Senior Scientist Jobs in Ventnor City, NJ

100% Onsite We are targeting for someone with more hands-on experience in histology techniques, specifically paraffin microtomy. Some one that has worked at a histology lab. The candidate must be able to be trained in a short period of time JOB SUMMARY: Histology Technician IV is responsible for proficiently performing routine histology technique, solution preparation, supply management, maintenance and operation of laboratory equipment and workstations, and good documentation practices (GDP) in recordkeeping, to support Quality Control Product Release Testing. This includes but is not limited to all aspects of routine histology, such as: sample receipt and accessioning, initial sample preparation (e.g., rehydration, rinsing, generating labels, etc.…), standard grossing and observations, fixation, paraffin and cryo-embedding, paraffin and cryo-microtomy, and Hematoxylin & Eosin (H&E) staining. Depending on skillset and training, the Histology Technician IV may also perform some histochemical stains (Special Stains) e.g., Verhoeff-Van Gieson (VVG) for product release testing; as well as routine histology testing of donor biopsies, explants, fresh, in-process, or final product samples for Tissue Services, Complaints, and Research & Development (R&D), as assigned. Compliance with standard operating procedures (SOPs), laboratory safety procedures, and maintenance of department databases/files are required. Additionally, the Histology Technician IV is responsible for troubleshooting histology technique and equipment issues; support equipment validations; cross-functional training activities; continuous/process improvement projects; and the Quality Management System. Education and Experience A.S. in Biology/related science or equivalent work experience Technical Certification (HT, HTL, QIHC, or related) preferred/eligible 5+ years Histology technique 3-5 years laboratory experience in a GXP environment 1-3 years in histochemistry (Special Stains)

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.

About the job Admera Health is seeking an Scientist I (Biopharma Lab, Temporary) to join our team! ADMERA - Entering the AD vanced M olecular ERA Admera Health provides genomic and bioinformatic services supporting discovery through clinical research stages. Our services include solutions for genomics, transcriptomics, epigenomics, and bioinformatics. Admera has deep expertise working with single-cell, FFPE, custom panels, and difficult or low-input samples. Corporate Culture Attributes: Innovative Collaborative Energetic Accountable Results-oriented Customer-centric Admera offers competitive health and financial benefits. In addition, we offer professional development and learning opportunities, rewarding bonus programs, and a wide range of work-life benefits. Title: Scientist I Department: Biopharma Services (Lab) Location: South Plainfield, NJ Responsibilities: Independently perform benchwork on projects to ensure successful product for all workflows. Take lead with fellow scientists in troubleshooting workflows. Assist in developing new workflows and take lead in improving current workflows. Train new associate scientists and scientists on laboratory workflows- documentation, benchwork, maintenance. Independently generate reports for results on benchwork and send to relevant customers, when necessary. Perform Next Generation based genomic assays on different workflows -Ex. RNA seq; Whole Genome Sequencing; Whole Exome Sequencing Detailed recordkeeping during project progress, procedures, deviations from standard protocols as necessary Assist Project Management team to provide technical support to customer Collaborate within the group, as well as cross departmental Qualifications: M.S. in Biological Sciences plus 2-3+ years of relevant laboratory experience required Ph.D. in Biological Scientist preferred Highly proficient in Molecular Biology principles and technologies including PCR, molecular cloning, and basic sequence analysis required Hands-on experience with Next Generation Sequencing platforms preferred Ability to multitask and meet deadlines in a fast-paced, customer-oriented environment Strong communication and interpersonal skills, both verbal and written For more information, please visit ********************* To review and apply to our open positions please visit ************************************

Job Title: Research Scientist Position Type: Full-Time Reports To: Director, Analytical R&D/QC We are seeking a highly motivated Research Scientist to join our Analytical R&D and QC department within the CDMO (Contract Development and Manufacturing Organization) industry. The ideal candidate will have a strong background in analytical chemistry and experience in method development, validation, and quality control testing. Key Responsibilities: Conduct analytical method development and validation independently. Troubleshoot analytical methods as needed and gain more experience in the related area. Conduct release testing for GMP regulatory starting materials, intermediates, and final APIs. Conduct testing for stability studies and cleaning verification. Review test data to ensure completion and accuracy. Write raw material test procedures as needed under supervision. Write SOPs and protocols as needed under supervision. Write instrument operating, maintenance, and qualification/calibration procedures as needed. Participate in OOS and deviation investigations, as needed. Support Quality Assurance as needed during internal audits and audits by clients and regulatory agencies. Assist in the development and implementation of corrective actions related to QC/AD. Troubleshoot and maintain analytical instruments. Ensure that instrument calibration and qualification intervals are current. Qualifications: BS, MS, or PhD in Analytical Chemistry, Chemistry, Pharmaceutical Sciences, or a related field. 3+ years of experience in analytical R&D and/or QC within the pharmaceutical or CDMO industry. Strong knowledge of analytical techniques, including HPLC, GC, UV-Vis spectroscopy, and dissolution testing. Familiarity with method validation protocols and regulatory requirements. Excellent problem-solving skills and attention to detail. Strong communication and interpersonal skills, with the ability to work effectively in a team environment. Proficient in data analysis software and laboratory information management systems (LIMS).

Bio Analytical scientist Duration: 12+ Months (Extendable) is Onsite Pay Rate: $38.00/hr on W2(Without Benefits included in the pay you will have you buy them separately by paying price for the benefits) Client: Pharmaceutical Bio-Analytical Scientist Warren, NJ- Onsite Work Schedule: Mon - Fri, Business Hours Summary: Executes experiments and analyzes data from flow cytometry analytical assays with limited supervision, as part of the Cell Therapy Analytical Development (CTAD) team. Executes experiments to support on-going method development to support drug product release. Responsible for ensuring compliance with good laboratory practices and other regulatory guidelines. Interfaces with internal research groups and clinical groups and assures laboratory productivity and technical research flexibility. Helps to oversee laboratory needs to ensure appropriate inventory/maintenance. Responsibilities • With limited supervision and/or oversight; design and execute analytical experiments of moderate complexity. • Perform data analysis, summarize and report experimental results. Present data in group meetings and work collaboratively to determine next steps. • Document/review laboratory work in e-notebooks that is detailed, accurate, timely, and in compliance with Good Documentation Practices. • Ensure proper operation and perform routine maintenance of laboratory equipment as needed. • Potentially could be working with biological material--no exposure to animals. Skills/Knowledge • Required B.S. with 2 - 4 years work experience or M.S. with 0 -2 years experience in Molecular & Cellular Biology, Immunology, or related discipline. • Experience working in a regulated (GLP/GMP) environment in preferred. • Flow cytometry assay development experience is preferred. • Experience with flow cytometry platforms is preferred: Miltenyi Macsquant, BD Symphony A5 and/or Canto, Beckman Coulter Cytoflex • Experience with flow cytometry software is preferred: Flowjo, FCS Express • Assay qualification/validation experience is preferred. • Excellent organization skills and ability to handle multiple tasks • Highly motivated, willingness to acquire new skills, and ability to work with minimal supervision. • Excellent verbal and written communication skills. • Must be proficient in microsoft suite

Job Details: Global Pharmaceutical Company Microbiologist Long Term Contract Skillman, NJ Microbiologist Individual should able to - Understanding of safety, cGMPs and documentation for a Microbiology Laboratory Understanding of general Microbiology laboratory procedures and Skillman campus procedures as related to routing sample management and testing, e.g. Fusion Understanding of Product / Process Microbiology including: Test Method Suitability and Validation Microbial Limits Water Activity Microorganism Identification Preservative Effectiveness (AET) Water Testing Growth Promotion Media Preparation Equipment Cleaning & Lab Cleaning Take on new assignments under direct supervision as required

Renaissance LLC All qualified applicants will receive consideration for employment without regard to race, color, sex, sexual orientation, gender identity, religion, national origin, disability, veteran status, age, marital status, pregnancy, genetic information, or other legally protected status. Scientist II, MS&T US-NJ-Lakewood Job ID: 2024-2765 Type: Regular Full-Time # of Openings: 1 Category: MS&T Lakewood, NJ Overview The purpose of MST Scientist II position is to perform MS&T functions with limited supervision such as process development, scale-up, technology transfer, commercialization and product lifecycle advancements. This individual will ensure he/she is trained in areas related to quality by design, scale-up, technology transfer, manufacturing scale-up and process improvement. Provide technical knowledge, influence and thorough planning to drive for timely and appropriate results with limited supervision. Responsibilities Perform MS&T activities with limited supervision for pharmaceutical products including parenteral and nasal products for all new products from scale-up to commercialization and process improvement beyond commercialization. Continue to grow in understanding the overall generic and new drug development processes, Agency requirements and CMC strategies. Understand and comply with all the Renaissance safety, environmental and quality practices and procedures as outlines in organization/departmental guidelines and SOPs, as well as applicable federal, state and local regulations. Ensure all department SOPs are in place and followed. Participate with supervision in the progress of project work with follow-ups, meeting timelines and providing appropriate technical info to the support team. Identify, develop, and foster good working relationships with cross-functional teams, external customers and support initiatives required to continually enhance Renaissance's reputation with customers. This role may also be a scientific team member for client calls regarding MS&T matters. Prepare project protocols, assess, and identify deliverables with limited supervision. Review technical data, documents and proposals. Provide technical guidance with limited supervision on both commercial products after launch and development products through technical communications, memos, and reports. Learn to trend data and look to continually achieve and meet specifications, providing Process Capability Analysis. Ensure batch records are written and accurate in a manner that Operations can follow them and ensure Operations are trained and feel confident in the process for commercial batches. Support any regulatory audits as assigned. Must have the ability to work in a team environment. Must comply with all company policies. Flexibility in schedule is required based on business needs. Other duties, as assigned. Qualifications Bachelor's Degree in Pharmaceutical Sciences, Formulation Chemistry, Chemical Engineering or similar degree AND a minimum of 3-5 years of related experience in MS&T or Product Development Master's Degree in Pharmaceutical Sciences, Formulation Chemistry, Chemical Engineering or similar degree AND a minimum of 1-3 years of related experience in MS&T or Product Development PhD in Pharmaceutical Sciences, Formulation Chemistry is a plus. Compensation details: 87200-102700 Yearly Salary PI188afebd8004-26***********4

Job Title: MS&T Scientist II Salary: $94,0000 MS&T Scientist II position will support the Company in the development and optimization of manufacturing processes, improving them and increasing the scale. The ultimate goal is to develop processes that optimize the product yield and minimize the cost of production. These products include injectables and nasal/sublingual sprays Responsibilities: Utilize and apply knowledge of basic scientific principles, theories and concepts to develop solutions to problems of moderate complexity. Design and conduct experiments at small and medium scales in co-ordination with R&D group. Collect and analyze data from development batches and provide process development reports and tech transfer reports. Provide input in developing robust process validation programs. Perform risk assessment and present ideas for modifying existing procedures and suggest alternative methods to improve results. Understand, keep current and apply current technology to include cGMP, sterile manufacturing techniques. Collaborate with Engineering, Operations, OpEx, and QA groups and prepare robust manufacturing records, technical reports and SOPs. Prepare, analyze and organize data for training, and meetings. Experience with API, small molecule is preferred. Qualifications: Bachelor's Degree (BS) in Engineering or Natural Sciences required with a minimum of 3 years of relevant experience in the pharmaceutical industry or equivalent combination of education and experience.

Open to: General Public Work Week: NL (35-hour) Work Week Salary: (P25) $74,534.83 - $105,943.75 Existing Vacancies: 1 Program/Location Department of Environmental Protection Office of the Deputy Commissioner Division of Science and Research 428 East State Street Trenton, NJ 08625 Scope of Eligibility Open to applicants who meet the requirements below. Description Under the direction of a Research Scientist 1 or other supervisory official in a state department, institution, or agency, conducts or participates in research projects or developed programs in a specified professional field; does other related work. Specific to the Position This scientist will assist with the coordination of research focused on ensuring safe and reliable water resources by designing, coordinating, and managing research projects and providing technical analysis focused on drinking water and wastewater treatment and evaluation. The appointee will also assist in determination of analytical capabilities of laboratories to measure contaminants for the development of standards in various media and provide technical support to water-related rule proposals. Evaluation of water quality characteristics that impact water treatment, methods for corrosion control treatment, and novel technologies capable of treating contaminants of emerging concern is essential. The appointee will review scientific publications and documents pertaining to new research, and assist in data compilation, analysis, and the preparation of reports. Tasks will include the preparation and management of research contracts and providing support to the Science Advisory Board. Preferred Skill Set Special consideration will be given to candidates with knowledge of the principles of modern research and statistical methods relevant to assessment of water and wastewater treatment, knowledge of organic and inorganic analytical chemistry methods, knowledge of essential quality assurance practices, and the ability to prepare clear and concise technical reports. Understanding of the release of lead and copper from distribution pipes is a plus. Requirements EDUCATION: Graduation from an accredited college or university with a Master's degree in a discipline appropriate to the position. EXPERIENCE: Two (2) years of experience in a field appropriate to the position. NOTE: A Doctorate in a discipline appropriate to the position may be substituted for two (2) years of experience indicated above. NOTE: All U.S. degrees and transcripts must be from an accredited college or university. All foreign degrees and transcripts must be evaluated for accreditation by a recognized evaluation service by the closing date of this posting. Failure to provide documentation may result in ineligibility. License Appointees will be required to possess a driver's license valid in New Jersey only if the operation of a vehicle, rather than employee mobility, is necessary to perform the essential duties of the position. SAME Applicants If you are applying under the NJ SAME program, your supporting documents (Schedule A or B letter) must be submitted along with your resume by the closing date indicated above. For more information on the SAME program, please visit SAME Program, email ***************, or call CSC at ************** and select Option #3. Veteran's Preference To qualify for New Jersey Veteran's Preference/status, you must establish Veteran's Preference through the Department of Military and Veteran's Affairs. Please submit proof of your Veteran's Preference along with your resume as indicated. For more information, please visit *********************************************************************** Residency All persons newly hired on or after September 1, 2011, have one year from the date of employment to establish, and then maintain principal residence in the State of New Jersey subject to the provisions of N.J.S.A. 52:14-7 (L.2011, Chapter 70), also known as the “New Jersey First Act”. Authorization to Work Selected candidates must be authorized to work in the United States per the Department of Homeland Security, United States Citizenship, and Immigration Services regulations. NOTE: The State of New Jersey does not provide sponsorship for citizenship to the United States. Equal Opportunity Employment The State of New Jersey seeks to increase the richness and diversity of its workforce, and in doing so, become the employer of choice for all people seeking to work in State Government. To evaluate the effectiveness of our efforts to attract and employ a diverse workforce, applicants are asked to voluntarily answer a few brief questions on the NJ Affirmative Action Information Form. All information is considered confidential and will be filed separately with the agency's affirmative action officer. This information will not be part of your application for employment and will not be considered in any hiring decision. The New Jersey Department of Environmental Protection is an Equal Opportunity Employer and is committed to inclusive hiring and a diverse workforce. We strongly encourage people from all backgrounds to apply. Accommodations under ADA will be provided upon request.

"All candidates must be directly contracted by ASK Consulting on their payroll and cannot be subcontracted. We are unable to provide sponsorship at this moment". Job Title: Associate Research Scientist Duration: 12 months Location: New Brunswick, NJ 08903 Pay Rate: $45-$47.47/Hr Job Description: 100% onsite(Possibility of some flexibility, need manager's approval) Work Schedule: Mon-Fri(normal business hours) Key Responsibilities: Support in-process analytical testing for monoclonal antibodies and fusion proteins, including HPLC/UPLC, isoelectric focusing, capillary electrophoresis, ELISA, qPCR, etc. Record, analyze, evaluate, and interpret data to support process development optimization. Maintain accurate and up to date laboratory e-notebook documentation. Ensure work is performed in accordance with established safety and quality protocols. Maintain a safe, clean, and high-performance laboratory environment. On-site presence is required to complete the primary responsibilities of this position. Qualifications & Experience: Required Bachelors degree in Analytical Biochemistry, Analytical Chemistry, Biotechnology, or related field with 1- 3 years of relevant industry experience. Experience in a variety of protein analytical techniques, including affinity chromatography, N-glycan characterization, charge variant analysis via iCIEF, size exclusion HPLC and UPLC, capillary electrophoresis, and ELISA, reverse phase chromatography. A basic understanding of cell line, upstream and downstream process development. Proficiency in Empower, SYMX, LIMS, and Microsoft applications. (recommended) Excellent communication, organizational skills, attention to detail, and problem-solving skills. Working knowledge of statistics, data analysis, and interpretation skills. Ability to work collaboratively in a team environment. About ASK: ASK Consulting is an award-winning technology and professional services recruiting firm servicing Fortune 500 organizations nationally. With 5 nationwide offices, two global delivery centers, and employees in 42 states-ASK Consulting connects people with amazing opportunities ASK Consulting is an equal opportunity employer. We celebrate diversity and are committed to creating an inclusive environment for all associates.

Development Scientist / Senior Scientist - Formulation *Must be fluent in speaking, writing, and reading Japanese* Do you have experience working with either generic or branded OSD products? Would you like to contribute that experience to a global pharmaceutical company? Our client is a global CDMO located in New Jersey. The site in New Jersey is focused on oral solid dose development and manufacturing of both generic and branded products. Globally the company has been in business since the 1980's and here in the US they have been growing their operations since the early 2000's. They are unique in the services they offer to be able to work with a pharmaceutical client from end to end on their drug product programs. This position is a new position for the research and development team and an instrumental one in being able to deliver timely results for the current and future clients. This position will report to the Senior Manager Technical Services. The Scientist professional should possess a strong background in oral solid dose formulation and scale -up and technical transfer activities from development to commercialization and lifecycle support. This is a hands on laboratory position. RESPONSIBILITIES: Develop junior personnel in both Technical Service and Operations departments for project support. Participate in new project opportunities by generating scientific expert content, hosting new customer visits or teleconferences, and attending conferences or customer visits to generate new leads. Responsible for maintaining GLP/GMP laboratory environment and maintaining a safe, clean laboratory. Execute laboratory work plan/schedule developed with input from supervisor or senior team member. Draft technical documents such as batch records, technical reports, and protocols with supervisor guidance. Perform parallel review of manufacturing documentation and may become qualified to perform technical review of documents for accuracy, thoroughness, and regulatory compliance. Train others on basic laboratory and manufacturing techniques. Assist in the execution of efficiency improvement project with guidance. Maintain high quality laboratory documentation in accordance with applicable regulatory guidance and Site SOPs. Performs physical testing as needed; bulk/tap density, flow analysis (Johanson and FT4) and sieve analysis. Executes procedures or methods of moderate complexity with high quality. Support novel manufacturing technology assessment to expand and improve technical capability according to the mid/long term investment plan. Perform bench marking and risk assessment of new manufacturing technologies working with vendors and prepare information summary for discussions. Reviewing manufacturing information (formulation compositions, processes, documentation) from a customer and develop/implement the manufacturing procedure into manufacturing area. Work with customer and operation group members to conduct tech-transfer batches under supervisor's directions. Provide a manufacturing procedure to the Operation Group for commercial production. Work with operation group members to conduct internal technical transfer batches. Prepare technical documents for execution of study protocol and study reports as required. Prepare and revise GMP documentation to manufacturing batch records, SOPs, etc. Assures experimental quality through sound experimental design and utilizes DOE. Promote the company's image through participation in conferences and seminars. Prepare batch records, specifications, procedures, and SOPs as needed. QUALIFICATIONS: Bachelor's degree in chemistry, biology, pharmacy, chemical engineering, or related field. At least 5-8 years' experience in a pharmaceutical process/product development environment. Working knowledge of the theories and manufacturing processes associated with the experimental manufacture of oral solid drug products specifically and pharmaceutical products in general. Familiar with technologies including Fluid Beds, High Shear Granulators, Tablet Presses, Tablet Coaters, Blenders, Mills, etc. Mechanical knowledge and hands on experience relating to fluid bed processor, granular, tablet press, encapsulation, and coating equipment. Formulation and process development for oral dosage forms. Technical transfer and scale up experience. NDA/ANDA filing experience including design space and DOE.

. The Upstream Manufacturing Scientist conducts mammalian cell culture processes and produces recombinant proteins for mammalian-based biosimilars, handling cell culture batches from 50 L to 1000 L in a cGMP environment. This role requires expertise in bioreactor operations, cell biology, and proficiency in batch records, protocols, and technical documentation. The individual must work collaboratively in teams and independently with minimal supervision. Key Responsibilities Collaborate with teams to execute upstream batches and operate bioreactors at various scales. Ensure timely completion of engineering and clinical batches. Develop equipment specifications and enhance manufacturing techniques. Monitor operating data and perform real-time adjustments. Interpret instructions in various formats and adhere to GMP and safety policies. Review manufacturing batch records and manage investigations as needed. Perform additional duties as assigned and comply with company policies. Qualifications Bachelor's or Master's degree in chemical, biological, or biochemical sciences with 3+ years in biopharmaceuticals. Experience with bioreactors or fermenters. Strong expertise in process development, batch execution, and analysis. Experience in GMP and aseptic environments, including use of single-use manufacturing tools. Proficient communication, teamwork, computer, and organizational skills. Knowledge of GMP documentation, cleaning verification, and validation.

Job Title: R&D Scientist Duration: 06 months contract EDUCATION AND EXPERIENCE: B.S.+ degree in Materials Science, Chemistry, or related engineering disciplines. Minimum 2 years direct laboratory experience. The R&D Scientist II reports directly to the R&D Manager and is responsible for delivering technical excellence in applied material/chemical sciences within the IDS R&D organization. The R&D Scientist II will support change to win activities such as interacting with material suppliers, conducting feasibility studies, and performing design verification/validation for blood collection devices. • Represents the R&D function as an Extended Team member in support of large technology and product development programs. • Design and execute experiments that further the development, verification, and evidence generation efforts across all assigned programs and projects. • Document and build technical knowledge within assigned business areas; with guidance, explore and recommend solution concepts and principles when applicable. • Drive aspects of product development work streams under guidance including but not limited to Requirements Management, Design Verification, and Design Transfer to Manufacturing for applicable assignments. • Ensure program success by working cross functionally with R&D-Engineering, Marketing, Medical Affairs, Manufacturing, Quality and Regulatory Affairs. • Participate in intellectual property growth; submit patent applications and Invention Disclosure Records. • Works under general and specific direction from manager and senior personnel to determine or develop potential approaches to solutions. • Adhere to Good Laboratory Practices, all relevant lab operational procedures, and actively participate in maintaining the setting and functionality of IDS laboratories and equipment. • Mentor and train junior team members and foster a collaborative work environment. • Travel as required to conferences, manufacturing sites, customer visits, etc. KNOWLEDGE AND SKILLS: • Knowledge on polymer formulation, processing and structure-property relationship. • Experience with handling clinical specimens (particularly human blood) is desired; blood-borne pathogen safety training is necessary and will be provided. • Must be proficient with MS Office, and experience with statistical analysis tools is desired. • Excellent written and verbal communication skills and interpersonal skills. Must be comfortable with complex team matrices. • Strong learning agility to facilitate strengthening core competency areas. • Self-motivated with a strong sense of urgency and willing to take hands-on work.

The position is on-site and lab-based, requiring relevant expertise in vibrational (FTIR and/or Raman) spectroscopy and compendial analytical techniques to support release testing of raw materials, excipients, intermediates, and starting materials used in the manufacturing of clinical drug substances and drug products. This position is located at New Brunswick, NJ (NBR) site, reporting directly to a Principal Scientist within the GxP Biologics and Pharma Raw Materials Group of the Analytical Strategy & Operations (ASO) department. DUTIES & RESPONSIBILITIES: Essential Duties and Responsibilities include, but are not limited to, the following: Independently perform analytical testing including but not limited to FTIR and Raman spectroscopy methods, color & physical appearance tests, pH and osmolality measurements, compendial wet chemistry identification methods (e.g., USP), and other general analytical lab techniques. Executed tests will support clinical release and stability testing of drug substances, drug products, excipients and raw materials used in the manufacturing and formulation of Clinical drug substances and drug products. Demonstrate practical knowledge of analytical techniques contributing to the development of phase-appropriate robust and reproducible analytical methods used in a GMP testing laboratory. Maintain clear, complete, accurate and GMP-compliant documentation for experiments. Independently execute analytical method qualifications, verifications, and validations (as applicable), carefully adhering to approved protocols. Contribute to study design and the authoring of analytical protocols and reports. Proactively provide clear, timely communication of potential issues to management. Organize and present data for internal meetings. Proactively provide clear, timely communication of potential issues to management. Professional Qualifications: The candidate must have a B.S. or equivalent with a degree in Analytical Chemistry, Chemistry, Biochemistry or equivalent; 1-2 years of analytical laboratory experience in a GMP environment is strongly preferred. An understanding of cGMP/GLP and GDPs practices and EHS requirements is essential for success in this position. Ability to comply with all applicable SOPs, internal and external (ICH, compendial) requirements/regulations is a must. The candidate must be able to deliver when working under assigned timelines and demonstrate good communication skills, particularly in documentation of data and writing reports and methods. Skill in communicating/escalating critical issues to appropriate team leaders and functional area management is necessary. Expertise in MS Office applications, in particular MS Word and Excel, is required. Familiarity with electronic documentation systems (e.g., Qumas, Infinity, Syncade-DCA) for routing protocols/reports, investigation reports for review and approval is a plus. Experience in use of scientific reporting applications and ELN software, e.g., VelQuest, Symyx and LIMS is preferred.

The incumbent will work in the development of oral solid dosage pharmaceutical products. Conducting formulation and process development, manufacturing clinical trial supplies, and supporting commercial product manufacturing when required. The incumbent will support implementation for the continuous process improvement efforts within the customer's business segment in the area of technology transfer and process scale up. Assist customers in evaluating technical needs and advise on equipment selection. The individual may also participate in continuous process improvement projects and support departmental initiatives, as well as evaluate new technologies to expand our service offering. There is an expectation of direct hands-on laboratory work and/or supervision of one or more direct reports and mentoring/training of other colleagues as needed. RESPONSIBILITIES Conduct physical and chemical property assessment (solubility, stability, particle size, etc.) of candidate compounds Conduct formulation and process development for oral solid dosage forms of new chemical entities and/or generic products. Perform lab and manufacturing experiment using key manufacturing equipment, including but not limited to, high shear granulator, fluid bed granulator/dryer/coater, blender, tableting machine, and film coating equipment. Conduct laboratory analysis on raw materials, in-process, and product formulations using key analytical apparatus, including but not limited to, scanning electron microscope, light microscope, laser particle size analyzer. Communicate results internally and externally through verbal and written updates and formal reports as necessary. Organize meetings and monitor all customer interactions independently. Participate in and lead cross-functional project teams to meet company and/or customer goals. Creates and/or revises new department-wide and site-wide procedures and company SOPs. Stay abreast of current scientific technologies to maintain the state of the art nature of CCU and will evaluate new technologies to expand our technical service offering. Proactively communicate strategy to customers and write and review new proposals and change orders, as appropriate. Support the business aspects of the position by taking responsibility for execution and communication of all work under their supervision. Develop junior personnel in both Technical Service and Operations departments for project support. Participate in new project opportunities by generating scientific expert content, hosting new customer visits or teleconferences, and attending conferences or customer visits to generate new leads. Responsible for maintaining GLP/GMP laboratory environment and maintaining a safe, clean laboratory. Execute laboratory work plan/schedule developed with input from supervisor or senior team member. Draft technical documents such as batch records, technical reports and protocols with supervisor guidance. Perform parallel review of manufacturing documentation and may become qualified to perform technical review of documents for accuracy, thoroughness and regulatory compliance. Train others on basic laboratory and manufacturing techniques. Assist in the execution of efficiency improvement project with guidance. Maintain high quality laboratory documentation in accordance with applicable regulatory guidance and Site SOPs. Performs physical testing as needed; bulk/tap density, flow analysis (Johanson and FT4) and sieve analysis. Executes procedures or methods of moderate complexity with high quality. Support novel manufacturing technology assessment to expand and improve CCU's technical capability according to the mid/long term investment plan. Perform bench marking and risk assessment of new manufacturing technologies working with vendors and prepare information summary for discussions. Reviewing manufacturing information (formulation compositions, processes, documentation) from a customer and develop/implement the manufacturing procedure into manufacturing area. Work with customer and CCU operation group members to conduct tech-transfer batches under Provide a manufacturing procedure to the Operation Group for commercial production. Work with CCU operation group members to conduct internal technical transfer batches. Prepare technical documents for execution of study protocol and study reports as required. Prepare and revise GMP documentation to manufacturing batch records, SOPs, etc. QUALIFICATIONS Must be fully bilingual (read, speak, write) in Japanese Working knowledge of the theories and manufacturing processes associated with the experimental manufacture of oral solid drug products specifically and pharmaceutical products in general. Bachelor's degree in chemistry, Biology, Chemical Engineering, or related field. At least 2 years' experience in pharmaceutical process/product development environment. Familiar with technologies including Fluid Beds, High Shear Granulators, Tablet Presses, Tablet Coaters, Blenders, Mills, etc. Mechanical knowledge and hands on experience relating to fluid bed processor, granular, tablet press, encapsulation, and coating equipment. Formulation and process development for oral dosage forms. Technical transfer and scale up experience. NDA/ANDA filing experience including design space and DOE. Ability to handle difficult situations produced by time constraints and customer demands, etc. Possess good knowledge of cGMPs and safety practices. Possess good interpersonal skills. Good verbal and written communication skills, computer skills in word processing, spreadsheets and some technical software.

A PE-backed Advanced Materials Company is seeking an Analytical Lab Scientist, a key role in ensuring the quality of raw materials and products through cutting-edge material characterization. You will be responsible for leading quality control initiatives, optimizing analytical methods, resolving customer quality issues, and supporting new product development teams. Key Responsibilities: Oversee laboratory safety, cleanliness, and organization, ensuring high operational standards. Develop and optimize analytical methods for raw materials and new product testing. Lead customer quality escalation projects, providing root cause analysis and clear presentations of findings. Work closely with R&D teams to develop new methods for material characterization in product development. Mentor junior staff and ensure accurate presentation of data and conclusions. Develop standard operating procedures (SOPs) for lab processes and review others' SOPs. Research and implement new analytical tools and instrumentation to enhance lab capabilities. Travel to support quality control and metrology processes at plant sites. Assist in the maintenance of chemical inventory and safety procedures. Qualifications: Ph.D., MS, or BS in Chemistry, Chemical Engineering, Materials Science, or a related field. 3-5+ years of experience in industrial chemical, polymer-based manufacturing, or advanced materials. Proficiency with analytical instruments like ICP-OES, FTIR, SEM-EDX, XRD, TGA, and DOE. Strong experience in Design of Experiments (DOE) and data analysis using statistical tools. Ability to work independently and communicate effectively with cross-functional teams. Experience with wet chemistry (acid/base/solvent) systems and advanced laboratory instrumentation. Additional Requirements: Must be able to work in a chemical and powder processing lab with various personal protective equipment (PPE) requirements. Physical capability to lift up to 50 lbs. Ideal Candidate Traits: Strong analytical and problem-solving skills. Excellent communication and presentation abilities. Ability to work in a fast-paced, evolving environment. A growth mindset with the flexibility to adapt to new challenges. Salary and Benefits: Competitive salary with performance-based bonus. Benefits package that includes health, dental, and vision coverage. Opportunity to work in a state-of-the-art R&D facility with advanced equipment. Collaborative and growth-oriented environment. Note: The salary range for this role takes into account the wide range of factors that are considered in making compensation decisions, including but not limited to skill set; experience and training; licensure and certifications; and other business and organizational needs. The disclosed range estimate has not been adjusted for the applicable geographic differential associated with the location at which the position may be filled. It is not common for an individual to be hired at or near the top of the range for their role, and compensation decisions are dependent on the facts and circumstances of each case. A reasonable estimate of the base range is $100,000.00 to $ 125,000.00 per year + 15% company performance bonus and benefits.

Exemplify BioPharma, Inc. a Symeres Company, is a global partner research organization (PRO) based in New Jersey, USA. We are a team of biopharma industry experts focused on delivering end-to-end Chemistry, Manufacturing and Controls (CMC) throughout the drug development and regulatory market application processes. Using a unique combination of program management, coupled with our New Jersey based process development laboratories we are ideally positioned to deliver CMC success to partner organizations. We are talent based team and our key asset is our experience, multidisciplinary expertise and proven track record. We strive to bring tangible value to our partners through provision of strategic, tactical and technical leadership to solve complex problems focused on reducing program timelines and costs. Position & Responsibilities Exemplify BioPharma is seeking a scientific leader to serve as Senior Analytical Chemist at our R&D laboratory located in Cranbury, New Jersey. The ideal candidate will have 0-3 years' experience and a proven record of sustained laboratory achievement and innovation. The professional in this position will lead analytical development for high priority drug candidates. You will identify and characterize key physical and chemical properties of pharmaceutical materials (e.g., active drug substances) and/or formulated drug products (e.g. tablets, injectable solutions). As an innovator, you will develop, validate and implement new analytical methods to guide product development and solve challenging technical problems related to purity, stability, packaging, and manufacturing. You will define strategies to address quality-related objectives, and will recommend the methods and specifications used to monitor pharmaceutical materials and/or the formulated product. You will then lead the transfer of these technologies to CRO, CMO manufacturing sites. This professional will lead and/or participate on multi-disciplinary product development teams and will supervise the studies and professional development of one or more laboratory professionals. You will develop new scientific ideas, methods and technologies that contribute to the responsibilities described above. Other responsibilities include statistical data analysis, compliance with pharmaceutical good manufacturing practices and the completion of technical reports and external publications (as appropriate). This visible and business-critical role demands excellent oral and written communication skills. This is an exceptional opportunity for motivated candidates who wish to be exposed to all aspects of CMC drug development in a fast moving, collaborative and learning environment. Qualifications A Ph.D. degree in analytical chemistry or a related discipline is preferred. The candidate must have a demonstrated ability to conduct independent research, solve scientific problems, and lead other professionals in a highly collaborative environment. Application If you are interested in applying for this exciting opportunity at Exemplify BioPharma please e-mail a cover letter and resume to ******************************.

EcolSciences, Inc., a 50 year old multi-disciplinary environmental consulting firm is seeking qualified individuals to fill the following position: SENIOR ENVIRONMENTAL SCIENTIST/GEOLOGIST/PROJECT MANAGER This is a senior-level position that will involve managing hazardous waste investigations including but not limited to environmental site assessments, ISRA investigations, soil/groundwater investigations and remediation studies. Qualifications: 7 to 10 years of relevant experience; Phase I and Phase II Experience; Strong experience with New Jersey Site Remediation Regulations and Guidance; Knowledge of NYSDEC and PADEP regulations; Bedrock groundwater investigation and remediation experience is desirable; Demonstrate excellent client management and communication skills; Demonstrate an ability to manage projects from initial proposal preparation through project completion; Excellent written and verbal communication skills; A degree in geology, engineering, or environmental sciences; 40 hour OSHA HAZWOPER training; Professional licenses such as LSRP, PE, PG, or CPG are desirable. EcolSciences offers an excellent salary and benefits package. Please respond through LinkedIn or send or email resume and salary history to: ECOLSCIENCES, INC. Attention: Peter A. Hansen, Principal 75 Fleetwood Drive, Suite 250 Rockaway, New Jersey 07866 ************************ EcolSciences, Inc. does not accept unsolicited resumes from individual recruiters or third party recruiting agencies in response to job postings. If Recruiters nevertheless submit one or more unsolicited resumes to any employee at EcolSciences, Inc. without a valid written agreement in place for the position, it will be deemed the sole property of EcolSciences, Inc. No fee will be owed or paid to Recruiters who submit unsolicited candidates, in the event the candidate is hired by EcolSciences, Inc. Benefits: Bonus Program 401(k) Dental insurance Health insurance Life insurance Paid time off Parental leave Professional development assistance Retirement plan Tuition reimbursement Vision insurance

Job Title: Material Scientist Cecilia is a NASA-backed start-up, upending the plastic waste crisis. We are commercializing a modular, microwave-based system that upcycles plastic waste into clean hydrogen and performance carbon, specifically carbon nanotubes. Join our innovative startup dedicated to advancing the frontier of nanocarbon materials. Leveraging a unique circular carbon approach, we are poised to transform industries with sustainable, high-performance solutions. As we gear up for our next phase of growth, we are seeking an in-lab Material Scientist to support our nanocarbon materials product development. Job Description: The Material Scientist will play a pivotal role in advancing the company's core materials development, particularly in carbon nanotube synthesis, functionalization, and applications. This is a full-time, in-person role based in our Newark, NJ laboratory, where the candidate will be responsible for hands-on experimentation, materials development, and data analysis. The successful candidate will innovate, optimize processes, and contribute to scalable material solutions. Responsibilities: - Integrate directly into our engineering and development team to synthesize and functionalize carbon nanotubes and nanocarbon-based materials, with a focus on improving properties and developing new applications. - Conduct hands-on lab experimentation including safe handling, purification, and functionalization of carbon nanotubes. - Experimental design, data analysis, and scientific reporting. - Directly work on our proprietary carbon nanotube synthesis, functionalization, and material productization. - Coordinate and analyze advanced characterization work with resources such as Raman spectroscopy, FTIR, TGA, TEM, and SEM. - Analyze experimental data, provide insights, and contribute to refining material processes for scalability. - Manage project timelines and deliverables, ensuring experimental data is well-documented and results are communicated clearly to the broader team. - Support collaborations with external partners and contribute to the scaling of lab-scale processes for commercialization efforts. - Follow all laboratory safety protocols and maintain high standards of cleanliness and organization. - Assist in general lab maintenance, including the setup of experiments and calibration of equipment. Required Qualifications: *Candidates must have experience in working with carbon nanotubes* - PhD in Materials Science, Physics, Chemistry, Chemical Engineering, or a related field, with a focus on nanocarbons, heterogeneous catalysis, thermochemistry, and specific experience with carbon nanotubes. - Ideal candidates will have completed their PhD within the last 12 months, candidates who are expected to defend their PhD dissertation within the next 12 months are also eligible. - Willingness to work in a hands-on, in-person laboratory role in Newark, NJ. - Expertise in carbon nanotube synthesis, purification, characterization, functionalization, and application development is highly desirable, with prior experience in CNT functionalization for specific applications, such as electronics, composites, or energy storage preferred. - Strong understanding of lab safety protocols, especially in the handling of nanomaterials and solid catalysts. - Proficiency in materials characterization techniques including (but not limited) Raman, FTIR, TGA, TEM, SEM, XRD, and AFM. - Ability to work safely and independently in a laboratory setting, with strong knowledge of lab safety protocols, especially in the handling of solid materials. - Strong problem-solving skills, creativity, and an eagerness to work in a fast-paced, innovative environment. - Excellent verbal and written communication skills to effectively document and share research findings. - Familiar with Microsoft and Google packages such as Word, Excel, Powerpoint. - Capable of performing physical tasks such as bending, reaching, lifting, and carrying materials up to 40 pounds. - Must be eligible to work in the US without company sponsorship