quality control chemist

Harba Solutions Inc.

<div>
 <p>
  <strong>
   Job Responsibilities:
  </strong>
 </p>
 <ul>
  <li>
   Perform qualitative and quantitative chemical analyses using techniques such as HPLC, GC, UV-Vis, FTIR, and titrations.
  </li>
  <li>
   Prepare and standardize reagents, solutions, and buffers.
  </li>
  <li>
   Conduct testing on raw materials, intermediates, and finished products according to approved methods and SOPs.
  </li>
  <li>
   Document all testing activities clearly and accurately in compliance with cGMP and ALCOA+ principles.
  </li>
  <li>
   Interpret and evaluate analytical data, ensuring results meet established specifications.
  </li>
  <li>
   Participate in method validation, equipment calibration, and troubleshooting as needed.
  </li>
  <li>
   Maintain laboratory equipment and ensure proper functioning through routine maintenance and calibration.
  </li>
  <li>
   Assist in investigations of OOS (Out of Specification), OOT (Out of Trend), and deviations.
  </li>
  <li>
   Collaborate with QA, production, and R&amp;D departments to support manufacturing and product release.
  </li>
 </ul>
 <p>
  <strong>
   Qualifications:
  </strong>
 </p>
 <ul>
  <li>
   Bachelor&rsquo;s degree in Chemistry, Biochemistry, Pharmaceutical Sciences, or related field.
  </li>
  <li>
   Minimum 2 years of hands-on experience in a QC laboratory within the pharmaceutical or biotech industry.
  </li>
  <li>
   Proficient in analytical techniques (e.g., HPLC, GC) and good laboratory practices.
  </li>
  <li>
   Solid understanding of cGMP, USP/EP, and FDA regulatory requirements.
  </li>
 </ul>
</div>


Quality Control Chemist

Cardinal Health

<div><div><p><b>Schedule: Second Shift - Anticipated Monday- Friday 3:00 pm - 12:00 am</b></p><p></p><p>
At Cardinal Health, we&rsquo;re developing the innovative products and services that make healthcare safer and more productive. Join a growing, global company genuinely committed to making a difference for our customers and communities.</p><p></p><h2 class="jobSectionHeader"><b>
What a Senior Specialist, Quality Control (Chemistry) contributes to Cardinal Health</b></h2><p>
Quality Control is responsible for the analysis and inspection of products or processes for compliance with specifications and standards.</p><ul><li>
Performs visual assessment and analytical evaluation or testing of products/processes.</li><li>
Demonstrates knowledge of testing methods, product usage, and applicable regulations and standards.</li><li>
Adheres to established policies and procedures.</li><li>
Establishes test methodology and may contribute to the development of policies and procedures.</li><li>
May provide technical guidance and training to others on SOPs and quality guidelines.</li></ul><h2 class="jobSectionHeader"><b>
Responsibilities</b></h2><ul><li>
Performs analysis of incoming materials, in-process, and product samples.</li><li>
Executes method verification, validation, and/or transfer protocols, analytical equipment qualification protocols, or computer system validation test scripts, as needed.</li><li>
Performs stability testing in alignment with stability protocols at the prescribed cadence.</li><li>
Performs laboratory investigations, change controls, deviations, and corrective/preventative actions as needed.</li><li>
Authors and optimizes SOPs, analytical testing forms, and other documents as necessary.</li><li>
Performs special projects or tasks as necessary based on skill set and/or development goals and business needs.</li><li>
Champion Quality, cGMP compliance, and EHS/Radiation Safety practices.</li><li>
Performs other job duties as assigned.</li><li>
The physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of this job.</li><li>
While performing the duties of this job, the employee is regularly required to talk or hear. The employee is frequently required to stand; walk; use hands to finger, handle or feel; and reach with hands and arms; balance; stoop, kneel, crouch or crawl. The employee must occasionally lift or move up to 25 pounds. Specific vision abilities required by the job include close vision, distance vision, color vision, peripheral vision, depth perception and the ability to adjust focus.</li><li>
The primary work environment consists of a professional office environment within a radiopharmaceutical manufacturing facility, the materials warehouse as well as the laboratory setting.</li><li>
The facility is operated under well-controlled and closely monitored conditions that are regulated by both State and Federal agencies, and that are enforced by the corporate internal quality and regulatory groups. Each staff member will receive specific training in keeping radiation exposures within regulatory guidelines and he/she will be routinely monitored for their exposure to radiation. Noise levels are considered low to moderate.</li></ul></div><h2 class="jobSectionHeader"><b>
Qualifications</b></h2><ul><li>
Bachelor&rsquo;s degree or previous work experience in a similar role or related science field preferred.</li><li>
2+ years of relevant work experience working with 21 CFR 210, 211 in the FDA regulated industry (Pharmaceutical or Medical Device) preferred.</li><li>
Has experience in authoring a variety of forms of documentation such as SOPs, Change Controls, CAPAs, Deviations and Laboratory Investigations preferred</li><li>
Proficient in Microsoft Word and Microsoft Excel and possess strong technical writing skills preferred</li></ul><p><b>
Schedule:</b></p><ul><li>
2nd Shift - Anticipated 3:00 pm - 12:00 am</li><li>
Potential to work 1st shift, to cover PTO of other analysts</li><li>
Initial training for this role will be provided on 1st shift.</li></ul><p></p><h2 class="jobSectionHeader"><b>
What is expected of you and others at this level</b></h2><ul><li>
Exhibits Cardinal Health's high ethical standards and code of conduct.</li><li>
Approaches work situations with a positive and energizing style.</li><li>
Possesses in-depth knowledge of work processes and tools within own area and can function as a Subject Matter Expert (SME) for processes, tools, and equipment.</li><li>
Gain awareness of other departments at site. Seek to understand the functions of those departments and the points of interaction between QC and your role.</li><li>
Exhibit professional conduct, respect for others, and understands how to be successful in a team environment.</li><li>
Is detail oriented, organized, has the ability to multi-task, and is self-motivated. Is aware of internal/external business issues and adapts work priorities in own area.</li><li>
Demonstrates strong communication skills. Effectively listens to and explains difficult issues to reach shared understanding and build alignment.</li><li>
Takes actions to continually improve quality and safety in daily work. Actively participates in improving work processes to meet and exceed expectations. Identifies opportunities for improvement based on process observations, outcome measures, and feedback.</li><li>
Reports errors in a timely and appropriate manner. Takes initiative and is accountable for areas of responsibility meeting regulatory requirements including but not limited to maintaining required trainings as appropriate to position requirements.</li><li>
Has the ability to act calmly and patiently when working under pressure and/conditions of stress. Maintains integrity, composure, communicates with honesty, transparency, clarity and promotes alternative perspectives.</li><li>
Actively builds relationships across functions/businesses that bring value to the company, encouraging the participation and perspectives of all team member, regardless of background.</li><li>
Identifies quality events and aids in any associated investigations.</li></ul><p></p><p><b>
Anticipated salary range:</b><b> </b>$67,500- $96,400</p><p><b>
Bonus eligible:</b><b> </b>No</p><p><b>
Benefits:</b> Cardinal Health offers a wide variety of benefits and programs to support health and well-being.</p><ul><li>
Medical, dental and vision coverage</li><li>
Paid time off plan</li><li>
Health savings account (HSA)</li><li>
401k savings plan</li><li>
Access to wages before pay day with myFlexPay</li><li>
Flexible spending accounts (FSAs)</li><li>
Short- and long-term disability coverage</li><li>
Work-Life resources</li><li>
Paid parental leave</li><li>
Healthy lifestyle programs</li></ul><p></p><p><b>
Application window anticipated to close:</b> 11/11/2025
</p><ul><li>if interested in opportunity, please submit application as soon as possible.</li></ul><p></p><p>
The salary range listed is an estimate. Pay at Cardinal Health is determined by multiple factors including, but not limited to, a candidate&rsquo;s geographical location, relevant education, experience and skills and an evaluation of internal pay equity.</p><p></p><p><i>
Candidates who are back-to-work, people with disabilities, without a college degree, and Veterans are encouraged to apply.</i></p>
<p><i>Cardinal Health supports an inclusive workplace that values diversity of thought, experience and background. We celebrate the power of our differences to create better solutions for our customers by ensuring employees can be their authentic selves each day. Cardinal Health is an Equal Opportunity/Affirmative Action employer. All qualified applicants will receive consideration for employment without regard to race, religion, color, national origin, ancestry, age, physical or mental disability, sex, sexual orientation, gender identity/expression, pregnancy, veteran status, marital status, creed, status with regard to public assistance, genetic status or any other status protected by federal, state or local law.</i></p></div>

Senior Specialist, Quality Control Chemist II

Najah Business Solutions

<p>Job Title: Chief Chemist (For Omani Only)</p><p>Educational Qualification: Bachelors/ Masters in Chemistry</p><p>Experience: 10 to 15 years of experience in Industrial chemical Analysis in Quality</p><p>Control Laboratory of a large Industry, preferably Chemical Fertiliser</p><p>or Petrochemical/ manufacturing unit.</p><p>Age: About 30 to 35 years, Male/Female candidate</p><p>Job Description: To work in SIUCI Quality Control Laboratory (QCL) as Chief Chemist</p><p>reporting to the Head of QCL department.</p><p>To be able to perform all the analyses conducted in the laboratory</p><p>and train the staff below and guide when they have doubts or</p><p>difficulties.</p><p>Analyze the deviations from normal procedure/diagnose the</p><p>problems in the analytical instruments/ deviation in the analysis</p><p>results and reporting to SM-QC for corrective action.</p><p>Implement the SOPs guidelines, periodic review and update the QHSE</p><p>documentation</p><p>Monitor the Daily Analysis Data as per Quality Plan and maintain the</p><p>record of analysis results.</p><p>Salary will be Negotiable</p><p>Job Types: Full-time, Permanent</p>

Chief Chemist (For Omani Only)

MARK INDUSTRIES

<p><b>Company Description</b></p><p><b>We are a leading stationery and manufacturing company dedicated to producing high-quality wooden pencils and related products. Our focus is on continuous innovation, ensuring superior finishes, vibrant colors, and durability in every product we deliver.</b></p><p><b>Role Description</b></p><p><b>This is a full-time on-site role for a Paint Chemist</b> located in Rawalpindi. The Paint Chemist will play a key role in developing and enhancing specialized paints used in wooden pencil manufacturing. Responsibilities include conducting laboratory tests, performing quality control assessments, and utilizing analytical skills to improve paint formulations. The role focuses on achieving high levels of shine and smooth finish for both matte and gloss coatings, as well as innovating with metallic and specialty colors. It also involves research and development (R&amp;D) activities such as designing experiments, analyzing data, and ensuring that all paint products meet required specifications and industry standards.</p><p><b>Qualifications</b></p><ul><li>Strong laboratory and analytical skills</li><li>Experience in quality control and maintaining product standards</li><li>R&amp;D capabilities, including designing and conducting experiments</li><li>Ability to develop and optimize coatings for wood surfaces (pencils) with improved shine, finish, and durability</li><li>Problem-solving and critical thinking abilities</li><li>Excellent communication and teamwork skills</li><li>Bachelor&rsquo;s degree in Chemistry, Chemical Engineering, or related field</li><li>Experience in the paint, coatings, or stationery industry is a strong plus</li></ul><p>Job Type: Full-time</p><p>Pay: Rs75,000.00 - Rs150,000.00 per month</p><p>Work Location: In person</p>

Paint Chemist

Mindlance

<div>
 <p>
  Chemist-III
 </p>
 <p>
  Duration-12months
 </p>
 <p>
  location- North Chicago, IL
 </p>
 <p>
  <br/>
 </p>
 <p>
  The Chemist is responsible for the coordination and organization of stability or reference standard studies to ensure uninterrupted daily operations associated with procurement, dispensing, studying, analyzing, and reporting of those studies while assuring compliance for Stability and Reference Standard Operations. This person will interface with various groups to request samples, resolve issues, and/or implement new studies.
 </p>
 <p>
  <br/>
 </p>
 <p>
  &bull; Provide timely stability services to ensure required studies are initiated according to filing strategies, and the needs of the business operations. This includes ensuring stability protocols are written, material is obtained for studies and placed in chambers in a timely manner. Revise studies as required to ensure no interruption or exceptions to protocols result, which includes loading, reviewing, and verifying static tables to ensure accuracy
 </p>
 <p>
  &bull; Review, analyze and trend results to detect potential significant negative or aberrant results or trends. Communicate concerns with management, customers, product quality, and laboratory personnel to ensure appropriate actions are taken and exception reports initiated. Compile clear and concise graphical and tabular data summaries.
 </p>
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  &bull; Author, review and approve change control documents.
 </p>
 <p>
  <br/>
 </p>
 <p>
  EEO:- Mindlance is an Equal Opportunity Employer and does not discriminate in employment on the basis of &ndash; Minority/Gender/Disability/Religion/LGBTQI/Age/Veterans
 </p>
</div>


Chemist

Weiman Products LLC

<div><p>Quality Control Chemist</p><p>
Onsite &ndash; Gurnee IL,</p><p><b>
Who We Are:</b></p><p>
PurposeBuilt Brands, rooted in a legacy dating back to Weiman, stands as a pioneer in crafting top-tier products for specialty surfaces. Our beloved brands, including Weiman, Goo Gone, Green Gobbler, Biokleen, Gonzo, Magic, Wright&rsquo;s, Stone Care International, Urnex, Five Star, and Micro-Scientific, are preferred choices among consumers and seasoned professionals alike.</p><p>
At PBB, we seek to hire employees who bring a level of engagement, drive, and performance that pushes business forward. We work together and are motivated by positive results, while continuously thriving in a scrappy environment. We believe our greatest assets are the talented and passionate employees who are motivated by our purposeful work. Our company may be 60 years old, but the real growth is just getting started.</p><p><b>
The Role:</b></p><p>
The Quality Control Chemist is responsible for ensuring finished products are made to quality specifications. This position will oversee the quality of a product from raw materials to finished product. The position will also be responsible for ensuring that the quality lab is maintained and sufficient to perform lab testing. The Quality Control Chemist will work directly with production, research and development, and supply chain departments.</p><p><b>
What You Will Do:</b></p><ul><li>
Perform chemical and microbial testing of batches and make adjustments as needed</li><li>
Inspect raw materials including chemicals, packaging components, and labels</li><li>
Assist Quality Technicians and production with finished product inspections</li><li>
Calibrate and maintain lab equipment</li><li>
Troubleshoot lab equipment</li><li>
Inspect and approve FDA product for release</li><li>
Assist in validation of lab equipment (IQ, OQ, PQ)</li><li>
Assist with product validations</li><li>
Maintain quality assurance lab</li><li>
Please note this job description is not designed to cover or contain a comprehensive listing of activities, duties or responsibilities that are required of the employee for this job. Duties, responsibilities, and activities may change at any time with or without notice.</li></ul><div></div><p><b><br>
What You Will Bring:</b></p><ul><li>
Bachelor&rsquo;s Degree in a science discipline or equivalent experience</li><li>
2-5 years previous lab experience</li><li>
Basic understanding of chemistry and laboratory equipment (e.g., pH meter, viscometer, UV-Vis, gas chromatograph, FTIR, auto titrator, etc.).</li><li>
Strong computer skills (proficient in MS Word, Excel, PowerPoint, and use of Access databases).</li><li>
Excellent verbal and written communication skills.</li><li>
Ability to problem solve and good math skills.</li><li>
Strong attention to detail and organizational skills.</li><li>
Understanding of manufacturing processes</li></ul><p></p><p><b><br>
Benefits:</b></p><p>
PBB offers a wide range of benefits because we understand no two employees are the same. We want our employees to feel empowered to set their day up for success, whether that's in the office or remote.</p><p><b><i>
What We Offer:</i></b></p><p></p><p><br>
Flexible work options (fully remote, hybrid, onsite)</p><p>
Generous paid time off</p><p>
Competitive salaries and bonus incentives</p><p>
401K company match</p><p>
Competitive medical, dental, &amp; vision insurance</p><p>
Pet insurance</p><p>
Annual fitness stipend</p><p>
Unmatched employee discount on all products</p><p>
Summer Hours</p><p>
LinkedIn learning membership</p><p></p><div><div><div><b><br>
Job Title:</b></div><div><br>
Quality Control Chemist</div><div><b><br>
PBB Job Code:</b></div><div><br>
QCCHEM</div></div><div><div><b><br>
Mercer Job Code:</b></div><div><br>
QLT.03.006.P20</div><div><b><br>
FLSA Status:</b></div><div><br>
Exempt</div></div><div><div><b><br>
Reports To:</b></div><div><br>
QA Manager</div><div><b><br>
Job Function:</b></div><div><br>
Quality</div></div><div><div><b><br>
Work Location:</b></div><div><br>
Somers, WI</div><div><b><br>
Travel Required:</b></div><div><br>
None</div></div></div><p></p><div><div><p><br>
Revision Number</p><p><br>
Date of Issue</p><p><br>
Author</p><p><br>
Approved by</p><p><br>
Brief Description of Change</p></div><div><p><br>
1.0</p><p><br>
6/10/2024</p><p><br>
Elem Tluczek</p><p></p><p><br>
Initial Draft</p></div></div></div><p></p>

QA Chemist Technician

Jindal Stainless

<div>
 <strong>
  Position Overview{{:}}-
  <br/>
  <br/>
 </strong>
 <strong>
  W
 </strong>
 <strong>
  e are seeking a skilled and dedicated Chemist to join our Central Quality Control team. The Chemist will be responsible for performing chemical analyses, ensuring quality control, and monitoring material composition to optimize the efficiency and output of the blast furnace and sinter plant. The role requires technical expertise in material chemistry, quality assurance, and process optimization to meet industry standards and production goals.
  <br/>
  <br/>
 </strong>
 <strong>
  Essential Duties and Responsibilities{{:}}-
  <br/>
  <br/>
 </strong>
 <strong>
  Monitor daily operation of laboratory and reporting results to all concerns
  <br/>
  <br/>
 </strong>
 <strong>
  Plan daily weekly monthly and annual maintenance required for the Instruments in the lab to ensure the availabilities through the year.
  <br/>
  <br/>
 </strong>
 <strong>
  Responsibilities{{:}}
  <br/>
  <br/>
 </strong>
 <ul>
  <li>
   Chemical Analysis of Materials{{:}}
  </li>
  <ul>
   <li>
    Collection of samples received from yard, rakes, and trucks in process and customer end samples.
   </li>
   <li>
    Thorough knowledge on Sample collection, preparation as per International standard methods.
   </li>
   <li>
    Well conversant with NABL (ISO/IEC 17025), prepare and develop and update ISO documents to comply with company policies.
   </li>
   <li>
    Plan and arrange to carry out calibration of typical Instruments to ensure accuracy of results reported.
   </li>
   <li>
    Conduct routine chemical analysis of raw materials (e.g., iron ore, limestone, coke, and fluxes) and sinter products to ensure compliance with quality specifications.
   </li>
   <li>
    Analyze blast furnace materials, including coke, sinter, slag, and hot metal, to monitor chemical properties and optimize production processes.
   </li>
   <li>
    Perform both wet chemical analysis and instrumental techniques such as XRF, ICP, OES ,C&amp;S- combustion analysis ,GC, Orsat, Microscopy and other methods as required for accurate material testing.
   </li>
   <li>
    Monitor the quality of sinter and blast furnace materials, ensuring they meet the required chemical, physical and metallurgical specifications for optimal performance.
   </li>
   <li>
    Carry out periodic inspections and tests to ensure that the sinter plant and blast furnace operations adhere to quality standards.
   </li>
   <li>
    Investigate and address any discrepancies in material quality, reporting findings and suggesting corrective actions to the production team.
   </li>
   <li>
    Maintain accurate and up-to-date records of all chemical analyses, test results, and quality control activities in both hard and soft form.
   </li>
   <li>
    Ensure strict adherence to safety protocols while handling chemicals, materials, and laboratory equipment.
   </li>
   <li>
    Comply with environmental regulations and company policies regarding waste disposal, emissions, and handling of hazardous materials.
   </li>
  </ul>
 </ul>
</div>


Junior Engineer

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