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<h3>Job Description</h3>
Ecolab, the&nbsp;global leader in premium cleaning, sanitizing and maintenance products and services for the hospitality, institutional and&nbsp;industrial markets&nbsp;is seeking a Clean Room roduction Technician. This Clean Room Production Technician is responsible for operating manufacturing equipment, documentation and maintaining quality standards.
What’s in it For You
<ul>
<li>The opportunity to take on some of the world’s most meaningful challenges, helping customers achieve clean water, safe food, and healthy environments</li>
<li>The ability to make an impact and shape your career with a company that is passionate about growth</li>
<li>The support of an organization that believes it is vital to include and engage diverse people, perspectives and ideas to achieve our best</li>
<li>Comprehensive benefits package starting day one of employment including medical, dental, vision, matching 401k, company paid pension, stock purchase plan, tuition reimbursement and more!</li>
</ul>
Click Here to see our benefits.
What You Will Do
<ul>
<li>Comply with aseptic gowning and hygiene requirements</li>
<li>Review filling and packaging instructions at beginning of line runs. Ensure&nbsp;the correct packaging materials are available. Ensure the correct Personal Protective Equipment is available and other safety procedures are understood and followed.</li>
<li>Perform material handling and transfer disinfection and complete required inventory transactions</li>
<li>Ensure the line is set up correctly per the filling and packaging instructions</li>
<li>Operate filling and packaging equipment in accordance with Good Manufacturing Practices (GMP), including performance of all line operations to ensure customer quality, operational safety and productivity requirements are met.</li>
<li>Complete changeover and line clearance according to SOP and batch record requirements.&nbsp; Collect samples and complete visual inspections as required</li>
<li>Actively participate in Kaizens, 5S, and special projects&nbsp;</li>
<li>Continuingly identify opportunities for system and process waste elimination&nbsp;</li>
<li>Perform basic, documented maintenance in accordance with department policy</li>
<li>Complete and document activities in accordance with department SOP and Good Documentation Practices. This could include performing basic quality tests. Enter results on paper or in&nbsp;electronic systems.</li>
<li>Complete packaging and filling assignment meeting or exceeding the standards.</li>
</ul>
Position Details
<ul>
<li>Plant Location: Greensboro, NC</li>
<li>Shift Options (Depending on business need): 1st Shift (6am - 2pm / Mon - Fri) + Required OT, as needed 2nd Shift (2pm - 10:30pm / Mon-Fri) + Required OT, as needed</li>
<li>Training: 10a-6:30p for 3-4 months (transition to 2p-10:30p after training)</li>
<li>Compensation: $19.00 / hour + $1.00 Shift Differential Clean Room personnel earn an additional $1.50 / hour upon completion of gowning qualification (within 30 days of start date)</li>
</ul>
Minimum Qualifications
<ul>
<li>High School Diploma or GED</li>
<li>1 year of previous Production Manufacturing experience</li>
<li>No immigration sponsorship available for this role&nbsp;</li>
</ul>
Physical Demands
Position requires the performance of all essential functions of the job, with or without reasonable accommodation, including:
<ul>
<li>Complying with the rigid requirements for operating in a clean room environment including maintaining exceptional personal hygiene and donning / doffing multiple layers of protective clean room attire numerous times during a shift</li>
<li>Lifting, shifting and carrying up to 50lbs</li>
</ul>
Preferred Qualifications
<ul>
<li>Previous clean room or other GMP environment experience is highly desirable</li>
<li>Experience understanding the mechanical movements of a machine&nbsp;</li>
<li>Ability to complete training and master skills that are required by position (including but not limited to Hazardous Material Safety and DOT training)&nbsp;</li>
<li>Ability to understand and track safety, quality and productivity data, including run rates, fill weights, and averages&nbsp;</li>
<li>Experience with Total Production Management (TPM) &amp; Continuous Improvement Systems&nbsp;</li>
<li>Ability to use basic math, including addition, subtraction, multiplication, division of whole numbers, fractions, percentages, and decimals&nbsp;</li>
</ul>
Annual or Hourly Compensation Range:
The pay range for this position is $19 / hour. Many factors are taken into consideration when determining compensation, such as experience, education, training, geography, etc. We comply with all minimum wage and overtime laws.
Benefits&nbsp;
Ecolab provides the following benefits: medical, dental, vision, life insurance, accident insurance, critical illness insurance, hospital indemnity insurance, auto insurance, home insurance, pet insurance, identity theft protection, short-term and long-term disability, 401k, pension plans, retirement health care benefits, short-term incentives, vacation (12 days), holidays, parental leave, employee stock purchase plans&nbsp;(Full-Time Associates), discount on day care services and caregiver services, adoption assistance, group legal services, employee assistance program, employee discount program, and education assistance program,&nbsp;on-Site childcare and fitness facilities may be available at select Ecolab locations.&nbsp;Click here for additional benefits information. If you are viewing this posting on a site other than our Ecolab Career website, view our benefits at&nbsp;jobs.ecolab.com/working-here.
Potential Customer Requirements Notice
To meet customer requirements and comply with local or state regulations, applicants for certain customer-facing roles may need to:
- Undergo additional background screens and/or drug/alcohol testing for customer credentialing.
- Be fully vaccinated for COVID-19, including a booster if eligible, unless a religious or medical accommodation is requested by the applicant and approved by Ecolab.
Americans with Disabilities Act (ADA)&nbsp;
Ecolab will provide reasonable accommodation (such as a qualified sign language interpreter or other personal assistance) with our application process upon request as required to comply with applicable laws. If you have a disability and require accommodation assistance in this application process, please visit the Recruiting Support link in the footer of each page of our career website.&nbsp;&nbsp;
 
Our Commitment to a Culture of Inclusion &amp; Belonging \nAt Ecolab, we believe the best teams are inclusive. We are on a journey to create a workplace where every associate can grow and achieve their best. We are committed to fair and equal treatment of associates and applicants and recruit, hire, promote, transfer and provide opportunities for advancement based on individual qualifications and job performance. In all matters affecting employment, compensation, benefits, working conditions, and opportunities for advancement, we will not discriminate against any associate or applicant for employment because of race, religion, color, creed, national origin, citizenship status, sex, sexual orientation, gender identity and expressions, genetic information, marital status, age, disability, or status as a covered veteran.
\n
In addition, we are committed to furthering the principles of Equal Employment Opportunity (EEO) through Affirmative Action (AA). 
\n
We will consider for employment all qualified applicants, including those with criminal histories, in a manner consistent with the requirements of applicable state and local laws, including the City of Los Angeles’ Fair Chance Initiative for Hiring Ordinance, the San Francisco Fair Chance Ordinance, and the New York City Fair Chance Act.

Clean Room Technician

<h3>Job Description</h3>
Amber Bio is a biotechnology company pioneering new gene editing modalities using multi-kilobase edits to reach previously undruggable patient populations. Founded by pioneers in the CRISPR field from leading institutions for gene editing research, the company is developing a first-of-its-kind RNA editing platform that can correct thousands of bases at once, thereby correcting genetic mutations safely and reversibly. If you are interested in building a new frontier in genetic medicine, we welcome you to apply.
 
Job Description: Research Associate III/ Senior Research Associate (Biodesigner), Assay Development / Bioanalytical Development
 
Position Overview: The Research Associate III/ Senior Research Associate in Assay Development and Bioanalytical Development will play a critical role in the development, qualification, and validation of bioanalytical methods to support our RNA editing programs. The successful candidate will work under the guidance of an assay development scientist to develop custom assays for the analysis of samples, including AAVs, cells, and tissues. This role also involves drafting key documents such as Standard Operating Procedures (SOPs) and method development reports.
 
Key Responsibilities:
<ul>
<li>Method Development, Qualification, and Validation:</li>
<li>Support the development, qualification, and validation of bioanalytical methods in accordance with regulatory guidelines.</li>
<li>Develop, optimize, and execute robust bioanalytical methods for the characterization, release, and stability testing of Amber's gene therapy. </li>
<li>Sample Analysis:</li>
<li>Support drug absorption, distribution, metabolism, and excretion studies.</li>
<li>Perform analysis of AAVs, cells, and tissues to support various stages of research and development.</li>
<li>Lead efforts to streamline and optimize sample storage and processing, as well as establishing and maintaining critical reagent stocks and cell banks.</li>
<li>Documentation Reporting:</li>
<li>Draft and review key documents such as SOPs, method development, and sample analysis reports.</li>
<li>Maintain accurate and detailed records of all experiments and analyses.</li>
<li>Collaboration &amp; Communication</li>
<li>Collaborate with manufacturing and preclinical teams to support pipeline needs.</li>
<li>Communicate and present findings clearly to internal stakeholders.</li>
</ul>
 
Qualifications:
<ul>
<li>B.A./B.S. or M.S. in Molecular Biology, Biochemistry, Analytical Chemistry, or a related field.</li>
<li>3+ years of experience in bioanalytical and assay development in the biotechnology or pharmaceutical industry.</li>
<li>Demonstrated strong proficiency in a wide range of molecular biology techniques such as molecular cloning, DNA/RNA extractions, RT-qPCR, ddPCR, and ELISA.</li>
<li>Experience with cell-based assays and detection methods such as fluorescence, luminescence, and ECL.</li>
<li>Hands-on experience using laboratory automated systems (e.g., liquid handlers, extraction robotics, etc.).</li>
<li>Background in RNA-based therapies is highly desirable.</li>
<li>Experience writing SOPs and reports supporting IND filings (e.g. development, qualification sample analysis reports, etc.)</li>
<li>Knowledge of FDA and ICH guidelines for method development, qualification, and validation. </li>
<li>Prior history in compiling and analyzing data and generating reports that are routinely presented to project teams.</li>
<li>Ability to work effectively in a collaborative, fast-paced environment.</li>
</ul>
 
Preference will be given to those who display:
 
<ul>
<li>High motivation, with a strong work ethic and dedication to generating impact.</li>
<li>Attention to detail, with the ability to extract deep insights from data.</li>
<li>Ability to go from ideation to data in an independent fashion.</li>
<li>Long-term personal vision with defined career goals.</li>
<li>Team-oriented thinking.</li>
<li>Demonstrated excellence in small team environments, including a “no task is too small” attitude. </li>
</ul>
 
If you have a passion for advancing gene editing technologies and desire to be part of a pioneering biotech company, we encourage you to apply and join our ambitious team.
 
Please apply directly through LinkedIn.
 
Amber Bio is an equal-opportunity employer and encourages applications from candidates of diverse backgrounds. We value diversity and are committed to creating an inclusive and supportive work environment for all employees.

Research Associate III/ Senior Research Associate (Biodesigner), Assay Development / Bioanalytica...

<h3>Job Description</h3>
On Line Design is looking for a full-time Fragrance Encapsulation Slurry Technician, in Hebron, KY working on-site. In this role, you will be responsible for the hands-on execution of microencapsulation processes, focusing on the preparation and testing of fragrance slurries. You will also be asked to assist in research and development activities to create new fragrance delivery systems, ensuring product stability and performance while adhering to strict safety and quality control standards. 
 
Responsibilities:
<ul>
<li>Formulate microencapsulation slurries for various applications for personal care, laundry and household applications.</li>
<li>Operate and maintain specialized lab equipment, such as mixing tanks, spray dryers, and other encapsulation machinery.</li>
<li>Conduct various tests on prepared fragrance slurries and microcapsules to evaluate performance.</li>
<li>Perform stability tests under different conditions (e.g., temperature, pH, pressure) to ensure product durability.</li>
<li>Analyze capsule properties, including size distribution, encapsulation efficiency, and fragrance release profiles.</li>
<li>Maintain detailed and accurate records of all experimental procedures, observations, and results. Record and report any deviations or inconsistencies in materials or process to the supervisor.</li>
<li>Assist in preparing technical reports and presentations for the R&amp;D team.</li>
<li>Ensure all laboratory equipment is properly calibrated, cleaned, and maintained.</li>
<li>Adhere to all company safety protocols, including proper handling of hazardous materials and wearing appropriate personal protective equipment (PPE).</li>
<li>Support the proper disposal of chemical waste in accordance with safety and environmental regulations.</li>
<li>Work closely with research scientists and the quality control team to ensure batch consistency and collaborate with production teams to scale up successful formulations from the lab to manufacturing. </li>
</ul>
 
Requirements:
<ul>
<li>Bachelor's degree in Chemistry, Polymer Science, Chemical Engineering, or a related scientific field expertise working in an R&amp;D process lab/pilot plant environment</li>
<li>3+ years of fragrance microencapsulation experience</li>
<li>Solid computer skills for data entry and analysis</li>
<li>Excellent communication and teamwork skills</li>
</ul>
 
Local candidates preferred, relocation assistance will be provided if needed for the correct candidate. 
 
On Line Design, Inc. is an equal opportunity employer and does not discriminate based on age, race, religion, color, sex, national origin, marital status, physical or mental disability, genetics, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state, or local laws.

Fragrance Encapsulation Slurry Technician

<h3>Job Description</h3>
Microbiology Laboratory Supervisor
Dade County, FL
Competitive Pay &amp; Benefits
 
The Microbiology Laboratory Supervisor will provide comprehensive testing for patients with infectious diseases. They will provide high-quality, state-of-the-art diagnostic services combined with readily available consultations with pathologists and laboratory scientists.
Microbiology Laboratory Supervisor Responsibilities:
<ul>
<li>Responsible for the technical and scientific oversight of the laboratory, day-to-day laboratory operation and personnel performing testing and reporting test results.</li>
<li>Participate in selection of test methodology appropriate for the clinical use of the test results.</li>
<li>Participate in the verification of the test procedures performed and the establishment of the laboratory's test performance characteristics, including the precision and accuracy of each test and test system.</li>
<li>Ensure enrollment and participation in an HHS-approved proficiency testing program commensurate with the services offered.</li>
<li>Establish a quality control program appropriate for the testing performed, establish the parameters for acceptable levels of analytic performance, and ensure that these levels are maintained throughout the entire testing process from the initial receipt of the specimen through sample analysis and reporting of test results.</li>
<li>Resolve technical and operational problems and ensure that remedial actions are taken whenever test systems deviate from the laboratory's established performance specifications.</li>
<li>Ensure that patient test results are not reported until all corrective actions have been taken and the test system is functioning properly.</li>
<li>Identify training needs and ensure that caregivers performing tests receive regular in-service training and education appropriate for the type and complexity of the laboratory services performed.</li>
<li>Evaluate the competency of all testing personnel and ensure that caregivers maintain their competency to perform test procedures and report test results promptly, accurately and proficiently.</li>
<li>Ensure the competency of testing personnel in the area of responsibility (i.e. moderately complexity and/or high complexity testing).</li>
<li>Evaluate and document competency assessment of testing personnel in laboratory area of responsibility at least semiannually during the first year the testing personnel tests patient specimens and annually thereafter.</li>
<li>Evaluate testing personnel competency through directly observing routine patient test performance, including patient preparation, specimen handling, processing and testing, monitoring the recording and reporting of test results, reviewing intermediate test results or worksheets, quality control records, proficiency testing results, and preventive maintenance records.</li>
<li>Supervise caregivers and handle staffing, hiring, orientation, scheduling, evaluating and developing caregivers.</li>
<li>Develop and maintain department objectives and services, assist with annual operating and capital budgets, and monitor, analyze and justify expense and revenue with departments.</li>
<li>Assist with policy and procedure development and ensure compliance.</li>
</ul>
Microbiology Laboratory Supervisor Qualifications:
<ul>
<li>Bachelor’s degree in chemical, physical, biological or clinical laboratory science or medical technology from a four-year college or university OR a bachelor’s degree from a four-year college or university, education and training equivalent to meet ASCP Board of Certification qualifications for Histotechnologist (HTL)/Cytotechnologist (CT) and meet the requirements and training of a Cytotechnologist as dictate by most current CLIA regulations. Diploma and/or transcripts must be provided and education will be verified.</li>
<li>State of Florida supervisor’s license in one or all disciplines or the ability to obtain the license.</li>
<li>Licensed as a Clinical Laboratory Technologist.</li>
<li>Microbiology experience in the specialty area you supervise.</li>
<li>National Certification by ASCP (SM(ASCP)).</li>
<li>Continued Education in Supervision and Administration.</li>
<li>Complete a HIV/AIDS Course.</li>
<li>8-10 years of experience in a Clinical Microbiology Laboratory.</li>
<li>American Society for Clinical Pathology (ASCP) certification is preferred.</li>
<li>Two years of clinical laboratory management or supervisory experience.</li>
</ul>

Microbiology Laboratory Supervisor

<h3>Job Description</h3>
DIRECTOR OF R&amp;D for Heavy Construction Equipment in Katy office. (Not remote position)
 
Fluent in Chinese and English required. 
 
SUMMARY
 
The Director of R&amp;D is responsible for the leadership of regional Research and Development for LiuGong’s Construction and Material Handling Product lines to achieve customer acceptance of quality and performance in North America to support strategic growth objectives. As department head, candidate will recruit and lead R&amp;D experts to develop and improve designs through collaboration with regional suppliers and Product Development engineers in China in these specific fields. Supports product development as a technical expert.
 
SPECIFIC RESPONSIBILITIES
 
<ul>
<li>Lead a technical development and quality assurance team responsible for:</li>
<li>Organizing people and financial resources to deliver annual objectives within allocated budgets</li>
<li>Supervising field research for LiuGong products on customer job sites to ensure detailed understanding of use cases and improvement opportunities</li>
<li>Converting functional specifications into design specifications.</li>
<li>Lead product development team responsible for: Prioritizing and defining development scopes of work.</li>
<li>Assist the headquarters' R&amp;D center in defining new products and conducting market research on technical requirements.</li>
<li>*Collect information on new technologies and standards emerging in the North American market and assist the HQ R&amp;D to do research on new technologies.</li>
<li>Lead key projects with research &amp; development to support business goals.</li>
<li>Develop concepts, products, and solutions by coordinating with R&amp;D business units in HQ.</li>
<li>Develop and execute improved product and industry technologies.</li>
<li>Recruit technical experts and develop R&amp;D personnel.</li>
<li>Research, design and evaluate materials, assemblies, processes, and equipment.</li>
<li>Monitor team metrics and objectives ensuring meeting of goals.</li>
<li>Represent departmental interests in all internal and external communication.</li>
<li>Document all phases of research and development.</li>
<li>Develop and monitor metrics as required to manage R&amp;D function.</li>
<li>Convey metrics to ensure appropriate alignment and executive awareness.</li>
<li>Other duties as required and requested by management.</li>
<li>Assisting with quality assurance to ensure applications are ready to be deployed to field.</li>
<li>Participating in industry events including conferences and committee meetings; authoring technical papers and patents.</li>
</ul>
 
The above job description is not intended to be an all-inclusive list of duties and standards of the position. Incumbents will follow any other instructions, and perform any other related duties, as assigned by their supervisor.
 
NO SPONSORSHIP - Must have valid work authorization and "in office" (not remote or flex) position. 
 
BACKGROUND &amp; SKILLS 
To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. The requirements listed below are representative of the knowledge, skill, and/or ability required. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.
 
<ul>
<li>Master’s Degree from an accredited college or university in Mechanical Engineering, Aerospace Engineering or equivalent.</li>
<li>Minimum 15+ years of progressive work experience in Engineering, of which at least 10 years must be in research and development for large equipment employed in Mining, Quarrying, or Heavy Construction.</li>
</ul>
 
PACKAGE
BENEFITS: Medical, dental, vision and life insurance packages offered. LGNA pays 100% medical, dental and vision insurance for employee only.
RETIREMENT: 401(K) plan, 100% match up to 6%, in accordance to company policy.
COMPENSATION: Competitive salary and bonus.
VACATION: 20 days of Paid Time Off (PTO) prorated the first year (until end of year / Dec)20 days of PTO on Jan 1 of next year.
HOLIDAYS: 10 paid holidays a year, in accordance to company policy.
EQUIPMENT: Branded Clothing, Laptop, Cell Phone.

DIRECTOR OF R&D for Heavy Construction Equipment (Mandarin/English required) In Katy, TX (Not re...

<h3>Job Description</h3>
About this Position:
 
Job Title: GIS Project Manager
 
Required Skills:
• Adept with complex project management.
• Strong oral and written communication skills.
• Business relationship management acumen.
• Core focuses on process improvement.
• Ability to solve problems and use critical thinking.
• Skilled with workflow mapping.
• Driven to innovate and foster adoption through organizational change management.
• Ensure GIS solutions meet compliance, security, and quality standards.
• Understanding of spatial data concepts
 
Preferred Skills:
• Strong Agile project management methodologies
• Document Management Systems, SharePoint
• Experience with ESRI ArcGIS, spatial databases, and data visualization tools
 
Note: For H-1B and OPT cases, we are seeking candidates from recognised organizations.
 
"No phone calls please."

GIS Project Manager

<h3>Job Description</h3>
The Pharma Method Development and Validation Chemist will perform studies for the development of immediate release and controlled release tablet and capsules dosage formulations, topical formulations (creams and gels) and liquid formulations.
Develop methods per ICH/USP requirements for excipient, API and final formulations of solid oral dosages form.
Writes method protocols for full validation and verifications to USP methods.
Does forced degradation studies.
Can make a method from scratch and or improves such by fine tuning the method parameters to meet USP or vendor specifications.
Works with QC to due testing . However, main job is taking a tech pack and making method validation protocols for submitting into ANDA .
Perform testing on raw materials and in-process and finished dosage forms.
Write technical documents including laboratory notebooks, batch records, project summaries, development reports, sampling and testing protocols, planned deviation reports, incident reports, and change control forms.
Maintain technical documents in the formulation development department.
Calibrate in-process testing equipment, interpret and analyze experimental data, identify the next steps to be taken and perform scale-up and technology transfers of formulations from research and development to the submission/clinical to production/commercial scale batches.
Direct the work of scientists and technicians in the formulation department, reviewing their laboratory notebooks, batch records, project summaries, product development reports and standard operating procedures.
Attend project meetings.
Manage R&amp;D projects and report project progress to the project manager.
Communicate the status of various batches to the production, QA, RA and QC departments and to clients, as needed.
Assist in FDA filings.
Review project contracts.
Assist IT in development and implementation of the database system.
Bachelor's Degree in Chemistry required.
Proficiency in computer usage and Microsoft Office required.
Job Type: Full-time
Required experience:&nbsp;Chemistry: 4 years

Analytical Development Chemist

<h3>Job Description</h3>
Job Description
 
Perform experiments pertaining to:
o Protein formulation/stability of various dosage forms (liquid/lyophilized) and configurations (vial/syringe), employing a variety of biochemical and biophysical analytical techniques, such as HPLC, capillary electrophoresis, and/or spectroscopy methods
o Scale-down/-up of biologics drug product processes
o In-use stability and administration
• Author protocols, technical summary reports/memos and tech transfer documentation defining the manufacturing process and parameters
• Review Master Batch Records for accuracy and trend process data supporting process development or fill/finish manufacturing operations
• Execute studies in support of drug product technology transfers to clinical and commercial manufacturing sites
• Be an effective communicator of ideas, project goals and results at departments/meetings in both written and presentation format.
• Be self-motivated, organized, thrive in team settings and enjoy scientific investigation and thinking, as well as be familiar with the relevant technical literature.
 
Knowledge, Experience and Skills:
 
• Degree in Chemical/Biochemical Engineering (or a related engineering discipline) or Pharmaceutical Sciences, and relevant industry experience that demonstrates expertise in drug product development as well as sustained excellence in performance and accomplishments that align to company goals.
• Excellent communication (both verbal and technical) and interpersonal skills are required.
• Demonstrates technical proficiency, scientific creativity, collaboration with others and independent thought in suggesting experimental design and research strategy.
 
Minimum Qualifications:
 
• A minimum of 5+ years of experience with BS degree or 3+ years of experience with MS degree in Pharmaceutical Sciences, Biology, Biochemistry, Biochemical Engineering or a related scientific discipline.
• A basic understanding of formulation and drug product process development for biologics (antibodies, fusion proteins, bi-specifics, vaccines, antibody drug conjugates, etc.).
• Previous experience interfacing with biologics drug product manufacturing sites and providing technical support during engineering runs/GMP operations is a plus.
 
Must Have Requirements/Skills:
• Experience working with Biologics molecules (proteins, mAbs); experience working with ADC is a plus
• Protein formulation/stability of various dosage forms (liquid/lyophilized) employing a variety of biochemical and biophysical analytical techniques, such as HPLC, capillary electrophoresis, and/or spectroscopy methods, analytical data analysis
• Experience with some scale-down/-up of biologics drug product process development activities; buffer preparations, testing using compendial methods (osmo, protein conc., pH, etc.) and UF/DF is a plus

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