OTHER

FEED

UNKNOWN

Founded in 2004, Pharmaron has invested in its people and facilities and established a broad spectrum of research, development, and manufacturing service capabilities throughout the entire drug discovery, preclinical, and clinical development process across multiple therapeutic modalities, including small molecules, biologics, and CGT products. PhD in Analytical Chemistry, Organic Chemistry, Pharmaceutical Sciences, or related discipline with 6+ years of industry experience OR MS with 8+ years of pharmaceutical industry experience OR BS with 10+ years of relevant pharmaceutical industry experience.

YEAR

<p><strong>Position</strong>: Associate Principal Scientist –  Analytical Chemistry</p><p><strong>Salary Range: </strong>$120k - $140k</p><p><strong>Location: </strong>Coventry, RI</p><p><strong>About Pharmaron</strong></p><p>Pharmaron is a global contract research and manufacturing organization (CRO/CDMO) helping pharma and biotech companies bring new therapies to life. With over 21,000 employees worldwide across 23 locations in the US, UK and China, we support drug discovery through to manufacturing with fully integrated, high-quality services.</p><p>We're proud of the impact we make and just last year, we supported over <strong>780 discovery projects</strong>, <strong>1,000+ CMC programmes</strong>, and <strong>1,000+ clinical trials </strong>across all phases. Our teams are involved in everything from small molecules, ADC's, biologics, and gene therapies and we work with more than <strong>3,000 global customers</strong>. To learn more, visit <a href="https://apc01.safelinks.protection.outlook.com/?url=http%3A%2F%2Fwww.pharmaron.com%2F&data=05%7C02%7CManuel.Chavez%40pharmaron.com%7C108b55e1f1974c9658a508ddceb40953%7Cad43cc9279994116bbb60a2bcc8776b3%7C1%7C0%7C638893994880380278%7CUnknown%7CTWFpbGZsb3d8eyJFbXB0eU1hcGkiOnRydWUsIlYiOiIwLjAuMDAwMCIsIlAiOiJXaW4zMiIsIkFOIjoiTWFpbCIsIldUIjoyfQ%3D%3D%7C0%7C%7C%7C&sdata=T%2FvyLMGKSoDpjKpFT5gLNDQYsPNZSNtnUro3FX%2FAduI%3D&reserved=0" rel="nofollow">www.pharmaron.com</a>.</p><p><strong>Job Overview </strong></p><p>Pharmaron is seeking an Associate Principal Scientist –  Analytical Chemistry to join our Analytical Chemistry team supporting API development and manufacturing at our Coventry, Rhode Island site.</p><p>This role provides scientific leadership in analytical method development and troubleshooting to support process chemistry, scale-up activities, and GMP manufacturing programs. The successful candidate will lead analytical strategies across multiple client projects while mentoring junior scientists and collaborating closely with cross-functional teams including process chemistry, manufacturing, and quality.</p><p><strong>Key Responsibilities</strong></p><ul><li>Lead analytical development strategies supporting <strong>API process development, scale-up, and manufacturing programs</strong>.</li><li>Design and implement <strong>robust analytical methods</strong> for characterization, impurity profiling, and quality control of APIs, intermediates, and starting materials.</li><li>Apply advanced analytical techniques including <strong>HPLC/UPLC, LC-MS, GC, NMR, and other characterization tools</strong> to support process development.</li><li>Troubleshoot complex analytical challenges and develop innovative solutions to support process chemistry and manufacturing teams.</li><li>Lead analytical activities across multiple client programs, ensuring timely delivery of high-quality data and technical reports.</li><li>Provide <strong>technical mentorship and scientific guidance</strong> to junior scientists and laboratory staff.</li><li>Collaborate cross-functionally with <strong>Process Chemistry, Manufacturing, Quality, and Regulatory teams</strong> to support development and GMP manufacturing activities.</li><li>Review experimental data, laboratory notebooks, and technical reports to ensure scientific accuracy and compliance.</li><li>Support proposal development and review <strong>RFPs</strong> to assess analytical requirements for new client programs.</li><li>Present analytical strategies and scientific findings to <strong>internal stakeholders and external clients</strong>.</li><li>Lead analytical investigations, root cause analysis, and troubleshooting for development and manufacturing challenges.</li><li>Author and review <strong>analytical protocols, reports, and SOPs</strong> in compliance with cGMP and regulatory expectations.</li><li>Contribute to continuous improvement initiatives that enhance analytical capabilities and operational efficiency.</li></ul><p><strong>What We're Looking For</strong></p><ul><li>PhD in Analytical Chemistry, Organic Chemistry, Pharmaceutical Sciences, or related discipline with 6+ years of industry experience OR MS with 8+ years of pharmaceutical industry experience OR BS with 10+ years of relevant pharmaceutical industry experience</li><li>Strong expertise in analytical techniques such as:<ul><li>HPLC / UPLC</li><li>LC-MS</li><li>GC / GC-MS</li><li>NMR</li><li>Impurity profiling and characterization</li></ul></li></ul><ul><li>Experience supporting API process development, scale-up, and GMP manufacturing</li><li>Demonstrated ability to troubleshoot complex analytical problems and develop innovative solutions</li><li>Experience mentoring or supervising scientists in a laboratory environment</li><li>Working knowledge of cGMP, ICH guidelines, and regulatory expectations</li><li>Experience working within pharmaceutical, biotech, or CDMO environments</li><li>Strong communication and presentation skills with the ability to interact effectively with clients and cross-functional teams</li><li>Ability to manage multiple priorities in a fast-paced scientific environment</li></ul><p><strong>Why Pharmaron?</strong></p><p>Pharmaron is a premier service provider for the life sciences industry. Founded in 2004, Pharmaron has invested in its people and facilities and established a broad spectrum of research, development, and manufacturing service capabilities throughout the entire drug discovery, preclinical, and clinical development process across multiple therapeutic modalities, including small molecules, biologics, and CGT products. With over 21,000 employees and operations in the U.S., the U.K. and China. Pharmaron has an excellent track record in delivering R&D solutions to its partners in North America, Europe, Japan, and China.</p><p><strong>Collaborative Culture:</strong> You will thrive in our inclusive and collaborative environment, where teamwork and innovation go hand in hand. Here, your voice matters, and your contributions make a real impact. "Employees Number One" and "Clients Centered" are the core cultural values at Pharmaron. Our culture, which sets Pharmaron apart from other organizations, has evolved from our deep commitment to our employees, partners, and collaborators.</p><p><strong>Benefits:</strong> As part of our commitment to your well-being, we offer a comprehensive benefits package:</p><ul><li>Insurance including Medical, Dental & Vision with significant employer contributions</li><li>Employer-funded Health Reimbursement Account</li><li>Healthcare & Dependent Care Flexible Spending Accounts</li><li>100% Employer-paid Employee Life and AD&D Insurance, Short- and Long-Term Disability Insurance</li><li>401k plan with generous employer match</li><li>Access to an Employee Assistance Program</li></ul><p><strong>How to Apply:</strong></p><p>Ready to seize this incredible opportunity? Join us at Pharmaron and be part of a dynamic team driving innovation and excellence in biopharmaceutical research and development. Apply online today!</p><p>As an Equal Employment Opportunity and Affirmative Action employer, Pharmaron values diversity and inclusion in the workplace, fostering an environment where all individuals are empowered to succeed. Join us in our mission to make a difference in the world of life sciences.</p><p>#LI-KS1</p>

Pharmaron

Associate Principal Scientist – Analytical Chemistry

Analysis Skills

Analytical Chemistry

Analytical Development

Analytical Method Development

Application Programming Interface (API)

Bid Analysis

Biology

Biotech and Pharmaceutical

Chemical Processes

Clinical Trial

Communication Skills

Continuous Improvement

Contract Manufacturing

Contract Research Organization (CRO)

Cross-Functional

Current Good Manufacturing Practice (cGMP)

Customer Relations

Customer/Client Research

Data Quality

Drug Development

Drug Discovery

Flexible Spending Accounts

GMP (Good Manufacturing Practices)

Gas Chromatography-Mass Spectrometry (GC-MS)

Healthcare

High Performance Liquid Chromatography (HPLC)

ICH Regulations

Identify Issues

Laboratory

Laboratory Notebook

Leadership

Liquid Chromatography-Mass Spectrometry (LC-MS)

Manufacturing

Mentoring

Multitasking

Nuclear Magnetic Resonance

Operational Audit

Organic Chemistry

Pre-Clinical Development

Presentation/Verbal Skills

Process Development

Process Manufacturing

Proposal Development

Quality Control

Regulations

Regulatory Compliance

Research & Development (R&D)

Research Contracts

Root Cause Analysis

Small Molecules

Standard Operating Procedures (SOP)

Strategic Planning

Team Player

Time Management

Writing Skills

Talent Acquisition

ADAPTED_NOW

The successful candidate will help to build Pfizer’s internal HTS capability in DBP by designing and executing automated data analysis and publishing workflows to enable HTS including primary, confirmation, counter screen, and selectivity assays in 384-well and 1536-well plate formats, all with minimal supervision. Independently design and execute protocols to upload, analyze, report and publish both internal and external data into corporate databases, Create workflows that can analyze and report plate level, layer-level, and well level calculations using data analysis software including Genedata screener.

<div><p><b>Use Your Power for Purpose</b></p><p>At Pfizer, our purpose is to deliver breakthroughs that change patients’ lives. Your work will have a profound impact on improving patients' lives globally. Whether you are involved in discovery sciences, ensuring drug safety and efficacy, or supporting clinical trials, you will leverage cutting-edge design and process development capabilities to accelerate and deliver best-in-class medicines to patients worldwide.</p><p><b>What You Will Achieve</b><br/> </p><p>We are seeking a Data Scientist with strong skills in programming, database architecture and tool development for the analysis of high throughput screening (HTS) data to join our HTS team within the Discovery Biology and Pharmacology (DBP) group in Groton, CT. The HTS team is building internal capabilities to support automated high-throughput screening to identify novel lead matter in support of Pfizer’s small molecule portfolio.  The successful candidate will combine his/her/their expertise in coding and data analysis with strong collaboration and organizational skills to partner with colleagues across functions and to support multiple disease areas of focus.</p><p><b>Key Responsibilities:</b></p><p>The successful candidate will help to build Pfizer’s internal HTS capability in DBP by designing and executing automated data analysis and publishing workflows to enable HTS including primary, confirmation, counter screen, and selectivity assays in 384-well and 1536-well plate formats, all with minimal supervision. This scientist will build and maintain a tracking dashboard that can organize and report the status of HTS campaigns, the output of screening efforts in terms of milestone achievement, and meta data associated with each project.</p><p>Successful candidates will be expected to:</p><ul><li><p>Ensure start-to-finish data flow encompassing registered compounds in source plates, data output from plate readers, QC analysis, etc. on fully and semi-automated platforms.</p></li><li><p>Independently design and execute protocols to upload, analyze, report and publish both internal and external data into corporate databases,</p></li><li><p>Create workflows that can analyze and report plate level, layer-level, and well level calculations using data analysis software including Genedata screener.</p></li><li><p>Test new versions of software and interact with software developers to ensure proper function in both development and production modes</p></li><li><p>Program automation systems using Cellario, Biomek, Echo, and other software platforms for efficient execution of HTS campaigns</p></li><li><p>Create and maintain a dashboard that captures the timelines of key milestones of HTS campaigns, allows for scheduling of multiple HTS projects on several different automation platforms and illustrates bottlenecks and areas for improvement.</p></li><li><p>Construct a reporting tool that informs senior management of the status and timelines of each HTS campaign.</p></li><li><p>Maintain a database of HTS results and meta data that can be queried to answer a variety of screening questions</p></li><li><p>Actively participate in the scouting, evaluation, creation, and implementation of new data solutions to enhance workflow efficiencies and/or capabilities. </p></li></ul><p><b>Here Is What You Need</b> (Minimum Requirements)</p><ul><li><p>BS or equivalent with 6+ years OR MS with 4+ years of experience relevant industry experience</p></li><li><p>Demonstrated experience writing codes, uploading data, publishing data, and managing databases</p></li><li><p>Knowledge of at least one language (python, Java, Excel VBA, C#, SQL) is required.</p></li><li><p>Familiarity with application programming interfaces (APIs)</p></li><li><p>Excellent customer service, time management, computer, verbal and written communication skills</p></li></ul><p><b>Bonus Points If You Have</b> (Preferred Requirements)</p><ul><li><p>BS in Biology, Biochemistry, Bioinformatics, Bioengineering or related life-sciences field</p></li><li><p>Ability to thrive in a fast-paced environment, whether working independently or as part of a team</p></li><li><p>Expertise in SQL and python</p></li><li><p>Knowledge of Genedata screener</p></li><li><p>Previous experience with project management software (Microsoft Project, Jira, Smartsheets or other)</p></li><li><p>Thorough understanding of different API architectures like REST and SOAP</p></li><li><p>Experience with Biomek I7, Echo acoustic liquid handlers, Tempest reagent dispensers, Pherastar plate readers and Envision plate readers</p></li><li><p>Experience with HighRes or other automated systems</p></li><li><p>Previous experience providing laboratory and automation support</p></li><li><p>Familiarity with in vitro assay data (fluorescence, HTRF, TR-FRET, SPA, luminescence) commonly used in pharmacology screening</p></li></ul><p>  </p><p><b>PHYSICAL/MENTAL REQUIREMENTS</b></p><ul><li><p>Lifting, sitting, standing, walking, bending</p></li><li><p>Ability to perform mathematical calculations</p></li></ul><p><b>NON-STANDARD WORK SCHEDULE, TRAVEL OR ENVIRONMENT REQUIREMENTS</b></p><ul><li><p>Majority of work will be performed during the standard workday, but ability to work flexible hours when needed is preferrable</p></li></ul><p><b>Other Job Details:</b></p><ul><li><p>Last Date to Apply: <b>August 07, 2025.</b></p></li><li><p>Work Location Assignment: On Premise</p></li><li><p>No relocation Support Available</p></li></ul><p style="text-align:inherit"><br/></p><p style="text-align:inherit">The annual base salary for this position ranges from $77,100.00 to $128,500.00. In addition, this position is eligible for participation in Pfizer’s Global Performance Plan with a bonus target of 7.5% of the base salary. We offer comprehensive and generous benefits and programs to help our colleagues lead healthy lives and to support each of life’s moments. Benefits offered include a 401(k) plan with Pfizer Matching Contributions and an additional Pfizer Retirement Savings Contribution, paid vacation, holiday and personal days, paid caregiver/parental and medical leave, and health benefits to include medical, prescription drug, dental and vision coverage. Learn more at Pfizer Candidate Site – U.S. Benefits | (uscandidates.mypfizerbenefits.com). Pfizer compensation structures and benefit packages are aligned based on the location of hire. The United States salary range provided does not apply to Tampa, FL or any location outside of the United States.</p><p style="text-align:inherit"/><p style="text-align:inherit"/><p style="text-align:inherit"/><p style="text-align:inherit"/><p style="text-align:left">Relocation assistance may be available based on business needs and/or eligibility.</p><p style="text-align:inherit"/><p style="text-align:inherit"/><div><div><div><div><div><div><div><div><p style="text-align:left"><b>Sunshine Act</b></p><p style="text-align:left">Pfizer reports payments and other transfers of value to health care providers as required by federal and state transparency laws and implementing regulations.  These laws and regulations require Pfizer to provide government agencies with information such as a health care provider’s name, address and the type of payments or other value received, generally for public disclosure.  Subject to further legal review and statutory or regulatory clarification, which Pfizer intends to pursue, reimbursement of recruiting expenses for licensed physicians may constitute a reportable transfer of value under the federal transparency law commonly known as the Sunshine Act.  Therefore, if you are a licensed physician who incurs recruiting expenses as a result of interviewing with Pfizer that we pay or reimburse, your name, address and the amount of payments made currently will be reported to the government.  If you have questions regarding this matter, please do not hesitate to contact your Talent Acquisition representative.</p></div></div></div></div></div></div></div></div><p style="text-align:inherit"/><p style="text-align:inherit"/><div><div><div><div><div><div><div><div><p><b>EEO & Employment Eligibility</b></p><p>Pfizer is committed to equal opportunity in the terms and conditions of employment for all employees and job applicants without regard to race, color, religion, sex, sexual orientation, age, gender identity or gender expression, national origin, disability or veteran status.  Pfizer also complies with all applicable national, state and local laws governing nondiscrimination in employment as well as work authorization and employment eligibility verification requirements of the Immigration and Nationality Act and IRCA.  Pfizer is an E-Verify employer.  This position requires permanent work authorization in the United States.</p></div></div></div></div></div></div></div></div><p style="text-align:inherit"/><p style="text-align:inherit">Research and Development</p><p style="text-align:inherit"/><p style="text-align:inherit">#LI-PFE</p></div>

A career at Pfizer offers opportunity, ownership and impact. All over the world, Pfizer colleagues work together to positively impact health for everyone, everywhere. Our colleagues have the opportunity to grow and develop a career that offers both individual and company success; be part of an ownership culture that values diversity and where all colleagues are energized and engaged; and the ability to impact the health and lives of millions of people. Pfizer, a global leader in the biopharmaceutical industry, is continuously seeking top talent who are inspired by our purpose to innovate to bring therapies to patients that significantly improve their lives.

Pfizer

Scientist, Assay Automation

Pfizer US

Join our innovative Sensing and Communications Department as a Senior Scientist, where you'll lead cutting-edge research and development programs in underwater acoustic systems, sonar technology, and maritime defense solutions. The area provides an excellent quality of life with coastal New England charm, affordable living compared to major metropolitan areas, access to beaches and outdoor recreation, and a thriving defense technology community.

<h4>Senior Scientist - Underwater Acoustic Systems & Maritime Technology Development</h4><p>Join our innovative Sensing and Communications Department as a Senior Scientist, where you'll lead cutting-edge research and development programs in underwater acoustic systems, sonar technology, and maritime defense solutions. This role offers the opportunity to work on technically-challenging national security projects while collaborating with multidisciplinary teams of subject matter experts in subsea technology, autonomous systems, and naval operations.</p><h4>Key Responsibilities</h4><ul><li>Lead and execute technology development programs in innovative maritime systems and underwater acoustic communications</li><li>Develop and manage strategic initiatives for the Sensing and Communications Department</li><li>Prepare and lead multidisciplinary proposals for novel maritime technology solutions and defense applications</li><li>Direct cross-functional engineering teams to solve complex system design challenges while meeting rigorous performance requirements</li><li>Apply advanced physics and mathematics principles to acoustic signal processing and sonar system development</li><li>Design and execute at-sea experiments and field testing of integrated subsea systems</li><li>Mentor and develop junior engineers and scientists in project execution and technical leadership</li><li>Collaborate with project managers, IPT leads, and government customers to deliver innovative solutions</li><li>Guide programs through the complete technology lifecycle from concept through prototype development and deployment</li></ul><h4>Required Qualifications</h4><ul><li>MS or PhD in Electrical Engineering, Mechanical Engineering, Ocean Engineering, Applied Mathematics, Applied Physics, or related technical discipline</li><li>Minimum 5 years of related engineering experience in research and development programs</li><li>Demonstrated experience developing innovative technology solutions in partnership with senior technical staff</li><li>Proven ability to technically lead and contribute to complex engineering tasks at a detailed level</li><li>Experience with acoustic communication systems design or implementation</li><li>Working knowledge of digital and analog circuit design</li><li>Excellent communication and interpersonal skills with diverse stakeholders including project managers and customers</li><li>Strong understanding of fundamental physics and mathematics principles</li></ul><h4>Preferred Qualifications</h4><ul><li>MS or PhD with 10+ years of experience in proposing, planning, and executing technology development programs</li><li>Track record successfully managing multiple multidisciplinary technical programs including scheduling, budgeting, resource coordination, and deliverable accountability</li><li>US Navy undersea warfare leadership and operational experience</li><li>Experience with subsea technology, sonar signal processing, and autonomous underwater systems</li><li>Background designing complex undersea systems including custom PCB design, embedded software development, data acquisition systems, and signal processing algorithms</li><li>Knowledge of Navy technologies, operations, and defense contracting environments</li><li>Experience guiding programs through various technology readiness levels from science and technology through deployment</li></ul><h4>About the Location</h4><p>This position offers flexibility to work from either our <strong>Groton, CT</strong> or <strong>Pawcatuck, CT</strong> locations. Groton, known as the "Submarine Capital of the World," sits along the scenic Thames River and Long Island Sound, offering a rich maritime heritage and close proximity to Naval Submarine Base New London. The area provides an excellent quality of life with coastal New England charm, affordable living compared to major metropolitan areas, access to beaches and outdoor recreation, and a thriving defense technology community. Pawcatuck offers small-town New England character on the Connecticut-Rhode Island border with easy access to coastal amenities and a collaborative professional environment.</p><h4>Why This Is a Great Opportunity</h4><ul><li>Work on mission-critical national security programs with direct impact on naval operations and undersea warfare capabilities</li><li>Engage in the full research and development lifecycle from first-principle analysis through prototyping and at-sea testing</li><li>Collaborate with recognized subject matter experts in acoustics, electronics, autonomous systems, and maritime technology</li><li>Lead and contribute to multidisciplinary teams addressing some of the most challenging technical problems in underwater systems</li><li>Competitive compensation package with annual salary ranging from $160,000 to $210,000 based on experience and qualifications</li><li>Professional growth opportunities through technical leadership roles and mentorship of emerging scientists and engineers</li><li>Access to state-of-the-art facilities and resources for advanced maritime technology development</li><li>Work in a dynamic environment where innovation meets practical application in defense technology</li></ul><h4>Apply Today</h4><p>If you're a motivated Senior Scientist with expertise in underwater acoustic systems, maritime technology, or defense research and development, we encourage you to apply for this immediate full-time opportunity. Join our team and make a meaningful contribution to advancing undersea warfare technology and national security capabilities. Qualified candidates should submit their application to be considered for this exciting role in cutting-edge maritime systems development.</p>

Great Bay Staffing Group

Senior Scientist Sensing and Communications

Acceptance Testing

Acoustics

Acoustics Systems

Analog Circuit Design

Applications Security

Applied Physics

Budgeting

Communication System Design

Digital Circuit Design

Electrical Engineering

Electronics

Embedded Software

Engineering

Field Trials

Government

Internet/IP Telephony

Interpersonal Skills

Mathematics

Mechanical Engineering

Physics

Printed Circuit Board Design

Product Lifecycle

Project Execution

Project/Program Management

Prototyping

Recreation

Signal Processing

Signal Processing Algorithms

Software Development

System Integration (SI)

System Operations

Technical Leadership

United States Navy (USN)

Manatal

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