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<p><strong>As the world leader in serving science, our work is more than something that fills our days – what we do has great purpose. Our industry-leading scale means unparalleled commercial reach, unique customer access and a global footprint. Our broad customer base, from research to clinical to commercial production means you can have a broad and meaningful impact here at Thermo Fisher Scientific. All while working in an environment where you will be supported, valued and rewarded for your performance.</strong></p><p><strong>Thermo Fisher Scientific Inc. is the world leader in serving science, with annual revenue of approximately $40 billion. Our Mission is to enable our customers to make the world healthier, cleaner, and safer. Whether our customers are accelerating life sciences research, solving sophisticated analytical challenges, growing efficiency in their laboratories, improving patient health through diagnostics, or the development and manufacture of life-changing therapies, we are here to support them. Our global team of more than 100,000 colleagues delivers an outstanding combination of innovative technologies, purchasing convenience, and pharmaceutical services through our industry-leading brands, including Thermo Scientific, Applied Biosystems, Invitrogen, Fisher Scientific, Unity Lab Services, Patheon, and PPD.</strong></p><h3><strong>Process &amp; Cleaning Validation Specialist II</strong></h3><p>As a Process &amp; Cleaning Validation Specialist II at Thermo Fisher Scientific, you will have the opportunity to be part of a world-class team and contribute to the flawless validation of manufacturing processes and cleaning procedures. Your expertise and proven experience will play a crucial role in ensuring the production of high-quality pharmaceutical products that meet strict regulatory requirements.</p><h4><strong>Responsibilities</strong></h4><ul><li>Evaluate manufacturing process documents and equipment cleaning procedures for validation purposes</li><li>Develop protocols and conduct process validation for product manufacturing and aseptic filling (Media fill)</li><li>Perform cleaning validation of cleaning procedures and ensure periodic cleaning verification</li><li>Manage validation protocols for cleaning, process, and Media Fill</li><li>Collaborate with other departments to define protocol contents and actions to be carried out</li><li>Validate manufacturing processes, cleaning procedures, and APS/Media Fill</li><li>Support the drafting and approval of documents for new product transfer and validation</li><li>Handle deviations related to validation activities</li><li>Ensure accurate execution of validation activities and detailed analysis of results</li><li>Draft validation reports and ensure proper archiving of all documentation</li><li>Provide quality support for new product transfer and process qualification</li><li>Actively participate in the design, construction, and implementation of new processes or manufacturing departments</li></ul><h4><strong>Requirements</strong></h4><ul><li>Bachelor's Degree or equivalent in a scientific/pharmaceutical area</li><li>2 years of previous related experience in the pharmaceutical sector</li><li>Knowledge of pharmaceutical techniques, production, and aseptic filling processes</li><li>Experience in risk management and client service/project management</li><li>Proficiency in Microsoft Office software</li><li>Fluent in English with advanced written and oral communication skills</li></ul><h4><strong>Work Schedule</strong></h4><ul><li>Standard (Mon-Fri)</li></ul><h4><strong>Environmental Conditions</strong></h4><ul><li>Office</li></ul><p><a target="_blank" rel="noopener noreferrer" href="http://jobs.thermofisher.com"><span style="color:#263238;"><strong>Apply today! </strong></span><span style="color:#0d47a1;"><strong>http://jobs.thermofisher.com</strong></span></a></p>

Process & Cleaning Validation Specialist II

<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><h3><strong>Manufacturing Associate</strong></h3><h4><strong>Job Description</strong></h4><p>As a Manufacturing Associate (Representative), you will check and schedule resources to ensure on-time delivery. Your scientific knowledge and background will be leveraged through your review of formulation documents and active ingredient dilution to ensure that products are manufactured to specification.</p><p>You will have an opportunity to become skilled in the use of a wide range of lab instruments, including but not limited to spectrophotometers, conductivity meters and auto-pipettors, all of which are essential to meeting our customers' requirements. Having the ability to learn quickly on the job, anticipate and resolve potential manufacturing and delivery issues and maintaining the highest level of quality are critical. Additionally, you will work on problems of diverse scope in which analysis of data requires evaluation of identifiable factors. You will also exercises judgment within generally defined practices and policies in selecting methods and techniques for obtaining solutions.</p><h4><strong>Key responsibilities include:</strong></h4><ul><li><span>The manufacturing of oligonucleotide APIs in a GMP environment.</span></li><li><span>Actively involved in aspects of technology transfer and scale-up of oligonucleotide manufacturing processes delivered from Manufacturing Technical Services into Manufacturing.</span></li><li><span>Write and revise standard operating procedures according to regulatory and procedural guidelines.</span></li><li><span>Work with Validation and Engineering personnel to validate new equipment and facilities.</span></li><li><span>Work with Manufacturing Management and Quality to resolve manufacturing problems including drafting quality documentation (CAPA, deviation, change control, etc.).</span></li><li><span>Maintain, calibrate, and trouble shoot critical process equipment.</span></li></ul><h4><strong>Shift Details:</strong></h4><p>During training, shift will be M-F, 8:30 AM - 5:00 PM. Training will be approximately 3 weeks. Post-training shift will transition to a night shift on Pitman Schedule.</p><p>The schedule will be Night shift (4:30pm – 5:00am)&nbsp;working a Pitman schedule: of 2 days working, 2 days off, 3 days working, 2 days off, 2 days working, then 3 days off.</p><h4><strong>Qualifications</strong></h4><ul><li><span>Bachelor’s or Master’s Degree or equivalent</span></li><li><span>1+ years of related manufacturing experience, pharmaceutical manufacturing environment preferred</span></li><li><span>Previous knowledge of oligonucleotide synthesis, HPLC, UF, conjugation, and lyophilization is advantageous</span></li><li><span>Detail-oriented and can perform technical duties following standard operating procedures and general laboratory safety rules</span></li><li><span>Excellent math, documentation, communication and operational troubleshooting skills</span></li><li><span>Mechanically inclined</span></li><li><span>Clean room environment experience desired</span></li><li><span>Experience working in a FDA regulated manufacturing environment is helpful</span></li></ul><h4><strong>Additional Details</strong></h4><p>This job has a full time weekly schedule. Applications for this job will be accepted until at least February 7, 2025 or until the job is no longer posted.</p><p>The full-time equivalent pay range for this position is $30.69 - $47.96/hr plus eligibility for bonus, stock and benefits. Our pay ranges are determined by role, level, and location. 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. Pay and benefit information by country are available at: <a target="_blank" rel="noopener noreferrer" href="https://careers.agilent.com/locations">https://careers.agilent.com/locations</a>.</p><p>Agilent Technologies, Inc. is an Equal Employment Opportunity and Affirmative Action employer. We value diversity at all levels. All individuals, regardless of personal characteristics, are encouraged to apply. All qualified applicants will receive consideration for employment without regard to sex, pregnancy, race, religion or religious creed, color, gender, gender identity, gender expression, national origin, ancestry, physical or mental disability, medical condition, genetic information, marital status, registered domestic partner status, age, sexual orientation, military or veteran status, protected veteran status, or any other basis protected by federal, state, local law, ordinance, or regulation and will not be discriminated against on these bases. Agilent Technologies, Inc., is committed to diversity in the workplace and strives to support candidates with disabilities. If you have a disability and need assistance with any part of the application or interview process or have questions about workplace accessibility, please email job_posting@agilent.com or contact +1-262-754-5030. For more information about equal employment opportunity protections, please visit <a target="_blank" rel="noopener noreferrer" href="https://www.agilent.com/en/accessibility">www.agilent.com/en/accessibility.</a></p><ul><li><strong>Travel Required:</strong> No</li><li><strong>Shift:</strong> Morning</li><li><strong>Duration:</strong> No End Date</li><li><strong>Job Function:</strong> Manufacturing</li></ul>

Manufacturing 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><h3><strong>Organic Chemist – Polymer &amp; Silica Particle Manufacturing</strong></h3><p>We are seeking an <strong>Organic Chemist</strong> to join our manufacturing centre of excellence based in <strong>Church Stretton</strong>, on the outskirts of Shrewsbury, Shropshire.</p><p><strong>This is an opportunity to join an expanding technical team demonstrating marketing leading quality and innovation in the production of liquid chromatography, peptide synthesis and clinical and diagnostics consumables for a rapidly growing Biopharmaceuticals market sector.</strong></p><p>Working on site within the technical team you will have the ability to make a real difference to one of Agilent’s most prominent consumables businesses. &nbsp;As an organisation we have embraced 6-sigma and Lean Manufacturing methodologies making for an engaging and rewarding mix of scientific discovery, process improvement and employee growth and development.</p><p><strong>You will be working as part of a multi-discipline, cross-functional team and your key responsibilities will include:</strong></p><ul><li>Work with production teams to analyse and troubleshoot existing production methods</li><li>Identify, design and implement production efficiency improvements</li><li>Scale existing processes to be able to meet rapidly growing market demands</li><li>Produce validation reports and statistical analysis that document process changes</li><li>Connect with industrial trends and new technologies to determine how these can integrate into existing processes to give competitive advantage</li><li>Represent the local team as part of global, cross disciplined project teams on new product introductions&nbsp;</li><li>Execute and support Management of Change control processes, determine the disposition of non-conforming materials, and create and execute preventative action plans to improve safety and quality.</li></ul><h4><strong>About Church Stretton</strong></h4><p>Church Stretton is in the heart of the south Shropshire Area of Outstanding Natural Beauty, within easy reach of Shrewsbury, Telford, Wolverhampton and Hereford. The area offers a high quality of life with excellent outdoor recreation opportunities. With affordable housing below the national average while local schools outperform the UK average.</p><p>The successful candidate can expect a fun place to work, exposure to new technologies and good career progression prospects. In addition, the things we value is work life balance, encouraging people to leave work when they should.</p><h3><strong>Qualifications</strong></h3><p>We are looking for a motivated individual with the following background:</p><ul><li><strong>University Degree</strong> in <strong>Organic / Polymer Chemistry</strong> or equivalent</li><li><strong>Hands on laboratory experience </strong>in <strong>process optimisation</strong>, <strong>scale up</strong> and<strong> technology deployment </strong>around <strong>organic </strong>and/or<strong> polymer chemistry</strong>.</li><li>Any<strong> project management experience</strong> would be a strong plus</li><li><strong>Proficiency </strong>in <strong>data analysis statistical tools </strong>and <strong>software </strong>is desired</li><li><strong>Experience </strong>of working in the <strong>Chemical Process industry</strong> and<strong> relevant tools </strong>(HAZOP, HAZID, Risk Assessment) would an advantage</li><li>Knowledge of <strong>Comprehensive Quality System</strong> would be preferable</li></ul><p>On a personal level, you are <strong>rigorous</strong>, <strong>eager to learn</strong> and <strong>able to adapt</strong> to different working <span style="text-decoration:inherit;">methods/environments.</span> You also have <strong>great communication skills</strong> to interact with both internal and external partners. You enjoy both <strong>working within a team</strong> and <strong>autonomously</strong>. You are also capable of <strong>taking ownership and leading a variety of projects</strong>. Finally, you possess a <strong>continuous improvement</strong> and <strong>digital mindset</strong>.</p><h3><strong>What we offer</strong></h3><ul><li>Outstanding company culture</li><li>Career development opportunities</li><li>Company pension scheme, yearly company bonus, private health care, stock purchase plan, medical &amp; life insurance…</li><li>A position within an international organisation, offering a dynamic working environment, with exciting challenges and opportunities</li></ul><p><strong>You will become part of a company that works according to these values:</strong><br>We move life sciences and diagnostics forward, care about the needs of our customers and strive to ensure people are treated consistently, fairly and with respect. We deliver effective life science and diagnostic solutions valued by our customers.</p><p><strong>We will make sure you get all the training and development opportunities you need to become the best in your field!</strong></p><h3><strong>Additional Details</strong></h3><p>This job has a full time weekly schedule.</p><p>Our pay ranges are determined by role, level, and location. 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. Pay and benefit information by country are available at: <a target="_blank" rel="noopener noreferrer" href="https://careers.agilent.com/locations"><span style="text-decoration:inherit;">https://careers.agilent.com/locations</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>Travel Required:</strong> Occasional</li><li><strong>Shift:</strong> Day</li><li><strong>Duration:</strong> No End Date</li><li><strong>Job Function:</strong> Manufacturing</li></ul>

Organic Chemist – Polymer & Silica Particle Manufacturing

<p><strong>As the world leader in serving science, our work is more than something that fills our days – what we do has great purpose. Our industry-leading scale means unparalleled commercial reach, unique customer access and a global footprint. Our broad customer base, from research to clinical to commercial production means you can have a broad and meaningful impact here at Thermo Fisher Scientific. All while working in an environment where you will be supported, valued and rewarded for your performance.</strong></p><h3><strong>QC Scientist I</strong></h3><div><div><div><p><span>As part of the Thermo Fisher Scientific team, you’ll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life every single day to enable our customers to make the world healthier, cleaner and safer. We provide our global teams with the resources needed to achieve individual career goals while helping to take science a step beyond by developing solutions for some of the world’s toughest challenges, like protecting the environment, making sure our food is safe or helping find cures for cancer.</span></p><h4><strong>Excellent Benefits Package</strong></h4><ul><li><span>Review our company’s </span><a target="_blank" rel="noopener noreferrer" href="https://jobs.thermofisher.com/global/en/total-rewards"><span>Total Rewards</span></a></li><li><span>Medical, Dental, &amp; Vision benefits-effective Day 1</span></li><li><span>Paid Time Off &amp; Holidays</span></li><li><span>401K Company Match up to 6%</span></li><li><span>Tuition Reimbursement – eligible after 90 days!</span></li><li><span>Employee Referral Bonus</span></li><li><span>Employee Discount Program</span></li><li><span>Recognition Program</span></li><li><span>Charitable Gift Matching</span></li><li><span>Company Paid Parental Leave</span></li><li><span>Career Advancement Opportunities</span></li></ul><h4><span><strong>Location/Division Specific Information</strong></span></h4><ul><li><span>Florence, SC</span></li><li><span>Hours: 8am-4:30pm</span></li></ul><h4><strong>How will I make an impact?</strong></h4><ul><li>Conducts moderately difficult chemical and physical testing of pharmaceutical raw materials, packaging components, finished products, microbiological, and stability samples by internally developed and completed test methods.</li><li>Performs validated test methods for pharmaceutical raw materials and finished products for strength, impurities, identity, and dissolution by HPLC, GC, dissolution, spectroscopy, and traditional quantitative analysis, using HPLC, GC, LC/MS, dissolution, spectroscopy, and/or traditional <span>quantitative analysis</span>.</li><li>Recognizes and reports out-of-specification or unexpected results and non-routine analytical and product problems; recommends solutions.</li><li>Maintains and troubleshoots analytical instrumentation as needed.</li><li>Clearly <span>and accurately communicate results by detailing testing/analysis data and acquired results, recording and reporting findings per prescribed lab procedures and systems. Collaborate with clients as needed.</span> ​</li><li>Prepares and assists in filing regulatory documents in support of internal projects. Provides communications with outside departments, corporate sites, agencies, and clients.</li><li>Writes SOPs and other instructional documents.</li><li>Cleans and coordinates work area, instrumentation, and testing materials., including HPLC and dissolution systems after use.</li><li>Performs all duties in strict compliance with Standard Operating Procedures, Good Manufacturing Practices, Good Laboratory Practices, and Safety guidelines. Maintains the vital compliance status required by company and facility standards.</li></ul><h4><strong>Education:</strong></h4><p>Bachelor's degree in physical science, preferably in Chemistry or Biology.</p><h4><strong>Experience:</strong></h4><p>No experience required, but prefer 2 years of experience performing tests or analyses for pharmaceutical raw materials, finished products, or microbiological samples. Experience with common office software and chromatographic data acquisition systems preferred.</p><h4><strong>Proficiencies:</strong></h4><ul><li>Solid foundation of chemistry and analytical instrumental technologies.</li><li>Good knowledge of qualitative and quantitative chemical or microbiological analysis.</li><li>Familiarity with quality and regulatory requirements in the pharmaceutical industry, including GMPs and descriptive organic chemistry.</li><li>Strong problem-solving skills and a logical approach to solving scientific problems.</li><li>Proficiency with HPLC, GC, LC/MS, and Dissolution techniques.</li><li>Effective interpersonal and communication skills (oral and written).</li><li>Competence in presenting information to customers, clients, and other employees.</li><li>Ability to read, analyze, and interpret technical procedures and governmental regulations.</li><li>Capability to write standard operating procedures, protocols, and reports.</li><li>Ability to address common inquiries or complaints from customers or regulatory agencies.</li><li>Proficiency in applying mathematical operations to determine test reliability, analyze variance, and apply correlation techniques.</li></ul></div></div></div><h4><strong>Work Schedule</strong></h4><ul><li>Standard (Mon-Fri)</li></ul><h4><strong>Environmental Conditions</strong></h4><ul><li><span>Laboratory Setting</span></li></ul>

QC Scientist I

<p><strong>As the world leader in serving science, our work is more than something that fills our days – what we do has great purpose. Our industry-leading scale means unparalleled commercial reach, unique customer access and a global footprint. Our broad customer base, from research to clinical to commercial production means you can have a broad and meaningful impact here at Thermo Fisher Scientific. All while working in an environment where you will be supported, valued and rewarded for your performance.</strong></p><h3><strong>Scientist - HPLC, GMP</strong></h3><div><div><div><p>At Thermo Fisher Scientific, you’ll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life - enabling our customers to make the world healthier, cleaner and safer. We provide our teams with the resources needed to achieve individual career goals while taking science a step beyond through research, development and delivery of life-changing therapies. With clinical trials conducted in 100+ countries and ongoing development of novel frameworks for clinical research through our PPD clinical research portfolio, our work spans laboratory, digital and decentralized clinical trial services. Your determination to deliver quality and accuracy will improve health outcomes that people and communities depend on – now and in the future.</p><p>Thermo Fisher's clinical research business is a leading global contract research organization and world leader in serving science. We are passionate, deliberate, and driven by our mission – to enable our customers to make the world healthier, safer, and cleaner.</p><p>Within our Analytical Services team, we have a functional service provider solution, which is a unique partnership that allows our customers to leverage the experience of our staff, while allowing you, the employee, to gain direct experience working onsite at a pharmaceutical/ biopharmaceutical company, all while maintaining full-time benefits.</p><h4><strong>Key responsibilities:</strong></h4><ul><li>Analytical characterization and assessment of clinical trial supplies (e.g. GMP compliant stability and release testing for both drug substances and drug products)</li><li>Understand corporate standards regarding code of conduct, safety, and GxP compliance.</li><li>Responsible for compliance with all applicable Client policies and procedures.</li><li>Document experimental data appropriately in laboratory documentation systems.</li><li>Maintains laboratory equipment and optimize laboratory operations for safe and efficient use of time and resources.</li><li>Troubleshoots equipment and experimental problems.</li><li>Laboratory operational support for the group’s experimental development and testing activities<ul><li>Complex solution preparation in a GxP environment</li><li>Laboratory balance checks and pH meter standardizations</li><li>Inventory/resource management (e.g. ordering supplies, stockkeeping, etc.)</li><li>Laboratory hygiene including waste disposal management and safety checks</li></ul></li><li>Document experimental data appropriately in an electronic laboratory notebook</li><li>Problem solving, either independently or with assistance, pertaining to experiment and/or instrumentation issues</li><li>Identify areas for improvement in laboratory operations to improve efficiency and resource usage and assist in continuous improvement activities</li></ul><h4><strong>Education and Experience:</strong></h4><ul><li>Bachelor's degree in lab sciences such as Chemistry, Biochemistry, Material Science, Immunology, Biology, Molecular Biology or similar</li><li><strong>Scientist:</strong> Previous experience that provides the knowledge, skills, and abilities to perform the job <strong>(comparable to 2-4 years’ experience)</strong></li><li>OR <strong>Masters</strong> degree with 0-2 years' experience</li></ul><p>In some cases, an equivalency, consisting of a combination of appropriate education, training and/or directly related experience, will be considered sufficient for an individual to meet the requirements of the role.</p><h4><strong>Knowledge, Skills and Abilities:</strong></h4><ul><li>Experience in a regulated cGMP Lab</li><li>Experience in analytical methodology, such as chromatography (HPLC/GC/IC), KF, UV and common compendial methods required. Experience in some specialty techniques required (LCMS, GCMS, PXRD, ICP, Dissolution, Disintegration).</li><li>Experienced in laboratory systems (LIMS, CDS, ELN) required.</li><li>Full understanding of laboratory requirements, PPD &amp; client SOPs, ICH guidelines, USP requirements and FDA guidance</li><li>Proven problem solving and troubleshooting abilities</li></ul><h4><strong>Working Environment:</strong></h4><p>Below is listed the working environment/requirements for this role:</p><ul><li>Able to communicate, receive, and understand information and ideas with diverse groups of people in a comprehensible and reasonable manner.</li><li>Able to work upright and stationary and/or standing for typical working hours.</li><li>Able to lift and move objects up to 25 pounds</li><li>Able to work in non-traditional work environments.</li><li>Able to use and learn standard office equipment and technology with proficiency.</li><li>May have exposure to potentially hazardous elements, including infectious agents, typically found in healthcare or laboratory environments.</li><li>Able to perform successfully under pressure while prioritizing and handling multiple projects or activities.</li></ul><h4><strong>Benefits</strong></h4><p>We offer competitive remuneration, annual incentive plan bonus, healthcare, and a range of employee benefits. Thermo Fisher Scientific offers employment with an innovative, forward-thinking organization, and outstanding career and development prospects. We offer an exciting company culture that stands for integrity, intensity, involvement, and innovation!</p><p>Our Mission is to enable our customers to make the world healthier, cleaner and safer. Watch as our colleagues explain 5 reasons to work with us. As one team of 100,000+ colleagues, we share a common set of values - Integrity, Intensity, Innovation and Involvement - working together to accelerate research, solve complex scientific challenges, drive technological innovation and support patients in need. #StartYourStory with PPD, part of Thermo Fisher Scientific, where diverse experiences, backgrounds and perspectives are valued.</p><p>Apply today! <a target="_blank" rel="noopener noreferrer" href="http://jobs.thermofisher.com">http://jobs.thermofisher.com</a></p><p>Thermo Fisher Scientific is an EEO/Affirmative Action Employer and does not discriminate on the basis of race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability or any other legally protected status.</p><h4><strong>Accessibility/Disability Access</strong></h4><p>Job Seekers with a Disability: Thermo Fisher Scientific offers accessibility service for job seekers requiring accommodations in the job application process. For example, this may include individuals requiring assistance because of hearing, vision, mobility, or cognitive impairments. If you are a job seeker with a disability, or assisting a person with a disability, and require accessibility assistance or an accommodation to apply for one of our jobs, please submit a request by telephone at 1-855-471-2255*. Please include your contact information and specific details about your required accommodation to support you during the job application process.</p><p>*This telephone line is reserved solely for job seekers with disabilities requiring accessibility assistance or an accommodation in the job application process. Messages left for other purposes, such as not being able to get into the career website, following up on an application, or other non-disability related technical issues will not receive a response.</p><h4><strong>Compensation and Benefits</strong></h4><p>The hourly pay range estimated for this position based in Illinois is $27.41–$45.68.</p><p style="text-align:left;">This position may also be eligible to receive a variable annual bonus based on company, team, and/or individual performance results in accordance with company policy. We offer a comprehensive Total Rewards package that our U.S. colleagues and their families can count on, which includes:</p><ul><li>A choice of national medical and dental plans, and a national vision plan, including health incentive programs</li><li>Employee assistance and family support programs, including commuter benefits and tuition reimbursement</li><li>At least 120 hours paid time off (PTO), 10 paid holidays annually, paid parental leave (3 weeks for bonding and 8 weeks for caregiver leave), accident and life insurance, and short- and long-term disability in accordance with company policy</li><li>Retirement and savings programs, such as our competitive 401(k) U.S. retirement savings plan</li><li>Employees’ Stock Purchase Plan (ESPP) offers eligible colleagues the opportunity to purchase company stock at a discount</li></ul><p style="text-align:left;"><span>For more information on our benefits, please visit: </span><a target="_blank" rel="noopener noreferrer" href="https://jobs.thermofisher.com/global/en/total-rewards"><span>https://jobs.thermofisher.com/global/en/total-rewards</span></a></p></div></div></div><h4><strong>Work Schedule</strong></h4><ul><li>First Shift (Days)</li></ul><h4><strong>Environmental Conditions</strong></h4><ul><li><span>Adherence to all Good Manufacturing Practices (GMP) Safety Standards</span></li></ul>

Scientist - HPLC, GMP

<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>We are here for people at every step, helping create, improve and prolong life. We deliver personalized treatments for serious diseases and enable people to achieve their dream of becoming parents. We empower the scientific community. Our tools, services, and digital platform make research simpler, more exact, and help to deliver breakthroughs more quickly. We provide progressive treatment solutions that help improve access to health thanks to the accuracy of our tests and the reliability of our medicine. As a company, we are at the forefront of digital living. Our science sits inside technologies that change the way we access, store, process, and display information. Our innovative technology drives human progress and opens new possibilities to transform life on Earth as we know it.</p>
<p>Thanks to the constant curiosity of our employees, we are making discoveries that can change the landscape of entire industries. For more than 350 years, we’ve been pushing the boundaries of what’s possible, and we’ll continue to do so in the years to come.</p>
<h3><strong>SENIOR LIPID SYNTHESIS CHEMIST</strong></h3>
<p>Work Your Magic with us!  Start your next chapter and join MilliporeSigma.</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&#39;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>
<h4><strong>Your Role:</strong></h4>
<ul>
<li><p>The Senior Lipid Synthesis Chemist at MilliporeSigma is a member of the targeted mRNA delivery group and will work on crafting a groundbreaking platform which will enable the therapeutic delivery of mRNA with high precision and safety.</p>
</li>
<li><p>Targeted mRNA delivery has the potential to change patient lives by enabling life changing therapies. </p>
</li>
<li><p>An M-Ventures funded biotech start-up is poised to seize the opportunity at the intersection between our Healthcare and Life Science Divisions. </p>
</li>
<li><p>Our mandate is to think big and reach across teams to leverage the full capabilities of the organization. </p>
</li>
<li><p>With the agility of a startup and the resources of a leading multinational organization, the targeted mRNA delivery team is transforming the way researchers develop mRNA therapies.</p>
</li>
</ul>
<h4><strong>Responsibilities include:</strong></h4>
<ul>
<li><p>Design of novel ionizable lipids, including cationic and anionic lipids, to deliver novel nucleic acid cargo to desired organ of interest</p>
</li>
<li><p>Designing novel shorter routes of synthesis to enable faster turnaround and higher yield</p>
</li>
<li><p>Synthesis and analysis of novel lipids</p>
</li>
<li><p>Active engagement with formulations and biology team to develop structure activity relationship (SAR) based-designs</p>
</li>
<li><p>Present study observations and data in cross-functional project meetings</p>
</li>
<li><p>Actively engage with legal/IP teams to determine patentability and freedom to operate on novel designs and enable the team to generate crucial intellectual property</p>
</li>
<li><p>The lab is located in Burlington, MA with a satellite location in Billerica, MA</p>
</li>
</ul>
<h4><strong>Who You Are:</strong></h4>
<h4><strong>Minimum Qualifications:</strong></h4>
<ul>
<li>PhD in Organic Chemistry, or other life science and 3+ years of experience in an academic or industrial setting</li>
</ul>
<p><strong>Preferred Qualifications:</strong></p>
<ul>
<li><p>Excellent track record of recent, active hands-on lab work involving organic synthesis</p>
</li>
<li><p>Experience with lipid synthesis</p>
</li>
<li><p>Experience with flow chemistry</p>
</li>
<li><p>Experience in <strong>NMR, LS-MS, HPLC, ELSD, CAD</strong> and varied purification strategies</p>
</li>
<li><p>Familiar with Pharma or Biopharmaceutical industry, especially drug discovery</p>
</li>
<li><p>Excellent verbal and written communication skills in English</p>
</li>
<li><p>Work experience in a non-viral delivery group</p>
</li>
<li><p>Ability to work under pressure in a global, matrixed organization across multiple time zones and geographies</p>
</li>
<li><p>Highly organized, detailed, creative, results-driven problem solver with demonstrated flexibility and collaborative working style</p>
</li>
</ul>
<h4><strong>What we offer:</strong></h4>
<ul>
<li><p>We are curious minds that come from a broad range of backgrounds, perspectives, and life experiences. </p>
</li>
<li><p>We celebrate all dimensions of diversity and believe that it drives excellence and innovation, strengthening our ability to lead in science and technology. </p>
</li>
<li><p>We are committed to creating access and opportunities for all to develop and grow at your own pace. </p>
</li>
<li><p>Join us in building a culture of inclusion and belonging that impacts millions and empowers everyone to work their magic and champion human progress!</p>
</li>
</ul>
<p>Apply now and become a part of our diverse team!  </p>
<p>If you would like to know more about what diversity, equity, and inclusion means to us, please <a href="https://www.emdgroup.com/en/company/press-positions.html"><strong>visit</strong></a> </p>
<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 href="https://www.merckgroup.com/en/careers/faqs.html"><strong>information</strong></a></p>


Senior Lipid Synthesis Chemist (NMR, LS-MS, HPLC, ELSD, CAD)

Lab technician

Liquid chromatography-mass spectrometry

Scientific and Research Fellow

Sales Representative

Academic staff

Laboratory services

Service engineer

Manager

Software

Molecular biology

Product Specialist

Application Specialist

Gas chromatography

Gas chromatography-mass spectrometry

Molecular spectroscopy UV-Vis, RAMAN, FTIR

Marketing

Analytical chemist

Technologist/Engineer

Laboratory instruments

Spectroscopy

Chemist

Quality Control (QC)

Microbiology

Liquid chromatography

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Jobs chemist - page 1

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