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Scientist I, Biomarker Assay Development, Translational Science
At Horizon Therapeutics, we define success by the number of lives touched, lives changed, and lives saved.$58k-88k yearly est.37d ago
QC Production Chemist
QC Production Chemist I
Essential Duties and Responsibilities
• Perform FDG and NaF synthesis according to Standard Operating Procedures (SOPs):
• Ensure all materials/reagents are accepted according to SOPs and within expiry
• Ensure all equipment is appropriately qualified prior to use
• Operate the synthesis unit according to SOPs
• Learn the basic operational principles of the synthesis unit and assist in routine maintenance of the synthesis unit
• Perform FDG and NaF quality control (QC) processes according to SOPs:
• Assist with basic maintenance of QC equipment
• Ensure all equipment is appropriately calibrated and qualified prior to use
• Operate the QC equipment according to SOPs
• Ensure completion of applicable cGMP documentation.
• Assist with inventory management:
• Maintain production/QC/cleaning supply levels as appropriate
• Assist with inventory reporting
• Perform material acceptance according to SOPs
• Communicate with local and Network support resources to troubleshoot equipment, production, or QC issues.
• Perform basic computer-controlled cyclotron operations for FDG and NaF production under the advisement of site Cyclotron and Facility Engineer.
• Maintain a clean and safe working environment.
• Perform radiation safety duties according Corporate Radiation Compliance Program and site licensing requirements.
• Maintain all qualification and validation requirements for entering ISO classified area.
• Clean classified and non-classified areas according to SOPs.
• Perform environmental monitoring of classified areas according to SOPs.
• Report manufacturing metrics into data repository as required.
• Complete cGMP documents as required and assist site and corporate Quality Assurance including, but not limited to:
• Corrective and Preventative Actions
• Out of Specifications
• No or Atypical Yields
• Manufacturing and QC Records
• Attend internal meetings as required.
• Other assigned duties as required.
• High school diploma required; associates degree in chemistry, engineering, or natural sciences preferred.
• Technical experience with computer-controlled automation preferred.
• Efficient in the use of MS Office Suite required.
• Ability to work various shifts and weekends required.
• Ability to be detail-oriented, accountable, patient, organized, and work in a team environment required.
• Ability to communicate professionally with colleagues and customers, have excellent attention to detail, and be dependable and responsible in a fast-paced, highly technical environment required.
• Ability to lift ~50 lbs. required.
• Up to 5% travel required.
$58k-78k yearly est.5d ago
Vulnerability Research and Development - US Citizens
To prevent limiting world-class talent to a single project, technical domain, or target space at Zetier we consider your full potential, background, and interests and align that to an engineering grade of Junior, Journeyman, Senior, xor Principal. Zetier hires skilled engineers and non-technical experts that are driven by mission success. Desired Technical Domains at Zetier:$74k-105k yearly est.17d ago
R&D Laboratory Technician
BNNT, LLC is seeking an R&D Laboratory Technician to support the development of new products for boron nitride nanotubes (BNNTs). Location : On-site at BNNT, LLC's headquarters (Newport News, VA)$21-35 hourly19d ago
Senior R&D Chemist
Insight Global is looking to hire a Senior R&D Chemist for a global manufacturing company located in Richmond, VA. For the first six months, this individual would be working in the lab formulating chemicals and oils for the Driveline business unit. Ability to relocate to Richmond, VA by August$85k-132k yearly est.16d ago
Product Management Consultant - Life Solutions
As a Product Management Consultant, you will deliver on complex assignments and initiatives for your assigned area.$65.7k-118.3k yearly60d+ ago
Associate Scientist - Immunology
Salubris Biotherapeutics, Inc. (or SalubrisBio) is a science-driven biotechnology company dedicated to the discovery and global development of novel antibody therapeutics for the treatment of cancer, cardiovascular and neurodegenerative diseases. Role Summary We are seeking a highly motivated full-time Associate Scientist to develop novel antibody therapeutics for the treatment of cancers.$63k-93k yearly est.12d ago
Bioinformatics Applications Scientist III
The Bioinformatics Applications Scientist III will develop and maintain bioinformatics pipelines for novel functional genomics applications, perform NGS data analysis and provide computational/data analytics support for research and product development. Job Title: Bioinformatics Applications Scientist III IDT is one of 10 Life Sciences companies of Danaher.$75k-90k yearly41d ago
URGENT Formulation Scientist
Job DescriptionDescription: JOB SUMMARY Under general supervision, performs formulation activities as required for, but not limited to, oral, transdermal, topical, oral, nasal, and ophthalmic route projects. Carries out laboratory work to support product formulation and development, stability work, excipient, and packaging sourcing. Job Responsibilities: * Developing complex pharmaceutical products, leading to successful ANDA filings and approval in a timely manner. * Managing and scheduling multiple projects, setting objectives, prioritizing activities to meet the milestones in a fast pace environment. * Designing, formulation and process development for various drug from project initiation to commercialization by following appropriate GMP regulations and safety requirements. * Participate in the set-up and operation of pilot scale equipment and instrumentation for the completion of small production runs in collaboration with the R&D technician. * Design and conduct pre-formulation and formulation studies, process development and optimization of prescription dosage form designs and ANDA oral Dosage forms using DOE * Perform Literature search and Evaluate patents to develop non-infringing strategies * Preparation of product manufacturing, batch records and protocols for different product development stages, including from R&D prototype formulations to process validations following SOPs and procedures, ensuring the detailed record and data keeping. * Utilize formulation techniques, processing equipment and unit operations including Wurster Coating, Tablet Coating, Compression, Blending, Encapsulation, HPLC, Spectrophotometry, Dissolution, Viscometer to develop Bio-Equivalent products * Review Analytical Data, draft SOP's, Process Evaluation protocols, IQ, OQ, PQ protocols and GMP Manufacturing Batch records, Packaging Batch Records. * Characterization of APIs, excipients and in process products; analysis of in-process samples or in-process products based on protocols and QbD concept, preparing various formulation samples to support cross-functional programs as needs. * Setting-up and cleaning equipment for experiments by following the SOPs, maintaining formulation Lab in a clean and safe working environment. * Establishing documentation management systems for CMC development and meeting FDA GMP, regulatory requirement, and FDA onsite inspections. * Comprehensive knowledge of Quality by Design (QbD) and Design of Experiments (DOE). * Professional knowledge of manufacturing principles, theories, and techniques. * Ensuring all regulatory documents in compliance with SOPs, FDA Regulations, and cGMP policy where applicable. OTHER or ADDITIONAL RESPONSIBILITIES Documentation * Completes documentation associated with manufacturing processes (e.g. batch record, protocols, and logbooks) with detail and accuracy. * Meets requirements for entries on all applicable Batch Production pages, completion and attachment of all dispensary and weight verification tickets. * Verifies the manufacturing process on BPR in an accurate and timely manner. * Provides status updates and operational challenges on status boards. Continuous Improvement * Assists in troubleshooting process issues; refers deviations from standard procedure to the supervisor. * Typically participates in at least one continuous improvement project of a moderate scope and complexity. Safety & Compliance * Adheres to all cGMP compliance/regulatory mandates and quality requirements. * Participates in safety teams, start-up discussions, incident debriefing sessions, etc. * Ensures compliance with SOPs, policies and procedures as required by the Company and regulatory agencies. * Maintain a clean, organized, work area. Training * Conforms to all training requirements, including company required and machine-specific training. Teamwork & Collaboration * Contributes to team and project success by sharing previously acquired knowledge. * Collaborates typically within own cross-functional work unit and occasionally with contacts outside own unit or department. Preferred Knowledge & Skills: * Knowledge of manufacturing regulatory programs and objectives (cGMP, CFR 210 and 211). * Maintaining formulation development notebook document work. * Maintaining compliance with GMP, SOPs and DEA regulations. * Coordinate with Regulatory Affairs, Operations, QC/QA, and Supply Departments to ensure that projects are planned and executed in a timely manner. Education & Experience: * BS or MS in Chemistry, Pharmacy, Biochemistry, Biology or Bio-technology or related field. * 2-3 years of experience in core formulation development and analytical instrument techniques. Physical Requirements/Working Environment: * Must be able to stand for long periods of time (up to 12 hour shifts), maneuver at least 50 pounds, climb ladders, wear a respirator and pass associated respirator tests and/or requirements, and be able to wear all required PPE, including safety glasses, ear plugs, and safety shoes * Stand, W$69k-103k yearly est.23d ago
Senior- Advanced Analytics
Not to mention all the other amazing rewards that working at DIRECTV, LLC offers. Our Senior- Advanced Analytics earn between $155,000 - $183,700 yearly. Senior- Advanced Analytics needed by DIRECTV, LLC in El Segundo, CA [and various unanticipated locations throughout the U.S.; may work from home] to utilize predictive modeling, multivariable analysis, data mining, test and control experimentation, and trend analysis to analyze large data sets from both internal and external sources.$155k-183.7k yearly1d ago
Manufacturing Scientist Process Validation (w/m/d) - Hybrid
Als Manufacturing Scientist Process Validation im PPQ Core Team, arbeitest du an spannenden Projekten im Bereich biologischer Herstellprozesse.$62k-85k yearly est.17d ago
Force Development Scientist & Engineer (S&E) Manager
QED Enterprises, Inc. (QED) is an SBA certified 8(a) small business and a Department of Veterans Affairs Center for Verification and Evaluation (CVE) certified service-disabled veteran-owned small-business (SDVOSB). Job DescriptionQED Enterprises (QED) was founded on the principles that we provide Quality services to our clients; we strive for Excellence in all that we do; and we are Driven to meet our customers' missions on time, within budget, and with the exceptional attention to detail our customers have come to expect of QED. Title: Force Development Scientist & Engineer (S&E) Manager - Subject Matter Expert Location: Arlington, VA *** MUST BE WILLING TO WORK ON SITE EVERY DAY *** Clearance Level: Secret Summary/Description: This position supports overarching acquisition workforce management as well as career field management for scientists, development engineers and program managers.$73k-106k yearly est.27d ago
Research Chemist - DIRECT HIRE
This position is located in the Office of Infrastructure R&D (HRDI) of the Federal Highway Administration (FHWA) Office of Research, Development, and Technology (HRT). The ideal candidate is a Research Chemist with experience planning, conducting, and reviewing research and development activities. Responsibilities As a Research Chemist, your responsibilities would include: Assisting manager of the FHWA Chemistry Laboratory.$89k-130k yearly est.12d ago
Product Development Scientist
Job DescriptionDescription: Kerecis seeks a Product Development Scientist to join a small but seasoned team of medical device professionals responsible for the development and commercialization of the company's next generation products across its wound, burn and surgery market.$65k-88k yearly est.15d ago
Lead Scientist I - Immunochemistry (Hybrid Work Model)
**What Labcorp Drug Development can offer you:** As the Lead Scientist, you will act as the Study Director, Responsible Scientist, or Principle Investigator for non-regulated, GLP-regulated, and GCP-regulated bioanalysis studies. The **Lead Scientist** supports the Immunochemistry team within the Bioanalysis division in Chantilly, VA. This is your chance to become part of a team that helps to bring the miracles of medicine to market sooner, as Labcorp Drug Development has helped pharmaceutical and biotech companies develop one-third of all prescriptions medicines in the market today. **Schedule:** This position will allow for the majority of the work week to be remote based with an on site presence in Chantilly 1 day out of the week following initial training/onboarding. At Labcorp, we offer opportunities to work on diverse, challenging projects with bright, interesting colleagues while building a flexible and rewarding career.$93k-118k yearly est.60d+ ago
Scientist I, Biomarker Assay Development, Translational Science
At Horizon Therapeutics, we define success by the number of lives touched, lives changed, and lives saved.$58k-88k yearly est.6d ago
Let Nationwide help create your career journey! As a team member in the Finance and Internal Audit department at Nationwide, the opportunities are endless! At Nationwide, our Analytic Scientists are responsible for modeling complex problems, discovering insights and identifying business opportunities using scientific research methods, statistics, machine learning, and data visualization techniques.$77k-100k yearly est.11d ago
Downstream Scientist - mRNA purification
Site Name: USA - Maryland - Rockville, USA - Delaware - Dover , USA - Delaware - Wilmington, USA - Virginia - Arlington, Washington DC$55k-82k yearly est.34d ago
Scientist 2, Enterprise Data Analytics & Data Intelligence
Comcast Technology Solutions is a fantastic place for bright minds and forward-thinkers looking to innovate and evolve with a company they can be proud of. Our roots - and our hearts - are in broadcast and digital video, but as part of Comcast NBCUniversal, we are so much more. Comcast Technology Solutions, a division of one of the world's leading media and technology companies, brings Comcast Corporation's proven technologies to an evolving list of industries worldwide. In most cases, Comcast prefers to have employees on-site collaborating unless the team has been designated as virtual due to the nature of their work. Comcast's Technology, Product & Experience organization works at the intersection of media and technology.$87.9k-131.8k yearly1d ago
Chemistry Laboratory: Research Spectroscopy Chemist
Full-Time in McLean, VA - TFHRC Genex Systems is looking for a Research Spectroscopy Chemists (RSC) to support the Chemistry Laboratory at the Federal Highway Administration (FHWA) Turner-Fairbank Highway Research Center (TFHRC) in McLean, VA.$94k-134k yearly est.60d+ ago
Based on recent jobs postings on Zippia, the average salary in the U.S. for an Analytical Scientist is $90,807 per year or $44 per hour.
The highest paying Analytical Scientist jobs have a salary over $125,000 per year while the lowest paying Analytical Scientist jobs pay $65,000 per year
A senior scientist is usually in charge of overseeing experiments and evaluating junior scientists' performance, especially in laboratory settings. Moreover, it is also their responsibility to assess every progress report to ensure it's accuracy and validity. As a senior scientist in the field, it is essential to lead and encourage fellow scientists in their joint pursuit for scientific innovations, all while adhering to the laboratory's standards and policies.
A Senior Research Associate works closely with research team members to implement research ideas. They diagnose, solve system/software problems, and install application software according to research needs.
A quality control manager is responsible for checking the quality of products and materials, especially for release and delivery, ensuring that the items are free of any defects. Quality control managers coordinate with other organization heads to develop effective processes to maintain and improve the products' efficiency, following the regulatory procedures and standard protocols. They monitor production, identify areas of improvement, inspect the finished products, and adjust product development techniques based on the client's specifications. A quality control manager must have excellent communication and leadership skills to handle the production team and address concerns immediately.
Illustrated Career Paths For an Analytical Scientist