qc analyst

Abbott

<div><p><b>Position:</b><b> QC Analyst
</b></p><p><b>Grade:</b> <b>12</b></p><p><b>
Reporting to: </b><b>Manager Chemical</b>
</p><p><b>Division:</b> <b>Established Pharmaceutical Division</b><b> - Operation
</b></p><p><b>Location:</b> <b>Karachi</b><b> - Landhi Plant
</b></p><p></p><p><b>Job Summary:</b></p><p></p><p>
Support the Manager Chemical by conducting all tests for conventional groups, new products, in-process products, and finished products on stability, as well as projects related to manufacturing. To assist Manager Chemical to support EHS Activities.</p><p></p><p><b>
Major Responsibilities:</b></p><p></p><ul><li>
Support section in charge for product releases, review Analytical Data on StarLims and manual data</li><li>
Assist Manager Chemical for all the activities taking place in FG, RM, TMV &amp; stability section</li><li>
Provide timely assistance to Manager Chemical in testing of all routine, Hold Time Study samples, stability products and validation samples</li><li>
Support Manager Chemical to support EHS Activities</li><li>
Assist Manager Chemical for all the activities taking place in respective section including SOP writing / QRA / CCP and TMV Protocols of related tasks</li><li>
Responsible to review Daily Balance Standardizations / pH meter Standardization in QC Lab with documentation</li><li>
Perform testing of Test Method Validation / Process Validation samples, fall in Conventional section</li></ul><p><b>
Education/Knowledge &amp; Experience:</b></p><ul><li>
Science Graduate/Master; preferably Chemist/Pharm D</li><li>
1-2 years&rsquo; experience in the same capacity</li><li>
Knowledge of technical problem resolution</li><li>
Proficient in MS Office</li><li>
Analytical Skills</li></ul></div>

QC Analyst

Rapid Job Sountions

<p><b>Job Title: </b>QC Data Analyst</p><p><b>Location: </b>Sangli, Maharashtra</p><p><b>Experience Level: </b>0-6 Years</p><p><b>Shift: </b>US Shift (Saturday and Sunday Off)</p><p>About Us:</p><p>We are a leader in the BPO industry, currently expanding our analytics divisions with a bold objective: to revolutionize the real estate and financial services sector through our proprietary suite of enterprise-grade solutions, powered by cutting-edge artificial intelligence. Join us in shaping the future with innovation and precision.</p><p><b>Role and Responsibilities of QC Data Analyst:</b></p><p>As a <b>QC Data Analyst </b>in Residential Appraisal Quality Control (QC), you will play acritical role in ensuring the accuracy, compliance, and quality of residential property appraisals.You will be responsible for reviewing, verifying, and optimizing appraisal reports to meet regulatory and industry standards. This role is essential for minimizing risks and ensuring accurate property valuations.</p><p><b>Key Responsibilities:</b></p><p><b>1. Reviewing and Verifying Appraisal Reports</b></p><p>o Ensure accuracy, consistency, and completeness of appraisal reports.</p><p>o Cross-check property details, such as size, layout, condition, and comparable properties.</p><p>o Assess the appropriateness of adjustments made to comparable sales.</p><p><b>2. Compliance and Regulatory Adherence</b></p><p>o Ensure adherence to the Uniform Standards of Professional Appraisal Practice (USPAP), federal guidelines, and lender requirements.</p><p>o Verify compliance with internal policies and client-specific standards.</p><p><b>3. Risk Assessment and Quality Control</b></p><p>o Identify red flags such as inconsistencies, questionable comparables, or potential appraisal bias.</p><p>o Detect and document signs of fraud or misrepresentation.</p><p>o Mitigate valuation risks to protect lenders from financial losses.</p><p><b>4. Collaboration with Stakeholders</b></p><p>o Provide constructive feedback to appraisers to improve report quality.</p><p>o Work closely with underwriters, loan officers, and compliance teams to resolve appraisal-related issues.</p><p><b>5. Documentation and Reporting</b></p><p>o Prepare detailed reports outlining discrepancies or areas requiring clarification.</p><p>o Maintain QC logs and track trends to refine quality control processes.</p><p><b>6. Training and Process Improvement</b></p><p>o Deliver training sessions for appraisal teams and QC staff on best practices and regulatory updates.</p><p>o Identify and implement process improvements to enhance efficiency and minimize errors.</p><p><b>7. Technology and Tools Usage</b></p><p>o Use specialized appraisal QC software and databases for efficient review and data management.</p><p>o Leverage data analytics to identify and address recurring appraisal errors.</p><p><b>8. Client Relationship Management</b></p><p>o Prepare customized quality control reports to meet client specifications.</p><p>o Assist with client audits by providing relevant documentation and analysis.</p><p><b>Core Skills and Qualities Required:</b></p><p>&middot; Exceptional attention to detail for identifying inconsistencies or errors in reports.</p><p>&middot; Strong analytical skills to critically assess data and ensure appraisal credibility.</p><p>&middot; Excellent communication skills for effective interaction with appraisers, underwriters, and clients.</p><p>&middot; Knowledge of USPAP, industry standards, and lending regulations.</p><p>&middot; Strong problem-solving abilities for resolving appraisal discrepancies.</p><p><b>What We Offer:</b></p><p>&middot; Opportunity to work on cutting-edge AI-driven solutions.</p><p>&middot; Exposure to the real estate and financial services industries.</p><p>&middot; Professional growth and development opportunities.</p><p>&middot; Collaborative and innovative work environment.</p><p>Ability to commute/relocate: Sangli, Maharashtra: Reliably commute or plan to relocate before starting work (Required)</p><p><b>Language: English (Required)</b></p><p><b>Shift Availability: Night Shift (Required)</b></p><p>Job Types: Full-time, Permanent, Fresher</p><p>Pay: &#8377;250,000.00 - &#8377;400,000.00 per year</p><p>Benefits:</p><ul><li>Health insurance</li><li>Paid time off</li><li>Provident Fund</li></ul><p>Experience:</p><ul><li>US Morgage: 1 year (Required)</li><li>Mortgage servicing: 1 year (Required)</li><li>Fresher: 1 year (Required)</li><li>Data analysis skills: 1 year (Required)</li></ul><p>Location:</p><ul><li>Sangli, Maharashtra (Preferred)</li></ul><p>Shift availability:</p><ul><li>Night Shift (Required)</li></ul>

QC Data Analyst

FujiFilm

<div>Position Overview:
<p>
The Microbiologist I will be responsible for assisting the QC microbiological aspects of cGMP compliance and testing at the FUJIFILM Biotechnologies Texas Quality Control Laboratory.</p><p><br>
</p>Company Overview:
<p>
The work we do at FUJIFILM Biotechnologies Texas has never been more important&mdash;and we are looking for passionate, mission-driven people like you who want to make a real difference in people&rsquo;s lives.</p><br>
<p><br>
From developing the next vaccine to advancing cell and gene therapies, we collaborate with industry leaders to tackle complex challenges and deliver meaningful solutions.</p><br>
<p><br>
If you&rsquo;re ready to help transform the future of medicine, join FUJIFILM Biotechnologies. We offer a flexible work environment and we&rsquo;re proud to cultivate a culture that will fuel your passion, energy, and drive&mdash;what we call Genki.</p><br>
<p><br>
Our state-of-the-art biomanufacturing facility is located in in College Station, Texas, which combines a small-town feel with vibrant culture, top-notch schools, and close proximity to big city life. Nestled between major hubs, it&rsquo;s a dynamic location that blends convenience with innovation.</p><br>
<p><br>
Fujifilm is globally headquartered in Tokyo with over 70,000 employees across four key business segments of healthcare, electronics, business innovation, and imaging. We are guided and united by our Group Purpose of &ldquo;giving our world more smiles.&rdquo; Visit: https://www.fujifilm.com/us/en/about/region/careers</p>
Job Description:
<p><b>
Primary Responsibilities:</b></p><ul><li>
Collect environmental monitoring (Total Air, Viable Air and Viable Surface) in a cleanroom/controlled environment.</li><li>
Collect Utility Monitoring Samples (RODI/WFI) routinely and for qualification of systems.</li><li>
Sample Compressed Gas/Process Gas system.</li><li>
Autoclave materials and components for use in the QC laboratory.</li><li>
Routine QC laboratory cleaning</li><li>
Management of inventory items for the laboratory</li><li>
Ensure the lab is maintained (organized, clean, &amp; properly supplied).</li><li>
Perform other duties as assigned.</li></ul><div><b>
Qualifications:
</b></div><ul><li>Associate&rsquo;s degree preferably in Biochemistry, Chemistry, Biology, or related field; OR,</li><li>
High School Diploma or GED and 1+ year of relevant experience.</li><li>
Ability to analyze raw data, assess assay and system suitability criteria.
</li><li>Ability to follow safety procedures outlined in the Chemical Hygiene Plan.</li><li>
Utilize SDS sheets to properly assess chemical hazards, spill response procedures, and PPE requirements if indicated.</li><li>
Good attention to detail and ability to utilize problem solving/trouble shooting skills.</li><li>
Good computer skills.</li><li>
Demonstrated written and oral communication skills.</li><li>
Strong organization and analytical skills.</li><li>
Role model for company core values of trust, delighting our customers, Gemba, and Genki.</li></ul><div><b>
Physical Requirements:</b></div><p>
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. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. While performing the duties of this job, the employee is regularly required to:</p><ul><li>
Experience prolonged standing, some bending, stooping, and stretching.</li><li>
Use hand-eye coordination and manual dexterity sufficient to operate a keyboard, photocopier, telephone, calculator, and other office equipment is required.</li><li>
Ability to sit for long periods to work on a computer.</li><li>
Potential for exposure to hazardous chemicals, gases, fumes, odors, mists, and dusts, and other hazardous materials.</li><li>
Ability to lift/pull/push 50 lbs on occasion and 15 lbs regularly.</li><li>
Ability to wear personal protective equipment including safety glasses, lab coat, and gloves.
</li><li>Attendance is mandatory.</li></ul><div><b>
Join us! FDB is advancing tomorrow&rsquo;s medicine, impassioning employees to chase the impossible and continually expand their potential. We are a company of emboldened goal seekers &ndash; driven by an innate desire to better ourselves, our families, our workplace, our company, our community and the world at large.</b></div><p></p><div><i><br>
To all agencies: Please, no phone calls or emails to any employee of FUJIFILM about this requisition. All resumes submitted by search firms/employment agencies to any employee at FUJIFILM via-email, the internet or in any form and/or method will be deemed the sole property of FUJIFILM, unless such search firms/employment agencies were engaged by FUJIFILM for this requisition and a valid agreement with FUJIFILM is in place. In the event a candidate who was submitted outside of the FUJIFILM agency engagement process is hired, no fee or payment of any kind will be paid.</i></div><br>
<div></div>
EEO Information:
<div>
Fujifilm is committed to providing equal opportunities in hiring, promotion and advancement, compensation, benefits, and training regardless of nationality, age, gender, sexual orientation or gender identity, race, ethnicity, religion, political creed, ideology, national, or social origin, disability, veteran status, etc.</div>
ADA Information:
<div>
If you require reasonable accommodation in completing this application, interviewing, completing any pre-employment testing, or otherwise participating in the employee selection process, please direct your inquiries to our HR Department (FDBTHR@fujifilm.com or (979) 431-3500).</div></div>

QC Analyst I, Microbiology

Novonesis

<div><p><b>Are you ready for a new beginning?
</b></p><p>We need your talent, knowledge and dedication to better our world with biology.
</p><p></p><p><b>Our purpose points the way
</b></p><p>In Novonesis, we know that solutions rooted in biology can help solve humanity&rsquo;s biggest challenges. Since we began more than a century ago, this has been our guide. It&rsquo;s how we've gotten so far. And it&rsquo;s how we'll impact the future. Now, more than ever, the world needs change. And with biosolutions, the possibilities for transformation are endless.
</p><p></p><p><b>We&rsquo;re here to better our world with biology.
</b></p><p></p><p>1. Experience - Minimum 3 years
</p><p>2. Education - Graduation in Science faculty - Chemistry
</p><p>3. Expert in Handling of Various Lab instrument like HPLC, PH meter, TDS Meter, UV Spectrophotometer, Hot Air Oven, Sieve Shaker .
</p><p>4. Wet lab analysis - Qualitative &amp; quantitative like titration, estimation, analysis of various types of water
</p><p>5. Handling of quality parameter of raw material, packaging material, Finished product Samples and reporting
</p><p>6. Hands of experience with Daily Verification &amp; calibration of instrument
</p><p>7. Knowledge of Computer Skill like Excel, Word, Power Point
</p><p></p><p><b>Could our purpose be yours? </b><b>Then apply today!
</b></p><p></p><p>At Novonesis we commit to an inclusive recruitment process and equality of opportunity for all our job applicants. We recommend you not to attach a cover letter to your application. Instead, please include a few sentences in your resume/CV about why you are applying. To ensure a fair recruitment process, please refrain from adding a photo in your resume/CV.
<br>
<br>
Novonesis is dedicated to fostering a unique community by embracing and respecting differences. We make all employment decisions based on business needs, ensuring that every individual can thrive, regardless of identity or background such as ethnicity, religion, gender, sexual orientation, age, disability, or veteran status.
<br>
<br>
<b>Want to learn more?
</b><br>
Learn more about Novonesis, our purpose, and your career opportunities at novonesis.com
<br>
<br>
<b>Not the right fit for you?
</b><br>
Even if this job isn't the right fit for you, perhaps you know someone who might find it interesting. If so, please feel free to share the job link and encourage them to apply. Thank you for your referral! Please check out our other open positions. The right fit for you could just be a few clicks away.
</p><p></p><p><b>Stay alert: Avoid recruitment scams
</b><br>
At Novonesis, we are committed to maintaining a safe and transparent recruitment process. Please be aware of potential scams targeting job seekers and take note of the following:
</p><ul><li><i>Novonesis will never ask for sensitive personal information, such as bank account details, Social Security numbers, or passwords, at any stage of the hiring process.
</i></li><li><i>Novonesis does not make employment offers without conducting interviews with candidates.
</i></li></ul><p></p><p><i>If you receive suspicious communication claiming to be from Novonesis, please do not share any personal or financial information. </i><i>We encourage you to verify the legitimacy of the message by contacting us directly through our official channels.</i></p></div><p></p>

Executive QC Analyst

Roquette

<div><div>Roquette is a family-owned global leader in plant-based ingredients and a leading provider of pharmaceutical excipients.</div><div></div><div>
Want to help us make a difference?<br>
Using plant-based resources, we collaborate with our customers and partners to imagine and offer ingredients to better feed people and treat patients.<br>
Each of our ingredients responds to unique and essential needs, and they enable healthier lifestyles.</div><div><div><div><div><div><div><div><div><div><div><div>
The Role:</div></div><div><div><div><div><div><div><div><div><div><div>
We are looking for our next QC Lab Analyst within our Quality Control team. The QC Lab Analyst will be responsible for performing routine and complex quality control tests to ensure that products meet defined specifications. This role involves working with various laboratory instruments, conducting validation studies, and supporting 24/7 Mini-Plant operations through rotating swing shifts.</div><div></div><div>
This position is located in Keokuk, IA.</div><div></div><div>
Compensation:</div><div>
The current hourly comp for this role is estimated to be $27/hourly. In addition, this position may also be eligible to earn performance-based incentive compensation. The specific compensation offered to a candidate will be influenced by a variety of factors including but not limited to skills, qualifications, experience, and location.</div><div>
What You&rsquo;ll Do:</div><ul><li>Perform quality control tests using lab instruments such as spectrophotometers, HPLC, and pH meters.</li><li>Follow and apply standard laboratory operating procedures for qualitative and quantitative assays.</li><li>Conduct calibration of analytical instruments and routine wet-chemistry and instrumental analysis on in-process and final products.</li><li>Execute validation studies and manage retained samples in accordance with established SOPs.</li><li>Maintain and troubleshoot basic lab equipment and instrumentation as needed.</li><li>Provide laboratory coverage on a rotating swing-shift schedule to support 24/7 Mini-Plant operations.</li><li>Work cross-functionally with Quality Assurance, Mini-Plants, Customer Care, Shipping, and external vendors.</li></ul><div></div><div>
What You&rsquo;ll Need:</div><div>
Education:</div><ul><li>BS Degree in Chemistry, Biology, or a related field.</li></ul><div>
Experience:</div><ul><li>Strong oral and written communication skills.</li><li>Demonstrated computer proficiency.</li><li>Strong problem solving, innovation, and analytical skills.</li></ul><div>
Supervisory Responsibility (if applicable)<br>
<ul><li>This position does not have direct reports.</li></ul></div><div>
Work Environment</div><ul><li>This role spends approximately 50% of the time in a laboratory/office environment and 50% in a plant setting.</li><li>Work environments may include high places, extreme heat/cold, poor ventilation, and areas with moving equipment and chemical/biological exposure.</li></ul><div>
Physical Demands</div><ul><li>While performing the duties of this job, the employee is required to speak or hear.</li><li>The employee is frequently required to stand, walk, climb stairs, use hands and fingers, reach with arms, and work in hot, cold, or loud environments.</li><li>Driving automotive equipment (e.g., golf cart) may be required.</li><li>Employee must be able to wear a respirator.</li></ul><div>
Position Type/Expected Hours of Work</div><ul><li>This is a full-time 8-hour Rotating swing-shift schedule.</li></ul><div></div><div>
Business Travel:</div><ul><li>Travel is not a regular requirement for this role.</li></ul><div></div><div>
AAP/EEO Statement</div><div>
Roquette is an Equal Opportunity Employer. Employment decisions are made without regard to race, color, religion, national origin, gender, sexual orientation, gender identity, age, physical or mental disability, genetic factors, military/veteran status or other characteristics protected by law. &ldquo;AAP, EEO, Drug-Free Workplace&rdquo;</div><div></div><div>
Other Duties</div><div>
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.</div></div></div></div></div></div></div></div></div></div></div></div></div></div></div></div></div></div></div><div>
If you identify yourself in this position, please apply by uploading your resume and let's start the journey together!</div><div></div><div>
Roquette is proud to be a global company where you can find personal and professional growth through multiple diverse experiences.</div><div></div><div>
Roquette strives to create a dynamic workforce while remaining firmly committed to equal opportunity by complying with EEO laws.</div><div><br>
As we continue to grow, Roquette understands that to be successful we must always be inclusive in our approach.</div><div></div><div>
To find out more about our products, values and sustainable development ambitions visit us at <div>www.roquette.com</div> and at <div>www.sustainability.roquette.com</div></div></div><div></div>

QC LAB Analyst

HR First Pvt Ltd

<p><b>Responsibilities:</b></p><ul><li>Prepare daily Plan Vs Actual execution along with analyst efficiency monitoring sheet.</li><li>To prepare product specifications and standard test methods of semi-finished &amp; finished products in accordance with the current compendia&rsquo;s.</li><li>To maintain accurate and detailed records of all testing procedures ,results and observations in compliance with Good Laboratory Practices (GLP) and regulatory requirements.</li><li>Troubleshooting equipment and method related issue to maintain efficient laboratory operation.</li><li>To prepare and revise standard operating procedure as per requirement.</li><li>To arrange laboratory chemicals, reagents and HPLC columns from appropriate suppliers in appropriate quantities to facilitate smooth testing of samples of products.</li><li>To help in preparation of monthly dash board of finished products.</li><li>To work closely with other QC team members, production and quality assurance to resolve quality related issues.</li><li>To monitor compliance in QC Section.</li><li>To participate in quality investigations and support batch release activities.</li><li>Suggest and implement process improvements to enhance laboratory efficiency.</li><li>To assist in implementing Company&rsquo;s EHS goals and objectives in one&rsquo;s specific area of work.</li></ul><p><b>Requirements:</b></p><ul><li>Bachelors in Pharmacy or D-Pharmacy</li><li>2 years of relevant experience from a pharmaceutical industry.</li></ul><p>Job Type: Full-time</p><p>Work Location: In person</p>

QC Executive

Acino International AG

<p>Acino is a Swiss pharmaceutical company, leader in advanced drug delivery technologies. We have a clear focus on selected emerging markets in the Middle East, Africa, the CIS Region, and Latin America, and we operate in some of the most dynamic countries of the world. We value courage, commitment, trust, and empathy and provide an environment that supports initiative and effort. We are proud to be action-oriented and open-minded, with a strong focus on quality and product availability, even in remote and hard-to-reach areas of the world.</p><p>We are constantly expanding our market position with a future-oriented international business strategy. Therefore, we are looking for a dedicated and motivated person to strengthen our Quality team in Dubai, UAE Site- Acino Pharmaceuticals FZ LLC </p><p>Quality Control Analyst will be responsible for performing analytical testing, maintaining laboratory resources, ensuring compliance with quality and safety standards, and supporting product release, method transfers, and validations. He /She will work with advanced analytical instruments, uphold data integrity principles, and ensure full compliance with GMP requirements to maintain product quality, safety, and efficacy.</p><p> Job Responsibilities </p><ul><li>Perform analysis of raw materials, packaging materials, bulk products, finished products, in-process samples, stability samples, process/cleaning validation samples, and miscellaneous samples as per approved methods and protocols.</li><li>Ensure all activities comply with GLP, GMP, and ALCOA  principles.</li><li>Operate major analytical instruments including HPLC, GC, Dissolution Apparatus, UV-Vis Spectrophotometer, and IR.</li><li>Perform daily verification, calibration, and routine maintenance of instruments as per SOPs.</li><li>Maintain an up-to-date inventory of reference standards, working standards, impurity standards, analytical columns, reagents, chemicals, and consumables.</li><li>Conduct qualification of working standards against reference or primary standards.</li><li>Prepare volumetric solutions and standardize them for routine use.</li><li>Prepare, review, and update SOPs, test methods, and specifications as needed.</li><li>Record all data accurately, clearly, and in real-time following GLP requirements.</li><li>Report and support investigations for any OOS, OOT, incidents, or non-compliance activities.</li><li>Initiate and support Change Control, CAPA, and Deviation processes as required.</li><li>Follow safety procedures and use the recommended PPE for all QC activities.</li><li>Ensure compliance with EHS policies and safe work practices in the laboratory.</li><li>Support analytical validation/verification and cleaning validation studies.</li><li>Participate in laboratory improvement initiatives.</li><li>Carry out additional tasks assigned by the QC Manager in line with department objectives.</li></ul><p> Qualifications & Skills: </p><ul><li>Bachelor's degree in chemistry, pharmaceutical sciences, or related discipline.</li><li>1-3 years of experience in a pharmaceutical QC laboratory.</li><li>Hands-on experience with HPLC, GC, Dissolution, UV, and IR instruments.</li><li>Knowledge of LIMS and SAP systems is preferred.</li><li>Good understanding of GMP, GLP, and data integrity principles (ALCOA ).</li><li>Strong attention to detail, analytical thinking, and problem-solving skills.</li><li>Effective communication and teamwork abilities.</li></ul><p>This is the opportunity to join a very dynamic organization, where decisions are taken fast and where you can actively participate in shaping our future. If this sounds exciting, we would love to hear more about you!</p><p> Please apply via our HR system here. </p>

Quality Control Analyst

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