Associate Scientist Jobs in Mauldin, SC

Lead the cross functional team to deliver on all program(s) deliverables within the terms and conditions of the contract and business case. Jobs at this level operate with some autonomy but are covered by well-defined Commercial policies or review of end results. The job allows modification of procedures and practices covering work as long as the end results meet standards of acceptability (typically annual volume, margin and compliance requirements). Responsible for medium-sized sales territories. **Job Description** We are seeking a highly motivated and accomplished Wind Energy Professional with a strong engineering background and an MBA to join our 2-year leadership training program. This individual will have the unique opportunity to gain comprehensive business experience across various functions within our organization, including product management, strategy, commercial operations, supply chain, services, and engineering. The ideal candidate will be a strategic thinker with a proven track record in wind energy and a demonstrated ability to lead and manage complex projects. **Key Responsibilities (depending on the rotation):** + **Product Management:** Collaborate with cross-functional teams to develop and launch new wind energy products, ensuring alignment with market needs and company goals. + **Strategy Development:** Participate in the development of strategic plans, including market analysis, competitive positioning, and business growth initiatives. + **Commercial Operations:** Support the execution of commercial strategies, including sales and marketing initiatives, customer engagement, and revenue growth. + **Supply Chain Management:** Work closely with supply chain teams to optimize procurement processes, manage inventory, and ensure timely delivery of components and materials. + **Services and Support:** Contribute to the development and delivery of services and support programs for our customers, including maintenance, repair, and technical support. + **Engineering:** Engage in engineering projects, including design, testing, and validation of wind energy systems, and contribute to continuous improvement initiatives. + **Leadership Development:** Actively participate in leadership training and development activities, including workshops, mentoring, and coaching sessions. + **Cross-functional Collaboration:** Foster collaboration and communication across all departments to ensure seamless integration and alignment of business strategies. **Required Qualifications:** + Bachelor's degree in engineering or science and an MBA. + At least 5 years of professional experience in the wind energy industry. **Desired Characteristics** **:** + Proven track record in leading and managing cross-functional projects + Strong analytical and problem-solving skills. + Excellent communication and interpersonal skills. + Proven ability to manage and mentor teams. + Familiarity with wind energy technology and industry standards. + Proficiency in project management methodologies and tools. + Experience in product management, strategy development, and commercial operations. + A background in supply chain management and services support. + A history of successful project management and team leadership in the wind energy sector. + Experience in international markets and cross-cultural team management. The salary range for this position is $104,000.00 - $173,400.00 USD Annual. The specific salary offered to a candidate may be influenced by a variety of factors including the candidate's experience, their education, and the work location. In addition, this role has variable compensation incentive of 10% . Available Health and Welfare benefits may include, Prescription drug, dental and vision coverage; saving account options (such as a Health Care Flexible Savings Account, Health Reimbursement Account, Limited Purpose Flexible Spending Account, and Dependent Care Flexible Spending Account); and an employee assistance program. Additional Benefits include a defined contribution 401(k) plan, employee life insurance, optional dependent life insurance, employee accidental death or dismemberment insurance coverage, short-disability, optional long-term disability, pre-tax transportation/commuter program, paid holidays, paid time off, parental leave, a layoff plan for salaried employees, tuition refund program, use of CareLoop, adoption assistance, optional identity theft prevention insurance, optional person legal assistance, and optional personal excess liability insurance. GE Vernova offers a great work environment, professional development, challenging careers, and competitive compensation. GE Vernova is an Equal Opportunity Employer (****************************************************************************************** . Employment decisions are made without regard to race, color, religion, national or ethnic origin, sex, sexual orientation, gender identity or expression, age, disability, protected veteran status or other characteristics protected by law. GE Vernova will only employ those who are legally authorized to work in the United States for this opening. Any offer of employment is conditioned upon the successful completion of a drug screen (as applicable). **Relocation Assistance Provided:** Yes GE Vernova is an Equal Opportunity Employer. Employment decisions are made without regard to race, color, religion, national or ethnic origin, sex, sexual orientation, gender identity or expression, age, disability, protected veteran status or other characteristics protected by law.

R&D Sr. Principal Scientist III will serve as technical lead/subject matter expert to support commercialization of soft-shell gelatin and gummy products. They will be responsible for scale up of new products, lead investigations on any bulk or product issues during product lifecycle, develop strategies to improve current manufacturing technologies, and develop new strategies for future gummy manufacturing. The candidate has excellent communication skills to meet with customers and lead technical discussions. They will be responsible for performing key development activities including authoring documentation, performing extended testing on pivotal batches, and training and troubleshooting were needed. In addition, this candidate must be able to review applicable test methods and use scientific rationale when investigating any out of specifications related to bulk manufacture. They must be able to generate new scientific proposals and lead efforts to investigate, identify, develop, and optimize new and existing formulations. The candidate should be certified in Six Sigma process and must have launched commercial supplement soft gel products. They must be knowledgeable of dietary supplement ingredients and excipient function. They must be able to calculate label claim for actives and determine appropriate overages. Having experience with process analytical technology is a plus. The candidate must be knowledgeable of cGMP and regulatory requirements and not debarred from activities related to food or drug manufacture (FDA). They must set an example by creating an open environment of mutual respect and honesty and by focusing on the facts and data. They must be comfortable with mentoring and supervising others. Preference will be given to those who also have extensive experience formulating and commercializing gummy and/or dosage forms. Responsibilities Specific Responsibilities · Leads and oversees full scale pivotal development batches completing all documentation in a timely manner with appropriate scientific rationale and justification where needed. · Trouble shoot existing methods and make appropriate timely recommendations on method development improvements; conducts work requiring judgment in the evaluation, selection, adaptation and modification of standard techniques, processes and criteria; review and provide technical guidance to technical challenges encountered, particularly unusual or complex problems. · Works closely with Quality and R&D colleagues to prepare, review master batch records, work instructions, specifications, position papers, CAPAs, MRBs and SOPs as needed. Write reports to capture all key data and rationale to validate manufacturing process for new products. · Periodically prepares research reports and technical recommendations by collecting, analyzing, and summarizing information and trends; gives presentations for both internal and external customers. · Attends seminars and workshops to expand knowledge of new technologies and practices related to soft gelatin encapsulation and related fields; communicate newly acquired knowledge to Team and Leadership for as necessary for continuous improvement, and other considerations. · Conducts scientific trials to support new raw sources and determine impact to product. · Develop strategies to effectively address project and company goals/needs; Collaborate with functional and technical experts to facilitate scientific achievement. · Responsible as a technical task leader within his/her area of expertise on company project teams, communications with corporate customer and 3rd party labs or for specific assignments; Demonstrate the ability to resolve key technical hurdles and questions by effectively utilizing available information and technical expertise. · Participate in establishing project goals and timeline for technical tasks and contribute to the generation of project-related documents and presentations. · Demonstrate the character of a science professional and a high degree of responsibility in maintaining scientific standards, cGMP compliance, and safe laboratory practices for self and reporting staff. · Responsible for compliance with applicable corporate policies and procedures; Follows safety guidelines and policies when performing duties in the laboratory or manufacturing. · Participates in dietary supplement related and science-based organizations, review industry updates, new guidance, new methods, etc. with these groups as the IVC representative. · Maintains ethical and good character as an IVC employee representing highest level of standards at all times as cited in our employee handbook. General Responsibilities · Poses no direct threat to the health or safety of himself/herself, of others, or to property. Defined as a significant risk of substantial harm that cannot be eliminated or reduced to an acceptable level by reasonable accommodation. · Requires regular attendance to perform essential element as contained herein between the assigned start and end times for work unless requested by management to fulfill a specific assigned duty to support manufacturing. · Performs such individual assignments as management may direct. · Other duties as assigned. Qualifications Education, Experience, and Licenses: · Graduate degree in food science formulation, chemistry, or pharmaceutics. · At least 15 years of experience developing soft gelatin encapsulated products. · At least 5 years of experience developing formulations for commercial gummy and/or confectionary dosage forms · Six Sigma certification preferred Knowledge, Skills, and Abilities · Excellent knowledge and experiences related to cGMP and regulatory requirements for NSF, USP and similar certifications. · Demonstrated good ability to resolve major technical challenges by effectively utilizing available information and technical expertise in soft gelatin manufacturing · Excellent time management, leadership, and communication skills (both oral and written). · Motivated leader for innovation and continuous improvements with colleagues, learns fast, grasps the "essence”, and can change course quickly as required · Ability to build excellent relationships with quality and other colleagues; proactive and motivated for best-in-class timely task completions and team performances International Vitamin Corporation (IVC) Is an Equal Opportunity Employer. Our organization remains steadfast in our commitment to fostering an inclusive and non-discriminatory work environment that welcomes individuals from all backgrounds. We firmly maintain the belief that every individual ought to be treated with respect and dignity, regardless of their race, color, religion, sex, sexual orientation, gender identity or expression, age, national origin, disability, veteran status, marital status, genetic information, or any other protected characteristic, as defined by the law. We pledge that all eligible job applicants shall receive an impartial and unbiased evaluation during the recruitment process, without any form of discrimination based on any of the protected class. Our dedication to promoting diversity and inclusivity remains unwavering, and we take immense pride in cultivating a workplace culture that values and celebrates differences. Our efforts towards creating an environment that is free from prejudice and discrimination are an integral part of our organizational philosophy, and we stand committed to upholding these principles.

**Genotyping Research Associate II** Ohalo Genetics ** Research Associate III - Genotyping **Type:** Full time **Desired start date****:** Aug 15th, 2024 **The Opportunity:** Ohalo Genetics is seeking a motivated Genotyping Research Associate III to contribute to our high throughput genotyping pipeline including using Next Generation Sequencing (NGS) and other molecular techniques. The successful candidate will have extensive experience in PCR setup, interpretation, genotyping and experience with NGS library preparation and sequencing. The candidate will work with other research associates and scientists to screen hundreds of plant tissue samples and conduct other molecular biology experiments to facilitate genotyping. They will be responsible for supporting day-to-day genotyping tasks and communicating progress and timelines to other teams. This role will ensure the proper operation of our high throughput genotyping pipeline. The genotyping Research Associate III will monitor the status of the genotyping pipeline and troubleshoot any issues in a timely manner. **Responsibilities:** * Perform DNA extraction, PCR and library preparation * Execute our high throughput genotyping workflow with automation. Identify problems and troubleshoot them * Communicate genotyping timelines, updates, and results to related teams * Careful execution of protocols for biotechnology/molecular biology experiments * Performing analytical assays for QC or research purposes * Detailed note-taking using an electronic lab notebook and accurate data entry into database * Maintaining a clean and safe laboratory and working environment * Monitor equipment status, minimizing downtime of the genotyping pipeline * Provide supervision and support for junior RA(s) in the team **Candidate Profile:** * Bachelor's or Master's degree in Biology, Plant Genetics, Molecular Biology, Biochemistry or a similar field * 5+ years experience or 2+ years experience with Master's degree in a similar role * Strong laboratory skills and experience with molecular biology techniques, such as DNA and RNA extraction, PCR, qPCR or dd PCR. * Strong understanding and experience of illumina sequencing, library preparation and QC * Strong understanding of molecular biology and genotyping methods * Exceptional organization & communication skills. Attention to detail and ability to maintain accurate laboratory records * Familiarity with plant breeding, genetic engineering and plant tissue culture/regeneration * Ability to work independently and as part of a team. Ability to work in a dynamic, fast-paced, start-up company environment * Proficiency with MS word and excel * Growth mindset, considers no limit to excellence ***Desired skills/experience:*** * Experience in designing and optimizing complex and multiplexed PCR * Advanced knowledge and experience of illumina library preparation and sequencing * Experience with automated liquid handling equipments * Demonstrated ability to follow lengthy and detailed protocols * Experience working with delicate analytical and assay instruments such as a Flow Cytometer, Nanodrop, Bioanalyzer, or Microplate reader. * Proven ability to take initiative in process optimization and troubleshooting * Some managing experience or proven leadership * Advanced data analysis skills using R or similar tools ***Demands*** * On site (one location) Monday through Friday * Standing 40-50% of the day * Intensive pipetting requiring dexterity and vision **About Ohalo Genetics:** Ohalo is using an evolutionary lens to reimagine the art and science of plant breeding. We seek to transform breeding and production systems with a goal of helping to sustainably support the world's growing population. *Notes: If you previously applied for a job at Ohalo Genetics, we encourage you to restate your interest in the position by submitting your application.* *No visa sponsorship is available for this position at this time.* *No recruiters please.*

Research Associate II - Genotyping Type: Full time The Opportunity: Ohalo Genetics is seeking a motivated Genotyping Research Associate II to join our high-throughput genotyping team. This position will focus on executing established genotyping workflows, including using Next Generation Sequencing (NGS) technologies and molecular biology techniques. The successful candidate will have a Bachelors degree in a related field with 3+ years experience or a Master's degree with more than 1 year relevant experience. This is a dynamic, hands-on role suited for individuals with a strong background in PCR, Illumina sequencing, and molecular biology workflows. Working closely with other research associates and scientists, the successful candidate will play a pivotal role in screening large sets of plant tissue samples and will contribute to the successful execution of our high throughput genotyping pipeline essential to Ohalo Genetics' production objectives. Responsibilities: Perform DNA extraction, PCR, and sequencing library preparation. Execute high-throughput genotyping workflows with automation, identifying and troubleshooting issues as they arise. Work with other scientists to develop and test new, customized genotyping workflows, including marker-based and whole-genome genotyping approaches. Communicate genotyping timelines, updates, and results with related teams. Carefully execute biotechnology/molecular biology protocols. Perform analytical assays for QC or research purposes. Maintain detailed lab records in an electronic notebook and ensure accurate data entry. Monitor equipment and minimize downtime in the genotyping pipeline. Supervise and support junior RAs in the team as needed. Candidate Profile: Bachelor's or Master's degree in Biology, Plant Genetics, Molecular Biology, Biochemistry, or a similar field. 3+ years in a relevant role (or 1+ with a Master's). Strong skills in molecular biology techniques, including DNA and RNA extraction, PCR, qPCR, or dd PCR. Proficiency in Illumina sequencing, library preparation, and QC. Detail-oriented with strong organizational and communication skills. Familiarity with plant breeding, genetic engineering, and plant tissue culture/regeneration. Ability to work independently and collaboratively in a fast-paced environment. Proficiency in MS Word and Excel. A growth mindset with a commitment to continuous improvement. Desired skills/experience: Experience designing and optimizing complex PCR workflows. Advanced Illumina library preparation and sequencing knowledge. Experience with automated liquid handling equipment. Familiarity with delicate analytical instruments, such as Flow Cytometer, Nanodrop, Bioanalyzer, or Microplate Reader. Demonstrated process optimization and troubleshooting abilities. Basic supervisory experience or proven leadership skills. Advanced data analysis skills using R or similar tools. Demands On site (one location) Monday through Friday Standing 40-50% of the day Intensive pipetting requiring dexterity and vision If you are passionate about molecular biology, plant genetics, and advancing genotyping technologies in a collaborative, startup environment, we encourage you to apply. Join us in driving innovation at the intersection of plant biotechnology and genomics. About Ohalo Genetics: Ohalo is accelerating evolution to unlock nature's potential. We seek to transform breeding and production systems with a goal of helping to sustainably support the world's growing population. Notes: If you previously applied for a job at Ohalo Genetics, we encourage you to restate your interest in the position by submitting your application. No visa sponsorship is available for this position at this time. No recruiters please.

**Employment Opportunity** **Criminalist - Firearms Laboratory** **Greenville County Department of Public Safety, Greenville, South Carolina** **Salary:** $52,980.22 - $87,417.35 per year Greenville County is seeking a Criminalist to perform a variety of duties related to the analysis of many types of evidence recovered at crime scenes including, but not limited to, firearms and tool mark analysis. Click to read more **Duties** This position is responsible for providing opinions and evaluations of evidence in an investigative capacity; preparing documentation reflecting the analysis and conclusions of the examiner; preparation of evidence to be used at trial; provide explanation of analysis procedures and conclusions in court as an expert witness; perform analysis of firearms, ammunition, ammunition components; conduct microscopic comparisons of questioned bullets and cartridge casings, examine various types of manufacturer, class and individual characteristics of tools and tool marks; examine captured material for any signs indicating make, model, modifications, place or origin, manufacturer of maker, and serial numbers; determine firearm operability; if safe to fire follow SOP's for the discharge of a firearm for the purposes of material recovery for comparison; perform administrative and technical reviews of reports and worksheets; and prepare written results suitable for intelligence or prosecutorial packages. The successful candidate will have good knowledge of acceptable practices and procedures for the analysis of evidence; working knowledge of the specialized machines, equipment and tools used in the collection and analysis of evidence; knowledge of LIMS and NIBIN systems; and knowledge of the demands and restraints that are imposed by the judicial system on the procedures and techniques used in forensic analysis. **Requirements** * Applicant must possess a minimum of a Bachelor of Science or advanced degree from an accredited university with a major in a natural or physical science. * Experience is required in the analysis of firearms, ammunition, and ammunition components; conducting microscopic comparisons of questioned bullets and cartridges casings; examining various types of manufacturers, class and individual characteristics of tools and tool marks on a variety of objects; providing training to other personnel in regard to firearm safety and proper handling techniques, and experience conducting examinations while maintaining chain of custody and formulating interpretation results for forensic an/or intelligence exploitation. * Applicant may be required to obtain a law enforcement certification, other certificates and licenses as determined by the Assistant County Administrator for the Department of Public Safety. * Must possess a valid driver's license. * Clear FBI/SLED background; good credit report and polygraph required. *See available now!* **How to apply:** **Click to receive job posting alerts** Posted: July 26, 2024 * To notified of job openings as they are posted, follow us on Twitter: or sign up for daily email alerts: * To sign up for the Crime Scene Investigator Newsletter, go to the page. * For more job listings, return to the page. * To learn how to get a job in crime scene investigations or forensic science, go to the page. * For a listing of colleges and universities offering degrees in crime scene investigations and forensics, go to the page. **NOTE:** The crime-scene-investigator.net is not responsible for typographical errors or omissions in employment notices on this web site. Often, employers change final filing dates, change duties and/or requirements, or close employment openings without notice. If you are interested in a job posted on this site be sure to contact the employer to see if changes in the filing date or job announcement have been made. Employers can also provide more information about open positions that does not appear in the announcements on these pages.

**Senior R&D Chemist (1733)** + Title:Senior R&D Chemist + Group Company: Mitsubishi Chemical Performance Polymers + Employment Type:Full time Group Company: + Mitsubishi Chemical Performance Polymers **Mitsubishi Chemical Performance Polymers, Inc. (MCPP)** a subsidiary of Mitsubishi Chemical is wholly owned, MCC and its twenty group companies provide products and services to customers in North and South America providing a broad range of businesses including chemical, petrochemical, composite materials, pharmaceuticals, electronics, and other businesses. MCPP has doubled in size over the past 5 years due to the organic growth with our customers as well as numerous positive acquisitions. This has allowed us to expand our product portfolio, global reach and create an exceptional team of 1000+ dedicated employees. MCPP operates a global network of 24 sites in 15 nations. In the Americas, MCPP has locations in Michigan, Ohio, South Carolina and Brazil. MCPP's goal to our associates is to create an environment that motivates people, creates teamwork and encourages close collaboration with our customer and suppliers. We maintain a strong investment in our associates and encourage an entrepreneurial spirit and growth. We offer our associates a competitive salary, benefits, vacation and incentive package. We encourage learning and development and offer our associates opportunity for advancement. Job Purpose The Senior Research & Development Chemist is the primary technical driving force for new product and application development for MCA-PPD, as well as providing sustaining technical support to current product line. This position will function as a key technical resource to all production locations as needed. The incumbent will work with Purchasing, Production, Sales and Marketing to supply technical knowledge and guidance regarding raw material, polymer and related problems and/or performance issues where materials may be a factor. The Senior R&D Chemist will supervise and mentor less-senior members of the technical team as needed. Principal Accountabilities 1. Drive targeted new product development efforts for our thermoplastic, polyvinyl, and 3DP-based compounds for major global strategic customers. 2. Responsible for technical integrity of the new product development cycle: + raw material selection and qualification including working knowledge of SDS and regulatory requirements + formulation development and establishment of processing criteria / requirements + establishment of intellectual property position + customer acceptance and quality control 1. Coordinate and validate each major step in the development system by providing technical leadership. Technical support will be given to MCA Purchasing, Production, Process & Project Engineering, Regulatory & Compliance, Quality Control, and key customers. 2. The incumbent must be familiar with physical property testing for specialty compounds, weathering, as well as plastic instrument characterization by FT-IR, TGA, DSC, etc. 3. Provide technical support to MCA-PPD's diverse product lines to sustain and grow current business. Support can be through working with: 4. Purchasing to qualify new or modified raw materials, 5. Production and Processing Engineering for technical analysis of nonconforming material and continuous improvement for reject reduction and/or cost improvements. 6. Marketing and Technical Service personnel to develop new and/or modified products to meet customer and marketplace needs including developing data, technical data sheets, engineering material testing and approval submittals to OEM. 7. Establish and maintain key technical relationships with other regions and divisions in MCG to leverage global know-how and best practices. 8. Lead and mentor less-senior members of the Technical Team, sharing know-how and overseeing critical projects and programs. Knowledge / Skills / Experience 1. Four-year technical degree from a four-year College or University. 1. Chemistry or Chemical Engineering 2. 5+ years' experience in compounding and product development 3. Excellent communication skills to effectively communicate at all levels of the organization. 4. Excellent computer skills - Microsoft Office (Word, Excel and PowerPoint). 5. Problem-solving skills demonstrated through utilization of tools such as 8D/5-Why/Six Sigma approach. 6. Demonstrated ability to lead individuals and teams through product/process development and problem-solving. 7. Experience with TEP is preferred. 8. Automotive experience is preferred. Pay Transparency (complete highlighted sections) + **The salary range for this position is $100,922 - $126,152. Factors such as scope and responsibilities of the position, candidate's work experience, education/training, job-related skills, internal peer equity, as well as market and business considerations may influence base pay offered. This salary will be subject to a geographic adjustment (according to a specific city and state), if an authorization is granted to work outside of the location listed in this posting.** + **Competitive Benefits** + **Benefits begin on DAY 1!** + **Employee Assistance Programs** + **Curated Self-Paced Learning & Development Programs for all Employees** **Mitsubishi Chemical Group (MCGC) and any of our subsidiaries do not accept unsolicited resumes from individual recruiters or third-party agencies. No fee will be paid to third parties who submit unsolicited candidates directly to our hiring managers or HR team. No placement fees will be paid to any firm unless specifically invited on the search by the MCGC Talent Acquisition team and such candidate was submitted to the MCGC Talent Acquisition Team via our Applicant Tracking System.** EEO Statement Mitsubishi Chemical Corporation values diversity in the workplace, is committed to a policy of equal employment opportunity and will not discriminate against an applicant or employee on the basis of race, color, religion, sex, sexual orientation, gender identity, national origin, disability, veteran status or any other legally recognized protected basis under applicable law. Applicants with disabilities may be entitled to a reasonable accommodation under the Americans with Disabilities Act and/or other applicable laws. If you require accommodation due to a disability at any time during the recruitment and/or assessment process, please contact Talent Acquisition.

Postdoctoral Scholar Location: Greenville, SOUTH CAROLINA Job Title Postdoctoral Scholar Working Title Postdoctoral Scholar Anticipated Recruitment Range. Salary offered may be outside of this range as impacted by budget, UNC salary administration, and/or candidate qualifications. $53,760 Position Location (City) Greenville Position Type Postdoctoral Scholars Job Category Postdoctoral Scholars Primary Function of Organizational Unit The Department of Microbiology and Immunology is a distinguished research and teaching facility of East Carolina University School of Medicine consisting of approximately 50 people. This department provides an academic base for teacher-scientists employed by the School of Medicine at East Carolina University in the disciplines of microbiology, immunology, molecular biology and other related disciplines. The department provides instruction to medical students, dental students, and graduate students. The department also provides guidance and research experience to graduate students seeking advanced degrees in microbiology and immunology. The department also offers a postdoctoral research training program. The department supports an array of faculty (16)-directed research programs of which many are supported by extramural grants and/or contracts. The department provides service to the school, university, state, nation, and to the profession by activities of faculty members on committees, study sections, in professional organizations, as consultants, and through other activities. Job Duties The postdoctoral scholar is responsible for independent and collaborative development, implementation, and analysis of scientific research in the discipline of immunology, autoimmunity, neurodegenerative disease, molecular genetics/ biology, biochemistry, and virology. Responsibilities include management of all aspects of vector construction, cell culture, protein expression, protein purification, protein characterization, bioassay, in vitro and in vivo experimentation, daily measurement of experimental autoimmune encephalomyelitis, and other inflammatory disease models. Duties include: hypothesis development, literature review, collection of pilot data, report writing, and supervising of undergraduate research students and graduate research students, overseeing data collection procedures, supervising experimental procedures, review of data for quality control, supervision of data entry/ data analysis, analysis of research hypothesis using descriptive and multivariate statistics, and the development of independent and collaborative presentations and publications. Scholars are expected to demonstrate compliance with established guidelines and regulatory standards for research including biosafety, responsible conduct of research, and human subjects training. Approximately 95% of the postdoctoral scholar's time will be devoted to experiments related to the project. Approximately 5% of the postdoctoral scholar's time will be devoted to managing the day-to-day activity of undergraduate and graduate research students in the laboratory. Minimum Education/Experience English Proficiency Excellent written and oral communication skills, PhD degree in Immunology or a closely-related field with at least 1 year of research experience in the area of Immunology Preferred Experience, Skills, Training/Education PhD degree in Immunology or closely-related field with at least 2 years of post-doctoral experience in the area of Immunology, Immunotherapy and/or Immunological Tolerance. Special Instructions to Applicant To be considered for this position, all applicants must apply through PeopleAdmin and attach their CV or resume, cover letter and names and contact information of 3 references. Appointments are typically for a one-year period. Five years (typically five appointments of one year) is typically the maximum total period that any individual may serve as a Scholar. The University, in its sole discretion has the option to renew or extend any appointment, subject to the availability of funds, past performance evaluations and/or any other lawful reasons. For other information on the ECU Office of Postdoctoral Affairs, please visit our website at: ********************************** Additional Instructions to Applicant In order to be considered for this position, applicants must complete a candidate profile online via the PeopleAdmin system and submit any requested documents. Additionally, applicants that possess the preferred education and experience must also possess the minimum education/experience, if applicable. Office of Human Resources Contact Information If you experience any problems accessing the system or have questions about the application process, please contact the Office of Human Resources at ************** or toll free at ************** or send an email to ******************. 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** Scientist - Applications Semi** **Job Details** Experienced Pacific North West Region - Portland, OR Fully Remote Full Time Up to 50% Day Science **Description** Rigaku Semiconductor Metrology Division is seeking an X‐ray Applications Scientist to support Rigaku's X‐ray metrology products. This position will work closely with Rigaku Service, Sales, Marketing, and the product development teams, and requires up to 30% travel for on‐site customer applications support and training. **Responsibilities:** * Provide applications support for Rigaku semiconductor metrology tools utilizing a variety of X-ray analytical techniques, e.g. X‐ray fluorescence (XRF), X‐ray diffraction (XRD), X‐ray reflectometry (XRR), and small angle X‐ray scattering (SAXS). * Assist customers remotely and on-site with recipe creation and optimization, tool operation and data analysis. Use expert technical knowledge of X-ray techniques to drive solutions to challenging customer applications. * Provide support to the Rigaku Service team for new tool installations and perform deep dive analysis to help troubleshoot tool issues as needed. * Provide support to the Rigaku Sales team to ensure customer satisfaction through all stages of the sales process. Work to understand customer application requirements and objectives, and act as technical lead for product demonstrations. * Write technical documentation and application notes, and create and maintain training material. Clearly and effectively communicate highly technical subject matter to a variety of audiences. * Maintain positive, productive work relationships with customers and colleagues at all levels. * Travel to customer sites located primarily within the United States, but with occasional international trips. **Qualifications** * Ph.D or M.S. in Material Science, Physics, Chemistry, Solid State, or related engineering fields. * Minimum of three years of work experience as an applications scientist or applications engineer in a semiconductor metrology tool manufacturer or as a process engineer in a semiconductor device manufacturer with thin film quality control/metrology experience. * Independent, hands-on experience with thin film analytical techniques. * Strong understanding of fundamentals of X-ray physics, spectroscopy, diffraction and scattering. * Strong understanding of semiconductor device manufacturing process. * Excellent analytical thinking and problem-solving skills, e.g. root cause analysis, 5 Whys. * Proficient in data analysis techniques and skills, including a working knowledge of statistics and statistical process control. * Proficient in speaking, reading, and writing in English. Ability to speak at an intermediate level in Japanese, Chinese, Korean, or Hebrew is a plus. * Excellent written and verbal technical communication skills. * Ability to travel up to 30% with occasional international travel. * U.S. Citizenship or U.S. Permanent Resident status required.

**Advancing food loss technologies and policies EUROPEAN PARLIAMENT, 13 FEBRUARY, 10:00AM** * 13 February 2024 * Posted by: Competere * Categories: events, highlights, News, Sustainable Nutrition **Advancing food loss technologies and policies** For this event, Competere is working in partnership with , and the discussion is hosted by MEP Rosa D'Amato. **February 13th, 2024, European Parliament** On **Tuesday, February 13th**, we organised the groundbreaking roundtable event “**Advancing food loss technologies and policies**” at the **European Parliament (Room A5E1)**, in Brussels. The discussion aimed to address the causes and impact of food loss and waste, introduce cutting-edge technologies, and showcase successful case studies. Outstanding speakers spotlighted business organisations that, by implementing innovative organisational processes and equipment/technologies, are contributing to the reduction of food loss and waste; finally, we will explored EU strategies and policies addressing this critical issue. . **Reducing food loss and waste** is a paramount for lowering GHG emission, preventing land degradation, safeguarding biodiversity, and ensuring food security. Food supply chains play a pivotal role through investments in the innovative processes and advanced technologies. ****Summary and policy recommendations**** ****Download the slides**** **REWATCH THE EVENT HERE** **PROGRAMME** > Welcome and Introduction **Rosa D'Amato**, MEP Data and causes of food loss and waste **Gyula Kasza**, University of Veterinary Medicine Budapest EU's policies and strategies **Alexandra Nikolakopoulou**, DG Sante Mitigating food loss: technology and solutions **Eva Sali**, Copa Cogeca **Federica Dolce**, Food&Drink Europe **Claudio Zanframundo**, Trane Technologies **Malte Piontek**, Schwarz Group **Christophe Diercxsens**, Too Good To Go **Federica Grassi**, SAFE - Safe Food Advocacy Europe **Vito Antonacci**, ZeroWaste Policies supporting technological innovation agains food waste **Rosa D'Amato**, MEP **Salvatore De Meo**, MEP **Inese Vaidere**, MEP Moderator **Pietro** **Paganini**, Competere.eu ****Download the flyer**** **SPEAKER BIO** To access the biographies of the speakers, Noi e terze parti selezionate raccogliamo informazioni personali e utilizziamo cookie o tecnologie simili per finalità tecniche e, con il tuo consenso, anche per le finalità di **esperienza e misurazione** come specificato nella . Puoi liberamente prestare, rifiutare o revocare il tuo consenso, in qualsiasi momento, accedendo al pannello delle preferenze. Il rifiuto del consenso può rendere non disponibili le relative funzioni. In caso di vendita di informazioni personali, puoi fare opt-out utilizzando il link "". Per saperne di più sulle categorie di informazioni personali raccolte e sulle finalità per le quali tali informazioni saranno utilizzate, si prega di fare riferimento alla nostra . Usa il pulsante “Accetta” per acconsentire. Usa il pulsante “Rifiuta” o chiudi questa informativa per continuare senza accettare.

**Please see Special Instructions for more details.** Positions are advertised for a minimum of five (5) business days on our job website. After five (5) business days, positions can be closed at the discretion of the department at any time. This employment site is updated on a regular basis. The length of the recruitment and screening process may vary from position to position, depending upon a variety of factors. Should review of your qualifications result in a decision to pursue your candidacy, you will be contacted by phone or email. We are only accepting applications submitted by January 2, 2025 **The University of South Carolina offers a valuable benefits package including but not limited to:** * Health and Life Insurance * Retirement Programs * Paid Tuition * Dependent Scholarships * Annual Leave * Sick Leave * 13 Paid Holidays (including an extended December holiday) * Paid Parental Leave * Professional Development Opportunities Click to learn more about why you should work at USC. USC Market Title Scientist Business Title (Internal Title) Scientist Advertised Salary Range Salary commensurate with qualifications. Location of Vacancy Greenville, SC Benefits for Research Grant or Time-Limited Positions Are Indicated Below The University of South Carolina (UofSC), through the State of SC and Public Employee Benefit Authority (PEBA), offers employees a valuable benefits package, including health and life insurance, generous paid leave and retirement programs. To learn more about UofSC benefits, access the "Working at USC" section on the Applicant Portal at *********************** Research Grant or Time-limited positions may be eligible for all, some, or no benefits, based on the grant or project funding. South Carolina Retirement No State Insurance Programs No Annual Leave No Sick Leave No Position Description Advertised Job Summary *The Scientist is responsible for overseeing the operations of multiple* *laboratories, ensuring a collaborative research environment, and adherence* *to safety and regulatory standards. This position entails working closely with* *the Prisma Health Cancer Institute and BMS Department research leadership* *to maintain operational efficiency and facilitate the onboarding process for* *new staff and tenants.* Job Related Minimum Required Education and Experience Requires a terminal degree (PhD or similar) in area of specialty and five years post-graduate experience. Required Certification, Licensure/Other Credentials Preferred Qualifications Experience working in Academic and/or Hospital environment. Knowledge/Skills/Abilities * Skills in research design, data analysis, inferential thinking, writing of research proposals and manuscripts, knowledge of appropriate quantitative and qualitative analytic techniques; ability to work in multidisciplinary environment and teams; * Ability to establish rapport with clinical and basic science colleagues and members of the community. * Knowledge of principles and practices of project management. * Ability to direct multiple diverse projects. * Ability to establish and maintain effective working relationships * Ability to always maintain a professional demeanor. * Ability to plan, organize and supervise the work of subordinate personnel. * Ability to communicate effectively and maintain respect, consistent with the principles of conscious leadership. * Ability to analyze data and present ideas effectively. * Ability to work independently * Ability to analyze complex data and data collection and develop methods to obtain accurate, useful output * Ability to design and modify report forms Ability to coordinate and schedule work between user groups * Ability to train and assist staff in use of systems. Job Duties Job Duty Operations Oversight and Onboarding: * Coordinate with the Cancer Institute and ITOR labs to facilitate new staff and/or tenant onboarding, Including badge and access requests, obtaining keys, and submitting work orders. * Ensure lab space availability, order or replace equipment, and resolve general laboratory issues as needed. Essential Function Yes Percentage of Time 35 Job Duty Laboratory Operations: * Ensure laboratory testing services are conducted safely and in compliance with quality protocols and project requirements. * Oversee or coordinate training and utilization of laboratory staff. * Facilitate maintenance, installation of equipment, and maintain workflow to meet deadlines and benchmarks. * Coordinate shared equipment usage and maintenance. * Maintain inventory, obtain supplies, and ensure proper organization and appearance of laboratory areas. * Confocal Microscope Operation: * Proficiently operate and maintain the confocal microscope system in the SOMG ITOR Laboratory. * Provide technical support, training, and ongoing guidance to lab members in using the microscope. * Ensure microscope calibration, alignment, and routine inspections for proper functioning. * Assist in data management, quality assurance, and documentation related to microscope usage. Essential Function Yes Percentage of Time 35 Job Duty Safety and Compliance: * Follow safety rules, guidelines, and standards for all projects, including waste disposal. * Coordinate orientation for new tenants and lab space availability. * Coordinate lab tenant meetings and serve as the resource for day-to-day needs and issues. * Coordinate equipment preventive maintenance, repairs, removal, and disposal. * Order new equipment as needed and approved and coordinate new equipment delivery and setup. Essential Function Yes Percentage of Time 30 Positions are advertised for a minimum of five (5) business days on our job website. After five (5) business days, positions can be closed at the discretion of the department at any time. This employment site is updated on a regular basis. The length of the recruitment and screening process may vary from position to position, depending upon a variety of factors. Should review of your qualifications result in a decision to pursue your candidacy, you will be contacted by phone or email. We are only accepting applications submitted by January 2, 2025 **The University of South Carolina offers a valuable benefits package including but not limited to:** * Health and Life Insurance * Retirement Programs * Paid Tuition * Dependent Scholarships * Annual Leave * Sick Leave * 13 Paid Holidays (including an extended December holiday) * Paid Parental Leave * Professional Development Opportunities Click to learn more about why you should work at USC . * * Yes * No

Research Associate III page is loaded **Research Associate III** **Research Associate III** locations Clark Laboratory-1st Floor time type Full time posted on Posted 30+ Days Ago job requisition id JR100068 **Job Summary** Woods Hole Oceanographic Institution is currently searching for a Research Associate to join the Geology and Geophysics Department. This is a regular, full-time, exempt position, and is eligible for full benefits. The initial appointment is for 12 months with the possibility of extension depending on performance and funding availability. The ideal candidate will lead development, calibration, and simulation of high-resolution coastal hydrodynamical models for coral reef/coastal environments. Online application forms should be submitted with a cover letter and full curriculum vitae including a list of three references.**Job Description** **ESSENTIAL FUNCTIONS:** Applicants are expected to * Develop nested high-resolution hydrodynamic models with existing community models, such as (but not limited to) SCHISM and Wave Watch III * Analyze field and satellite observational data to understand coastal hydrodynamical processes and to evaluate the performance of hydrodynamic model * Test different model configurations and parameters, and adjust model set up to improve model performance * Carry out long-term model simulations and synthesize model output * Collaborate with an interdisciplinary team of scientists and effectively communicate scientific findings with scientists in different fields * Provide technical reports and other documentation of methods and procedures * Be able to work on tasks requiring creativity and independent thinking along with a deep understanding of fundamental research and science principles * Be able to work independently and effectively manage his/her own schedule to meet deadlines * Experience with data assimilation, forecasting, cross scale modelling, and/or sediment transport modelling would be an advantage * Experience with “what-if scenario” testing would be an advantage **NON-ESSENTIAL FUNCTIONS:** Preparation of scientific articles for publication, development of research proposals, and participation in fieldwork **Education and Experience** * PhD degree in physical oceanography with several years of ocean hydrodynamic modeling experience, or demonstrated competency as a postdoctoral researcher or research associate in a related field * Proficiency in Matlab/Python and Linux is required * Experience with oceanography or coral reef field work is advantageous, but not required. **Additional Job Requirements** **PHYSICAL REQUIREMENTS:** * Physical duties for this position include but are not limited to the ability to work around others. This position is mostly sedentary by nature. **Affirmative Action/EEO Statement** Woods Hole Oceanographic Institution (WHOI) provides equal employment opportunities to all employees and applicants for employment and prohibits discrimination and harassment of any type without regard to race, color, religion, age, sex, national origin, disability status, genetics, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state or local laws. Welcome, WHOI's growth is opening doors to exciting opportunities. Connecting the right people with the right roles not only strengthens us, but also promotes better collaboration. After you've explored our current openings, please apply to roles that you believe are the best match based on your education and experience. Visit your profile to update your resume, apply to saved jobs, and check the status of your job-related activities. We appreciate your interest in becoming a part of WHOI. As a leading non-profit organization, we are dedicated to ocean research, exploration, and education. Our scientists and engineers are at the forefront of understanding the ocean's complex interactions with our planet. With a diverse and passionate team, we are a global leader in ocean science and engineering. At WHOI, discovery and innovation are not the only things we excel at; we are also committed to our people, our local community, and the world around us. If you share our commitment to exploring the ocean's mysteries and its profound impact on the Earth and humanity, consider joining our team to make a difference in the world.

**Job Details** Entry Optional Work from Home Part Time **Description** Activated Insights (formerly HCP) is a B2B software-as-a-service company serving North America's fastest-growing labor market, in-home senior care. As the market leader in North America, our technology, survey, and training solutions are used by everyone from mom-and-pop small businesses to billion-dollar care organizations. Ultimately, our services impact the lives of hundreds of thousands of seniors every year. * Build an exciting career in the SaaS, healthcare technology, and home care industry with an award-winning, fast-growing company. * Experience a startup/agency culture but with the stability of a company that has been in business for 15+ years * Work with some of the largest agencies, technology vendors, and healthcare tech on the planet! * Be a part of a company that has been recognized multiple times as the best place to work. **What will you'll be doing** * Our Satisfaction Research Associate performs surveys over the phone with home care recipients, their families, and caregivers across the country. * Accurately type their responses that are then passed on to their home care provider, who use it to improve the care of the individuals and the jobs of their employees. **What we offer** * Flexible schedule that you create (no late nights or weekends) * 25+ hours per week start at $11 + bonuses * 16-24 hours per week start at $10 + bonuses * Raise upon graduating 1st Month Training Program * Part time 16-40 hours * 3 days of paid training * Monthly Bonuses & Incentives * Work from home options * Raises every 4 months * Paid time off We also offer bilingual Russian and Spanish speaking positions! If you want a purposeful job with co-workers, supervisors, and managers who believe in what they do and want to see you grow, we'd love to visit with you **Qualifications** * Speaks Russian * High attention to detail * Basic computer literacy required * Typing speed of at least 40 words per minute * Commitment to efficiency and accuracy * Previous surveying experience a plus * Excellent communication skills, both written and verbal

Share If you are unable to complete this application due to a disability, contact this employer to ask for an accommodation or an alternative application process. **QC Chemist I** Full Time Science Eng Spec 30+ days ago Requisition ID: 2363 **GENERAL DESCRIPTION OF POSITION** The primary responsibility of this position is to analyze drug substances, drug products, and/or stability samples using approved laboratory monographs/specifications, Standard Operating Procedures, and USP/NF methodologies to ensure drug products manufactured at and distributed by Pharmaceutical Associates, Inc. meet all quality and compliance requirements. ESSENTIAL DUTIES AND RESPONSIBILITIES * Follows all policies, procedures, SOPs, cGMPS, Work Instructions, and supervisor instructions. * HPLC/GC Chemists: Shall have an emphasis in HPLC and/or GC methodology and analyses including all applicable preparations (extractions, dissolution, ISE separation, etc.), and training or experience in chromatographic software and instrument troubleshooting. * Wet Chemists: Shall have an emphasis in wet chemistry methodology and analyses such as various titrations, dissolution, USP/NF limit tests, Identifications, TLC, etc. * Responsible for performing analysis of raw materials, bulk, finished product, and stability samples in a timely and compliant manner, as instructed by QC Supervisor, per applicable SOPs, PAI monographs/specifications, and USP methodology to ensure finished goods are acceptable for distribution. * Responsible for documentation of all analyses per applicable SOPs. * Responsible for performance of routine laboratory functions to support manufacturing/production and assure that production schedule is met. * Responsible for the timely testing and release of manufactured bulk drug products for packaging. * Responsible for maintaining clean and organized laboratories. Wash labware and pipettes by loading/unloading dishwasher/pipette washer. * Notify Laboratory Coordinator when reagents, standards, and other materials need to be ordered to ensure all resources available for testing. * Assist in training and evaluating laboratory personnel to run laboratory equipment for established methods. * Assist in documentation review of laboratory notebooks. * Accountable for the accuracy and timeliness of work, attention to detail, and adherence to test method monograph/specifications. For following applicable Standard Operating Procedures, including all safety procedures and policies. For working safely in an effective work team. * Perform any other related duties as required or assigned. **EDUCATION / EXPERIENCE** * BS in Science + 0 years' experience **ADDITIONAL INFORMATION** To perform this job successfully, an individual must be able to perform the essential job functions satisfactorily. PAI is an Equal Opportunity Employer. In compliance with the Americans with Disabilities Act, PAI will provide reasonable accommodations to qualified individuals with disabilities and encourages both prospective and current employees to discuss potential accommodations with the employer. PAI uses E-Verify. EEO Employer / Veteran / Disabl ed 2nd Shift: Monday through Thursday, 4pm - 2:30am

PL Developments, also known as PLD, is a leading manufacturer, packager, and distributor of over-the-counter (OTC) pharmaceutical products and consumer healthcare goods. We are seeking a skilled and detail-oriented chemist with a strong background in analytical chemistry and laboratory operations to join our team. This role is ideal for a motivated individual with a passion for science, problem-solving, and collaboration in a dynamic laboratory setting. Work Schedule: Monday - Friday 8am-5pm JOB QUALIFICATIONS: Bachelor's degree in Chemistry or a related science from an accredited institution, with 2-4 years of relevant laboratory experience in the pharmaceutical industry, or 2+ years of experience as a Chemist I; or an equivalent combination of education and experience. Expertise of GLP, cGMP, FDA and other regulatory requirements. Proficiency in laboratory instrumentation, including UV/Vis, FTIR, HPLC, and GC. Strong foundation in analytical chemistry. Experience with laboratory software and applications such as HPLC, FTIR, UV, LIMS, Lab Calc, and GC. Knowledge of sampling methods and quality control systems. Proficiency in quantitative and qualitative analysis, including the application of statistical methods. Knowledge of sample preparation techniques. Excellent communication skills, both written and verbal. Ability to establish and maintain cooperative working relations. Ability to manage multiple projects, duties and assignments. POSITION RESPONSIBILITIES: Adhere to organizational policies and procedures, as well as state, federal, and local laws. Ensure compliance with current Good Laboratory Practices (cGLP), current Good Manufacturing Practices (cGMP), safety requirements, and laboratory Standard Operating Procedures (SOPs). Conduct scheduled preventive maintenance and calibration of laboratory instrumentation (i.e., pH meter, HPLC, dissolution equipment, etc.). Prepare standard and sample solutions as required by the test methods. Operate general analytical instruments for all routine testing (i.e., HPLC, GC, UV/Vis, automatic titrator, and FTIR). Perform wet chemistry tests on raw material (i.e., LOD, Assays, pH, titration, etc.). Perform analyses on intermediate and finished products. Maintain appropriate documentation (records and lab notebooks) as required by SOPs. Comply with good housekeeping and safety practices. Participate in troubleshooting of analytical test methods and laboratory instruments. Take part in the training program as a qualified trainer, as requested. Assist in troubleshooting and problem solving. Accurately and precisely perform testing. Perform related duties as assigned. PHYSICAL REQUIREMENTS: Employees in this class are subject to extended periods of sitting, standing, walking, lifting materials weighing up to 50 pounds, vision to monitor, moderate to loud noise levels. Incumbents may be exposed to or work with toxic materials, toxic gases, electrical hazards, and dangerous tools and equipment. Work is performed in an office or laboratory environment. Incumbents must be able to use personal protective equipment (e.g. respirators, gloves, etc.). BENEFITS: PLD is a proud equal opportunity employer offering many corporate benefits, including: ⠁ Medical and Dental Benefits ⠁ 401K with employer match ⠁ Group Life Insurance ⠁ Flex Spending Accounts ⠁ Paid Time Off and Paid Holidays ⠁ Tuition Assistance ⠁ Corporate Discount Program ⠁ Opportunities to Flourish Within the Company #HP1

SynTerra is looking for a qualified Project Scientist/Hydrogeologist who can offer our clients their expertise. This position requires 2-4 years of experience with groundwater flow and transport modeling; environmental sampling, assessment, and remediation; or other relevant areas of expertise and experience in an applicable discipline. This position requires the ability to work independently on specific tasks and in collaboration with clients and other environmental professionals. The position requires the ability to work in an outdoor environment and to travel. We provide assessment and remediation services on a wide variety of projects for a very diverse set of clients, primarily within the Southeastern United States. Responsibilities: Constructing numerical fate and transport models (MODFLOW/MT3DMS/MODPATH) to characterize and quantify groundwater flow patterns and mobile constituent transport processes. Evaluating complex geologic and hydrogeologic systems using various tools and methodologies. Assisting in the design and optimization of monitoring programs and engineered systems including landfills, drainage channels, stability features, and groundwater remedial systems. Preparing and performing technical reviews of reports on groundwater modeling, groundwater monitoring, site characterization, risk assessment, permit application, and remediation. Preparing a wide variety of recurring and nonrecurring correspondence, reports, and other documents from information obtained from coworkers, files, and other sources. Using varied and advanced functions of “office suite automation” to include diagramming, e-mail, GIS, presentation, word processing, and spreadsheet software. Create, format, modify, edit, and print a variety of outputs from the automation listed in a professional and timely manner. Coordinating with leadership on business development, project management, and proposal writing. Demonstrating willingness to travel throughout our market area for field work, as necessary. Requirements Bachelor's degree in hydrogeology, geology, hydrology, environmental science, engineering (environmental, civil, hydraulic, agricultural or water resource engineering), or related field. Master's degree or Doctorate degree greatly preferred. Software proficiency (including but not limited to): GMS, Surfer, Adobe Acrobat, ESRI ArcGIS Pro, Google Earth Pro, and Microsoft Office Suite. Experience in flow and transport modeling 40 hr. OSHA HAZWOPER trained a plus Must be able to work in both indoor and outdoor settings in environments ranging from climate controlled office space to foul weather, heat, and rain. May sit or stand for several hours at a time and climb inclines (terrains, ladders, etc.). Required to lift objects up to 50 lbs. Must be able to work in a team environment. We are interested in every qualified candidate who is eligible to work in the United States. However, we are not able to sponsor visas for this position. SynTerra is an equal opportunity employer. Hiring, promotion, transfer, compensation, benefits, discipline, termination and all other employment decisions are made without regard to race, color, religion, sex, sexual orientation, creed, age, disability, national origin, genetic information, veteran status, pregnancy, childbirth, medical needs arising from pregnancy or childbirth, medical conditions related to pregnancy or childbirth, including, but not limited to, lactation, or any other characteristics protected by law, unless a bona fide occupational qualification applies.

Today, Lonza is a global leader in life sciences operating across five continents. While we work in science, there's no magic formula to how we do it. Our greatest scientific solution is talented people working together, devising ideas that help businesses to help people. In exchange, we let our people own their careers. Their ideas, big and small, genuinely improve the world. And that's the kind of work we want to be part of. Goal of the Supply Chain Project Manager is to support the strategic growth initiatives of the company. This would include maintaining and intensifying as well as identifying and implementing long term partnership with customers through outstanding Supply Chain Programs for the Capsules and Health Ingredients product portfolio. This position will also be responsible for setting up the ingredients' flow in AMER with global and regional alignment from end to end. Additionally, this position will be identifying and implementing, with the support of other areas, value stream mapping and lean initiatives as well as any other project that can increase value or reduce cost on the supply chain continuum. Key Responsibilities: Carries out responsibilities in accordance with the organization's policies, procedures, and state, federal and local laws and regulations. Train, and demonstrate proficiency, on primary laboratory processes and instrumentation. Train on, and implement testing of, raw materials and finished goods following written in-house and compendium procedures. Maintain accurate and complete logbooks, verification logs and user logs following good laboratory documentation practices. Perform routine preventative maintenance and/or requalification of analytical instrumentation. After proficiency is established, operate analytical instruments; HPLC, ICP, GC, UV/Vis, HPTLC, FTIR and automatic titrator, to release raw materials, product development samples and finished goods. Conduct laboratory activities with moderate supervision. Write/revise Standard Operating Procedures and implement special projects, as the need arises. Prioritize workload to align with the needs of the business. Conduct and document Out of Specification investigations, as necessary. Peer review laboratory data generated by other chemists. Key Requirements: Bachelors in Chemistry or Biology (with strong lab experience) Working in a cGMP laboratory supporting manufacturing operations Maintain good laboratory practices following ISO and cGMP guidelines Enforce to all laboratory and plant safety procedures HPLC (Required) GC (Required) FTIR (Required) Wet Chemistry (Required) ICP-MS (Preferred) Good written and oral abilities Every day, Lonza's products and services have a positive impact on millions of people. For us, this is not only a great privilege, but also a great responsibility. How we achieve our business results is just as important as the achievements themselves. At Lonza, we respect and protect our people and our environment. Any success we achieve is no success at all if not achieved ethically. People come to Lonza for the challenge and creativity of solving complex problems and developing new ideas in life sciences. In return, we offer the satisfaction that comes with improving lives all around the world. The satisfaction that comes with making a meaningful difference. Lonza is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, religion, color, national origin, sex, sexual orientation, gender identity, age, status as a qualified individual with disability, protected veteran status, or any other characteristic protected by law.

Today, Lonza is a global leader in life sciences operating across five continents. While we work in science, there's no magic formula to how we do it. Our greatest scientific solution is talented people working together, devising ideas that help businesses to help people. In exchange, we let our people own their careers. Their ideas, big and small, genuinely improve the world. And that's the kind of work we want to be part of. Goal of the Supply Chain Project Manager is to support the strategic growth initiatives of the company. This would include maintaining and intensifying as well as identifying and implementing long term partnership with customers through outstanding Supply Chain Programs for the Capsules and Health Ingredients product portfolio. This position will also be responsible for setting up the ingredients' flow in AMER with global and regional alignment from end to end. Additionally, this position will be identifying and implementing, with the support of other areas, value stream mapping and lean initiatives as well as any other project that can increase value or reduce cost on the supply chain continuum. Key Responsibilities: * Carries out responsibilities in accordance with the organization's policies, procedures, and state, federal and local laws and regulations. * Train, and demonstrate proficiency, on primary laboratory processes and instrumentation. * Train on, and implement testing of, raw materials and finished goods following written in-house and compendium procedures. * Maintain accurate and complete logbooks, verification logs and user logs following good laboratory documentation practices. * Perform routine preventative maintenance and/or requalification of analytical instrumentation. * After proficiency is established, operate analytical instruments; HPLC, ICP, GC, UV/Vis, HPTLC, FTIR and automatic titrator, to release raw materials, product development samples and finished goods. * Conduct laboratory activities with moderate supervision. * Write/revise Standard Operating Procedures and implement special projects, as the need arises. * Prioritize workload to align with the needs of the business. * Conduct and document Out of Specification investigations, as necessary. * Peer review laboratory data generated by other chemists. Key Requirements: * Bachelors in Chemistry or Biology (with strong lab experience) * Working in a cGMP laboratory supporting manufacturing operations * Maintain good laboratory practices following ISO and cGMP guidelines * Enforce to all laboratory and plant safety procedures * HPLC (Required) * GC (Required) * FTIR (Required) * Wet Chemistry (Required) * ICP-MS (Preferred) * Good written and oral abilities Every day, Lonza's products and services have a positive impact on millions of people. For us, this is not only a great privilege, but also a great responsibility. How we achieve our business results is just as important as the achievements themselves. At Lonza, we respect and protect our people and our environment. Any success we achieve is no success at all if not achieved ethically. People come to Lonza for the challenge and creativity of solving complex problems and developing new ideas in life sciences. In return, we offer the satisfaction that comes with improving lives all around the world. The satisfaction that comes with making a meaningful difference. Lonza is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, religion, color, national origin, sex, sexual orientation, gender identity, age, status as a qualified individual with disability, protected veteran status, or any other characteristic protected by law.

The One Health Entomology group of the Laboratory of Entomology at Wageningen University and Research is looking for an ambitious postdoctoral researcher with experience in the ecology and population dynamics of blood-feeding insects. The research interests of the group are to understand the factors that determine the presence and/or emergence of vector-borne diseases and to unravel the underlying mechanisms from molecular to ecosystem level. With this knowledge, the group ultimately aims to design novel strategies for vector control that are affordable, safe for use, and sustainable in the context of our changing environment. The team consists of ambitious scientists that employ interdisciplinary approaches, both in the lab as well as in the field. The postdoctoral position will involve the coordination of and data collection for a new European project, funded via the European Biodiversity Initiative (Biodiversa+), with partners in France, Spain and Morocco. The position is for 3 years. **About the Project** By 2050, 70% of the global population will live in urban areas, leading to increased environmental challenges such as pollution and biodiversity loss. The "greening" of cities, through green spaces and water bodies, offers a nature-based solution to promote sustainability, biodiversity, and human health, for example by reducing heat island effects, air pollution, and improving physical and mental well-being. However, they may also provide habitats for disease-transmitting vectors, such as mosquitoes and sandflies. The impact of urban greening on vector populations is expected to depend on local conditions, highlighting the need for effective surveillance and control, particularly in both public and private spaces. Wageningen University is now leading a new project that aims to explore the relationships between public and private urban green spaces on the one hand, and diversity of blood-feeding arthropods and their implications for vector-borne disease transmission to humans and animals on the other. **Your responsibilities** You will be responsible for developing and executing vector sampling protocols in collaboration with the European partner institutes. Within the Netherlands, you will be coordinating field sampling activities in diverse urban areas across the country. Your work will involve the use of molecular approaches for vector identification and for assessing biodiversity indices, e.g. via eDNA techniques. You are expected to integrate and analyze findings from different country settings and write scientific publications. In collaboration with the head of the One Health Entomology group, you will facilitate national and international meetings for partner institutes and stakeholders.* an excellent academic record (PhD) in medical/veterinary entomology or related ecological discipline; * experience with (field-based) research on mosquito/vector (community) ecology; * experience with diverse molecular lab techniques * good knowledge of statistical methods, including multivariate analyses * excellent oral and written English communication skills; * a good organizer and team player. **Your job** **Your qualities** The successful candidate is/has: In our international working environment there is an increasing amount of communication in English. For this position it is about C1 .**We offer you** Wageningen University & Research offers excellent . A few highlights from our Collective Labour Agreement include: * sabbatical leave, study leave, and partially paid parental leave; * working hours that can be discussed and arranged so that they allow for the best possible work-life balance; * there is a strong focus on vitality and you can make use of the sports facilities available on campus for a small fee; * a fixed December bonus of 8.3%; * excellent pension scheme. In addition to these first-rate employee benefits, you will of course receive a good salary. Depending on your experience, we offer a competitive gross salary of between € 3.378,- and € 5.331,- for a full-time working week of 38 hours, in accordance with the (scale 10). Additionally, a contract for 0,8 FTE can be discussed. As for your contract, we initially offer a one-year contract that can be extended on good performance. Wageningen University & Research encourages internal advancement opportunities and mobility with an internal recruitment policy. There are plenty of options for personal initiative in a learning environment, and we provide excellent training opportunities. We are offering a unique position in an international environment with a pleasant and open working atmosphere. You are going to work at the greenest and most innovative campus in Holland, and at a university that has been chosen as the “” in the Netherlands for the 19th consecutive time. **Coming from abroad** Wageningen University & Research is the university and research centre for life sciences. The themes we deal with are relevant to everyone around the world and Wageningen, therefore, has a large international community and a lot to offer to international employees. Because we expect you to work and live in the Netherlands our team of advisors on Dutch immigration procedures will help you with the visa application procedures for yourself and, if applicable, for your family. Feeling welcome also has everything to do with being well informed. Wageningen University & Research's page contains practical information about what we can do to support international employees coming to Wageningen. Furthermore, our can assist you with any additional advice and information about for example housing, opening a bank account, dual career programs or schooling. Finally, certain categories of international staff may be eligible for a tax exemption on a part of their salary during the first five years in the NetherlandsFor more information about this position, please contact, Sander Koenraadt, Professor at the Laboratory of Entomology, by email: *********************** For more information about the procedure, please contact **************************** You can apply directly using the apply button on the vacancy page on our website which will allow us to process your personal information with your approval. This vacancy will be listed up to and including 13 January 2025. We hope to schedule the first job interviews in the last week of January 2025. **Procedure** As part of our selection process, an assessment may be incorporated within the procedure **Welcome, safe, and valued** Wageningen University & Research (WUR) highly values diversity and inclusion because we believe that different insights lead to innovative solutions. We create a work environment where everyone feels welcome, safe, and appreciated, regardless of background, identity, or experience. Together, we are building a culture where everyone's unique contribution adds to the success of our organization. **We are** The mission of Wageningen University & Research is “To explore the potential of nature to improve the quality of life”. Under the banner Wageningen University & Research, Wageningen University and the specialised research institutes of the Wageningen Research Foundation have joined forces in contributing to finding solutions to important questions in the domain of healthy food and living environment. With its roughly 30 branches, 7,600 employees (6,700 fte) and 13,100 students and over 150,000 participants to WUR's Life Long Learning, Wageningen University & Research is one of the leading organisations in its domain. The unique Wageningen approach lies in its integrated approach to issues and the collaboration between different disciplines. Read the why your future colleagues enjoy working at WUR and watch the video below to get an idea of our green campus! *We will recruit for the vacancy ourselves, so no employment agencies please.

At **Haley & Aldrich**, a 900+ person national engineering and environmental consulting firm, our creative, technically strong staff work collaboratively to deliver exceptional value to clients. We look for professionals with a passion for solving complex challenges and for creating change, which is a vital part of our culture, no matter what role a staff member holds. We are looking to add new talent to our growing team! We are currently seeking a **Geochemical Scientist** to work in a technical support role with highly skilled professionals on diverse project teams in a dynamic environment. This is an excellent opportunity to join a growing group and company and get involved in a variety of projects for a diverse range of clients. This is a **full-time** position located in our **Greenville, SC** office. **DUTIES/RESPONSIBILITIES** **The successful candidate will:*** Support large project teams throughout the US, focusing on the characterization and assessment of inorganic constituents in the environment. * Be classically trained in geochemical modelling software PHREEQC or Geochemists Workbench. * Have a strong conceptual understanding of fate and transport mechanisms for inorganic constituents in groundwater and surface water. * Work in the field 30-40% collecting environmental samples, document logging cores in situ, mineralogic characterization, redox investigations, environmental tracer investigations, formulation of conceptual site models, drilling oversight, groundwater monitoring well installations, and performing geochemical field investigations of abandoned mine lands, legacy mining sites, and active mining sites. * Summarize details, observations, technical procedures and/or project assignment requirements for senior or project personnel. * Partner with and support Haley & Aldrich staff members on a wide variety of the geochemical aspects of the projects to address client goals and objectives. * Work and schedule resources collaboratively with project teams. * Assist in the planning, coordination, and execution of geochemical field investigation programs, including subsurface explorations and laboratory testing. * Compile, reduce, analyze, visualize, manage, and report geochemical data, using data management software and other tools. * Assist in identifying technical issues and the development design recommendations. * Conduct geochemical analyses. * Draft written reports, memoranda, daily/weekly field reports and specifications. * Contribute to development of proposals and cost estimates to clients. * Perform all work in accordance with company and client Health & Safety protocols. * Comply with the Guiding Principles and Code of Behavior articulated in our Company Charter. **SKILLS/EXPERIENCE** * Minimum B.S. degree in Inorganic Geochemistry (Environmental Chemistry and other Geoscience's degrees will be considered). * 0-3 years of professional services consulting experience that includes construction quality control/documentation, evaluation of environmental data, and presentation of technical solutions in a variety of written and oral formats. * Have a base knowledge of mineralogy and the concepts of rock-forming minerals. * Foundational chemistry background. * Experience with geochemical modeling. * Experience with database and database processing. * Python coding or other computer coding. * OSHA 40-hour HAZWOPER training and MSHA Training preferred. * Excellent organizational, written, and verbal communication and problem-solving skills and attention to detail. * Ability to convey observations and produce accurate and concise field notes, logs, data sheets and reports on daily activities including construction projects. * Experience in planning, coordinating, and executing subsurface investigation and laboratory testing programs. * Familiarity and interest with geology, mineralogy, environmental remediation and construction is a plus. * Must possess a valid driver's license, have a reliable form of transportation to travel to job sites and the office, and the ability to travel out of town for temporary work assignments. * Positive attitude, self-motivated, strong work ethic, flexibility, and willingness to work with project teams spread across many geographies. * Self starter. * Strong computer literacy skills including proficiency in all MS Office software. * Ability to lift 30 lbs. unassisted. **About Haley & Aldrich** Haley & Aldrich is committed to delivering the value our clients need from their capital, operations, and environmental projects. Our one-team approach allows us to draw from our 900 engineers, scientists, and constructors in more than 35 offices for creative collaboration and expert perspectives. Since our founding in 1957, we have had one goal in all we do: deliver long-term value efficiently, no matter how straightforward or complex the challenge. Learn more at Haley & Aldrich is an equal opportunity employer. All qualified applications will receive consideration for employment without regard to gender, race, age, disability, veteran, or any other legally protected status. We offer excellent career growth, a highly competitive total compensation plan, and a solid Interested candidates should apply on our **Note to external search firms:** Haley & Aldrich does not accept unsolicited resumes and will not be obligated to pay a placement fee for unsolicited resumes. Please do not send resumes to Haley & Aldrich employees. Please work through a Talent Acquisition Manager. #LI-BG1