qc analyst

Star Laboratories (Pvt.) Ltd.

<ul><li>Perform <b>bulk product analysis</b> as per specifications</li><li>Conduct <b>finished product (final pack) testing</b> before release</li><li>Execute <b>stability studies and testing</b> as per protocols</li><li>Prepare and maintain <b>stability reports &amp; QC documentation</b></li><li>Follow <b>SOPs, GMP, and data integrity practices</b></li><li>Operate lab instruments (<b>HPLC, UV, pH meter, etc.</b>)</li><li>Record, review, and report test results accurately</li><li>Support <b>method development / trial testing activities</b></li><li>Assist in routine lab work and audits</li></ul><p><b>Qualification &amp; Experience: </b></p><p><b>Education:</b> BS Chemistry</p><p><b>Experience:</b> Fresh / 0&ndash;1 year</p><p>Job Type: Full-time</p><p>Work Location: In person</p>

QC Analyst

Werfen

<div><div><div><h3 class="jobSectionHeader"><b>Job Information</b></h3><div>
Number</div>
<div>ICIMS-2026-10156</div>
<div>Job function</div>
<div>QA&amp;RA</div>
<div>Job type</div>
<div>Full-time</div>
<div>Location</div>
<div>Werfen - Orangeburg - 526 Route 303 Orangeburg, New York 10962 United States
</div><div>Country</div>
<div>United States</div>
<div>Shift</div>
<div>1st</div>
<h3 class="jobSectionHeader"><b>About the Position</b></h3><div><div><h4 class="jobSectionHeader"><b>
Introduction</b></h4>
<div><p><b>Werfen</b></p><p><br>
</p><p>Werfen is a growing, family-owned, innovative company founded in 1966 in Barcelona, Spain. We are a worldwide leader in specialized diagnostics in the areas of Hemostasis, Acute Care Diagnostics, Transfusion, Autoimmunity, and Transplant. Through our Original Equipment Manufacturing (OEM) business line, we research, develop, and manufacture customized assays and biomaterials. We operate directly in 30 countries, and in more than 100 territories through distributors. Our Headquarters and Technology Centers are located in the US and Europe, and our workforce is more than 7,000 strong.</p><p></p><p><br>
Our success comes from a specific focus in these rapidly evolving diagnostic areas, our commitment to customers, and our dedication to innovation and quality. We&rsquo;re passionate about providing healthcare professionals the most valuable and complete solutions to improve hospital efficiency and enhance patient care.</p></div>
</div></div><div><div><h4 class="jobSectionHeader"><b>Overview</b></h4>
<div><p><b>Position Summary:</b></p><p>
Performs analyses of Clinical Chemistry, Critical Care, Coagulation and/or Microbiology controls and reagents using various automated and manual techniques in accordance with established Quality standards and GMP requirements</p></div>
</div></div><div><div><h4 class="jobSectionHeader"><b>Responsibilities</b></h4>
<div><p><b>Key Accountabilities</b></p><p><b>
Essential Functions:</b></p><ul><li>
Performs automated and manual assays as detailed in departmental/plant SOPs and QC Monographs including raw material, in-process and finished product.</li><li>
Interprets test results against specifications and decides if assays pass or fail.</li><li>
Maintains documentation of all work performed in accordance with GMP requirements.</li><li>
Evaluates product complaints upon Team Leader or Team Champion's request.</li><li>
Performs product stability, proficiency, environmental testing and water system testing.</li><li>
Responsible for routine preventive maintenance, general trouble shooting, general cleanliness and calibration of Lab equipment.</li><li>
Updates departmental SOP's and QC Monographs as directed by Team Leader or Senior QC Analyst. Performs microbial testing per SOP's and QC Monographs.</li><li>
Orders required laboratory supplies, reagents and other consumables.</li><li>
Monitors proper storage conditions and expiration dates.</li><li>
Disposes hazardous and biohazardous materials.</li><li>
Other duties as directed by Team Leader or Sr. QC Analyst.</li><li>
Maintains samples in accordance with established procedures.</li><li>
Maintains statistical process control charts and other tracking reports</li></ul><p><b>
Budget Managed</b> (if applicable):
</p><ul><li>N/A</li></ul><p><b>
Internal Networking/Key Relationships:</b></p><ul><li>
To be determined based on department needs</li></ul><p><b>
Skills &amp; Capabilities:</b>
</p><ul><li>Functional/technical skills</li></ul><p>
The hourly wage range Werfen reasonably expects to pay for the position is $24 to $29. Compensation is reasonably based upon multiple factors including education, relevant experience, skillset, knowledge, and specific needs of the business.</p></div>
</div></div><div><div><h4 class="jobSectionHeader"><b>Qualifications</b></h4>
<div><p><b>Min Knowledge &amp; Experience Required for the Position:</b></p><ul><li>
B.S./B.A. Degree in Science or Medical Technology or equivalent required, plus 2 years clinical laboratory experience with a basic knowledge of quality control principles.</li></ul><p><b>
Physical Requirements:</b></p><ul><li>
This position requires the ability to lift and move materials per current OSHA standards.</li></ul><p><b>
International Mobility: Required:</b>
</p><ul><li>No</li></ul><p><b>
Travel requirements:</b>
</p><ul><li>No</li></ul></div><br>
</div></div><p></p><div><div><div><p>If you are interested in constantly learning and being challenged on a daily basis we encourage you to submit your resume or CV.</p><p></p><p><br>
Werfen is an Equal Opportunity employer and is committed to a diverse workplace. Werfen strictly prohibits unlawful discrimination, harassment or retaliation based upon an individual&rsquo;s race, color, religion, gender, sexual orientation, gender identity/expression, national origin/ancestry, age, mental/physical disability, medical condition, marital status, veteran status, or any other protected characteristic as defined by applicable state or federal law. If you have a disability and need an accommodation in relation to the online application process, please contact NAtalentacquisition@werfen.com for assistance.</p><p></p><p><br>
We operate directly in over 30 countries, and in more than 100 territories through distributors. Annual revenue is approximately $2 billion and more than 7,000 employees around the world comprise our Werfen team.</p><p></p><p><br>
www.werfen.com</p></div></div></div></div></div></div><p></p>

QC Analyst II

Lonza

<div><p><b>QC Analyst I - Environmental Monitoring (2nd Shift)</b></p><p><b>
Location:</b> Portsmouth, NH, USA. The actual location of this job is in Portsmouth, NH, USA.</p><p>
Join our Quality Microbial Control team on a specialized Sunday &ndash; Wednesday (1:00 PM &ndash; 11:30 PM) shift. In this role, you will support our 2k asset by performing critical environmental and utility monitoring, ensuring our manufacturing environment meets the rigorous standards required for life-saving drug production.</p><p><b>
What you will get:</b></p><ul><li><p>
An agile career and dynamic working culture.</p></li><li><p>
An inclusive and ethical workplace.</p></li><li><p>
Competitive salary and performance-based bonuses.</p></li><li><p>
401(k) matching plan.</p></li><li><p>
Competitive compensation programs that reward high performance.</p></li><li><p>
Comprehensive medical, dental, and vision insurance.</p></li></ul><p>
Access to our full list of global benefits: https://www.lonza.com/careers/benefits</p><p><b>
What you will do:</b></p><ul><li><p>
Execute routine test samples for In-Process, Lot Release, and Stability studies to support the 2k asset production schedule.</p></li><li><p>
Support the monitoring and sampling of critical utilities and HVAC systems throughout the facility to ensure a state of microbial control.</p></li><li><p>
Apply Data Integrity principles in all aspects of work, ensuring compliance with Lonza policies and cGMP standards.</p></li><li><p>
Work on assignments that are semi-routine in nature, recognizing and escalating deviations from accepted practices as required.</p></li><li><p>
Utilize laboratory computer systems and Microsoft Office (Word, Excel) to accurately record and report high-quality results.</p></li><li><p>
Take personal responsibility for safety and maintain a &quot;Quality First&quot; mindset, notifying management of any potential GMP deficiencies or process deviations.</p></li><li><p>
Act as an engaged member of the Microbial Control team, maintaining a positive attitude and ensuring all tasks are completed accurately and on time.</p></li></ul><p><b>
What we are looking for:</b></p><ul><li><p>
High School Diploma or equivalent is required. An Associate&rsquo;s Degree in Microbiology, Biochemistry, or a related Science field is preferred.</p></li><li><p>
Strong ability to interpret data and follow complex instructions within defined procedures and practices.</p></li><li><p>
A desire to learn from experience and treat errors as opportunities for professional growth.</p></li><li><p>
Commitment to adherence to cGMPs and the ability to exercise sound judgment to determine appropriate actions.</p></li><li><p>
Strong verbal and written communication skills, necessary for reporting and collaborating within a shift-based team.</p></li><li><p>
Ability to work the assigned Sunday &ndash; Wednesday, 1:00 PM &ndash; 11:30 PM shift, arriving on time and maintaining focus on manufacturing demands.</p></li></ul><p><b>
About Lonza</b></p><p>
At Lonza, our people are our greatest strength. With 30+ sites across five continents, our globally connected teams work together every day to manufacture the medicines of tomorrow. Our core values of Collaboration, Accountability, Excellence, Passion and Integrity reflect who we are and how we work together. Everyone&rsquo;s ideas, big or small, have the potential to improve millions of lives, and that&rsquo;s the kind of work we want you to be part of.</p><p>
Innovation thrives when people from all backgrounds bring their unique perspectives to the table. At Lonza, we offer equal employment opportunities to all qualified applicants regardless of race, religion, color, national origin, sex, sexual orientation, gender identity, age, disability, veteran status, or any other characteristic protected by law. If you&rsquo;re ready to help turn our customers&rsquo; breakthrough ideas into viable therapies, we look forward to welcoming you on board.</p><p><b>
Ready to shape the future of life sciences? Apply now.</b></p></div>

QC Analyst Level I - Environmental Monitoring (2nd Shift)

<ul><li>Basic knowledge of <b>stability studies (ICH guidelines preferred)</b></li><li>Strong <b>documentation and reporting skills</b></li><li>Familiarity with <b>QC instruments (HPLC, UV, etc.)</b> is a plus</li><li>Attention to detail and data accuracy</li><li>Good communication and teamwork skills</li></ul><p><b>Qualification &amp; Experience:</b></p><ul><li><b>Education:</b> BS Chemistry / M.Sc Chemistry (preferred)</li><li><b>Experience:</b> Fresh to 1 year (Fresh candidates are encouraged to apply)</li></ul><p>Job Type: Full-time</p><p>Work Location: In person</p>

QC Stability Analyst / Executive – Testing & Documentation

Goulston

<p></p><div><p><b>Join a company that has more than 75 years of experience!</b></p>
<p><b>
Goulston </b>is a market leader in the chemicals sector. While much of our experience and history is in the synthetic fibers area, we also have developed expertise in other surface modification technologies. Our mission at Goulston is to be the global leader in surface modification technologies by providing our customers with innovative products and services that are consistently superior in technology, quality, performance and value.</p><br>
<p></p>
<p><b>
We are seeking a passionate and skilled individual to take on exciting opportunities as a QC Analyst in Monroe, NC</b>. Whether you are starting your career or bringing years of experience, this is your chance to thrive in a dynamic, collaborative environment where your contributions make a global impact.</p><br>
<p></p>
<p><b>
Why Choose Goulston:</b></p>
<ul><li>
Competitive salary based on position and experience level</li><li>
Two Medical insurance plans (PPO &amp; HDHP)</li><li>
Dental &amp; Vision Insurance</li><li>
Paid time off (start off earning 1.25 days per month)</li><li>
401K with employer matching</li><li>
Defined Contribution Retirement Savings Plan</li><li>
Excellent on-going training</li><li>
Growth opportunities</li><li>
We take pride in being a good corporate citizen and supporting our community in its social, cultural, educational and environmental initiatives</li></ul><br>
<p></p>
<p><b>
JOB SUMMARY :</b></p>
<p>
Compiles, tabulates and analyzes lab test data and summarizes by creating reports that describe deviation from the product's specifications.</p>
<ul><li><b>
Night Shift Only (Sunday - Thursday; 10:00pm - 6:30am)</b></li></ul><br>
<p></p>
<p><b>
ESSENTIAL DUTIES AND RESPONSIBILITIES:
</b></p><ul><li>Complete testing in accordance to test sheet instructions for finished products, raw materials, and samples submitted to the QC Lab.</li><li>
Maintain records for all data generated; sign and date all work performed. Keep and maintain any records deemed necessary to QC operation.</li><li>
Operation and calibration of equipment as directed.
</li><li>Competent in the routine operation as indicated by written procedures for the analysis of products and raw materials for which training has been completed.</li><li>
Maintain lab through housekeeping, waste disposal and taking inventory of lab supplies.</li><li>
Performs other duties as assigned.</li></ul><br>
<p></p>
<p><b>
EDUCATION</b>:
</p><p>High school diploma or general education degree (GED).</p><br>
<p></p>
<p><b>
EXPERIENCE:</b></p>
<p>
1+ years of related quality experience, Chemical lab experience preferred.</p><br>
<p></p>
<p><b>
Ready to Build Your Career with Goulston?</b><br>
If you&rsquo;re seeking an opportunity to grow your career, APPLY TODAY! Be sure to attach your resume for consideration.</p><br>
<p></p>
<p><i>
Goulston is </i><i>a</i><i>n equal opportunity employer. All applicants will be considered for employment without attention to race, color, religion, sex, sexual orientation, gender identity, national origin, veteran or disability status.</i></p></div><p></p>

Quality Control Analyst

Julphar

<div></div><div><div><div><div><div><p>At Julphar, we are on a journey of culture transformation &amp; our mission is to provide a better quality of life for the entire family by delivering best in class solutions and real value with compassion and professionalism.</p>
<p>Our core values: Respect, Collaboration, innovation, Integrity and Compassion - Combined with a focus on diversity, inclusion, and equal opportunities - are key drivers in our aim to make a positive impact on the lives of the patients we serve, enable Talents , create a healthy work environment, and accomplish our goals through world-class research and with the compassion and commitment of our employees.</p>
<p><b>
Job Summary/Main Purpose</b></p><br>
<p></p>
<p>
The Specialist in the Quality Control division at Julphar HQ - RAK is responsible for adhering to cGMP principles and maintaining them effectively. The role involves carrying out chemical and physical analysis of finished products, raw materials, and stability samples, as well as process validation. The Specialist operates various QC equipment, follows GLP, GMP, and safety procedures, and maintains hygienic conditions in the lab. Additionally, the Specialist is responsible for entering data on SAP, recording all working data, assisting supervisors, training newly joined staff, and ensuring final products adhere to all specifications and regulations. The role also includes creating and processing HPLC &amp; GC analytical methods, performing investigations for lab incidents, and supporting external and internal audits.</p><br>
<p></p>
<p><b>
Key Responsibilities</b></p>
<ul>
<li>To adhere with the cGMP principles and to maintain them in an effective manner.</li>
<li>Responsible to carry-out chemical and physical analysis of FP/RM/Stability, process validation</li>
<li>Responsible for the operation of various QC equipment (depending on the section)</li>
<li>Prepare to follow GLP, GMP and safety procedures and maintain hygienic conditions in lab</li>
<li>Entering data on SAP.</li>
<li>Responsible for recording all working data.</li>
<li>Helps supervisors in assigned tasks</li>
<li>To ensure and follow GLP, GMP, safety procedures and maintain hygienic conditions in lab.</li>
<li>Training newly joined staff</li>
<li>Entering and checking data of analyst on SAP</li>
<li>Assist in trouble shooting and solving problems that may come up in the day-to-day operation of the department.</li>
<li>Ensure Final Products adhere to all specifications and regulations.</li>
<li>Create HPLC &amp; GC analytical methods from approved STM/Pharmacopeia for all analysts before starting analysis</li>
<li>Processing and approval for all HPLC &amp;GC analytical data for all analysts, review and check all the Audit trial for all the instruments.</li>
<li>To train the QC personnel on all the applicable procedures, specifications, testing methods and qualify analysts to perform various QC analysis.</li>
<li>To ensure the analysis is performed correctly as per applicable procedures</li>
<li>To perform investigation for the lab incidents, OOS, OOT results, deviations and take appropriate corrective and preventive actions.</li>
<li>To lock the results in SAP, to create notifications &amp; reservations for maintaining enough stock of chemicals &amp; consumables.</li>
<li>To involve and support external and internal audits and to close the audit observations on time.</li>
<li>Review and approve protocols and reports such as method validation, method transfer, process validation and stability.</li>
<li>To handle and close the Quality management system actions like Deviations, OOS, CAPAs, AMS and Change controls using Amplelogic system.</li>
<li>To follow and ensure data integrity and good documentation practices are implemented in the QC labs.</li>
<li>Apart from the above, the works assigned by the Head of the department/designee.</li></ul><br>
<p></p>
<p><b>
Core Competency</b></p>
<ul>
<li>In terms of competency, you are highly oriented with a strong sense of accountability &amp; ownership.</li>
<li>High on process compliance and implementation skills with strong attention to details.</li>
<li>Strong communication, interpersonal and problem-solving skills are required.</li>
<li>Business acumen partnered with a dedication to legality.</li>
<li>Must be able to manage tasks and priorities and easily adapt to changing situations.</li>
<li>Highly disciplined and must be organized, self-motivated to learn new learnings and implement them at workplace.</li>
<li>Must be able to work in a cross-functional environment interacting with other internal and external departments</li></ul><br>
<p></p>
<p><b>
Qualifications, Key Experiences / Functional Knowledge Requirements:</b></p><br>
<p>
</p><ul><li>Bachelor&rsquo;s degree in pharmacy/science.</li>
<li>Minimum 2 years&rsquo; experience in the same field.</li>
<li>Proficient with computer software applications.</li>
<li>Adhering to cGMP principles and maintaining them effectively.</li>
<li>Conducting chemical and physical analysis for RM, FP and stability</li>
<li>Operating various QC equipment and ensuring compliance with GLP, GMP, and safety procedures.</li>
</ul><p>
We value people from different backgrounds. Could this be your story? Apply today or visit www.Julphar.net to read more about us and the journey of Julphar</p></div></div></div></div></div><p></p>

Sr. Specialist - Quality Control

US Tech Solutions

<div>
 <p>
  <strong>
   Duration: 12 months contract
  </strong>
 </p>
 <p>
  <strong>
   Shift:
  </strong>
  <strong>
   2pm - 10pm Sunday - Wednesday or Wednesday-Saturday
  </strong>
 </p>
 <p>
  <br/>
 </p>
 <p>
  <strong>
   <u>
    Job Description:
   </u>
  </strong>
 </p>
 <p>
  First few weeks of the training will be on Dayshift schedule
 </p>
 <ul>
  <li>
   Execute QC activities, working with the day and night shift managers, including sample receipt, prioritization, and accurate entry into LIMS.
  </li>
  <li>
   Perform routine and complex analytical testing in chemistry, bioassay, and/or microbiology, including STAT testing as required.
  </li>
  <li>
   Ensure accurate, compliant documentation in accordance with GDP, GMP, and 21 CFR Part 11 requirements.
  </li>
  <li>
   Support laboratory investigations related to deviations or OOS results and communicate shift-level risks to QC leadership.
  </li>
  <li>
   Utilize electronic systems including LIMS, Biovia (LES, ELN, CIMS/CISPro), and Veeva Vault (QualityDocs, QMS).
  </li>
  <li>
   Collaborate cross-functionally to meet testing timelines and contribute to continuous improvement initiatives.
  </li>
  <li>
   Preferred - Bachelor&rsquo;s degree in a scientific discipline or equivalent experience, entry level will be considered.
  </li>
  <li>
   Experience working in a GMP-regulated environment and ability to work independently.
  </li>
 </ul>
 <p>
  <br/>
 </p>
 <p>
  <strong>
   <u>
    Basic Qualifications:
   </u>
  </strong>
 </p>
 <ul>
  <li>
   High school/GED + 2 years work experience or
  </li>
  <li>
   Associates degree and 6 months work experience or
  </li>
  <li>
   Bachelors degree
  </li>
 </ul>
 <p>
  <br/>
 </p>
 <p>
  <strong>
   <u>
    Must Have Skill Sets:
   </u>
  </strong>
 </p>
 <ul>
  <li>
   Experience working in a GMP-regulated environment
  </li>
  <li>
   Ability to work independently
  </li>
  <li>
   Laboratory or aseptic knowledge
  </li>
 </ul>
 <p>
  <br/>
 </p>
 <p>
  <strong>
   <u>
    About US Tech Solutions:
   </u>
  </strong>
 </p>
 <p>
  US Tech Solutions is a global staff augmentation firm providing a wide range of talent on-demand and total workforce solutions. To know more about US Tech Solutions, please visit www.ustechsolutions.com.
 </p>
 <p>
 </p>
 <p>
  <br/>
 </p>
 <p>
  "US Tech Solutions is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, colour, religion, sex, sexual orientation, gender identity, national origin, disability, or status as a protected veteran"
 </p>
 <p>
  <br/>
 </p>
 <p>
  <strong>
   Thanks and Regards,
  </strong>
 </p>
 <p>
  Bilal Ahmed
 </p>
 <p>
  <strong>
   Email
  </strong>
  : bilal.ahmed@ustechsolutionsinc.com
 </p>
 <p>
  <strong>
   Internal Job ID: 26-06439
  </strong>
 </p>
</div>


Quality Control Associate

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