Chemist Jobs in Haddon, NJ

LHH Recruitment Solutions has a Development Chemist opening for our client in the Burlington, NJ area. This direct hire role allows you to collaborate with numerous departments to facilitate new formulations for new compounds through customer specifications in accordance with regulations. This direct hire role allows you to collaborate closely with the research and development team to facilitate quality control, trials, and issuance of new formulations. Candidates MUST have a minimum of 3 years' professional experience in rigid formulation with polyvinyl chloride and familiar with extrusion and/or injection molding. This fully on-site position requires a bachelor's degree preferably in a chemistry or related field and a minimum 3-year development experience. Ideal candidates will have extensive experience in PVC material application as well as a proven track record of understanding and utilization of surface to interface properties a s well as surface characterization. You will be responsible for customer interfacing as well. Salary range: $75,000 to $80,000 DOE. Job Summary: Conduct development work for new compounds in new product developments, and improves current compounds in performance, efficiency, and price competitiveness in accordance with all regulatory requirements. Responsibilities: Analyze compounds and manage corresponding data tracking. Define and determine physical and chemical properties for compounds. Oversee development and issuance of new formulations for new compounds based on requirements and specifications from clientele. Conduct investigation of new and old formulations in replacement of raw materials to enhance performance and minimize cost. Maintain quality standards. Responsible overseeing raw material substitutions as required. Collaborate with HSE in updating and maintaining SDS. Prepare technical data information for customers. Generate ideas for new product development. Manage tests performed with accuracy, completeness and in regulatory compliance. Make recommendations regarding for production line or production lines and trial formulations. Attend and oversee production trials to ensure formulations are being utilized as intended. Attends monthly QA/QC meetings as scheduled. Attend customer trial(s) per request from R&D Manager to validate the performance of the new compound and make necessary adjustments per customer trial(s) feedback. Collaborate internally with various departments for R&D related issues. Provides technical support internally/externally to Production, QC/QA, Sales and customers as needed. Responsible for managing regulatory files including, but not limited to, NSF and UL qualifications and certifications. Annual audit participation. Oversee monitoring of equipment to ensure safety precautions are being followed. Assist in ISO Audits. Assist in creating, maintaining, and updating of R&D ISO documents. Required Qualifications: Bachelor's degree (B.S.) in chemistry - NOT BIOLOGY. Minimum of three years of relevant experience in a manufacturing environment of PVC Material. Highly preferred - experience in a PVC (Polyvinyl Chloride) compounding setting. ASQ Certified Quality Engineer, with a desired ASQ Six Sigma Green Belt highly preferred. Possesses in-depth knowledge of quality control/quality assurance procedures and legal standards. Proven expertise in chemistry relating to surface-interface properties as well as surface characterization. Proficiency in Microsoft Excel and competence in other Microsoft Office 365 applications or related programs. Effective promoter of positive culture and relationships utilizing clear and positive communication across the board. Highly detail oriented. Expert in time management, capable of working under pressure as well as meeting deadlines. Excellent verbal and written communication skills. Oversee task prioritization and delegation when necessary. This posting is a representative sample of the types of roles we typically place with our clients. Depending on the specific client, location, and role, the salary range is estimated to be $75,000 to $80,000 DOE and benefits may include medical, dental, vision, 401k+match and PTO.

Innovative company is seeking an innovative and team-oriented surfactant and water treatment chemist in their facility located in the Philadelphia area. Chemist will be responsible for R&D projects covering a variety of formulation development and modification as well as leachate, condensate treatability study. The position will work closely with other R&D and QC Chemists as well as manufacturing technicians. This position will be located in West Chester, PA and report to the VP of Technology. Essential Functions & Responsibilities: Set-up internal standard test procedures New product development Leachate, condensate treatability study using various physical/chemical as well as biological processes. Scope, design and execute product performance improvement projects Formulation tailoring for unique customer specifications Operating bench scale or pilot scale leachate, condensate treatment systems Conduct water quality analysis. Support Manufacturing, Quality, Sales and Product Management functions Operation of analytical and application equipment Developing and implementation of quality control specifications and standards Project management and documentation including laboratory notebook documentation and project report writing Strong laboratory skills required including both scientific practices and housekeeping Job Specifications: Bachelors of Science in Chemistry, Chemical Engineering (or related technical discipline) is preferred. Candidates with other relevant industry experience may be considered 5 or more years lab experience in product development/application is desirable Experience in operating bench scale or pilot scale water treatment system is desirable. Foam formulation experience is required Understanding of polymer chemistry and structure property relationships Strong mechanical aptitude Experience in data collection, manipulation and analysis (Microsoft Suite, etc.) Company offers a salary of 90-115K, bonus opportunities, extensive benefits package.

Bioanalytical Associate- Wilmington, Delaware This role will focus on supporting in-vitro ADME (Absorption, Distribution, Metabolism, and Excretion) studies and plasma sample analysis in preclinical drug development. The successful candidate will play a pivotal role in the analysis and interpretation of bioanalytical data to support early-stage drug discovery. Key Responsibilities: Support ADME Studies: Conduct routine ADME assays, such as protein binding and metabolic stability, to generate key data supporting drug development decisions. Plasma Sample Analysis: Prepare and analyze plasma samples for pharmacokinetic studies, including the measurement of drug concentration, metabolite profiling, and related biomarkers. Data Interpretation & Reporting: Analyze data sets, provide scientific interpretation, and communicate results to cross-functional teams in a clear and concise manner. Record-Keeping: Maintain concise and accurate records of all study activities in accordance with industry guidelines and company policies. Troubleshooting and Continuous Improvement: Troubleshoot assay issues, propose corrective actions, and implement process improvements to enhance the efficiency and reliability of bioanalytical data. Qualifications: Bachelor's degree in Analytical Chemistry, Biochemistry, or a related field. 1+ years of hands-on lab experience in bioanalysis, with a focus on ADME/PK studies and plasma sample analysis. Technical Expertise: Hands-on lab experience with ADME screening assays, such as protein binding and microsomal stability. Experience with plasma sample bioanalysis in support of non-clinical pharmacokinetic studies. Experience with LC-MS/MS, HPLC, UPLC, and related analytical techniques for the quantification and characterization of drug candidates in biological samples is a plus. Strong analytical and troubleshooting skills with the ability to interpret complex datasets. Preferred Qualifications: Familiarity with drug discovery and development, especially within preclinical research. Experience with quantitative LC-MS/MS bioanalytical techniques and ABSciex mass spectrometers. Knowledge of relevant bioanalytical software (e.g., Analyst, Prism) is a plus.

Franklin Biolabs emerges from the esteemed legacy of Dr. Jim Wilson's laboratory, a beacon of innovation in vector technology for over three decades. Building on this rich heritage, Franklin Biolabs is poised to redefine the landscape of the global genetic medicines industry. As a Contract Research Organization (CRO), Franklin Biolabs offers a comprehensive suite of services spanning from discovery through clinical manufacturing. Our goal is to empower our partners by providing unparalleled solutions that drive the advancement of genetic medicines. Leveraging decades of expertise and a commitment to excellence, we bridge the gap between groundbreaking research and ensuring that transformative therapies reach those who need them most. Job Summary As an Upstream GMP Scientist I you will have a strong background in cell culture and bioreactor operations at pilot and GMP scale, preferably in rAAV production. You will receive processes transferred into GMP, and author batch records, SOPs as well as deviation investigations. You will execute GMP processes in appropriate grade clean rooms trained in gowning and all relevant GMP processes and procedures. Personnel in this position will mentor and train associates as well. Unlike traditional manufacturing personnel, our model aims to train GMP personnel to be process science experts as well and there will be times when they will work closely with PD/MS&T to perform development work as well. The Upstream GMP Scientist I will have mastered the skills and responsibilities of a GMP Associate Scientist and will be mastering the skills and responsibilities of a GMP Scientist. Qualifications B.S. in Biology, Biochemistry, Engineering or related field preferred but not required with 3-5 years' experience. Understanding of relevant science and proficiency in laboratory/GMP space techniques. Strong attention to detail and ability to document activities and follow protocols. Preparation of buffers and solutions. Comfort with routine calculations, tracking and interpreting data. Proficient with Microsoft Office, lab and equipment software. Familiarity with statistical analysis software preferred. Ability to follow GMP and execute in GMP environment when needed. Mastered GMP execution of all relevant areas. Understands regulations applicable to area and how to conduct deviation investigations. Understanding of GMP materials controls, facilities, and equipment. Strong problem-solving skills, planning and mitigation of risks. Strong understanding of data measurements and variability. Ability to troubleshoot and involve/communicate with management and QA as required. Involved in technology transfer. Strong communication, ability to present and write technical instructions and deviation reports. Ability to train and assist Associate level scientists. Analyze data and interpret results to identify trends and work with development scientists to make improvements. Assist in preparing documents for regulatory submissions. Strong understanding of cell culture and bioreactor operations. Strong understanding of in-process monitoring equipment, probes and assays. Understanding of analytics testing results, including AAV quality and purity. Proficiency in AAV production, and an understanding of stability and impact of process variable on AAV yield and quality. Application note Franklin Biolabs is not accepting unsolicited resumes from search or staffing firms. All resumes submitted by search or staffing firms to any employee at Franklin Biolabs via email, the Internet, or directly without a valid written search agreement for this role will be deemed the sole property of Franklin Biolabs and no fee will be paid in the event the candidate is hired

JOB TITLE: US Medical, Promotional Review Scientist, Portfolio Duration: 6 months (re-evaluate extension needs at 6 months) Work Schedule: 40 hours a week Top 3-5 skills: Strong scientific acumen Medical writing, and communication skills Prior promotional review experience preferred. Purpose and Scope of the Position • As a Medical Promotional Review (PReP) scientist, this individual is responsible for providing input and advice to conduct the review of promotional materials for scientific/medical validity across BMS' oncology portfolio. • Critical review and recommend changes to promotional materials/activities to ensure balance of the messages, medical accuracy, and appropriateness of the content of the materials/activities in accordance with relevant guidance. • Proactively align and build strong relationships with champions and other advisors/stakeholders on strategic priorities and issues or concerns to provide medical advice to ensure balance of messages in accordance with relevant guidelines. • Participate in internal and external meetings (training, educational and other matrix meetings) to remain current on ever changing regulations, relevant new medical/scientific information, and strategy. • Determine acceptability of data/references used to support promotional claims and provide expert guidance as well as effective negotiation leading to resolution for approval of pieces. Required Competencies • PharmD, MD, PhD preferred with minimum of 3 years' experience in clinical practice or the pharmaceutical industry. • Demonstrates thorough understanding of medical writing. • Demonstrates ability to manage various projects, solve problems, deliver on commitments, and work with multidisciplinary teams. • Strong scientific/medical writing and verbal communication skills required. • Developed business acumen and ability to impact and influence senior internal stakeholders. • Strong leadership and organizational skills with demonstrated success in driving optimal business results in a complex matrix organization required. • Prior promotional review experience preferred. If hired, you will enjoy the following Eclaro Benefits: 401k Retirement Savings Plan administered by Merrill Lynch Commuter Check Pretax Commuter Benefits Eligibility to purchase Medical, Dental & Vision Insurance through Eclaro If you feel you are qualified with the required skills and if you are interested, please free to send your word version most updated resume TAILORED to the job description above to *************** or call *************. Equal Opportunity Employer: Eclaro values diversity and does not discriminate based on Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status.

Upstream Associate Scientist - Contract - King of Prussia, PA Proclinical is working alongside a global pharmaceutical who are seeking an Upstream Associate Scientist to join our team in King of Prussia, PA. Primary Responsibilities: In this role, you will focus on completing daily manufacturing tasks, documenting activities, and ensuring all production activities are safe and compliant. This position requires a strong ability to work within a highly matrixed organization and multi-functional team environment. Skills & Requirements: Ability to work in a highly matrixed organization. Ability to multi-task within a multi-functional team environment. Troubleshooting skills. Capable of following written instructions and clear written communication skills. Computer literacy. Familiarity with basic scientific principles and experience in routine bench work and/or instrumental analysis. Ability to author, revise, and/or support SOPs, change controls, and deviations. Bachelor of Science degree in Chemical Engineering, Biology, Chemistry, or other engineering or scientific field. The Upstream Associate Scientist's responsibilities will be: Complete daily manufacturing tasks per standard operating procedures and batch document instructions. Document all manufacturing activities clearly and accurately. Ensure all production activities are completed in a safe and compliant manner. Maintain and prepare high-quality documentation. Dispense large and small amounts of raw materials. Perform CIP (Clean-in-Place) and SIP (Sterilize-in-Place) of product tanks. Work with hazardous materials under appropriate safety procedures. Perform other functions as necessary or as assigned. If you are having difficulty in applying or if you have any questions, please contact Jackie Cerchio at j.cerchio@proclinical.com Proclinical is a specialist employment agency and recruitment business, providing job opportunities within major pharmaceutical, biopharmaceutical, biotechnology and medical device companies. Proclinical Staffing is an equal opportunity employer. INDSCIC

The Scientific Team at Russell Tobin & Associates is hiring a Biophysics Scientist for a world-class client in Collegeville, PA 19426 Required top skills: -Biophysical Assays & Data Analysis -Bachelor's degree (BS) in a life sciences discipline, such as biophysics, analytical chemistry, or biochemistry. -Experience in laboratory research, especially in quantitative or analytical science fields, is preferred. (Not Mandatory) -knowledge of protein biochemistry and biophysics Additional Details: -3+ months contract with Possibility for extension or conversion to FTE Based on business need -Pay: $30 to $34/ hr

Responsibilities: Should be able to work flexible hours; Setup process equipment for lab-scale experiments. Prepare laboratory reagents, solutions and culture media. Perform lab-scale downstream processing of vaccine process intermediates. Perform process monitoring assays. Analyze, collate, track, and report data back to client staff members. Maintain records and test results following good laboratory practices (GLP). Work independently and efficiently. Document work clearly and perform tests accurately. Communicate effectively with client staff members. Qualifications: Education: B.S. in Bio/ Chemical Engineering, Biochemistry, or related science. 0-5 years work experience with at least six months related laboratory experience preferably performing biologics purification steps. General laboratory skills, experience with pipettes. Operation of tangential flow filtration experience is preferred. Experience using formulas and linking spreadsheets in Excel. Excellent communication (oral and written) and attention to detail. Ability to work independently and as part of a team, self-motivation, adaptability, and a positive attitude. Ability to learn new techniques, perform multiple tasks simultaneously, keep accurate records, follow instructions, and comply with company policies.

Key responsibilities: Employee will be expected to participate in all aspects of department visual inspection program, including preparation of the inspection suite, stocking of related supplies, performance of inspection of injectable products, completion of associated logbooks and batch documentation, and storage of finished product. Individual can pass color-blindness and vision testing (must achieve 20/20 with or without vision correction such as glasses or contact lenses). Must be able to pass visual appearance testing method competencies within 90 days of hire. When not inspecting, employee will be asked to complete training in and perform functions in manufacturing operations, which may include vial washing, component rinsing and preparation, Container Closure Integrity testing, and other manufacturing tasks as requested. Employee will also assist with department consumables storage and stocking programs. Employee may be asked to perform administrative tasks such as procedure revision, template revision, records filing, records archiving, and other tasks as needed. All job functions will be performed according to procedure and in accordance with cGMP, Standard Operating Procedures, and safety codes and regulations. Identifies risks to business for consideration by management. Assist and contribute to GMP and safety self-inspection activities. Accountable for delivering innovation in the Clinical Supply Chain to deliver cost savings, reduce risk and improve service. Accountable for reporting and maintaining metrics as appropriate. Zero instances of data falsification or data integrity issues by staff. Employee has basic computer skills including Word, Outlook, and ability to navigate simple website interfaces. Education and Experience: Bachelor's degree in lab sciences such as Chemistry, Biochemistry, Material Science, Immunology, Biology, Molecular Biology or similar Knowledge, Skills and Abilities: Application of knowledge and leveraging of continuous improvement activities utilizing available tools where applicable that support continued adherence with industry regulations,

Our large pharmaceutical client is seeking an Associate Scientist to join their growing team within the R&D Immunology Translational Science organization in Spring House, PA. The Immunology Therapeutic Area is focused on developing new cutting-edge therapies to treat dermatology, GI, and rheumatic diseases. This team is responsible for generating Next Generation Sequencing (NGS) data and passing it to the computational group for analysis. The role of this lab-based Scientist will primarily be focused on Next Generation Sequencing (NGS) including QC of RNA, normalizing the RNA, bringing it down to specific concentration, then moving into library prep. The ideal candidate will have strong molecular biology skills and hands-on experience in the lab doing RNA QC work. They will also need to demonstrate strong attention to detail and organization as they will be responsible for hundreds of samples at any given time. Qualifications: Bachelor's or Master's Degree in Biology or related field 3+ years of experience in the lab with Next Generation Sequencing (NGS) RNA sequencing experience Salary: $75,000-$100,000 (flexible based on experience) Hours: Monday-Friday, 8:00am-4:30pm Hiring Method: Multiyear contract - After 1 year on contract, the individual will have the opportunity to apply for a permanent role or have their contract renewed for another year PTO: 10 PTO days & 6 paid sick days annually Benefits: Medical, Dental, Vision and 401K plans available 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.

Hi, My name is Gaurav and I am a recruiter with Net2Source Inc. Our direct client is looking to hire a Scientist - II (Associate) - PA/NJ Only Only in their growing team. Please find below the job description. Title : Scientist - II (Associate) Location : Lower Gwynedd, PA 19002 or Rahway NJ 07065 Duration : 12 months Rate : $35/hr on W2 without any benefits Key skills: • HPLC and dissolution experience is required. • Analytical chemistry background is required. • Empower expertise is preferred • Pharma industry is preferred Description • We are currently seeking a temporary scientist for an immediate onsite position within the Analytical Sciences (AS) laboratory within Science and Technology at Organon. • The successful candidate will be expected to perform analytical testing of drug products and APIs under the supervision of a senior scientist. • The candidate will have a good understanding of the technical, regulatory, and GMP needs related to drug product development. • The position will report to the Senior Leadership of the Analytical Sciences laboratory. • Strong technical background with a problem-solving skill set as well as the ability to work in teams are considered essential. Position Responsibilities: • Perform analytical testing (e.g., HPLC/UPLC and dissolution) of drug products • Perform data analysis (chromatography/spectroscopy) and present them to the team in a timely manner Qualifications Education and experience: BS with 4-6 years or MS with 1-3 years or Ph.D with 0-2 years of relevant experience in Analytical Chemistry. Required Experience and Skills • Hands-on analytical laboratory experience-e.g., wet chemistry, chromatography. • Expertise in Liquid Chromatography (HPLC/UPLC) and dissolution • Hands-on experience with chromatographic integration and with Empower software (or other chromatographic data acquisition systems) and Electronic Laboratory Notebook (ELN) • Experience collecting and analyzing raw data, preparing graphs and other visualization tools to help interpret results • Demonstrated strong verbal as well as written communication skills and ability to work in an interdisciplinary team environment. Preferred Experience and Skills: • Expertise in UV. • Working knowledge of laboratory GMP, quality, compliance and data integrity requirements and related recent industry trends • Working knowledge of troubleshooting analytical techniques (e.g., chromatography, dissolution, spectroscopy, etc). • Demonstrated ability to work independently in the laboratory • Working knowledge of statistics and tools, e.g., statistical data treatment and/or Excel or Minitab. • Experienced in conducting comparative and or multi-media dissolution studies. Thanks Gaurav Gupta Sr. Pharma Recruiter *************************** **************

in Doylestown, PA: We seek a highly motivated and innovative scientist with immunology research experience and a passion to develop antibody-based therapeutics. You will play an integral role in the pre-clinical development of novel autoimmunity and inflammation therapeutics. The ideal candidate will have a proven track record of experience with core immunological assays and models (e.g., T cell proliferation, antigen recall, in vivo models of inflammatory disease) and techniques (immune cell culture, flow cytometry, ELISA, RT-PCR, etc.) The candidate will be required to coordinate and execute on research projects across multiple functional teams, both internal of IGMS and external vendors and collaborators. Strong communication skills and organizational skills are essential. A key initial responsibility will be the set up and establishment of core capabilities in the AI lab. This role involves delivering on programs through proof- of-concept in vitro and in vivo studies and advancing therapeutic candidates from early discovery to IND- enabling studies. Responsibilities: Establish core capabilities in AI lab Lead research efforts to generate proof-of-concept in vitro and in vivo data for early-stage autoimmune and inflammation programs Lead therapeutic candidate selection and perform IND-enabling studies Work closely with team members and CROs to develop assays and models to assess biological activity Present results at internal and external meetings Qualifications: Ph.D. with 2-7 years of industry experience or with equivalent postdoctoral research experience or a Bachelor's/ Master's degree with 10+ years of industry experience in the field of immunology. Must have hands-on experience and proficiency in one or more of the following areas: multi-color flow cytometry, complex cell-based functional assays, in vivo mouse models of disease. Must be proficient with Microsoft Word, Excel, and PowerPoint, GraphPad Prism, and FlowJo. Experience establishing mechanistic in vitro and ex vivo immune cell-based assays with primary immune cells from human and relevant animal species. Understanding of and ability to select relevant in vivo models for mechanistic and efficacy studies. Demonstrated track record of independence, critical thinking, and scientific research achievements in immunology and/or significant contributions to a discovery program or therapeutic development. Highly organized with reliable time-keeping skills and able to maintain a detailed and well organized electronic notebook. Must have strong interpersonal, collaboration, and communication skills. Being a team player and respectful of others is a must. Able to thrive in a fast-paced, start-up environment. Able to commute to Doylestown.

Coordinates the development implementation and ongoing maintenance of the integrated Laboratory Information System to support the delivery of laboratory services and laboratory information. Duties and Responsibilities Oversees and develops the operation, installation and ongoing support of the Laboratory Information System (LIS} Performs the maintenance of the LIS tables, files and dictionaries insuring the LIS is updates with current laboratory information Assists the laboratory departments in defining and updating the database Assists in the development of instrument interfaces Develops/revises the systems to ensure efficient laboratory work flow Works with the vendor to ensure any changes to the database do not adversely affect the LIS or laboratory operations Validates any changes/updates to the database to ensure performance as designed Assists and developing and delivers training programs on the system Assists in the implementation of updates/upgrades to the LIS and/or interfaces Assists in the implementation of new instrument/system interfaces Manages the development of testing plans for any changes to the LIS or any other areas where a change in the systems, software, interfaces, forms, formats, policies, procedures, etc. would affect the LIS or any computer supported functions related to laboratory Assists in the execution of the testing plans and the validation of the proper operation of the LIS and any interfaced systems or instruments Participates and provides input on all decisions related to the LIS Participates in ongoing meetings to address issues and problems related to LIS Develops procedures as related to LIS system build Ensures system security measures meet HIPAA requirements Other related work as assigned Skills Required Excellent verbal, written, presentation and communication skills Strong organizational and problem solving skills Ability to collaborate with and integrate the interests of various laboratory disciplines Commitment to strong customer service objectives Ability to collaborate with or integrate interests of various Health Department entities and disciplines LIS programming Software Quality Assurance testing System to System interface design, development and troubleshooting Education and Experience Baccalaureate degree in Medical Technology, Biology, Chemistry or related sciences. Second degree or demonstrated studies in computer science or management information systems desirable. Schedule Monday-Friday, 8:30a-5p Physical Demands Ability to sit for long periods of time Ability to spend long hours staring at a computer monitor

Hatfield, PA may support two sites and candidates must be able to travel to our sites as needed At Biolyst Scientific, we understand the evolving needs of clinicians and scientists in a world of supply chain disruptions and the demand for scientific advancements. We offer more than just order fulfillment, we provide partnership, expertise, and a genuine investment in your success. Our team blends industry knowledge with passion to deliver innovative solutions that drive medical and scientific progress. We are big enough to deliver, small enough to care. POSITION SUMMARY The Quality Control Chemist Lead oversees the quality control (QC) processes at Biolyst Scientific, ensuring that products meet all regulatory standards and internal quality benchmarks. This role involves managing QC operations and implementing robust quality systems to ensure the highest standards of product integrity and compliance. ESSENTIAL JOB FUNCTIONS Quality Control Oversight: Perform chemical and physical testing of raw materials, in-process materials, and finished products in accordance with established procedures and specifications. Operate and maintain laboratory equipment, including HPLC, gas chromatography, sonicator, UV-Vis, viscosity meter, centrifugator, refactometer, microscopy, pH meter, titration pole, spectrophotometers, and other analytical instruments. Manage Stability Program, including resources, tests, trends and reports. Ensure all testing is performed accurately and documented in compliance with GMP, GLP, GDP and FDA regulations. Regulatory Compliance: Support during audits and inspections by regulatory agencies. Stay current with industry regulations and best practices and ensure that all QC processes adhere to these standards. Method Development and Validation: Develop, validate, and optimize analytical methods for product testing. Troubleshoot and resolve issues related to analytical methods and equipment. Collaborate with research and development teams to support product development and improve existing methods. Data Analysis and Reporting: Analyze and interpret QC data to identify trends, potential issues, and areas for improvement. Prepare and present detailed reports on QC activities, test results, and performance metrics to senior management. Implement corrective and preventive actions (CAPAs) based on data analysis and feedback. Continuous Improvement: Drive continuous improvement initiatives within the QC department to enhance efficiency, accuracy, and product quality. Participate in cross-functional teams to address quality issues and implement solutions. Inventory and Resource Management: Manage the inventory of QC supplies and reagents, ensuring availability and proper storage. Oversee the maintenance and calibration of QC instruments and equipment. Prepare and review laboratory documentation, including test methods, protocols, reports, and standard operating procedures (SOPs). SKILLS AND ABILITIES Strong knowledge of QC methodologies, USP requirements, FDA regulatory requirements, and industry best practices. Proven team and leadership management skills. Excellent analytical, problem-solving, and organizational abilities. Proficiency in analytical instruments and techniques (e.g., HPLC, GC, spectroscopy). Effective communication and interpersonal skills. MINIMUM REQUIREMENTS Education: Bachelor's or Master's degree in Chemistry, Biochemistry, Pharmaceutical Sciences, or a related field. Experience: Minimum of 5-7 years of experience in quality control or regulatory within the life sciences or diagnostics industry. Relevant certifications (e.g., ASQ Certified Quality Auditor) are a plus. Biolyst Scientific provides equal employment opportunities to all persons and prohibits employment decisions based on race, religion, color, creed, national origin, sex, age, disability, political affiliation, protected veteran status, or sexual orientation.

QC Analyst I or QC Analyst II Philadelphia, PA (100% Onsite) Pay: $38-45/hr *Shift will be either Sunday-Thursday OR Tuesday-Saturday 8am-5pm MUST HAVE: QC experience in the the pharmaceutical industry, ELISA, and Flow Cytometry!! Overview The Quality Control Analyst I supports quality control testing operations. The Quality Control testing programs include but are not limited to, in-process, final drug product, and stability testing with a focus on cell therapy products. This role requires hands-on laboratory experience in at least one of the following: cell culture / maintenance and cell count determination (NC-200), cell based potency assays utilizing various immunoassays (ELISA, ELLA, etc.) platforms, and or identification / characterization / potency assays using multicolor flow cytometry platforms. This position supports the ramp-up of QC analytical release assays and other activities in a newly built facility for cell therapy products. This position works across different shifts. Depending on your assigned shift, you may be required to work overtime, weekends, and holidays to meet target turn around times. Essential Functions and Responsibilities Perform daily GMP Quality Control laboratory testing activities at the facility with minimal to no errors while ensuring testing is completed in compliance with all applicable procedures, standards, and GMP regulations. Perform data analysis and final result reporting to support product lot release with adherence to turnaround times. Act as a subject matter expert (SME) on one or more assays and train new laboratory personnel Support thorough GMP investigations for out-of-specification test results and other quality events. Support technical problem-solving for issues pertaining to GMP Quality Control Support product stability programs, including execution of stability testing and final reporting of stability data. Initiate and support revisions of documentation, such as SOP, protocols and reports. Initiate and support quality records such as deviations, laboratory investigations, CAPAs, and change controls Perform peer review of laboratory data and logbooks. Update trending data sheet, as required. Operate at a consistent and high level of efficiency, while producing high-quality and accurate results. Support Health Authority inspections. Provide input to functional laboratory team meetings. Comply with Safety SOPs, SDS sheets, and laboratory procedures per company policy and OSHA regulations. Perform miscellaneous duties as assigned. Required Education, Skills, and Knowledge Minimum of a bachelor's degree in biology, Biochemistry, Microbiology, Chemistry, or related scientific field or equivalent combination of education and experience. Minimum two (2) years of GMP experience in the pharmaceutical industry within a Quality Control role. Solid understanding and functional knowledge with hands-on experience with at least one of the following: Multicolor Flow Cytometry, Cell-based ELISA, cell culture with cell enumeration (NC-200) Experience in technical writing (e.g., test methods, SOPs, protocols, etc.) Detail-oriented with strong technical skills High level of ownership and accountability Demonstrate a sense of urgency; ability to recognize time sensitivity. Proficient with using Microsoft Office applications (Outlook, Excel, Word, and PowerPoint) Preferred Education, Skills, and Knowledge Experience with cell therapy products is a plus and/or relevant technical skills (NC 200, ELISA, and/or Flow). Physical Demands and Activities Required: Must be able to wear appropriate clean room attire and all Personal Protective Equipment (PPE), i.e., scrubs, gowning coveralls, masks, gloves, etc. Must meet requirements for and be able to wear a half-face respirator. Able to stand and/or walk 90% (and sit 10%) of the scheduled workday which may include climbing ladders or steps. Must be able to use near vision to view samples at close range. Able to crouch, bend, twist, reach, and perform activities with repetitive motions. Must be able to lift and carry objects weighing 30 pounds. The physical demands described here represent those that an employee must meet to perform the essential functions of this job successfully. Reasonable accommodations may be made upon request to enable individuals to perform essential functions. Please contact Human Resources to request an accommodation. Mental: Clear and conceptual thinking ability; excellent judgment, troubleshooting, problem-solving, analysis, and discretion; ability to handle work-related stress; ability to handle multiple priorities simultaneously; and ability to meet deadline. Work Environment: This position will work in both an office and a manufacturing setting. When in the lab, you may be exposed to various chemicals/biochemical, including latex and bleach. Additionally, there is potential for variable noise levels, equipment hazards, strong odors, and other detergents/sanitizers. The statements contained in this document are intended to describe the general nature and level of work being performed by a colleague assigned to this description. They are not intended to constitute a comprehensive list of functions, duties, or local variances. Management retains the discretion to add or to change the duties of the position at any time.

The Coriell Institute for Medical Research is seeking an ambitious and highly skilled Research Technician III to play a critical leadership role within our Research and Development (R&D) team. This position is integral to advancing Coriell's mission to innovate in the areas of stem cell research, genome editing, and supporting the Camden Cancer Research Center (CCRC) biobank. In addition to contributing to cutting-edge research, you will oversee the day-to-day laboratory activities, ensuring smooth operations, mentoring research technicians, and promoting a culture of collaboration and scientific rigor. This role demands a combination of strong leadership, laboratory management, independent problem-solving, and teamwork to maintain high productivity and precision in the lab. As a key member of the R&D team, you will collaborate with top scientists and researchers, playing a direct role in generating induced pluripotent stem cell (iPSC) lines, differentiated cellular models, organoids, and isogenic controls using CRISPR-Cas9 technology. You will also support and manage activities that ensure quality control. Key Responsibilities: Leadership & Oversight: Lead and support research technicians by overseeing day-to-day laboratory activities, mentoring team members, and ensuring adherence to safety and quality protocols. iPSC Reprogramming: Reprogram primary human cell lines into iPSCs, ensuring adherence to best practices and high-quality standards. Cell Line Management: Perform routine maintenance, expansion, and cryopreservation of various human cell lines. This includes documenting cell culture processes and ensuring traceability. Characterization & Quality Control: Utilize a range of techniques (such as immunohistochemistry, flow cytometry, and qPCR) to characterize iPSC and differentiated cell lines, ensuring consistency and reproducibility in experimental data. Flow Cytometry: Plan, execute, and analyze flow cytometry experiments to characterize cell surface markers and evaluate the quality and purity of iPSCs and differentiated cell types. Ensure accurate data analysis and interpretation to support ongoing R&D efforts. CRISPR-Cas9 Genome Editing: Execute precise CRISPR-Cas9 protocols for genome modification, contributing to the creation of isogenic cell lines. Laboratory Recordkeeping: Maintain detailed, accurate, and up-to-date laboratory records, ensuring all data are traceable and can be used in future projects and publications. Inventory & Reagent Management: Oversee the maintenance and organization of lab inventories, reagents, media, and various instruments. Ensure all laboratory functions run smoothly by assisting in routine equipment maintenance and compliance with safety standards. Cross-Team Collaboration: Work closely with other members of the R&D team and other departments within the institute to share insights and develop best practices in cell biology and molecular genetics. Continuous Learning: Stay up to date with advancements in stem cell technologies, genome editing, flow cytometry techniques, and related fields to enhance your contributions to the R&D team. Continuous Learning: Stay at the forefront of developments in stem cell technology, genome editing, biobanking practices, and related fields, applying new knowledge to enhance ongoing R&D and biobank efforts. Qualifications: Master's or Ph.D. degree in Cell/Molecular Biology, Biotechnology, or a related field. Minimum of 5 years of hands-on experience with iPSCs and human cell lines. Proficiency in aseptic cell culture techniques and ability to troubleshoot and optimize protocols. Expertise in molecular and cell biology techniques, including ELISA, qPCR, DNA/RNA isolation, immunohistochemistry, and flow cytometry. Strong working knowledge of CRISPR-Cas9 genome editing with proven ability to validate and troubleshoot experiments. Experience or familiarity with biobanking practices and cellular quality control standards. Proven leadership and laboratory management experience, with the ability to mentor and guide research technicians. Exceptional attention to detail, analytical skills, and ability to manage multiple projects in a dynamic research environment. Meticulous recordkeeping and organizational skills, with a commitment to maintaining laboratory and biobank best practices. Excellent communication skills and ability to work collaboratively within interdisciplinary teams. Preferred Skills: Experience working within non-profit, medical, or academic research settings. Knowledge of biobanking practices. Experience in handling high-throughput data, contributing to publications, or presenting at scientific conferences. Coriell & Recruitment Founded in 1953, the Coriell Institute for Medical Research is a nonprofit research institute dedicated to improving human health through biomedical research. Coriell scientists lead research in personalized medicine, cancer biology, epigenetics, and the genomics of opioid use disorder. Coriell also hosts one of the world's leading biobanks-comprised of collections for the National Institutes of Health, disease foundations and private clients-and distributes biological samples and offers research and biobanking services to scientists around the globe. To facilitate drug discovery and disease study, the Institute also develops and distributes collections of induced pluripotent stem cells. To learn more, visit **************** Any offer of employment extended by Coriell is contingent on an applicant's ability to be Authorized to Work in the United States of America. Upon date of hire, all employees are required to provide whichever valid Employment Authorization Documents they wish, as long as it is in compliance with Federal Regulations. This /posting is to provide general guidance on the nature of work that will be performed in this position. It is not represented to be a full or exhaustive list of the duties, responsibilities, or qualifications needed for this role. Due to the nature of our work, the duties, responsibilities, and qualifications listed on this job description/posting are subject to change. Coriell is an Equal Opportunity Employer, who values a diverse work environment, who is committed to providing reasonable accommodations to individuals with disabilities. Coriell is an at-will employer.

To clean the production, lab, and warehouse areas according to site procedures and complying to safety and quality requirements. Conduct GMP Cleaning operations in accordance with Biopharm Safety Procedures and cGMPs. GMP Cleaners are responsible for providing support to the production operations. It is essential the individual have a thorough understanding of the tasks required and the repercussions of their actions. Minimum level of education required - Intermediate School - Reading and comprehension skills required to execute GMP Cleaning activities and ensure operations occur in safe, compliant and efficient manner. Minimum of 1 year experience in Sterile or GMP Cleaning operations within Pharmaceutical or Biotechnology industry or 5 or more years of equivalent experience Prior experience with pharmaceutical manufacturing SHIFT: 12 hour shifts - 3 or 4 days/week including holidays and every other weekend. It's still TBD on the exact hours but it will primarily be geared towards nights (i.e., 12pm-12am or 2pm-2am)

Our large pharmaceutical client is seeking a Scientist to join the Immunomics team within the R&D Immunology Translational Science organization in Spring House, PA. The Immunology Therapeutic Area is focused on developing new cutting-edge therapies to treat dermatology, GI, and rheumatic diseases. This team is responsible for generating Next Generation Sequencing (NGS) data and passing it to the computational group for analysis. The role of this lab-based Scientist will primarily be focused on Next Generation Sequencing (NGS) including QC of RNA. Main responsibilities include: * Extracting RNA from tissue, cells, blood * RNAseq library preparation using Roche Kapa kits and sc RNAseq library preparation using 10X Genomics kits * QC of RNA/DNA samples using qPCR, Agilent TS and updating team with progress of library generation/QC * Lab sample/freezer management The ideal candidate will have strong molecular biology skills and hands-on experience in the lab doing RNA QC work. They will also need to demonstrate strong attention to detail and organization as they will be responsible for hundreds of samples at any given time. REQUIRED SKILLS AND EXPERIENCE -Bachelor's or Master's Degree in Biology or related field -3+ years of experience in the lab with Next Generation Sequencing (NGS) -RNA sequencing experience -Pipetting skills NICE TO HAVE SKILLS AND EXPERIENCE -Single cell experience -Tecan automation experience -Experience working with tissues -Olink experience -Immunology experience -Experience working with frozen PPMC -Flow cytometry Compensation: $40-48/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.

QC Environmental Monitoring Scientist - Contract - King of Prussia, PA Proclinical is working alongside global pharmaceutical company who are seeking a QC Environmental Monitoring Scientist. Primary Responsibilities: The successful candidate will focus on performing Environmental Monitoring in GMP Classified areas, including viable air, non-viable air, surface sampling, and settling plate analysis. This position requires immediate attention to detail and adherence to GMP standards. Skills & Requirements: A minimum of 3 - 5 years' experience in Environmental Monitoring within GMP areas. Minimum of a BS in biology, microbiology, or a related science field. Proficiency in using GMP systems for data entry. The QC Environmental Monitoring Scientist's responsibilities will be: Perform Environmental Monitoring in GMP Classified areas. Prepare Environmental Monitoring samples for analysis. Participate in laboratory investigations related to Environmental Monitoring. Enter data into GMP systems (LIMS/LES, Veeva, SAP/ERP). Complete necessary SOP and hands-on training for Environmental Monitoring. If you are having difficulty in applying or if you have any questions, please contact Jackie Cerchio at j.cerchio@proclinical.com Proclinical is a specialist employment agency and recruitment business, providing job opportunities within major pharmaceutical, biopharmaceutical, biotechnology and medical device companies. Proclinical Staffing is an equal opportunity employer. INDSCIC