postdoctoral fellow is expected to be highly self-motivated and independent. They will be joining a highly collaborative, multidisciplinary training environment. Essential Functions The candidate will perform CRISPR-based gene editing to study pathways related to energy acquisition of the malaria parasites and energy exchange at the host-parasite interface. The position offers opportunities to Cultivate malaria parasites in the long-term Perform CRISPR/Cas9 mediated gene editing Analyze phenotypic changes upon conditional knockdown or knockout of genes Understand the mechanisms of parasite bioenergetics and biology Required Qualifications Minimum of PhD or Doctorate in Life science or related field. Minimum of 1 year of experience. Preferred Qualifications • Evidence of publication record in genetics, biology, and/or infectious diseases, with experience performing parasite culture and gene editing. • Excellent communication and written skills to enhance interactions and collaborations among different research teams. Physical Demands Typically sitting at a desk/table Typically standing, walking Location The Ke Lab is located on the Queen Lane Campus Additional Information This position is classified as Exempt, grade K. Compensation for this grade ranges from $54,630.00 to $81,940.00 per 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. Applicants are encouraged to explore the Professional Staff salary structure and Compensation Guidelines & Policies for more details on Drexel's compensation framework. For information about benefits, please review Drexel's Benefits Brochure. Special Instructions to the Applicant Please make sure you upload your CV/resume and cover letter when submitting your application. A review of applicants will begin once a suitable candidate pool is identified.

Scientist, Biologics Full-time Frontage Laboratories Inc. is an award winning, full-service, CRO/Contract Research Organization operating over 25 state-of-the-art laboratories across the US, Canada and China. Our core competencies include drug metabolism, pharmacokinetics/ pharmacodynamics (PK/PD), safety and toxicology, bioanalytical services, chemistry and manufacturing controls for drug development, and core laboratory services for clinical trials. Responsibilities : Primary responsibilities include, but are not limited to the following: Perform analytical and biological sample testing• Conduct method development and validation studies• Perform immunoassay techniques: (ligand binding assays, ELISA, MSD, and/or RIA applicable to Pharmacokinetic and Immunogenicity studies), with proficiency• Prepare and handle various cell lines, tissue culture media and other reagents for cell-based assays such as Neutralizing Antibody (NAb) assays• Maintenance of instruments, and address technical and instrumental issues• Assist the Principal Investigator with study conduct• Maintain study documentation• Meet regulatory compliance requirements• Maintain a safe work environment Requirements : Bachelor's degree in related scientific discipline or Bachelors degree with relevant experience• At least 2 years working in a laboratory preferred Salary and Benefits : Frontage Laboratories offers a competitive compensation and benefits package including health and dental insurance, a 401(k) plan, disability insurance, and life insurance. Frontage Laboratories Inc. is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, religion, color, national origin, sex, sexual orientation, gender identity, age, status as a protected veteran, among other things, or status as a qualified individual with disability.

A world leader in the field of in vitro diagnostics for over 55 years, bioMérieux provides diagnostic solutions which determine the source of disease and contamination to improve patient health and ensure consumer safety. In North America we have more than 5,000 team members across 11 sites or subsidiaries, including Salt Lake City-based BioFire Diagnostics and one subsidiary in Montreal, Canada. Come and join a family-owned global company with a long-term vision, and a human-centered culture. Position Summary: The Molecular Biologist is responsible for planning, implementation and management of PCR and qPCR processes and products. This individual will be expected to provide scientific guidance and molecular expertise in transferring completed development projects from research to operations and production. They will ensure operations has accurate and detailed SOPs as well as lead troubleshooting projects that arise in Operations. His/her direct reporting will be to The Director of Manufacturing. Responsibilities: Responsible for production and filling of PCR solutions in accordance with standard work instructions Leading technology transfer from R&D to Operations from assay development to production SOP generation and scaling from R&D to Operations from assay development to production Design and develop troubleshooting and root cause identification of Operations related issues, specifically related to PCR and molecular diagnostics Assist with design, implementation, and maintenance of PCR automation Proactively implement quality and productivity improvements Maintain knowledge of company operations, departments, organization, and executive's direct reports Studies and Experience: MS or Ph.D. in Molecular Biology and between 2 to 5 years of industry experience or equivalent experience in GMP related industry 2 years managerial experience Quality Assurance and Quality Control experience in a regulated (FDA, GMP) industry is highly desirable Skills and Qualifications: In depth knowledge of molecular diagnostics & PCR Excellent computer, communication, interpersonal, and organizational skills required. Must be results oriented, and self-motivated Lean six sigma knowledge a plus BioMérieux Inc. and its affiliates are Equal Opportunity/Affirmative Action Employers. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, age, protected veteran or disabled status, or genetic information. Please be advised that the receipt of satisfactory responses to reference requests and the provision of satisfactory proof of an applicant's identity and legal authorization to work in the United States are required of all new hires. Any misrepresentation, falsification, or material omission may result in the failure to receive an offer, the retraction of an offer, or if already hired, dismissal. If you are a qualified individual with a disability, you may request a reasonable accommodation in BioMérieux's or its affiliates' application process by contacting us via telephone at **************, by email at **************************, or by dialing 711 for access to Telecommunications Relay Services (TRS).

Scientist II Department: Regulatory In Vitro ADME FLSA status: Exempt Are you ready to embark on an exhilarating journey with a team that's passionate about making a difference? Pharmaron is thrilled to invite you to join us as our newest Scientist II! If you're craving a role that offers challenges, growth, and meaningful impact, then this is the opportunity you've been waiting for. Job Overview: Scientist II within our Regulatory In Vitro ADME Laboratory team in Exton, PA plays an integral role in growing the operations and customer base by supporting drug metabolism (DM), ADME, and Drug-Drug interaction (DDI) studies. The Scientist II will work in a team-based environment to execute the studies, and their timely completion. Additional tasks: * Function as analyst for DM and DDI studies. * Design, and prepare ADME/DM/DDI protocols, SOPs, and procedures. * Perform drug metabolism and DDI studies, evaluate and interpret the experimental data. * Conduct studies according to appropriate study protocols/plans. * Conduct routine maintenance of room and instruments. * Review and comment on draft protocols. What We're Looking For: We are seeking individuals who have strong communication skills with attention to detail who thrive in fast-paced environments. * Master's or advanced degree in biology, biochemistry or related discipline. * 2+ years of industry experience. * Knowledge and experience with in vitro ADME assays, cell biology and maintenance, cytotoxicity assays, molecular biology experiments like RNA extraction, cDNA preparation and PCR experiments. * Ability to prioritize and manage multiple tasks concurrently, ensuring critical issues are addressed promptly while maintaining a high quality of work. Why Pharmaron? Pharmaron is a premier service provider for the life sciences industry. Founded in 2004, Pharmaron has invested in its people and facilities and established a broad spectrum of research, development, and manufacturing service capabilities throughout the entire drug discovery, preclinical, and clinical development process across multiple therapeutic modalities, including small molecules, biologics, and CGT products. With over 21,000 employees and operations in the U.S., the U.K. and China. Pharmaron has an excellent track record in delivering R&D solutions to its partners in North America, Europe, Japan, and China. Collaborative Culture: You'll thrive in our inclusive and collaborative environment, where teamwork and innovation go hand in hand. Here, your voice matters, and your contributions make a real impact. "Employees Number One" and "Clients Centered" are the core cultural values at Pharmaron. Our culture, which sets Pharmaron apart from other organizations, has evolved from our deep commitment to our employees, partners and collaborators. Comprehensive benefit package: As part of our commitment to your well-being, we offer a comprehensive benefits package: * Insurance including Medical, Dental & Vision with significant employer contributions * Employer-funded Health Reimbursement Account * Healthcare & Dependent Care Flexible Spending Accounts * 100% Employer-paid Employee Life and AD&D Insurance, Short and Long Term Disability Insurance * 401k plan with generous employer match * Access to an Employee Assistance Program How to Apply: Ready to seize this incredible opportunity? Join us at Pharmaron and be part of a dynamic team driving innovation and excellence in biopharmaceutical research and development. Apply online today! #LI-JB1

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 The Technical Operations Contractor is responsible for technical aspects of the Lifecycle Management structure and strategy for parenteral drug products including SIMPONI pre-filled syringes, STELARA pre-filled syringes, and Risperdal Consta Injection. The candidate will provide this technical support at U.S. based contract manufacturing sites such as Baxter Bloomington, IN and Alkermes, Wilmington, OH. The candidate will support technology transfers, implementation of continuous process verification programs, investigations, change control initiatives, and continuous process improvement programs. FUNCTIONAL KNOWLEDGE, SKILLS, AND ABILITIES: • Strong expertise with regard to pharmaceutical products & manufacturing processes with a focus on parenteral products • Good knowledge regulatory requirements and GMP's understands the technical aspect of the lifecycle strategy of products • applies the science based risk approach and regulatory/GMP intelligence • ability to create, maintain, and upgrade product technical knowledge and author documentation regarding these activities • ability to monitor technical process and product performance across internal and external manufacturing sites and employ statistical methods to assess • ability to participate in risk assessments with a quality and compliance perspective PERSONAL & INTERPERSONAL SKILLS / LEADERSHIP SKILLS: • Ability to participate on cross functional / cross-region project teams • Ability to manage complexity and change • Ability to interact at different levels of the organization (including Sr. Management) • Ability to work under pressure and resolve conflicts • Ability to work independently under general direction, having a good sense of prioritization of assigned tasks and manage time accordingly • Ability to participate in a result oriented project team PERSONAL ATTITUDE & MINDSET: • Can-do mentality, agility & flexibility able to work with stretched goals and deadlines • Works with others towards the project team's goals • Understands culture differences • Communicates, motivates, negotiates and is an assertive person having impact • Shows a high sense of responsibility regarding professional activities Qualifications DEGREE REQUIREMENT: Minimum requirements: BS/BA with 3 to 5 years' experience in pharmaceutical development or pharmaceutical manufacturing or related post graduate academic experience/education. Additional Information This is a time sensitive and critical position a quick response would be of great help. Contact Information: Sneha Shrivastava Technical Recrutier **************

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. 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: Competitive pay Comprehensive training Medical, dental, vision, and 401(k) matching Generous paid time off and holidays Retirement plan Tuition assistance Ability to make an impact in the communities we serve Relocation Assistance Sign on bonus 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.

Carlisle Weatherproofing Technologies (CWT) is a leading supplier of building envelope solutions that effectively drive energy efficiency and sustainability in commercial and residential applications. We are looking for a Scientist II - Asphalt in our Kimberton, PA facility. Job Summary: Looking for a bright, hard-working scientist to join our dynamic research and development team. This role is responsible for participating in the execution of laboratory work across a variety of product lines including asphalts. The scientist is to assist with manufacturing of new and existing products, and to solve factory and field problems. The scientist plans their work, under the guidance of senior scientists, to meet objectives established by R&D Director. Duties and Responsibilities: * Conduct research in the areas of formulation modifications and potential new product development * Develop new applications or customize existing applications to meet specific scientific project needs * Summarize and communicate data results to the broader technology team and recommend new systems and processes to improve operations * Document all work product in a clear and logical manner using standard scientific reports * Provide input into quality control testing protocols as necessary * Other duties as assigned Required Knowledge/Skills/Abilities: * The individual will have preferable 3+ years laboratory work experience formulating asphalt blends, and asphalt emulsions * Familiar with ASTM and AASHTO standard methods * The individual will have a track record of executing technology projects from inception through completion. * Demonstrated ability to take product concepts from the laboratory to the plant and ultimately to commercialization. * Comfortable working and communicating with Operations/Manufacturing to facilitate scale-up; * Possess an understanding of the chemistry, physical properties, processing and storage of finished product formulations and their potential utilization in other applications, as well as aging mechanisms; * Experience in DSC, TGA, DSR, Instron, Iatroscan, and SEM a plus. Essential Full Performance Skills: * Ability to work independently and take initiative, with the ability to evaluate new, unconventional ideas and apply them for improvement of the product performance. * Proficiency in Microsoft products and laboratory tools. * Demonstrated knowledge in laboratory safety. * Exceptional attention to detail in all aspects of work with the ability to handle multiple projects simultaneously. * Ability to communicate effectively. Education and Experience: * Required: * Bachelors Degree in Chemistry, Chemical Engineering, Polymer Chemistry, Material Science, or equivalent * 3+ years of relevant laboratory experience specific to formulations Working Conditions: * In addition to the standard laboratory and office environments, this position involves occasional work off-site at manufacturing facilities and job sites typical of the industrial trade. Physical Requirements: * Sitting, standing, walking. #LI-MW1 Education and Experience: * Required: * Candidates should possess a degree in Chemistry, Chemical Engineering, or Materials Science. * Work experience: BS/MS >10 years, PhD with >5 years. * Experience with adhesive or coatings for water and/or weather proofing applications. * Experience with Hot Melt Pressure Sensitive Adhesives (HMPSA), Butyl based adhesives, or Silyl-Terminated Polyether (STPE) / Silyl-Terminated Polyurethanes (STPU) preferred.

Our mission is to inspire children through science, sparking lifelong imagination and curiosity. For over 25 years, we have delivered unique, hands-on science experiences for children through our after-school programs, birthday parties, workshops, special events, and summer camps. Our innovative programs are as entertaining as they are educational! Mad Science is the world's leading provider of fun science programs for elementary-aged children. As a Mad Scientist, you will lead students through an inquiry-based discovery method involving instructor demonstrations, hands-on activities, and amazing take-home projects that will illustrate how science affects the world around us. Build and fly rockets, demonstrate lasers, explore the states of matter using dry ice, and create slime and other polymers. You will inspire the next generation of scientists through our innovative activities that show kids what science is really about. Responsibilities Facilitate a one-hour after-school science enrichment program using a pre-set curriculum. · Attend orientation and training prior to starting your programs.· Ensure the safety of the kids during programs· Engage with the kids during the activities and experiments. The goal is for the the kids to have fun, not sit through a lecture.· Must be able to lift equipment in kits, can vary in size and weight (heavier kits have wheels). Your vehicle must be able to accommodate the equipment. · Must be able to drive to and from the program with your own vehicle. Programs near you include locations in Haddonfield, Moorestown, and more. Schedule and Pay- You will be scheduled at a school close to you where you will report to at the same day and time each week for either 6 or 8 consecutive weeks. Programs typically start at between 3-3:45PM and last 1.5 hours. - $40 for a 1.5 hour program- Mileage is compensated for any program over 25 miles round trip. Qualifications- Must have experience working with children.- Your own reliable car and license.- Must be over 18 years of age. - Must be vaccinated for COVID-19.- A background in science and/or experiencing performing is a plus! Compensation: $40.00 per hour Mad Science is a powerhouse brand with locations around the globe! For over 35 years, we have sparked imaginative learning through our summer camps, birthday parties, in-class workshops, after-school programs, and special events for kids ages 3-12. Become part of our team and help us inspire the next generation of scientists and engineers. Our locations are always looking for part-time instructors and full-time office staff.

Mindlance is a national recruiting company which partners with many of the leading employers in the Life Sciences, IT, and Financial Services sectors, feel free to check us out at ************************* Job Description The successful candidate will be responsible for performing multiple biochemical assays to screen compounds and profile lead candidates for pharmaceutical targets. Job requirements include ability to work with purified proteins, compound plate creation and tracking and perform biochemical assays. The successful candidate will work as part of an interactive research team; will report results of studies back to team members and in a timely, thorough, and coherent manner. Such a position requires an energetic, highly organized and motivated person. Requirements include compound plate creation using dispensers such as ECHO, compound ordering and tracking, execution of biochemical assays using automated liquid handlers and spectroscopic readers and generation of electronic notebooks that document all performed work. Good communication skills as well as an aptitude to perform research activities in a collaborative and result-driven setting are a must. Qualifications The successful candidate will possess an M.S. with 1-3 years of experience or a B.S. /B.A. with 2-4 years of experience or the equivalent training/experience. Additional Information All your information will be kept confidential according to EEO guidelines.

• Carry out standard operating procedures involving basic laboratory techniques, operation of laboratory equipment and record keeping necessary to a research laboratory. • Responsible for E-notebook records. Quals-- Education: Bachelor's Degree/ Master's Degree in life science related fields with at least 4 years of lab experience. Skills: • Requires at least 2 year experience in the application of Molecular Biology laboratory techniques in industrial or academic settings. • Experience in the use of basic laboratory techniques, including ELISA, DNA extraction, PCR, Nucleic acid gel electrophoresis, cloning, restriction enzyme digests, transformations, etc. Personality: • Detail Oriented • Flexible • Team player • Optimistic Note: • 100% lab based onsite role at WestPoint,PA

Responsibilities Develop, validate, and troubleshoot bioanalytical methods (e.g., ELISA, MSD, qPCR/RT-qPCR, etc.) for sample testing and data reporting, serving as the Principal Investigator (PI) as required. Present and interpret data both internally and externally, ensuring clarity and scientific rigor. Maintain client satisfaction through timely communication, responsiveness, and on-schedule delivery of high-quality results. Prepare and review laboratory data and controlled documents, including study plans and final reports. Support laboratory operations and provide mentorship to junior staff members. Contribute to the development and refinement of policies, procedures, work instructions, and standard operating procedures (SOPs). Ensure compliance with company standards, including Code of Conduct, Environmental Health and Safety (EHS), and GLP/GCP/GDP regulations. Perform additional duties as assigned to support team and organizational goals. Skills, Education & Qualifications BA/BS or higher with 7-8 years lab experience; all experiences will be evaluated Knowledge and understanding of regulatory requirements; GLP, GCP, 21CFR Part 11, GDP, GMP Able to independently perform complex lab work Able to work in a regulated environment Able to work effectively and contribute within a team Able to work with computer systems Able to document clearly Knowledge of and experience in a regulatory environment

Scientist, Biologics Full-time Frontage Laboratories Inc. is an award winning, full-service, CRO/Contract Research Organization operating over 25 state-of-the-art laboratories across the US, Canada and China. Our core competencies include drug metabolism, pharmacokinetics/ pharmacodynamics (PK/PD), safety and toxicology, bioanalytical services, chemistry and manufacturing controls for drug development, and core laboratory services for clinical trials. Responsibilities: Primary responsibilities include, but are not limited to the following: Perform analytical and biological sample testing • Conduct method development and validation studies • Perform immunoassay techniques: (ligand binding assays, ELISA, MSD, and/or RIA applicable to Pharmacokinetic and Immunogenicity studies), with proficiency • Prepare and handle various cell lines, tissue culture media and other reagents for cell-based assays such as Neutralizing Antibody (NAb) assays • Maintenance of instruments, and address technical and instrumental issues • Assist the Principal Investigator with study conduct • Maintain study documentation • Meet regulatory compliance requirements • Maintain a safe work environment Requirements: Bachelor's degree in related scientific discipline or Bachelors degree with relevant experience • At least 2 years working in a laboratory preferred Salary and Benefits: Frontage Laboratories offers a competitive compensation and benefits package including health and dental insurance, a 401(k) plan, disability insurance, and life insurance. Frontage Laboratories Inc. is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, religion, color, national origin, sex, sexual orientation, gender identity, age, status as a protected veteran, among other things, or status as a qualified individual with disability.

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 • The scientist will be responsible for activities that support protein expression in E.coli, baculovirus/insect, and/or mammalian expression system, such as cell culture, small scale expression evaluation and large scale expression in flasks and wave bags. • The scientist will also be responsible for establishing Client purification protocols or follow established protocol using IMAC, SEC and other purification media to provide protein for high-throughput screening and crystallography studies. • Additional responsibilities include experimental design, data analysis, troubleshooting, participation in project teams and maintaining detailed records. Qualifications • The qualified candidate will have a BS, MS in biological sciences, biochemistry or related scientific discipline. • A minimum of 3-5 year of experience in a laboratory setting is required (with preferably 2 years in industry). • Experience in expression in the three expression systems mentioned above is preferred. Experience in protein purification techniques is required. • Familiarity with the use of the AKTA purification systems would be a plus. Additional Information Anuj Mehta Technical Recruiter (Clinical/Scientific) Artech Information Systems LLC 360 Mt. Kemble Avenue, Suite 2000 | Morristown, NJ 07960 Office: ************ | Fax: ************ Connect with us on - LinkedIn | Facebook | Twitter

Hello Jobseekers Net2Source is hiring for its direct client a Scientist - II (Associate) for their growing team. Please find below the job description. Title : Scientist - II (Associate) Duration : 12 months Rate : $40/hr - $52.00/hr on W2 No Benefits Note : PhD will be overqualification Responsibilities/ Duties: • Carry out standard operating procedures involving basic laboratory techniques, operation of laboratory equipment and record keeping necessary to a research laboratory. • Responsible for E-notebook records. Qualifications Education: Bachelor's Degree/ Master's Degree in life science related fields with at least 4 years of lab experience. Skills: • Requires at least 2 year experience in the application of Molecular Biology laboratory techniques in industrial or academic settings. • Experience in the use of basic laboratory techniques, including ELISA, DNA extraction, PCR, Nucleic acid gel electrophoresis, cloning, restriction enzyme digests, transformations, etc.

Scientist, Biologics Full-time Frontage Laboratories Inc. is an award winning, full-service, CRO/Contract Research Organization operating over 25 state-of-the-art laboratories across the US, Canada and China. Our core competencies include drug metabolism, pharmacokinetics/ pharmacodynamics (PK/PD), safety and toxicology, bioanalytical services, chemistry and manufacturing controls for drug development, and core laboratory services for clinical trials. Responsibilities: Primary responsibilities include, but are not limited to the following: * Perform analytical and biological sample testing * Conduct method development and validation studies * Perform immunoassay techniques: (ligand binding assays, ELISA, MSD, and/or RIA applicable to Pharmacokinetic and Immunogenicity studies), with proficiency * Prepare and handle various cell lines, tissue culture media and other reagents for cell-based assays such as Neutralizing Antibody (NAb) assays * Maintenance of instruments, and address technical and instrumental issues * Assist the Principal Investigator with study conduct * Maintain study documentation * Meet regulatory compliance requirements * Maintain a safe work environment Requirements: * Bachelor's degree in related scientific discipline or Bachelors degree with relevant experience * At least 2 years working in a laboratory preferred Salary and Benefits: Frontage Laboratories offers a competitive compensation and benefits package including health and dental insurance, a 401(k) plan, disability insurance, and life insurance. Frontage Laboratories Inc. is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, religion, color, national origin, sex, sexual orientation, gender identity, age, status as a protected veteran, among other things, or status as a qualified individual with disability. *

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: • Working within the Prostate/IO drug discovery team to execute in vitro and ex vivo experiments to be used for compound candidate selection and to explore the therapeutic potential of drug targets. • Contribute to development, optimization and troubleshooting of immunological-based assays • Works with minimal supervision on projects of moderate to complex scope • Uses good verbal communication skills and interpersonal skills to communicate with other team members Other duties include data analyses, maintain electronic notebook records of experimental data, summarize and communicate results in internal meetings Must have experience in: • Flow cytometry techniques and flow cytometry analysis. Multicolor flow cytometry experience is strongly desirable.\ • Basic aseptic cell culture technique, such as maintaining cell lines and primary cells, cell banking, etc . • Basic skills in molecular biology including transfection and viral transduction, DNA isolation, cloning, etc . • Experience with cell-based immunoassays, and working with primary cells and ex- vivo analyses is desired . • Familiarity with basic cell purification techniques and immunological phenotyping procedures, as well as processing blood and primary human and rodent tissues, is also desired Demonstrated creativity and Client approaches to solving technical problems • Strong organizational skills including the ability to manage several projects simultaneously • Excellent interpersonal skills with the ability to interact effectively with people, internally and externally Methodical, reliable and comfortable working under fixed timelines Detail-oriented, with excellent record-keeping skills Qualifications Requirements: BA/BS or MA/MS degree in immunology, pharmacology, molecular biology, cancer biology, or related field. 2-5 years of experience (MS/MA) or 2-8 years (BA/BS) years of experience, performing progressively advanced duties at the Associate Scientist I level, or the equivalent training/experience Additional Information Best Regards, Sneha Shrivastava ************