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chemist i

ADMA Biologics

<div></div><div><div><div><div><div><div><p><b>ADMA Biologics </b>is a biopharmaceutical company relentlessly committed to creating superior products for immunodeficient patients at risk for infection. It is our devotion to this underserved population that fuels us and our hands-on approach to production and development that sets us apart. If you are looking for a dynamic, innovative, growing company in the biopharmaceutical industry that is committed to excellence and integrity, then consider ADMA Biologics. We currently have an exciting opportunity available for a <b>Chemist I in Boca Raton, Florida!
</b></p></div></div></div></div><div><div><div><div>Job Title: Chemist I
</div></div></div></div><div><div><div><div>Job Description:
<div><div><div><h2 class="jobSectionHeader"><b>Position Summary<br>
</b></h2></div><p></p><div><p>The <b>Chemist I </b>will perform quality control testing of raw materials, in-process and final products; following general instructions on routine work and detailed instructions on new assignments.
</p></div></div><div><div><h2 class="jobSectionHeader"><b>Essential Functions (ES) and Responsibilities<br>
</b></h2></div><p></p><div><ul><li>Perform quality control chemistry and/or Immunoassays for raw materials, in-process and final products according to approved Standard Operating Procedures (SOPs).
</li></ul><ul><li>Perform instrument calibration or qualification according to written procedures.
</li></ul><ul><li>Perform testing as needed to generate data for method validations and other special projects, following general instructions on routine work and detailed instructions on new assignments.
</li></ul><ul><li>Fulfill requests from management for assistance in other matters as needed.
</li></ul><ul><li>Accountable for following Standard Operating Procedures (SOPs) and adhering to cGMP guidelines.
</li></ul><ul><li>Utilize cGMP practices in documentation and execution of job functions.
</li></ul><ul><li>Review documentation on trained tasks as assigned by manager.
</li></ul></div></div><div><div><h2 class="jobSectionHeader"><b>Job Responsibilities or Job Requirements
</b></h2></div></div><div></div><div><div><h2 class="jobSectionHeader"><b>Competencies
</b></h2></div><div><div>Ability to follow the cGMP&rsquo;s and procedures with great attention to detail
</div><div>Able to work in high-pressure, deadline-driven environment
</div><div>Demonstrated ability to achieve goals, overcome obstacles, and meet deadlines
</div><div>Possess time management skills and be able to balance multiple job assignments at once
</div><div>Possesses excellent oral and written communication skills with close attention to detail and accuracy to collaborate effectively with cross-functional teams and communicate findings and recommendations
</div></div></div><div><div><h2 class="jobSectionHeader"><b>Experience Requirements<br>
</b></h2></div><p></p><div><p><b>Education Requirements:
</b></p><p>B.S. in Chemistry, Biochemistry, Molecular Biology or related science discipline is required.<br>
</p><p></p><p><b>Experience Requirements:
</b></p><p>This position requires experience in a laboratory setting. Work experience in a regulated environment (FDA, EPA, etc.) is preferred.
</p></div></div><div><div><h2 class="jobSectionHeader"><b>Preferred Experience
</b></h2></div></div><div></div><div><div><h2 class="jobSectionHeader"><b>Compliance Requirements (ES)<br>
</b></h2></div><p></p><div><p>The minimum compliance expectation for this role entails strict adherence to FDA regulations and company policies governing sales and marketing activities. This includes completion of required compliance training, accurate documentation of sales interactions, and adherence to data privacy regulations. Additionally, the role requires proactive participation in compliance reviews, prompt reporting of any potential issues, and ongoing education to stay updated on relevant FDA regulations.
</p></div></div></div></div></div></div></div><div><div><div><div>Job Description Footer:
<p><b><i>In addition to competitive compensation, we offer a comprehensive benefits package including:
</i></b></p><ul><li>401K plan with employer match and immediate vesting
</li><li>Medical, Vision, Life and Dental Insurance
</li><li>Pet Insurance
</li><li>Company paid STD and LTD
</li><li>Company Paid Holidays
</li><li>3 Weeks&rsquo; Paid Time Off (within the first year)
</li><li>Tuition Assistance (after the first year)
</li><li>Easily accessible to Tri-Rail
</li>Free shuttle to the Boca Tri-Rail station<br>
<li>
</li></ul><p></p><p><b>ADMA Biologics </b>uses E-Verify to confirm the employment eligibility of all newly hired employees. To learn more about E-Verify, including your rights and responsibilities, please visit www.dhs.gov/E-Verify .<br>
</p><p></p><p><b>ADMA Biologics </b>is an Equal Opportunity Employer.
</p></div></div></div></div><div><div>Apply now</div></div></div></div>

Chemist I

University of Florida

<p></p><div><div><p><b>JOB NO:</b></p>
<div>537026</div><br>
<p><b>WORK TYPE:</b></p>
<div>Staff Full-Time</div><br>
<p><b>LOCATION:</b></p>
<div>Palm Beach</div><br>
<p><b>CATEGORIES:</b></p>
<div>Veteran's Preference Eligible, Physical/Mathematical Sciences</div><br>
<p><b>DEPARTMENT:</b></p><div>
60740000 - AG-EREC-BELLE GLADE</div></div><br>
<div>
<div><div><div><div><b>CLASSIFICATION TITLE:</b></div>
<div>
<p>Chemist I</p></div><br>
</div><br>
<div><div><b>CLASSIFICATION MINIMUM REQUIREMENTS:</b></div>
<div>
<p>Bachelor&rsquo;s degree in chemistry or a closely related field; no experience required.</p></div><br>
</div><br>
<div><div><b>JOB DESCRIPTION:</b></div>
<div>
<div>Instrumental Analysis<br>
<ul><li>Measure soil pH using a calibrated pH meter following laboratory protocols.</li><li>Perform chemical analyses using multiple analytical instruments, including:</li></ul>
o Colorimeter for rapid nutrient and parameter testing.<br>
o Discrete Analyzer for multi-parameter soil solution analysis.<br>
o Inductively Coupled Plasma (ICP) Spectrometer for elemental analysis of soil extracts.<br>
<ul><li>Operate, calibrate, and maintain analytical instruments in compliance with QC/QA standards.</li><li>Document results in laboratory records and ensure accuracy before submission.</li></ul></div>
<div>
Reagent Preparation and Soil Extractions<br>
<ul><li>Prepare chemical reagents and extraction solutions according to standard operating procedures (SOPs)
</li></ul> and safety guidelines.<br>
<ul><li>Conduct soil extractions using established methods
</li><li>Filter extracts to remove particulates prior to analytical testing.</li><li>Label and store extracts appropriately to ensure sample integrity.</li></ul></div>
<div>
Data Management and Reporting<br>
<ul><li>Enter analytical data into laboratory databases with high attention to accuracy and consistency.</li><li>Monitor QC/QA performance by reviewing calibration data, blanks, duplicates, and control samples.</li><li>Generate fertilizer recommendations based on analytical results, following laboratory guidelines.</li><li>Compile data into tables, charts, and graphs for client reports, research summaries, and presentations.</li><li>Utilize software such as Microsoft Word, Excel, and Access to manage and process laboratory data.</li></ul></div>
<div>
Sample Preparation<br>
<ul><li>Receive, log, and organize soil samples according to laboratory protocols.</li><li>Sort samples based on project requirements and testing schedules.</li><li>Dry samples in designated drying ovens to remove moisture prior to analysis.</li><li>Use mechanical and manual methods to sieve samples to specified particle size fractions.</li><li>Sift and scoop prepared samples into labeled containers for extractions and analysis.</li><li>Maintain cleanliness and prevent cross-contamination between samples during preparation.</li></ul></div>
<div>
Laboratory Maintenance and General Support<br>
<ul><li>Wash glassware to ensure contamination-free analysis.</li><li>Maintain a clean and organized laboratory workspace in compliance with safety regulations.</li><li>Assist in routine maintenance of laboratory equipment.</li><li>Support other laboratory functions and projects assigned by the Laboratory Manager.</li></ul></div></div><br>
</div><br>
<div><div><b>EXPECTED SALARY:</b></div>
<div>
<p>$23.07 hourly commensurate with education and experience</p></div><br>
</div><br>
<div><div><b>REQUIRED QUALIFICATIONS:</b></div>
<div>
<p>Bachelor&rsquo;s degree in chemistry or a closely related field; no experience required.</p></div><br>
</div><br>
<div><div><b>PREFERRED:</b></div>
<div>
<p>Experience in soil-testing and/or soil research, a good facility with common word processing and spreadsheet/charting software, and an aptitude to learn new software.</p></div><br>
</div><br>
<div><div><b>SPECIAL INSTRUCTIONS TO APPLICANTS:</b></div>
<div>
<p>In order to be considered, you must upload your cover letter and resume.</p>
<p>
Application must be submitted by 11:55 p.m. (ET) of the posting end date.</p>
<p>
This position is eligible for veteran&rsquo;s preference. If you are claiming veteran&rsquo;s preference, please upload a copy of your DD 214 Member Copy 4 with your application for consideration. See our Veteran's Preference Page for more specific information.</p></div><br>
</div><br>
<div><div><b>HEALTH ASSESSMENT REQUIRED:</b></div> <div>No</div></div></div><br>
</div>
</div><p></p><div><p><b>ADVERTISED:</b></p>
<div>04 Sep 2025</div> Eastern Daylight Time<br>
<p><b>APPLICATIONS CLOSE:</b></p>
<div><div>18 Sep 2025</div></div>
Eastern Daylight Time</div></div><p></p>

Ampac Fine Chemicals

<div><p>The Quality Control Chemist I will be responsible for analyzing and making determinations as to the quality of a product, using analytical equipment pertinent to the appropriate application of skills. This position provides solutions to a variety of technical problems of moderate scope and complexity. Work is closely supervised.</p><p>
This position is day shift, Monday through Friday. On-site required.</p><p>
Job Duties:</p><ul><li>
Analysis of bulk chemicals, pharmaceutical compounds, and environmental monitoring samples which require a comprehensive knowledge of chemistry or microbiology and laboratory techniques.</li><li>
General housekeeping including maintaining general cleanliness of laboratories and restocking reagents and laboratory consumables.</li><li>
May conduct review of peer data from less complex analysis.</li><li>
Maintain a through and neat laboratory notebook.</li><li>
Compilation of data obtained from analytical tests, analysis of the data, and reporting of results to appropriate departments.</li><li>
May be responsible for communicating status and timing of analytical testing to internal clients.</li><li>
May participate in investigations of laboratory samples and help determine appropriate corrective and preventive actions (CAPA) to address mitigation of investigation assignable cause.</li></ul><p><b>
EDUCATION AND EXPERIENCE</b></p><ul><li>
Bachelors degree Chemistry, Microbiology or Related Field required.</li><li>
0-1 years directly related technical experience or equivalent combination of education and experience.</li></ul><p><b>
COMPETENCIES/SKILLS</b></p><ul><li>
Strong interpersonal and verbal communication skills.</li><li>
Must have a high consciousness for personal and laboratory safety.</li><li>
Strong attention to detail.</li><li>
Team oriented.</li><li>
Good judgement and an understanding of chemistry theories and concepts.</li></ul><p><b>
CERTIFICATIONS and LICENSES</b></p><ul><li>
Not Applicable</li></ul><p>
This job description does not constitute a contract of employment or otherwise limit employment at will rights at any time.</p></div><p></p>

Quality Chemist I

VERO Biotech

<div>
 <strong>
  Description
 </strong>
 <strong>
  Description
  <br/>
  <br/>
 </strong>
 Performs specifically prescribed tasks of a routine nature to meet company and regulatory quality standards for a combination product (drug/device). Performs testing according to Standard Operating Procedures (SOP&rsquo;s). Exhibits basic knowledge of laboratory tests. Work is closely supervised and checked for accuracy, neatness and progression. Completes tasks accurately and timely.
 <br/>
 <br/>
 <ul>
  <li>
   Independently performs analytical testing for some release and raw material testing according to SOP&rsquo;s and / or USP methods.
  </li>
  <li>
   Ensures that all equipment used for testing purposes is within calibration and preventative maintenance schedules.
  </li>
  <li>
   Ensures that all reagents and chemicals used for testing are being stored appropriately and are within their shelf-life or expiry.
  </li>
  <li>
   Clearly and accurately records data and supporting test information related to tasks performed in lab per GDP and data integrity requirements
  </li>
  <li>
   Contributes to summary reports &amp; investigations
  </li>
  <li>
   Notifies management of any data excursions, such as out of specification results, equipment failures, and environmental conditions that could affect testing
  </li>
  <li>
   Performs daily, weekly or monthly equipment verifications, as assigned
  </li>
  <li>
   Adheres to all relevant lab safety rules / requirements for working in the laboratory as well as those specified for chemicals / reagents and equipment used for testing
  </li>
  <li>
   May be responsible for one or two areas of the lab, such as inventory management
  </li>
  <li>
   May train entry level employees on a few tasks and assays
  </li>
  <li>
   Other related duties as assigned
   <br/>
   <br/>
  </li>
 </ul>
 <strong>
  Qualifications
  <br/>
  <br/>
 </strong>
 Academic Qualification: Associate Degree (Chemistry or related field)
 <br/>
 <br/>
 Years of experience: 0-1 year
 <br/>
 <br/>
 Laboratory Skills: understanding of basic chemistry
 <br/>
 <br/>
 Quality Compliance / Good Lab Practice Experience: awareness of the importance of GxP practices (e.g. GMP, GLP, GDP, etc.)
</div>


QC Chemist I

Quagen Pharmaceuticals

<div>
 <p>
  <strong>
   POSITION SUMMARY:
  </strong>
 </p>
 <p>
  Analytical Chemist will be engaged in the different laboratory testing using a range of analytical equipment and techniques within GMP laboratory.
 </p>
 <p>
  <strong>
   MAJOR DUTIES/RESPONSIBILITIES:
  </strong>
 </p>
 <ul>
  <li>
   Perform assigned testing including but not limited to the physical, chemical tests per in-house written procedures and compendial monograph for the raw materials, active pharmaceutical ingredients, in-process, finished and stability products, using various wet chemistry, physical and instrumental techniques such as LC, GC, UV-Vis Spectrophotometer, dissolution, IR, Particle Size Analyzer, KF Auto titrator, Bulk Density, and other routine QC instruments.
  </li>
  <li>
   Document work clearly and perform tests accurately. Record data and results as specified in documentation procedures.
  </li>
  <li>
   Maintain proper laboratory logbooks, notebooks and other records all the time. Report and participate in the deviations and investigations.
  </li>
  <li>
   Comply with all regulatory/in-house requirements (may include but not limited to safety, housekeeping, laboratory chemical waste, cGMP, cGLP, documentation) when performing the assigned activity.
  </li>
 </ul>
 <p>
  &middot;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;Labels, transcribes and records documentation such as report sheets and laboratory notebooks as required by Standard Operating Procedures (SOPs).
 </p>
 <p>
  &middot;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;Perform laboratory related other duties as assigned.
 </p>
 <p>
  <strong>
   MINIMUM/PREFERRED REQUIREMENTS:
  </strong>
 </p>
 <p>
  <strong>
   Education:
  </strong>
  &nbsp;Bachelor&rsquo;s Degree in Science/Chemistry
 </p>
 <p>
  <strong>
   Experience:
  </strong>
  &nbsp;Based on the position level, must require minimum 2-10 years prior experience working in the Quality Control Laboratory in a cGMP environment, preferably in pharmaceutical industry.
 </p>
 <p>
  Hands on Empower-3 experience is plus.
 </p>
 <p>
  QC experience in Generic Pharmaceutical industries would be preferable
 </p>
 <p>
  Knowledge in Good Documentation practices. Knowledge in USP/ FDA
 </p>
 <p>
  BENEFITS: Offers a comprehensive benefits package to employees
 </p>
</div>


Analytical Chemist I/II/III

ARL Bio Pharma

<div>
 Chemist I - Analytical
 <br/>
 <br/>
 Position Summary
 <br/>
 <br/>
 Join a company where you can make a difference from day one and help make the world a better and safer place. ARL Bio Pharma provides analytical and microbiological testing for the pharmaceutical industry. Our laboratory works with pharmaceutical companies, compounding and hospital pharmacies, drug manufacturers, and raw material suppliers bringing excellence to pharmaceutical sciences and making pharmaceuticals safer. This position is a fantastic stepping-stone for those with some basic experience looking to expand their career in the interesting world of the pharmaceutical industry. The Chemist I is responsible for utilizing established methods and standard lab equipment/instrumentation (HPLC, IC) to qualitatively and quantitatively analyze routine pharmaceutical substances and formulations.
 <br/>
 <br/>
 <strong>
  Some highlights...
  <br/>
  <br/>
 </strong>
 <ul>
  <li>
   Paid Training
  </li>
  <li>
   Work in a comfortable office setting with casual dress code
  </li>
  <li>
   Have your own workspace where you can work largely independently
  </li>
  <li>
   Free Medical and Dental insurance
  </li>
  <li>
   401K Retirement with Company Match
  </li>
  <li>
   Excellent Work/Life Balance
   <br/>
   <br/>
  </li>
 </ul>
 This is a full-time role with a great benefits package.
 <br/>
 <br/>
 <strong>
  Work Schedule:
 </strong>
 7:00 am - 4:30pm
 <br/>
 <br/>
 <strong>
  Restrictions:
 </strong>
 Because of vital nature of this work, we do not allow medical marijuana cards and we do random drug testing on all of our employees.
 <br/>
 <br/>
 <strong>
  Essential Functions
  <br/>
  <br/>
 </strong>
 <ul>
  <li>
   Adhere to Quality Management System (QMS)
  </li>
  <li>
   Follow prescribed safety rules and regulations in performing all assigned duties
  </li>
  <li>
   Follow written and oral instruction
  </li>
  <li>
   Prepare reagents and solutions required for testing
  </li>
  <li>
   Perform laboratory testing and record results in compliance with cGMP&rsquo;s (if applicable) and internal QMS
  </li>
  <li>
   Work and think independently, yet share ideas and work towards team goals
  </li>
  <li>
   Use a personal computer including word processing, spreadsheets, email and database applications
  </li>
  <li>
   Express thoughts in a clear concise manner both orally and written
  </li>
  <li>
   Work to establish the ability to effectively prioritize and plan multiple work activities with varying deadlines and complexities
  </li>
  <li>
   Adherence to all ARL safety standards, protocols, policies and procedures
   <br/>
   <br/>
  </li>
 </ul>
 <strong>
  Position Requirements...
  <br/>
  <br/>
 </strong>
 <ul>
  <li>
   An associate degree in chemistry or related science with 2+ years industrial experience OR...
  </li>
  <li>
   Bachelor&rsquo;s degree in chemistry or related science with 1-2 years&rsquo; experience in the Pharmaceutical industry.
  </li>
  <li>
   Communication Proficiency
  </li>
  <li>
   Problem Solving/Analysis
  </li>
  <li>
   Organization/Multi-tasking
  </li>
  <li>
   Collaboration Skills
  </li>
  <li>
   Thoroughness
   <br/>
   <br/>
  </li>
 </ul>
 <strong>
  Work Environment...
  <br/>
  <br/>
 </strong>
 This job operates in a laboratory environment.
 <br/>
 <br/>
 <strong>
  Physical Demands...
  <br/>
  <br/>
 </strong>
 The role requires standing for prolonged periods of time; dexterity in fingers and hands to perform complex and precise manipulations; ability to walk and stoop; ability to lift and move up to 50 pounds; see in the normal visual range including the ability to distinguish colors and shades and hear in the normal audio range with or without correction.
 <br/>
 <br/>
 AAP/EEO Statement
 <br/>
 <br/>
 ARL Bio Pharma, Inc. provides equal employment opportunity to all individuals regardless of their race, color, creed, religion, gender, age, sexual orientation, gender identity, national origin, disability, veteran status, genetics or any other characteristic protected by state, federal, or local law. ARL Bio Pharma, Inc. expressly prohibits any form of workplace harassment based on race, color, creed, religion, gender, age, sexual orientation, gender identity, national origin, disability, veteran status, genetics or any other characteristic protected by state, federal, or local law. Improper interference with the ability of ARL Bio Pharma, Inc. employees to perform their job duties may result in discipline up to and including discharge. Further, the company takes affirmative action to ensure that applicants and employees are treated without regard to any of these characteristics.
 <br/>
 <br/>
 Employment Type: Full Time
 <br/>
 <br/>
 Years Experience: 1 - 3 years
 <br/>
 <br/>
 Salary: $24 - $30 Hourly
 <br/>
 <br/>
 Bonus/Commission: No
 <br/>
 <br/>
</div>


Analytical Chemist

Germer International - Pharmaceutical Recruiting

<div>
 <p>
  Our pharmaceutical client is looking for a chemist to join their growing organization! If you are someone who wants to be a part of a highly technical team, this may be the role for you!
 </p>
 <p>
  <br/>
 </p>
 <p>
  The Chemist II/III will conduct release and stability testing for pharmaceutical products with specific focus on LC and GC chromatographic analyses as well as dissolution testing.
  <strong>
  </strong>
  This position involves conducting various analytical tests to ensure the quality and performance of solid dosage forms while maintaining a high level of laboratory safety and compliance.
 </p>
 <p>
  <br/>
 </p>
 <p>
  <strong>
   Key Responsibilities
  </strong>
  :
 </p>
 <p>
  <br/>
 </p>
 <ul>
  <li>
   Prepare solid dosage samples for analysis by accurately weighing, blending, and homogenizing materials to ensure representative samples for testing.
  </li>
  <li>
   Conduct dissolution testing of solid oral drug products using USP Apparatus I and Apparatus II.
  </li>
  <li>
   Perform HPLC assays for the quantitative analysis of pharmaceutical components, including potency, purity, and samples from dissolution testing.
  </li>
  <li>
   Ensure analytical instrumentation is properly maintained.
  </li>
  <li>
   Ensure that all laboratory work complies with Good Laboratory Practices (GLP) and Good Manufacturing Practices (GMP), following established Standard Operating Procedures (SOPs).
  </li>
  <li>
   Maintain accurate and detailed records of experiments, results, and procedures in laboratory notebooks and electronic systems, ensuring data integrity.
  </li>
  <li>
   Adhere to safety protocols and participate in laboratory safety initiatives, ensuring a safe and compliant work environment.
  </li>
 </ul>
 <p>
  <br/>
 </p>
 <p>
  <strong>
   Minimum Qualifications
  </strong>
  :
 </p>
 <p>
  <br/>
 </p>
 <ul>
  <li>
   Bachelor&rsquo;s degree in chemistry with at least two (2) years of experience in the pharmaceutical industry.
  </li>
  <li>
   Hands-on experience with HPLC, GC, Dissolution, and use of Empower software
  </li>
  <li>
   Strong analytical and problem-solving skills.
  </li>
  <li>
   Excellent communication and teamwork skills.
  </li>
  <li>
   Attention to detail and commitment to maintaining data integrity.
  </li>
 </ul>
 <p>
 </p>
</div>


Explore 1677+ Chemist i in Person Jobs In Person Jobs In Person Jobs In Training Jobs In Person Jobs In Training Jobs In United States this September. Find roles across top companies and apply now to boost your career.

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Chemist I

Chemist I

Quality Chemist I

QC Chemist I

Analytical Chemist I/II/III

Analytical Chemist

Analytical Chemist