Lab Technician – Contract or CTP – Seattle, WAA Pharmaceutical Company is seeking a Lab Technician in Seattle, WA. Role Description The primary purpose of this position will be to support daily lab operations and to manage lab equipment within Cell Therapy Development Operations. • Learn and follow lab specific procedures and policies • Maintain regular contact with supervisor • Routine maintenance and calibration of lab equipment (i.e., biosafety cabinets, water baths, cellometers, etc.) • Lab equipment service coordination with third party suppliers • Monitor and maintain cold storage equipment • General maintenance of the CTDO laboratories • Documentation of calibration and maintenance activities • Troubleshooting equipment issues • Preparation of stock solutions for routine testing Skills & Requirements • 0-5 years of experience in BSL2 lab operations or lab management • Excellent communication skills • Detail and customer service oriented • Able to work independently upon instruction, document work and communicate honestly and openl
HAYS PLC • Seattle, U.S.
Job Overview and Responsibilities: Field sampling of various product and process streams. Seek and follow guidance provided by Team Leads, Senior PM’s and Supervisor. Ensure the production of high quality, legally defensible data and reports, safely and on time. Provide excellent customer service. Providing limited or specific technical expertise to our customers. Primary responsibilities include the following (but are not limited to): Conduct basic field sampling projects in conjunction with a more senior technologist.Review field data with assistance from supervisor or more senior field staff to ensure sampling is completed as per applicable test methods and protocols.Prepare equipment and chemicals, client confirmation and site-specific safety training, field sampling, field QA/QC of data, collection of field data, fill out daily WHA forms and daily field reports, turns over completed data to senior technologist on project in a timely manner.Perform equipment maintenance, repair and calibration at direction of Supervisor or senior field staff, with training from Senior Project Managers.Provide excellent customer service by always presenting a professional attitude and representing Bureau Veritas in a positive way; comply with all client and Bureau Veritas safety initiatives and rules; provides technical support and expertise to our clients; ensure that all Client requests and expectations are met.Ensure vehicle fleet is maintained in clean, working order and Bays are kept clean at all times.Perform QA/QC of data as required by Reporting or Management.Ensure daily use of personal monitors, gas monitors during field projects, and use of all required PPE.Support and comply with all Bureau Veritas policies, Quality System and Health & Safety program.Participate, when requested in lab and Health & Safety meetings and internal and external audits.Provide general lab support to other departments as required.All other responsibilities as assigned. Is there a mutual fit? You ideally have: 2-year technical diploma or 2-3 years relevant chemistry related or relevant work experience.Basic understanding of well and plant processing techniques and concepts.Basic knowledge of sampling methods and theories.Basic understanding of chemistry, plumbing, and electrical techniques and concepts.Willingness to travel and work extended hours in the field.Knowledge of safe work procedures and requirements.Good driving record with less than 6 demerits and meets federal carrier driver requirements. Schedule:Monday to Friday May require flexible workings hours and overtimeEvenings, week-ends and out of town travel may be required
Receptix • Edmonton, Canada
NMC Royal Hospital KLFJob Summary:Assist the Laboratory Supervisor in the coordination of laboratory activities. Provide accurate, timely and cost effective testing of patient samples to aid in the diagnosis and treatment of disease in compliance and harmony with the quality management system. The Lab Technician has supervisory responsibility, limited to his / her work departmentMedical technologist may be rotated through the various laboratory departments in order to keep himself / herself familiarized with those laboratory procedures which may be ordered on an emergency basis when working shifts.Duties & Responsibilities:Technical:Lab Procedures: Performs a variety of technical laboratory procedures according to Medical Center, laboratory and national standards to obtain patient specimens using to ensure specimen quality used to aid in the diagnosis and treatment of disease. Responsible for performing and observing hematological, biochemical, serological and specially requested tests on patients specimens and correctly records all results.Administrative:Documentation: Responsible for accurately completing records and reports and other statistical information for master files or databases. Follows laboratory policy for data retrieval, record keeping, specimen, and identification, requisition, reporting, charting, and billing procedures. Updates Records and Documents on a daily basisCommunication/Teamwork: Maintains positive working relationship with the medical staff and hospital personnel. Uses positive interpersonal skills to educate/support lab customers and promote success of team members. Uses clear and concise verbal and written communication with staff and the public. Acts independently on supervisor’s direction and accepts responsibility of the adopted policy and procedures of the hospital and the laboratory. Shares call duty and works different shifts as required. Immediately notifies the patient care unit or physician of any critical test results, within 20 mints of the result generation. Interacts professionally with all department members, physicians’ staff, administration and the Administrator of Clinical Laboratory and Pathology. Quality Control/Quality Improvement: To perform and follow quality assurance programs for various laboratory sub departments. Participates in Internal and external QC/QI for area of specialty and Lab indicators. Does not report patient results unless quality control data are within accepted parameters. Recognizes out of control values, takes corrective action, and notifies others of changes to the laboratory supervisor.Safety & Education: Complies with laboratory safety procedures. Possesses adequate knowledge of instrumentation, theory, and application of new and existing tests. Completes education necessary to maintain licensure or certification for the job. Uses and maintains all laboratory equipment correctly. Problem Solving/Critical Thinking: Assumes responsibility to resolve problems. Performs required preventative maintenance procedures in laboratory instrumentation. Investigates and resolves technical problems, consults supervisor if resolution involves policy or procedure modification. Identifies real or potential situations or equipment failure, attempts to resolve within area of specialty or knowledge and refers complex issues to appropriate source. May be a key analyzer operator with proper training and documentation of skills.Follows the laboratory safety policies and participates in safety education programs. To attend and follow continuous medical training and education program.Comply with all OSH and infection control policies, standards and procedures and cooperate with hospital management to comply those requirementsWork accordance with the documented OSH procedures and instructions, specific responsibilitiesBe familiar with emergency and evacuation proceduresNotifying OSH Hazards, incidents, Near misses and issues and assistance with the preparation of risk assessments, incident reportsComply with Waste management procedures and policiesAttend applicable OSH/Infection control training programs, mock drills and awareness programsUse of appropriate personal protective equipment and safety systemsTraining: Attends departmental and organizational training as when required to keep him/ herself updated on the laboratory policies and SOPs.Qualifications Qualification, Licensure, Education, Experience, Special Skills:Associate Degree in Medical Laboratory TechnologyAt least two (2) years of Medical Laboratory experience.Currently licensed in country of origin and with HAAD license to practice in Abu-Dubai UAE.Fluent in spoken & written English, Arabic language is desirable, but not essential.Primary Location: Royal Hospital - Khalifa City - Abudhabi Work Locations: Royal Hospital - Khalifa City - Abudhabi Abu Dhabi Abu Dhabi Job: Medical Organization: NMC Royal Hospital KLFFull-time
Alliance Employment Services • Abu Dhabi, United Arab Emirates
RoleHours and days are dependent on timetable, however there is flexibilty for negotiation.Performs and/or supervises tasks that are carried out in accordance with guidelines, accepted practice and school policy. This may include the supervision and coordination of other education support class staff within the work area or educational program. Supervision and coordination would be limited to ensuring routine tasks are performed to required standards. Input into identifying training needs and development of education support class staff within the work area or educational program becomes an important feature at range 2.Specialised support to achieve specific outcomes is a feature of range 2. Typically this will involve accountability for a single function, (e.g. ensuring data is properly maintained) or the operation of a work area (e.g. managing the day to day operation of a school office) under the direction of the principal or another senior manager.Provides support to teachers and students that is beyond the routine support provided at education support class Level 1, range 1. Within an educational program assists teachers with the coordination of the support function, such as directing/organising the work of other support staff or providing a specialist support role. Undertakes medical intervention support tasks or other specialised student/teacher support roles that require specific training that must be updated from time to time. The role is for a specific purpose for which there will be direct accountability as opposed to support roles that are carried out by a range of staff performing routine tasks under direction.Performs technical tasks that require a sound knowledge of basic technical and/or scientific principles that are used to develop and adapt work methods and make judgements where there are clear guidelines and limited options. Routine technical support in libraries, science and information technology laboratories would be typical examples.An education support class position supports the educational services being provided to students, but must not include duties of teaching as defined in clause 2.6.1 of the Education and Training Reform Act 2006 (Vic) or its successor. Supervision of students cannot be required except where it is an integral part of the employee's position or involves supervision of students individually or in small groups, in controlled circumstances, where the responsibility for students remains clearly with a teacher.Responsibilities· Maintain science storerooms ensuring as far as practicable that these areas are kept clean and tidy. Label and keep materials secure from unauthorised access. Be responsible for stock control and ordering of chemicals, biological supplies, equipment and other materials. Be responsible for laboratory documentation systems, stock inventories, cataloguing work sheets, filing resource materials etc.· Maintain an efficient system of allocation of materials and equipment by consulting with science teachers on their practical work requirements. Advise on chemical and equipment safety matters where appropriate. Perform routine tasks in preparation for science practical classes including the preparation of chemical solutions, trialling experiments and conducting chemical and physical tests. Prepare chemicals and equipment by the requested date and place on trolleys. Assist science staff with demonstrations and practical classes when required.· Pack away practical chemicals and equipment after practical completion. Clean and maintain laboratory equipment in working order.· Maintain a safe chemical storage and labelling system and dispose of hazardous materials in accordance with current hazardous chemical regulations. Maintain Material Safety Data Sheets (MSDS) and Risk Assessment forms of chemicals as used by the College Laboratory.· Arrange for manufacture, maintain, repair and service equipment as required.· Assist in care of animals and plants in the science area in accordance with current DET handling and animal ethics guidelines.· Contribute significantly to the overall organisation and maintenance of laboratories, preparation areas and Science rooms.· Other duties as directed by the Principal.Selection Criteria1. Demonstrated ability and competency as outlined in the role description below.2. Demonstrated high level of organisation and communication skills and the ability to relate to both students and staff.3. Demonstrated sound knowledge of laboratory procedures and techniques involving chemicals and associated equipment.4. Demonstrated sound knowledge of Occupational Health and Safety principles, in particular first aid treatment and procedures.5. Demonstrated ability to work independently and to prioritise and manage tasks to meet work deadlines.6. Demonstrated ability to work effectively in a team environment.7. Demonstrated commitment to professional learning and growth for both self and others.
JORA • Melbourne, Australia
Position Description: As a Laboratory Technician, you will be responsible for supporting the manufacturing process in one of Goodyear's Chemical manufacturing plants. Goodyear Chemical is a division of The Goodyear Tire & Rubber Company which manufactures and markets rubber-related chemicals for various applications. You will also promote safety, environmental stewardship and housekeeping throughout the facility. Responsibilities will include, but not be limited to: Gather and analyze in-process and finished product samples to provide quality assurance and process control information for the manufacturing process using specific laboratory test methods and techniques Perform routine maintenance (e.g., change septums, gas cylinders) Run miscellaneous test methods (e.g., specific gravity, Brookfield viscosity, refractive index, flow index, density, melt point) Communicate clearly and concisely, both orally and in writing Ability to comprehend and employ both written and verbal instruction Abide by safe work standards including Lock Out Tag Out (LOTO), Fall Protection, Confined Spaces, and appropriate use of Personal Protective Equipment (PPE) Adhere to Goodyear's attendance policy Perform a variety of manual tasks in varying temperatures for extended periods of time, which may include lifting light to heavy materials, climbing, standing, squatting, bending, and working at heights and/or confined spaces when applicable. Basic Qualifications: HS Diploma/GED Must have completed a minimum of 20 semester hours of college level chemistry including: General Chemistry Organic Chemistry Quantitative Chemistry, and/or Instrumental Analytical Chemistry *Previous experience in instrumental laboratory testing can be substituted for up to four (4) hours of the required chemistry hours Must be at least 18 years of age Must be legally authorized to work in the US without company sponsorship now or in the future Must be able to successfully complete all post-offer, pre-employment contingencies Ability to work any and/or rotating shifts, weekends, holidays, or overtime if applicable Basic computer skills. Preferred Qualifications: BS degree in Chemistry or other science Previous experience in instrumental laboratory testing Previous military service experience within a technical specialty Candidate Criteria: Self-motivated: demonstrates appropriate initiative with or without direct supervision Hard worker: someone who works diligently to get tasks done Adaptability: the ability to make changes, and to be successful in changing environments Team player: an associate who can be counted on to assist the company in being successful whether working on a team or individual projects Ability to review, analyze, and interpret information, identify problems, and make decisions in routine and non-routine situations Commitment to working safely.
Goodyear Tire & Rubber Company • Houston, U.S.
A Pharmaceutical Company is seeking a Research Associate in Frederick, MD. Role Description This role will provide process engineering and analytical support for commercial manufacturing of cell therapy. Working cross functionally with quality, operations, material management, facility and engineering functions, the role is expected to provide technical input for product/process response and investigations, technology implementation, technology transfers, process validation and regulatory filings. • Execute scientific laboratory studies to support process/product understanding and continuous improvement projects • Execute analytical testing of cell therapy products – flow cytometry, ELISA and PCR assays. • Ability to follow laboratory procedures with attention to detail, and successfully execute experiments at the bench • Provide technical input to the execution of process validation and comparability campaigns. • Participate in evaluation of new technology and process automation for introduction into GMP manufacturing • Participate and support process FMEAs to understand process and product risks as a pre-requisite for process validation. • Participate and report to a cross-functional team to advance production activities. • Participate in Operational Excellence activities within Tier Structure. • Participate continuous improvement projects supporting commercial manufacturing site • Ensure systematic DMAIC based approach utilization for process/product related investigations to identify root cause and provide impact assessment to maintain routine manufacturing operations and determine process improvements for manufacturing. • Support technology transfers of launch and commercial cell therapy products • Effectively & efficiently communicate manufacturing process performance internally. • Support the implementation of automation and IT infrastructure projects • Assist in writing technical documentation (protocols & reports for equipment/instrument qualifications, comparability, and cell therapy manufacturing process validation) Skills & Requirements • Bachelors Degree in Biochemical Engineering, Tumor Immunology, Biotechnology or Life Sciences. • Basic understanding in Bioprocessing, Cell Culture and Biochemistry. • Knowledge of ELISA and/or PCR testing • Knowledge in flow cytometry and data analysis (FACSDiva, FlowJo, GraphPad Prism, Excel) is a plus • Ability to think critically, demonstrate troubleshooting and problem-solving skills • Excellent interpersonal, verbal and written communication skills are essential in this collaborative work environment • Previous experience with other technologies is a plus • Experience with the use of Microsoft word, Excel, Power Point, Smartsheet, Prism, JMP, and other data analysis applications • Highly collaborative with excellent interpersonal, verbal and written communication skills • Ability to think critically with demonstrated problem-solving and troubleshooting skills • Comfortable working in a fast-paced company environment with minimal direction and able to adjust workload/assignments based upon changing priorities • Self-motivated, detail-oriented, and willing to accept temporary responsibilities outside of initial job description
HAYS PLC • Frederick, U.S.
About the PositionThe purpose of the position is to support Goodyear's business by managing the day to day testing operations within the facility by motivating team members to meet department safety expectations, quality standards, productivity goals, and Goodyear policies. This position requires a balance of supervisory skills and strong communication including Supervising APMA Reinforcement Testing lab. This position will be required to interact with customers to address questions or inquiries about tests and results Primary ResponsibilitiesManage day to day operation of the department/lab during their shift. Schedule incoming testing requests. Ensure & validate that the output of the work meets current quality standards. Address customer questions about test status, results, or special timing. Plan, organize, coordiate and direct the work force to achieve department/shift goals and objectives daily.Ensure work is completed in a timely manner. Ensure quality and safety processes are being followed. Drive On Time Delivery. Actively manage the Performance Management Process for direct reports by giving constructive, timely feedback. Promote Continuous Improvement. Responsible for housekeeping standardManage people working on their shift. Track attendance. Responsible for the PMP process for their department/shift: performance reviews, training and development plans. Investigate & manage resolution of personnel issues associated with performance, attendance, teamwork, work responsibilities, & safety. Support customer requests that may require special set-up, customer visits and tours, and fast track test requests. Maintain and update departments procedures. Create and maintain shift metrics, which may include logbooks, assignments sheets, attendance, lab performance and machine performance parameters. Schedule resources to maximize operational effectivenessLiason with customers. Address customer questions about test status, results, or special timing. Coordinate special testing requests. Act as primary contact person for operational issues that may occor throughout the day. Communicate effectively with team members, leaders, and customers (both written and oral). Ensure adherence and compliance to established company policies and proceduresMake sure test procedures and equipment operations in area do not hinder associates' ability to work in a safe manner. Where issues are found, work with EHS and Management to find resolutions. Lead training programs by actively reviewing current and future needs to support knowledge management and team flexibility. Lead projects and teams focused on improving operational effeciencies, standardization, process improvements, quality initiatives and teamwork Required Education and ExperienceAssociates Degree with 2 years experience in testing environment; OR HS diploma/GED with 7 years experience in testing environment is requiredWork experience related to lab operations/department functionKnowledge of equipmentDemonstrated leadership skills and experienceAbility to understand and discuss technical concepts as they relate to testing Skills and AbilitiesDemonstrated leadership skills through assiged projects, or process improvements such as lean, CIS or other departmental initiativesIn depth knowledge and understanding of work being performed by the work force and ability to adjust, modity or correct. Internal Goodyear Safety standards and OSHA regulations.Working knowledge of administrative tools and systems for timekeeping, attendance, performance metrics, lab automation and scheduling as well as other tools to support an efficient work group. Solid computer skills (e-mail, SAP, TDIS, Microsoft office)
Goodyear Tire & Rubber Company • Akron, u.s.
Our client, one of the largest Contract Development & Manufacturing Organizations (CDMO) in Europe is currently looking for their future Analytical Development Labs Head. Your responsibilities:Based in the Innovation and Development group, you will bring a deep understanding of development and validation of modern analytical methods, with a passion for leading dynamic and high performing teams in an evolving environment (internally, externally). External collaboration with clients and technology partners is an important part of the role.Lead and support a team of technicians and scientists.Maintain an up-to-date understanding of trends, requirements, and regulations in analytical methods.Ensure that a comprehensive analytical platform is in place for all aspects of Safety, Identity, Strength, Purity and Quality.Provide quality, on time, analytics for external client projects in various phases of development (pre-clinical, clinical), and ensure the transferability of methods into QC labs to support clinical and commercial release testing. Your profile:PhD in Life Sciences preferred, with a focus on proteins or biochemistry.Ideally 8+ years of experience in an applied setting, with experience of working in multi-disciplinary teams.Previous experience in management of teams.Strong understanding of biological production processes.Solid understanding of analytical method development and validation (accuracy, precision, robustness, etc), including regulatory expectations (e.g., ICH, EP, etc).Great experience in Project Management.Strong oral and written English skills Business fluent English (B2-C1 level); similar level in French (B1-C2).
Approach People Recruitment • Paris, France
LabCorp is seeking a Clinical Laboratory Supervisor to join our team in Charlotte, NC. In this position, you will work in a fast paced, customer focused, and challenging environment, and will be a part of our overall mission at LabCorp: "Improving Health, Improving Lives" as we combat the COVID-19 pandemic.Job Duties/ResponsibilitiesSupervise the day to day operations of the laboratoryEnsure laboratory tests are accurately performed and results are reported in a timely mannerDirectly supervise, train, and mentor laboratory personnel of the departmentMonitor daily workflow in the lab and schedule adequate assay coverageResponsible for ensuring all shifts in the department are properly staffedResearch and resolve any production errors while escalating when necessaryEngage in continuous process and service level improvementsEnsure all equipment is being properly maintained through Quality ControlPrepare and maintain Quality Assurance records and documentsEvaluate new process improvements and make appropriate recommendationsMeet regularly with direct reports to provide coaching and feedback for their developmentPerform bench work as needed and maintain proficiency/competency in technical operationsEnsure all work is in accordance with state and Federal regulationsResponsible for administering and managing policies and proceduresProcess and maintain payroll and personnel filesPerform administrative duties as neededBachelor's degree in Medical Technology or a Science related majorMinimum 2 years of experience as a Medical Technologist in a clinical laboratoryPrior experience in Chemistry, Hematology and Urinalysis is highly preferredPrevious supervisor experience is preferredASCP and/or AMT Certifications are a plusStrong working knowledge of CLIA, CAP and relevant state regulationsUnderstanding of laboratory operations as well as policies and proceduresProficient with Laboratory Information Systems and Microsoft OfficeStrong communication skills; both written and verbalHigh level of attention to detail with strong organizational skillsComfortability making decisions in a changing environmentAbility to handle the physical requirements of the position
Careerbuilder • Charlotte, U.S.
Description de l'offreOur client¸ a leading pharmaceutical company is currently looking for their future Field Application Specialist. Your responsibilities:Support Account and Key Account Managers analysing customers’ technical or organizational difficulties.Elaborating and presenting relevant solutions. In the pre-sales phase, recommends technical solutions, including answering customers’ questions about the use of the systems, on site or by remote access. Organizing and conducting demos.Organizing and executing on-site Customer training and initial instrument set-up, if needed. Explaining technical solutions and benefits, helping customers implementing the solution by supporting the installation and go live process (reagents, instruments, LIMS connection…).Supporting the Sales Team and Distributors’ sales activities to ensure territory and regional sales targets are achieved.Collects field feedback and information on the product line e.g. application, hardware and software features requested by customers. Your profile:University Scientific degree (bachelor +) in biology+ 2 or more years of experience in the scientific field (healthcare industry, laboratory).Scientific background coupled with business acumen.Ability to identify customer needs and elaborate relevant technical solutions.English fluent.
Approach People Recruitment • Paris, France
JOB SUMMARY: Conduct biological research associated with one or more complex projects within the NASA Ames Research Center’s Bioengineering Branch. Primary focus will be on designing, building, and analyzing a microbiology experiment for the International Space Station (ISS). The goal of the experiment is to complete multi-omics analysis of Arthrospira platensis during 6-months of continuous photoautotrophic growth. BASIC REQUIREMENTS: ● Master's degree from an accredited university in a biological discipline with 3+ years’ professional experience or a Doctoral degree with 0-3 years’ of experience. ● Laboratory experience in genomics, molecular biology, microbiology/plant biology, biochemistry/analytical chemistry, omics sample preparation, and omics data analysis. ● Familiarity with best practices for working with hazardous materials and willingness to adhere to NASA-defined processes. ● Experience with Microsoft Office and command line computer operating systems such as Linux, Unix, or R. ● Ability to communicate effectively with scientists, engineers, and external scientific service providers from a wide range of technical backgrounds. ● Excellent written and verbal communication skills as well as analytical problem-solving abilities. ● Track record of communicating scientific results through conference presentations and peer-reviewed journal articles. ● Capacity to work independently and efficiently with minimal instruction. ● Demonstrated ability to work in a team environment. ESSENTIAL FUNCTIONS: ● Complete experimental research to determine spaceflight experiment design requirements, develop/build the flight payload, and prepare samples for omics analysis. ● Support science components of flight operations that may require travel and/or extended hours. ● Conceive and design laboratory experiments and actively participate in project planning. ● Generate, record, analyze, and compile experimental data. ● Complete statistical analysis of whole genome sequences, transcriptome sequences, proteomics, and metabolomics data. ● Submit data to appropriate public databases. ● Prepare figures for presentation/publication and collaborate with other scientists in publishing research findings. ● Draft scientific materials for public outreach and/or publication. ● Present research at scientific conferences. ● Maintain a safe and organized laboratory area. ● Perform laboratory duties including management of materials and supplies, equipment, and operations. ● Identify materials and equipment needed for experiments, obtain product information, identify vendors, and assist in the preparation of material and supply acquisition. ● Oversee general state of the laboratory, including scheduled waste removal, decontamination of surfaces, and instrument calibration/upkeep. ● Carry out assigned duties in a manner consistent with defined safety policies and report any safety incidents, potential hazards, or close calls. Assist with identifying and eliminating any unsafe conditions.
Careerbuilder • Mountain View, U.S.
A Pharmaceutical Company is seeking a Lipid Nanoparticle Scientist in San Diego, CA. Role Description The successful candidate will design, manufacture and characterize lipid nanoparticles for the delivery of nucleic acids as well as other novel nanoparticle-based drug delivery formulations containing small molecules, RNA, DNA and proteins. The work is multi-functional and includes formulation design, analytical methods development, physical characterization, experimental design, sample analysis and interpretation of results. The candidate with be expected to bring prior experience in the field and interact closely with other researchers in the design of lipid nanoparticle delivery formulations. This is a hands-on, laboratory-based role in a highly collaborative early development environment. Job Description: • Must have experience with lipid nanoparticle delivery of RNA or DNA for transfection to mammalian cells or in-vivo models. • Must have experience in nanoparticle formulation and nanoparticle drug delivery. • Must have experience in development of methods to analyze and characterize nanoparticle formulations, components and functionality. • Background in the biology of gene transfection and expression is a plus. • Experience and technical proficiency with HPLC and other methods for analysis and quantification of small molecules, DNA and proteins is preferred. • Previous experience and technical proficiency in the physical characterization of nanoparticles, including particle sizing is a plus. • Familiarity with lab-scale nanoparticle preparation techniques, including microfluidics technology, is preferred. • Experience with alternate pharmaceutical manufacturing technologies homogenization, lyophilization, micronization, etc. is a plus. • Strong interpersonal, communication, collaboration and problem solving skills. • Ability to document work and proven record of scientific technical writing. Skills & Requirements • Qualifications: Ph.D. in Chemistry, Biochemistry, Pharmaceutical Sciences, Chemical Engineering, Biomedical Engineering or closely-related discipline with an emphasis in delivery of nucleic acids. M.S. or B.S. in similar fields acceptable with a minimum of 6+ years of relevant industrial experience.
HAYS PLC • San Diego, U.S.