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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.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.<h3>Process &amp; Cleaning Validation Specialist II</h3>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.<h4>Responsibilities</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>Requirements</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>Work Schedule</h4><ul><li>Standard (Mon-Fri)</li></ul><h4>Environmental Conditions</h4><ul><li>Office</li></ul><a target="_blank" rel="noopener noreferrer" href="http://jobs.thermofisher.com">Apply today! http://jobs.thermofisher.com</a>

Process & Cleaning Validation Specialist II

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 <a target="_blank" rel="noopener noreferrer" href="https://www.agilent.com/">Agilent</a>.<h3>Manufacturing Associate</h3><h4>Job Description</h4>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.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.<h4>Key responsibilities include:</h4><ul><li>The manufacturing of oligonucleotide APIs in a GMP environment.</li><li>Actively involved in aspects of technology transfer and scale-up of oligonucleotide manufacturing processes delivered from Manufacturing Technical Services into Manufacturing.</li><li>Write and revise standard operating procedures according to regulatory and procedural guidelines.</li><li>Work with Validation and Engineering personnel to validate new equipment and facilities.</li><li>Work with Manufacturing Management and Quality to resolve manufacturing problems including drafting quality documentation (CAPA, deviation, change control, etc.).</li><li>Maintain, calibrate, and trouble shoot critical process equipment.</li></ul><h4>Shift Details:</h4>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.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.<h4>Qualifications</h4><ul><li>Bachelor’s or Master’s Degree or equivalent</li><li>1+ years of related manufacturing experience, pharmaceutical manufacturing environment preferred</li><li>Previous knowledge of oligonucleotide synthesis, HPLC, UF, conjugation, and lyophilization is advantageous</li><li>Detail-oriented and can perform technical duties following standard operating procedures and general laboratory safety rules</li><li>Excellent math, documentation, communication and operational troubleshooting skills</li><li>Mechanically inclined</li><li>Clean room environment experience desired</li><li>Experience working in a FDA regulated manufacturing environment is helpful</li></ul><h4>Additional Details</h4>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.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>.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><ul><li>Travel Required: No</li><li>Shift: Morning</li><li>Duration: No End Date</li><li>Job Function: Manufacturing</li></ul>

Manufacturing Associate

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 <a target="_blank" rel="noopener noreferrer" href="https://www.agilent.com/">Agilent</a>.<h3>Organic Chemist – Polymer &amp; Silica Particle Manufacturing</h3>We are seeking an Organic Chemist to join our manufacturing centre of excellence based in Church Stretton, on the outskirts of Shrewsbury, Shropshire.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.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.You will be working as part of a multi-discipline, cross-functional team and your key responsibilities will include:<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>About Church Stretton</h4>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.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.<h3>Qualifications</h3>We are looking for a motivated individual with the following background:<ul><li>University Degree in Organic / Polymer Chemistry or equivalent</li><li>Hands on laboratory experience in process optimisation, scale up and technology deployment around organic and/or polymer chemistry.</li><li>Any project management experience would be a strong plus</li><li>Proficiency in data analysis statistical tools and software is desired</li><li>Experience of working in the Chemical Process industry and relevant tools (HAZOP, HAZID, Risk Assessment) would an advantage</li><li>Knowledge of Comprehensive Quality System would be preferable</li></ul>On a personal level, you are rigorous, eager to learn and able to adapt to different working methods/environments. You also have great communication skills to interact with both internal and external partners. You enjoy both working within a team and autonomously. You are also capable of taking ownership and leading a variety of projects. Finally, you possess a continuous improvement and digital mindset.<h3>What we offer</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>You will become part of a company that works according to these values: 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.We will make sure you get all the training and development opportunities you need to become the best in your field!<h3>Additional Details</h3>This job has a full time weekly schedule.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>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.<ul><li>Travel Required: Occasional</li><li>Shift: Day</li><li>Duration: No End Date</li><li>Job Function: Manufacturing</li></ul>

Organic Chemist – Polymer & Silica Particle Manufacturing

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.<h3>QC Scientist I</h3><div><div><div>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.<h4>Excellent Benefits Package</h4><ul><li>Review our company’s <a target="_blank" rel="noopener noreferrer" href="https://jobs.thermofisher.com/global/en/total-rewards">Total Rewards</a></li><li>Medical, Dental, &amp; Vision benefits-effective Day 1</li><li>Paid Time Off &amp; Holidays</li><li>401K Company Match up to 6%</li><li>Tuition Reimbursement – eligible after 90 days!</li><li>Employee Referral Bonus</li><li>Employee Discount Program</li><li>Recognition Program</li><li>Charitable Gift Matching</li><li>Company Paid Parental Leave</li><li>Career Advancement Opportunities</li></ul><h4>Location/Division Specific Information</h4><ul><li>Florence, SC</li><li>Hours: 8am-4:30pm</li></ul><h4>How will I make an impact?</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 quantitative analysis.</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 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. ​</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>Education:</h4>Bachelor's degree in physical science, preferably in Chemistry or Biology.<h4>Experience:</h4>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.<h4>Proficiencies:</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>Work Schedule</h4><ul><li>Standard (Mon-Fri)</li></ul><h4>Environmental Conditions</h4><ul><li>Laboratory Setting</li></ul>

QC Scientist I

Restek is a world leader in the development and manufacturing of chromatography products — designed by chromatographers — that offer increased sample throughput, faster separations, and reduced cycle times. The Restek portfolio includes gas chromatography (capillary) columns, columns for high-performance and ultra-high-performance liquid chromatography (HPLC and UHPLC), reference standards and other chromatography standards and accessories. Their products are designed by chromatographers for chromatographers, engineered for durability and performance, and supported by a database of applications data.<h2 style="color:rgb(38, 35, 33);font-family:Circular, -apple-system, BlinkMacSystemFont, &quot;Segoe UI&quot;, Roboto, Oxygen, Ubuntu, Cantarell, &quot;Fira Sans&quot;, &quot;Droid Sans&quot;, &quot;Helvetica Neue&quot;, sans-serif;font-style:normal;letter-spacing:normal;text-align:start;text-indent:0px;text-transform:none;">Operations Technician I - GCQC</h2>At Restek, our core values—We Care, Better Every Day, Respectfor All, and Win Together—are at theheart of everything we do.&nbsp;We care&nbsp;deeplyabout our employee-owners, our customers, and the communities we serve aroundthe world. We strive to be&nbsp;better every day&nbsp;byfostering personal and professional growth while delivering solutions thatdrive positive global change. We value&nbsp;respect for all,creating a workplace where every voice matters and diverse perspectives driveinnovation. And we believe we&nbsp;win together,celebrating shared success as a 100% employee-owned company.&nbsp;Restek Corporation is seeking an Operations Technician I to join our Gas Chromatography Quality Control (GCQC) department. This role is pivotal in ensuring the performance and quality of GC columns through rigorous testing and adherence to analytical techniques. The successful candidate will need a high level of attention to detail, effective multi-tasking abilities, and a strong willingness to learn about gas chromatography and its metrics. This position will be scheduled&nbsp;Sunday&nbsp;through Friday 10:30 pm to 6:30 am&nbsp;after a training period.<h4>Key Responsibilities:</h4><ul><li>GC Column Preparation:&nbsp;Prepare and install GC capillary columns.</li><li>Performance Testing:&nbsp;Utilize GC and custom software to assess GC column performance.</li><li>Procedure Adherence:&nbsp;Follow Standard Operating Procedures (SOPs) meticulously.</li><li>Material Tracking:&nbsp;Track and manage raw materials necessary for the testing process.</li><li>Record Keeping:&nbsp;Maintain accurate records and databases, including Statistical Product Control (SPC) or other quality records.</li><li>Quality Review:&nbsp;Evaluate product requirements and assess performance against quality standards.</li><li>Safety Compliance:&nbsp;Adhere to safe handling procedures for chemicals and equipment, consult safety resources when needed, and follow Restek’s safety codes and regulations.</li><li>Team Collaboration:&nbsp;Attend and participate in departmental and team meetings.</li><li>Additional Duties:&nbsp;Execute other assigned tasks as required.</li></ul><h4>Physical Requirements:</h4><ul><li>Work Duration:&nbsp;Standing or sitting 8-10 hours per shift with occasional breaks.</li><li>Physical Activities:&nbsp;Reaching, pulling, fingering, pinching, grasping, typing, repetitive motion.</li><li>Lifting:&nbsp;Occasionally exert up to 20 lbs of pressure/frequently up to 10 lbs.</li><li>Exposure:&nbsp;Work environment may include fumes, odors, dust, or gases.</li></ul><h4>Qualifications:</h4>Typical requirements are a high school diploma or GED. Preferably 2 years of specialized training in a science-related technology or relevant experience. Previous manufacturing experience a plus.<ul><li>Technical Skills:&nbsp;Basic problem-solving using math and scientific principles. Familiarity with Microsoft Office Suite and basic ERP systems is preferred.</li><li>Knowledge &amp; Abilities:<ul><li>Attention to Detail:&nbsp;Strong focus on accuracy and precision.</li><li>Problem-Solving:&nbsp;Effective problem-solving skills.</li><li>Communication:&nbsp;Ability to understand and follow both oral and written instructions and to communicate effectively with team members.</li><li>Teamwork:&nbsp;Friendly demeanor and ability to work well in a team setting.</li></ul></li></ul>This position will require the successful completion of a standard background check in accordance with Restek policy. Employment with Restek will require successful completion of a pre-employment drug screen.<h4>What Makes Restek Unique</h4>We prioritize work-life balance and well-being with offerings like generous PTO, unlimited sick time, onsite fitness center and wellness program with incentives, childcare reimbursement, and adoption assistance—giving you the tools to&nbsp;Own Your Well-Being. Through our Employee Stock Ownership Plan (ESOP) and robust 8% retirement contributions, you can&nbsp;Own Your Financial Future&nbsp;while sharing in the success you help create. Our commitment to development ensures you can&nbsp;Own Your Growth&nbsp;through learning opportunities, career advancement programs, and a collaborative culture that values innovation and teamwork.We are an equal opportunity employer, considering applicants without regard to race, ethnicity, national origin, sex, sexual orientation, gender identity or expression, age, disability, religion, military or veteran status, or any other protected characteristic. Restek provides reasonable accommodations for individuals with disabilities in accordance with the Americans with Disabilities Act and applicable laws.If you’re ready to join a team that lives its values and empowers you to&nbsp;Own Your Future, we’d love to hear your story. Apply today.

Operations Technician I - GCQC

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

Technologist/Engineer

Laboratory instruments

Spectroscopy

Chemist

Quality Control (QC)

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