qc analyst

Lonza

<div><p><b>QC Analyst I &ndash; Analytical (Cell Therapy, Night Shift)</b></p><p><b>
Location: Portsmouth, NH, USA.</b></p><p>
As a <b>QC Analyst I</b> on our Cell Therapy Analytical team, you are responsible for the high-precision testing that confirms the safety and potency of personalized medicines. Working on the night shift, you provide the critical data needed to move patient treatments forward. This is a foundational role for a scientifically minded individual who wants to master complex analytical methods in a fast-paced, high-stakes environment.</p><p><b>
Schedule &amp; Shift</b></p><ul><li><p><b>
Shift:</b> Night Shift (<b>8:00 PM &ndash; 6:30 AM</b>)</p></li><li><p><b>
Days:</b> Wednesday through Saturday (4-day, 10-hour schedule)</p></li><li><p><b>
Orientation:</b> Your first 2 weeks of training will be held on the day shift.</p></li><li><p><b>
Differentials:</b> This role includes competitive night and weekend shift pay.</p></li></ul><p><b>
What You&rsquo;ll Get</b></p><ul><li><p><b>
Specialized Technical Training:</b> Master foundational analytical techniques (such as Flow Cytometry, ELISA, or qPCR) used in the release of cell-based therapies.</p></li><li><p><b>
Direct Impact:</b> Your work directly verifies that a patient&rsquo;s custom treatment is safe and effective before it reaches them.</p></li><li><p><b>
Predictable Balance:</b> The 4x10 schedule offers three consistent days off per week.</p></li><li><p><b>
Full Lonza Benefits:</b> Medical, dental, vision, 401(k), and performance-based incentives. Our full list of global benefits: lonza.com/careers/benefits.</p></li></ul><p><b>
What You&rsquo;ll Do</b></p><ul><li><p><b>
Analytical Testing:</b> Perform routine analytical assays to support in-process, lot release, and stability testing for Cell Therapy products.</p></li><li><p><b>
Aseptic Handling:</b> Maintain the highest standards of sterility when handling sensitive biological samples to ensure data integrity and prevent contamination.</p></li><li><p><b>
Data Recording:</b> Document all results in real-time, following <b>Good Documentation Practices (GDP)</b> and ensuring 100% compliance with cGMP standards.</p></li><li><p><b>
Lab Support:</b> Assist in the maintenance of laboratory equipment, the preparation of reagents, and ensuring the lab remains in an audit-ready state.</p></li><li><p><b>
Collaborative Quality:</b> Work closely with your night shift team to meet manufacturing deadlines and participate in clear, detailed shift handovers.</p></li><li><p><b>
Problem Recognition:</b> Learn to identify and escalate any results that deviate from expected ranges, supporting the team in maintaining total process control.</p></li></ul><p><b>
What We&rsquo;re Looking For</b></p><ul><li><p><b>
Education:</b> Associate&rsquo;s or Bachelor&rsquo;s degree in a Scientific Discipline (Biology, Chemistry, Biochemistry, or related field) is required.</p></li><li><p><b>
Experience:</b> This is an <b>entry-level (Level I) role</b>. We are looking for individuals with strong foundational lab skills, whether from an academic setting or prior industry experience.</p></li><li><p><b>
Technical Aptitude:</b> A strong desire to learn complex analytical instrumentation and laboratory computer systems (LIMS).</p></li><li><p><b>
Attention to Detail:</b> The ability to follow detailed Standard Operating Procedures (SOPs) with 100% accuracy.</p></li><li><p><b>
Reliability:</b> Ability to consistently work the 8 PM &ndash; 6:30 AM schedule and contribute to a high-performing night team.</p></li><li><p><b>
Attributes:</b> Self-motivated, positive attitude, and a deep commitment to the patient-first mission of Cell Therapy.</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 start your career in QC? Apply now.</b></p></div>

QC Analyst I - Analytical (Nights)

<div><p><b>QC Analyst IV &ndash; Environmental Monitoring</b></p><p><b>
Location: Portsmouth, NH, USA.
</b></p><p>As a <b>QC Analyst IV</b>, you are a Subject Matter Expert (SME) and a primary technical lead for the Environmental Monitoring team. This senior role is critical for maintaining the microbial control strategy of our multi-modal facility. You will be responsible for leading complex investigations, driving continuous improvement projects, and ensuring our EM program remains in a permanent state of compliance with global regulatory standards.</p><p><b>
Schedule: Day Shift, Monday &ndash; Friday, 8:00 AM &ndash; 5:00 PM</b></p><p><b>
What You&rsquo;ll Get</b></p><ul><li><p><b>
Technical Leadership:</b> Act as a lead for the EM department, influencing site-wide quality culture and operational strategy.</p></li><li><p><b>
Audit Frontline:</b> Represent the EM program as a Subject Matter Expert during internal and external regulatory inspections (FDA, EMA, etc.).</p></li><li><p><b>
Advanced Project Ownership:</b> Lead the implementation of new technologies, such as rapid microbiological methods or paperless data systems.</p></li><li><p><b>
Comprehensive Benefits:</b> Medical, dental, vision, 401(k), and performance-based incentives. Our full list of global benefits: lonza.com/careers/benefits.</p></li></ul><p><b>
What You&rsquo;ll Do</b></p><ul><li><p><b>
Technical SME Ownership:</b> Serve as the technical lead for the site&rsquo;s EM and Utility monitoring programs. Provide high-level guidance on sampling plans, risk assessments, and the qualification of new cleanrooms.</p></li><li><p><b>
Complex Investigations:</b> Lead and author high-complexity environmental excursion investigations. Utilize root cause analysis (RCA) tools to identify systemic issues and implement effective CAPAs.</p></li><li><p><b>
Data Trending &amp; Strategy:</b> Perform advanced analysis of environmental and utility data. Identify long-term trends and present findings to site leadership and the Quality Council to drive proactive contamination control.</p></li><li><p><b>
Regulatory &amp; Audit Excellence:</b> Prepare, review, and defend EM data and procedures during regulatory audits. Ensure all department SOPs and sampling protocols meet current Annex 1 and global cGMP expectations.</p></li><li><p><b>
Mentorship &amp; Coaching:</b> Provide advanced technical training and mentorship to Level I, II, and III analysts. Foster a culture of technical excellence and &quot;Right First Time&quot; performance.</p></li><li><p><b>
Continuous Improvement:</b> Identify and execute Lean Laboratory initiatives to increase efficiency, reduce lead times, and enhance data integrity across the EM program.</p></li><li><p><b>
Review &amp; Approval:</b> Act as a final technical reviewer for complex laboratory records, validation protocols, and summary reports.</p></li></ul><p><b>
Who We&rsquo;re Looking For</b></p><ul><li><p><b>
Education:</b> Bachelor&rsquo;s degree (BS) in a Life Sciences discipline (Microbiology, Biology, or related field) is <b>required</b>.</p></li><li><p><b>
Experience:</b> <b>5&ndash;10 years of advanced experience</b> in Quality Control Microbiology or Environmental Monitoring within a cGMP manufacturing environment is <b>required</b>.</p></li><li><p><b>
Technical Mastery:</b> * Expert-level knowledge of cleanroom classifications (Grade A&ndash;D) and aseptic processing.</p><ul><li><p>
Deep understanding of global regulatory requirements (FDA, EMA, ICH) for environmental and utility monitoring.</p></li><li><p>
Proficiency in utilizing Laboratory Information Management Systems (LIMS) and data trending software.</p></li></ul></li><li><p><b>
Leadership Attributes:</b> A proven track record of leading projects, managing timelines, and influencing cross-functional teams without direct authority.</p></li><li><p><b>
Communication:</b> Exceptional technical writing skills and the ability to present complex scientific data clearly to senior management and auditors.</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 lead the standard of excellence in QC? Apply now.</b></p></div>

QC Analyst Level IV - Environmental Monitoring

MacroGenics

<div><p><b>Responsibilities and Job Duties:</b></p><br>
<p></p>
<ul>
<li>Collects routine environmental monitoring (EM) samples and water samples and performs plate enumeration on a daily basis in accordance with all protocols and procedures.</li>
<li>Performs basic water testing such as pH and conductivity in accordance with standard operating procedures.</li>
<li>Enters sampling and testing data into laboratory data system, and ensure adherence to standard operating procedures and cGMPs.</li>
<li>Performs routine lab cleaning and equipment maintenance activities in accordance with SOPS as scheduled, and escalates potential equipment issues to supervisor.</li>
<li>Reports out of specification results from the sampling and testing to supervisor and assists with performing laboratory investigations to determine the root cause and possible resolution.</li>
<li>Revises and updates standard operating procedures, as assigned with guidance from senior analysts and/or supervisor.</li></ul><br>
<p></p>
<p><b>
Qualifications</b></p>
<p><i>
Education, Experience, &amp; Credentials</i></p><br>
<p></p>
<ul>
<li>High School Diploma and minimum of one year experience in performing Environmental Monitoring and Microbiology testing.</li>
<li>Bachelor&rsquo;s Degree in a scientific discipline</li></ul><br>
<p></p>
<p><i>
Knowledge, Skills and Abilities</i></p>
<ul>
<li>Working knowledge of good in performing Environmental Monitoring or Microbiology testing.</li>
<li>Needs to be able to follow directions that are outlined in SOPs and other quality guidelines.</li>
<li>Ability to organize daily activities to meet internal customer needs in a fast-paced environment</li>
<li> Ability to understand when he/she should seek advice and guidance</li>
<li> Data entry skills
 </li><li>Be able to work in a team environment in a cooperative and respectful manner.</li>
<li> Ability to stand for periods of time when performing tasks on the floor.</li>
<li> Ability to work a varied schedule including off shift and weekends.</li>
<li>Ability to lift up to 50 pounds.</li>
</ul>
<p><b>Supervisory Responsibilities</b></p>
<p>
None</p>
<p><b>
Additional Information</b></p>
<p>
The annual equivalent of pay for the Quality Control Analyst I position ranges from $50,250-83,750. For non-exempt roles, and according to applicable regulations, there may be the possibility for overtime pay. This role is eligible for the Company&rsquo;s discretionary bonus and discretionary equity incentives. Eligible employees may participate in the Company&rsquo;s benefits programs, including medical / dental / vision / prescription coverage, employee wellness resources, 401(k) plan with employer match, access to an Employee Stock Purchase Plan, (ESPP), paid time off &amp; paid parental leave benefits, and disability benefits.</p>
<p>
The annual pay rate range is described in good faith, and the Company believes is the range of possible compensation for this role at the time of this posting depending on the candidate&rsquo;s experience, qualifications, geographic location, and other factors permitted by law. The Company may ultimately pay more or less than the posted range, and this range may be modified in the future. No amount is considered to be wages or compensation until such amount is earned, vested, and determinable under the terms and conditions of the applicable policies and plans. The amount and availability of any bonus, commission, benefits, or any other form of compensation and benefits that are allocable to a particular employee remains in the Company's sole discretion unless and until paid and may be modified at the Company&rsquo;s sole discretion, consistent with the law.</p>
<div>
<div><p><b>Statement</b></p>
<p>
MacroGenics is proud to be an equal opportunity employer. Employment selection and related decisions are made without regard to race, color, national origin, sex, gender identity, sexual orientation, religion, age, disability, protected veteran status, or any other characteristic protected by federal, state or local law. We are committed to working with and providing reasonable accommodation to individuals with disabilities. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the employment process, please email info@macrogenics.com or call (301) 354-3566 and/or 711 for TTD/TTY service.</p>
<p><b>
Equal Opportunity Employer/Veterans/Disabled</b></p>
<p><b>
We do not</b><b> </b><b>accept non-solicited resumes or candidate submittals from search/recruiting agencies.</b></p></div></div></div>

QC Analyst I - Environmental Monitoring

Wipro

<div>Job Description<p></p><div><div><ul><li><div><b><br>
</b><br>
</div></li></ul></div></div><div><div><div><div>Job Title: QUALITY ANALYST L3
</div></div></div></div><div><div><div><div>City: Hyderabad
</div></div></div></div><div><div><div><div>State/Province: Telangana
</div></div></div></div><div><div><div><div>Posting Start Date: 2/20/26
</div></div></div></div><div><div><div><div>Wipro Limited (NYSE: WIT, BSE: 507685, NSE: WIPRO) is a leading technology services and consulting company focused on building innovative solutions that address clients&rsquo; most complex digital transformation needs. Leveraging our holistic portfolio of capabilities in consulting, design, engineering, and operations, we help clients realize their boldest ambitions and build future-ready, sustainable businesses. With over 230,000 employees and business partners across 65 countries, we deliver on the promise of helping our customers, colleagues, and communities thrive in an ever-changing world. For additional information, visit us at www.wipro.com.
</div></div></div></div><div><div><div><div>Job Description:
<div><div><div><h2 class="jobSectionHeader"><b>Job Description
</b></h2></div><div><p><b>Role Purpose
</b></p><p>The purpose o central quality analyst role is to conduct quality audits and perform analytics in different areas as defined by central quality team, supporting the project teams in ensuring higher client satisfaction
</p></div></div><div><div><h2 class="jobSectionHeader"><b>͏
</b></h2></div><div><p><b>Do
</b></p><p>1. Conduct process quality audits as per plan
</p><ul><li>Conduct various process audits as per guidelines and SPO&Atilde;&cent;&Acirc;&Acirc;s defined in QMS
</li><li>Prepare findings from the report and share it with the account/ project leadership on daily/ weekly/ monthly, as required
</li><li>Conduct weekly analysis to identify the error trends and for top 2 errors, conduct root cause analysis (RCA)
</li>Conduct calibration communication to communicate any changes from the client and conduct refresher trainings to bridge any skill gap due to these changes<br>
<li>
</li></ul><p></p><p>2. Conduct analysis, report generation and process compliance in different areas like metrics office, CAG, Process Definition
</p><ul><li>Ensure processes to be followed in Wipro in terms of all quality norms in the areas of project management and highlight potential risks
</li><li>Provide insights and process guidance to the projects as per the need
</li><li>Prepare timely dashboards, reports, insights and share with the central quality and delivery teams to ensure minimum client escalation
</li><li>From time to time highlight any critical escalations where the central quality team&Atilde;&cent;&Acirc;&Acirc;s intervention is required in any BU project team
</li><li>Automate the report generations etc to ensure minimization of non-value added tasks, ensuring maximum utilization of existing platforms and their increased adoption
</li></ul></div></div><div><div><h2 class="jobSectionHeader"><b>͏
</b></h2></div><div><p><b>Deliver
</b></p><div><div><div><div><b>No. </b></div><div><b>Performance Parameter </b></div><div><b>Measure
</b></div></div><br>
<div><div>1. </div><div>Quality Standards
</div><div><ul><li>Timely generation of reports, dashboards, insights to the respective team
</li><li>Accuracy of the data
</li><li>Feedback from the project teams on the insights
</li><li>Quality of insights shared with the team
</li></ul></div></div><br>
</div></div></div></div><div><div><h2 class="jobSectionHeader"><b>͏
</b></h2></div></div><div></div><div><div><h2 class="jobSectionHeader"><b>͏
</b></h2></div></div></div></div></div></div></div><div></div><div><div><div><div>Mandatory Skills: QC - ALM Admin .<br>
<p></p>Experience: 8-10 Years .<br>
<p></p>Reinvent your world. We are building a modern Wipro. We are an end-to-end digital transformation partner with the boldest ambitions. To realize them, we need people inspired by reinvention. Of yourself, your career, and your skills. We want to see the constant evolution of our business and our industry. It has always been in our DNA - as the world around us changes, so do we. Join a business powered by purpose and a place that empowers you to design your own reinvention.</div></div></div></div></div><p></p>

QUALITY ANALYST L3

Novixs Web Services

<p><b>Job Type:</b></p><p>Full-time | On-site (Hybrid)<br/>Location: Pune<br/>Working Hours: 8 hours/day</p><p><b>Job Description</b></p><p>We are hiring <b>Quality Checking Analysts</b> for a <b>Banking KYC Form Filling Project</b>. The role involves reviewing and validating data entered by Data Entry Operators to ensure <b>high accuracy, compliance, and billing eligibility</b> as per client standards.</p><p>This is a <b>quality-critical role</b> that directly impacts monthly revenue and client billing.</p><p><b>Key Responsibilities</b></p><ul><li>Perform <b>quality checks</b> on KYC data entered by Data Entry Operators</li><li>Identify, classify, and document errors accurately</li><li>Verify <b>critical fields</b> such as Name, DOB, PAN, Aadhaar, Address, Bank details, etc.</li><li>Ensure compliance with defined <b>accuracy calculation standards</b></li><li>Send error forms back to respective Data Entry Operators for correction</li><li>Re-verify corrected forms and confirm accuracy</li><li>Maintain daily and monthly quality reports</li><li>Ensure that overall team accuracy meets <b>billing thresholds</b></li><li>Follow SOPs and client quality guidelines strictly</li><li>Focus on <b>error prevention</b>, not error correction</li></ul><p><b>Quality Standards &amp; Accountability</b></p><ul><li>Accuracy is calculated using the formula: <b>Accuracy (%) = 100 &minus; (Total Errors Found &divide; Total QC-ed Forms) &times; 100</b></li><li>All errors identified are counted once, even after correction</li><li>QC decisions are final unless excluded under defined exception rules</li><li>Missed critical errors may lead to performance review or deduction</li></ul><p><b>Required Skills &amp; Qualifications</b></p><ul><li><b>Minimum 1 year experience</b> in:</li><li>KYC processing</li><li>Banking operations</li><li>Data quality / audit / BPO projects</li><li>Prior QC experience is <b>highly preferred</b></li><li>Strong attention to detail</li><li>Good understanding of KYC documents and banking data</li><li>Ability to read and understand English clearly</li><li>Basic computer proficiency</li><li>Knowledge of data accuracy metrics and reporting</li><li>Ability to work independently and make objective decisions</li></ul><p><b>Mandatory Selection Process</b></p><ul><li>Candidates must clear a <b>QC accuracy and error-identification test</b></li><li>Practical assessment will be conducted before final selection</li></ul><p><b>Confidentiality &amp; Compliance</b></p><ul><li>Must sign <b>NDA and Data Confidentiality Agreement</b></li></ul><p>Any data misuse or manipulation will lead to immediate termination</p><p>Job Type: Full-time</p><p>Pay: ₹15,000.00 - ₹25,000.00 per month</p><p>Benefits:</p><ul><li>Paid sick time</li></ul><p>Experience:</p><ul><li>QA/QC: 1 year (Preferred)</li></ul><p>Work Location: In person</p>

Quality Analyst

Symrise

<div><b>About us</b><p><br>
Symrise is a global supplier of fragrances and flavors, cosmetic active ingredients as well as functional ingredients. Its customers include perfume, cosmetics, food and beverage manufacturers, the pharmaceutical industry and producers of dietary supplements and pet food.</p>
<p>
With sales of around &euro;5.0 billion in the 2024 financial year, the company is one of the world's leading providers. The Group, headquartered in Holzminden, Germany, has more than 100 locations in Europe, Africa and the Middle East, Asia, the USA and Latin America.</p>
<p>
Together with its customers, Symrise develops new ideas and market-ready concepts for products that form an indispensable part of everyday life. Economic success and corporate responsibility are inextricably linked.</p>
<p>
Symrise &ndash; always inspiring more...</p><p></p><b><br>
Your role</b><p><br>
Essential Functions:
<br>
A. Analyze raw materials, intermediates, and finished products according to Symrise, FCC, USP, ISO or AOAC testing methods. Enter all relative data into SAP or other quality databases. Support QC Sensory and QC Systems data administration as needed.
<br>
<br>
B. Assist other departments and members of the lab in their requests for analytical testing and results.
<br>
<br>
C. Perform project analysis in support of QC, QA, Divisional and Regulatory requirements.
<br>
<br>
D. Provide first line operation and day-to-day instrument and data system maintenance and calibration.
<br>
<br>
Other Functions:
<br>
A: Conform to documented Roles and Responsibilities for this position
<br>
B: Maintain timely and complete conformance to established test method certification for this position</p><b><br>
About you</b><p><br>
BS or BA in Chemistry, Food Science, Biology or a related field<br>
Knowledge and functional understanding of Quality Systems: GLP, SQF, ISO-9001, HACCP, SAP preferred</p><div><br>
Skills &amp; Abilities:
<br>
<ul><li>Expertise in performing accurate, consistent and timely testing according to established methods</li><li>Able to work under pressure, determine priorities, organize resources and meet QC timelines</li><li>Strong organizational ability with attention to detail</li><li>Professional, clear, concise and effective communication in verbal and written format.</li><li>Proficient skills with Microsoft office, SAP and collateral QC computer systems</li><li>Based on subjective and objective results, able to recognize trends that may impact product quality or Symrise operational performance.</li><li>No dietary restrictions that would prohibit tasting of savory, sweet, and other natural and artificial flavor chemicals</li></ul></div><b><br>
Our offer</b><p><br>
Become part of our open and transparent culture. It will give you the opportunity to flourish and to develop inspiring experiences that contribute to the health and well-being of consumers in 160 countries around the world. Putting our employees in focus fuels our strong company growth above market rates and makes us an excellent place to develop your career.</p>
<p><b>
Come join us and embark on a fascinating journey with Symrise.</b></p>
<p>
If you feel that you fit the above criteria, then please apply by using our online application system. Your application will be treated confidentially.</p>
<p><i>
We are an Equal Opportunity Employer. We do not discriminate on the basis of race, religion, color, sex, gender identity, sexual orientation, age, non-disqualifying physical or mental disability, national origin, veteran status or any other basis covered by appropriate law. All employment is decided on the basis of qualifications, merit, and business need.</i></p>
<p><i>
Pay Transparency Disclosure: The expected annual salary range for this position is USD $66,000.00 &ndash; USD $80,000.00. Actual pay will be determined based on experience, qualifications, geographic location, and other job-related factors permitted by law. A discretionary annual bonus may be available based on individual and company performance.</i></p><br>
Job Reference: NA01427</div>

Quality Control Chemist

G NINE BIOCEUTICALS PVT LTD

<p>GNINE is a third party manufacturing unit in beta-lactum (TABLET/DRY SYRUP &amp; DRY POWDER INJ).</p><p>Requirement of Quality Control Analyst.</p><p>Job Type: Full-time</p><p>Pay: ₹12,000.00 - ₹30,000.00 per month</p><p>Work Location: In person</p>

Quality Control Analyst

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