quality control analyst

Caraway Pharmaceutical

<ul><li>Perform routine and non-routine chemical and physical testing of raw materials, in-process samples, and finished products.</li><li>Conduct stability studies and prepare stability reports in compliance with guidelines.</li><li>Operate, calibrate, and troubleshoot analytical instruments such as HPLC, GC, UV-Vis, FTIR, dissolution testers.</li><li>Review test results, identify deviations and assist in root cause analysis and CAPA implementation.</li><li>Ensure strict compliance with GMP, GLP, DRAP, and pharmacopeial standards (USP/BP/EP).</li><li>Document all activities in laboratory records &amp; logbooks with accuracy and timeliness.</li><li>Participate in internal and external audits, providing required documentation and support.</li><li>Collaborate with QA, Production, and R&amp;D teams to resolve quality related issues and improve processes.</li><li>Maintain stock of reagents, chemicals, and consumables required for smooth lab operations.</li></ul>Job Type: Full-timePay: Rs40,000.00 - Rs45,000.00 per monthApplication Question(s):<ul><li>Only apply if you have 1 to 2 years of pharmaceuticals QC experience</li></ul>Experience:<ul><li>QC Analyst: 2 years (Required)</li></ul>Work Location: In person

Quality Control Analyst

Crest Pharma

We are looking for a pharmacist who is able to;<ul><li>Perform routine physical, chemical, and analytical testing of raw materials, intermediates, and finished products.</li><li>Operate and maintain laboratory equipment such as HPLC, UV-Vis spectrophotometer, dissolution apparatus, and balances.</li><li>Prepare reagents, standard solutions, and samples for analysis.</li><li>Accurately record test results in laboratory notebooks, worksheets, or electronic systems as per SOPs.</li></ul>Job Type: Full-timePay: Rs45,000.00 - Rs65,000.00 per monthAbility to commute/relocate:<ul><li>Industrial Estate: Reliably commute or planning to relocate before starting work (Preferred)</li></ul>Work Location: In person

Quality Control Analyst/Pharmacist

Swift HR World

Job Position: Quality AnalystJob Location: Vadapalani , Chennai Gender: Female only Shift: Day Shift onlyShift Time: 9:00 am - 5:30 pmWorking Days: Monday to Saturday Experience: Fresher to 6 Months experience Work type: Work From Office onlyJob Summary:We are seeking a detail-oriented Handwritten Data Entry Quality Analyst to ensure the accuracy and quality of data extracted from handwritten documents. The ideal candidate will possess strong attention to detail, excellent analytical skills, and a thorough understanding of data validation and quality control processes.Key Responsibilities:<ul><li>Review and validate data entered from handwritten documents for accuracy and completeness.</li><li>Identify and flag discrepancies, errors, and inconsistencies in data entry.</li><li>Work closely with the data entry team to provide feedback and improve data accuracy.</li><li>Develop and maintain quality control checklists and procedures for handwritten data.</li><li>Collaborate with data processing and IT teams to suggest automation or process improvements.</li><li>Ensure compliance with data privacy and confidentiality standards.</li></ul>Required Qualifications:<ul><li>High school diploma or equivalent; bachelor&rsquo;s degree preferred.</li><li>Excellent attention to detail and problem-solving skills.</li><li>Strong typing and proofreading skills.</li><li>Proficiency in using data entry tools, spreadsheets (Excel/Google Sheets), and quality tracking systems.</li><li>Ability to work independently and manage time effectively.</li></ul>Job Types: Full-time, PermanentPay: Up to &#8377;10,000.00 per monthApplication Question(s):<ul><li>Are you OK with monthly package of 10k / month? (Without ESI &amp; PF)</li></ul>Education:<ul><li>Bachelor's (Required)</li></ul>Work Location: In person

Quality Analyst

Great Learning

<div><div>Job Description
Great Learning is hiring experienced quality analysts to work full-time with us. We are looking for a Quality Analyst to join our team and help check our programs/courses that meet our organization&rsquo;s quality standards. The responsibility of quality analysts is to create and execute test plans to ensure our processes function properly. Identify and remedy problems, recommend actions to meet quality assurance standards, and ensure that industry rules and regulations are followed. Quality analysts also investigate any learner queries or complaints and ensure the user&rsquo;s expectations are met during testing before programs are consumed by the learners. Implementing and monitoring test scripts to assess functionality, reliability, performance, and quality of the service or product. We&rsquo;re looking for dependable, detail-oriented candidates with keen analytical thinking skills and the ability to adapt. If you have good communication skills and at least three years of experience in quality assurance, our company could be the perfect fit for you. 
<ul><li>
Proficient in reviewing content to align with specified standards and guidelines generating accurate edits.</li><li>
Gathering and documenting evidence of product performance during reviews in accordance with product specifications.</li><li>
Meeting weekly, monthly, and quarterly targets while promptly notifying the manager of associated risks.</li><li>
Preparing edit logs and review reports detailing error types identified by the development team.</li><li>
Identifying recurring content issues within project teams and proposing corrective and preventive actions.</li><li>
Compiling and analyzing statistical data.</li><li>
Ensuring testing processes meet user expectations.</li><li>
Drafting quality assurance policies and procedures.</li><li>
Investigating customer complaints and program-related issues.</li></ul>
</div><div>Qualifications
<div><ul><li>Years of Experience: 2 to 5 years 
</li><li>
Scrutinizing data to pinpoint patterns and opportunities for enhancement.</li><li>
Devising and executing quality control protocols.</li><li>
Working alongside internal teams to address quality concerns.</li><li>
Recording and conveying test outcomes to internal stakeholders.</li><li>
Engaging in ongoing efforts to enhance operational excellence.</li><li>
Proven work experience as a quality analyst or in a similar role.</li><li>
Experience in quality inspection, auditing, and testing.</li><li>
Document QA testing processes.</li><li>
Good communication skills, both written and verbal.</li><li>
Strong computer skills and knowledge of QA databases and applications.</li><li>
Strong analytical and problem-solving skills.</li><li>
Relevant training and/or certifications as a Quality Analyst.</li></ul></div></div></div>

noon

<div>
 
 
 Job Title:
 
 Quality Analyst
 
 
 
 Location:
 
 Gurgaon, India
 
 
 
 Reporting to:
 
 Assistant Manager Quality
 
 
 
 
 
 
 
 
 
 About noon
 
 
 
 
 
 
 We&rsquo;re building an ecosystem of digital products and services that power everyday life across the Middle East&mdash;fast, scalable, and deeply customer-centric. Our mission is to deliver to every door every day. We want to redefine what technology can do in this region, and we&rsquo;re looking for a Quality Analyst who can help us move even faster.
 
 
 
 
 
 noon&rsquo;s mission: Every door, every day.
 
 
 
 
 
 Launched in 2022, noon Minutes is noon&rsquo;s quick-commerce platform, delivering everyday essentials in just minutes across Saudi Arabia, the UAE, and Egypt. Leveraging cutting-edge technology and real-time logistics, we are redefining convenience in the region &mdash; one order at a time.
 
 
 
 
 
 
 What You&rsquo;ll Do
 
 
 
 As a Quality Analyst at noon Minutes, you&rsquo;ll play a critical role in ensuring top-notch customer service delivery by evaluating and improving our agents&rsquo; interactions across various channels. You&rsquo;ll be responsible for identifying trends, delivering actionable insights, and partnering with operations to maintain the highest standards.
 
 
 
 
 
 
 Responsibilities
 
 
 
 
 
 <ul>
 <li>
 Monitor customer interactions (Calls, Chats, Emails, and Tickets), either remotely or side-by-side.
 </li>
 <li>
 Conduct regular briefings with operational staff to share insights and updates.
 </li>
 <li>
 Analyze quality audits and testing results to recommend actionable improvements.
 </li>
 <li>
 Perform trend and root-cause analysis to identify top errors and advisor-level performance gaps.
 </li>
 <li>
 Conduct random disposition audits of agent interactions.
 </li>
 <li>
 Provide timely and constructive feedback to Customer Service Representatives (CSRs).
 </li>
 <li>
 Facilitate focus groups and performance evaluations to drive improvement.
 </li>
 <li>
 Prepare and share regular internal reports, including call monitoring data and agent performance metrics.
 </li>
 <li>
 Ensure adherence to Quality SLAs and internal quality benchmarks.
 </li>
 <li>
 Collaborate closely with Team Leaders and Training teams to address performance and process gaps.
 </li>
 </ul>
 
 
 
 
 
 What You&rsquo;ll Need
 
 
 
 
 
 <ul>
 <li>
 Minimum 2 years of experience as Quality Analyst
 </li>
 <li>
 Fluent in English (both written and spoken).
 </li>
 <li>
 Previous experience auditing customer service interactions and providing direct feedback to agents is a plus.
 </li>
 <li>
 Strong attention to detail with a customer-first mindset.
 </li>
 <li>
 Proficiency in Microsoft Excel and Word (basic level required).
 </li>
 <li>
 Ability to adapt quickly to dynamic environments and shifting priorities.
 </li>
 <li>
 A data-driven mindset with a passion for operational excellence.
 </li>
 </ul>
 
 
 
 
 
 Who will excel?
 
 
 
 
 
 <ul>
 <li>
 We&rsquo;re looking for people with high standards, who understand that hard work matters.
 </li>
 <li>
 You need to be relentlessly resourceful and operate with a deep bias for action.
 </li>
 <li>
 We need people with the courage to be fiercely original.
 </li>
 <li>
 noon is not for everyone; readiness to adapt, pivot, and learn is essential.
 </li>
 </ul>
 
 
</div>

Star Laboratories (Pvt.) Ltd.

Basic Function: To supervise analytical activities of QC analysts, ensure data accuracy, and maintain proper documentation for the raw material section of Quality Control.Key Responsibilities:<ul><li>Organize and manage the raw material section of the QC department.</li><li>Supervise day-to-day analytical activities of QC analysts.</li><li>Review and verify analytical/testing data, including calculations, before material release.</li><li>Ensure accuracy, completeness, and compliance of QC documentation as per SOPs and regulatory standards.</li><li>Maintain proper record-keeping and ensure data integrity across all QC processes.</li><li>Contribute to improving the overall performance and efficiency of the QC department.</li></ul>Qualifications:<ul><li>Pharm D, M.Sc. Chemistry.</li></ul>Experience:<ul><li>4&ndash;6 years of relevant experience in Quality Control.</li></ul>Location:23km, Multan Road, LahoreJob Type: Full-timeWork Location: In person

Sr. QC Analyst

Johnson & Johnson

<div>At Johnson &amp; Johnson, we believe health is everything. Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at https://www.jnj.com
Job Function:
Quality
Job Sub Function:
Quality Control
Job Category:
Professional
All Job Posting Locations:
Raritan, New Jersey, United States of America
Job Description:
Janssen Pharmaceuticals, Inc., a member of Johnson &amp; Johnson's Family of Companies, is recruiting for an Analyst, Quality Control Analytics - CAR-T in Raritan, NJ! This shift is going to be scheduled 8:00am - 6:00pm through Sunday - Wednesday.
At Johnson &amp; Johnson, we believe health is everything. Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at https://www.jnj.com/.
Are you interested in joining a team that is positively impacting patients' lives by ensuring high quality in our cell therapy products? Apply today for this exciting opportunity to be part of the #CAR-T team!
The QC Analyst is responsible for conducting biochemical, microbiological, and/or general testing of final product samples submitted to the QC laboratories. They are responsible for ensuring testing is completed in compliance with all applicable procedures, standards, and GMP regulations. They typically work with a team of 5 &ndash; 15 other Analysts within the functional laboratory of the Quality Control department.<h3 class="jobSectionHeader">
Key Responsibilities:</h3><ul><li>
Perform analytical testing and maintain a safe work environment in compliance with all applicable procedures, EHS, and GMP regulations</li><li>
Perform peer review/approval of laboratory data and logbooks</li><li>
Use electronic systems (e.g., LIMS, iLAB) for execution and documentation of testing</li><li>
Build, review, and approve relevant QC documents, SOPs, and WIs</li><li>
Complete invalid assay and general laboratory investigation records, CAPAs, change controls</li><li>
Support Health Authority inspections</li><li>
Provide input to functional laboratory meetings</li></ul><h3 class="jobSectionHeader">
Qualifications:
</h3><h3 class="jobSectionHeader">Education:</h3><ul><li>
Minimum of a Bachelor&rsquo;s or equivalent University Degree required; advanced degree (MSc., Ph.D.) or focused degree in Biology, Biochemistry, Chemistry, or related scientific field is preferred</li></ul><h3 class="jobSectionHeader">
Experience and Skills:</h3>
Required:<ul><li>
Minimum of two (2) years of relevant work experience</li><li>
Experience performing one or more of the following cellular and/or molecular based techniques: qPCR, Flow Cytometry, ELISA, Cell Culture, and/or Potency assays</li><li>
Experience within Biopharmaceutical or Pharmaceutical industry</li><li>
Experience with aseptic processing in biosafety cabinets and/or ISO 5 clean room</li><li>
Demonstrated experience successfully working in an analyst role/level and proficiency using analytical methodologies within a functional laboratory</li><li>
Knowledge of cGMP regulations and Good Documentation Practices (GDP)</li><li>
Experience with Quality Control document reviews and regulatory inspection processes</li><li>
Proficient in performing technical writing (e.g., test methods, SOP's, protocols, etc.)</li><li>
Excellent written and verbal communication skills</li></ul>
Preferred:<ul><li>
Work experience in Cell and/or Gene Therapy or Biologics</li><li>
Basic knowledge of Compendial (e.g., USP, EP, JP, etc.) requirements and standards</li><li>
Experience with LIMs and SAP or equivalent systems</li><li>
Experience, training, or certification with Process Excellence tools and methodologies</li></ul><h3 class="jobSectionHeader">
Other:</h3><ul><li>
Requires ability and flexibility to work 10-hour shifts between the operational hours of 8:00am - 6:00pm (Sunday - Wednesday), and provide occasional support on the weekends or other shifts</li><li>
Requires the ability to meet the physical demands (lift up to 20 lbs, stand or sit for extended periods of time in a laboratory setting), to perform visual inspections of materials (color, appearance, particles, etc.), and to document observations during laboratory testing</li><li>
Requires up to 5% domestic travel to other sites/locations</li></ul>
For more information on how we support the whole health of our employees throughout their wellness, career and life journey, please visit www.careers.jnj.com.
Johnson &amp; Johnson is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, age, national origin, disability, protected veteran status or other characteristics protected by federal, state or local law. We actively seek qualified candidates who are protected veterans and individuals with disabilities as defined under VEVRAA and Section 503 of the Rehabilitation Act.
Johnson &amp; Johnson is committed to providing an interview process that is inclusive of our applicants&rsquo; needs. If you are an individual with a disability and would like to request an accommodation, external applicants please contact us via https://www.jnj.com/contact-us/careers, internal employees contact AskGS to be directed to your accommodation resource.<h3 class="jobSectionHeader">
#car-t</h3>
The anticipated base pay range for this position is :
$69,500-$102,350
Additional Description for Pay Transparency:
Subject to the terms of their respective plans, employees and/or eligible dependents are eligible to participate in the following Company sponsored employee benefit programs: medical, dental, vision, life insurance, short- and long-term disability, business accident insurance, and group legal insurance. Subject to the terms of their respective plans, employees are eligible to participate in the Company&rsquo;s consolidated retirement plan (pension) and savings plan (401(k)). Subject to the terms of their respective policies and date of hire, Employees are eligible for the following time off benefits: Vacation &ndash;120 hours per calendar year Sick time - 40 hours per calendar year; for employees who reside in the State of Washington &ndash;56 hours per calendar year Holiday pay, including Floating Holidays &ndash;13 days per calendar year Work, Personal and Family Time - up to 40 hours per calendar year Parental Leave &ndash; 480 hours within one year of the birth/adoption/foster care of a child Condolence Leave &ndash; 30 days for an immediate family member: 5 days for an extended family member Caregiver Leave &ndash; 10 days Volunteer Leave &ndash; 4 days Military Spouse Time-Off &ndash; 80 hours Additional information can be found through the link below. https://www.careers.jnj.com/employee-benefits</div>

Analyst, QC CAR-T (PG24)

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Analyst, QC CAR-T (PG24)