Chemist jobs in Baltimore, MD

Works with customers and AR teams to identify unmet needs, collect design input and develop new product design strategies. Technical and laboratory lead in developing new polymers, robust products, and basic production processes that can be successfully commercialized. Essential Functions: Conducts required laboratory work; including polymerization, formulation, coating and testing Develops new products that lead to sustainable commercial revenue Functions as a technical lead on product development teams Develops design strategies based on robust design input Meets technical commitments in order to complete project progression dates and milestones Contributes to product scale up and development through reproducibility and validation testing support Detailed knowledge of required chemical and physical test methods May supervise and teach other laboratory staff Responsible for the proper disposal of hazardous waste into the proper labeled containers and drums Interfaces with customers on new product applications Interfaces with associates from other departments as needed (e.g. cross-functional teams) Documents lab work in electronic notebook and project reports Performs all duties consistent with established AR guidelines, ISO-9001, and elements of GMP deemed necessary to support the business (as outlined in the Quality Manual) Actively complies with and endorses Department and Company objectives Additional Responsibilities: Performs other duties and responsibilities as assigned. Job Specifications: BS, MS, or PhD in chemistry, polymer science or materials science; adhesive polymerization, formulation, and coating experience preferred Ability to perform duties with minimal or no supervision Ability to manage multiple priorities Requires an demonstrated ability to use sensitive test equipment Ability to employ statistical analysis techniques Ability to manage and supervise laboratory staff Ability to maintain confidentiality of AR information Must communicate fluently in English Excellent oral & written communication skills Excellent interpersonal skills Knowledge of computers & related word processing, spreadsheet & e-mail software-Microsoft preferred

Job Title Semiconductor Nanocalorimetry Senior Researcher Division Research & Economic Development Department NIST PREP Work Status Full Time Position Category Contractual Faculty Rank Open Rank FLSA Pay Range Contractual Salary Range $100,000 / year Fund Source Federal/Grant Job Summary A research scientist role working to advance our capabilities in nanocalorimetry, including developing methods for applying the technique to in situ monitoring of semiconductor processes. The major responsibilities of the candidate will include implementing chip-based nanocalorimeters on atomic layer deposition (ALD) processes to measure the thermochemistry of surface reactions. Job Duties * Operating and maintaining research-grade ALD equipment * Maintaining vacuum system, including precursors and pumps * Setting up and operating calorimetric and optical instrumentation, including data collection systems * Setting up and operating complementary in situ measurements to aid in calorimetric data interpretation * Modeling time-resolved calorimeter thermal response to extract physical quantities (e.g. heats of adsorption, reaction, etc.) * Analyzing deposited films using analytical techniques, as needed * Working in a multi-disciplinary team comprised of experts in ALD processes, metrology development, and computational modeling * Regularly reporting research findings to project team and advisor(s) * Publishing in peer-reviewed scientific journals and presenting at conferences Knowledge, Skills, Abilities & Other Characteristics * Expertise in building and operating custom lab instrumentation * Expertise in vapor phase deposition processes, such as ALD * Strong written and oral communication skills * Ability to work as part of a team and independently Required Minimum Qualifications * Ph.D. or equivalent experience in chemistry, physics, materials science, or related field Other Preferences for Consideration

We are looking to fill a **Scientist II or III - Metrology Specialist** position working as a full-time employee of Parexel FSP on long-term assignment onsite at one of our clients located in **Rahway, NJ.** This position offers full benefits, sick time, 401K, paid holidays, and paid time off. **This position does not offer sponsorship.** **Metrology specialist is responsible for the oversight of regulated and non-regulated laboratory equipment** . This role will oversee the lifecycle of the lab instrumentation covering acquisition and installation, performance or coordination of routine maintenance, computer system validation, and regulated systems retirement **Qualifications -** B.S./M.S. in Chemistry, Biochemistry, Engineering, or a related discipline + **Scientist II** - B.S. with 1-2 years of relevant experience or M.S. with 0-1 years of relevant experience + **Scientist III** - B.S. with 3-5 years of relevant experience or M.S. with 1-2 years of relevant experience **Responsibilities** + Prepare, review, and approve instrument/equipment documentation such as master equipment lists, qualification documentation, and calibration documentation + Coordinate service activities across a variety of vendors and service engineers while building and maintaining strong working relationships + Gain a working knowledge of laboratory equipment to facilitate with troubleshooting and/or perform maintenance or calibration activities + Participate in computer system validation activities associated with new or upgraded equipment or software packages + Support the purchase, installation, and equipment qualification of new laboratory equipment + Collaborate with metrology staff across multiple testing labs and sites for process improvement, cross-training and cross-site support + Originate and progress Notice of Event (NOE) and Change Management (CM) records + Perform and document investigations and assist in developing/implementing CAPA plans + Represent the laboratory on all aspects of laboratory equipment during audits + Ensure compliance with all regulatory requirements (cGMP) and internal policies and procedures **Required Skills and Experience** + Experience working within a regulated (GMP) laboratory + **Experience maintaining or operating laboratory equipment including HPLCs, GCs, UVs, dissolution systems, or other specialized computerized systems** + Familiarity with standalone computer system validation requirements + Highly organized, and capable of multi-tasking to manage a variety of laboratory equipment or system related schedules, documents, and maintenance tasks + Capable of working independently under moderate supervision + Strong verbal and written communication skills + Strong interpersonal skills. Comfortable interacting with a variety of on-site and off-site collaborators **Desired Skills and Experience** + Experience with maintenance of analytical instrumentation such as HPLC, UPLC, GC, UV, IR, Karl Fischer, and dissolution with ability to troubleshoot them. + Experience with computerized standalone systems GMP validation requirements + Familiarity with authoring relevant instrument standard operating procedures (SOPs) **About Parexel** Parexel FSP includes the CMC Operations group. We provide pharmaceutical and biopharmaceutical companies with qualified and talented technical professionals to support the development and delivery of new therapies. For results-driven and caring individuals who want to make a meaningful difference in the world, Parexel is trusted by life sciences companies to meet their long-term staffing needs for scientists and engineers and related professionals in discovery and development of novel therapies, keeping patients at the center of everything we do, and where an inclusive community helps you be your best, transforming any career into a life-changing achievement. **Come join us!** \#LI-DK1 EEO Disclaimer Parexel is an equal opportunity employer. Qualified applicants will receive consideration for employment without regard to legally protected status, which in the US includes race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or protected veteran status.

Full-time Description The Analytical Chemist plays a fundamental role in Sterilex R&D by enabling New Product Development and Product Stewardship initiatives. This role is responsible for developing and validating new analytical methods to support new product development and manufacturing quality control processes. The ideal candidate has experience with basic wet chemistry quality control methods, analytical chemistry instrumentation, method development, statistics, and validation of those methods under Good Laboratory Practices. The candidate works closely with R&D Formulation Chemists and key contacts in Operations. This position is regularly scheduled to be staffed Monday through Friday, 8:30 a.m. to 5:00 p.m. with occasional overtime as needed to support department and company business needs. KEY RESPONSIBILITIES 1. Analytical Chemistry Method Development & Validation Improve existing analytical methods and develop new methods to support new product development and product stewardship initiatives. Validate and maintain the portfolio of current analytical methods utilized in Sterilex chemistry labs. 2. R&D Product Stewardship & Technical Support Lead initiatives to support existing products, such as qualification of new and equivalent raw materials or locally sourced raw materials in new geographies. Identify key raw material characteristics, contaminants, unreacted byproducts, etc. using sound analytical techniques. Conduct and/or oversee GLP chemical characterization studies of current or in-development products Serve as GLP study director or sponsor as needed in studies supporting regulatory approval. Respond to field / customer technical support inquiries as needed. 3. Quality Control Method Transfer & Support Lead or co-lead the qualification of manufacturing QC procedures, specifications and processes. Provide on-going support of manufacturing QC methods & quality control troubleshooting, working jointly with Sterilex Operations. Identify cost effective and relatively simple analytical methods for co-packers, especially for critical chemical components in raw materials and finished goods. 4. Analytical Chemistry Laboratory Quality Management & Operations Work jointly with QA to maintain the analytical chemistry lab quality program in full compliance with Sterilex QMS practices Develop, implement, and maintain laboratory safety protocols, ensuring compliance with all laboratory safety rules and regulations. Oversee regular maintenance as well as scheduling and execution of annual preventative maintenance/calibrations of Sterilex analytical instruments within chemistry and analytical labs Identify analytical equipment gaps for the Sterilex laboratory with the ability to propose cost effective equipment solutions. Identify and cooperatively manage third-party analytical lab relationships when outsourcing is required. 5. Uphold R&D Process Rigor & Foster Talent Development Conduct and oversee essential training of new technician hires Use experience to propose improvements to R&D processes and contribute innovative ideas for product improvements and new product concepts. Prepare and present written and oral reports on research findings, project status, literature reviews, and technical issues that affect the business. Survey scientific literature to remain current with developments and stay abreast of current trends, practices, regulatory changes that would impact Sterilex products. Interface effectively with Sterilex scientific, business development, and management staff to understand Sterilex markets, innovation and product development goals. Document and protect intellectual property by maintaining laboratory notebooks and timely completion of other patent-related documentation. Adhere to Sterilex's Stage Gate and Quality Management processes, use of associated tools, and documentation of research, project status, recommendations, and decisions made. Requirements QUALIFICATIONS · Education: B.S. or M.S. degree in Chemistry or related degree from an accredited college or university. Ideally a degree is in Analytical Chemistry and/or with an emphasis on Analytical Chemistry. · Experience: 5+ years of independent research or development experience in an academic or industrial analytical chemistry or QC laboratory setting Moderate+ experience with chromatographic (HPLC, GC) and spectroscopic (MS, UV/Vis) analytical techniques and basic wet chemistry methods (titrations, pH, surface tension measurements, foam tests, etc.) In-depth working knowledge of analytical method development, method transfer, and method validation. Experience working in a Good Laboratory Program (GLP) environment and validation of methods under GLPs. · Skills: Ability to draw scientifically supportable conclusions and recommendations, and develop follow-up experiments as appropriate. Demonstratable organizational skills and ability to maintain a clean and orderly working environment Demonstrate ability to understand chemical interactions and reactions and propose analytical methods to confirm. Utilize industry standard statistical software and methods when reporting results. Ability to execute written procedures and experiments with minimal supervision. · Key Competencies: Ability to recognize inconsistencies in data and execute corrective actions in consultation with R&D management to mitigate issues Understanding of industrial laboratory processes and procedures including proper maintenance of laboratory notebooks and general laboratory safety procedures Ability to read, comprehend and follow documents, including standard operating procedures, test methods, safety rules and regulations, and instrument operating and maintenance instructions. Motivated to take full ownership of assigned tasks Competent to prepare and carefully review figures, computations, tests, reports, etc., and ensure internal consistency. Good written and oral communication skills and effective interpersonal skills Computer literate: MS Office, statistical software, programs to operate equipment, other related software, email etc. Ability to work independently, multi-task and balance priorities

Job DescriptionDescription: The Analytical Chemist plays a fundamental role in Sterilex R&D by enabling New Product Development and Product Stewardship initiatives. This role is responsible for developing and validating new analytical methods to support new product development and manufacturing quality control processes. The ideal candidate has experience with basic wet chemistry quality control methods, analytical chemistry instrumentation, method development, statistics, and validation of those methods under Good Laboratory Practices. The candidate works closely with R&D Formulation Chemists and key contacts in Operations. This position is regularly scheduled to be staffed Monday through Friday, 8:30 a.m. to 5:00 p.m. with occasional overtime as needed to support department and company business needs. KEY RESPONSIBILITIES 1. Analytical Chemistry Method Development & Validation Improve existing analytical methods and develop new methods to support new product development and product stewardship initiatives. Validate and maintain the portfolio of current analytical methods utilized in Sterilex chemistry labs. 2. R&D Product Stewardship & Technical Support Lead initiatives to support existing products, such as qualification of new and equivalent raw materials or locally sourced raw materials in new geographies. Identify key raw material characteristics, contaminants, unreacted byproducts, etc. using sound analytical techniques. Conduct and/or oversee GLP chemical characterization studies of current or in-development products Serve as GLP study director or sponsor as needed in studies supporting regulatory approval. Respond to field / customer technical support inquiries as needed. 3. Quality Control Method Transfer & Support Lead or co-lead the qualification of manufacturing QC procedures, specifications and processes. Provide on-going support of manufacturing QC methods & quality control troubleshooting, working jointly with Sterilex Operations. Identify cost effective and relatively simple analytical methods for co-packers, especially for critical chemical components in raw materials and finished goods. 4. Analytical Chemistry Laboratory Quality Management & Operations Work jointly with QA to maintain the analytical chemistry lab quality program in full compliance with Sterilex QMS practices Develop, implement, and maintain laboratory safety protocols, ensuring compliance with all laboratory safety rules and regulations. Oversee regular maintenance as well as scheduling and execution of annual preventative maintenance/calibrations of Sterilex analytical instruments within chemistry and analytical labs Identify analytical equipment gaps for the Sterilex laboratory with the ability to propose cost effective equipment solutions. Identify and cooperatively manage third-party analytical lab relationships when outsourcing is required. 5. Uphold R&D Process Rigor & Foster Talent Development Conduct and oversee essential training of new technician hires Use experience to propose improvements to R&D processes and contribute innovative ideas for product improvements and new product concepts. Prepare and present written and oral reports on research findings, project status, literature reviews, and technical issues that affect the business. Survey scientific literature to remain current with developments and stay abreast of current trends, practices, regulatory changes that would impact Sterilex products. Interface effectively with Sterilex scientific, business development, and management staff to understand Sterilex markets, innovation and product development goals. Document and protect intellectual property by maintaining laboratory notebooks and timely completion of other patent-related documentation. Adhere to Sterilex's Stage Gate and Quality Management processes, use of associated tools, and documentation of research, project status, recommendations, and decisions made. Requirements:QUALIFICATIONS · Education: B.S. or M.S. degree in Chemistry or related degree from an accredited college or university. Ideally a degree is in Analytical Chemistry and/or with an emphasis on Analytical Chemistry. · Experience: 5+ years of independent research or development experience in an academic or industrial analytical chemistry or QC laboratory setting Moderate+ experience with chromatographic (HPLC, GC) and spectroscopic (MS, UV/Vis) analytical techniques and basic wet chemistry methods (titrations, pH, surface tension measurements, foam tests, etc.) In-depth working knowledge of analytical method development, method transfer, and method validation. Experience working in a Good Laboratory Program (GLP) environment and validation of methods under GLPs. · Skills: Ability to draw scientifically supportable conclusions and recommendations, and develop follow-up experiments as appropriate. Demonstratable organizational skills and ability to maintain a clean and orderly working environment Demonstrate ability to understand chemical interactions and reactions and propose analytical methods to confirm. Utilize industry standard statistical software and methods when reporting results. Ability to execute written procedures and experiments with minimal supervision. · Key Competencies: Ability to recognize inconsistencies in data and execute corrective actions in consultation with R&D management to mitigate issues Understanding of industrial laboratory processes and procedures including proper maintenance of laboratory notebooks and general laboratory safety procedures Ability to read, comprehend and follow documents, including standard operating procedures, test methods, safety rules and regulations, and instrument operating and maintenance instructions. Motivated to take full ownership of assigned tasks Competent to prepare and carefully review figures, computations, tests, reports, etc., and ensure internal consistency. Good written and oral communication skills and effective interpersonal skills Computer literate: MS Office, statistical software, programs to operate equipment, other related software, email etc. Ability to work independently, multi-task and balance priorities

JRAD has an immediate opening for an Analytical Chemist in Washington DC. J Analyzes environmental and/or air samples for Chemical contamination Operates and maintains laboratory equipment (e.g., Gas and Liquid Chromatography, Mass Spectrometers, and performs basic maintenance and checks on common laboratory systems Uses Laboratory Information Management System (LIMS) software for managing analytical data Participates in laboratory proficiency testing activities and maintains QAQC records to include performance charts, control limits, and detection and reporting limits for analytical methods governing use of laboratory instrumentation Maintains operator manuals and procedures, providing training to new staff in the operation and use of Lab equipment and LIMS Meticulously adheres to laboratory procedures, data management practices and safety protocols in accordance with Laboratory Quality Assurance Plans and safety policies/regulations Supports formal audits of laboratory quality control systems and practices, the inspection of safety practices and the review of Job Hazard Analyses Maintains inventory of lab supplies Required Skills and Education: Bachelor's Degree in Chemistry, Biochemistry, or similar, from an accredited college or university More than 3 year of experience with quantitative analysis of chemical compounds, and 2 years' experience with screening environmental samples for toxic industrial compounds (TICs) Must have demonstrated analytical laboratory skills as evidenced by participation in a Proficiency Test such as a Precision and Accuracy performance test or equivalent Must have experience with quality management standards (e.g., ISO 17025 or similar), sample preparation methods, techniques, regulations, protocols, safety measures, and the operation and maintenance of chemical laboratory instrumentation Working knowledge of Microsoft Office products including Excel, Project, Word, Access and Power Point Excellent written and oral communication skills Multiple experience level positions available for Journeyman to Senior level Chemists Minimum of 10 years of experience with a Bachelors Degree, or 6 years of experience with a Masters Degree Security Clearance Ability to obtain and maintain a secret security clearance When you work for JRAD you will never be just a number. We put people before profits! JRAD is committed to the health and well-being of its employees. We offer more paid time off than the average company upon hire, and the following benefits are available to all full-time employees: Health Insurance Dental Insurance Vision Insurance Life & Accidental Death and Dismemberment Insurance Section 125 Flexible Spending Accounts for unreimbursed Medical & Dependent Day Care Disability Insurance 401K Plan Tuition Reimbursement JRAD is an equal opportunity employer as to all protected groups, including protected veterans and individuals with disabilities. Please note this job description in no way states or implies that these are the only duties to be performed by this employee. The employee will be required to follow any other instructions and to perform any other duties requested by the supervisor. The JRAD salary range for this position is a general guideline only and not a guarantee of compensation or salary. There are many factors considered when determining the compensation provided in an offer. These factors include, but are not limited to position responsibilities, education, experience, knowledge, skills, and contract terms and conditions.

Analytical Chemist I Duration: 12+ Months Contract Total Hours/week: 40.00 1st Shift: Work days/hours: M - F 8:30am -- 5pm Client: Medical Device Company Employment Type: Contract on W2 (Need US Citizens Or GC Holders Only) No H1B's Onsite daily Description: Work within a team to provide Analytical Chemistry support to our customers using various analytical instruments and techniques. Develop and follow protocols for analytical testing and reporting results following current good laboratory practices. Duties And Responsibilities: 1. Develop, follow protocols and perform analytical testing using wet chemistry analysis, UV/VIS Spectroscopy, UPLC/MS, FTIR, ICP-MS and other techniques as required. 2. Use office and instrumentation specific computer software. 3. Perform tasks according to existing protocols, applying basic scientific principles to assigned tasks, developing experiments and documenting the performed work as required. 4. Identify and troubleshoot problems, collect and record data, report data. 5. Participate in technical meetings and data reviews. 6. Make sure Lab supplies are properly ordered, labeled, and stored. 7. Make sure required safety and other training is completed and training records are maintained according to department policies. 8. Perform laboratory work and documentation in accordance with GLP and company guidelines. 9. Perform tasks under general supervision. Qualifications: Knowledge And Skills: • Basic understanding in the use of liquid chromatography systems. • Basic understanding of chromatography theory and hands-on experience with HPLC or UPLC. • Excellent verbal and written communication skills are necessary together with the ability to interact effectively in team and cross-functional environments. • Understanding of GLP laboratory guidelines. • Optional experience includes the use of UPLC/MS using Empower software, FTIR and ICP-MS. • Experience in method development. Education And Experience • Minimum of a Bachelor's degree in Chemistry, Biochemistry, Biology or related discipline. • Prefer a minimum of 1 year of industrial or academic experience in Analytical Chemistry testing.

General Job Information This position is located in the Department of Forensic Sciences (DFS), Public Health Laboratory (PHL) Division. The mission of the DFS is to provide high-quality, timely, accurate, and reliable forensic science services using best practices and best available technology, focusing on unbiased science and transparency to enhance public safety and health. The incumbent serves as a Supervisory Clinical Chemist who supports the chemical terrorism (CT) initiative under Centers for Disease Control and Prevention (CDC) cooperative agreement and performs as the CT Coordinator for the District. Duties and Responsibilities Performs specific analytical tests utilizing protocols transferred from the Centers for Disease Control and other general methods where there are established protocols and practices available. Under minimal supervision, modifies existing methodologies for new testing compounds, matrixes or testing instrumentation. Acts as lead technical specialist in two of three analytical platforms (GC-MS, LC-MS/MS, high resolution mass spectrometry or ICP MS), provides training and acts as a subject matter expert (SME) for the method and instrumentation. Performs technical review of data collected from unit staff; Independently leads projects including but not limited to: method development, research projects, and training programs. Leads validation of new methods and protocols; maintains journals, logs and other records pertinent to method validation. Reviews scientific literature to determine the chemical and biological characteristics of samples to be analyzed to facilitate sample preparation and analysis. Leads in interpretation and evaluation of test results to determine validity and scientific significance. Performs periodic maintenance and calibration of instruments and related equipment within the chemistry laboratory. Performs preventive maintenance and quality control on instruments as outlined in the manufacturer's instructions and Standard Operating Procedures. Leads in the training of lower-level personnel and students in the theoretical and practical aspects of chemistry and quality assurance. Prepares reports and maintains records of work performed on patient specimens and samples; maintains reagent lot numbers for quality control and files such records in an appropriate manner. Provides the full range of supervisory services, as required to manage and direct the work efforts of subordinate staff and activities of assigned operations. Develop quantitative and qualitative measures for evaluating the work performance of staff. Supervises and assigns duties and responsibilities; formulates overall plans for resources; approves and disapproves leave requests; recommends job selections, promotions, incentive recognition and corrective or adverse actions; establishes work standards; and identifies developmental and training needs. Qualifications and Education Degree: physical sciences, life sciences, or engineering that included 30 semester hours in chemistry, supplemented by course work in mathematics through differential and integral calculus, and at least 6 semester hours of physics. Or Combination of education and experience -- course work equivalent to a major as shown in A above, including at least 30 semester hours in chemistry, supplemented by mathematics through differential and integral calculus, and at least 6 semester hours of physics, plus appropriate experience or additional education. Licenses and Certifications None Working Conditions/Environment The work is performed in an office setting and laboratory setting. The office setting is when preparing documentation and the laboratory setting is during the testing and analysis phase. The incumbent may be exposed to hazardous materials, toxic substances, and blood borne pathogens and is required to follow safe laboratory practices and wear protective clothing gear such as laboratory coats, fume hoods, safety goggles, radiation badges, aprons, gloves, and shields, etc. and to adopt sterile techniques. The nature of the DFS mission necessarily involves the potential risks associated with biological or chemical hazards, including morgue functions. Although contact with these functions is intended to be minimal, the risks are nevertheless possible; training to recognize, address, and mitigate these risks is required as is dealing with potentially personally difficult topics, such as crime, death, and disease. Other Significant Factors Tour of Duty: Monday - Friday, 8:30am to 5:00pm Pay Plan, Series and Grade: MS-1320-13 Promotion Potential: No known promotion potential Type of Appointment: Management Supervisory Service (MSS). Positions in the Management Supervisory Service (MSS) serve at the pleasure of the appointing authority and may be terminated at any time with or without cause. Collective Bargaining Unit: This position is not covered under a collective bargaining agreement. Position Suitability: This position has been deemed Safety Sensitive under the guidelines of the DC Personnel Manual and is subject to mandatory pre-employment and periodic criminal background checks and traffic records checks (as applicable). This position is also subject to mandatory pre-employment and random drug and alcohol testing. In this position, you may be disqualified from employment based on the presence of marijuana in test results, even if you possess a medical card authorizing the use of medical marijuana. Position Designation: This position has been designated as Essential and acceptance of this offer confirms you agree to adhere to the policies in sections 1271 and 1274 of DPM Chapter 12, regarding essential/emergency employees. As an emergency employee, you will be required to either report to work, stay at work, or telework (if directed to do so) during a declared emergency or during a period of non-emergency where your duties have been deemed as critical District government functions/operations. You may be required to perform other duties outside of your position description during a period of a declared emergency (such as manual labor, shelter services, etc.). Residency Preference: Applicants claiming "Residency Preference" will be required to maintain residency in the District of Columbia for a minimum of seven (7) years. Failure to do so may result in forfeiture of employment. EEO Statement: The District of Columbia Government is an Equal Opportunity Employer. All qualified candidates will receive consideration without regard to race, color, religion, national origin, sex, age, marital status, personal appearance, sexual orientation, family responsibilities, matriculation, physical handicap, or political affiliation.

MacroGenics is a leader in the discovery and development of innovative medicines that utilize our next generation antibody-based technologies. Our team of 350+ dedicated individuals is advancing a pipeline of product candidates to treat patients with cancer. Our products and platforms have attracted multiple partnerships with leading pharmaceutical and biotechnology companies around the globe. The Company considers its employees to be its most valuable asset and we are committed to providing opportunities for individuals to learn and grow as a means to further their professional development. MacroGenics' corporate culture promotes an atmosphere of innovation, open communication and teamwork where employees can see firsthand how they contribute to the success of the organization. Summary of Position As a member of the Protein Science team, this individual will set up transfections to express proteins in mammalian cells followed by their purification and characterization to support the Biologics discovery pipeline. Job duties * Culture of mammalian cells in suspension following aseptic techniques and cell-line specific protocols. * Transient transfection of cell lines or expansion of stable cell pools, from 3 ml - 10 L scale, to express proteins of interest. Monitor and optimize culture conditions to maximize protein quality and expression. * Protein purification from milligram to gram scale using semi-automated FPLC systems. * Analytical characterization of purified proteins to support research projects for drug discovery. * Collect, analyze, and summarize experimental data in electronic lab notebook for archiving and sharing. * Maintain lab and lab equipment in optimal functioning condition. Report any problems to supervisor. Qualifications: Education/Experience Associate Scientist II * Bachelor's degree in Biology or Biochemistry or a related field of study with a minimum of 2 years of bench-related experience Scientist I * Bachelor's degree in Biology or Biochemistry or a related field of study with a minimum of 3 years of bench-related experience or Master's degree in Biology or Biochemistry or a related field of study. Laboratory experience gained through undergraduate coursework, graduate research, or an internship is required. A minimum of 1 year of bench-related experience, strongly preferred. Knowledge, Skills and Abilities * Experience with mammalian cell culture, transfections, maintaining cell lines, etc. with meticulous sterile technique and lab practices. * Experience with recombinant protein purification and analytical characterization (CE or SDS-PAGE, SEC). * Experience with experimental design and execution with minimal supervision. * Experience with standard lab software for data analysis (MS Excel, Prism, etc.). Good organizational skills and ability to multi-task. * Good verbal and written communication skills. Demonstrated ability to work in a collaborative environment with other team members. * Willingness to work on occasional weekends. Preferred Experience * Experience with antibody purification using automated FPLC system. * Experience with quantitative assays (BLI Octet, ELISA, etc.). Supervisory Responsibilities: None Additional Information The annual rate of pay for the Associate Scientist II position ranges from $67,200 - $102,500. The annual rate of pay for the Scientist I position ranges from $84,400 - $128,800. For non-exempt roles, and according to applicable regulations, there may be the possibility for overtime pay. This role is eligible for the Company's discretionary bonus and discretionary equity incentives. Eligible employees may participate in the Company's benefits programs, including medical / dental / vision / prescription coverage, employee wellness resources, 401(k) plan with employer match, access to an Employee Stock Purchase Plan, (ESPP), paid time off & paid parental leave benefits, and disability benefits. The annual pay rate range is described in good faith, and the Company believes is the range of possible compensation for this role at the time of this posting depending on the candidate's experience, qualifications, geographic location, and other factors permitted by law. The Company may ultimately pay more or less than the posted range, and this range may be modified in the future. No amount is considered to be wages or compensation until such amount is earned, vested, and determinable under the terms and conditions of the applicable policies and plans. The amount and availability of any bonus, commission, benefits, or any other form of compensation and benefits that are allocable to a particular employee remains in the Company's sole discretion unless and until paid and may be modified at the Company's sole discretion, consistent with the law. Statement MacroGenics is proud to be an equal opportunity employer. Employment selection and related decisions are made without regard to race, color, national origin, sex, gender identity, sexual orientation, religion, age, disability, protected veteran status, or any other characteristic protected by federal, state or local law. We are committed to working with and providing reasonable accommodation to individuals with disabilities. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the employment process, please email ******************** or call ************** and/or 711 for TTD/TTY service. Equal Opportunity Employer/Veterans/Disabled We do not accept non-solicited resumes or candidate submittals from search/recruiting agencies.

Milliken & Company is a global manufacturing leader whose focus on materials science delivers tomorrow's breakthroughs today. From industry-leading molecules to sustainable innovations, Milliken creates products that enhance people's lives and deliver solutions for its customers and communities. Drawing on thousands of patents and a portfolio with applications across the textile, flooring, chemical and healthcare businesses, the company harnesses a shared sense of integrity and excellence to positively impact the world for generations. Discover more about Milliken's curious minds and inspired solutions at Milliken.com and on Facebook, Instagram, LinkedIn and Twitter. POSITION OVERVIEW Milliken's Laurel Plant in Gainesville, FL, is seeking a qualified individual to join its manufacturing team as an R&D laboratory technician. The technician performs routine work in the Research and Development Laboratory to safely develop chemical processes and produce products on a small scale. JOB RESPONSIBILITIES • Operate and maintain mechanical laboratory equipment, including vacuum pumps, stirrers, and pressurized systems. • Safely set up and operate lab-scale glassware, distillation columns, and instrumentation for tests, research, process development, or small-scale manufacturing. • Operate and maintain electronic laboratory equipment, such as temperature controllers, timers, and distillation controllers. • Develop familiarity with standard analytical procedures used for material characterization, including IR spectrometry, UV spectrometry, gas chromatography, Refractive Index, Specific Gravity, Viscosity, Flash Point, and % Solids. • Document records completely, accurately, neatly, and legibly. • Learn basic functions of other departments, such as Quality, Analytical, Shipping, Customer Service, EHS, Production, Maintenance, and Purchasing, to work with respective areas. QUALIFICATIONS • High School Diploma or GED, along with some work experience in a lab setting. • Experience using Microsoft Office suite applications. • Ability to plan and prioritize daily tasks. Milliken is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to actual or perceived race, color, creed, religion, sex or gender (including pregnancy, childbirth or related medical condition, including but not limited to lactation), sexual orientation, gender identity or gender expression (including transgender status), ancestry, national origin, citizenship, age physical or mental disability, genetic information, marital status, veteran or military status or any other characteristic protected by applicable law.

Under minimal supervision of QC management, the QC Chemist performs physical and chemical testing on raw materials, in-process and finished products, as well as stability samples. Utilizes established methods and standard operating procedures and laboratory equipment to perform testing of materials. Prepares high quality written documentation, such as notebooks, logbooks, standard operating procedures (SOPs) and LIMS reports. Trouble shoots analytical equipment. Provides training on analytical methods and new technologies. Responsibilities: Performs analytical testing of raw materials, in-process materials, finished products and stability samples. Operates laboratory equipment such as balances, pH meters, hardness testers, particle size analysis, LOD, Karl Fischer, Melting Point, etc. in accordance with laboratory SOPs and test methods. Effectively performs routine testing using HPLCs, GCs, UV-VIS, FT-IR and ICP-MS equipment in accordance with SOPs and test methods. Performs data analysis and evaluation of test results. Prepares reports and reviews data. Maintains accurate records of test data, maintains laboratory notebooks and logbooks in accordance with company guidelines and GDPs. Assists in writing and revising SOPs and tests methods as needed. Follows documented procedures: SOPs, test methods, and transfer protocols. Performs routine maintenance, calibration, and performance verification on applicable instruments. Performs investigation activities and writes deviation and investigation reports. Suggests and writes CAPAs. Follows lab safety procedures. Perform other duties as assigned. Qualifications: Bachelors in chemistry or related physical/biological science, or equivalent combination of education, training and professional experience that provides the individual with the required knowledge, skills, and abilities. Minimum of 3 years' experience in Pharmaceutical Analysis Must understand analytical chemistry. Demonstrated knowledge of cGMP regulations and ICH guidelines Computer literacy and ability to use data acquisition and processing software, such as EMPOWER 3 Demonstrate the ability to read, analyze, and interpret USP/NF methods, SOPs and technical procedures manuals, and batch records. Demonstrate the ability to define problems, collect data, establish facts, and draw valid conclusions; interpret an extensive variety of technical instruction in mathematical or diagram form. Knowledge of basic laboratory practices, methods, and techniques Demonstrate the ability to carry out work assignments communicated orally or in writing. Demonstrate familiarity with Lean Six Sigma Methodologies and proven analytical/ problem solving capabilities. Demonstrates the ability to establish good working relationships with other departments, including vendors, colleagues, and subordinates. Demonstrates the appropriate technical knowledge necessary to make sound decisions on development issues with minimal supervision. Demonstrate the ability to analyze data and information and assess and resolve complex problems/issues as required. Must be able to comprehend and follow all applicable SOPs. Demonstrate ability to acquire the appropriate knowledge from resources on with electronic Quality Management Systems such as MasterControl and Trackwise. Demonstrate understanding of the current federal, local, and international regulations regarding the production, testing, and release of drug substances and products. Good understanding of cGMPs, industry, and regulatory standards and guidelines. Demonstrate familiarity with Microsoft programs like Word, Excel, PowerPoint, Project, Teams, Outlook, etc. Demonstrate the ability to portray the appropriate level of integrity and professionalism. Demonstrate the ability to communicate effectively with management, staff, regulators, and client representatives in written and verbal formats. Demonstrate the ability to complete tasks accurately and according to established and shifting timelines. Demonstrate the ability to make quality scheduling, resource allocation, and priorities decisions. Energetic, execution-focused, self-motivated, and organized individual who is accustomed to working in a deadline-focused, high-pressure entrepreneurial environment. Results-oriented and efficient. Creative and open-minded who fosters an environment in which sharing of ideas is encouraged. Demonstrate the ability to work closely with a diverse customer and employee base (internally and externally). Demonstrate the ability to work well in a cross-functional team environment. Must communicate fluently in English and have legible handwriting. Physical Demands: Ability to travel between and within facilities to visit staff, operations, and projects, as needed. Ability to sit, stand, climb stairs, and climb ladders to mezzanines (when necessary). Ability to lift up to 40 pounds on occasion. Ability to use PPE (safety shoes, goggles, respirators, gloves, etc. when necessary).

Who We Are Arcellx is a public, clinical-stage biotechnology company reimagining cell therapy by engineering innovative immunotherapies for patients with cancer and other incurable diseases. We believe that cell therapies are one of the forward pillars of medicine and our mission is to destroy cancer and advance humanity by developing cell therapies that are safer, more effective, and more broadly accessible. Our team members are made up of talented innovators and dreamers working from our offices in Gaithersburg, Maryland, and Redwood City, California. At Arcellx, we hire exceptional people and create a fun, diverse, supportive, and informal environment that allows everyone to do their best work. What Matters to Us Living our core values is essential to maintaining a work environment that is high-performing, inclusive, and collaborative. We look for candidates who demonstrate strong values alignment and bring different backgrounds, viewpoints, and abilities to the team. Arcellx Core Values Start with authenticity: We foster an inclusive environment where each person can bring their authentic self to work. Think ‘we' before ‘me': We prioritize collective success, collaborating and supporting one another to achieve our shared goals. Embrace the challenge: We deliver exceptional results by working with shared determination and a commitment to doing what's right. How You'll Make a Difference As an Associate Scientist , you will use molecular biology, protein purification and characterization methods to support Discovery's protein engineering and technology development efforts. Engaging with a cross-functional team in a fast-paced environment, you'll identify and develop Arcellx's lead therapeutic candidates. Our potentially life-saving treatments would not exist without the work of our talented Discovery scientists; this role will have a tremendous impact on our pipeline and ability to deliver novel and effective drugs to patients. The “Fine Print” - What You'll Do Work with other scientists to design, generate and characterize recombinant proteins to be used in cancer therapy discovery and development. Assist with selection and/or screening strategies used in protein discovery workflows employing phage display, yeast display, ELISA, BLI and flow cytometry as needed. Communicate detailed observations on experiments and assist in the preparation of technical reports, summaries, and protocols. Skills and Experience We Look For Bachelor's or master's degree in the life sciences (e.g., biology, genetics, biochemistry, chemistry, chemical engineering, bioengineering). Minimum of 3 years of experience in a laboratory setting. Ability to work both independently and collaboratively. Ability to effectively plan, organize, and prioritize work activities. Must demonstrate proficiency with molecular biology methods , including primer design, PCR, gel electrophoresis, plasmid DNA preparation, cloning and sequence analysis using SnapGene or similar software. Preferred skills include those related to recombinant protein expression (e.g. transient transfection), purification (e.g. nickel and Protein A affinity chromatography) and characterization (e.g. ELISA, BLI, SDS-PAGE, protein quantitation and flow cytometry). Rewards at Arcellx Our people are our greatest asset, and supporting their well-being is an essential part of delivering on our mission and impacting the lives of patients. Putting this belief into practice means offering strong compensation and benefits. The base salary range for this position is $75,000 - $95,000 per year. Where a candidate falls within that range is determined by factors such as years of experience. Our compensation package also includes an annual bonus based on company goals and an equity (RSU) grant. We do offer relocation assistance for roles if required. Our market-leading benefits package includes: 100% coverage for medical, dental and vision for team members and dependents, unlimited vacation, a 3-day weekend every month, fully-paid parental leave for up to 6 months, tuition reimbursement, 401k employer contribution and more. Join us in our quest to reimagine cell therapy and destroy cancer. For more on our technology, culture, and team, go to **************** #LI-Onsite

US Tech Solutions is a global staff augmentation firm providing a wide-range of talent on-demand and total workforce solutions. To know more about US Tech Solutions, please visit our website ************************ We are constantly on the lookout for professionals to fulfill the staffing needs of our clients, sets the correct expectation and thus becomes an accelerator in the mutual growth of the individual and the organization as well. Keeping the same intent in mind, we would like you to consider the job opening with US Tech Solutions that fits your expertise and skillset. Job Description • BioProcess Engineering (BPE) department is responsible for scale up, tech transfer, and facility fit of clinical and commercial processes to manufacturing. BPE is also responsible for producing development drug substance material and data from pilot facilities. Members of Development Scale-up Center (DSC), within BPE, produce materials up to 500L scale for toxicology and process development studies, to confirm process performance and to troubleshoot issues in GMP facility, and work with cross functional team on technology evaluations. • This position is focused on upstream cell culture and fermentation processes supporting scalability and production of therapeutic proteins in DSC. Position is a hands-on laboratory and production-based role. Responsibilities include but are not limited to media preparations, routine sub-culturing of cells and fermentations. The candidate will assist in adaptation of transferred information for scale-up processes from late stage development to DSC as well as assisting in the production of various tox and development materials, troubleshooting and resolving technical issues with the production processes and/or equipment, identifying root causes for deviations, implementing corrective/preventative actions, assisting in implementing new technologies, and trending/analyzing data. • The candidate will assist in compiling data and expected to summarize and assist in interpreting results. The candidate will also maintain production and laboratory equipment. Qualifications Education: • Bachelor of Science (BS) or Master of Science (MS) in scientific, engineering or related field. Experience: • For the RA, we require a BS with 2 - 5 years or a MS with 0 - 2 years of relevant experience. • For the AS, we require a BS with a minimum of 5 years or MS with a minimum of 2 years of relevant experience. Additional Information Special Skills/ Abilities • Hands on proficiency in cell culture and/or fermentation and good aseptic techniques. Bioreactor/fermenter operation experience is preferred. • Good documentation, writing and communication skills in a team based setting are essential.

• Adherence to laboratory health and safety procedures * Adherence to Standard Operating Procedures (SOPs) * Adherence to applicable company policies and guidelines * Adherence to federal and/or local regulations, as applicable * Perform a wide variety of in vitro assays or tests required to characterize product or material safety, including but not limited to the HPRT Mutagenesis assay and the Mouse Lymphoma Assay. * Maintain sterile and good cell/tissue culture techniques * Prepare study reagents in accordance with SOPs and study instructions * Use and maintain scientific equipment, instrumentation and computer systems * Conduct pre-designed assays using basic laboratory techniques and skills * Make scientific observations, maintain detailed data books/documentation and ensure all documentation fulfills generally accepted professional/industry standards and GLP regulations * Perform peer review of data and lab support records * Keep the next level manager and Study Director informed of study status, technical problems and other issues which impact the lab/study * Address quality audit findings and generate deviations using the quality system, as needed * Receive instructions on new assignments from the laboratory manager or designee and study directors * Attend pre-planning, or operational team meetings, as needed * Perform other job duties, as assigned Additional Position Responsibilities: Additional Requirements: * Ability to multi-task and participate in multiple nonclinical research studies concurrently. * Ability to function effectively in a team-oriented atmosphere and work independently when necessary. * Plans assigned workload on a daily basis and effectively schedule multiple assignments. * Ability to produce high quality data while working under the pressure of strict deadlines. * Overtime, weekend and holiday work as required. * Ability to lift at least 50 lb * Work requires use of PPE (personal protective equipment). * Other special projects and duties as assigned, Professional Responsibilities:(if applicable) * Attend continuing education courses or webinars, as appropriate Minimum Requirements: Bachelor's degree in a scientific discipline (i.e., Biology, Chemistry, Biochemistry, etc.) with 1+ years experience working in a research laboratory. - OR - Associate degree in a scientific discipline (i.e., Biology, Chemistry, Biochemistry, etc.) with 3+ years experience working in a research laboratory. Effective written and oral communication skills. Proficiency in basic computer applications such as email, MS Word and Excel. The anticipated base salary for this position could range between $60,600 to $ 75,000 and will depend, in part, on the successful candidate's qualifications for the role, including education and experience. Preferences: * Knowledge of Good Laboratory Practices (GLP) preferred. * Life Science, Chemicals or Healthcare industry knowledge preferred * Experience in cell/tissue culture and aseptic technique * Good written and verbal communication skills * Ability to prioritize, organize and manage time effectively Working Conditions & Physical Requirements * Extended computer and display screen equipment usage * Ability to push, pull, lift pounds unassisted. * Stand / walk for extended period of time. * Fine manipulation including handle touch object or tools and ability to handled controls to perform work. * Ability to read and interpret materials, verbally communicate, and hear required. Critical Success Factors * Customer Focus. Identifies, prioritizes and anticipates customer needs and delivers relevant, value-add, solutions to meet and exceed them * Results Driven. Internal drive toward action to efficiently, timely, and accurately achieve results. Sets high but achievable standards for self and others. Seeks opportunities to improve process and outcomes. Constantly reviews performance to identify areas to develop. * Efficient. Takes responsibility for own time and effectiveness. Identifies what needs to be done and does it before being asked or before the situation requires it. Able to work things out without having to be shown too often. Seeks opportunities to contribute appropriately without direction. * Communication. Able to communicate information and ideas clearly and articulately both in oral and written form. Uses appropriate language, style and methods depending on audience and the purpose of communication. Able to convey complex information clearly. Anticipates the information that others will need. Expresses ideas effectively. Practices attentive and active listening. * Collaboration. Actively supports and contributes to the success of the team. Actively encourages and practices collaboration and cooperation on the team. Shares information and supports other team members. Can get things done with and through others and set realistic objectives. Seeks opportunities to develop others. * Relationship Builder. Develops, maintains, and strengthens strong partnerships with others internally and externally, cross functionally, in person and remotely. * Critical Thinking and Problem Solving. Able to identify and separate out the key components of problems and situations. Able to manipulate and interpret information from a range of sources to spot patterns and trends in information and to deduce cause and effect from this. Can generate a range of creative solutions, evaluate, and choose the most appropriate option * Improvement Driven. Inspires and generates new solutions and approaches to issues and challenges to maximize efficiency and effectiveness through everyday practice of root cause analysis and critical thinking problem solving; Continually works to refine skills and abilities; Builds on ideas of others to come up with new ways to address issues or problems; Generates creative new solutions and approaches to issues and processes. * Organization and time Management. Plans and prioritizes work, manages time appropriately to meet deadlines, follows up with others to ensure one's own work and commitments are completed on time, deals with pressure and deadlines through good planning. * This position could be offered at different levels for candidates who qualify with a combination of advanced levels of education and/or years of experience. The salary range will adjust along with the level of the role to match the person's relevant experience and/or education level. Inotiv is a growing contemporary drug discovery and development company where we "Play to Win" in an industry rich with opportunity. Together, we face challenges and together we win in the delivery of world-class drug discovery and development solutions that impact the health and well-being of people all over the world. There's an opportunity for everyone at all phases of a career, each individual's unique skill set has an impact on the work we conduct. If you have the talent and desire to impact the quality of people's lives, we have the career opportunities to make it happen. Join us in embracing research and science to impact the health and well-being of people all over the world. Salary will be commensurate with experience and responsibilities. Benefits include health and dental coverage, short- and long-term disability, paid time off, paid parental leave, 401K, and more! Inotiv is an Equal Opportunity Employer. It is our policy to provide a fair and equal employment opportunity to all persons, regardless of age, race, color, religion, sex, gender, gender identity, gender expression, sexual orientation, genetic information, disability, national origin, veteran status, or any other basis prohibited by law. This policy governs all aspects of employment, including selection, job assignment, compensation, discipline, termination and access to benefits and training.

Mahalo for your interest in this role! Please see the full position description below and click Start Your Application when ready. For more information about DAWSON, please visit dawsonohana.com. This position is intended to support the Naval Treaty Implementation Program (NTIP) in its role for implementation and compliance of the specific arms control treaties and agreements under NTIP s purview. The work for this position will be located at the Washington Naval Yard, Washington District of Columbia (D.C.) Job Description Work with the Government to identify and assign qualified personnel to critical functions in support of the assistance team Accompany Department of the Navy (DON) personnel to the DON facility designated for inspection Store, periodically test, maintain, and rapidly deploy inspection support equipment to the Point of Entry at Dulles International Airport and to the DON installation designated for a Challenge Inspection s (CI) or CI exercise Provide day-to-day support to the NTIP staff in the conduct of routine business Attend meetings, draft Memoranda for Record, prepare presentations, and reports Monitor the arms control treaty community for movement toward any type of new or altered framework or arms control agreements Provide research and analytical support to program and resource management decision making Assess impacts to the Department of the Navy, as required Prepare and deliver all technical studies, analysis, research, documentation Qualifications Secret Security Clearance Bachelor s degree from an accredited institution Seven (7) plus years of experience in arms control, international relations, national security, or a related field Available to deploy to an affected DON installation as directed *Position is Contingent Upon Award DAWSON is an Equal Opportunity/Affirmative Action/VEVRAA federal contractor. All qualified applicants will receive consideration for employment without regard to race, color, religion, gender, national origin, disability status, protected veteran status, or any other characteristic protected by law. DAWSON offers a best-in-class benefits program including medical, dental, and vision insurance; a 401(k) program with employer match; paid vacation and sick leave; employer-paid basic life and AD&D insurance; an Employee Assistance Program; and a flexible work environment. Additionally, employees can choose from several voluntary benefits including critical illness coverage; accident insurance; identity theft coverage; pet insurance, and more. DAWSON gives preference to internal candidates. If no internal candidate meets our qualifications, external candidates will be given consideration.

Chimera Enterprises International is seeking a Chemical and Nuclear Surety Analyst to support the Army Treaty Compliance and Surety Division (DAMO-SSD), Deputy Assistant Secretary of the Army for Environment Safety & Occupational Health (DASA(ESOH)), and U.S. Army Nuclear and Countering Weapons of Mass Destruction Agency (USANCA) Description The ideal candidate will have substantial experience in chemical and nuclear surety, as well as familiarity with Department of Defense (DoD) guidelines and regulations. The Chemical and Nuclear Surety Analyst will support DAMO-SSD by ensuring compliance with U.S. laws and DoD directives related to chemical and nuclear surety, providing technical and policy support, participating in related meetings, and maintaining oversight of surety-related activities. Mission To ensure the Army's adherence to chemical and nuclear surety requirements by providing expert analysis, strategic guidance, and comprehensive support. This role involves implementing surety programs and policies in alignment with DoD and Army guidelines to ensure the safety, security, and accountability of chemical agents and special nuclear materials (SNM). Clearance Level Required: SECRET JOB DESCRIPTION AND RESPONSIBILITIES: Provide continuous support to DAMO-SSD, including the study and assessment of USG, DoD, Joint, and Army surety guidance issues. Determine the impact of chemical and nuclear surety and accident and incident response on Army operations, plans, force structure, training, and resources. Provide operations, program oversight, and staff support to DAMO-SSD to assist in the execution of its responsibilities for developing, implementing, and overseeing compliance with surety guidance measures. Utilize database management systems to collect, analyze, present, communicate, and file information related to surety guidance and surety I&C planning. Attend and participate in meetings, conferences, briefings, seminars, training courses, and guidance meetings. Support and accompany the Department of the Army Inspector General (DAIG) on surety-related inspections. Monitor available information sources for surety-related matters and provide regular updates and reports. Prepare synopses, after-action reports (AAR), trip reports, significant activity reports (SIGACT), information memorandums, and information papers as required. Recommend special studies and research and analysis topics pertaining to surety issues for approval and assignment by the Government. Review and comment on U.S. government, DoD, and Army documents and publications related to chemical and nuclear surety. Support the revision of formal Army surety-related guidance documents such as AR 50-5, AR 50-6, AR 190-17, and DA Pam 50-5. Assist with implementation of chemical and surety-related guidance, including reviewing requests for exceptions and surety status termination. Knowledge, Skills, and Abilities: Minimum of two (2) years of experience interacting with Service Staff, Joint Staff, and Office of the Secretary of Defense (OSD) organizations. Strong knowledge of chemical and nuclear surety operations and compliance measures. Proficiency in database management and the ability to utilize them for surety analysis. Excellent analytical skills with the capability to develop and implement compliance measures. Strong communication and interpersonal skills for effective collaboration with various stakeholders. Ability to draft, review, and update technical and policy documents related to surety. Minimum Qualifications: Education: Bachelor's Degree in engineering, scientific, technical, management, or a related discipline relevant to this PWS. Experience: 2 to 5 years' experience in managing and overseeing chemical and nuclear surety programs and interacting with high-level DoD personnel. Clearance: SECRET Location: Primarily on-site in the National Capital Region (NCR), with occasional travel as required. Chimera Enterprises International is committed to equal opportunity and affirmative action in hiring and retaining a diverse workforce, including protected veterans and individuals with disabilities.

Job DescriptionWho we are REGENXBIO is an exceptional place to work. You'll have the opportunity to collaborate with some of the best and the brightest people, touch amazing science, and be a part of extraordinary plans. Our core values: Trust, Accountability, Perseverance, and Innovation drive everything we do. We aim to bring these values to life every day with all that we do, and we believe that what we do matters - to patients, to their families, and to their communities. As a member of our Bioanalytical Sciences team, you will be responsible for performing nonclinical and clinical sample testing (PK, Immunogenicity, PCR, etc.) following developed, qualified, and/or validated bioanalytical methods in support of REGENXBIO projects and programs. You will also be responsible for developing and validating bioanalytical methods for gene therapy products. You will also be responsible for performing QC review of documentation produced in the Bioanalytical laboratory, including assay runs, summary tables, reports, protocols and collaborate with various departments to ensure compliance with regulatory expectations.What you'll be doing Conduct assay operations and maintains accurate testing records. Review technical documents. Perform QC peer reviews and manages project-related activities. Troubleshoot analytical method issues and maintains lab inventories. Support Sample receipt/Accession, buffer preparation and lab maintenance Performs additional tasks or assist with special projects as assigned or needed. We set our employees up for success. To be successful in this role and help us achieve our goals, we are looking for someone with the following skills and qualifications: Bachelor's degree in a relevant scientific field with 2+ years of industry experience, or Master's with 1+ year. Hands-on experience with immunoassays (ELISA, MSD), cell-based assays, qPCR, and/or LC-MS. Analytical, problem-solving, and organizational skills with excellent attention to detail. Collaborative team player with strong written and verbal communication skills. Proficient in data analysis software (e.g., SoftMax) and Microsoft Office applications. By joining REGENXBIO, you will have the opportunity to be a part of a growing company and incredible team passionate about developing novel AAV gene therapy products to our patients. In addition, professional development is important to us. By joining our team, you'll have the opportunity to be exposed to challenging projects and development resources to help you grow personally and professionally. We are proud to offer a comprehensive rewards package which includes a market-competitive base salary, an annual performance-based bonus program, stock grants at all levels, and benefits such as health, dental, and vision insurance, retirement plan with 401(k) match, summer hours, and more! The estimated compensation range for this role is $66,000-$89,000 annually. The actual salary offered to the final candidate depends on a number of factors such as relevant work experience, skills, education, and years of experience.

Under minimal supervision of QC management, the QC Chemist performs physical and chemical testing on raw materials, in-process and finished products, as well as stability samples. Utilizes established methods and standard operating procedures and laboratory equipment to perform testing of materials. Prepares high quality written documentation, such as notebooks, logbooks, standard operating procedures (SOPs) and LIMS reports. Trouble shoots analytical equipment. Provides training on analytical methods and new technologies. Responsibilities: Performs analytical testing of raw materials, in-process materials, finished products and stability samples. Operates laboratory equipment such as balances, pH meters, hardness testers, particle size analysis, LOD, Karl Fischer, Melting Point, etc. in accordance with laboratory SOPs and test methods. Effectively performs routine testing using HPLCs, GCs, UV-VIS, FT-IR and ICP-MS equipment in accordance with SOPs and test methods. Performs data analysis and evaluation of test results. Prepares reports and reviews data. Maintains accurate records of test data, maintains laboratory notebooks and logbooks in accordance with company guidelines and GDPs. Assists in writing and revising SOPs and tests methods as needed. Follows documented procedures: SOPs, test methods, and transfer protocols. Performs routine maintenance, calibration, and performance verification on applicable instruments. Performs investigation activities and writes deviation and investigation reports. Suggests and writes CAPAs. Follows lab safety procedures. Perform other duties as assigned. Qualifications: Bachelors in chemistry or related physical/biological science, or equivalent combination of education, training and professional experience that provides the individual with the required knowledge, skills, and abilities. Minimum of 3 years' experience in Pharmaceutical Analysis Must understand analytical chemistry. Demonstrated knowledge of cGMP regulations and ICH guidelines Computer literacy and ability to use data acquisition and processing software, such as EMPOWER 3 Demonstrate the ability to read, analyze, and interpret USP/NF methods, SOPs and technical procedures manuals, and batch records. Demonstrate the ability to define problems, collect data, establish facts, and draw valid conclusions; interpret an extensive variety of technical instruction in mathematical or diagram form. Knowledge of basic laboratory practices, methods, and techniques Demonstrate the ability to carry out work assignments communicated orally or in writing. Demonstrate familiarity with Lean Six Sigma Methodologies and proven analytical/ problem solving capabilities. Demonstrates the ability to establish good working relationships with other departments, including vendors, colleagues, and subordinates. Demonstrates the appropriate technical knowledge necessary to make sound decisions on development issues with minimal supervision. Demonstrate the ability to analyze data and information and assess and resolve complex problems/issues as required. Must be able to comprehend and follow all applicable SOPs. Demonstrate ability to acquire the appropriate knowledge from resources on with electronic Quality Management Systems such as MasterControl and Trackwise. Demonstrate understanding of the current federal, local, and international regulations regarding the production, testing, and release of drug substances and products. Good understanding of cGMPs, industry, and regulatory standards and guidelines. Demonstrate familiarity with Microsoft programs like Word, Excel, PowerPoint, Project, Teams, Outlook, etc. Demonstrate the ability to portray the appropriate level of integrity and professionalism. Demonstrate the ability to communicate effectively with management, staff, regulators, and client representatives in written and verbal formats. Demonstrate the ability to complete tasks accurately and according to established and shifting timelines. Demonstrate the ability to make quality scheduling, resource allocation, and priorities decisions. Energetic, execution-focused, self-motivated, and organized individual who is accustomed to working in a deadline-focused, high-pressure entrepreneurial environment. Results-oriented and efficient. Creative and open-minded who fosters an environment in which sharing of ideas is encouraged. Demonstrate the ability to work closely with a diverse customer and employee base (internally and externally). Demonstrate the ability to work well in a cross-functional team environment. Must communicate fluently in English and have legible handwriting. Physical Demands: Ability to travel between and within facilities to visit staff, operations, and projects, as needed. Ability to sit, stand, climb stairs, and climb ladders to mezzanines (when necessary). Ability to lift up to 40 pounds on occasion. Ability to use PPE (safety shoes, goggles, respirators, gloves, etc. when necessary).

US Tech Solutions is a global staff augmentation firm providing a wide-range of talent on-demand and total workforce solutions. To know more about US Tech Solutions, please visit our website ************************ We are constantly on the lookout for professionals to fulfill the staffing needs of our clients, sets the correct expectation and thus becomes an accelerator in the mutual growth of the individual and the organization as well. Keeping the same intent in mind, we would like you to consider the job opening with US Tech Solutions that fits your expertise and skillset. Job Description • BioProcess Engineering (BPE) department is responsible for scale up, tech transfer, and facility fit of clinical and commercial processes to manufacturing. BPE is also responsible for producing development drug substance material and data from pilot facilities. Members of Development Scale-up Center (DSC), within BPE, produce materials up to 500L scale for toxicology and process development studies, to confirm process performance and to troubleshoot issues in GMP facility, and work with cross functional team on technology evaluations. • This position is focused on upstream cell culture and fermentation processes supporting scalability and production of therapeutic proteins in DSC. Position is a hands-on laboratory and production-based role. Responsibilities include but are not limited to media preparations, routine sub-culturing of cells and fermentations. The candidate will assist in adaptation of transferred information for scale-up processes from late stage development to DSC as well as assisting in the production of various tox and development materials, troubleshooting and resolving technical issues with the production processes and/or equipment, identifying root causes for deviations, implementing corrective/preventative actions, assisting in implementing new technologies, and trending/analyzing data. • The candidate will assist in compiling data and expected to summarize and assist in interpreting results. The candidate will also maintain production and laboratory equipment. Qualifications Education: • Bachelor of Science (BS) or Master of Science (MS) in scientific, engineering or related field. Experience: • For the RA, we require a BS with 2 - 5 years or a MS with 0 - 2 years of relevant experience. • For the AS, we require a BS with a minimum of 5 years or MS with a minimum of 2 years of relevant experience. Additional Information Special Skills/ Abilities • Hands on proficiency in cell culture and/or fermentation and good aseptic techniques. Bioreactor/fermenter operation experience is preferred. • Good documentation, writing and communication skills in a team based setting are essential.