Senior scientist jobs in Upper Darby, PA

Job Title: Equipment Validation Scientist Hours: Monday-Friday, 9:00am-5:00pm Hiring Method: 3 Year Contract Pay Range: $40.00 - $45.00/hr Benefits: Health, Dental, Vision Insurance + 10 Days PTO, 6 Sick Days, and all company paid holidays annually Job Description Our Bio-pharmaceutical Client is seeking an Equipment Validation Scientist to join their team in West Point, PA. This individual will be a part of the Discovery, Preclinical and Translational Medicine Operations organization and will be responsible for supporting process automation systems in clinical and non-clinical Regulated Bioanalytic, Vaccine Modernization laboratories. This position may provide direct support to lab equipment maintenance, system security, data management, obsolescence initiatives, and all SDLC and Compliance needs. They will work closely with divisional/enterprise Information teams, global infrastructure, and risk/security organizations to ensure that project deliverables and ongoing operations receive appropriate support. They will also be responsible for the successful implementation of Automation solutions, system and equipment validation, Change Control and testing documentation. The Equipment Validation Scientist will develop a suite of reporting, analytics and visualization solutions that support local clinical operations and administrative business processes; ensure automation systems are maintained in a validated state, as part of an active/ongoing lifecycle management program and in compliance with Current GXP requirements; And will be accountable for implementing system changes and conducting system investigations. They will have active and engaged participation in the routine operations support processes as well as supporting a culture of continuous improvement at the site. This will include trouble-shooting challenging equipment/automation issues to improve performance, engaging in vendor and IT support needs, responding to alarms, and implementing future AI/ML capabilities as available. They will be providing support or leading a small startup or existing production team providing technical assistance in fulfilling the automation requirements for the team and reviewing automation documents, preventive maintenance, and Standard Operating Procedures to ensure compliance with GXP Practice and corporate safety requirements. In addition, they will be developing and supporting corrective actions for investigations related to automation systems, using technical knowledge to assure the efficient operation of a variety of automated processing and operational and informational technology systems and participating in compliance audits and training programs including providing client services support for business area laboratory applications. Required Skills and Experience Laboratory Experience Lab Equipment Maintenance experience SDLC Experience GLP or GXP experience Bachelor's degree in Scientific or Engineering field Nice to Have Skills and Experience Master's Degree Automation Experience Compensation: $40.00/hr to $45.00/hr. Exact compensation may vary based on several factors, including skills, experience, and education. Healthcare benefit packages for this role will start on the 1st day of employment and include medical, dental, and vision insurance, financial protection benefits, as well as HSA, FSA, and DCFSA account options. 401k retirement account access is offered starting on the 90th day with employer matching after one year of service. Employees in this role are also entitled to paid sick leave and/or other paid time off as provided by applicable law.

Responsibilities · Prepare reagents, standards, and control samples · Analyze samples using various techniques specific to department · Independently design and develop methods · Perform method validation or qualification · Operate analytical equipment · Technical resource for 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 · Collaborate across teams, departments, and sites · Evaluate and establish processes to improve quality and efficiency · Record tasks in accordance with Good Documentation Practices (GDP) · Knowledge of regulatory requirements; GLP, GCP, 21CFR Part 11 · Follow applicable SOPs and procedural documents · Other tasks as assigned Education, Experience & Skills Required · BA/BS or higher with 11-12 years lab experience; all experiences will be evaluated · PhD in relevant field with 3-5 years lab experience · Knowledge and understanding of regulatory requirements; GLP, GCP, 21CFR Part 11, GDP, GMP · Able to independently develop and 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 · Able to communicate clearly Physical Demands · Must be able to sit at a desk for up to 6 hours per day · Walking and/or standing as required for the rest of the working day · Must be able to occasionally lift 15 lbs.; this includes lifting boxes, equipment, etc. · Bending or standing as necessary · The length of time of these tasks may vary from day to day and task to task

Preparation of samples, reagents and standards for analysis, following standard procedures. XRD data acquisition and assessing basic data quality. X-ray tomography data acquisition and assessing basic data quality. Electron microscopy data acquisition and assessing basic data quality. Particle and Energetics data acquisition and assessing basic data quality. (e.g. particle size, density, contact angle, surface tension, surface area) Performing routine instrument operation. Disposal of lab waste, following a set protocol. Cleaning and restocking lab areas as needed. Minimum Qualifications: B.S. in chemistry, materials science, physics, or engineering or demonstration of equivalent knowledge acquired in on-the-job training. Skills in sample preparation, safely handling chemicals, and experience with a variety of lab equipment in a chemical laboratory setting are essential to this position. An ability to work well with other people under tight timelines and conflicting priorities is critical.

Since 1869, we've connected people through food they love. We're proud to be stewards of amazing brands that people trust. Our portfolio includes the iconic Campbell's brand, as well as Cape Cod, Chunky, Goldfish, Kettle Brand, Lance, Late July, Pacific Foods, Pepperidge Farm, Prego, Pace, Rao's Homemade, Snack Factory, Snyder's of Hanover. Swanson, and V8. Here, you will make a difference every day. You will be supported to build a rewarding career with opportunities to grow, innovate and inspire. Make history with us. Why Campbell's… Benefits begin on day one and include medical, dental, short and long-term disability, AD&D, and life insurance (for individual, families, and domestic partners). Employees are eligible for our matching 401(k) plan and can enroll on the first day of employment with immediate vesting. Campbell's offers unlimited sick time along with paid time off and holiday pay. If in WHQ - free access to the fitness center. Access to on-site day care (operated by Bright Horizons) and company store. Giving back to the communities where our employees work and live is very important to Campbell's. Our “Campbell's Cares” program matches employee donations and/or volunteer activity up to $1,500 annually. Campbell's has a variety of Employee Resource Groups (ERGs) to support employees. How you will make history… Imagine...working for a company that knows that its people are the key to its success in the marketplace. A company in which achieving extraordinary results and having a stimulating work experience are part of the same process. We cultivate and embrace a diverse employee population. We recognize that people with diverse backgrounds, experiences and perspectives fuel our growth and enrich our global culture. We are looking for an individual who enjoys working in a fast-paced, team-oriented environment, likes to be challenged, and values the opportunity to make a difference. The Associate Scientist R&D will be responsible for supporting the Research & Development activities on the RTS Soup & Innovation Product Development Team. In this role you will be executing projects across the Soup & Broth portfolio, including ready to serve soup and innovation. The scope of the job encompasses the entire Product Development process from idea conception through plant commercialization. What you will do… Execute work plans for the Ready to Serve Soup Business supporting one or more projects of low to moderate complexity and technical risk. Demonstrate organizational and planning skills. Assist with the development and execution of project timelines, which include contingency planning. Leverage vendor capabilities to expand formulation possibilities and ingredient solves to increase speed to market. With guidance, develop prototypes to support concept and ideation exploration work and continue to refine the prototypes based on consumer feedback. Work on the bench and pilot plant line to understand initial feasibility of new products and conduct ingredient screenings during benchtop evaluation. Conduct trials in the Pilot Plant and/or manufacturing facilities to assess manufacturing capability and consumer acceptability. Incorporate nutritional and cost parameters into product design. Demonstrate flexibility and agility by being able to adapt quickly to changes in direction. Partner with team members to advance projects and be able to function effectively in a cross-functional team environment. Lead cross-functional tastings with business partners and stakeholders. Communicate plans, results and project risks to vendors, senior functional staff and/or business teams as required. Work independently to create new concepts based on research, benchmark and creativity solutions. Who you will work with… In this role you will report to the Manager of Research and Development - Soup & Broth. What you bring to the table… (Must Haves) Bachelor of Science or higher in Food Science or related field. Minimum of 6 months in CPG or Foodservice industry or related experience with basic or Co-Op food product development experience. It would be nice if you have… (Preferred Skills) Demonstrated skills in commercializing products/processes in the manufacturing environment are desired. Creative problem-solving skills. Technical, culinary, and new product curiosity for food. Ability to work with ambiguity and seek creative solutions. Inclination to work in a team environment. Strong planning and organizing skills. Ability to synthesize data, interpret, and provide recommendations. Highly capable with lab practices, running & improving test methods, material preparation, and batch assessment. Strong planning and organizational skills. Good written and oral communication skills. Basic understanding of consumer testing methodologies. Computer skills include basic fluency in Microsoft Office, and database management. Working Conditions: Anticipated travel of up to 30% to locations which may include the following: World Headquarters (WHQ) Office, Research Kitchen, Pilot Plant, and Manufacturing Plants (Campbell Soup Company (CSC), co-manufacturers and vendors). A significant portion of the job is in the thermal production environment; thus, the work exposes the employee to heat and hot food products, coolers, and freezers requiring the use of personal protective equipment. Ability to walk or stand up at times for up to ¾ of the workday. Physical ability to handle weights of up to approximately thirty pounds. Handle allergens including dairy, peanuts, tree nuts, soy, wheat, eggs and other food ingredient chemicals and allergens while wearing appropriate PPE. Willingness and ability to taste and evaluate a wide range of food products and ingredients. Compensation and Benefits: The target base salary range for this full-time, salaried position is between $57,800-$83,100 Individual base pay depends on work location and additional factors such as experience, job-related skills, and relevant education or training. Total pay may include other forms of compensation. In addition, we offer competitive health, dental, 401k and wellness benefits beginning on the first day of employment. Please ask your Talent Acquisition Partner for more information about our total rewards package. The Company is committed to providing equal opportunity for employees and qualified applicants in all aspects of the employment relationship, including consideration for employment, without regard to race, color, sex, sexual orientation, gender identity, national origin, citizenship, marital status, protected veteran status, disability, age, religion, or any other classification protected by law.

At Lilly, we unite caring with discovery to make life better for people around the world. We are a global healthcare leader headquartered in Indianapolis, Indiana. Our employees around the world work to discover and bring life-changing medicines to those who need them, improve the understanding and management of disease, and give back to our communities through philanthropy and volunteerism. We give our best effort to our work, and we put people first. We're looking for people who are determined to make life better for people around the world. Organization Overview: At Lilly, we unite caring with discovery to make life better for people around the world. We are a global healthcare leader headquartered in Indianapolis, Indiana. Our 35,000 employees around the world work to discover and bring life-changing medicines to those who need them, improve the understanding and management of disease, and give back to our communities through philanthropy and volunteerism. We give our best effort to our work, and we put people first. We're looking for people who are determined to make life better for people around the world. Responsibilities: Lilly Imaging/Avid Radiopharmaceuticals provides technical expertise for molecular imaging to Lilly Research Laboratories. The scientist will provide expertise for biological assay development for the discovery and characterization of novel PET imaging agents, with a focus on neuroscience or oncology imaging and other therapeutic areas. This scientist will work independently, coordinating experimental details of internal and external partnered projects, conducting experiments him/herself, performing data analysis, and presenting data to internal teams and the international scientific community. Establish and execute imaging research projects supporting oncology, neuroscience or other drug discovery and biomarker projects Design and conduct novel binding assays, including radioligand binding assays Characterize and purify biological targets Collaborate with internal project teams, implement translatable imaging biomarker assays and ensure seamless translation of projects Publish results of research projects as appropriate Participate in extramural scientific organizations and attend scientific symposia as well as workshops in order to continue educational/professional development Other duties as assigned Basic Requirements: Degree in physical or biological sciences or imaging-related field Bachelor's degree with min of 15 years' experience, master's with a min of 12 years' experience, or PhD in scientific field. Experience with in vitro assay development Peer-reviewed publications Additional Skills/Preferences: PhD degree preferred Experience in Oncology or Neuroscience, preferably in molecular imaging Experience designing and executing novel biochemical, cellular and tissue assays, including radioligand binding assays (e.g. filtration binding, ELISA/AlphaLISA, SPR and LC/MS) Experience working with amyloidogenic proteins Demonstrated ability to independently conceive, design and execute the characterization and purification of biological targets Experience in drug discovery of PET molecular imaging agents Peer reviewed publications Willingness/desire to learn and incorporate additional technologies or therapeutic area biology to address imaging needs Excellent communication skills (both written and verbal) Excellent presentation skills Strong organizational skills and ability to effectively manage multiple priorities Creativity and critical thinking skills Team Player Additional Information: Lilly is an EEO/Affirmative Action Employer and does not discriminate on the basis of age, race, color, religion, gender, sexual orientation, gender identity, gender expression, national origin, protected veteran status, disability or any other legally protected status Eli Lilly and Company, Lilly USA, LLC and our wholly owned subsidiaries (collectively “Lilly”) are committed to help individuals with disabilities participate in the workforce and ensure equal opportunity to compete for jobs. If you are an individual with a disability and require a reasonable accommodation to participate in the application process, please email Lilly Recruiting Compliance. Please note, this email address is intended for use only to request a disability accommodation, please email Lilly Recruiting Compliance for further assistance. Inquiries which are not requests for accommodations may not receive a response. Lilly is dedicated to helping individuals with disabilities to actively engage in the workforce, ensuring equal opportunities when vying for positions. If you require accommodation to submit a resume for a position at Lilly, please complete the accommodation request form (******************************************************** for further assistance. Please note this is for individuals to request an accommodation as part of the application process and any other correspondence will not receive a response. Lilly is proud to be an EEO Employer and does not discriminate on the basis of age, race, color, religion, gender identity, sex, gender expression, sexual orientation, genetic information, ancestry, national origin, protected veteran status, disability, or any other legally protected status. Our employee resource groups (ERGs) offer strong support networks for their members and are open to all employees. Our current groups include: Africa, Middle East, Central Asia Network, Black Employees at Lilly, Chinese Culture Network, Japanese International Leadership Network (JILN), Lilly India Network, Organization of Latinx at Lilly (OLA), PRIDE (LGBTQ+ Allies), Veterans Leadership Network (VLN), Women's Initiative for Leading at Lilly (WILL), en Able (for people with disabilities). Learn more about all of our groups. Actual compensation will depend on a candidate's education, experience, skills, and geographic location. The anticipated wage for this position is $121,500 - $198,000 Full-time equivalent employees also will be eligible for a company bonus (depending, in part, on company and individual performance). In addition, Lilly offers a comprehensive benefit program to eligible employees, including eligibility to participate in a company-sponsored 401(k); pension; vacation benefits; eligibility for medical, dental, vision and prescription drug benefits; flexible benefits (e.g., healthcare and/or dependent day care flexible spending accounts); life insurance and death benefits; certain time off and leave of absence benefits; and well-being benefits (e.g., employee assistance program, fitness benefits, and employee clubs and activities).Lilly reserves the right to amend, modify, or terminate its compensation and benefit programs in its sole discretion and Lilly's compensation practices and guidelines will apply regarding the details of any promotion or transfer of Lilly employees. #WeAreLilly

Legend Biotech is a global biotechnology company dedicated to treating, and one day curing, life-threatening diseases. Headquartered in Somerset, New Jersey, we are developing advanced cell therapies across a diverse array of technology platforms, including autologous and allogenic chimeric antigen receptor T-cell, T-cell receptor (TCR-T), and natural killer (NK) cell-based immunotherapy. From our three R&D sites around the world, we apply these innovative technologies to pursue the discovery of safe, efficacious and cutting-edge therapeutics for patients worldwide. Legend Biotech entered into a global collaboration agreement with Janssen, one of the pharmaceutical companies of Johnson & Johnson, to jointly develop and commercialize ciltacabtagene autolecuel (cilta-cel). Our strategic partnership is designed to combine the strengths and expertise of both companies to advance the promise of an immunotherapy in the treatment of multiple myeloma. Legend Biotech is seeking a Scientist II as part of the R&D Novel Car Design team based in Philadelphia, PA. Role Overview We are seeking a highly motivated and creative scientist to grow our pipeline efforts. The successful candidate will be part of Legend Biotech, a leading cell therapy company with commercial CAR drug product CARVYKTI and an attractive pipeline portfolio. The candidate will be an integral part of our R&D team, whose aim is to research, develop and advance the next generation of cell therapies using cutting edge in vivo gene delivery technologies and create innovative novel CAR designs for a wide range of human indications. This position will focus on in-vivo CAR. The position requires enthusiasm, passion, outstanding skills in the art, attention to detail, and a desire to create new medicines for patients. Key Responsibilities Be able to work independently under minimal supervision. Lead, design and optimize research with aims of exploring next generation cell therapies using in-vivo CAR virus Perform functional characterization of T cells transduced with in-vivo CAR virus using multiple functional assays but not limited to cytotoxicity assay, serial cytotoxicity assay, and cytokine release assay etc. Help execute the evaluation of in-vivo CAR virus using in-vitro assays and in-vivo mice models. Design, execute and interpret research requiring molecular biology techniques including PCR/DDPCR/ qPCR, NGS, RNA and DNA analysis. Perform research requiring cell biology techniques including cell culture, transfection, FACS, and cellbased assays. Analyze and present data to a wide range of audiences of internal group meetings and other forums. Dissect published literature to find novel solutions to in-vivo cell therapy problems. Generate, manage, evaluate, and maintain critical data in a highly organized manner. Requirements PhD in Biology or related discipline 3 years of experience in the field of cell therapy with cell culture methods (T cells, CAR-T or TCR-T preferred), quantitative PCR and functional characterization of T cells (Cytotoxicity assay using Incucyte or xCelligence, and MLR assay). Prior experience with in-vivo CAR virus evaluation will be preferred. Proficient in cell-based assays with various read out technologies such as flowcytometer, Incucyte, Xcelligence. Experience with transfection and lentivirus or retrovirus transduction. Experience/ working knowledge (molecular biology and cellular biology) in design and evaluation of modified viruses. Individual should be go-getter and be able to work independently. Excellent written and oral communication skills. #Li-JR1 #Li-Hybrid The anticipated base pay range is $107,482 - $141,070 USD Benefits We are committed to creating a workplace where employees can thrive - both professionally and personally. To attract and retain top talent in a highly competitive industry, we offer a best-in-class benefits package that supports well-being, financial stability, and long-term career growth. Our offerings are designed to meet the diverse needs of our team members and their families, ensuring they feel valued and supported every step of the way. Highlights include medical, dental, and vision insurance as well as a 401(k)-retirement plan with company match that vest fully on day one. Equity and stock options are available to employees in eligible roles, we offer eight weeks of paid parental leave after just three months of employment, and a paid time off policy that includes 15 vacation days, 5 personal days, 5 sick days, 11 U.S. national holidays, and 3 floating holidays. Additional benefits include flexible spending and health savings accounts, life and AD&D insurance, short- and long-term disability coverage, legal assistance, and supplemental plans such as pet, critical illness, accident, and hospital indemnity insurance. We also provide commuter benefits, family planning and care resources, well-being initiatives, and peer-to-peer recognition programs - demonstrating our ongoing commitment to building a culture where our people feel empowered, supported, and inspired to do their best work. EEO Statement Legend Biotech is a proud equal opportunity/affirmative action employer committed to attracting, retaining, and maximizing the performance of a diverse and inclusive workforce. It is Legend's policy to ensure equal employment opportunity without discrimination or harassment based on race, color, religion, sex (including pregnancy, childbirth, or related medical conditions), sexual orientation, gender identity or expression, age, disability, national origin, marital or domestic/civil partnership status, genetic information, citizenship status, uniformed service member or veteran status, or any other characteristic protected by applicable law. Employment is at-will and may be terminated at any time with or without cause or notice by the employee or the company. Legend may adjust base salary or other discretionary compensation at any time based on individual, team, performance, or market conditions. Legend Biotech maintains a drug-free workplace.

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: Scientist II Location: Fort Washington, PA Duration: 12 Months Job Description: II. Position Summary: Provides testing, technical and troubleshooting support in the QC laboratories. These functions include: Collection, processing, method development and testing of chemical components, bulk products, raw materials, packaging components, finished products, marketed product stability, in-process materials, scale up, validation and cleaning validations to conform with specifications and standard operating procedures (SOPs). Thorough knowledge of SOPs, USP and other applicable pharmacopeia. Possess foresight to recognize task needs and performs the trained task without the request of management. Reviews and/or writes the following documents: APR, SOPs, QSRs, Instrument qualification, protocol/report writing, trending and review/analysis of data. Performs statistical analysis in support of APRs, Stability, and Product Release. Complies with cGMPs, safety training and regulations. Performs more advance technical projects under the supervision of management. Maintains an environment of respect and teamwork with all coworkers. The Company's management reserves the right to add, delete or otherwise alter assigned duties at any time. To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. The requirements listed are representative of the knowledge, skill, and/or ability required. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. III. Responsibilities : (Define key accountabilities and/or activities.) Under limited supervision and in accordance with all applicable federal, state and local laws/regulations, the Companies' policies, procedures and guidelines, this position: Ensure quality and compliance in all my actions by: o Attend GMP training on the schedule designated for my role and as appropriate for my role o Adhere to strict compliance with procedures applicable to my role. o Exercise the highest level of integrity in the tasks that I perform o In a timely and prompt manner, identify report and seek correction for deviations noted in my workplace. o Embrace a behavior of employee involvement and commitment to doing the job right the first time Systems Knowledge • Be a Power User in the applicable systems and roles assigned. • Trained to the role in which you are assigned as required for your job function in the applicable systems • Utilize tools within MS office and other systems to improve business effectiveness • Exposure to & working knowledge of electronic batch records and/or other automated processes/systems (labs) • Working knowledge of SAP or ERP system; including other relevant systems per role • Working knowledge of an automated system. Product Knowledge • Understanding of product family, product size and put-up, and product characteristics (color, viscosity) associated active and excipient. Critical parameter associated with all processing steps. Training • Can act as SME and be a curriculum owner. • Partner with training department to create training materials including curricula. • Can act as qualified trainer in specific areas. • Participate in all trainings. • Ensure all trainings are completed on-time. Investigations • Assists in gathering information and documentation as required. • Participates in investigations as required. Compliance - Safety, GMP, Facilities • Provide support during regulatory inspections /audits as directed. Support may be in the form of scribes, runner, and document gathering. • Attend GMP training on the schedule designated for the role and as appropriate for the role. • May provide statistical analysis in support of the APR and Stability processes. • Adhering to strict compliance with procedures according to the roles and responsibilities. • Exercises the highest level of integrity in the tasks performed • In a timely and prompt manner, identify report and seek correction for deviations noted in the workplace. • Embrace a behavior of employee involvement and commitment to doing the job right the first time. • Strong working GMP knowledge. Communicates and identifies GMP gaps. • Can participate in all types of audits & Inspections. • Leads areas in ensuring all operations (processes) are completed in a compliant and safe manner. • Assists in coordination efforts in case of emergency- spill, fire etc. • Takes necessary action to eliminate and immediately address safety hazards. Communicate any observed unsafe behaviors immediately. • Understands the safety concerns and promotes a safety conscience culture for their job function. • Wears the appropriate PPE when working in manufacturing and other hazardous working environments and advocates standards of safety. • Contributes and attends all EHS programs as assigned. • Promptly communicates deficiencies to management. • Maintains facility and work area in good working condition. • Works with team to ensure all aspects of business remain compliant. Documentation Management • Edits documentation (i.e. Standard Operating Procedures, work instructions) as necessary. • Perform/assist in the completion and documentation of the process steps as per the documentation directives. • Complete visual verification of the process and document these steps in the appropriate system. • Document all activities per the GMP requirements. Process Excellence, Lean, Continuous Improvement, ME2 • Completes PE/ Lean awareness training. • Proactively identifies opportunities for continuous improvement and proposes actions to address these opportunities. • Participates and leads continuous improvement implementations and kaizen events. Understands and applies PE tools in daily work activities. Leadership • Job expert that less experienced personnel can go to for assistance. • Provides leadership in absence of supervisors (for short periods). • Assist management through change and transformation activities. • Facilitates departmental meetings and may assist in the coordination of other scheduled meetings. In absence of management, attends meetings on his/her behalf. • Continuously demonstrates all GLP values; specifically: integrity and credo based actions, self awareness and adaptability, results and performance driven, organization and talent development, and collaboration and teaming. Demonstrated behaviors include: fairness, honesty, consistent and ethical behaviors, empathy and collaboration. • Contributes and supports an environment that fosters diversity and inclusion. • Exhibits and lives core values and behaviors. • Contributes to a climate of open communication, engagement and ownership within team. • Builds working relationships • Provides feedback to site management • Supports strategic and tactical plans in alignment with site's mission and plans. IV. Requirements : Education: Bachelor's Degree in Microbiology, Chemistry, Biology, Natural Science, Medical Technology, or related science is required Experience: Minimum 2 years of GMP/GLP quality control lab experience in a pharmaceutical and/or OTC and/or regulated environment is required. Physical Demands: Capable of performing routine laboratory activities. Light to moderate lifting Knowledge, Skills and Abilities: Basic knowledge/exposure of a LIMS system is preferred Additional Information Regards, Anuj Mehta ************

Who We Need We are seeking a Senior Scientist to join our R&D Inks & Coatings group. You will work alongside an outstanding team in designing and formulating both water and solvent based inks ad coatings for printing applications (primarily for rotogravure and flexography). Responsibilities: Design and formulate water & solvent based inks and coatings. Modify existing inks and coatings to meet customer requirements. Lead and support projects from lab formulation to commercialization. Work closely with raw material suppliers and internal procurement department for bringing alternate raw materials or for qualifying new raw materials. Generate and analyze data after conducting standard tests on inks and coatings. Occasional domestic travel to customers for attending technical meetings or print trials. Interact with customers to understand and define the scope of project. Regularly interact with sales, procurement and production during various stages of new product development. Other duties as assigned. Knowledge/Skills/Experience: 5-8 years minimum experience in formulating inks for printing applications. Prefer experience in ink formulation for rotogravure printing process. Experience or familiarity with printing processes such as rotogravure, flexography, screen printing and industrial digital printing. Knowledge on working with film/substrates like PVC, BOPP or PET. Able to work in highly customer focused laboratory settings. Proficient in DOE and able to work with R&D management workflow software. Ability to work in 5S and safe environment. Displays good verbal and written skills. What WE Can Do For You Penn Color offers many tangible and intangible benefits to our full time employees: Tangible benefits include: Highly competitive compensation A choice between 3 outstanding medical plans 401K with a strong company match PTO to balance your life Additional company perks And More! Our intangible benefits really set us apart: Unmatched company stability Long-term career opportunity True open door, friendly environment Ability to "own" your role Company events that bring us all together If you desire a long-term career, want to work alongside an exceptional group of people, and wish to use your talents to shape a world-class company, then we are your employer of choice! Together, we will illuminate the world! Penn Color, Inc. is an Equal Employment Opportunity employer. We adhere to a policy of making employment decisions without regards to race, color, religion, sex, age, disability or any other protected categories. It is our intention that all qualified applicants be given an equal opportunity and that selection decisions be based on job-related factors.

Since 1869, we've connected people through food they love. We're proud to be stewards of amazing brands that people trust. Our portfolio includes the iconic Campbell's brand, as well as Cape Cod, Chunky, Goldfish, Kettle Brand, Lance, Late July, Pacific Foods, Pepperidge Farm, Prego, Pace, Rao's Homemade, Snack Factory, Snyder's of Hanover. Swanson, and V8. Here, you will make a difference every day. You will be supported to build a rewarding career with opportunities to grow, innovate and inspire. Make history with us. Why Campbell's… * Benefits begin on day one and include medical, dental, short and long-term disability, AD&D, and life insurance (for individual, families, and domestic partners). * Employees are eligible for our matching 401(k) plan and can enroll on the first day of employment with immediate vesting. * Campbell's offers unlimited sick time along with paid time off and holiday pay. * If in WHQ - free access to the fitness center. Access to on-site day care (operated by Bright Horizons) and company store. * Giving back to the communities where our employees work and live is very important to Campbell's. Our "Campbell's Cares" program matches employee donations and/or volunteer activity up to $1,500 annually. * Campbell's has a variety of Employee Resource Groups (ERGs) to support employees. How you will make history… The Sensory Scientist will support sensory and consumer research projects for the Snacks Division with guidance from Senior Sensory Design team members. Reporting to the Director for Sensory Design, this individual will support sensory projects, driving innovation and renovation for the Snacks categories and other businesses as needed. You will be responsible for supporting, planning, and providing sensory expertise to technical research programs throughout the stage-gate process and delivering actionable insights to impact and fuel business growth. We are seeking an individual who can make an impact to help shape the future of some of our iconic brands What you will do… * Becoming familiar with the range of sensory profiles and attributes seen in Snacks categories. * Providing continuous Sensory and consumer insights to ensure robust team evaluations and product development guidance. * Supporting sensory projects (planning, data collection, analysis, product launch, and post-launch). * Developing project objectives and strategies in response to business needs, executing studies, and recommending actions. * Co-facilitate internal tasting experience of products across categories, developing and communicating critical sensory insights leveraging our "Mind the Gap" philosophy. * Conducting sensory tests and analyzing data using appropriate statistical methods to guide enablers, business continuity projects, and quality initiatives. * Continually investigate the quantifiable dimensions of flavor and texture. * Coordinate and assist in audits of research vendors. * Create actionable design of experiments (DoEs) in conjunction with key stakeholders. * Perform other duties as needed. Who you will work with… The Sensory Scientist will work cross-functionally with members of Research and Development, Business Quality Assurance, Regulatory, Legal, Brand, Sales, Consumer Insights, and Operations, promoting the use of Sensory and Consumer/Product Research to influence, guide, and unlock product differentiation to deliver the desired consumer experience. This role reports to the Director of Sensory. What you bring to the table… (Must Haves) * Bachelor's degree * 2 years of experience with sensory analysis and market research on either the vendor or customer side It would be nice if you have… (Preferred Skills) * Education discipline in Food Science, Sensory Science, Consumer Science, Market Research, Statistics, Food Technology or related field or disciplines. * Experience working at or with a CPG company. * Knowledge of sensory science as a discipline - including experience of discrimination, descriptive analysis, and consumer research techniques. * Knowledge of technical tools that support sensory testing and data analysis such as SIMS, Compusense, FIZZ, SAS, JMP, and Minitab. * Ability to manage multiple projects concurrently. * Software knowledge: Microsoft Excel, Word, PowerPoint, and Outlook. * Statistical skills, basic understanding of multivariate analysis. Fluency in the use of statistical software is a plus. * Strong written and oral communication skills with an emphasis on effective visual storytelling * Strong organizational skills. * Able to work well in a team environment. * Independently motivated. * Good interpersonal/teamwork skills and a sense of business/ technical interrelationships. WORKING CONDITIONS: * Headquarters (HQ) Office, Research Kitchen, Pilot Plant, and Manufacturing Plants (Campbell's Soup Company (CSC), co-manufacturers and vendors). * Willingness and ability to taste and evaluate a wide range of food products and ingredients. * The work exposes the employee to heat and hot food products, coolers, and freezers requiring the use of personal protective equipment. * Must be available to travel to various customers, suppliers, and production facilities (Anticipated travel at around 20%). Compensation and Benefits: The target base salary range for this full-time, salaried position is between $73,500-$105,700 Individual base pay depends on work location and additional factors such as experience, job-related skills, and relevant education or training. Total pay may include other forms of compensation. In addition, we offer competitive health, dental, 401k and wellness benefits beginning on the first day of employment. Please ask your Talent Acquisition Partner for more information about our total rewards package. The Company is committed to providing equal opportunity for employees and qualified applicants in all aspects of the employment relationship, including consideration for employment, without regard to race, color, sex, sexual orientation, gender identity, national origin, citizenship, marital status, protected veteran status, disability, age, religion, or any other classification protected by law.

The Scientist role is primarily responsible for aggregate safety analyses and aggregate report writing. He/she will contribute or will be responsible for report writing and/or report ownership related to core safety deliverables including scheduled and ad hoc post-marketing aggregate reports. Daily activities involve database searching, aggregate safety analysis and case level review, writing, planning, conducting meetings, and project management/coordination of strategic safety documents. The Scientist will partner with team members, stakeholders such as safety physicians, and a vendor. The Scientist must be able to work on multiple projects simultaneously and prioritize tasks. Responsibilities: Scientist would be responsible to contribute to or serve as report owner for scheduled and non-scheduled post-marketing safety reports and other deliverables as applicable. Scheduled reports include PBRERs/PSURs, PADERs, Addendums to Clinical Overview, and PBRER/PSUR Addendum Reports. Non-scheduled reports include Ad hoc reports in response to health authority queries or internal requests, health hazard evaluations, and labeling support documents. Ensure timely, quality deliverables for assigned tasks related to core deliverables with oversight as appropriate Initiate/conduct searches of internal and external databases Perform aggregate safety analysis and case level review Present results at Safety Management Team meetings as needed Author/contribute to the preparation of core safety deliverables Partner with vendor to develop reports/deliverables Comply with processes and ensure appropriate documentation Utilize technical skills and programs to analyze and organize data (e.g., Excel pivot tables, SAS JMP) Adhere to report timelines and escalate issues to management as appropriate Qualifications/Experience Required Bachelor s degree in health or biomedical science (3+ years industry experience or equivalent) or Advanced degree preferred in health or biomedical science (2+ years industry experience or equivalent) Clinical/medical writing and/or PV experience Strong English verbal and written communication skills Strongly Preferred: Aggregate safety report writing and aggregate safety analysis Project management of safety/regulatory documents Awareness of applicable regulations and guidance related to post-marketing aggregate safety requirements Experience using Microsoft word templates Qualifications Bachelor s degree in health or biomedical science (3+ years industry experience or equivalent) or Advanced degree preferred in health or biomedical science (2+ years industry experience or equivalent) Additional Information All your information will be kept confidential according to EEO guidelines.

R&D Assistant Scientist - In vivo Full-Time position Level: Assistant Scientist Location: On site (Philadelphia, PA) Start date: Available immediately Why Join Verismo? Our team is small but driven, with the single focus of bringing life-changing cell therapies to patients with cancer. With a solid pipeline built around the novel KIR-CAR platform, and two clinical trials underway, our technology has found a way to circumvent the barriers in solid cancer where other CAR therapies have had limited success. KIR-CARs eliminate the artificial recombinant chimeric receptors used in CAR T cells and instead use a natural NK cell derived signaling system. This system is potent against both hematologic and solid tumors, and in preclinical models is superior to current CAR T in conferring long-term, sustained anti-tumor function to overcome T cell exhaustion. We have a strong team for pre-clinical development, CMC with PD and AD, clinical product manufacture, and lead clinical investigators bringing KIR-CARs to patients in need. Our company is comprised of individuals who each bring something unique to the table and are valued for their contributions. Our culture is based on the concept of ‘love what you do' and the dedication that builds a team where people do their best and support one another. Because we believe our people are our greatest asset, career development is an encouraged as an investment in our team and we encourage a healthy work/life balance. Overall Job Purpose: An Assistant Scientist will first and foremost be a people-person, with the necessary scientific background to assist the senior Scientist with conducting scientific studies in the cutting-edge gene-engineered T cell therapy. The candidate will be working closely with our KIR-CAR translational science team in managing daily operations in the laboratory, and assisting with in vivo preclinical studies and ensuring Quality and Data Integrity are preserved in preparation for IND application and transition to first-in-human clinical trials. Additional responsibilities will include assisting with lentivirus preparation, cell line maintenance and related tasks. This role will also be fluent in communicating with our internal scientific team. The candidate will report directly to our Executive Director of Translational Science and assist R&D senior scientists with our in vivo experiments, by preparing materials, designing experiments, acquiring and analyzing data for IND-enabling studies and other translational studies. This individual will help manage daily operations in the laboratory and contribute to studies across R&D functions when needed. The candidate will be a team player who is eager to work in a fast-paced environment. Job summary: Assist R&D scientists with all in vivo experiments including, design, data acquisition, and data analysis to support pre-clinical development of Verismo's pipeline candidates in potential cancer indications. (70%) Manage the daily operation in the Verismo's translational science laboratory, including but not limited to ordering laboratory consumables and reagents, monitoring and maintaining the inventories, maintaining laboratory equipment, following safety procedures, and maintaining compliance records and lab notebooks in an industry setting. (15%) Assist R&D scientists with other lab tasks as assigned (15%). Essential Duties & Responsibilities: General scientific knowledge and laboratory skills. Hands-on lab work in a flexible, fast-paced industry setting is essential. Aseptic cell culture techniques are required. Working knowledge in mouse handling, IV/IP/SubQ injections, and blood and tissue collection is preferred. Experience in problem solving ability and ability to apply risk-based critical thinking in a technical environment. Ability to collaborate across R&D teams and good interpersonal skills. Technical written and oral communication skills are essential. Ability to prioritize, independently manage and complete deliverables within given timelines. Good organizational skills and attention to detail with high quality output. Appropriately document research findings in lab notebooks. Takes responsibility for laboratory efficiency, compliance and cleanliness. Required Qualifications, Experience & Abilities: B.A./B.S. in molecular biology, cell biology or related field with at least 2-3 year research experience. Working experience with cell culture and mice is a must. Molecular biology and flow cytometry experience is preferred. Prior industry experience with adoptive cell therapies is preferred. Prior experience working in a team setting. Well-organized and has experience documenting protocols and recording the data generated from them in an industry setting. Willingness to take other duties as assigned. * Please note that we cannot reimburse travel expenses for candidate interviews.

Scientist, Bioanalytical Services Title: Scientist, Bioanalytical Services Scientist / Bioanalytical Services Essential Functions Run sensitive, reliable and efficient LC-MS/MS bioanalytical assays for TK/PK assessment. Responsibilities: Perform high-volume sample analysis and/or data analysis, data QC, and data interpretation Maintain schedule of projects and timelines Coordinate study activities with Principal Investigator to ensure efficiency and quality Aid in the preparation of study summaries and/or reports Maintain the proper level of regulatory compliance for each study, helping to address QA audit findings. Maintain tools, computer programs, and SOPs required for studies Ensure that GLP regulations and SOPs are followed in all bioanalytical service activities. Follow safety precautions. Job Requirements: Experience using Sciex Analyst software, and Watson LIMS, a plus. Ability to successfully work in a team environment. Excellent oral and written communication skills. Master's degree in Analytical Chemistry, Biochemistry, Pharmacology or related scientific discipline with 1+ years direct experience, OR Bachelor's degree in same discipline with 4+ years direct experience. Salary and Benefits: Frontage Laboratories offers a competitive compensation and generous benefits package including health and dental insurance, a 401(k) plan, health insurance, short and long-term disability insurance, life insurance etc. 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.

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.

JobID: 210689616 JobSchedule: Full time JobShift: Day : The Workforce Planning (WFP) organization is a part of Consumer and Community (CCB) Operations division. The WFP Data Science organization is tasked with delivering quantitatively driven solutions to support the core WFP functions (demand forecasting, capacity planning, resource scheduling, and business analysis & support). The WFP organization supports Chase's call centers, back office, and ~5,200 retail branches. As a Data Scientist Lead - WFP Machine Learning Scientist, within JPMorganChase, you will engage in projects by the Artificial Intelligence(AI)/Machine Learning(ML) team that can be complex, data intensive, and of a high level of difficulty, each having significant impact on the business. You will typically encounter these problems which will be of an unstructured nature, whereby the employee will be expected to quickly assess and comprehend the situation then develop a practical problem solving strategy. You will be expected to analyze the topic in question, develop solution proposals and review their results and next steps with management for prioritization, timing, and delivery. The AI/ML team is tasked with building next-gen data science solutions that move us closer to real-time inference and decision making. Job Responsibilities * Design and development of Machine Learning, Artificial Intelligence and Statistical models. * Participate in the full model development lifecycle, from framing the problem to prepare documentation and passing independent model review (MRGR). * Lead AI/ML projects along with mentor and coach junior team members. * Collaborate with stakeholders to understand the business requirements and clearly define the objectives of any solution. * Identify and select the correct method to solve the problem while staying up to data on the latest AI/ML research * Ensure the robustness of any data science solution. * Develop and communicate recommendations and data science solutions in easy-to-understand-way leveraging data to tell a story. * Lead and persuade others while positively influencing the outcome of team efforts and help frame a business problem into a technical problem resulting in a feasible solution. Required Qualifications, Capabilities, and Skills * Master's Degree with 5+ years or Doctorate (PhD) with 3+ years of experience operating as an data science professional (e.g. data scientist, statistician, or related professions) in a quantitative field: Statistics, Analytics, Data Science, Engineering, Operations Research, Economics, Mathematics, Machine Learning, Artificial Intelligence, and related disciplines. * 2+ years of experience leading AI/ML projects with multiple team members * Hands-on experience developing statistical models, machine learning models, and/or artificial intelligence models. * Deep understanding of math and theory behind AI/ML algorithms. * Proficient in data science programming languages like Python, R or Scala. * Experience with big-data technologies such as Hadoop, Spark, SparkML, etc. & familiarity with basic data table operations (SQL, Hive, etc.). * Demonstrated relationship building skills, with a superior ability to make things happen through the use of positive influence. Preferred Qualifications, Capabilities, and Skills * Advanced expertise with Time Series and Operations Research techniques. * Natural Language Processing(NLP)/Natural Language Generation(NLG), Neural Nets, or other ML/AI skills. * Prior experience with public cloud technologies such as Amazon Web Services(AWS), Azure or Google Cloud Platform(GCP). * Previous experience leading highly complex cross-functional technical projects with multiple stakeholders This position is full time in office Monday - Friday. This position is not hybrid nor remote.

Piper Companies is currently looking for an experienced Bioconjugation Scientist in Philadelphia, Pennsylvania (PA) to work for an innovative and growing pharmaceutical company. The Bioconjugation Scientist will play a significant role in developing innovative conjugates for the treatment of serious life threating diseases. Responsibilities for the Bioconjugation Scientist include: * Design, plan, and execute experiments focused on bioconjugate synthesis (e.g., protein-small molecule, protein-peptide, protein-oligonucleotide, and protein-fluorophore conjugates). * Analyze conjugates and biomolecules using LC-MS, HPLC, UV-Vis, SDS-PAGE gels, and RNA gels to assess purity, integrity, and molecular composition. * Maintain proper laboratory documentation within ELM in accordance with GLP/GDP guidelines Qualifications for the Bioconjugation Scientist include: * 1- 2 years' experience with AKTA purification or conjugation * 1-2 years of experience within pharmaceutical research or manufacturing * B.S. in Molecular Biology or scientific field Compensation for the Bioconjugation Scientist include: * Salary Range is $65,000-$70,000 dependent upon experience * Comprehensive benefits package Keywords Bioconjugation, conjugation, pharmaceutical research, AKTA purification, HPLC, LC-MS, SDS Page, RNA gels, science, design of experiment, DOE, Philadelphia, PA, Pennsylvania, ELN, electric lab notebooks, comprehensive benefits package, Health, Vision, Dental. #LI-ONSITE #LI-DF1

Associate Scientist - (25003184) Description Temple University's School of Medicine is searching for an Associate Scientist!Salary Range: $60,000 - 70,000A variety of important factors are reviewed by HR when considering salary, including job duties, the applicant's education and experience, all relevant internal equity considerations, department budget, and funding source. Become a part of the Temple family and you will have access to the following:Full medical, dental, vision coverage Paid time off9 Federally Observed Paid Holidays3 Personal DaysTuition remission - eligible employees and their dependents can obtain a degree TUITION FREEA generous retirement plan and so much more!Position Summary:The Associate Scientist reports to Dr. Skorski. He/She will perform scientific experiments, have an in-depth technical and theoretical knowledge and expertise in molecular biology, leukemogenesis, DNA repair, and animal model study Job Details:* This is a grant funded position Required Education and Experience:* Ph. D. in biology with at least 3 years of relevant experience. An equivalent combination of education and experience will be considered. Required Skills and Abilities:* Demonstrated ability to supervise students at the undergraduate level. * Must be able to work with potentially hazardous specimens. * Ability to keep accurate records of research performed to NIH standards. * Ability to operate standard office equipment and software including MS office. * Excellent written, oral and interpersonal communication skills. * Ability to interact with a diverse population of students, faculty, and staff. * Demonstrated organization skills with the ability to handle multiple tasks. * Must prioritize well and focus on completion of tasks and objects while under stress of a demanding work schedule. Essential Duties:* Responsible for independently performing a wide range of research functions based on agreed protocols and objectives. * The candidate will study the mechanism of DNA repair in leukemia and solid tumor cells in various tissue-specific microenvironments. The methods to be used include tissue culture, molecular and cell biology procedures, DNA repair, flow cytometry, and in vivo experiments in various mouse models. * Perform literary research and participating in the development of research protocols. * Performs other duties as assigned Temple University is committed to a policy of equal opportunity for all in every aspect of its operations, including employment, service, and educational programs. The University has pledged not to discriminate on the basis of age, color, disability, marital status, national origin or ethnic origin, race, religion, sex (including pregnancy), sexual orientation, gender identity, genetic information or veteran status. Compliance Statement: In the performance of their functions as detailed in the position description employees have an obligation to avoid ethical, legal, financial and other conflicts of interest to ensure that their actions and outside activities do not conflict with their primary employment responsibilities at the institution. Employees are also expected to understand and be in compliance with applicable laws, University and employment policies and regulations, including NCAA regulations for areas and departments which their essential functions cause them to interact. Temple University's Annual Security and Fire Safety Report contains statistics, policies, and procedures related to campus safety. Go here to review: *************** temple. edu/reports-logs/annual-security-report You may request a copy of the report by calling Temple University's Department of Public Safety at ************. Primary Location: Pennsylvania-Philadelphia-Health Sciences Campus (HSC)-Pharmacy - Allied HealthJob: StaffSchedule: Full-time Shift: Day JobEmployee Status: Regular

Job Description Associate Scientist / Scientist I Salary Range: $45K - $58K Pharmaron is a global CRO (Contract Research Organization) helping pharma and biotech companies bring new therapies to life. With over 21,000 employees worldwide across 23 locations in the US, UK and China, we support drug discovery through to manufacturing with fully integrated, high-quality services. We're proud of the impact we make and just last year, we supported over 780 discovery projects, 1,000+ CMC programmes, and 1,000+ clinical trials across all phases. Our teams are involved in everything from small molecules, ADC's, biologics, and gene therapies and we work with more than 3,000 global customers. To learn more, visit ****************** Job Overview: Pharmaron (Exton) Lab Services LLC is seeking a motivated Associate Scientist / Scientist I with strong molecular biology and bioassay experience to join our growing Cell and Gene Therapy (CGT) bioassay team. Key Responsibilities: Perform DNA and RNA isolation from diverse sample types (cells, tissues, biofluids) using both manual and high throughput systems Conduct qPCR and digital PCR (dd PCR, QIAcuity) analyses to quantify gene expression, vector copy number, and other molecular parameters. Execute experiments following standard operating procedures (SOPs) and project-specific protocols under regulated (GxP) or research conditions. Maintain accurate, detailed, and timely documentation of all experimental activities in electronic and/or laboratory notebooks. Assist with laboratory inventory management, reagent preparation, and instrument maintenance. Collaborate with cross-functional teams to ensure data quality, reproducibility, and compliance with quality system requirements. Perform additional duties and responsibilities as assigned by management. What We're Looking For: 1-3+ years of hands-on molecular biology or bioassay laboratory experience required; the exact requirement may vary based on educational background (B.S., M.S., or Ph.D.). Demonstrated experience isolating DNA/RNA from biological matrices (cells, tissues, biofluids). Solid understanding of PCR principles and practical experience with qPCR and/or digital PCR (dd PCR, QIAcuity) platforms. Experience with automated extraction systems such as QIAcube HT or KingFisher Flex preferred. Familiarity with method development or validation in a regulated (GLP or GxP) environment is a plus. Highly detail-oriented, organized, and capable of managing multiple projects simultaneously. Strong communication and teamwork skills in a collaborative, fast-paced lab environment. 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 will 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. Benefits: 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! As an Equal Employment Opportunity and Affirmative Action employer, Pharmaron values diversity and inclusion in the workplace, fostering an environment where all individuals are empowered to succeed. Join us in our mission to make a difference in the world of life sciences. #LI-MC1

Job Title: Scientist - Proteomics & Mass Spectrometry Employment Type: Full-Time About the Role The Molecular Modalities Discovery group is seeking a highly motivated scientist with expertise in proteomics and informatics to support capability development in the mass spectrometry (MS)-omics space, with a particular focus on oligonucleotides and single-point mutations. This is a bench-focused role requiring hands-on experience in biological mass spectrometry workflows. Key Responsibilities Perform biological mass spectrometry workflows with a primary focus on proteomics. Support small molecule discovery, including identification and progression of molecules that interact with drug targets. Execute sample preparation steps, including: Handling cryogenically preserved cells (not chemically fixed). Buffer treatment for cell lysis and protein extraction. Enrichment steps (e.g., amino precipitation). Protein digestion and peptide processing. Reconstitution and loading samples onto MS tips for automated analysis. Learn and apply core workflows for MS-based proteomics. Collaborate with partners for occasional live-cell handling. Maintain accurate documentation and adhere to standard operating procedures. Qualifications Bachelor's degree in Biology, Biochemistry, or related field (advanced degree preferred). Hands-on experience with mass spectrometry in a biological context. Strong understanding of proteomics MS workflows and sample preparation techniques. Familiarity with informatics tools for data analysis is a plus. Ability to work independently at the bench and troubleshoot technical challenges. Preferred Skills Background in biology and handling biological materials. Knowledge of oligos analysis and mutation detection. Experience with MS automation Compensation: $45-70/hr Exact compensation may vary 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.

Prepare reagents, standards, and control samples Analyze samples using various techniques specific to department Operate analytical equipment Maintain analytical equipment Ensure lab area is clean and inspection ready at all times Remove lab waste Record tasks in accordance with Good Documentation Practices (GDP) Learn and apply regulatory requirements; GLP, GCP, 21CFR Part 11 Follow applicable SOPs and procedural documents Learn how to review and evaluate data results Other tasks as assigned Education, Experience & Skills Required BA/BS or higher in Chemistry; all experiences will be evaluated 1-2 years experience in LCMS Able to perform basic lab work Able to work in a regulated environment Able to work effectively and contribute within a team Able to work with computer systems & document clearly About Us Are you interested in working in science for a leading global Contract Research Organization that is expanding rapidly and delivering best in class service to its clients? If you are ambitious and hard working then keep reading, as we are looking for talented individuals like you. We are globally recognised for our leadership in science and, as a result, you will have the opportunity to work with some of our industries smartest and most inquisitive people, in a flexible and supportive environment. It is the ideal place to expand your knowledge, take on new responsibilities and make ambitious strides in your career. If you want to join us to help us deliver our mission of using our scientific capabilities to improve the quality of life of people, then we would love to hear from you.