lab analyst

ICON plc

<div>Lab Analyst 3- Lenexa, KS- Onsite; Full-Time<div></div><div>
ICON plc is a world-leading healthcare intelligence and clinical research organization. We&rsquo;re proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development</div><div></div><div>
We are currently seeking a Lab Analyst 3 to join our diverse and dynamic team. As a Lab Analyst 3 at ICON, you will play a critical role in conducting complex laboratory analyses and supporting the delivery of high-quality data for clinical research studies. You will be responsible for performing advanced testing procedures, maintaining accurate records, and ensuring compliance with regulatory and quality standards.</div><div></div><div>
What You Will Be Doing:</div><div></div><ul><li><div>
Performing complex laboratory tests and analyses in accordance with established protocols and procedures.</div></li><li><div>
Documenting test results and maintaining detailed records to ensure data accuracy and integrity.</div></li><li><div>
Conducting quality control checks and calibrations of laboratory equipment to maintain compliance with regulatory standards.</div></li><li><div>
Collaborating with cross-functional teams to troubleshoot and resolve technical issues and ensure timely delivery of results.</div></li><li><div>
Participating in the development and validation of new laboratory methods and procedures to support ongoing research projects.</div></li><li><div>
Planning, handling and delivering laboratory training.</div></li><li><div>
Planning and organizing assay validation/qualification in conjunction with the method development team.</div></li><li><div>
Identifying all applicable regulatory requirements and ensuring compliance.</div></li><li><div>
Leading troubleshooting and investigation efforts as well as performing retraining and impact assessments if applicable.</div></li><li><div>
Acting as subject matter expert, performing study support, and taking part in sponsor communications.</div></li><li><div>
Driving process improvements and evaluating effectiveness for process changes.</div></li><li><div>
Providing education sessions in a group setting.</div></li></ul><div></div><div>
Your Profile:</div><ul><li>
Bachelor&rsquo;s degree in biology, chemistry, or a related scientific field; advanced degree preferred.</li><li>
3-5 years of experience in a laboratory environment, with a focus on advanced analytical techniques and procedures.</li><li>
Strong technical skills, with proficiency in using laboratory equipment and software for data analysis and reporting.</li><li>
Excellent attention to detail and organizational abilities, with a commitment to maintaining high-quality standards.</li><li>
Strong communication and teamwork skills, with the ability to work effectively in a collaborative environment.</li></ul><div></div><div>
Preferred Qualifications:</div><ul><li>
Ability to work independently within the lab</li><li>
Experience working with FACTSDIVA or FlowJO</li><li>
4+ years of experience working with flow cytometry</li><li>
Strong communicator and a team player</li></ul><div></div><div>
#LI-Onsite</div><div>
#LI-HP1</div><div></div><div>
What ICON can offer you:</div><div></div><div><div><div><div><div>
Our success depends on the quality of our people. That&rsquo;s why we&rsquo;ve made it a priority to build a diverse culture that rewards high performance and nurtures talent.</div><div></div><div>
In addition to your competitive salary, ICON offers a range of additional benefits. Our benefits are designed to be competitive within each country and are focused on well-being and work life balance opportunities for you and your family.</div><div></div><div>
Our benefits examples include:</div><ul><li><div>
Various annual leave entitlements</div></li><li><div>
A range of health insurance offerings to suit you and your family&rsquo;s needs.</div></li><li><div>
Competitive retirement planning offerings to maximize savings and plan with confidence for the years ahead.</div></li><li><div>
Global Employee Assistance Programme, TELUS Health, offering 24-hour access to a global network of over 80,000 independent specialised professionals who are there to support you and your family&rsquo;s well-being.</div></li><li><div>
Life assurance</div></li><li><div>
Flexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidised travel passes, health assessments, among others.</div></li></ul></div></div></div></div><div></div><div>
Visit our <div>careers site</div> to read more about the benefits ICON offers.</div><div></div><div>
At ICON, inclusion &amp; belonging are fundamental to our culture and values. We&rsquo;re dedicated to providing an inclusive and accessible environment for all candidates. ICON is committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status.</div><div></div><div><div><div><div><div>
If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or in order to perform the essential functions of a position, please let us know</div><div></div><div><div>
Interested in the role, but unsure if you meet all of the requirements? We would encourage you to apply regardless &ndash; there&rsquo;s every chance you&rsquo;re exactly what we&rsquo;re looking for here at ICON whether it is for this or other roles.</div></div></div></div></div></div></div><div></div>

Lab Analyst 3

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

Petrolabs India Private Limited

<p>Degree - B.Sc Chemistry, Bio Chemistry, Micro Biology<br/>Test or analyze used oil samples to detect presence of water, contaminants, wear indicating potential issues for the critical equipment or to determine physical or chemical properties to ensure that products meet quality standards.</p><p>Job Types: Full-time, Fresher</p><p>Pay: &#8377;14,000.00 - &#8377;15,000.00 per month</p><p>Ability to commute/relocate:</p><ul><li>Kukatpally, Hyderabad, Telangana: Reliably commute or planning to relocate before starting work (Preferred)</li></ul><p>Education:</p><ul><li>Bachelor's (Preferred)</li></ul><p>Language:</p><ul><li>Telugu, English &amp; Hindi (Preferred)</li></ul><p>Location:</p><ul><li>Kukatpally, Hyderabad, Telangana (Preferred)</li></ul><p>Work Location: In person</p>

Lab Analyst

ACZ Laboratories, Inc

<div><p>ACZ Laboratories, Inc. is an environmental testing laboratory located in the beautiful mountain town of Steamboat Springs, CO. Founded in 1980, ACZ Laboratories is an accredited environmental testing laboratory with inorganic, organic, and radiochemical capabilities. We specialize in the analysis of trace-level contaminants in water, soil, sediment, sludge, waste, biota, and tissue.</p>
<p>
We are seeking a dedicated and detail-oriented Environmental Lab Analyst / Chemist to join our team and provide clients and communities with high quality data to ensure a healthy environment for present and future generations. The Environmental Lab Analyst /Chemist reports directly to and works with the Lab Supervisor.
</p><p>As an Environmental Lab Analyst / Chemist, you will be responsible for conducting chemical analyses and testing of environmental samples including soil, water, air, and hazardous waste. You will play a crucial role in ensuring compliance with environmental regulations and providing accurate data to support environmental assessments and projects. The ideal candidate will have strong technical knowledge in analytical chemistry, attention to detail, and a passion for environmental sustainability.</p>
<p><b>
Key Accountabilities</b>
</p><ul><li>Conduct accurate and timely environmental sample analysis
 </li><li>Ensure compliance with environmental regulations and quality standards
</li><li>Maintain and calibrate laboratory instruments
</li><li>Document, review and report test results
</li><li>Support laboratory safety and environmental protection</li>
</ul>
<p><b>Job Responsibilities</b>
</p><p><i>Conduct accurate and timely environmental sample analysis</i>
</p><ul><li>Prepare samples for analysis, including digestion, filtration, and dilution as required by standard operating procedures.
</li><li>Perform chemical analyses of environmental samples using various laboratory techniques and instruments (e.g., GC-MS, HPLC, ICP-MS).
</li><li>Ensure accurate analysis on environmental samples for various constituents to provide high-quality data that supports environmental monitoring and regulatory reporting.</li>
</ul>
<p><i>Ensure compliance with environmental regulations and quality standards</i></p>
<ul>
<li>Stay current with industry trends, regulations, and advancements in analytical chemistry.
</li><li>Participate in the development and validation of new laboratory methods and procedures.
</li><li>Perform quality control checks and maintain records of laboratory activities.</li>
<li>Execute EPA approved methods according to laboratory standard operating procedures.</li>
</ul>
<p><i>Maintain and calibrate laboratory instruments</i></p>
<ul>
<li>Maintain and calibrate laboratory equipment to ensure accuracy and reliability of results.
</li><li>Monitor and maintain support equipment such as balances, ovens, and thermometers.
</li><li>Clean laboratory equipment and facilities.</li>
</ul>
<p><i>Document, review and report test results</i></p>
<ul>
<li>Analyze and interpret data and prepare comprehensive reports summarizing findings and methodologies.
</li><li>Collaborate with project managers and other team members to meet project deadlines and deliverables.</li>
<li>Maintain complete and accurate records of laboratory activities.
</li><li>Prepare and review data.</li>
</ul>
<p><i>Support laboratory safety, environmental protection and mission</i></p>
<ul>
<li>Ensure compliance with environmental regulations and laboratory safety protocols.
</li><li>Perform other duties as instructed.</li>
<li>Learn, embrace, and adhere to ACZ's mission, core values, and quality system.</li>
</ul>
<p><b>Qualifications</b>
</p><ul><li>Bachelor&rsquo;s degree in chemistry, environmental science, or a related field.
</li><li>Previous experience in an environmental lab or analytical chemistry role is highly desirable.
</li><li>Proficiency in laboratory instruments and techniques relevant to environmental analysis.
</li><li>Strong understanding of environmental regulations (e.g., EPA, ASTM standards).
</li><li>Excellent organizational skills and attention to detail.
</li><li>Ability to take initiative and complete tasks with minimal supervision
</li><li>Can work independently and as part of a team in a fast-paced environment
</li><li>Strong verbal and written communication skills.
</li><li>Proficient in data analysis software and Microsoft Office Suite.
</li><li>Strong work ethic.
</li><li>Desire and ability to work in a team environment.</li>
</ul>
<p><b>What We Offer</b>
</p><ul><li>Full-time, fully benefited position; paid time off, paid holidays, health, dental, 401k, profit sharing, disability and accident insurance
</li><li>$22.50 &ndash; $25.00/hour DOQ
</li><li>Flexible work schedule</li>
</ul>
<p>ACZ is an equal opportunity employer. We celebrate diversity and are committed to creating an inclusive environment for all employees. Position will be open until filled.</p></div>

Environmental Lab Analyst / Chemist

<div><b>Site Name:</b> Pakistan - Sindh - Karachi<br>
<b>Posted Date:</b> Nov 17 2025<p><br>
To ensure compliance of the Training Management system at Site by liaising with the departments, ensuring all the employees are trained, competent and the compliance needs are met.</p><p></p><p>
Release of good quality packaging material in line with approved standards and specification to support business and ensure smooth production operations by timely release of packaging components.</p><p></p><p><b>
Education, Skills &amp; Experience</b></p><ul><li>
Bachelor&rsquo;s degree in sciences, Engineering, Business or Pharm&#8209;D is required for this role.</li><li>
1- 3 years of experience in a preferred role.</li><li>
 Understanding of regulatory requirements including GMP and compliance training where required. Train the trainer certification would be beneficial.</li><li>
Good communication and presentation skills.</li><li>
Stakeholder and conflict management.</li><li>
Strong public speaking ability and conducting ILT session (small and large scale).</li><li>
Experience of handling groups of people including non- management.</li><li>
Proficient in MS Office (Word, PowerPoint and Excel).</li></ul><p></p><p><b>
Responsibilities</b></p><p><b>
Training Coordinator:</b></p><ul><li>
Implementation of the organization, personnel and training management system at the Site in- line with the global/ QMS training standards and policies, ensuring the in- place and in- use of the local procedure, policies and QMS requirements, obtaining TC 02 access in myLearning, smooth handling of the system and execution of the projects</li><li>
Ensure timely completion of trainings on monthly basis through periodic follow ups with the individuals, dept managers and learning reps across the Site, assessing the impact in case of any overdue, escalating to the relevant stakeholders and reporting to the SQC including mandatory and annual GMP refreshers</li><li>
Ensure monthly KPIs are monitored, managed and reported throughout the month, to the SQC and regional governance forums along with attending all the site- based or regional forums with timely provision of the data and completion of the actions as per the timelines, share knowledge of the forums and implement actions at the site level.</li><li>
Perform the management monitoring and participation in the independent business monitoring of the training system at site to ensure effectiveness.</li><li>
Analysis of the training needs in collaboration with the departments based on criteria defined in the TNA, updating the TNA on monthly basis with the SOPs included or deleted, change in the roles &amp; responsibilities and training delivery method.</li><li>
Ensure all the SOPs and OJTs are existing in myLearning as learning items with timely assignment of the questionnaires, curricula are updated electronically in-line with the TNA in VQD as well as in myLearning.</li><li>
Support the delivery/ facilitation of learning &amp; development interventions such as deviation investigation and root cause, customer complaints, recalls, out of specs or where appropriate.</li><li>
Conduction of the new employee&rsquo;s induction on timely basis, review of job descriptions and their assignment, job codes in myLearning and organograms are updated.</li><li>
Timely closure of all the CAPAs/ actions for risks, deviations, management monitoring, independent business management, change controls, annual reviews etc</li><li>
Development, adherence and approval of the learning calendar based on different systemic reviews and outcomes of the previous year, assigning, scheduling ILTs, marking in myLearning and reporting in the SQC</li><li>
Facilitate and ensure TtT of all trainers at the Site.</li><li>
Perform periodic review of all training related material such as packages, job descriptions, TNA, curricula, organograms and others to ensure they meet the minimum GMP requirements.</li><li>
Develop capability frameworks to ensure the right capability is embedded across the organization and to support the site in the 70/20/10 development of the employees based on the capability models and their outcomes.</li><li>
Perform annual review of the compliance training system and drive continuous improvement through employee&rsquo;s performance reviews and projects to simplify and modernize the training methodology.</li></ul><p></p><p><b>
Pack Lab Analyst:</b></p><ul><li>
Checking of artworks, bromides, machine proof, &amp; buying samples as per standards and regulatory requirements with respect to formulation RN &amp; ML Nos., Storage conditions&amp; Address to ensure GSK requirements are met and to avoid any Regulatory sanctions. To check the total artwork after the input of concerned Departments so that all the requirements are fulfilled in the Artworks</li><li>
Conduct Management monitoring audits to ensure compliance. Meeting with Supplier&rsquo;s for on-line complaint and rejections in order to facilitate the supplier in CAPA so to avoid recurrence in future supplies</li><li>
Preparation of monthly report of the section, Vendor complaints &amp; rejection data for supply review meetings and site quality council</li><li>
Preparation /Review of specifications /test methods, SOP&rsquo;s of packaging material to ensure compliance and ensure in-use of SOPs</li><li>
To manage calibrations and proper use of all equipment to ensure compliance.</li><li>
Updating of specification of new &amp; revised Packaging material in LIMS</li><li>
Update specifications and requirements of Packaging Materials in SAP (d-MERP)</li><li>
Look after the Pack Management Lab as designate in absence of Pack Management Manager</li><li>
To ensure that the all the SOPs related to training, QMS, change control, risk management Record Retention activities are in place and in use</li><li>
Maintains a safe and healthy work environment</li><li>
Ensure implementation of EHS standards and guidelines in the area of responsibility.</li><li>
Reporting EHS adverse events (Near misses, Incidents and Accidents) timely.</li></ul><p>
To ensure compliance of the Training Management system at Site by liaising with the departments, ensuring all the employees are trained, competent and the compliance needs are met.</p><p></p><p>
Release of good quality packaging material in line with approved standards and specification to support business and ensure smooth production operations by timely release of packaging components.</p><p></p><p><b>
Education, Skills &amp; Experience</b></p><ul><li>
Bachelor&rsquo;s degree in sciences, Engineering, Business or Pharm&#8209;D is required for this role.</li><li>
1- 3 years of experience in a preferred role.</li><li>
 Understanding of regulatory requirements including GMP and compliance training where required. Train the trainer certification would be beneficial.</li><li>
Good communication and presentation skills.</li><li>
Stakeholder and conflict management.</li><li>
Strong public speaking ability and conducting ILT session (small and large scale).</li><li>
Experience of handling groups of people including non- management.</li><li>
Proficient in MS Office (Word, PowerPoint and Excel).</li></ul><p></p><p><b>
Responsibilities</b></p><p><b>
Training Coordinator:</b></p><ul><li>
Implementation of the organization, personnel and training management system at the Site in- line with the global/ QMS training standards and policies, ensuring the in- place and in- use of the local procedure, policies and QMS requirements, obtaining TC 02 access in myLearning, smooth handling of the system and execution of the projects</li><li>
Ensure timely completion of trainings on monthly basis through periodic follow ups with the individuals, dept managers and learning reps across the Site, assessing the impact in case of any overdue, escalating to the relevant stakeholders and reporting to the SQC including mandatory and annual GMP refreshers</li><li>
Ensure monthly KPIs are monitored, managed and reported throughout the month, to the SQC and regional governance forums along with attending all the site- based or regional forums with timely provision of the data and completion of the actions as per the timelines, share knowledge of the forums and implement actions at the site level.</li><li>
Perform the management monitoring and participation in the independent business monitoring of the training system at site to ensure effectiveness.</li><li>
Analysis of the training needs in collaboration with the departments based on criteria defined in the TNA, updating the TNA on monthly basis with the SOPs included or deleted, change in the roles &amp; responsibilities and training delivery method.</li><li>
Ensure all the SOPs and OJTs are existing in myLearning as learning items with timely assignment of the questionnaires, curricula are updated electronically in-line with the TNA in VQD as well as in myLearning.</li><li>
Support the delivery/ facilitation of learning &amp; development interventions such as deviation investigation and root cause, customer complaints, recalls, out of specs or where appropriate.</li><li>
Conduction of the new employee&rsquo;s induction on timely basis, review of job descriptions and their assignment, job codes in myLearning and organograms are updated.</li><li>
Timely closure of all the CAPAs/ actions for risks, deviations, management monitoring, independent business management, change controls, annual reviews etc</li><li>
Development, adherence and approval of the learning calendar based on different systemic reviews and outcomes of the previous year, assigning, scheduling ILTs, marking in myLearning and reporting in the SQC</li><li>
Facilitate and ensure TtT of all trainers at the Site.</li><li>
Perform periodic review of all training related material such as packages, job descriptions, TNA, curricula, organograms and others to ensure they meet the minimum GMP requirements.</li><li>
Develop capability frameworks to ensure the right capability is embedded across the organization and to support the site in the 70/20/10 development of the employees based on the capability models and their outcomes.</li><li>
Perform annual review of the compliance training system and drive continuous improvement through employee&rsquo;s performance reviews and projects to simplify and modernize the training methodology.</li></ul><p></p><p><b>
Pack Lab Analyst:</b></p><ul><li>
Checking of artworks, bromides, machine proof, &amp; buying samples as per standards and regulatory requirements with respect to formulation RN &amp; ML Nos., Storage conditions&amp; Address to ensure GSK requirements are met and to avoid any Regulatory sanctions. To check the total artwork after the input of concerned Departments so that all the requirements are fulfilled in the Artworks</li><li>
Conduct Management monitoring audits to ensure compliance. Meeting with Supplier&rsquo;s for on-line complaint and rejections in order to facilitate the supplier in CAPA so to avoid recurrence in future supplies</li><li>
Preparation of monthly report of the section, Vendor complaints &amp; rejection data for supply review meetings and site quality council</li><li>
Preparation /Review of specifications /test methods, SOP&rsquo;s of packaging material to ensure compliance and ensure in-use of SOPs</li><li>
To manage calibrations and proper use of all equipment to ensure compliance.</li><li>
Updating of specification of new &amp; revised Packaging material in LIMS</li><li>
Update specifications and requirements of Packaging Materials in SAP (d-MERP)</li><li>
Look after the Pack Management Lab as designate in absence of Pack Management Manager</li><li>
To ensure that the all the SOPs related to training, QMS, change control, risk management Record Retention activities are in place and in use</li><li>
Maintains a safe and healthy work environment</li><li>
Ensure implementation of EHS standards and guidelines in the area of responsibility.</li><li>
Reporting EHS adverse events (Near misses, Incidents and Accidents) timely.</li></ul><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 and Training Coordinator

Zifo

<div><p>Location: Cambridge, MA</p><p><b>
*This role will require regular presence at our client sites in Cambridge, MA*</b></p><p><b>
**This role is not eligible for relocation assistance**</b></p><p></p><p>
The Zifo Lab Automation Analyst provides technical laboratory automation services, including multivendor instrument, information technology and validation/compliance services when applicable. The individual will work as part of Zifo&rsquo;s Lab Automation team to implement customer needs and address gaps to propose solutions for the desired automated state. He or she will work with business users and managers of customers in conjunction with the internal Zifo support teams.</p><p><b>
Requirements</b></p><ul>
<li>Provides technical support of customer laboratory environments</li>
<li>Ensure that common automation equipment is properly maintained and in good working order. This includes stand-alone liquid handlers (Hamilton, Echo, Tecan, etc), plate readers (SpectraMax, Envision, Neo2, etc) plate washers/dispensers, as well as several fully integrated robotic systems.</li>
<li>Install, operate, maintain, QC, troubleshoot problems, create methods/scripts, and train users on instruments is required.</li>
<li>Configured in-lab settings for automation software (eg: Cellario, Green Button Go) as required to train robotic equipment.</li>
<li>Perform unit test scripts for in-Lab automation equipment to validate the remote programmed software.</li>
<li>Able to build and operate debugging scripts and perform simple parallel development in the production environment.</li>
<li>Modify existing systems, instruments, methods and software to meet evolving needs.</li>
<li>Work collaboratively with discovery, engineering and expression groups at the local sites to optimize research efficiencies through implementation of automation process improvements and novel technologies</li>
<li>Ensures adherence to client&rsquo;s corporate policies through periodic reporting and compliance programs</li>
<li>Document procedures, policies, troubleshooting and best practices</li>
<li>Perform system preventative maintenances based on client&rsquo;s schedule, if applicable</li></ul><p><br>
</p><p>Required Skills:</p><ul>
<li>Knowledge of laboratory safety practices as defined by the company and/or customer&rsquo;s site safety code</li>
<li>Experience in the operation, maintenance, troubleshooting and scripting for liquid handlers, dispensers, plate washers, plate readers, Octet, etc. required.</li>
<li>Programming experience using Python, Java, C# or VB.NET</li>
<li>Experience with scheduling, operation, training and troubleshooting of fully integrated robotic systems</li>
<li>Expertise with Hi-Res BioSolutions&rsquo; Cellario or Biosero&rsquo;s Green Button Go scheduling software is a plus.</li>
<li>Experience with Titian Mosaic is a plus</li>
<li>Exemplary interpersonal skills including the ability to work with other automation engineers and non-automation scientists.</li>
<li>Excellent organizational skills, as exemplified by an aptitude for clear record-keeping and data analysis, and the ability to prioritize work across multiple projects.</li>
<li>Excellent customer service skills complemented by an ability to listen to and interpret client requests</li>
<li>Ability to troubleshoot complex instrument and technology issues</li>
<li>Strong oral and written communication skills</li>
<li>Ability to identify, track and complete tasks for multiple projects</li></ul><p><br>
</p><p>About you:</p><ul>
<li>Independent, self-motivated &amp; results driven individual</li>
<li>Willingness &amp; ability to acquire quickly new technical skills &amp; business principles</li>
<li>Ability for Critical Thinking and Logical Reasoning</li>
<li>Good understanding of pharmaceutical research and drug Discovery &amp; development processes and biologics workflows (preferred, not required)</li></ul><p><br>
</p><p>Required Education/Experience:</p><ul>
<li>Bachelor of Science in computer science, life science or equivalent industry experience</li>
<li>2+ years of relevant technical experience including (but not limited to); biotech/pharmaceutical company or an automation provider.</li>
<li>Experience with scientific instrumentation (preferred)</li>
</ul><p><b>Benefits</b></p><p>
About Zifo:</p><p>
CURIOSITY DRIVEN, SCIENCE FOCUSED, EMPLOYEE BUILT. Our culture is unlike any other, one where we debate, challenge ourselves, and interact with all alike. We are a curious bunch, characterized by our passion to learn and spirit of teamwork. Zifo is a global R&amp;D solutions provider focused on the industries of Pharma, Biotech, Manufacturing QC, Medical Devices, specialty chemicals and other research-based organizations. Our team&rsquo;s knowledge of science and expertise in technology help Zifo better serve our customers around the globe, including 7 of the Top 10 Biopharma companies.</p><p>
We look for Science &ndash; Biotechnology, Pharmaceutical Technology, Biomedical Engineering, Microbiology etc. We possess scientific and technical knowledge and bear professional and personal goals. While we have a &ldquo;no doors&rdquo; policy to promote free access within, we do have a tough door to walk in. We search with a two-point agenda &ndash; technical competency and cultural adaptability.</p><p>
We offer a competitive compensation package including accrued vacation, medical, dental, vision, 401k with company matching, life insurance, and flexible spending accounts.</p><p>
If you share these sentiments and are prepared for the atypical, then Zifo is your calling!</p><p>
Zifo is an equal opportunity employer, and we value diversity at our company. We do not discriminate on the basis of race, religion, color, national origin, gender, sexual orientation, age, marital status, veteran status, or disability status.</p></div>

Lab Automation Analyst

Manappuram healthcare ltd

<p><b>Key Responsibilities</b></p><ul><li><b>Conduct laboratory tests and experiments</b> following established protocols</li><li><b>Prepare and analyze samples</b> such as blood, tissue, or chemical compounds</li><li><b>Operate and calibrate lab equipment</b> including microscopes, centrifuges, and spectrometers</li><li><b>Record and interpret data</b> accurately for reporting and research purposes</li><li><b>Maintain cleanliness and safety</b> in the lab by following health and safety regulations</li><li><b>Label, store, and dispose of specimens</b> properly</li><li><b>Assist scientists and medical professionals</b> in research and diagnostic procedures</li></ul><p><b>Required Skills and Qualifications</b></p><ul><li><b>Attention to detail</b> and strong analytical skills</li><li><b>Knowledge of lab procedures and safety protocols</b></li><li><b>Familiarity with lab equipment and software</b></li><li><b>Ability to follow strict guidelines and document findings</b></li><li><b>Teamwork and communication skills</b></li><li>Education BSC MLT</li></ul><p><b>Typical Work Environment</b></p><ul><li>Hospitals, clinics, research institutions, pharmaceutical companies, or industrial labs</li><li>May involve working with hazardous materials or infectious samples</li><li>Often requires wearing protective gear and adhering to strict hygiene standards</li></ul><p><b>Job Titles and Variants</b></p><ul><li>Medical Laboratory Technician</li><li>Clinical Lab Technician</li><li>Research Lab Assistant</li><li>Quality Control Technician</li></ul><p>Job Types: Full-time, Permanent</p><p>Pay: &#8377;10,086.00 - &#8377;20,539.93 per month</p><p>Work Location: In person</p>

Lab Technician

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