quality control analyst

Premier Explosives Limited

<p><b>Company Name : Premier Explosives Limited,</b></p><p><b>Function : Quality control </b></p><p><b>Title : Quality control Analyst</b></p><p><b>Work Location : Unit : Peddakandukuru, Yadadri Bhongiri District, </b></p><p><b>Near Hyderabad 60 km from Uppal</b></p><p><b>Qualification : M.Sc Chemistry with minimum 60% marks </b></p><p><b>Experience : Fresh or 1 year experience in relevant field </b></p><p><b>Industry / domain from : Chemical Industry with Volumetric analysis experience</b></p><p><b>Age : Less than 30 years</b></p><p><b>Gender : Male</b></p><p><b>Languages known : Telugu-English-Hindi</b></p><p><b>Key Role &amp; Responsibilities : </b></p><p><b>Chemist and chemical analysis in the lab</b></p><p><b>Time line for joining : Immediately or 15 days maximum.</b></p><p><b>CTC : As per experience and company norms.</b></p><p><b>If you match the above criteria you can apply through indeed. </b></p><p>Job Types: Full-time, Permanent, Fresher</p><p>Pay: &#8377;20,000.00 - &#8377;25,000.00 per month</p><p>Benefits:</p><ul><li>Health insurance</li><li>Provident Fund</li></ul><p>Application Question(s):</p><ul><li>Are you willing to work in our Unit : Peddakandukuru, Yadadri-Bhongiri District nearly 60 Km away from Hyderabad?</li></ul><p>Education:</p><ul><li>Master's (Required)</li></ul><p>Experience:</p><ul><li>Quality Anayst : 1 year (Required)</li><li>Quality Analyst: 1 year (Required)</li></ul><p>Language:</p><ul><li>Telugu- English- Hindi  (Required)</li></ul><p>Shift availability:</p><ul><li>Day Shift (Required)</li></ul><p>Work Location: In person</p><p>Application Deadline: 18/10/2025<br/>Expected Start Date: 01/11/2025</p>

Quality Control Analyst

Sun moon Pharmaceuticals

<p>Required fresher for Quality Control</p><p>Required experiencenced for Quality Control</p><p>Job Types: Full-time, Fresher</p><p>Pay: &#8377;11,674.62 - &#8377;42,310.76 per month</p><p>Work Location: In person</p>

Ingredion

<div><p><b>About Ingredion:</b></p><p>
Join Ingredion, where innovation impacts lives worldwide! Without even realizing it, you&rsquo;ve experienced our work in your favorite chocolate, your pet&rsquo;s food, the paper you write on, and your everyday snacks. As a global powerhouse across more than 60 industries, we harness the potential of natural ingredients to transform lives. Whether you&rsquo;re just starting your career or bringing years of experience, there's a place for you here to make a real difference. Be part of our team that values a wide range of perspectives and is committed to shaping a better world with every product we create.</p><p></p><p><br>
Location: Belcamp, MD</p><p>
Workplace type: Onsite</p><p></p><p>
As an <b>Associate QC Analyst</b>, you will develop quality standards for the organization&rsquo;s raw materials, in-process products, and finished products and design new, complex, or innovative measures, tests, sampling methods, and other procedures that ensure that these standards are met.</p><p></p><p><b>
What you will do:
</b></p><ul><li>Demonstrate growing competency in organizational skills, task prioritization, written, verbal and computer skills</li><li>
Ability to work in a diverse team environment</li><li>
Follow all safety guidelines and quality systems established by Ingredion</li><li>
Perform methods from the United States Pharmacopeia (USP), American Chemical Society (ACS), Food Chemical Codex (FCC), CMMEF and other validated procedures independently</li><li>
Perform a variety of tasks and procedures in a fast-paced environment</li><li>
Maintain complete, accurate and legible test records, in accordance with Company policy and ISO requirements</li><li>
Prioritize testing based on business needs and ensure testing is performed in an appropriate and timely manner</li><li>
Collect samples for in process and/or finished products testing needs</li><li>
Disposition product against established specifications</li><li>
Assist in routine maintenance of equipment using established procedures</li><li>
Perform other work as assigned with minimal supervision</li><li>
Learn new skills and assist in the training of others</li><li>
Assist in completing investigations as assigned for OOSs, customer complaints, process upsets</li><li>
Follow 5S principles and guidelines</li></ul><p></p><p><b>
What you will bring:
</b></p><ul><li>Bachelor's degree in Chemistry, Biology, Microbiology, Food Science, or related sciences</li><li>
Possess knowledge of laboratory practices</li></ul><p></p><p><b>
Who you are:
</b></p><ul><li>Cover shifts as needed. Must be available for weekends, holidays and after-hours coverage</li><li>
Self-starter with a strong work ethic</li><li>
High level of integrity and sincerity</li><li>
Proactive and innovative with a strong will to succeed</li><li>
Ability to follow verbal and written instructions</li></ul><p></p><p><b>
Why Join Ingredion?
</b></p><p>Discover why Ingredion is the ideal place to advance your career with our exceptional rewards and benefits package designed to help you thrive. Create the future with us and enjoy:</p><ul><li><b>
Total Rewards Package</b> &ndash; Competitive salary and performance-based pay recognizing your contributions to our success</li><li><b>
Comprehensive Benefits &amp; Wellness Support</b><b> &ndash;</b> Health, long-term savings, and resources for your physical, mental, and emotional well-being</li><li>
Career Growth &ndash; Learning, training, and development opportunities, including tuition reimbursement</li><li>
Employee Recognition Program &ndash; A culture of real-time appreciation, with personalized recognition rewards globally</li><li><b>
Employee Discount Program &ndash; Provides exclusive discounts on everyday products, services, and travel</b></li></ul><p></p><p>
#LI-ONSITE</p><p>
#LI-KJ1</p><p></p><p>
We are an equal opportunity employer and value diversity at our company. Ingredion seeks to provide a work environment that is free from harassment and discrimination. We will not tolerate any form of discrimination based on race, color, religion, age, gender, gender identity, gender expression, national origin, ancestry, handicap or disability&mdash;mental or physical&mdash;marital status, sexual orientation, veteran status, disability resulting from military service, or any other classification protected by law (&ldquo;protected classifications&rdquo;). We are committed to establishing and maintaining a work environment where everyone is treated with dignity and respect.</p><p></p><p>
Ingredion provides accommodations to job applicants with disabilities throughout the hiring process. If a job applicant requires an accommodation during the application process or through the selection process, we will work with the applicant to meet the job applicant's accommodation needs.</p><p></p><p><b>
Relocation Available:</b></p>
No<p></p><p><b>
Pay Range:</b></p>
$50,000.00-$66,666.67 Annual<p></p><p>
This pay range is not a guarantee of compensation or salary. Final base salary will be determined based on several factors which may include but are not limited to responsibilities of the job, education, experience, knowledge, skills, and abilities, as well as internal equity, alignment with market data and applicable bargaining agreement (if any).</p><p></p><p><b>
Incentive Compensation:</b></p><p>
As a part of the total compensation package, this role may be eligible for the Ingredion Annual Incentive Plan or a role-specific commission/bonus.</p><p></p><p><b>
Benefits:</b></p><p>
Full-time roles are eligible for our comprehensive benefits package which includes medical, dental and vision coverage as well as a 401(k) plan with an competitive company match.</p></div>

Associate Quality Control Analyst

City of Norfolk, VA

<div><div><div><h2 class="jobSectionHeader"><b>Description</b></h2></div><br>
<p></p><div><br>
<br>
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<p>The Ryan White Part A Program is a federally funded program that funds and provides medical and supportive services for people living with HIV and AIDS. The program consists of two major components: the Planning Council and Grantee Administration. The Planning Council determines the services needed and the amount of funding dedicated to each service. The Grantee's Office is responsible for program administration.</p><p>
The CAREWare Database Coordinator will manage Ryan White Part A Program data management system; CAREWare. This position is responsible for collecting and analyzing data, interpreting and tracking trends, and preparing reports presentations while ensuring accuracy, integrity, security, and consistency of data. The Database Coordinator will also identify and resolve data-related issues, discrepancies and concerts and provide training to new and existing Part A subrecipients.</p><p><b><br>
Department Hiring Salary Range: $55,000 - $60,000</b></p></div><br>
<p></p>
<div><h2 class="jobSectionHeader"><b>Essential Functions</b></h2></div>
<p></p><div><div>Essential functions include but are not limited to:</div><br>
<ul><li>
Oversee and maintain the Norfolk TGA RWPA CAREWare data system</li><li>
Responsible for CAREWare database development and maintenance to ensure Ryan White data reporting requirements are met.</li><li>
Administer the CAREWare database, including creating user accounts, managing data entry, deleting duplicating clients, troubleshooting problems</li><li>
Recommend system-wide improvements for CAREWare</li><li>
Prepare service-specific custom data reports as needed by the Recipient, CQM, Planning Council and other Stakeholders as necessary</li><li>
Will develop and implement methodologies to enable local providers meet data reporting requirements.</li><li>
Provide CQM data-related technical assistance</li><li>
Reviews subrecipients Ryan White Services Reports (RSR) to ensure data completeness</li><li>
Provide consultation and technical assistance to Ryan White Part A subrecipients to ensure that their data collection and reporting mechanisms are in compliance with data reporting needs.</li><li>
Design procedures for the collection and evaluation of data.</li></ul></div><p></p>
<div><h2 class="jobSectionHeader"><b>Education/Experience</b></h2></div>
<p></p><div><div>Work requires knowledge of a specific vocational, administrative, or technical nature which may be obtained with a two-year associate's degree, diploma or equivalent from a college, technical, business, vocational, or correspondence school or equivalent experience. Concentration in Information Technology, Public Health, Statistics, or related area of study preferred.<br>
<br>
Two years of relevant experience in health, social, or community-based organizations serving indigent populations.</div><br>
Must possess proficient computer skills to operate business software, including Microsoft Office products.<br>
<br>
Experience with CAREWare is a plus.</div><p></p>
<div><h2 class="jobSectionHeader"><b>Additional Information &amp; Requirements</b></h2></div>
<div><p><b>Work Location: </b>741 Monticello Ave, Norfolk, VA 23510<br>
<br>
<b>Work Hours:</b> Monday-Friday; 8:30-5pm</p></div></div></div>

CAREWare Database Coordinator (Data Quality Control Analyst)

Tap Growth ai

<div>
 <strong>
  🌟 We're Hiring: Quality Control (QCO) Analyst III Contractor! 🌟
  <br/>
  <br/>
 </strong>
 We are seeking an experienced
 <strong>
  Quality Control Analyst III
 </strong>
 to ensure product quality and compliance through rigorous testing and analysis. The ideal candidate will have expertise in quality assurance methodologies, analytical testing, and regulatory standards to maintain our high-quality standards.
 <br/>
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 <strong>
  📍 Location:
 </strong>
 Norton, MA
 <br/>
 <br/>
 <strong>
  ⏰ Work Mode:
 </strong>
 Work From Office
 <br/>
 <br/>
 <strong>
  💼 Role:
 </strong>
 Quality Control (QCO) Analyst III Contractor
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 <br/>
 <strong>
  Pay Scale:
 </strong>
 Up to $95, 056 (Dependent on Experience)
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 <br/>
 <strong>
  What You'll Do
  <br/>
  <br/>
 </strong>
 <ul>
  <li>
   Perform routine and non-routine analytical and/or microbiological assays to support raw materials, in-process
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   <br/>
  </li>
 </ul>
 samples, product release, and stability studies, following established SOPs
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 <ul>
  <li>
   Support a continuous operational schedule by supporting weekend laboratory operations (Analytical,
   <br/>
   <br/>
  </li>
 </ul>
 Microbiology, Raw Materials).
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 <ul>
  <li>
   Maintain up-to-date training records, adhere to the testing schedule, and ensure the timely completion of all
   <br/>
   <br/>
  </li>
 </ul>
 assignments to support the seamless operation of QC activities and uphold the department's commitment to
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 <br/>
 meeting project timelines and quality metrics
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  <li>
   Assist in the maintenance of laboratory equipment and inventory, including the preparation of reagents and
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  </li>
 </ul>
 samples to ensure smooth laboratory operations
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  <li>
   Ensure data are reviewed timely; qualify as a data reviewer to ensure timely and efficient data availability.
   <br/>
   <br/>
  </li>
 </ul>
 <strong>
  What We're Looking For
  <br/>
  <br/>
 </strong>
 ✅ B.S. in chemistry, biology, or biochemistry, or related scientific field;
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 <br/>
 ✅ Pharmaceutical/Biotech industry experience with 4 years in a GMP Quality Control function or equivalent,
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 <br/>
 relevant industry experience
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 <br/>
 ✅ Experience in method transfer and/or analytical method implementation; solid understanding of method
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 <br/>
 lifecycle management and phase-appropriate approach is desirable
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 ✅ Demonstrated technical writing skills, with preference for technical writing of investigations
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 <br/>
 ✅ Proficient in data analysis and interpretation, with excellent attention to detail to inform decision-making
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 <em>
  <strong>
   Ready to make an impact? 🚀 Apply now and let's grow together!
  </strong>
 </em>
</div>


Quality Control Chemist / GMP QC Data Reviewer – Contract Role

Nutrifactor Laboratories (Pvt) Limited

<p>We are seeking a detail-oriented and motivated <b>QC Analyst</b> to join our team at Nutrifactor.</p><p><b>Qualification</b>: BS Chemistry or Pharm-D from a recognized university</p><p><b>Experience</b>: 1 to 3 years in HPLC operations</p><p><b>Responsibilities:</b></p><ul><li>Conduct testing using HPLC and UV methods.</li><li>Perform thorough RAW material testing to ensure compliance with quality standards.</li><li>Execute finishing testing procedures for the final product.</li><li>Monitor and analyses product samples to ensure they meet quality specifications.</li><li>Conduct routine inspections and audits to identify areas for improvement.</li><li>Ensure adherence to safety protocols and quality control regulations.</li><li>Maintain accurate records of testing, inspections, and results.</li><li>Identify and report any deviations from established quality standards.</li><li>Assist in the development and implementation of quality control procedures.</li><li>Provide training to lab technicians and other relevant staff.</li><li>Collaborate with cross-functional teams to continuously improve quality processes.</li></ul><p><b>Requirements:</b></p><ul><li>Strong knowledge of RAW material testing.</li><li>Proficiency in finishing testing processes.</li><li>Ability to handle multiple tasks simultaneously.</li><li>Excellent organizational and multitasking skills.</li><li>Effective written and verbal communication for preparing daily reports</li></ul><p><b>Note</b>: This position is based in Khurrianwala, Faisalabad. Only apply if you are willing to relocate or are currently residing in the area.</p><p>Job Type: Full-time</p><p>Work Location: In person</p>

QC Analyst

Newport Medical Solutions

<div><div><b>Job Title: Quality Analyst - Charge Entry</b></div><div><b>
Years of Experience: 2 -4 years</b></div><div><b>
Shift Timings: day shift (9:00 AM to 6:00 PM)</b></div><div><b>
Location: Hyderabad, Telangana</b></div><div>
</div><div><b>
Job Description</b></div><div></div><div><br>
We are seeking a highly skilled Quality Analyst with a minimum 2-4 years of experience in the Charge Entry department. The ideal candidate will be responsible for ensuring the accuracy and efficiency of charge entry processes, identifying areas for improvement, and implementing quality control measures to enhance overall performance.</div><div></div><div><b><br>
Roles and Responsibilities:</b></div><div></div><ul><li><br>
Conduct regular audits of charge entry processes to identify discrepancies and errors</li><li>Develop and implement quality control procedures to improve accuracy and efficiency</li><li>Collaborate with team members to address issues and provide training as needed</li><li>Analyze data and generate reports to track performance metrics and identify trends</li><li>Communicate findings and recommendations to management for process improvement</li><li>Stay updated on industry best practices and regulatory requirements to ensure compliance</li><li>Participate in cross-functional teams to support process improvement initiatives</li></ul><div>
</div><div><b>
Qualifications:</b></div><div></div><ul><li><br>
Bachelor's degree in healthcare administration or related field</li><li>Minimum of 2-4 years of experience in Charge Entry department</li><li>Strong analytical skills and attention to detail</li><li>Proficiency in using charge entry software and tools</li><li>Excellent communication and interpersonal skills</li><li>Ability to work independently and as part of a team</li><li>Certification in Quality Management or related field is a plus</li></ul><div>
If you meet the qualifications and are passionate about ensuring quality in charge entry processes, we encourage you to apply for this exciting opportunity.</div><div>
</div><div><b>
Additional Comments</b></div><div>
Candidate who carries different practice management systems with specialties Ortho &amp; ObGyn</div></div>

Quality Analyst - Charge Entry - CE-QA-2510-001

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Quality Control Analyst

Quality Control Analyst

Associate Quality Control Analyst

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Quality Control Chemist / GMP QC Data Reviewer – Contract Role

QC Analyst

Quality Analyst - Charge Entry - CE-QA-2510-001