<h3>Job Description</h3>
Job DescriptionSalary: 
DB Environmental, Inc. (DBE) is accepting resumes for a full-time Chemist to support a contracted position with the South Florida Water Management District (District), located at 8894 Belvedere Road, West Palm Beach, Florida. 
Position Summary
This is a staff level chemist position responsible performing various tasks in an environmental laboratory certified under the National Environmental Laboratory Accreditation Program (NELAP). Tasks will include:
<ul>
<li>sample preparation and inorganic analyses using automated and manual methods, which may utilize imaging multi-mode plate readers, HPLC systems, flow injection analyzers, plasma emission spectrophotometers, ion chromatographs, and carbon analyzers,</li>
<li>calibration and monitoring of instrument output to ensure quality control standards are met,</li>
<li>routine instrument maintenance,</li>
<li>instrumentation troubleshooting as needed,</li>
<li>data entry into the laboratory information management system (LIMS),</li>
<li>general support for laboratory washing and decontamination of field and lab equipment, and</li>
<li>sample receiving and log-in support.</li>
</ul>
All work will be performed according to the current standard operating procedures (SOP) using established protocols that ensure turnaround time, quality, and productivity expectations are met. 
Employment Guidelines
<ul>
<li>Minimum of a bachelors degree in a natural or physical science, or related field.</li>
<li>At least 2 years related work experience in a scientific discipline is desired.</li>
<li>Familiarity with basic environmental laboratory procedures, including sample log-in, sample preparation, inorganic laboratory analysis, and automated analytical laboratory instruments.</li>
<li>Experience in following certified laboratory QA/QC requirements and good laboratory practices.</li>
<li>Knowledge of basic laboratory safety and chemical hygiene.</li>
<li>Experience in using Laboratory Information Management Systems (LIMS) is desired.</li>
<li>Strong oral and written communication skills and proven organizational, time, and self-management skills.</li>
<li>Proficient in Microsoft Office Products (Excel, Word, Outlook, etc.).</li>
</ul>
Physical Requirements/Working Environment
The position requires lifting (up to 40 pounds), prolonged standing, repetitive bending and reaching, and periodic exposure to refrigerated conditions to retrieve samples. Primary activities are performed in a laboratory where employees routinely use numerous chemical compounds, reagents, gases, acids and bases.
Compensation and Benefits
Compensation for the position is based on individual experience and qualifications. DBE offers competitive pay, paid vacation and holidays, health/dental insurance, and life insurance. DBE is an equal opportunity employer.
Submission
Please email your resume and cover letter by May 14, 2025.
 
We would like to thank all applicants for their interest. However, only those selected for an interview will be contacted.

Chemist

<h3>Job Description</h3>
Job DescriptionCompany Description 
<ul>
<li>Katalyst Healthcares &amp; Life Sciences is hiring entry level candidates for several positions for contract research in Clinical trials of drugs, biologics and medical devices.</li>
<li>We have a few immediate job opportunities available in Drug Safety and Pharmacovigilance and Clinical Research field. We work with University hospitals, pharmaceutical companies and recruiting partners.</li>
</ul>
Job Description 
Job description: Uses scientific education and analytical chemistry experience to perform simple to moderately complex laboratory testing within a good manufacturing practices laboratory to generate results. Interprets data output to determine conformance to specifications. Acts as a team member in the API/ Raw Material/ In-Process/Drug Product testing laboratories. Responsibilities:
<ul>
<li>Independently performs and verifies a multitude of laboratory techniques for which they are trained on while adjusting to unforeseen technical or logistical obstacles to accomplish assignments.</li>
<li>Understands multiple laboratory techniques and principles and can independently trouble-shoot and resolve analytical techniques and instrument issues.</li>
<li>Takes initiative to be a key player in team activities and decision making including proactive identification, development, and implementation of improvement plans.</li>
<li>Budgets their time independently and effectively to carry out assigned tasks and makes recommendations for improvement.</li>
<li>Recognizes obstacles to completion of assigned testing and can independently resolve them. Consistently achieves commitments despite obstacles.</li>
<li>Takes ownership of special projects as needed to support overall laboratory needs and requirements.</li>
<li>Communicates proactively with supervisor and team members on frequent basis to ensure timely product release.</li>
<li>Interfaces with regulatory agencies during audit activities as needed.</li>
</ul>
Requirements:
<ul>
<li>Bachelor's Degree in the sciences with 0-4 years of laboratory experience.</li>
<li>Associate degree with at least 3 years of laboratory experience.</li>
<li>Flexibility in shift and workdays highly desirable.</li>
<li>Ability to work with general supervision but effectively manages their own time to multi-task based upon their completed training matrix.</li>
<li>Good interpersonal, documentation, and communication skills.</li>
<li>Desired technical competencies (not all required): LC, LCMS, GC, GCMS, ICP, Empower, Karl Fischer, dissolution, IR, titrations, and common wet chemical testing.</li>
</ul>
Top skills:
<ul>
<li>attention to detail.</li>
<li>direct lab experience.</li>
<li>GMP experience.</li>
<li>problem solving skills.</li>
</ul>
Additional Information 
All your information will be kept confidential according to EEO guidelines.

Chemist I

<h3>Job Description</h3>
Job Descriptionjob summary: 
The level I Chemist will perform standard chemical and physical analysis of inner and outer nutritional products in the quality control lab using wet chemistry techniques and instrumental analyses.
 location: Winston Salem, North Carolina job type: Temporary salary: $18 - 21 per hour work hours: 8 to 4 education: No Degree Required responsibilities: 
<ul>
<li>Performs qualitative and quantitative chemical and physical analysis of raw materials and finished products.</li>
<li>Prepares standards and reagents; calibrates and operates sophisticated laboratory instrumentation such as HPLC, FTIR, UV- Visible spectrophotometer.</li>
<li>Interprets test results and compares with determined standards and limits.</li>
<li>Interprets and compares data and historical records and trend verification under general supervision - Solves practical problems and carry out responsibilities under general supervision.</li>
<li>Documents data in lab notebook and follow basic cGMP guidelines.</li>
<li>Assists laboratory staff by training chemists and laboratory technicians as needed.</li>
<li>Reviews product certificates of analysis for accuracy and conformance and maintain C of A files.</li>
<li>Maintains a safe, clean and efficient laboratory.</li>
</ul>
 qualifications: 
Required:
<ul>
<li>Hands on lab experience with HPLC, FTIR, UV- Visible spectrophotometer</li>
<li> Ability to follow basic cGMP guidelines </li>
</ul>
#LI-HK1
 skills: HPLC, Chemistry, GMP (Good Manufacturing Practice) 
 Equal Opportunity Employer: Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status. At Randstad, we welcome people of all abilities and want to ensure that our hiring and interview process meets the needs of all applicants. If you require a reasonable accommodation to make your application or interview experience a great one, please contact <a href="mailto:HRsupport@randstadusa.com" target="_blank">HRsupport@randstadusa.com</a>. Pay offered to a successful candidate will be based on several factors including the candidate's education, work experience, work location, specific job duties, certifications, etc. In addition, Randstad offers a comprehensive benefits package, including health, an incentive and recognition program, and 401K contribution (all benefits are based on eligibility). This posting is open for thirty (30) days.

<h3>Job Description</h3>
Job Description
Description:
<ul>
<li>
Uses scientific education and analytical chemistry experience to perform simple to moderately complex laboratory testing within a good manufacturing practices laboratory to generate results.
</li>
<li>
Interprets data output to determine conformance to specifications.
</li>
<li>
Acts as a team member in the API/ Raw Material/ In-Process/Drug Product testing laboratories.
</li>
<li>
Independently performs and verifies a multitude of laboratory techniques for which they are trained on while adjusting to unforeseen technical or logistical obstacles to accomplish assignments.
</li>
<li>
Understands multiple laboratory techniques and principles and can independently trouble-shoot and resolve analytical techniques and instrument issues.
</li>
<li>
Takes initiative to be a key player in team activities and decision making including proactive identification, development, and implementation of improvement plans.
</li>
<li>
Budgets their time independently and effectively to carry out assigned tasks and makes recommendations for improvement.
</li>
<li>
Recognizes obstacles to completion of assigned testing and can independently resolve them. Consistently achieves commitments despite obstacles.
</li>
<li>
Takes ownership of special projects as needed to support overall laboratory needs and requirements.
</li>
<li>
Communicates proactively with supervisor and team members on frequent basis to ensure timely product release.
</li>
<li>
Interfaces with regulatory agencies during audit activities as needed.
</li>
</ul>
Qualifications:
<ul>
<li>
Bachelor's Degree in the sciences with 0-4 years of laboratory experience; OR
</li>
<li>
Associate degree with at least 3 years of laboratory experience
</li>
<li>
Open to an MS degree 
</li>
<li>
Ability to work with general supervision but effectively manages their own time to multi-task based upon their completed training matrix.
</li>
<li>
Good interpersonal, documentation, and communication skills.
</li>
<li>
Desired technical competencies (not all required): LC, LCMS, GC, GCMS, ICP, Empower, Karl Fischer, dissolution, IR, titrations, and common wet chemical testing
</li>
<li>
Attention to detail
</li>
<li>
Direct lab experience
</li>
<li>
GMP experience
</li>
<li>
Problem solving skills
</li>
</ul>
Benefits:
Healthcare Insurance: Synectics offers eligible employees and their dependents healthcare coverage through BlueCross BlueShield of Illinois. Eligibility begins on the 1st day of the calendar month following 60 days of continuous full time employment with Synectics. Premiums are subsidized by Synectics. 
Dental Insurance: Synectics offers eligible employees and their dependents a dental plan through MetLife. Eligibility begins on the 1st day of the calendar month following 60 days of continuous full time employment with Synectics. 
Vision Insurance: Synectics offers eligible employees vision insurance through VSP. Eligibility begins on the 1st day of the calendar month following 60 days of continuous full time employment with Synectics.401(k) Plan: The Synectics Inc. Investment Savings Retirement Plan. Synectics offers all employees who are 21 years of age or older the opportunity to invest in the 401(k) Plan on the first enrollment date that is at least 30 days after employment begins. Enrollment dates are each January 1st, April 1st, July 1st, and October 1st.
Technical Certification Bonus: Synectics is pleased to award its employees a bonus of up to $500 for an approved professional certification. In determining the bonus amount, Synectics will consider the cost of the test(s) for any certification relating to your current position, achieved during your employment with us. Only one Certification Bonus per calendar year may be awarded per employee. Only current, active employees will be eligible to receive this bonus. It will be awarded 90 days after the Synectics office has received documentation confirming the successful completion of the certification.
Synectics is an equal opportunity employer.

<h3>Job Description</h3>
Job DescriptionJob Title: Chemist Job Location: Milwaukee, WI Job Duration: 12 Months+ Job Description:
<ul>
<li>As an integral part of our innovation team, the Chemist provides much needed new product development and scale-up capacity for the realization of R&amp;D mission. Under the supervision of a Sr. Scientist (or R&amp;D leaders), the Chemist will contribute to the new chemistry development and scale-up for a reproducible and sustainable production methods and procedures. The Chemist is expected to set a high-quality standard for accuracy, in following good laboratory practices, and in complying with all safety regulations.</li>
<li>Maintain knowledge &amp; expertise in technical areas of organic and organometallic chemistry.</li>
<li>Engage with internal innovation team in formulating project concepts.</li>
<li>Develop hands-on expertise in chemical synthesis, catalysis and Organometallic chemistry.</li>
<li>Validate technical prototypes.</li>
<li>Document all the innovation work.</li>
<li>Support product launch and post-launch follow ups.</li>
<li>Create workable and sustainable production solutions.</li>
<li>Transfer workable solutions to designated production group.</li>
<li>Provide needed technical support to production.</li>
</ul>
 Preferred Qualifications:
<ul>
<li>Work experience in chemistry R&amp;D or chemical manufacturing is preferred.</li>
<li>Experience in chemical synthesis with reasonable knowledge in catalysis, organometallics, ligand synthesis etc. is a plus.</li>
<li>Experience with catalysis screening applications is a plus.</li>
<li>Offer technical training to production group as needed.</li>
<li>Collaborate with different departments such as safety, quality, sales &amp; marketing to introduce new products &amp; processes.</li>
<li>Serve as a technical liaison with the other R&amp;D or technical groups.</li>
</ul>
 Minimum Qualifications:
<ul>
<li>Ph.D. Chemistry.</li>
</ul>
 Preferred Qualifications:
<ul>
<li>Work experience in chemistry R&amp;D or chemical manufacturing is preferred.</li>
<li>Experience in chemical synthesis with reasonable knowledge in catalysis, organometallics, ligand synthesis etc. is a plus.</li>
<li>Experience with catalysis screening applications is a plus.</li>
</ul>
 #sczr2

<h3>Job Description</h3>
Job Title: QC Scientist - Pharmaceutical Manufacturing Support \nJob Summary: \nWe are seeking a skilled and experienced QC Scientist to support the manufacturing of pharmaceutical products. The primary responsibilities include routine testing and analysis of finished products (tablets, capsules, sub-gels) and raw materials, utilizing a variety of laboratory instruments and techniques. This position requires hands-on experience with a range of analytical instruments and the ability to perform stability testing, assay testing, and other essential chemical analyses in compliance with internal SOPs and USP monographs. The ideal candidate will have a strong background in pharmaceutical testing and a proven track record working with oral solid dosage forms and raw materials. \nKey Responsibilities:\n
<ul>\n\t
<li>Routine Testing and Analysis: \n\tConduct routine analysis of finished products and raw materials, including weight, chemistry tests for raw materials, and stability sample testing under different ICH conditions.\n\t</li>
<li>Testing and Assays: \n\tPerform a range of tests, including assay, identity (ID), content uniformity, blending uniformity, impurity testing, water content determination, content resolution, disintegration, and hardness testing.\n\t</li>
<li>Instrument Proficiency: \n\tOperate and troubleshoot laboratory instruments such as HPLC, UPLC, GC, Karl Fischer, FTIR, visualization testers, and pH meters. Experience with chromatography software (e.g., Empower 3) is highly preferred.\n\t</li>
<li>Methodology Compliance: \n\tFollow approved testing procedures and methods according to internal SOPs and USP monographs. Report data accurately and promptly.\n\t</li>
<li>Data Review and Trending: \n\tConduct peer data reviews and analyze data trends to ensure consistent results. Participate in laboratory investigations using TrackWise software.\n\t</li>
<li>Collaboration and Support: \n\tAssist other scientists and laboratory personnel to ensure timely completion of projects. Support routine lab activities such as balance calibration, pH calculations, and other day-to-day tasks.\n\t</li>
<li>Stability and Medical Testing: \n\tPerform stability testing of pharmaceutical products and excipients under ICH conditions, and assist with medical testing as necessary.\n\t</li>
<li>Software Utilization: \n\tUtilize Empower 3 chromatography software for HPLC and UPLC analysis.\n</li>
</ul>
\nPosition Requirements:\n\n
<ul>\n\t
<li>Education and Experience:\n\n\t
<ul>\n\t\t</ul>
</li>
<li>4-8 years of hands-on experience in a laboratory setting, with a focus on oral solid dosage forms (tablets, capsules, sub-gels) and raw materials.\n\t\t</li>
<li>Strong working knowledge of pharmaceutical testing, including stability testing and compliance with USP standards.\n\t\t</li>
<li>Experience with laboratory instrumentation such as HPLC, UPLC, GC, Karl Fischer, FTIR, and pH meters.\n\t\t</li>
<li>Prior experience with Empower 3 software or similar chromatography software is a significant advantage.\n\t</li>
</ul>
\n\t\n\t
<ul>
<li>Skills and Knowledge:\n\t
<ul>\n\t\t</ul>
</li>
<li>Strong understanding of pharmaceutical testing methods, including assay, identity testing, content uniformity, and impurity analysis.\n\t\t</li>
<li>Ability to perform digital testing using HPLC and UPLC, and the ability to troubleshoot and calibrate equipment as needed.\n\t\t</li>
<li>Knowledge of data review processes, trending, and documentation of test results.\n\t\t</li>
<li>Ability to adhere to SOPs, USP monographs, and GMP regulations.\n\t\t</li>
<li>Strong communication and teamwork skills to collaborate with other lab personnel and ensure project completion.\n\t\n\t \n\t\t\t\t\n\t\t\t\t\t\n\t\t\t\t\n\t\t\t\t\n\t\t\t\tAs part of our promise to talent, Kelly supports those who work with us through a variety of benefits, perks, and work-related resources. Kelly offers eligible employees voluntary benefit plans including medical, dental, vision, telemedicine, term life, whole life, accident insurance, critical illness, a legal plan, and short-term disability. As a Kelly employee, you will have access to a retirement savings plan, service bonus and holiday pay plans (earn up to eight paid holidays per benefit year), and a transit spending account. In addition, employees are entitled to earn paid sick leave under the applicable state or local plan. Click here for more information on benefits and perks that may be available to you as a member of the Kelly Talent Community. 
Why Kelly® Science &amp; Clinical? 
 Kelly Science &amp; Clinical is your connection to premier scientific and clinical companies looking to hire industry experts just like you. Our team creates expert talent solutions to solve the world’s most critical challenges. Every day, we match science professionals with dream jobs that fit their skills, interests, and career goals—it’s the way we think job searching should be. Nearly 100 percent of our science recruiters have a professional background and education in science, so we know a thing or two about the science market and how to get your expertise noticed.\n\t\t\t \n\t\t\t \n\t\t\t\t\n\t\t\t\t\t\n\t\t\t\t\n\t\t\t\t\n\t\t\t\t
About Kelly
 Work changes everything. And at Kelly, we’re obsessed with where it can take you. To us, it’s about more than simply accepting your next job opportunity. It’s the fuel that powers every next step of your life. It’s the ripple effect that changes and improves everything for your family, your community, and the world. Which is why, here at Kelly, we are dedicated to providing you with limitless opportunities to enrich your life—just ask the 300,000 people we employ each year. Kelly is committed to providing equal employment opportunities to all qualified employees and applicants regardless of race, color, sex, sexual orientation, gender identity, religion, national origin, disability, veteran status, age, marital status, pregnancy, genetic information, or any other legally protected status, and we take affirmative action to recruit, employ, and advance qualified individuals with disabilities and protected veterans in the workforce. Requests for accommodation related to our application process can be directed to the Kelly Human Resource Knowledge Center. Kelly complies with the requirements of California’s state and local Fair Chance laws. A conviction does not automatically bar individuals from employment. Kelly participates in E-Verify and will provide the federal government with your Form I-9 information to confirm that you are authorized to work in the U.S. \n\t\t\t \n\t\t\t</li>
</ul>

<h3>Job Description</h3>
QC Chemist &nbsp;– Plano, TX area \n \nSeeking a detail-oriented and highly motivated QC Chemist to join the growing Quality Control team with pharmaceutical company located near Plano, TX.&nbsp; &nbsp;You will be responsible for conducting cGMP-compliant testing of pharmaceutical products and materials to ensure their quality and compliance with regulatory standards. \n \nJob Responsibilities:\n
<ul>\n\t
<li>Perform comprehensive testing on final products, in-process materials, raw materials, and stability samples according to established procedures.\n\t</li>
<li>Execute a variety of analytical testing methods, including but not limited to: \n\t
<ul>\n\t</ul>
\n\t\n\t</li>
<li>Chromatography (e.g., HPLC, UPLC, GC)\n\t</li>
<li>Spectroscopy (e.g., UV-Vis, IR)\n\t</li>
<li>Wet chemistry techniques (e.g., titrations, loss on drying)\n</li>
</ul>
\n\n
<ul>\n\t
<li>Complete and meticulously review all test records, ensuring accuracy, completeness, and adherence to Good Documentation Practices (GDP).\n\t</li>
<li>Promptly report any quality anomalies, out-of-specification (OOS) results, or deviations according to established Standard Operating Procedures (SOPs).\n\t</li>
<li>Participate in deviation and laboratory investigations, contributing to root cause analysis and corrective/preventive actions (CAPAs).\n\t</li>
<li>Draft clear and concise data summaries, including Certificates of Analysis (COA’s) and stability summary tables.\n\t</li>
<li>Contribute to the maintenance and updates of analytical methods, technical reports, and investigation documentation.\n\t</li>
<li>Prepare necessary testing reagents, standards, and maintain adequate laboratory supplies and chemicals.\n\t</li>
<li>Conduct environmental monitoring (EM) sampling within the laboratory, perform incubation, and execute associated testing.\n\t</li>
<li>Assist in the validation and/or development of analytical methods and techniques, ensuring their suitability and reliability.\n\t</li>
<li>Participate in the qualification, calibration, and maintenance of QC laboratory equipment.\n\t</li>
<li>Package and ship samples to contract testing laboratories as required, ensuring proper handling and documentation.\n\t</li>
<li>Undertake additional responsibilities and tasks as assigned by QC management to support the overall function of the Quality Control department.\n</li>
</ul>
\nRequirements:\n\n
<ul>\n\t
<li>Bachelor's degree in Chemistry, Biochemistry, Pharmaceutical Sciences, or a related scientific discipline.\n\t</li>
<li>Proven experience working in a regulated laboratory environment, preferably within the pharmaceutical or biotechnology industry.\n\t</li>
<li>Demonstrated proficiency with a variety of analytical techniques, including High-Performance Liquid Chromatography (HPLC), Mass Spectrometry (MS), and Capillary Electrophoresis (CE) methods.\n\t</li>
<li>Comprehensive understanding of current Good Manufacturing Practices (cGMPs), proper documentation practices, and data integrity principles.\n\t</li>
<li>Strong analytical and problem-solving skills with a keen attention to detail and accuracy.\n\t</li>
<li>Excellent written and verbal communication abilities, with the capacity to clearly articulate technical information.\n\t</li>
<li>Demonstrated ability to work independently and collaboratively within a team-based setting.\n\t</li>
<li>Capability to function effectively and adapt to changes in a rapidly evolving environment.\n\t</li>
<li>Strong organizational skills with the ability to balance multiple priorities simultaneously and meet deadlines.\n\t</li>
<li>Flexibility to easily switch between multiple ongoing projects and adjust priorities based on business needs.\n</li>
</ul>
\nAdditional Notes:\n\n
<ul>\n\t
<li>Direct hire with full benefits\n\t</li>
<li>Hours may vary depending on dose schedule and clinical site requirements.\n\t</li>
<li>Salary range: $60,000 - $80,000 per year, commensurate with experience.\n</li>
</ul>
\n \n&nbsp; \n\t\t\t\t\n\t\t\t\t\t\n\t\t\t\t\n\t\t\t\t\n\t\t\t\tAs part of our promise to talent, Kelly supports those who work with us through a variety of benefits, perks, and work-related resources. Kelly offers eligible employees voluntary benefit plans including medical, dental, vision, telemedicine, term life, whole life, accident insurance, critical illness, a legal plan, and short-term disability. As a Kelly employee, you will have access to a retirement savings plan, service bonus and holiday pay plans (earn up to eight paid holidays per benefit year), and a transit spending account. In addition, employees are entitled to earn paid sick leave under the applicable state or local plan. Click here for more information on benefits and perks that may be available to you as a member of the Kelly Talent Community. 
Why Kelly® Science &amp; Clinical? 
 Kelly Science &amp; Clinical is your connection to premier scientific and clinical companies looking to hire industry experts just like you. Our team creates expert talent solutions to solve the world’s most critical challenges. Every day, we match science professionals with dream jobs that fit their skills, interests, and career goals—it’s the way we think job searching should be. Nearly 100 percent of our science recruiters have a professional background and education in science, so we know a thing or two about the science market and how to get your expertise noticed.\n\t\t\t \n\t\t\t \n\t\t\t\t\n\t\t\t\t\t\n\t\t\t\t\n\t\t\t\t\n\t\t\t\t
About Kelly
 Work changes everything. And at Kelly, we’re obsessed with where it can take you. To us, it’s about more than simply accepting your next job opportunity. It’s the fuel that powers every next step of your life. It’s the ripple effect that changes and improves everything for your family, your community, and the world. Which is why, here at Kelly, we are dedicated to providing you with limitless opportunities to enrich your life—just ask the 300,000 people we employ each year. Kelly is committed to providing equal employment opportunities to all qualified employees and applicants regardless of race, color, sex, sexual orientation, gender identity, religion, national origin, disability, veteran status, age, marital status, pregnancy, genetic information, or any other legally protected status, and we take affirmative action to recruit, employ, and advance qualified individuals with disabilities and protected veterans in the workforce. Requests for accommodation related to our application process can be directed to the Kelly Human Resource Knowledge Center. Kelly complies with the requirements of California’s state and local Fair Chance laws. A conviction does not automatically bar individuals from employment. Kelly participates in E-Verify and will provide the federal government with your Form I-9 information to confirm that you are authorized to work in the U.S. \n\t\t\t \n\t\t\t

QC Chemist

<h3>Job Description</h3>
Job Description
We are looking for a highly motivated Analytical Bench Chemist with hands-on experience in at least one of the following analytical instruments: FTIR, HPLC, GC, ICP-OES, Mass Spectrometry (MS), or Ion Chromatography (IC). The ideal candidate will also have experience with wet chemistry techniques and a strong understanding of USP monographs and FDA regulatory testing.
Key Responsibilities:
<ul>
<li>Perform qualitative and quantitative analyses using various analytical techniques, including HPLC, GC, ICP-OES, MS, IC, and wet chemistry.</li>
<li>Conduct routine and non-routine testing of raw materials, in-process materials, and finished products according to USP monographs and FDA regulations.</li>
<li>Develop, validate, and optimize analytical methods for testing products.</li>
<li>Interpret analytical data and prepare detailed laboratory reports.</li>
<li>Ensure compliance with Good Manufacturing Practices (GMP), Good Laboratory Practices (GLP), FDA, and ISO standards.</li>
<li>Troubleshoot instrumentation issues and provide technical support for laboratory operations.</li>
<li>Conduct calibration, qualification, and routine maintenance of analytical instruments.</li>
<li>Maintain accurate records of laboratory activities, including sample preparation, testing protocols, and instrument maintenance logs.</li>
</ul>
Qualifications:
<ul>
<li>Bachelor’s degree in chemistry, Biochemistry, or a related field.</li>
<li>3-4 years of hands-on experience with at least one analytical instrument: HPLC, GC, ICP-OES, MS, IC, or wet chemistry techniques.</li>
<li>Familiarity with USP monographs and FDA regulatory testing procedures.</li>
<li>Strong problem-solving skills with the ability to troubleshoot instrument issues and improve method performance.</li>
<li>Experience working in a GMP/GLP regulated environment.</li>
<li>Excellent data analysis skills and experience with chromatography and spectroscopy software.</li>
<li>Strong organizational skills with attention to detail.</li>
<li>Ability to work independently and as part of a collaborative team.</li>
</ul>
Preferred Skills:
<ul>
<li>Familiarity with method development and validation techniques.</li>
<li>Experience with data acquisition software (e.g., Chromeleon, Qtegra).</li>
<li>Experience using LIMS (Laboratory Information Management System) or other data acquisition and management software.</li>
</ul>
Excellent written and verbal communication skills

<h3>Job Description</h3>
Job DescriptionBenefits: 
<ul>
<li>401(k)</li>
<li>Dental insurance</li>
<li>Health insurance</li>
<li>Paid time off</li>
<li>Vision insurance</li>
</ul>
 Bayport Laboratories LLC is a leading company in the cosmetic manufacturing industry, dedicated to producing high-quality, innovative products that meet the needs of our customers. We are seeking a motivated Quality Chemist eager to begin their career in the quality field and contribute to our commitment to excellence. Job Summary: The Quality Chemist will play a key role in supporting our quality assurance and control processes in the laboratory. This entry-level position is perfect for a chemist passionate about quality and interested in developing their expertise within the cosmetic industry. The role involves performing tests, analyzing results, and assisting in the implementation of quality protocols to ensure our products meet regulatory and industry standards. Key Responsibilities: Conduct routine testing and analysis of raw materials, in-process samples, and finished cosmetic products to ensure compliance with established quality standards. Assist in the development and validation of analytical methods specific to cosmetic formulations. Maintain accurate and detailed records of all testing procedures, results, and observations. Collaborate with production, R&amp;D, and regulatory teams to identify and resolve quality issues. Participate in internal audits and support external regulatory inspections as needed. Assist in the calibration, maintenance, and troubleshooting of laboratory equipment to ensure consistent and reliable results. Help implement and maintain quality control and assurance procedures in accordance with GMP, ISO, and other relevant cosmetic industry regulations. Contribute to continuous improvement initiatives by identifying opportunities for process optimization and efficiency in the quality department. Support the preparation, review, and revision of quality documentation, including SOPs, test methods, and batch records related to cosmetic products. Qualifications: Bachelors degree in Chemistry, Cosmetic Science, Biochemistry, or a related field. Strong interest in quality assurance and control; prior experience in a quality-related role within the cosmetic industry is a plus but not required. Basic knowledge of laboratory techniques and instrumentation, including pH , viscosity , appearance and stability test methods relevant to cosmetics. Excellent attention to detail, strong analytical skills, and a proactive approach to problem-solving. Ability to work independently as well as part of a team in a fast-paced, dynamic environment. Good communication skills, both written and verbal. Proficiency in Spanish is required; bilingual candidates preferred. Familiarity with GMP, ISO, and other cosmetic industry quality standards is preferred. What We Offer: Opportunities for professional growth and development in the quality field within the cosmetic industry. A collaborative and supportive work environment with a focus on innovation. Comprehensive training and mentorship programs to help you advance your career.

Quality Chemist

<h3>Job Description</h3>
Job Description
Red Spot Paint &amp; Varnish was founded in 1903 in Evansville, Indiana. We supply interior and exterior high performance coatings for a world of plastics and automotive markets. We pride ourselves on being a company that has continued to thrive and grow in our community for over 120 years! Red Spot strives to provide an exciting work environment and avenues to give back to our community. If you have a strong desire to work for a leading, global coatings company in the development of new, innovative products, then Red Spot is where you want to be!
We are currently seeking a skilled and detail-oriented person to join our Research &amp; Development team as a Coatings Chemist in our Evansville, IN research facility. The main purpose of this position is to develop, modify and/or improve coatings for automotive and non-automotive applications. This includes but is not limited to primers, basecoats, topcoats, and clearcoats.
Responsibilities:
<ul>
<li>Develop and formulate coatings using knowledge of chemistry and materials science.</li>
<li>Utilize DOEs to build new products and improve existing coatings.</li>
<li>Conduct laboratory experiments to optimize formulations for performance, durability, and cost-effectiveness.</li>
<li>Analyze and interpret test data and make recommendations for adjustments to formulations as needed.</li>
<li>Collaborate with internal teams to transfer products from laboratory scale to production.</li>
<li>Document and record research findings and procedures.</li>
</ul>
Qualifications:
<ul>
<li>Bachelor’s degree in chemistry or a related science discipline with at least two intermediates to advanced chemistry laboratory courses or laboratory research experience.</li>
<li>0 - 5+ years coatings experience.</li>
<li>Ability to problem solve on coatings projects and issues and adequately communicate with the supervisors.</li>
<li>Ability to pass Ishihara Test for Color Deficiency.</li>
<li>Strong analytical skills.</li>
<li>Utilization of design of experiment approach (DOE).</li>
<li>Ability to document, report, present, and interpret findings as well as design follow-up experiments for results.</li>
<li>Ability to concentrate on details and work independently.</li>
<li>Ability to learn and apply technical concepts quickly.</li>
<li>Knowledge/understanding of general chemical principles/properties.</li>
<li>Ability to apply basic statistical techniques.</li>
<li>Excellent computer skills.</li>
<li>Excellent interpersonal skills.</li>
<li>Effective oral/written communication skills.</li>
<li>Ability to organize and prioritize a variety of projects and multiple tasks in an effective and timely manner.</li>
</ul>
Red Spot offers:
<ul>
<li>Competitive pay commensurate with experience.</li>
<li>Comprehensive benefits package including health, dental, and vision insurance.</li>
<li>Retirement savings plan (401k) with company match</li>
<li>On-site &amp; near site medical clinics at no cost to employees and dependents</li>
<li>Paid Holidays and Vacation Time</li>
<li>Employee Assistance Program</li>
<li>Tuition Reimbursement</li>
<li>Long Term Disability</li>
<li>Voluntary Life Insurance for employees and dependents</li>
</ul>
Red Spot Paint &amp; Varnish Co., Inc. is an equal opportunity employer. We do not and will not discriminate against any applicant or employee based on race, religion, color, national origin, gender, gender identity, sexual orientation, age, military status, disability, genetic information, citizenship status, or any other basis prohibited by law. Red Spot Paint &amp; Varnish Co., Inc. will comply with its legal obligation to provide reasonable accommodation to qualified individuals and applicants.
For more information, visit <a href="http://www.redspot.com/careers/" target="_blank">www.redspot.com/careers/</a>
Company DescriptionRed Spot's success the past 121 years is rooted in three fundamental values - Innovation, Integrity, and Ingenuity! While the market, and our customers, are finding new products and applications for our coatings on a routine basis, the attributes they demand haven't changed—performance, function, appearance, competitiveness, quality, and availability, to name a few. Red Spot manufactures a full line of specialty, high performance coatings for plastic and select other materials, including glass, film, and metal. We tend to categorize our products offerings by cure technology—air, thermal, ultra violet, and in-mold curing, to name the most common. 
<h3>Company Description</h3>
Red Spot's success the past 121 years is rooted in three fundamental values - Innovation, Integrity, and Ingenuity! While the market, and our customers, are finding new products and applications for our coatings on a routine basis, the attributes they demand haven't changed—performance, function, appearance, competitiveness, quality, and availability, to name a few.\r\n\r\nRed Spot manufactures a full line of specialty, high performance coatings for plastic and select other materials, including glass, film, and metal. We tend to categorize our products offerings by cure technology—air, thermal, ultra violet, and in-mold curing, to name the most common.

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