lab analyst

CVR Labs

<div><p>We recognize that a company&rsquo;s success is driven by its team member&rsquo;s combined efforts and strategies. CVR Labs strives to recruit and maintain an enthusiastic team with knowledge, experience, and a good attitude. Whether you are interested in building your career by joining our analytical, field, marketing/sales, or management department, we always welcome resumes and employment applications. CVR Labs values its employees and offers competitive benefits to show appreciation to its team members.</p><p>
There&rsquo;s never been a better time to join our truly dynamic enterprise &ndash; and to be all you can be. You can use this section to access details on our general vacancies within each business.</p></div><p></p>
<br><p>Job Title Lab Analyst (Immediate Requirement)</p>
<br><p>Qualification M.Sc. Chemistry<br>
Qualification M.Sc. Chemistry</p>
<br>Experience 2&ndash;4 Years

Lab Analyst (Immediate Requirement)

<div><div>You will perform analytical testing to help ensure quality and safety at our Pakistan laboratory. You will work closely with laboratory colleagues, production, and quality teams to deliver timely and accurate test results. We value clear procedures, careful records, and a willingness to learn and improve. This role offers practical growth, cross-team collaboration, and the chance to make meaningful contributions that align with our mission of uniting science, technology and talent to get ahead of disease together.
<br>
<br>
<b>Responsibilities
</b><br>
<ul><li>Perform routine testing of raw materials, in-process samples, finished products and stability samples using approved methods and laboratory instruments.
</li><li>Record, review and report test data clearly and accurately in laboratory records and the laboratory information system.
</li><li>Support investigations into atypical or out-of-specification results and help implement corrective actions.
</li><li>Maintain reagent, reference standard and consumable inventories and perform routine equipment checks and basic calibrations.
</li><li>Support method transfers, validation activities and on-the-job training for laboratory colleagues.
</li><li>Follow good manufacturing and laboratory practices, safety procedures and participate in workplace inclusion and EHS activities.
</li></ul><br>
<b>Education, Experience &amp; Skills
</b><br>
<ul><li>Pharm &ndash; D, Bachelor&rsquo;s or Master&rsquo;s degree in Chemistry, Applied Chemistry, Industrial Chemistry, or a related science discipline.
</li><li>Fresh to 2 years of laboratory experience in quality control, analytical testing, or a similar regulated environment.
</li><li>Practical experience with common laboratory techniques and instruments such as HPLC, GC, UV-visible spectrophotometry, or comparable analytical equipment.
</li><li>Basic computer skills including MS Office and willingness to learn laboratory information systems and SAP.
</li><li>Clear written and verbal communication skills and ability to work collaboratively in diverse teams.
</li><li>Understanding of good laboratory and good manufacturing practices and commitment to following procedures.
</li><li>Experience using LIMS and SAP for sample release, inventory transactions, or reporting.
</li><li>Experience supporting investigations, root cause analysis, and corrective actions.
</li><li>Familiarity with quality management systems and document control processes.
</li><li>Strong attention to detail, organization and basic data calculation skills.
</li></ul><br>
<b>What we value
</b><br>
We welcome people who bring curiosity, respect and a collaborative mindset. We support inclusion and fair opportunities for all candidates. If you are ready to grow your laboratory career, care about quality and want to make a meaningful impact, we encourage you to apply.
<br>
<br>
Apply now and help us get ahead of disease together.
</div><p></p><p><b>Why GSK?
</b><br>
<b>Uniting science, technology and talent to get ahead of disease together.
</b></p><p></p><p>GSK is a global biopharma company with a purpose to unite science, technology and talent to get ahead of disease together. We aim to positively impact the health of 2.5 billion people by the end of the decade, as a successful, growing company where people can thrive. We get ahead of disease by preventing and treating it with innovation in specialty medicines and vaccines. We focus on four therapeutic areas: respiratory, immunology and inflammation; oncology; HIV; and infectious diseases &ndash; to impact health at scale.
</p><p></p><p>People and patients around the world count on the medicines and vaccines we make, so we&rsquo;re committed to creating an environment where our people can thrive and focus on what matters most. Our culture of being ambitious for patients, accountable for impact and doing the right thing is the foundation for how, together, we deliver for patients, shareholders and our people.
</p><p></p><p><b>Contact information:
</b><br>
You may apply for this position online by selecting the <b>Apply now </b>button.
</p><p></p><p><b>Important notice to Employment businesses/ Agencies
</b></p><p>GSK does not accept referrals from employment businesses and/or employment agencies in respect of the vacancies posted on this site. All employment businesses/agencies are required to contact GSK's commercial and general procurement/human resources department to obtain prior written authorization before referring any candidates to GSK. The obtaining of prior written authorization is a condition precedent to any agreement (verbal or written) between the employment business/ agency and GSK. In the absence of such written authorization being obtained any actions undertaken by the employment business/agency shall be deemed to have been performed without the consent or contractual agreement of GSK. GSK shall therefore not be liable for any fees arising from such actions or any fees arising from any referrals by employment businesses/agencies in respect of the vacancies posted on this site.</p></div>

Lab Analyst

PepsiCo

<b>Responsibilities:</b><br>
1. Carry out and record chemical and physical, microbiological laboratory testing of products both work in progress and finished products by following the correct methods of analysis and SOPs.
<br>2. Chemical and physical, microbiological testing for all the raw and packaging materials to be released.
<br>3. Responsible for the waste water anlysis .
<br>4. Implementing the hold and release procedure.
<br>5. Perform and record internal calibration check of the lab equipments and instruments as per the required intervals.
<br>6. Sending daily, weekly and monthly reports showing the Weak Link performance
<br>7. Participate in investigations into product issues, customer complaints.
<br>8. Following and ensuring Global PepsiCo Standards "GEHSMS" compliance.
<br>9. Esclate problems to the attention of Lab manager , in addition to providing advices on quality issuesز
<br>10. Perform sanitation and hygiene test procedures to ensure compliance to PI standards and local authority standards.
<br>11. Communication of any OOS result to the top management and implement the corrective actions.
<br>12. Commply with Good Laboratory Practice (GLP) within the lab and follow all the Lab documented procedures and instructions regarding HACCP, ISO, Hygiene, and EHS.
<br><br>
13. Achieve the best quality of the product over our competitors regarding FLC (FritoLay Challenge).
<br>14. Keep the consistency of being (pass) in all regional proficiency tests.
<br>Ensure retained/shelf life samples are stored effectively for traceability and testing as required.
<br>15. Ensure producing safe products and applying key food safety attributes in his/her area of concern.
<br>Carry out any other tasks relevant to the department as requested by department managers or other related departments e.g. R&D.
<br>16. Perfrom and report Trade & retail ausit for All DCs
<br><br>
<b>Qualifications:</b><br>
1. University Degree in Quality, Chemistry, Food Science or Agricuture , Science.
<br>2. 1 -2 year experience in FMCG. Is preferred
<br>3. Very good verbal, spoken and written communication skills in English and Arabic languages.
<br>4. Very good in Microsoft office (Excel, Word, Power Point, Outlook).
<br>5. GMP,GLP and al food safety standards
<br>6. Quality systems knowledge

SC QC Associate - Lab Analyst

<div>
 <strong>
  Responsibilities
  <br/>
  <br/>
 </strong>
 <ul>
  <li>
   Carry out and record chemical and physical, microbiological laboratory testing of products both work in progress and finished products by following the correct methods of analysis and SOPs.
  </li>
  <li>
   Chemical and physical, microbiological testing for all the raw and packaging materials to be released.
  </li>
  <li>
   Responsible for the waste water anlysis .
  </li>
  <li>
   Implementing the hold and release procedure.
  </li>
  <li>
   Perform and record internal calibration check of the lab equipments and instruments as per the required intervals.
  </li>
  <li>
   Sending daily, weekly and monthly reports showing the Weak Link performance
  </li>
  <li>
   Participate in investigations into product issues, customer complaints.
  </li>
  <li>
   Following and ensuring Global PepsiCo Standards "GEHSMS" compliance.
  </li>
  <li>
   Esclate problems to the attention of Lab manager , in addition to providing advices on quality issuesز
  </li>
  <li>
   Perform sanitation and hygiene test procedures to ensure compliance to PI standards and local authority standards.
  </li>
  <li>
   Communication of any OOS result to the top management and implement the corrective actions.
  </li>
  <li>
   Commply with Good Laboratory Practice (GLP) within the lab and follow all the Lab documented procedures and instructions regarding HACCP, ISO, Hygiene, and EHS.
  </li>
  <li>
   Achieve the best quality of the product over our competitors regarding FLC (FritoLay Challenge).
  </li>
  <li>
   Keep the consistency of being (pass) in all regional proficiency tests.
   <br/>
   <br/>
  </li>
 </ul>
 Ensure retained/shelf life samples are stored effectively for traceability and testing as required.
 <br/>
 <br/>
 <ul>
  <li>
   Ensure producing safe products and applying key food safety attributes in his/her area of concern.
   <br/>
   <br/>
  </li>
 </ul>
 Carry out any other tasks relevant to the department as requested by department managers or other related departments e.g. R&amp;D.
 <br/>
 <br/>
 <ul>
  <li>
   Perfrom and report Trade &amp; retail ausit for All DCs
   <br/>
   <br/>
  </li>
 </ul>
 <strong>
  Qualifications
  <br/>
  <br/>
 </strong>
 <ul>
  <li>
   University Degree in Quality, Chemistry, Food Science or Agricuture , Science.
  </li>
  <li>
   1 -2 year experience in FMCG. Is preferred
  </li>
  <li>
   Very good verbal, spoken and written communication skills in English and Arabic languages.
  </li>
  <li>
   Very good in Microsoft office (Excel, Word, Power Point, Outlook).
  </li>
  <li>
   GMP,GLP and al food safety standards
  </li>
  <li>
   Quality systems knowledge
  </li>
 </ul>
</div>


T. Marzetti Company

<div>About Us:
<div>
The Marzetti Company (Nasdaq: MZTI) manufactures and sells specialty food products. Our retail brands include Marzetti&reg; dressings and dips, New York Bakery&trade; garlic breads, and Sister Schubert&rsquo;s&reg; dinner rolls, in addition to exclusive license agreements for Olive Garden&reg; dressings, Chick-fil-A&reg; sauces and dressings, Buffalo Wild Wings&reg; sauces, Arby&rsquo;s&reg; sauces, Subway&reg; sauces, and Texas Roadhouse&reg; steak sauces and frozen rolls. Our foodservice business supplies sauces, dressings, breads, and pasta to many of the top restaurant chains in the United States.
<br>
<br>
At Marzetti, our mission is to make every meal better through high-quality, flavorful food. Led by our purpose, to nourish growth with all that we do, our team members are dedicated to creating great tasting food and cultivating deep and lasting relationships.</div><br>
<div></div>
Overview:
<div>
The analyst position is key in maintaining the quality of incoming ingredients, in line product, and finished product. This person shall report any non conformance of finished product to the QA Supervisor or Manager. Excellent opportunity to expand your skillset and advance your career within the Quality group within Marzetti.</div><div></div><div><i><br>
We kindly request that recruitment agencies and staffing firms refrain from submitting unsolicited resumes to our company. Any resumes sent without a prior agreement and access to proper submittal into the ATS will be considered the property of T. Marzetti, and we reserve the right to contact those candidates without any obligation to pay a fee.</i></div>
Responsibilities:<br>
<div></div><ul><li>
Basic Understanding of the key testing attributes and following the Work Practices in the Quality Assurance Manual.</li><li>
Reports processing problems or packaging line issues immediately to Production Supervisor and QA Manager.</li><li>
Reports packaging line problems or potential problems immediately to Production Supervisor and QA Manager.</li><li>
Collects retain samples at prescribed frequency and maintains samples in an organized fashion. Maintains adequate inventory of lab-prepared colors and flavors.</li><li>
Maintains lab work area in a clean and orderly fashion and performs calibration of lab equipment when assigned.</li><li>
Monitors critical control points (CCPs) for PH, water activity and metal detection.</li><li>
Follows and maintains awareness of the plant Good Manufacturing Practices (GMPs) and reports anything which might have a negative impact.</li><li>
Follows Good Laboratory Practices (GLPs) established by QA Manager and Safety guidelines established by plant management.</li><li>
Ensures quality, food safety 5S, OSHA, and HACCP support programs, assures conformity to all company, customer and government standards.</li><li>
Participates in activities related to Marzetti Operational Excellence.</li><li>
Basic science skills; math, accurate data collection, general lab, and computer data entry. Ability to be dependable and timely.</li><li>
Strong written and verbal communication skills. Detailed oriented with the ability to follow detailed instructions and specifications.</li><li>
Ability to work independently on pre-assigned task and multi-task, organize job tasks and the workspace.</li><li>
Any and all other duties assigned due to business needs.</li></ul><div></div><div><br>
#TMZ23</div>
Qualifications:
<ul><li>Bachelor&rsquo;s degree in food science, Microbiology, or related field preferred but not required: or 2 years&rsquo; experience.</li><li>
Ability to work cooperatively with a team.</li><li>
Strong oral and written communication skills and computer skills required.</li></ul>
Working Conditions/Environment:
<div>
Works in a laboratory and manufacturing environment where the employee is regularly required to speak, read, sit, stand, walk, climb, crouch, lift, reach, grasp and bend while moving about the facility. Requires some lifting of moderately heavy items such as test equipment and product cases. Must be able to stand for an 8&ndash;10-hour shift (sometimes longer) with regular breaks while performing repetitive tasks. May be required to work overtime and / or weekends as needed. The employee may be exposed to non-ambient temperatures, odors, dust, oil, slippery floors, moving parts / equipment, and handling hazardous testing and sanitation chemicals. The Noise level in the lab is moderate and loud in the plant. Ear protection, eye/face protection, hair/beard nets, steel-toed/slip-resistant shoes, and gloves are required as necessary in accordance with company GMP and safety standards.</div>
Cultivate Your Career:
<div>
Lancaster Colony Corporation and its wholly owned subsidiary T. Marzetti Company are committed to a policy of equal opportunity for all associates without regard to race, color, religion, gender, national origin, age, disability, sexual orientation, or gender identity. It is our goal to provide opportunities that nourish the growth of each individual team member.</div></div>

Quality Assurance Analyst - 3rd Shift

Mass General Brigham

<div>Site: The Brigham and Women's Hospital, Inc.<br>
<p></p><br>
<p>Mass General Brigham relies on a wide range of professionals, including doctors, nurses, business people, tech experts, researchers, and systems analysts to advance our mission. As a not-for-profit, we support patient care, research, teaching, and community service, striving to provide exceptional care. We believe that high-performing teams drive groundbreaking medical discoveries and invite all applicants to join us and experience what it means to be part of Mass General Brigham.<br>
</p><p></p><br>
<br>
<p><b>Job Summary
</b></p>GENERAL SUMMARY:
<br>
The Cardiac Imaging Core Lab (CICL), Directed by Scott D. Solomon, MD, is an academic research organization located within the Brigham and Women&rsquo;s Hospital, a Harvard-affiliated hospital. Through close collaboration with academic, NIH, and industry partners, the CICL supports a wide range of activities including echocardiographic study design, analysis, and central core lab operations for primarily large-scale national and international clinical trials. There are approximately 40 staff supporting 40+ clinical trials ongoing at any given time with a typical volume of 1000 &ndash; 1500 echos received each month.
<br>
Reporting to the CICL Executive Director and working under the supervision of Harvard Faculty Directors, the Sr. Echo Analyst is responsible for especially complex overreading of assigned studies. This overreading is a critical quality check of analysis already performed and requires expert judgement and skill which is over and above Echo Analyst level.<br>
<p></p><br>
<div><div><div><div><div><div><div><p><b>Qualifications
 </b></p></div></div></div></div></div></div></div><p><b>PRINCIPAL DUTIES AND RESPONSIBILITIES:
</b></p><p>1. Serves as an integral part of the research team providing echocardiographic overreading for assigned studies.
</p><p>2. Performs echocardiographic strain analysis of heart size and function in a high quality, scientific, and reproducible manner. These analyses may include but are not limited to: 2D, 3D, M Mode, Color Doppler, strain, etc.
</p><p>3. Is an integral member of the QA review process of analyzed data and requests re-review as needed of assigned Echo Analysts.
</p><p>4. Advises CICL Executive Director with technical research direction as it relates to the overall research scope of the CICL.
</p><p>6. Participates in lab wide and/or project specific meetings.
</p><p>7. Adheres to all CICL SOPs as well as internal system and technical requirements for performing within this role.
</p><p><b>QUALIFICATIONS:
</b></p><p>MD with cardiovascular experience or PhD with cardiovascular research experience in human subject clinical trials is required.
</p><p>Candidate requires either 5 years leadership experience within CICL or at least 10 years prior leadership experience overseeing echo analysis.
</p><p>Knowledge of cardiac anatomy, physiology, cardiac pathophysiology hemodynamics and echocardiography assessment of heart disease is required. Advanced knowledge in echocardiography including but not limited to: 3-D, gradient analysis, etc. is preferred.
</p><p></p><p><b>SKILLS/ABILITIES/COMPETENCIES REQUIRED:
</b></p><ul><li>Ability to perform echocardiographic analysis analyze 2D, M Mode, Color Doppler, strain, etc. is required.
</li></ul><ul><li>Strong research design and analytical skills.
</li></ul><ul><li>Strong computer and database statistical skills.
</li></ul><ul><li>Excellent time management/organizational skills.
</li></ul><ul><li>Able to multitask and assign priorities in a busy, challenging environment.
</li></ul><ul><li>Ability to work as part of an interdisciplinary research team.<br>
</li></ul><p></p><br>
<div><div><div><div><div><div><div><p><b>Additional Job Details (if applicable)<br>
</b></p></div></div></div></div></div></div></div><p></p><br>
<div><div><div><div><div><div><div><p><b>Remote Type
</b></p></div></div></div></div></div></div></div>Hybrid<br>
<p></p><br>
<div><div><div><div><div><div><div><p><b>Work Location
</b></p></div></div></div></div></div></div></div>75 Francis Street<br>
<p></p><br>
<div><div><div><div><div><div><div><p><b>Scheduled Weekly Hours
</b></p></div></div></div></div></div></div></div>0<br>
<p></p><br>
<div><div><div><div><div><div><div><p><b>Employee Type
</b></p></div></div></div></div></div></div></div>Per Diem<br>
<p></p><br>
<div><div><div><div><div><div><div><p><b>Work Shift
</b></p></div></div></div></div></div></div></div>Day (United States of America)<br>
<p></p><br>
<br>
<p><b>Pay Range
</b></p>$29.81 - $43.63/Hourly<br>
<p></p><br>
<p><b>Grade
</b></p>7<br>
<p></p><br>
At Mass General Brigham, we believe in recognizing and rewarding the unique value each team member brings to our organization. Our approach to determining base pay is comprehensive, and any offer extended will take into account your skills, relevant experience if applicable, education, certifications and other essential factors. The base pay information provided offers an estimate based on the minimum job qualifications; however, it does not encompass all elements contributing to your total compensation package. In addition to competitive base pay, we offer comprehensive benefits, career advancement opportunities, differentials, premiums and bonuses as applicable and recognition programs designed to celebrate your contributions and support your professional growth. We invite you to apply, and our Talent Acquisition team will provide an overview of your potential compensation and benefits package.<br>
<p></p><br>
<div><div><div><div><div><div><div><p><b>EEO Statement:
</b></p></div></div></div></div></div></div></div>2200 The Brigham and Women's Hospital, Inc. is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religious creed, national origin, sex, age, gender identity, disability, sexual orientation, military service, genetic information, and/or other status protected under law. We will ensure that all individuals with a disability are provided a reasonable accommodation to participate in the job application or interview process, to perform essential job functions, and to receive other benefits and privileges of employment. To ensure reasonable accommodation for individuals protected by Section 503 of the Rehabilitation Act of 1973, the Vietnam Veteran&rsquo;s Readjustment Act of 1974, and Title I of the Americans with Disabilities Act of 1990, applicants who require accommodation in the job application process may contact Human Resources at (857)-282-7642.<br>
<p></p><br>
<h2 class="jobSectionHeader"><b>Mass General Brigham Competency Framework
</b></h2><div><div><p>At Mass General Brigham, our competency framework defines what effective leadership &ldquo;looks like&rdquo; by specifying which behaviors are most critical for successful performance at each job level. The framework is comprised of ten competencies (half People-Focused, half Performance-Focused) and are defined by observable and measurable skills and behaviors that contribute to workplace effectiveness and career success. These competencies are used to evaluate performance, make hiring decisions, identify development needs, mobilize employees across our system, and establish a strong talent pipeline.</p></div></div></div>

Echo Cardiac Analyst

Haleon

<div>
 Welcome to Haleon. We&rsquo;re a purpose-driven, world-class consumer company putting everyday health in the hands of millions. In just three years since our launch, we&rsquo;ve grown, evolved and are now entering an exciting new chapter &ndash; one filled with bold ambitions and enormous opportunity.
 <br/>
 <br/>
 Our trusted portfolio of brands &ndash; including Sensodyne&reg;, Panadol&reg;, Advil&reg;, Voltaren&reg;, Theraflu&reg;, Otrivin&reg;, and Centrum&reg; &ndash; lead in resilient and growing categories. What sets us apart is our unique blend of deep human understanding and trusted science.
 <br/>
 <br/>
 Now it&rsquo;s time to fully realise the full potential of our business and our people. We do this through our Win as One strategy. It puts our purpose &ndash; to deliver better everyday health with humanity &ndash; at the heart of everything we do. It unites us, inspires us, and challenges us to be better every day, driven by our agile, performance-focused culture.
 <br/>
 <br/>
 <strong>
  Job Purpose:
  <br/>
  <br/>
 </strong>
 To carry out the analysis of stability samples in accordance with stability schedules, conduct analytical method validation/verification, monitor stability chambers, prepare stability protocols and reports, and maintain the archiving of raw data.
 <br/>
 <br/>
 <strong>
  Key Responsibilities:
  <br/>
  <br/>
 </strong>
 <ul>
  <li>
   Perform timely analysis of stability samples (accelerated, ongoing, and long-term) to meet the schedule and achieve 100% KPI compliance.
  </li>
  <li>
   Conduct analysis of NPI (New Product Introduction) batches, analytical method validation/verification, and testing of reference standards for qualification.
  </li>
  <li>
   Prepare stability protocols and reports, receive stability samples, update stability schedules, label samples, and pull stability samples as per schedules.
  </li>
  <li>
   Complete and maintain all related documents (worksheets, logbooks, protocols, reports, etc.) in accordance with data integrity principles (ALCOA+).
  </li>
  <li>
   Monitor all stability chambers and report any malfunctions in a timely manner.
  </li>
  <li>
   Report any OOT (Out of Trend), OOS (Out of Specification), atypical results, events, or deviations promptly.
  </li>
  <li>
   Ensure proper disposal of waste.
  </li>
  <li>
   Provide timely stability data to the QS (Quality Systems) department for PPR (Periodic Product Review) reports.
  </li>
  <li>
   Properly archive stability data and maintain the tracker to ensure easy retrieval and compliance.
  </li>
  <li>
   Support the Finished Goods Testing department in achieving CTR (Confirms to Release) targets.
  </li>
  <li>
   Support audit preparation activities in collaboration with the reporting manager.
  </li>
  <li>
   Ensure compliance with GMP (Good Manufacturing Practices), Quality, and other relevant policies and legal requirements, as well as Haleon Guidelines.
  </li>
  <li>
   Ensure compliance with Environmental, Health, and Safety (EHS) policies and legal requirements, as well as Haleon Guidelines.
  </li>
  <li>
   Perform any other responsibilities assigned as needed to meet business requirements.
   <br/>
   <br/>
   <br/>
  </li>
 </ul>
 <strong>
  Skills &amp; Competencies:
  <br/>
  <br/>
 </strong>
 <ul>
  <li>
   M.Sc.(Chemistry) / Pharm D
  </li>
  <li>
   Analyst with 1-2 years of experience in a Quality Control (QC) lab with strong analytical skills and knowledge of the pharmaceutical industry or a relevant field.
   <br/>
   <br/>
   <br/>
  </li>
 </ul>
 <strong>
  Why Join Us?
  <br/>
  <br/>
 </strong>
 The future of everyday health is changing. And we&rsquo;re the people changing it. In front of us is an incredible opportunity to go beyond what any of us have done before. And make everyday health more achievable, more inclusive and more sustainable. For more and more people.
 <br/>
 <br/>
 So join us, as we build one of the world&rsquo;s leading consumer companies. Join us to innovate our category-leading brands. To better understand people&rsquo;s everyday health needs. To tackle the biggest barriers that stand in their way. To change individual and societal behavior.
 <br/>
 <br/>
 In our efforts to further tackle barriers that may be standing in our way, we have implemented what we call a Hybrid Working model, known as Home office. Home office in the country of employment is permitted for all employees whose position allows it. The employee and the manager agree on the circumstances in which working from the office is required and in which the employee can work remotely or specific local arrangements. This helps us with ensuring that we maintain a healthy work-life balance, and give our best to our people.
 <br/>
 <br/>
 Join us to work with colleagues who share your restless energy. To explore your interests. To stretch yourself to do the best work of your career. And join us, as together we build a working experience that encourages us all to lead happier, healthier, more productive lives.
 <br/>
 <br/>
 The way we see it, every day is an opportunity for better. And we&rsquo;re going all in to realize it.
 <br/>
 <br/>
 <strong>
  Job Posting End Date
  <br/>
  <br/>
 </strong>
 2026-01-01
 <br/>
 <br/>
 <strong>
  Equal Opportunities
  <br/>
  <br/>
 </strong>
 Haleon are committed to mobilising our purpose in a way that represents the diverse consumers and communities who rely on our brands every day. It guides us in creating an inclusive culture, where different backgrounds and views are valued and respected &ndash; all in support of understanding and best serving the needs of our consumers and unleashing the full potential of our people. It&rsquo;s important to us that Haleon is a place where all our employees feel they truly belong.
 <br/>
 <br/>
 During the application process, we may ask you to share some personal information, which is entirely voluntary. This information ensures we meet certain regulatory and reporting obligations and supports the development, refinement, and execution of our inclusion and belonging programmes that are open to all Haleon employees.
 <br/>
 <br/>
 The personal information you provide will be kept confidential, used only for legitimate business purposes, and will never be used in making any employment decisions, including hiring decisions.
 <br/>
 <br/>
 <strong>
  Adjustment or Accommodations Request
  <br/>
  <br/>
 </strong>
 If you require a reasonable adjustment or accommodation or other assistance to apply for a job at Haleon at any stage of the application process, please let your recruiter know by providing them with a description of specific adjustments you are requesting. We&rsquo;ll provide all reasonable adjustments to support you throughout the recruitment process and treat all information you provide us in confidence.
 <br/>
 <br/>
 <strong>
  Note to candidates
  <br/>
  <br/>
 </strong>
 The Haleon recruitment team will contact you using a Haleon email account (@haleon.com). If you are not sure whether the email you received is from Haleon, please get in touch.
</div>


Analyst Stability Lab

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