United Kingdom

Belgium

Germany

Japan

Spain

 China

Taiwan

Singapore

Australia

Thailand

Czech Republic

India

Malaysia

Switzerland

Sweden

Poland

Lithuania

Norway

Finland 

Austria

Netherlands

South Korea

Canada

France

Denmark

Mexico

Brazil

Slovakia

South Africa

Scotland

Romania

Vietnam

Ireland

Philippines

Israel

Slovenia

United Arab Emirates

Greece

Hungary

New Zealand

Costa Rica

Argentina

Italy

Indonesia

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Türkiye

<p><strong>Peak Scientific is a global leader in developing innovative gas generation solutions for analytical laboratories in a wide variety of industries including life sciences, biomedical, pharma, petrochemical and environmental.  With over 20 years of sustained growth, Peak has firmly established itself as a dominant player in laboratory gas generation - a market which is estimated to be worth over £250m globally, and still growing. This success is a result of a continual focus on manufacturing cutting-edge products and directly supporting customers across the world with industry-leading service and maintenance. With over 20 overseas offices across every continent and over 600 staff globally, Peak is one of Scotland’s manufacturing success stories of the past decade.</strong></p>
<h3><strong>HEAD OF ENGINEERING - GLASGOW</strong></h3>
<ul>
<li><p>An exciting opportunity has arisen for a <strong>Head of Engineering</strong> at Peak HQ, Inchinnan. Reporting to the COO, you will be responsible for the successful Research, Design and Development of new products and technologies. </p>
</li>
<li><p>Owning the Product and Technology Development Process (PDP) you will ensure all stakeholders are engaged and contributing towards the success of new products and technologies.</p>
</li>
</ul>
<h4><strong>Additionally, you will be responsible for</strong></h4>
<ul>
<li><p>Managing team leads (9) including Research and Development, Design and Development, Test and Validation, Product Compliance and New Product Integration.</p>
</li>
<li><p>Actively monitoring and driving the Product and Technology Roadmap through market awareness of applications and complementary market sectors.</p>
</li>
<li><p>Financial and business accountability by ensuring all projects are on time and in budget.</p>
</li>
<li><p>Making technical decisions and setting technical direction.</p>
</li>
<li><p>Chairing and reviewing business project priority meetings with the COO and reporting updates to the Executive Board as required.</p>
</li>
<li><p>Accountability for the Product Change Process ensuring changes are implemented with minimal disruption to the business and its remains fit for purpose.</p>
</li>
<li><p>Protecting business continuity through multi source supply whilst retaining key compliance.</p>
</li>
<li><p>Driving a culture of Continuous Improvement and Engineering Excellence especially with considering of IoT opportunities for reliability and faster innovation.</p>
</li>
<li><p>Developing and mentoring the teams by sharing knowledge and best practice, modern ways of working.</p>
</li>
</ul>
<p>You must have a proven track record in a similar role of leading and driving teams in a fast-paced Engineering environment (in a £100M+ company), with knowledge of engineering best practices including Design for Manufacture and Design for Assembly and opportunities for engineering patents. Candidates should also have a degree in a relevant engineering discipline or sufficient experience.</p>
<h4><strong>You will have an understanding of the following</strong></h4>
<ul>
<li><p>Mechanical, pneumatical and electrical engineering principles.</p>
</li>
<li><p>Validation Testing and End of Life Product Management.</p>
</li>
<li><p>Structuring Research and Development projects and potential patents.</p>
</li>
<li><p>Future proofing products with product data collection and consideration of sustainability credentials.</p>
</li>
<li><p>Championing Continuous Improvement activities on product or process.</p>
</li>
<li><p>Awareness of EN 61010, UL and ISTA certifications.</p>
</li>
</ul>
<p>At Peak we strive to attract individuals who will enjoy and align with our culture and values: to put customers first, be innovative, stay agile, always respectful, and show pride and passion. </p>
<p>Our customers are at the heart of everything we do, and we’re passionate about supporting our employees to reach their full potential and exceed our customers’ expectations.</p>
<p><strong>We offer a competitive package and opportunities to develop within an expanding international company.</strong></p>


Head of Engineering

<p><strong>AstraZeneca. We are a global, science-led, patient-focused pharmaceutical company. We are dedicated to transforming the future of healthcare by unlocking the power of what science can do for people, society and the planet.</strong></p>
<h3><strong>EXECUTIVE DIRECTOR, HEAD OF BIOANALYTICAL- BIOPHARMA DEVELOPMENT</strong></h3>
<p><strong>This job is available in 4 locations</strong></p>
<ul>
<li>Gaithersburg, Maryland, United States </li>
<li>Cambridge, England, United Kingdom </li>
<li>Waltham, Massachusetts, United States Gothenburg, </li>
<li>Västra Götaland County, Sweden</li>
</ul>
<p>Do you have expertise in, and passion for science? Are you ready to work at the cutting-edge, where scientific innovations and an entrepreneurial spirit are the norm?  We’re looking for dynamic thought leaders with curious minds, who are comfortable taking smart risks and constantly challenging the boundaries of science all the while learning and developing core skills and experiences. Locations: Gaithersburg, MD; Waltham, MA; Gothenburg (Sweden); Cambridge (UK)</p>
<h4><strong>What we do</strong></h4>
<p>We are a global, science-led Biopharmaceutical business and our innovative medicines are used by millions of patients worldwide. The iBA group within Clinical Pharmacology and Safety Sciences provides broad discovery, preclinical, and clinical support including life cycle management across all therapeutic areas enabling pipeline delivery, decision making, innovation and advancement to improve the lives of patients through life-changing medicines.</p>
<h4><strong>Why we love it</strong></h4>
<p>The future is bright at AstraZeneca as we bring ground-breaking therapies to complex disease to patients with critical needs.  Scientific innovations are at the core of what we do across our industry leading portfolio which drive exciting opportunities and varied work. We’re on an exciting journey to pioneer the future of healthcare!</p>
<h4><strong>What you&#39;ll do</strong></h4>
<p>As part of the Integrated Bioanalysis (iBA) Global Team, you will report to the global head of iBA. You&#39;ll have responsibilities for leading a team of scientists designing and driving execution of complex bioanalytical strategies while making a direct and tangible impact on all aspect of AstraZeneca’s Biopharmaceutical portfolio, including therapeutic areas such as Cardiovascular and renal metabolism (CVRM), Vaccines and immunology (V&amp;I),  Neuroscience (NSc.) as well as Respiratory and Immunology (R&amp;I).</p>
<ul>
<li><p>You will also be responsible for driving the scientific strategic interface with our CRO partner.   </p>
</li>
<li><p>You will drive interactions with key stakeholders across the business including but not limited to Safety Science, Clinical Pharmacology, Business Process Operations, Therapeutic areas, Patient Safety, Quality Assurance and Regulatory Affairs.  </p>
</li>
<li><p>The ideal leader will design and implement ways of operating to ensure effective collaboration and delivery of robust bioanalytical strategies, including but not limited to, endpoints such as PK/CK, immunogenicity and biomarkers when required to support the AstraZeneca pipeline.</p>
</li>
<li><p>Working with a dynamic team you will be responsible providing solution to complex challenges while also building a dynamic team of scientist with diverse technical expertise and an innovative mindset.</p>
</li>
<li><p>You will have the opportunity to have an immediate and lasting impact to our diverse pipeline.</p>
</li>
<li><p>This is a role that requires a high level of collaboration across other strategy leads within Bioanalysis to ensure effective relationship with CROs.</p>
</li>
</ul>
<h4><strong>Education/Experience required:</strong></h4>
<ul>
<li><p>PhD in Biochemistry, immunology, molecular biology, bioengineering or related studies.</p>
</li>
<li><p>10+ years of relevant experience with at least 2 years&#39; experience driving teams to to bring drugs to market</p>
</li>
</ul>
<h4><strong>Essential for the role:</strong></h4>
<ul>
<li><p>Ability to build effective partnerships across all therapeutic areas and key stakeholders within and outside AZ</p>
</li>
<li><p>Ability to manage change in a fast past environment where bringing effective therapies to patients is our number one priority</p>
</li>
<li><p>Establish and drive strategies on how iBA will ensure delivery of scientific and operational excellence across all modalities</p>
</li>
<li><p>Proven track record driving scientific innovation</p>
</li>
<li><p>Proven ability to develop   assets through all stages of drug development</p>
</li>
<li><p>Proven experience as a Subject Matter Expert in pre-clinical and clinical bioanalysis capable of designing and driving bioanalytical strategies for PK/CK, PD biomarkers and immunogenicity assessments (humoral and cellular)</p>
</li>
<li><p>Experienced leader with a proven track record of working with dynamic teams and driving talent development</p>
</li>
<li><p>Experienced development bioanalysis leader capable of working across diverse fast-moving team, leading and implementing robust bioanalytical strategy to advance the portfolio</p>
</li>
<li><p>Worked collaboratively with stakeholders, providing solutions to challenges and mitigating risk</p>
</li>
<li><p>Experience across a range of bioanalytical applications and technical formats including but not limited to, <strong>Flow Cytometry</strong>,  <strong>Mass Spectrometry</strong>, <strong>ELISpot, viral assays, molecular assays</strong> (ddPCR, qPCR, RT-qPCR, NGS) cytokine assays, ligand binding assays etc.</p>
</li>
<li><p>Lead a team that act as subject matter experts working with colleagues supporting assay transfer, scientific quality and study conduct at CRO partners</p>
</li>
<li><p>Well-developed understanding of trends in the industry and deep knowledge of global regulatory expectations and guidance</p>
</li>
<li><p>Collaborate with colleagues to ensure data and scientific insight are available for regulatory submission documentation such as INDs, CTAs, IBs, ISI and/or NDAs/BLAs</p>
</li>
<li><p>Ability to interpret and integrated complex datasets to draw conclusions that drive key portfolio decisions</p>
</li>
<li><p>Ability to handle multiple projects and / or tasks concurrently in a fast-paced environment</p>
</li>
<li><p>Ability to develop, coach and mentor</p>
</li>
<li><p>Background in pharmaceutical development</p>
</li>
<li><p>Proven publication and presentation record</p>
</li>
<li><p>Exceptional verbal and written communication skills</p>
</li>
</ul>
<h4><strong>Desirable for the role:</strong></h4>
<ul>
<li><p>Matrix or line management experience</p>
</li>
<li><p>Experienced in discovery bioanalysis for other drug modalities</p>
</li>
</ul>
<h4><strong>So, what’s next?</strong></h4>
<ul>
<li><p>Are you already imagining yourself joining us? Good, because we can’t wait to hear from you!</p>
</li>
<li><p>If you’re curious to know more then please reach out to (contact person) We welcome with your application, no later than <strong>November 13, 2024</strong>.</p>
</li>
</ul>
<p>AstraZeneca embraces diversity and equality of opportunity. We are committed to building an inclusive and diverse team representing all backgrounds, with as wide a range of perspectives as possible, and harnessing industry-leading skills. We believe that the more inclusive we are, the better our work will be. We welcome and consider applications to join our team from all qualified candidates, regardless of their characteristics. We comply with all applicable laws and regulations on non-discrimination in employment (and recruitment), as well as work authorization and employment eligibility verification requirements.</p>


Executive Director, Head of Bioanalytical - BioPharma Development

<p><strong>ALS is a global leader in scientific testing, providing comprehensive testing solutions to clients in more than 60 countries across a wide range of industries, including environment, food and beverage, mining, personal care, pharmaceutical, healthcare and equipment reliability. Using state-of-the-art technologies and innovative methodologies, our dedicated international teams deliver the highest-quality testing services and personalised solutions supported by local expertise. We help our clients leverage the power of data-driven insights for a safer and healthier world.</strong></p>
<p><strong>Imagine your future with us!</strong></p>
<p>At ALS, we encourage you to dream big. When you join ALS, you join a purpose and values-driven team that empowers you to innovate, create, and thrive. Our global team turns up each day with passion and commitment to do amazing things, always challenging our thinking to find ways to solve some of the world’s most complex problems for a safer, healthier world. </p>
<h3><strong>DEPUTY LABORATORY MANAGER UK</strong></h3>
<p>The Deputy Laboratory Manager will work at the ALS Inspection Prescot Site. Reporting to the Laboratory Manager UK, the Deputy Laboratory Manager will be responsible for the management, quality and operational performance of the UK analytical laboratory. Encompassing all services, operations, processes and controls from sample receipt through to the approval stage within the Analytical Services function to deliver profitable, efficient and highly accurate laboratory services. </p>
<ul>
<li><p><strong>Basis:</strong> Full Time , Monday to Friday, Working hours TBC.</p>
</li>
<li><p><strong>Salary:</strong> Competitite + bonus scheme</p>
</li>
</ul>
<h4><strong>About you</strong></h4>
<p><strong>To be successful in this role you will have:</strong></p>
<ul>
<li><p>A degree level qualification in Chemistry.</p>
</li>
<li><p>Have a minimum of 10 years’ experience within the metals and minerals industry.</p>
</li>
<li><p>Minimum of 3 years working at senior management level.</p>
</li>
<li><p>Able to liaise professionally at ALL levels with internal and external customers.</p>
</li>
<li><p>Able to deliver overall and individual commodity analysis services.</p>
</li>
<li><p>Good commercial understanding and appreciation of factors involved in delivery, quality services and profitably.</p>
</li>
<li><p>Good understanding of quality and appreciation of factors involved in delivery a quality service.</p>
</li>
<li><p>Competence with standard Microsoft software packages and well-practiced in preparing Management information and reports.</p>
</li>
<li><p>Working knowledge of analysis in the commodity sectors (minerals and metals).</p>
</li>
<li><p>Working of the factors involved in delivering a quality service to ISO 9001 and ISO 17025 standards.</p>
</li>
<li><p>Working knowledge of profit &amp; loss systems and the factors involved in delivery a profitable service.</p>
</li>
<li><p>Professional or academic understanding of science ideally in a scientific discipline.</p>
</li>
<li><p>Working knowledge of LIMS (Laboratory Information and Management System).</p>
</li>
<li><p>Sufficient technical understanding and awareness of laboratory services to be able to communicate technical solutions and methods to reflect best practice.</p>
</li>
<li><p>Able to manage a large team and build positive morale.</p>
</li>
</ul>
<h4><strong>Position duties</strong></h4>
<ul>
<li><p>Strategic business contribution, planning, and execution within the ALS Inspection Division.</p>
</li>
<li><p>Delivery of ALS Inspection UK business objectives and targets in cooperation with Finance – Commercial – Inspection – Assay Customer Services departments- Quality.</p>
</li>
<li><p>Aid in the allocation of work to laboratory team according to their competence and skill set, knowledge, availability of equipment and customer requirements.</p>
</li>
<li><p>Monitor and aid delivery of Key Performance Indicators and targets; liaise with all departments with a view to improving the efficiency and effectiveness of the processes involved.</p>
</li>
<li><p>Work directly with departmental laboratory heads as required to maintain and monitor quality, TAT and productivity.</p>
</li>
<li><p>Take part in and contribute to on-going development programmes to continuously improve efficiency and effectiveness of the Laboratory.</p>
</li>
<li><p>Work directly with departmental laboratory heads to plan workflow, and resolve any technical, personnel or quality issues.</p>
</li>
<li><p>Undertake other line management responsibilities as required and in accordance with the seniority of the position.</p>
</li>
<li><p>Responsible for quality of results and laboratory service provision.</p>
</li>
<li><p>Delivery of customer requirements within required specification and time frame.</p>
</li>
<li><p>Attend client meetings when requested and respond to clients queries within authorised parameters in a timely manner.</p>
</li>
<li><p>Escalate client issues as appropriate. Complaint and dispute investigation and resolution.</p>
</li>
<li><p>To manage and ensure compliance with the clauses of the accreditation standards, ISO 9001:2015 and ISO 17025:2017.</p>
</li>
<li><p>To participate where required in UKAS/ISO audits of the Quality Management System.</p>
</li>
<li><p>Assist implementation of effective corrective actions to any non-conformances raised.</p>
</li>
<li><p>Technical consultancy as required either within the laboratory, to ALS satellite laboratories or for external customers.</p>
</li>
<li><p>Aid in the recruitment, training and development of the laboratory team to maintain optimum levels of laboratory workforce and skills across all departments to meet the business needs.</p>
</li>
<li><p>Evaluate and improve the Laboratory department’s skills using performance reviews and monitoring training plans in conjunction with HR Manager, Technical Manager and Laboratory departmental managers.</p>
</li>
<li><p>To act and undertake all duties with respect to the lab manager when they are absent.</p>
</li>
</ul>
<h4><strong>Employee Benefits</strong></h4>
<p><strong>This role will also come with the following fantastic benefits:</strong></p>
<ul>
<li><p>Attractive Salary 25 days holiday plus bank holidays Free parking 6% employer pension</p>
</li>
<li><p>Shift Allowance Free staff canteen Life Assurance</p>
</li>
<li><p>This is an excellent opportunity for a motivated and highly skilled person looking to develop their career in an international company.</p>
</li>
</ul>


Deputy Laboratory Manager UK

<p><strong>Waters Corporation (NYSE: WAT), the world's leading specialty measurement company, has pioneered chromatography, mass spectrometry and thermal analysis innovations serving the life, materials, and food sciences for more than 60 years. With more than 7,000 employees worldwide, Waters operates directly in 35 countries, including 15 manufacturing facilities, with products available in more than 100 countries. Our team focuses on creating business advantages for laboratory-dependent organizations to enable significant advancement in healthcare delivery, environmental management, food safety, and water quality.</strong></p><p>Working at Waters enables our employees to unlock the potential of their careers. Our global team is driven by purpose. We strive to be better, learn and improve every day in everything we do. We’re the problem solvers and innovators that aren’t afraid to take risks to transform the world of human health and well-being. We’re all in it together delivering benefit as one to provide the insights needed today in order to solve the challenges of tomorrow.</p><h3><strong>China Distribution Manager/ Sr. Manager</strong></h3><h4><strong>Overview</strong></h4><p>The Manager China Distribution is a critical position in the Global Fulfilment &amp; Distribution organization leading the distribution of all Waters Division &amp; Clinical products to customers and service organization in China. In addition, this is one of the key leadership positions on a global team with an opportunity to make an impact at the enterprise level and influence Waters’ strategies by designing and optimizing a global distribution network to support future business growth. &nbsp;This position requires high interaction with stakeholders across levels in multiple functions of the company - Global Planning, Global Procurement, Trade Compliance, Data &amp; Systems, China Commercial, China Finance, China Service, China Clinical, Manufacturing sites and other Tier-1 DCs and is responsible for approx. 15% of Waters revenue.</p><p>This position requires a highly experienced leader with demonstrated subject matter expertise who can act as the go-to individual in the field of distribution. This position requires a combination of technical skills, supply chain knowledge, and emotional intelligence to lead change management initiatives and achieve consensus amongst cross functional stakeholders.</p><h4><strong>Responsibilities</strong></h4><ul><li>Lead the China Distribution Team to execute the primary acitivty of Order fulfilment, by providing the external and internal clients with the ordered products, on time, complete, and using the most efficient and effective processes and distribution methods.</li><li>Manage a team of seven employees spanning the functions of Warehouse Operations, Trade Operations (Import/Export), Logistics, Supply Chain coordination &amp; Planning/Buying.<br>Maintain and develop the work force of the China DC in line with the services required and using the processes and practices of Waters corporation.</li><li>Manage inbound and outbound flows from the DC, day-to-day warehouse operations and minimize the freight costs.<br>Build and own strong relationships with 3rd party warehouse and logistic vendors (transportation, IE, brokers etc.), manage their performance according to established KPIs and drive improvements.</li><li>Actively manage inventory working with Global Planning; responsible for optimizing inventory levels, E&amp;O and warehouse space.</li><li>Create annual operating plans and ensure warehousing &amp; logistics costs are in line with those plans.</li><li>Liaise with finance to analyze cost variance, prepare forecast and define action plans on monthly basis.</li><li>Work seamlessly with Greater China WD team and participate in S&amp;OP to address stock shortage risk and allocation, ensuring the supply plan is aligned with sales target.</li><li>Maintain and uphold compliance standards for quality, trade/customs and IVD products; provide solutions to mitigate compliance risk</li><li>Actively engage in advancement &amp; adoption of SAP and other tools to enhance distribution services and promote efficient processes.</li><li>Track and communicate impact of external developments in China, events and trends in the transportation area.<br>Identify and lead Continuous Improvement projects using Lean methodologies to enhance efficiency and optimize costs in logistics and distribution operations (OTIF, on time delivery etc.)</li><li>Further expand and modernize Waters global distribution and logistics capabilities in China in conjunction with other global operations &amp; WD functions.</li><li>Key member of global freight RFQ team and all Waters division freight improvements.</li><li>Develop and implement multi-year logistics strategy for the organization to meet China business growth needs.</li><li>Lead and/or actively participate in global programs; oversee implementation of transformational strategies in multiple regions.</li></ul><h4><strong>Qualifications</strong></h4><ul><li>Bachelor’s degree in supply chain, logistics or business</li><li>Minimum of 10 years’ experience in supply chain, distribution, logistics</li><li>Experience in a managerial role with a logistics service provider or the logistics organization of a manufacturing company<br>People leader who leads by example and can implement processes &amp; drive performance</li><li>Self-starter, responsible, reliable, self-motivated and able to work with minimal supervision</li><li>Ability to handle data, perform analyses for decisions and generate insightful reports and presentations</li><li>Must possess excellent communication skills, both verbal and written plus an ability to interact with a wide range of people – across functions and countries; with internal and external parties</li><li>Experience with financial processes: budgeting, reporting, analysis of results</li><li>Experience with an ERP system and planning concepts</li><li>Ability to manage and prioritize multiple projects, tasks &amp; day-to-day operations</li><li>Flexible in thinking, can connect business requirements with operational possibilities</li></ul>

China Distribution Manager/ Sr. Manager

<p><strong>Our passion for science and technology is what drives our more than 64,000 employees across 66 countries to find solutions to some of today’s toughest challenges and create more sustainable ways to live.</strong></p><p>Work Your Magic with us! Start your next chapter and join <i>MilliporeSigma</i>.</p><p>Ready to explore, break barriers, and discover more? We know you’ve got big plans – so do we! Our colleagues across the globe love innovating with science and technology to enrich people’s lives with our solutions in Healthcare, Life Science, and Electronics. Together, we dream big and are passionate about caring for our rich mix of people, customers, patients, and planet. That's why we are always looking for curious minds that see themselves imagining the unimaginable with us.</p><p>This role does not offer sponsorship for work authorization. External applicants must be eligible to work in the US.</p><h3><strong>Supervisor, Analytical Quality Control Scientist</strong></h3><h4><strong>Your Role:</strong></h4><p>Millipore Sigma, Round Rock, is seeking to hire an experienced Analytical Scientist/Supervisor for its Analytical Quality Control (AQC) operations. The individual will be responsible for assisting the Quality Control Manager for oversight of operations within Quality Control. &nbsp;This includes personnel management, safety, quality, scheduling, budgets, metrics, regulatory compliance, and testing. Specific responsibilities include:&nbsp;</p><ul><li>Solve problems, optimize processes, develop new processes and prepare procedures</li><li>Scheduling production project</li><li>Reviewing test and validation plans</li><li>Leading out-of-specification investigations</li><li>Providing guidance and oversight to direct reports</li><li>Help develop strategies and plans to optimize group performance</li><li>Support the development of team members</li><li>Oversee the maintenance and qualification of analytical instrumentation</li><li>Review data to ensure completeness, accuracy, and compliance with quality requirements</li><li>Manage method development and validation</li><li>Respond efficiently to evolving priorities</li></ul><h4><strong>Physical Attributes:</strong></h4><ul><li>Work near moving mechanical parts, fumes, airborne particles, toxic or hazardous chemicals</li><li>Particular vision specifications: close, distance, color, peripheral, depth vision, and adjust focus</li><li>May wear: air helmet, mask, safety shoes, apron, rubber and Tyvek suits, protective gloves, safety glasses, or goggles</li><li>Occasionally lift/move up to 40 pounds</li></ul><h4><strong>Who You Are</strong></h4><h5><strong>&nbsp;Minimum Qualifications</strong></h5><ul><li>Bachelor's Degree in Chemistry, Chemical Engineering, or other Life Sciences discipline</li><li>10+ years experience performing quality control and/or analytical chemistry in a regulated environment (i.e. GLP, GMP, ISO)</li><li>1+ years of experience directly supervising or managing personnel&nbsp;</li></ul><p>OR</p><ul><li>Experience in an analytical lab analyzing neat materials and finished product in Quality Control</li><li>Proficiency in technical fundamentals, organizational skills, documentation, and effective communication</li><li>Experience in analytical chemistry techniques including HPLC, GC, LC-MS, GC-MS, IR, ROI, LOD, Karl Fischer, NMR, ICP, IC and GC-Headspace</li></ul><h5><strong>&nbsp;Preferred Qualifications</strong></h5><ul><li>Excellent written and verbal communication skills</li><li>Ability to work in a team environment</li><li>Experience working in an analytical testing lab with hazardous and toxic chemicals</li><li>Effective technical writing skills to generate development reports</li></ul><h4><strong>Notice on Fraudulent Job Offers</strong></h4><p>Unfortunately, we are aware of third parties that pretend to represent our company offering unauthorized employment opportunities. If you think a fraudulent source is offering you a job, please have a look at the following <a target="_blank" rel="noopener noreferrer" href="https://www.merckgroup.com/en/careers/faqs.html"><strong>information</strong></a>.</p>

Supervisor, Analytical Quality Control Scientist

<p><strong>Our passion for science and technology is what drives our more than 64,000 employees across 66 countries to find solutions to some of today’s toughest challenges and create more sustainable ways to live.</strong></p><p>Work Your Magic with us! Start your next chapter and join <i>MilliporeSigma</i>.</p><p>Ready to explore, break barriers, and discover more? We know you’ve got big plans – so do we! Our colleagues across the globe love innovating with science and technology to enrich people’s lives with our solutions in Healthcare, Life Science, and Electronics. Together, we dream big and are passionate about caring for our rich mix of people, customers, patients, and planet. That's why we are always looking for curious minds that see themselves imagining the unimaginable with us.</p><p>This role does not offer sponsorship for work authorization. External applicants must be eligible to work in the US.</p><h3><strong>Manager, QC Chemistry Lab</strong></h3><h4><strong>Your Role:</strong></h4><ul style="margin-bottom:11.0px;"><li>Lead, hire, develop, and manage a team of chemists and laboratory scientists.</li><li>Oversees the analysis and release of raw materials, intermediates, and finished products to determine their chemical and physical properties.</li><li>Delivers QC operational performance. Ensure QC capacity and capability is in place to meet demand, ensuring all vital testing is carried out.</li><li>Provides analytical&nbsp;knowledge and support to the Quality Control team for troubleshooting issues, complex situations and oversees the delivery of initial and ongoing training and mentoring.</li><li>Collaborates with cross-functional teams to investigate and resolve quality-related issues.</li><li>Leads and directs the introduction of new technology, coordinates and leads initiative to ensure that Quality Control remains contemporary and driven.</li><li>Is accountable for ensuring safety and compliance is understood and maintained across the QC labs.</li><li>Uses knowledge to support regulatory inspections and client audits.</li><li>Manages laboratory equipment, supplies, and maintenance activities.</li><li>Provides technical expertise and guidance on analytical methodologies and instrumentation.</li></ul><h4><strong>Who You Are</strong></h4><h5><strong>&nbsp;Minimum Qualifications</strong></h5><ul style="margin-bottom:11.0px;"><li>Bachelors Degree in Chemistry, Biochemistry, or other Life Science discipline.</li><li>4+&nbsp;years of experience in a quality control or analytical laboratory setting.</li><li>2+ years of leadership experience.</li></ul><h5><strong>&nbsp;Preferred Qualifications</strong></h5><ul style="margin-bottom:11.0px;"><li>Experience with analytical techniques, such as UPLC/HPLC, GC, titrations, and spectroscopy.</li><li>Masters Degree in Chemistry.</li><li>9+&nbsp;years of experience in a quality control or analytical laboratory setting.</li><li>Experience with Product Quality, Quality Control Lab Operation and Regulatory requirements, including FDA, cGMP, and ICH guidelines.&nbsp;</li></ul><h4><strong>Notice on Fraudulent Job Offers</strong></h4><p>Unfortunately, we are aware of third parties that pretend to represent our company offering unauthorized employment opportunities. If you think a fraudulent source is offering you a job, please have a look at the following <a target="_blank" rel="noopener noreferrer" href="https://www.merckgroup.com/en/careers/faqs.html"><strong>information</strong></a>.</p>

Manager, QC Chemistry Lab

<p><strong>Chromatography, the science of separation, affects the lives of almost everyone. Phenomenex’s chromatography products advance the future of scientific analysis and investigation, ensuring the quality of essentials like your food, water, shampoo, and even cold medication. We strive to provide the best tools and resources possible to help scientists improve global health and well-being, including award-winning liquid chromatography, gas chromatography, and sample preparation products. Be part of our global success, centered on a commitment to developing novel analytical chemistry solutions, unique marketing, and exceptional customer service and support.</strong></p><p>Phenomenex is one of 10 Life Sciences companies of Danaher. Together, we accelerate the discovery, development and delivery of solutions that safeguard and improve human health.</p><p>Learn about the <a target="_blank" rel="noopener noreferrer" href="https://www.danaher.com/how-we-work/danaher-business-system">Danaher Business System</a> which makes everything possible.</p><h3><strong>Channel Manager</strong></h3><h4><strong>In this role, you will have the opportunity to:</strong>&nbsp;</h4><div><ul><li>Responsible to manage channel partners and continuously improve &amp; optimize channel management policy and process including channel partner selecting, onboarding, partnering, managing and leveraging to drive business growth.</li><li>Manages channel conflict with other sales channels by fostering excellent communication internally and externally, and through strict adherence to channel rules of engagement.</li><li>Raise gaps and improvements on channel management operations policies and procedures, discuss improvement solutions with partners and implement follow up actions to optimize overall procedure.</li><li>Manage existing channel partner relationships in conjunction with the sales and sales leadership teams according to the set goals. Develop and evaluate for channel managments.</li><li>Lead team to optimize channel management operations excellence aligned with business developing trend, brand, and sales strategies, and set clear priorities for team across channels.</li><li>Set up and optimize controlling tools to ensure proper implementation of policy and tools for efficient follow up with channel management team. Measure essential KPIs at organizational and individual level.</li><li>Improvement and Optimization on distributors evaluations systems, Set up and optimize controlling tools to ensure proper implementation of channel manangement and developemnt, Reduce un-qualified channel partners. Work with operation to ensure that the quality standards and business controls are in place and Communicate system, policy and process changes.</li></ul></div><p>At Danaher we bring together science, technology and operational capabilities to accelerate the real-life impact of tomorrow’s science and technology. We partner with customers across the globe to help them solve their most complex challenges, architecting solutions that bring the power of science to life. Our global teams are pioneering what’s next across Life Sciences, Diagnostics, Biotechnology and beyond. For more information, visit <a target="_blank" rel="noopener noreferrer" href="http://www.danaher.com">www.danaher.com</a>.</p><p>At Danaher, we value diversity and the existence of similarities and differences, both visible and not, found in our workforce, workplace and throughout the markets we serve. Our associates, customers and shareholders contribute unique and different perspectives as a result of these diverse attributes.</p>

Channel Manager

<p><strong>Agilent inspires and supports discoveries that advance the quality of life. We provide life science, diagnostic and applied market laboratories worldwide with instruments, services, consumables, applications and expertise. Agilent enables customers to gain the answers and insights they seek - so they can do what they do best: improve the world around us. Information about </strong><a target="_blank" rel="noopener noreferrer" href="https://www.agilent.com/"><strong>Agilent</strong></a><strong>.</strong></p><p>Agilent is a global leader in laboratory and clinical technologies; we are passionate about bringing great science to life. &nbsp;Our commitment to quality and innovation supports cutting-edge life science research, patient diagnostics, and ensures the safety of water, food, and pharmaceuticals. As scientists and clinicians pursue small, everyday advances and life-changing discoveries, we provide trusted answers to their most critical questions and challenges. We can’t wait for you to join us as we continue our mission to improve the world around us.</p><h3><strong>Clinical Research Associate</strong></h3><h4><strong>Job Description</strong></h4><div><div><p><span>The Clinical Research Associate (CRA) will support successful and timely start-up and&nbsp;completion of clinical trials and be a key member of the Organization of Chief Medical Officer&nbsp;(OCMO) Global Clinical Affairs team. This will include oversight and management of assigned studies associated with investigator sites and monitoring activities.</span></p><p><span>The CRA will monitor clinical trials in accordance with Good Clinical Practice (GCP), Agilent procedures, and all applicable regulations. The CRA works closely with the Clinical Trial Manager (CTM) and/or lead CRA to&nbsp;ensure all monitoring activities are conducted according to study requirements and Monitoring Plan. The CRA may report to a CTM or people manager and has no direct reports.</span></p></div></div><h4><strong>Primary Responsibilities (all levels)</strong></h4><ul><li>Performs all study monitoring visits and completes supporting visit reports, including applicable visits such as site/investigator qualification, site initiation, interim monitoring, remote monitoring, and close-out visits</li><li>Trains investigator(s) and site staff on study protocol and all relevant study procedures</li><li>Support study start-up, conduct, and closeout activities. May assist in developing study-related plans and documents including clinical protocol, clinical brochures/IFUs, development of CRFs, reviewing informed consent forms, monitoring plan, etc. May coordinate IRB/EC approvals</li><li>Functions independently in the field and interacts professionally with all levels of medical and scientific professionals</li><li>Identify early on any unsatisfactory results, operations or specific problems and take immediate action to appropriate groups including escalating and assisting in resolving any study related issues that arise during study conduct</li><li>Assures adherence to GCP, study protocol, procedures, all applicable requirements, and regulations throughout the study monitoring visits. Responsible for implementing and maintaining the effectiveness of the quality system</li><li>Collect and review site regulatory and essential documents for accuracy and completion. Maintain the study Trial Master File (TMF)/or eTMF and ensure the Investigator Site Files (ISFs) are current and maintained</li><li>Perform Source Data Verification (SDV) and data cleaning in accordance with study monitoring plan. Reviewing all study logs and documentation ensuring audit trail and chain of custody is maintained</li><li>Performs Investigation Use Only (IUO) or Research Use Only (RUO) inventory and accountability, in accordance with study monitoring plan. Facilitates return or destruction of any unused IUO/RUO material as required</li><li>Serve as the primary point of contact for assigned sites and works with sites to resolve data queries and monitoring findings. Maintains accurate and timely communications with sites and ensures records are filed in TMF/ISF</li><li>Ensures TMF/ISF is audit ready. Assists with site audit(s) and site quality management activities, as needed. Tracks site progress against contractual agreements</li><li>Contribute to organizational and departmental process development, improvement, and Implementation</li></ul><h4><strong>Qualifications</strong></h4><ul><li>Bachelor's degree or higher, or equivalent credentials</li><li>Knowledge of International Council for Harmonisation (ICH)/GCP guidelines, 21 CFR (Code of Federal Regulations) part 812 (Investigational Device Exemption) (IDE), and monitoring procedures/best practices (ICH E6(R2)</li><li>Demonstrating strong written and verbal communication skills and presentation skills</li><li>Track record demonstrating strong organizational and problem-solving skills</li><li>Track record demonstrating a strong work ethic and ability to deliver tasks on time</li><li>Proficient with Microsoft Office Suite including automation tools</li><li>For CRA I: 1+ years direct clinical research experience at a sponsor, CRO, device manufacturer, IVD, companion diagnostics or investigator site</li><li>Experience with Electronic Data Capture (EDC) systems and eTMF systems</li></ul><p><strong>Ideal candidate must reside in the Carpinteria, CA area. This is not a remote position.</strong></p><p><span>The US pay range for this full-time position is $61,200.00 - $100,406.00/yr, plus eligibility for bonus, stock and benefits. Our pay ranges are determined by role, level, and location. The range displayed on each job posting reflects the minimum and maximum new hire pay for the position across the relevant US locations. Within the range, individual pay is determined by work location and additional factors, including job-related skills, experience, and relevant education or training. During the hiring process, a recruiter can share more about the specific pay range for a preferred location. Additional details are available at: </span><a target="_blank" rel="noopener noreferrer" href="https://careers.agilent.com/locations/americas/united-states/"><span>https://careers.agilent.com/locations/americas/united-states/</span></a></p><p>Agilent Technologies Inc. is an equal opportunity employer. Qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability or any other protected categories under all applicable laws.</p><ul><li><strong>Option to Work Remote:</strong> Yes</li><li><strong>Travel Required:</strong> 35% of the Time</li><li><strong>Schedule:</strong> Full time</li><li><strong>Shift:</strong> Day</li><li><strong>Duration:</strong> No End Date</li><li><strong>Job Function:</strong> Marketing</li></ul>

Clinical Research Associate

<p><strong>Agilent inspires and supports discoveries that advance the quality of life. We provide life science, diagnostic and applied market laboratories worldwide with instruments, services, consumables, applications and expertise. Agilent enables customers to gain the answers and insights they seek - so they can do what they do best: improve the world around us. Information about </strong><a target="_blank" rel="noopener noreferrer" href="https://www.agilent.com/"><strong>Agilent</strong></a><strong>.</strong></p><p>Agilent is a global leader in laboratory and clinical technologies; we are passionate about bringing great science to life. &nbsp;Our commitment to quality and innovation supports cutting-edge life science research, patient diagnostics, and ensures the safety of water, food, and pharmaceuticals. As scientists and clinicians pursue small, everyday advances and life-changing discoveries, we provide trusted answers to their most critical questions and challenges. We can’t wait for you to join us as we continue our mission to improve the world around us.</p><h3><strong>Clinical Research Associate</strong></h3><h4><strong>Job Description</strong></h4><div><div><div><p><span>The Clinical Research Associate (CRA) will support successful and timely start-up and&nbsp;completion of clinical trials and be a key member of the Organization of Chief Medical Officer&nbsp;(OCMO) Global Clinical Affairs team. This will include oversight and management of assigned studies associated with investigator sites and monitoring activities.</span></p><p><span>The CRA will monitor clinical trials in accordance with Good Clinical Practice (GCP), Agilent procedures, and all applicable regulations. The CRA works closely with the Clinical Trial Manager (CTM) and/or lead CRA to&nbsp;ensure all monitoring activities are conducted according to study requirements and Monitoring Plan. The CRA may report to a CTM or people manager and has no direct reports.</span></p></div></div></div><h4><strong>Primary Responsibilities (all levels)</strong></h4><ul><li>Performs all study monitoring visits and completes supporting visit reports, including applicable visits such as site/investigator qualification, site initiation, interim monitoring, remote monitoring, and close-out visits</li><li>Trains investigator(s) and site staff on study protocol and all relevant study procedures</li><li>Support study start-up, conduct, and closeout activities. May assist in developing study-related plans and documents including clinical protocol, clinical brochures/IFUs, development of CRFs, reviewing informed consent forms, monitoring plan, etc. May coordinate IRB/EC approvals</li><li>Functions independently in the field and interacts professionally with all levels of medical and scientific professionals</li><li>Identify early on any unsatisfactory results, operations or specific problems and take immediate action to appropriate groups including escalating and assisting in resolving any study related issues that arise during study conduct</li><li>Assures adherence to GCP, study protocol, procedures, all applicable requirements, and regulations throughout the study monitoring visits. Responsible for implementing and maintaining the effectiveness of the quality system</li><li>Collect and review site regulatory and essential documents for accuracy and completion. Maintain the study Trial Master File (TMF)/or eTMF and ensure the Investigator Site Files (ISFs) are current and maintained</li><li>Perform Source Data Verification (SDV) and data cleaning in accordance with study monitoring plan. Reviewing all study logs and documentation ensuring audit trail and chain of custody is maintained</li><li>Performs Investigation Use Only (IUO) or Research Use Only (RUO) inventory and accountability, in accordance with study monitoring plan. Facilitates return or destruction of any unused IUO/RUO material as required</li><li>Serve as the primary point of contact for assigned sites and works with sites to resolve data queries and monitoring findings. Maintains accurate and timely communications with sites and ensures records are filed in TMF/ISF</li><li>Ensures TMF/ISF is audit ready. Assists with site audit(s) and site quality management activities, as needed. Tracks site progress against contractual agreements</li><li>Contribute to organizational and departmental process development, improvement, and Implementation</li></ul><h4><strong>Qualifications</strong></h4><ul><li>Bachelor's degree or higher, or equivalent credentials</li><li>Knowledge of International Council for Harmonisation (ICH)/GCP guidelines, 21 CFR (Code of Federal Regulations) part 812 (Investigational Device Exemption) (IDE), and monitoring procedures/best practices (ICH E6(R2)</li><li>Demonstrating strong written and verbal communication skills and presentation skills</li><li>Track record demonstrating strong organizational and problem-solving skills</li><li>Track record demonstrating a strong work ethic and ability to deliver tasks on time</li><li>Proficient with Microsoft Office Suite including automation tools</li><li>For CRA I: 1+ years direct clinical research experience at a sponsor, CRO, device manufacturer, IVD, companion diagnostics or investigator site</li><li>Experience with Electronic Data Capture (EDC) systems and eTMF systems</li></ul><p><strong>Ideal candidate must reside in the Carpinteria, CA area. This is not a remote position.</strong></p><p><span>The US pay range for this full-time position is $61,200.00 - $100,406.00/yr, plus eligibility for bonus, stock and benefits. Our pay ranges are determined by role, level, and location. The range displayed on each job posting reflects the minimum and maximum new hire pay for the position across the relevant US locations. Within the range, individual pay is determined by work location and additional factors, including job-related skills, experience, and relevant education or training. During the hiring process, a recruiter can share more about the specific pay range for a preferred location. Additional details are available at: </span><a target="_blank" rel="noopener noreferrer" href="https://careers.agilent.com/locations/americas/united-states/"><span>https://careers.agilent.com/locations/americas/united-states/</span></a></p><p>Agilent Technologies Inc. is an equal opportunity employer. Qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability or any other protected categories under all applicable laws.</p><ul><li><strong>Option to Work Remote:</strong> Yes</li><li><strong>Travel Required:</strong> 35% of the Time</li><li><strong>Schedule:</strong> Full time</li><li><strong>Shift:</strong> Day</li><li><strong>Duration:</strong> No End Date</li><li><strong>Job Function:</strong> Marketing</li></ul>

<p><strong>Agilent inspires and supports discoveries that advance the quality of life. We provide life science, diagnostic and applied market laboratories worldwide with instruments, services, consumables, applications and expertise. Agilent enables customers to gain the answers and insights they seek - so they can do what they do best: improve the world around us. Information about </strong><a target="_blank" rel="noopener noreferrer" href="https://www.agilent.com/"><strong>Agilent</strong></a><strong>.</strong></p><p>Agilent is a global leader in laboratory and clinical technologies; we are passionate about bringing great science to life. &nbsp;Our commitment to quality and innovation supports cutting-edge life science research, patient diagnostics, and ensures the safety of water, food, and pharmaceuticals. As scientists and clinicians pursue small, everyday advances and life-changing discoveries, we provide trusted answers to their most critical questions and challenges. We can’t wait for you to join us as we continue our mission to improve the world around us.</p><h3><strong>GC/Energy &amp; Chemical Marketing Program Manager</strong></h3><h4><strong>Job Description</strong></h4><ul><li>Responsible for the development of marketing plans and strategic marketing programs of GC/Energy &amp; Chemical Market, to support sales in designated market segments, identify volume and strategic customers, and develop partnerships.</li><li>Analyzes market data to identify trends/opportunities, develop strategic direction from market information, and create compelling market analysis presentations in GC/Energy &amp; Chemical Market.</li><li>Enables sales by identifying and developing business opportunities and providing information and support for the sales force in GC/Energy &amp; Chemical Market.</li><li>May be responsible for interfacing with customers through company channels marketing program.</li><li>Co-work with cross-functional teams on strategic projects and build up KOLs relationship.</li></ul><h4><strong>Qualifications</strong></h4><ul><li>Bachelor's or Master's Degree or equivalent, energy &amp; chemical industry, petrochemical engineering is preferred.</li><li>Post-graduate, certification, and/or license may be required.</li><li>Typically, at least 8+ years relevant experience in sales or marketing or applications in this field.</li></ul><p>Agilent Technologies Inc. is an equal opportunity employer. Qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability or any other protected categories under all applicable laws.</p><ul><li><strong>Travel Required:</strong> NO</li><li><strong>Schedule:</strong> 50% of the Time</li><li><strong>Shift:</strong> Day</li><li><strong>Duration:</strong> No End Date</li><li><strong>Job Function:</strong> Marketing</li></ul>

GC/Energy & Chemical Marketing Program Manager

Lab technician

Liquid chromatography-mass spectrometry

Scientific and Research Fellow

Sales Representative

Academic staff

Laboratory services

Service engineer

Manager

Software

Product Specialist

Application Specialist

Gas chromatography

Gas chromatography-mass spectrometry

Molecular spectroscopy UV-Vis, RAMAN, FTIR

Marketing

Analytical chemist

AAS, ICP/OES, ICP/MS

Technologist/Engineer

Laboratory instruments

Spectroscopy

Chemist

Quality Control (QC)

Liquid chromatography

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Jobs manager - page 7

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