analytical chemist

Viatris

<div>Mylan Technologies, Inc.<p></p><p>
Viatris is a global healthcare company uniquely positioned to bridge the traditional divide between generics and brands, combining the best of both to more holistically address healthcare needs globally. With a mission to empower people worldwide to live healthier at every stage of life, we provide access at scale, currently supplying high-quality medicines to approximately 1 billion patients around the world annually and touching all of life's moments, from birth to the end of life, acute conditions to chronic diseases.
</p><p></p><p>We have been included on number of award lists that demonstrate the impact we are making.
</p><p></p><p>Every day, we rise to the challenge to make a difference and here&rsquo;s how the Senior Chemist role will make an impact:</p><p></p><p>
Key responsibilities for this role include:</p><ul><li><p>
Perform general instrumental analysis.</p></li><li><p>
Calculate, check, and/or review analytical data.</p></li><li><p>
Support method development, validation and transfer though drafting and execution of associated protocols and reports.</p></li><li><p>
Perform / oversee instrument calibrations and maintenance.</p></li><li><p>
Perform troubleshooting of analytical methods, instrumentation and equipment.</p></li><li><p>
Provide training in analytical procedures and techniques.</p></li><li><p>
Completes analytical projects with limited supervision.</p></li><li><p>
Develop and implement methods for the automation of current or revised QC methods using new equipment and instrumentation.</p></li><li><p>
Document activities and check documentation of other laboratory personnel.</p></li><li><p>
Assist in the investigation of aberrant results. Provide written summary reports of such investigations.</p></li></ul><p></p><p>
The minimum qualifications for this role are:</p><ul><li><p>
Minimum of a Bachelor of Science degree and two years of experience as a chemist or equivalent. Bachelor of Science degree and 4 years of experience and proficiency of a range of analytical techniques is preferred. However, a combination of experience and/or education will be taken into consideration.</p></li><li><p>
Must possess knowledge of Various laboratory instrumentation including; dissolution baths, HPLC&rsquo;s, GC&rsquo;s, FTIR, UV-Vis Spectrophotometers, Instron, balances, pH meter, etc. Knowledge of scientific software, basic word processing, and spreadsheets.</p></li><li><p>
Ability to solve problems with a variety of concrete variables through semi-standardized solutions that require some ingenuity and analysis. Ability to draw inferences and follow prescribed and detailed procedures to solve moderately complex problems.</p></li></ul><p></p><p>
Exact compensation may vary based on skills, experience, and location. The salary range for this position is $55,000.00 - $105,000.00 USD.</p><p></p><p>
At Viatris, we offer competitive salaries, benefits and an inclusive environment where you can use your experiences, perspectives and skills to help make an impact on the lives of others.
</p><p></p><p>Viatris is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, national origin, religion, age, color, sex, sexual orientation, gender identity, gender expression, disability, or protected veteran status, or any other characteristic protected by local, state, or federal laws, rules, or regulations.</p></div><p></p>

Senior Chemist, Quality - Weekend Shift, 5:00am – 3:30pm Wed - Saturday

Ecolab

<div>
 Ecolab is seeking a Chemist to execute technical laboratory activities in support of technical platform development.
 <br/>
 <br/>
 <strong>
  What&rsquo;s In It For You
  <br/>
  <br/>
 </strong>
 <ul>
  <li>
   The opportunity to take on some of the world&rsquo;s most meaningful challenges, helping customers achieve clean water, safe food, abundant energy 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
   <br/>
   <br/>
  </li>
 </ul>
 <strong>
  What You Will Do
  <br/>
  <br/>
 </strong>
 <ul>
  <li>
   Conducts analyses and experiments on organic and inorganic substances to determine and evaluate their applications
  </li>
  <li>
   Conducts experiments to improve upon or to duplicate various materials and substances
  </li>
  <li>
   Engages in research to develop new methods of processing or production
  </li>
  <li>
   Examines potential new uses for technical platforms
  </li>
  <li>
   Assignments involve data collection, technical analysis, summarizing findings in written technical reports and at key project check points and recommendations for proceeding to project conclusions
  </li>
  <li>
   Contributes to the development of differentiated technology, products, processes, or systems
  </li>
  <li>
   Provides professional divisional support
  </li>
  <li>
   Conducts analyses and experiments in support of product applications
  </li>
  <li>
   Maintain accurate lab notebook records and file reports for experimental work.
  </li>
  <li>
   Assignments may require the development and selection of appropriate methods, tests and procedures.
  </li>
  <li>
   Develop innovative applications and extensions of existing or new products, processes, systems or methods having major importance to the business.
  </li>
  <li>
   Ensure that proprietary project innovations are protected with proper legal instruments (e.g. patents).
   <br/>
   <br/>
  </li>
 </ul>
 <strong>
  Basic Qualifications
  <br/>
  <br/>
 </strong>
 <ul>
  <li>
   Bachelor's degree in Chemistry, Biology or Biochemistry
  </li>
  <li>
   2 years of Chemistry experience
  </li>
  <li>
   Sponsorship is not offered for this role
   <br/>
   <br/>
  </li>
 </ul>
 <strong>
  Preferred Qualifications
  <br/>
  <br/>
 </strong>
 <ul>
  <li>
   Experience applying principles of scientific thinking to define problems, collect data, analyze potential solutions, and draw valid conclusions
  </li>
  <li>
   Demonstrated success in working on complex, multi-function project teams
  </li>
  <li>
   Excellent people and team building skills, interacting with a wide range of individuals and grade levels.
  </li>
  <li>
   Strong presentation skills with ability to clearly articulate technical subject matter
  </li>
  <li>
   Ability to create innovative solutions toward key application issues for the business
  </li>
  <li>
   Must have demonstrated initiative and ability to work independently and handle multiple tasks
  </li>
  <li>
   Experience in WWTP ,R.O., cooling towers and steam boilers (quality control , chemical and biological analysis and operations)
   <br/>
   <br/>
  </li>
 </ul>
 Location:
 <br/>
 <br/>
 <ul>
  <li>
   Job location King Abdullah economic city (KAEC) - Located in close proximity to Thuwal, almost 100 km (62 mi) north of Jeddah.
   <br/>
   <br/>
  </li>
 </ul>
 <strong>
  Our Commitment to a Culture of Inclusion &amp; Belonging
  <br/>
  <br/>
 </strong>
 Ecolab is committed to fair and equal treatment of associates and applicants and furthering the principles of Equal Opportunity to Employment. We will 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. Ecolab 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, or disability.
 <br/>
 <br/>
</div>


Chemist

Hikma

<p></p><div><div><div><div><div><div><div>Description:
<div><b>Location: Saudi Arabia, Riyadh</b></div>
<div><b>
Job Type: [Full-time]</b></div>
<div><b>
Hashtag: #LI-NA1</b></div><br>
<div></div>
<div><b>
About Us:</b></div>
<div>
For over 45 years, Hikma Pharmaceuticals has been putting better health within reach, every day, by creating high-quality medicines and making them accessible to those who need them. We are helping to shape a healthier world that enriches all our communities, and our global team of 9,500+ empowered employees are central to this mission.</div><br>
<div></div>
<div>
As a trusted and reliable partner of over 800 high-quality generics, specialty and branded pharmaceutical products, we are driven to improve access to medicine. Through our 29 manufacturing plants, 9 R&amp;D centers across the MENA, North America and Europe, our footprint allows us to play a critical role in serving patients.</div><br>
<div></div>
<div><b>
Description:</b></div><br>
<div></div>
<div>
We are looking for a talented <b>Quality Control Analyst </b>to join us. At Hikma you&rsquo;ll be supported by a culture of progress and belonging where people are encouraged to develop, wellbeing is prioritised and our inclusive approach values contributions from all. We&rsquo;re seeking candidates who embody our values: Innovative, driven to keep learning; Caring, genuinely compassionate in their work; and Collaborative, eager to solve problems together.</div><br>
<div></div>
<div>
If you want to be part of a team that cares about impact, this is the place for you.</div><br>
<div></div>
<p><b>
Key Responsibilities:</b></p>
<ul>
<li>Implement standard operating procedures.</li>
<li>Perform all the desired tests.</li>
<li>Follow the cGMPs, GLPs and safety precautions.</li>
<li>Follow the documentation system requirements.</li>
<li>Perform calibration &amp; calibration checks as needed.</li>
<li>Perform analytical method validation.</li>
<li>Perform in-process control tests.</li>
<li>Perform cleaning verification.</li>
<li>Perform sampling verification.</li>
<li>Perform testing.</li>
<li>Affixing quarantine / release labels.</li>
<li>Follow and preparing reagent solutions and other analytical requirements.</li>
<li>All required activities to ensure quality and quantity of work and cost effectiveness with compliance of cGMPs, GLPs and safety requirement.</li>
<li>Result recording on SAP computer system.</li>
<li>Creating and Updating certificate of analysis and method of analysis.</li></ul><br>
<div></div>
<div><b>
Qualifications:</b></div>
<div><b>
We are looking for candidates whose experience and skills align closely with the qualifications outlined below:</b></div><br>
<div></div>
<div><b>
Education: </b>Bachelor&rsquo;s degree in chemistry.</div>
<div><b>
Experience</b>: 0-3 years.</div>
<div><b>
Background:</b> Sufficient knowledge/training and experience in routine laboratory work. Sufficient knowledge &amp; experience in the use of instruments used in analytical laboratory.</div><br>
<div></div>
<div><b>
Learn more about Hikma in KSA </b><b>hikma-ksa-factsheet-aug-2025-en.pdf</b></div><br>
<div></div>
</div></div></div></div><div><div><div><div>Location:
Riyadh, SA, 11564</div></div></div></div></div></div></div><p></p>

Quality Control Analyst

Thermo Fisher Scientific

<div><p><b>Work Schedule</b></p>
Standard (Mon-Fri)<p></p><p><b>
Environmental Conditions</b></p>
Adherence to all Good Manufacturing Practices (GMP) Safety Standards, Laboratory Setting, Office<p></p><p><b>
Job Description</b></p><p></p><p>
Shift: Full-Time; Monday &ndash; Friday; 8am-5pm PT</p><p><b>
ONSITE:
</b></p><p>This is a fully onsite role based at our customer&rsquo;s site in <b><i>South San Francisco, CA.</i></b> We welcome applicants from all locations within the US. Please note that relocation assistance is not provided for this position, and any relocation costs will be the responsibility of the candidate.</p><p>
Must be legally authorized to work in the United States without sponsorship.</p><p>
Must be able to pass a comprehensive background check, which includes a drug screening.</p><p>
At Thermo Fisher Scientific, you&rsquo;ll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life - enabling our customers to make the world healthier, cleaner and safer. We provide our teams with the resources needed to achieve individual career goals while taking science a step beyond through research, development and delivery of life-changing therapies. With clinical trials conducted in 100+ countries and ongoing development of novel frameworks for clinical research through our PPD clinical research portfolio, our work spans laboratory, digital and decentralized clinical trial services. Your determination to deliver quality and accuracy will improve health outcomes that people and communities depend on &ndash; now and in the future.</p><p>
Thermo Fisher's clinical research business is a leading global contract research organization and world leader in serving science. We are passionate, deliberate, and driven by our mission &ndash; to enable our customers to make the world healthier, safer, and cleaner.</p><p>
Our Laboratories Functional Service Partnership (FSP) team plays a direct role in advancing drug development by creating sustained groups of talent within our customers&rsquo; organizations to provide long-term support. Through this collaborative approach, our professionals bring their commitment to excellence, industry knowledge, and operational strength directly into customer environments, helping to enhance capabilities and advance the delivery of life-changing therapies.</p><p><b>
Key responsibilities:</b></p><ul><li>
Initiate and maintain the lifecycle of multiple analytical instruments used in testing synthetic molecules. The lifecycle includes initial qualification, calibration, preventative maintenance, troubleshooting and repair, and decommissioning of analytical instrumentation.</li><li>
Provide support to multiple laboratories by ordering supplies, managing inventories, coordinating vendor visits, and helping to maintain GMP status for analytical instrumentation.</li><li>
Provide documentation support in the form of proof-reading, formatting, document control (Condor), and technical writing. Document Control Specialist will support documentation needs for controlled documents throughout the creation, revision, and final approval process</li><li>
Act as a change owner (Trackwise/Veeva) to create change control records for analytical equipment and documents, and review of proposed changes to documents to ensure traceability throughout the document change control process</li><li>
Ensure on-time completion of all routine activities related to instrument lifecycle (e.g., preventative maintenance activities) and change records.</li><li>
Ensure all work is completed efficiently under GMP compliance to maximize operations.</li><li>
Help ensure laboratory compliance by performing routine walk-throughs to detect and mitigate potential environmental, health and safety issues</li></ul><p><b>
Education and Experience:
</b></p><ul><li>Bachelor's degree in lab sciences such as Chemistry, Biochemistry, Material Science, Immunology, Biology, Molecular Biology or similar</li><li><b>
Assoc Scientist:</b> Previous experience that provides the knowledge, skills, and abilities to perform the job <b>(comparable to 0-2 years&rsquo;)</b></li><li><b>
Scientist: </b>Previous experience that provides the knowledge, skills, and abilities to perform the job <b>(comparable to 2-4 years&rsquo;)</b></li><li><b>
OR </b>Master's degree</li></ul><p>
In some cases, an equivalency, consisting of a combination of appropriate education, training and/or directly related experience, will be considered sufficient for an individual to meet the requirements of the role.</p><p><b>
Knowledge, Skills and Abilities:
</b></p><ul><li>Experience in the qualification, calibration, maintenance, and troubleshooting of GMP instrumentation including, but not limited to, HPLC, GC, LCMS, dissolution testers, titrators, and FTIR.</li><li>
Experience with Document Control processes preferred</li><li>
Strong word processing and proofreading skills a must.</li><li>
Extensive knowledge/experience using MS Word.</li><li>
Experience with Change Records (Trackwise/Veeva) strongly preferred</li><li>
Basic understanding of change control process</li><li>
Exceptional attention to detail and turnaround time</li><li>
Strong understanding of regulatory requirements around FDA 21 CFR Part 11, EU Annex 11, GAMP 5, GLP and GMP regulations as well as ISO 9001 QMS requirements. Experience working with lab systems (ELN, LIMS, Empower, Chemstation) and processes in a GxP environment is highly desirable</li><li>
Experience serving and developing a strong partnership with clients in a fast-paced environment</li><li>
Laboratory support for analytical chemistry laboratories</li><li>
Ability to work independently or as part of a team utilizing self-motivation, adaptability, and a positive attitude</li><li>
Strong computer skills. Strong Windows OS and permissions skills a plus</li><li>
proactive communication (oral and written); excellent organizational skills including the ability to manage project resource requirements (material, time, etc.), and ability to elevate relevant issues to appropriate leadership</li><li>
Ability to learn new techniques, perform and prioritize multiple tasks simultaneously, keep accurate records, follow instructions, and comply with company policies and procedures</li><li>
Excellent judgment, troubleshooting and problem solving skills</li><li>
Familiarity with risk based assessments and decision making is highly desirable</li></ul><p><b>
Working Environment:
</b></p><p>Below is listed the working environment/requirements for this role:</p><p>
Able to communicate, receive, and understand information and ideas with diverse groups of people in a comprehensible and reasonable manner.</p><p>
Able to work upright and stationary and/or standing for typical working hours.</p><p>
Able to lift and move objects up to 25 pounds</p><p>
Able to work in non-traditional work environments.</p><p>
Able to use and learn standard office equipment and technology with</p><p>
proficiency.</p><p>
May have exposure to potentially hazardous elements, including infectious agents, typically found in healthcare or laboratory environments.</p><p>
Able to perform successfully under pressure while prioritizing and handling multiple projects or activities.</p><p><b>
Benefits</b></p><p>
We offer competitive remuneration, annual incentive plan bonus, healthcare, and a range of employee benefits. Thermo Fisher Scientific offers employment with an innovative, forward-thinking organization, and outstanding career and development prospects. We offer an exciting company culture that stands for integrity, intensity, involvement, and innovation!</p><p></p><p><b>
Compensation and Benefits</b></p>
The hourly pay range estimated for this position based in California is $35.00&ndash;$39.50.<p></p><p>
This position may also be eligible to receive a variable annual bonus based on company, team, and/or individual performance results in accordance with company policy. We offer a comprehensive Total Rewards package that our U.S. colleagues and their families can count on, which includes:</p><ul><li><p>
A choice of national medical and dental plans, and a national vision plan, including health incentive programs</p></li><li><p>
Employee assistance and family support programs, including commuter benefits and tuition reimbursement</p></li><li><p>
At least 120 hours paid time off (PTO), 10 paid holidays annually, paid parental leave (3 weeks for bonding and 8 weeks for caregiver leave), accident and life insurance, and short- and long-term disability in accordance with company policy</p></li><li><p>
Retirement and savings programs, such as our competitive 401(k) U.S. retirement savings plan</p></li><li><p>
Employees&rsquo; Stock Purchase Plan (ESPP) offers eligible colleagues the opportunity to purchase company stock at a discount</p></li></ul><p></p><p>
For more information on our benefits, please visit: https://jobs.thermofisher.com/global/en/total-rewards</p><p></p>
This job posting is for multiple levels:<p></p>
The salary range estimated for the second level is: $26.00&ndash;$34.50</div><p></p>

FSP - Scientist - Analytical Chemistry Lab Instrument Support

ENDO INTERNATIONAL PLC

<div><p><b>Why Us?</b></p><p></p><p>
At Par Health, we believe great healthcare is built on getting the essentials right. We&rsquo;re looking for passionate, talented individuals who share our commitment to improving lives. With 4,000+ team members worldwide, we lead with pride and purpose&mdash;prioritizing quality and safety while fostering a culture of continuous improvement, accountability, and teamwork. Elevating the Essentials isn&rsquo;t just our tagline, it&rsquo;s the higher standard we live by every day.</p><p></p><p><b>
Job Description Summary</b></p><p></p>
Provides technical support at an elevated level by developing solutions to routine problems of limited scope and complexity. Depending on the laboratory area, will perform analysis on Raw Materials, Intermediates, In-Process, Finished Product, or Stability samples using established analytical methods.<p></p><p><b>
Job Description</b></p><p></p><p><b>
ESSENTIAL FUNCTIONS:
</b></p><ul><li>Follow good documentation practices for the accurate and timely documentation of all activities</li><li>
Perform wet chemistry and instrumentation testing</li><li>
Follow site HSE Policies</li><li>
Assist with establishing &amp; maintaining safe work standards in the lab</li><li>
Peer-review all levels of work</li><li>
Conducts lab investigation and root cause analysis, providing solutions to issues</li><li>
Regularly uses communication skills to exchange information, especially technical information within the lab</li></ul><p></p><p><b>
DEPARTMENT </b><b>SPECIFIC/NON-ESSENTIAL</b><b> FUNCTIONS</b><b>:</b></p><ul><li>
LIMS entry, approval, and data release of products</li><li>
Use of analytical balances, HPLC, GC, ICP, KF Titrator, IR, UV, pH Meter, volumetric glassware</li><li>
Wet testing like assay titrations, colorimetric tests, TLC, heavy metals, and sieves</li><li>
Maintain instrument readiness</li><li>
Ability to troubleshoot equipment and methods in areas of proficiency</li><li>
Trainer for all areas of proficiency</li><li>
Provides guidance and support to team members</li><li>
Design Gage R&amp;R experiments</li><li>
Identify method improvements and perform change controls</li><li>
Ordering of lab supplies</li><li>
Identification of cost savings opportunities</li><li>
Actively sustains laboratory housekeeping and identifies improvement opportunities</li><li>
Completion of hands-on and electronic training</li><li>
Participates and leads area huddles or shift meetings</li><li>
Other duties as assigned</li></ul><p></p><p><b>
MINIMUM REQUIREMENTS</b><b>:</b></p><p><i>
Education:</i></p><p>
High School Diploma or equivalent required. Bachelor's Degree in science related field (Chemistry, Biology) is preferred or Associate's Degree with equivalent combination of education, experience, and competencies accepted.</p><p></p><p><i>
Experience:</i></p><p>
Minimum 1-3 years of experience in a cGMP facility</p><p><i>
Preferred </i><i>Skills/Qualifications:</i></p><ul><li>
Adept at wet chemistry testing</li><li>
Working knowledge of analytical instrumentation and troubleshooting (GC/LC especially)</li><li>
Good technical writing and oral communication skills</li><li>
Basic computer skills and familiarity with Microsoft Office Suite</li><li>
Substantial acquaintance with and understanding of application of basic lab/analytical principles, theories and concept</li><li>
Use and/or Basic knowledge of industry practices and standards</li><li>
Use of Chromeleon or other chromatography software</li><li>
Previous Pharmaceutical experience is a plus</li></ul><p></p><p><b>
COMPETENCIES:</b></p><p>
Informing, Customer Focus, Listening, Perseverance, Organizing, function/technical skills, Peer Relationships, Comfort around Higher Management, Multi-tasking
</p><p></p><p><b>ORGANIZATIONL RELATIONSHIP/SCOPE:</b></p><p>
Reports to the Supervisor Quality Testing. Contacts involve matters of moderate importance to the organization and include R&amp;D, Marketing, Production employees including Engineers, Supervisors, and Operators, Logistics, EHS, and DEA. Infrequent customer contacts on routine matters.</p><p></p><p><b>
WORKING CONDITIONS:</b></p><ul><li>
80% Laboratory exposure to plant products, solvents and reagents, some of which are hazardous or potent compounds<ul><li>
Requires use of PPE for lab environment and potential handling of controlled substances</li><li>
Primarily standing and walking within the building, but also requires some walking between buildings, stairs, and lifting.</li></ul></li><li>
20% Office environment</li><li>
This position works 12-hour shifts on our Weekday Days schedule.</li></ul><p></p><p><b>
DISCLAIMER:</b></p><p><i>
The above statements are intended to describe the general nature and level of work being performed by employees assigned to this classification. They are not intended to be construed as an exhaustive list of all responsibilities, duties and skills require</i></p><p></p><p><b>
EEO Statement:</b></p><p></p><p>
We comply with all applicable federal, state, and local laws prohibiting discrimination and harassment, and provides equal employment opportunities (EEO) to all employees and applicants for employment without regard to race, color, religion, gender, sexual orientation, gender identity, national origin, age, disability, veteran status, or genetic information, or any other classification protected by federal, state or local law. This policy applies to all terms and conditions of employment, including recruiting, hiring, placement, promotion, termination, layoff, recall, transfer, leaves of absence, compensation and training.</p></div><p></p>

Quality Tech III

Avid Bioservices

<div><div>Looking to join a passionate team dedicated to developing and manufacturing life-saving biopharmaceuticals? Avid Bioservices is a leading clinical and commercial biologics CDMO focused on creating innovative solutions to meet the needs of our clients and improve patient outcomes.<br>
</div><div><b>Your Role:</b>
</div><div>The <b>Analyst, Quality Control</b> will perform testing and sampling to support manufacturing, validation, process development and stability studies in a GMP environment.</div><ul><li>
Perform and review routine assays for HPLC, ELISA/cell-based immunoassays, and/or electrophoresis (SDS-PAGE/IEF) with strict adherence to written analytical test procedures.</li><li>
Perform aseptic sampling, visual inspection, pH, conductivity, osmolality, and spectrophotometry.</li><li>
Review, revise and write test methods, standard operating procedures. In addition to performing QC testing, the Analyst may support validation projects, investigations, and method development projects.</li><li>
Other functions include but are not limited to writing study protocols and reports; training other analysts; working with other departments in developing, revising, and implementing QC procedures and policies.</li><li>
Knowledgeable of company cGMPs as well as industry regulations that apply to all job functions.</li><li>
Participate in regulatory inspections.</li><li>
Support continuous improvement initiatives.</li><li>
Other duties as assigned.</li></ul><div><b>
Minimum Qualifications:</b></div><ul><li>
Bachelor&rsquo;s degree in biology, biochemistry, chemistry or equivalent scientific field or a minimum of 2 years of relevant, hands-on experience working in a QC or analytical lab or equivalent combination of education/experience.</li><li>
Experience with analytical testing and equipment, writing reports/procedures/specifications, GMPs and regulatory audits are essential.</li><li>
Must be proficient with ELISA, Analytical Biochemistry or chemistry.</li></ul><div><b>
Position Type/Expected Hours of Work:</b>
</div><div>This role is a full-time onsite position. Days and hours of work are Monday through Friday, 8:00a.m. to 5:00p.m. unless otherwise stated by Supervisor. The employee must also, if instructed, have the ability to work overtime and/or weekends when necessary.</div><div></div><div><b>
Compensation:</b>
</div><div>We offer competitive compensation packages for this role, including a base salary, performance-based bonuses, and comprehensive benefits such as health, dental, and vision insurance, 401(k) matching, and paid time off.
</div><div></div><div>The compensation range for this role is $26.73-$30.00 hourly depending on experience and qualifications. Additionally, we offer opportunities for career growth and development as well as a supportive and inclusive work environment.
</div><div></div><div><b>Who you are:</b>
</div><ul><li>You have a &quot;bring it on!&quot; team player approach and an unshakable positive attitude, always ready to tackle anything that comes your way.</li></ul><ul><li>
Your written and verbal skills are out of this world, and you communicate with clarity and confidence.</li><li>
You have exceptional multitasking skills and an unparalleled attention to detail that ensure the smooth running of everything.</li><li>
You are a master at building relationships, capable of establishing connections with anyone, be it team members, clients, vendors, or suppliers.</li></ul><div><b>
Physical Demands &amp; Work Environment:</b>
</div><div>In this dynamic role, expect a blend of regular activities like sitting, standing, and walking, with occasional physically engaging tasks such as lifting objects up to 20 pounds. The work environment might expose you to electrical shocks, toxic chemicals, vibrations, or loud noise levels occasionally. However, reasonable accommodations are available to enable individuals with different abilities to perform effectively, ensuring a supportive and adaptable work setting. Your visual acuity, including close, distance, and color vision, will be essential in navigating through the diverse day-to-day demands of this position.</div></div>

Analyst, Quality Control (Airway)

Louis Dreyfus Company

<div><b>Company Description</b><p><br>
Louis Dreyfus Company is a leading merchant and processor of agricultural goods. Our activities span the entire value chain from farm to fork, across a broad range of business lines, we leverage our global reach and extensive asset network to serve our customers and consumers around the world. Structured as a matrix organization of six geographical regions and ten platforms, Louis Dreyfus Company is active in over 100 countries and employs approximately 18,000 people globally.</p><b><br>
Job Description</b><p><br>
This position ensures the safety, quality and complaints of products manufactured and distributed by a fully integrated soybean processing facility. This role is expected to perform accurate and timely lab analysis on raw materials, in-process samples, finished products, and other samples as required to support operational decisions to maintain company standards, meet regulatory requirements, and maintain food/feed safety programs.</p><p><b>
Laboratory Operations:</b></p><ul><li>
Perform and lead daily testing to ensure food safety and quality of the final product within the Quality Control laboratory of a fully integrated soybean processing facility.</li><li>
Operate all laboratory equipment and conduct routine analyses on raw materials, finished products, and inprocess samples.</li><li>
Manage multiple tasks efficiently to meet testing deadlines.</li><li>
Understand Official Methods used for testing (e.g., ASTM, EN, AOCS, USP, etc.).</li><li>
Follow established Standard Operating Procedures (SOPs) for testing methods.</li><li>
Accurately enter test data into Laboratory Information Management System (LIMS).</li><li>
Generate all Certificates of Analysis (COAs) on finished products and special COAs requested by commercial (e.g., transloads, commingles, 3rd party, customer requests, data sheets, etc.).</li><li>
Collect samples from operational areas as required (e.g., final tanks, microbiological samples, etc.).</li><li>
Collect and ship samples as needed (e.g., referee sample, customer requests, 3rd party testing, etc.).</li><li>
Maintain a clean and organized lab environment in compliance with 5S and housekeeping standards.</li><li>
Maintain skill levels as training is completed through the level progression system.</li><li>
Performs basic troubleshooting and maintenance of laboratory equipment.</li><li>
Accepts/carries out/completes other duties as assigned by the Laboratory Supervisor or Quality Manger.</li></ul><p><b>
Process Control &amp; Improvement:
</b></p><ul><li>Analyze production and certification samples and communicate results promptly to operations personnel.</li><li>
Report out of spec or out of trend results to management.</li><li>
Collect samples as required to maintain the environmental monitoring program.</li><li>
Perform ATP and allergen testing as required in operational areas to ensure cleanliness.</li><li>
Participates in cross-check testing with internal and external laboratories. Quality and Food/Feed Safety Programs:</li><li>
Comply with Good Manufacturing Practices (GMPs), Good Laboratory Practices (GLPs), and Food Safety Management Systems, including FSSC 22000.</li><li>
Understand and adhere to BQ9000 Producer Requirements and NOPA Trading Rules.</li></ul><p><b>
Equipment Used</b></p><ul><li>
Standard laboratory equipment and machinery (e.g., FTIR, GC, ICP-OES, ICP-MS Karl Fisher, NIR, analytical balance, colorimeter).</li><li>
Typical office equipment: PC, telephone, printer/scanner, fax machine.</li><li>
Personal protective equipment as required.</li></ul><br>
<b>
Qualifications</b><p><b><br>
Basic Qualifications
</b></p><ul><li>Strong analytical skills</li><li>
Ability to learn and follow testing procedures.</li><li>
Ability to handle multiple tasks with accuracy and prioritize workload.</li><li>
Proficiency with spreadsheet and word processing software, (e.g., Excel and MS Word)</li><li>
Strong mathematical skills</li><li>
Ability to work in a safe manner and follow all safety standards and procedures.</li></ul><p><b>
Preferred Qualifications</b></p><ul><li><b>
Education:</b> 2-year or 4-year technical diploma or degree in chemistry, food science, biochemistry, microbiology related field.</li><li>
Experience: 1-year or more of analytical chemistry laboratory experience in the food, feed, pharmaceuticals, food ingredients, or related industry. Consideration will be given to laboratory experience gained through the duration of the education.</li><li>
Prior quality inspection or testing experience.</li><li>
Laboratory, chemical, or quality certifications preferred.</li></ul><br>
<b>
Additional Information</b><p><br>
Additional Information for the job</p><div></div><p><b>
What We Offer</b></p><p>
We provide a dynamic and stimulating international environment, which will stretch and develop your abilities and channel your skills and expertise with outstanding career development opportunities in one of the largest and most solid private companies in the world.</p><ul><li>Comprehensive benefits program including medical, dental and vision care coverage, flexible spending account plans, employee assistance program, life insurance and disability coverage</li><li>401k with Company Match</li><li>Family Friendly Benefits including childbirth and parental leave, fertility and family building benefits</li><li>Paid Time Off (PTO) and Paid Holidays</li><li>Flexible work available (not applicable to all roles)</li></ul>
<p><b>
Diversity &amp; Inclusion</b><br>
<br>
LDC is driven by a set of shared values and high ethical standards, with diversity and inclusion being part of our DNA. LDC is an equal opportunity employer committed to providing a working environment that embraces and values diversity, equity and inclusion.<br>
<br>
LDC encourages diversity, supports local communities and environmental initiatives. We encourage people of all backgrounds to apply.</p>
<p><b>
Equal employment opportunity (EEO)</b></p><p>
Louis Dreyfus Company provides equal employment opportunities to all employees and applicants for employment and prohibits discrimination and harassment of any type without regard to race, color, religion, age, sex, national origin, disability status, genetics, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state or local laws.</p><p>
This policy applies to all terms and conditions of employment, including recruiting, hiring, placement, promotion, termination, layoff, recall, transfer, leaves of absence, compensation and training.</p>
<p><b>
Sustainability</b><br>
<br>
Sustainable value is at the heart of our purpose as a company.<br>
<br>
We are passionate about creating fair and sustainable value, both for our business and for other value chain stakeholders: our people, our business partners, the communities we touch and the environment around us</p></div>

Laboratory Technician - Nights

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