quality control scientist

Gilead Sciences

<div><div>At Gilead, we&rsquo;re creating a healthier world for all people. For more than 35 years, we&rsquo;ve tackled diseases such as HIV, viral hepatitis, COVID-19 and cancer &ndash; working relentlessly to develop therapies that help improve lives and to ensure access to these therapies across the globe. We continue to fight against the world&rsquo;s biggest health challenges, and our mission requires collaboration, determination and a relentless drive to make a difference.</div><div><br>
Every member of Gilead&rsquo;s team plays a critical role in the discovery and development of life-changing scientific innovations. Our employees are our greatest asset as we work to achieve our bold ambitions, and we&rsquo;re looking for the next wave of passionate and ambitious people ready to make a direct impact.</div><div><br>
We believe every employee deserves a great leader. People Leaders are the cornerstone to the employee experience at Gilead and Kite. As a people leader now or in the future, you are the key driver in evolving our culture and creating an environment where every employee feels included, developed and empowered to fulfil their aspirations. Join Gilead and help create possible, together.<br>
<br>
Job Description</div><div></div><div><br>
At Gilead our pursuit of a healthier world for all people has yielded a cure for hepatitis C, revolutionary improvements in HIV treatment and prevention as well as advancements in therapies for viral and inflammatory diseases and certain cancers.</div><div></div><div>
We set and achieve bold ambitions in our fight against the world&rsquo;s most devastating diseases, united in our commitment to confronting the largest public health challenges of our day and improving the lives of patients for generations to come.</div><div></div><div>
As a Senior Scientist, Raw Materials at Gilead you will be vital for the success of Clinical Biologics QC, providing strategic leadership and overseeing daily operations raw materials.</div><div></div><div>
Focus Areas:</div><ul><li><div>
Manage the end to end lifecycle of GMP raw materials, including receipt, quarantine, sampling, testing coordination, release, storage, requalification, and expiry/disposal. ‑to‑end lifecycle of GMP raw materials, including receipt, quarantine, sampling, testing coordination, release, storage, requalification, and expiry/disposal.</div></li><li><div>
Ensure uninterrupted availability of raw materials to support manufacturing and laboratory testing through proactive inventory planning and risk management.</div></li><li><div>
Coordinate GMP sampling and testing activities for raw materials (e.g., chemicals, excipients, buffers, solvents, reagents), including internal QC and external laboratories.</div></li><li><div>
Review and maintain raw material specifications, Certificates of Analysis (CoAs), quality agreements, and supplier change notifications; support supplier and material qualification and requalification.</div></li><li><div>
Oversee storage, labeling, segregation, and status control of materials under appropriate environmental conditions; manage excursions and related investigations.</div></li><li><div>
Maintain accurate raw material records in electronic systems (e.g., LIMS, ERP, EDMS); perform inventory reconciliations, cycle counts, and data trending.</div></li><li><div>
Serve as a key point of contact for externally tested materials, coordinating internal stakeholders and external laboratories to ensure timely release.</div></li><li><div>
Review and manage deviations, OOS/OOT results, risk assessments, and CAPAs.</div></li><li><div>
Ensure inspection readiness and support internal and external audits.</div></li><li><div>
Collaborate cross‑functionally with Quality Control, Analytical Development, Regulatory Affairs, Quality Assurance, and Supply Chain to support method lifecycle, regulatory filings, and health authority inquiries.</div></li><li><div>
Author, review, and maintain GMP documentation, including protocols, reports, SOPs, deviations, change controls, CAPAs, and study closeout documentation.</div></li><li><div>
Collaborate cross‑functionally with QC, CMC, Regulatory Affairs, Manufacturing, and Supply Chain to support raw material commitments, filings, and health authority responses.</div></li></ul><div></div><div>
Qualifications:</div><ul><li><div>
Experience with Biologics Quality Control with knowledge of industry best practices and trends for raw materials.</div></li><li><div>
In-depth understanding and application of GMP principles, concepts, practices and standards in the US and internationally.</div></li><li><div>
Must be able to develop and improve complex concepts, techniques, standards and new applications based on quality principles and theories.</div></li><li><div>
Must be able to develop solutions to complex problems, which require a high degree of ingenuity, creativity and innovation.</div></li><li><div>
Must be able to exercise judgment and independently determine and take appropriate action where precedent may not exist.</div></li><li><div>
Proven ability to work with senior management to develop and ensure the implementation of Company-wide long-term solutions.</div></li><li><div>
Demonstrated an ability to develop a vision for Quality Control functions and have shaped the capabilities of the function to fulfill that vision.</div></li><li><div>
Demonstrated the ability to influence process and outcomes across functions.</div></li></ul><div></div><div>
Requirements:</div><ul><li><div>
8+ Years experience with BS in Chemistry, Biochemistry or related field OR</div></li><li><div>
6 + Years with MS in Chemistry, Biochemistry or related field OR</div></li><li><div>
2+ Years with PhD in Chemistry, Biochemistry or related field</div></li><li><div>
Deep knowledge and experience in Biologics quality control.</div></li><li><div>
Stays ahead of shifting trends in industry.</div></li><li><div>
Must think critically and creatively and be able to work independently to determine appropriate resources for resolution of problems.</div></li><li><div>
Strong organizational and planning skills.</div></li><li><div>
Shows excellent verbal and written communication skills and collaborative interpersonal skills.</div></li></ul><div></div><div>
People Leader Accountabilities:</div><ul><li><div>
Create Inclusion - knowing the business value of diverse teams, modeling inclusion, and embedding the value of diversity in the way they manage their teams.</div></li><li><div>
Develop Talent - understand the skills, experience, aspirations and potential of their employees and coach them on current performance and future potential. They ensure employees are receiving the feedback and insight needed to grow, develop and realize their purpose.</div></li><li><div>
Empower Teams - connect the team to the organization by aligning goals, purpose, and organizational objectives, and holding them to account. They provide the support needed to remove barriers and connect their team to the broader ecosystem.</div></li></ul><br>
<div></div>
The salary range for this position is: $169,320.00 - $219,120.00. Gilead considers a variety of factors when determining base compensation, including experience, qualifications, and geographic location. These considerations mean actual compensation will vary. This position may also be eligible for a discretionary annual bonus, discretionary stock-based long-term incentives (eligibility may vary based on role), paid time off, and a benefits package. Benefits include company-sponsored medical, dental, vision, and life insurance plans*.<div></div><div>
For additional benefits information, visit:</div><div><div>
https://www.gilead.com/careers/compensation-benefits-and-wellbeing</div></div><div></div><ul><li>Eligible employees may participate in benefit plans, subject to the terms and conditions of the applicable plans.</li></ul><div><br>
For jobs in the United States:</div><div>
Gilead Sciences Inc. is committed to providing equal employment opportunities to all employees and applicants for employment, and is dedicated to fostering an inclusive work environment comprised of diverse perspectives, backgrounds, and experiences. Employment decisions regarding recruitment and selection will be made without discrimination based on race, color, religion, national origin, sex, age, sexual orientation, physical or mental disability, genetic information or characteristic, gender identity and expression, veteran status, or other non-job related characteristics or other prohibited grounds specified in applicable federal, state and local laws. In order to ensure reasonable accommodation for individuals protected by Section 503 of the Rehabilitation Act of 1973, the Vietnam Era Veterans' Readjustment Act of 1974, and Title I of the Americans with Disabilities Act of 1990, applicants who require accommodation in the job application process may contact <div>ApplicantAccommodations@gilead.com</div> for assistance.</div><div><br>
For more information about equal employment opportunity protections, please view the <div>'Know Your Rights'</div> poster.</div><div></div><div><div>
NOTICE: EMPLOYEE POLYGRAPH PROTECTION ACT</div><br>
<div>YOUR RIGHTS UNDER THE FAMILY AND MEDICAL LEAVE ACT</div></div><div><br>
Gilead Sciences will not discharge or in any other manner discriminate against employees or applicants because they have inquired about, discussed, or disclosed their own pay or the pay of another employee or applicant. However, employees who have access to the compensation information of other employees or applicants as a part of their essential job functions cannot disclose the pay of other employees or applicants to individuals who do not otherwise have access to compensation information, unless the disclosure is (a) in response to a formal complaint or charge, (b) in furtherance of an investigation, proceeding, hearing, or action, including an investigation conducted by the employer, (c) consistent with the legal duty to furnish information; or (d) otherwise protected by law.</div><div><br>
Our environment respects individual differences and recognizes each employee as an integral member of our company. Our workforce reflects these values and celebrates the individuals who make up our growing team.</div><div><br>
Gilead provides a work environment free of harassment and prohibited conduct. We promote and support individual differences and diversity of thoughts and opinion.</div><div><br>
For Current Gilead Employees and Contractors:</div><div>
Please apply via the Internal Career Opportunities portal in Workday.</div></div>

Senior Scientist, Raw Materials

US Pharmacopeia

<div>
 <strong>
  Description
  <br/>
  <br/>
 </strong>
 <strong>
  Who is USP?
  <br/>
  <br/>
 </strong>
 The U.S. Pharmacopeial Convention (USP) is an independent scientific organization that collaborates with the world&rsquo;s leading health and science experts to develop rigorous quality standards for medicines, dietary supplements, and food ingredients. At USP, we believe that scientific excellence is driven by a commitment to fairness, integrity, and global collaboration. This belief is embedded in our core value of Passion for Quality and is demonstrated through the contributions of more than 1,300 professionals across twenty global locations, working to strengthen the supply of safe, high-quality medicines worldwide.
 <br/>
 <br/>
 At USP, we value inclusive scientific collaboration and recognize that attracting diverse expertise strengthens our ability to develop trusted public health standards. We foster an organizational culture that supports equitable access to mentorship, professional development, and leadership opportunities. Our partnerships, standards, and research reflect our belief that ensuring broad participation in scientific leadership results in stronger, more impactful outcomes for global health.
 <br/>
 <br/>
 USP is proud to be an equal employment opportunity employer (EEOE) and is committed to ensuring fair, merit-based selection processes that enable the best scientific minds&mdash;regardless of background&mdash;to contribute to advancing public health solutions worldwide. We provide reasonable accommodations to individuals with disabilities and uphold policies that create an inclusive and collaborative work environment.
 <br/>
 <br/>
 <strong>
  Brief Job Overview
  <br/>
  <br/>
 </strong>
 This is a hands-on, non-supervisory position in USP&rsquo;s Reference Standards Laboratory. The Scientist I will contribute to the scientific expertise and work ethic of the laboratory through a broad range of technical support and knowledge. A Scientist I has mastered many common techniques in the laboratory and is able to contribute their own observations and input to difficult projects. The incumbent will provide technical assistance to collaborative testing and the continued suitability for use program by performing analytical tests, reviewing analytical data, and preparing summary reports. The incumbent may execute 90% - 100% of their work at the bench level.
 <br/>
 <br/>
 <strong>
  How will YOU create impact here at USP?
  <br/>
  <br/>
 </strong>
 As part of our mission to advance scientific rigor and public health standards, you will play a vital role in increasing global access to high-quality medicines through public standards and related programs. USP prioritizes scientific integrity, regulatory excellence, and evidence-based decision-making to ensure health systems worldwide can rely on strong, tested, and globally relevant quality standards.
 <br/>
 <br/>
 Additionally, USP&rsquo;s People and Culture division, in partnership with the Equity Office, invests in leadership and workforce development to equip all employees with the skills to create high-performing, inclusive teams. This includes training in equitable management practices and tools to promote engaged, collaborative, and results-driven work environments.
 <br/>
 <br/>
 <strong>
  The Scientist I Has The Following Responsibilities
  <br/>
  <br/>
 </strong>
 <ul>
  <li>
   Demonstrates solid scientific approach to analysis in the laboratory.
  </li>
  <li>
   Routinely applies personal experience, academic training, and technical insights &ndash; including emerging sciences &ndash; to solve complex technical problems within the laboratory.
  </li>
  <li>
   Conducts analysis of reference standard candidates using a broad range of analytical methodologies.
  </li>
  <li>
   Organizes, implements, and evaluates testing of reference standards materials.
  </li>
  <li>
   Records experimental data, ensuring clear and accurate transcription of results and calculations.
  </li>
  <li>
   Reviews literature for analytical test methods, as well as interprets and evaluates data.
  </li>
  <li>
   Executes all testing and analysis of data with excellence and essentially no errors.
  </li>
  <li>
   Demonstrates a strong desire to continue learning and grow personal capability.
  </li>
  <li>
   Pursues, recommends, and implements new approaches or processes to improve laboratory operations.
  </li>
  <li>
   Positively influences project direction by ensuring their own work is congruent with overall direction of laboratory projects.
  </li>
  <li>
   Assists with other testing programs and duties in the laboratory as needed.
   <br/>
   <br/>
  </li>
 </ul>
 <strong>
  Who is USP Looking For?
  <br/>
  <br/>
 </strong>
 The Successful Candidate Will Have a Demonstrated Understanding Of Our Mission, Commitment To Excellence Through Inclusive And Equitable Behaviors And Practices, Ability To Quickly Build Credibility With Stakeholders, Along With The Following Competencies And Experience
 <br/>
 <br/>
 <ul>
  <li>
   B.A. /B.S. in Science and 2 years of relevant laboratory experience.
  </li>
  <li>
   Working knowledge of common analytical methods and procedures [examples include: Infrared Spectroscopy (IR), Ultraviolet Spectroscopy (UV), Chromatography (TLC, HPLC, GC)], and expertise in calibrating and operating analytical instruments are required.
  </li>
  <li>
   Extensive understanding of chromatographic analyses, as well as other general analytical chemistry principles required.
   <br/>
   <br/>
  </li>
 </ul>
 <strong>
  Additional Desired Preferences
  <br/>
  <br/>
 </strong>
 <ul>
  <li>
   Strong communication and presentation skills, both verbal and written.
  </li>
  <li>
   Experience working in the pharmaceutical and/or biotechnology industry is strongly preferred.
  </li>
  <li>
   Knowledge of DEA, ICH guidelines and FDA regulations, and experience with compendial procedures and compliance strongly preferred.
  </li>
  <li>
   Proficiency with electronic documentation systems is strongly preferred.
  </li>
  <li>
   Takes personal responsibility to ensure work is delivered on time and is the highest possible quality.
  </li>
  <li>
   Skills to anticipate, troubleshoot, and solve technical problems.
   <br/>
   <br/>
  </li>
 </ul>
 <strong>
  Supervisory Responsibilities
  <br/>
  <br/>
 </strong>
 None, this is an individual contributor role.
 <br/>
 <br/>
 <strong>
  Benefits
  <br/>
  <br/>
 </strong>
 USP provides the benefits to protect yourself and your family today and tomorrow. From company-paid time off and comprehensive healthcare options to retirement savings, you can have peace of mind that your personal and financial well-being is protected.
 <br/>
 <br/>
 <strong>
  Compensation
  <br/>
  <br/>
 </strong>
 Base Salary Range: USD $58,000.00 &ndash; $74,000.00 annually.
 <br/>
 <br/>
 Target Annual Bonus: % Varies based on level of role.
 <br/>
 <br/>
 Individual compensation packages are based on various factors unique to each candidate&rsquo;s skill set, experience, qualifications, equity, and other job-related reasons.
 <br/>
 <br/>
 Note: USP does not accept unsolicited resumes from 3rd party recruitment agencies and is not responsible for fees from recruiters or other agencies except under specific written agreement with USP.
 <br/>
 <br/>
 Equal Opportunity Employer/Protected Veterans/Individuals with Disabilities
 <br/>
 <br/>
 This employer is required to notify all applicants of their rights pursuant to federal employment laws.
 <br/>
 <br/>
 For further information, please review the Know Your Rights (https://www.eeoc.gov/poster) notice from the Department of Labor.
 <br/>
 <br/>
 <strong>
  Job Category
 </strong>
 Chemistry &amp; Scientific Standards
 <br/>
 <br/>
 <strong>
  Job Type
 </strong>
 Full-Time
</div>


Scientist I

FujiFilm

<div><h2 class="jobSectionHeader"><b>Position Overview
</b></h2><div><div><div><div>The Scientist 2, QC Analytical Development (AD) Chemistry is responsible for coordinating the transfer of analytical methods for Technology Transfer (TT) of drug substance (DS) and drug product (DP) into the Quality Control laboratories of FUJIFILM Biotechnologies, Holly Springs. The QC AD Chemistry Scientist 2 ensures GMP compliant laboratory operations in accordance with regulatory guidelines. This role coordinates analytical method transfers from clients, including the following analytical methods: chromatography (GC, HPLC, UPLC, SEC), spectroscopy (MS, GC/MS, LC-MS/MS, UV, UV-Vis, FTIR), electrophoresis (GE, non-reducing and reducing CE-SDS, imaged capillary isoelectric focusing (icIEF)), wet chemistry, glycan analysis, sub-visible particle analysis, peptide mapping, and physical appearance, etc.</div>
</div></div></div><h2 class="jobSectionHeader"><b>Company Overview
</b></h2><div><div><div><p>FUJIFILM Biotechnologies is building the future of bioproduction in Holly Springs, North Carolina. By end of 2025, we&rsquo;ll open North America&rsquo;s largest end-to-end CDMO biopharmaceutical manufacturing facility, offering drug substance production, fill-finish, and packaging under one roof.</p><br>
<p>We&rsquo;re looking for passionate, mission-driven people to help us realize this exciting vision and deliver the next vaccine, cure, or therapy. We offer a dynamic work environment and we&rsquo;re proud to cultivate a culture that will fuel your purpose, energy, and drive&mdash;what we call Genki. Ready to shape the future of medicine? Let&rsquo;s transform healthcare together!</p><br>
<p><br>
Holly Springs, North Carolina, combines small-town warmth with proximity to Raleigh&rsquo;s thriving tech scene, making it the perfect blend of community and opportunity.</p><br>
<p><br>
Fujifilm is globally headquartered in Tokyo with over 70,000 employees across four key business segments of healthcare, electronics, business innovation, and imaging. We are guided and united by our Group Purpose of &ldquo;giving our world more smiles.&rdquo; Visit: https://www.fujifilm.com/us/en/about/region/careers</p>
</div></div></div><h2 class="jobSectionHeader"><b>Job Description
</b></h2><div><div><div><div><b>What You&rsquo;ll Do</b></div><ul><li>
In-depth technical knowledge of Analytical Chemistry and ability to analyze raw data, assess assay and system suitability criteria.</li><li>
Relevant experience in analytical method development and validation.</li><li>
Demonstrated application and knowledge of ICH guidelines on analytical method validation.</li><li>
Experience with customers and analytical method transfers.</li><li>
Experience with project management and demonstrated ability to monitor project progress and provide status updates.</li><li>
Demonstrated communication skills, technical proficiency, scientific creativity, collaboration with others and independent thought.</li><li>
Planning of projects in terms of timing, execution of deliverables and resource allocation.</li><li>
Excellent interpersonal skills including the ability to work as part of a cross-functional team, collaborate with external clients, adapt to changing business needs, communicate with confidence, challenge others when necessary and display strong problem-solving capabilities.</li><li>
Excellent English oral and written communication skills as well as demonstrated expertise with Microsoft Excel, Project, Word and SmartSheet.</li><li>
Familiarity with LIMS Software.</li><li>
Proficient in physical and chemical testing methods for biological products, including chromatography (GC, HPLC, UPLC, SEC), spectroscopy (MS, GC/MS, LC-MS/MS, UV, UV-Vis, FTIR), electrophoresis (GE, non-reducing and reducing CE-SDS, imaged capillary isoelectric focusing (icIEF)), wet chemistry sub-visible particle analysis, and glycan analysis, and peptide mapping.</li><li>
Displays an advanced knowledge of GMP requirements for laboratory operations.</li><li>
Possesses a broad knowledge of quality control operations, systems, and directives.</li></ul><p><b>
Minimum Qualifications</b></p><ul><li>
Bachelor&rsquo;s Degree in Chemistry, Biochemistry, Biological Sciences, Engineering, or related science field with 9+ years of analytical laboratory experience preferably in Biotechnology, Pharma, Contract Research Organization (CRO), or Contract Laboratory Organization (CLO).</li><li>
4-6 years of experience in a GMP environment</li></ul><div></div><p><b><br>
Preferred Qualifications</b></p><ul><li>
Master&rsquo;s Degree in Chemistry, Biochemistry, Biological Sciences, Engineering, or related science field with 7+ years of experience; OR,</li><li>
Ph.D. in Chemistry, Biochemistry, Biological Sciences, Engineering, or related science field with 5+ years of experience.</li><li>
Experience with Customer Relationship Management.</li><li>
Prior drug substance or manufacturing experience, including process validation, transfer, commercialization, and manufacturing support and troubleshooting.</li><li>
Experience using quality systems (e.g., deviation management system, change control, corrective and preventive action (CAPA), document management system).</li></ul><p></p><p><b><br>
Physical Requirements:</b></p><div>
The physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform essential functions. While performing the duties of this job, the employee is required on a regular basis to:</div><ul><li>
Will work in environment which may necessitate respiratory protection</li><li>
Ability to discern audible cues.</li><li>
Ability to inspect or perform a task with 20/20 corrected vision, visual acuity, including distinguishing color.</li><li>
Ability to stand for prolonged periods of time up to 120 minutes</li><li>
Ability to sit for prolonged periods of time up to 120 minutes</li><li>
Ability to conduct activities using repetitive motions that include writs, hands and/or fingers.</li><li>
Ability to conduct work that includes moving objects up to 10 pounds.</li><li>
Will work in warm/cold environments.</li></ul><div></div><div><i><br>
To all agencies: Please, no phone calls or emails to any employee of FUJIFILM about this requisition. All resumes submitted by search firms/employment agencies to any employee at FUJIFILM via-email, the internet or in any form and/or method will be deemed the sole property of FUJIFILM, unless such search firms/employment agencies were engaged by FUJIFILM for this requisition and a valid agreement with FUJIFILM is in place. In the event a candidate who was submitted outside of the FUJIFILM agency engagement process is hired, no fee or payment of any kind will be paid.</i></div><p></p><ul><li><br>
LI-Onsite</li></ul>
</div></div></div><h2 class="jobSectionHeader"><b>EEO Information
</b></h2><div><div><div><div>Fujifilm is committed to providing equal opportunities in hiring, promotion and advancement, compensation, benefits, and training regardless of nationality, age, gender, sexual orientation or gender identity, race, ethnicity, religion, political creed, ideology, national, or social origin, disability, veteran status, etc.</div>
</div></div></div><h2 class="jobSectionHeader"><b>ADA Information
</b></h2><div><div><div><div>If you require reasonable accommodation in completing this application, interviewing, completing any pre-employment testing, or otherwise participating in the employee selection process, please direct your inquiries to our HR Department (FDBN_PNC@fujifilm.com).</div></div></div></div></div>

Scientist 2, QC Analytical Development - Chemistry

<div><div>At Gilead, we&rsquo;re creating a healthier world for all people. For more than 35 years, we&rsquo;ve tackled diseases such as HIV, viral hepatitis, COVID-19 and cancer &ndash; working relentlessly to develop therapies that help improve lives and to ensure access to these therapies across the globe. We continue to fight against the world&rsquo;s biggest health challenges, and our mission requires collaboration, determination and a relentless drive to make a difference.</div><div><br>
Every member of Gilead&rsquo;s team plays a critical role in the discovery and development of life-changing scientific innovations. Our employees are our greatest asset as we work to achieve our bold ambitions, and we&rsquo;re looking for the next wave of passionate and ambitious people ready to make a direct impact.</div><div><br>
We believe every employee deserves a great leader. People Leaders are the cornerstone to the employee experience at Gilead and Kite. As a people leader now or in the future, you are the key driver in evolving our culture and creating an environment where every employee feels included, developed and empowered to fulfil their aspirations. Join Gilead and help create possible, together.<br>
<br>
Job Description</div><div><br>
At Gilead our pursuit of a healthier world for all people has yielded a cure for hepatitis C, revolutionary improvements in HIV treatment and prevention as well as advancements in therapies for viral and inflammatory diseases and certain cancers.</div><div></div><div>
We set and achieve bold ambitions in our fight against the world&rsquo;s most devastating diseases, united in our commitment to confronting the largest public health challenges of our day and improving the lives of patients for generations to come.</div><div></div><div>
As a Senior Scientist, Stability at Gilead you will be vital for the success of Clinical Biologics QC, providing strategic leadership and overseeing daily operations for stability.</div><div></div><div>
Focus Areas:</div><ul><li><div>
Manage stability strategy for assigned products. Coordinate and oversee GMP stability studies for clinical and commercial products, ensuring compliance with FDA, ICH, and global regulatory requirements.</div></li><li><div>
Manage stability study setup and execution, including protocols, storage conditions (ICH long-term, intermediate, accelerated), pull schedules, testing panels, and acceptance criteria.</div></li><li><div>
Oversee stability sample management, including receipt, labeling verification, controlled storage, chain of custody, and timely sample pulls.</div></li><li><div>
Monitor stability chamber conditions (temperature/humidity), support maintenance and qualification activities, and manage excursions and related investigations.</div></li><li><div>
Compile, review, trend, and statistically analyze stability data to identify product risks and support shelf-life assignments, APR/PQRs, and regulatory submissions.</div></li><li><div>
Maintain stability programs and records in electronic systems.</div></li><li><div>
Author and review stability sections of regulatory submissions</div></li><li><div>
Review and manage deviations, OOS/OOT results, risk assessments, and CAPAs.</div></li><li><div>
Ensure inspection readiness and support internal and external audits.</div></li><li><div>
Author, review, and maintain GMP documentation, including protocols, reports, SOPs, deviations, change controls, CAPAs, and study closeout documentation.</div></li><li><div>
Collaborate cross functionally with Quality Control, Quality Assurance, Analytical Development, CMC, Regulatory Affairs, Manufacturing, and Supply Chain to support stability commitments, filings, and health authority responses.</div></li></ul><div></div><div>
Qualifications:</div><ul><li><div>
Experience with Biologics Quality Control with knowledge of industry best practices and trends for Stability.</div></li><li><div>
In-depth understanding and application of GMP principles, concepts, practices and standards in the US and internationally.</div></li><li><div>
Must be able to develop and improve complex concepts, techniques, standards and new applications based on quality principles and theories. Must be able to develop solutions to complex problems, which require a high degree of ingenuity, creativity and innovation.</div></li><li><div>
Must be able to exercise judgment and independently determine and take appropriate action where precedent may not exist.</div></li><li><div>
Proven ability to work with senior management to develop and ensure the implementation of Company-wide long-term solutions.</div></li><li><div>
Demonstrated an ability to develop a vision for Quality Control functions and have shaped the capabilities of the function to fulfill that vision.</div></li><li><div>
Demonstrated the ability to influence process and outcomes across functions.</div></li></ul><div></div><div>
Requirements:</div><ul><li><div>
8+ Years experience with BS in Chemistry, Biochemistry or related field OR</div></li><li><div>
6 + Years with MS in Chemistry, Biochemistry or related field OR</div></li><li><div>
2+ Years with PhD in Chemistry, Biochemistry or related field</div></li><li><div>
Deep knowledge and experience in Biologics quality control.</div></li><li><div>
Stays ahead of shifting trends in industry.</div></li><li><div>
Must think critically and creatively and be able to work independently to determine appropriate resources for resolution of problems.</div></li><li><div>
Strong organizational and planning skills.</div></li><li><div>
Shows excellent verbal and written communication skills and collaborative interpersonal skills.</div></li></ul><div></div><div>
People Leader Accountabilities:</div><ul><li><div>
Create Inclusion - knowing the business value of diverse teams, modeling inclusion, and embedding the value of diversity in the way they manage their teams.</div></li><li><div>
Develop Talent - understand the skills, experience, aspirations and potential of their employees and coach them on current performance and future potential. They ensure employees are receiving the feedback and insight needed to grow, develop and realize their purpose.</div></li><li><div>
Empower Teams - connect the team to the organization by aligning goals, purpose, and organizational objectives, and holding them to account. They provide the support needed to remove barriers and connect their team to the broader ecosystem.</div></li></ul><br>
<div></div>
The salary range for this position is: $169,320.00 - $219,120.00. Gilead considers a variety of factors when determining base compensation, including experience, qualifications, and geographic location. These considerations mean actual compensation will vary. This position may also be eligible for a discretionary annual bonus, discretionary stock-based long-term incentives (eligibility may vary based on role), paid time off, and a benefits package. Benefits include company-sponsored medical, dental, vision, and life insurance plans*.<div></div><div>
For additional benefits information, visit:</div><div><div>
https://www.gilead.com/careers/compensation-benefits-and-wellbeing</div></div><div></div><ul><li>Eligible employees may participate in benefit plans, subject to the terms and conditions of the applicable plans.</li></ul><div><br>
For jobs in the United States:</div><div>
Gilead Sciences Inc. is committed to providing equal employment opportunities to all employees and applicants for employment, and is dedicated to fostering an inclusive work environment comprised of diverse perspectives, backgrounds, and experiences. Employment decisions regarding recruitment and selection will be made without discrimination based on race, color, religion, national origin, sex, age, sexual orientation, physical or mental disability, genetic information or characteristic, gender identity and expression, veteran status, or other non-job related characteristics or other prohibited grounds specified in applicable federal, state and local laws. In order to ensure reasonable accommodation for individuals protected by Section 503 of the Rehabilitation Act of 1973, the Vietnam Era Veterans' Readjustment Act of 1974, and Title I of the Americans with Disabilities Act of 1990, applicants who require accommodation in the job application process may contact <div>ApplicantAccommodations@gilead.com</div> for assistance.</div><div><br>
For more information about equal employment opportunity protections, please view the <div>'Know Your Rights'</div> poster.</div><div></div><div><div>
NOTICE: EMPLOYEE POLYGRAPH PROTECTION ACT</div><br>
<div>YOUR RIGHTS UNDER THE FAMILY AND MEDICAL LEAVE ACT</div></div><div><br>
Gilead Sciences will not discharge or in any other manner discriminate against employees or applicants because they have inquired about, discussed, or disclosed their own pay or the pay of another employee or applicant. However, employees who have access to the compensation information of other employees or applicants as a part of their essential job functions cannot disclose the pay of other employees or applicants to individuals who do not otherwise have access to compensation information, unless the disclosure is (a) in response to a formal complaint or charge, (b) in furtherance of an investigation, proceeding, hearing, or action, including an investigation conducted by the employer, (c) consistent with the legal duty to furnish information; or (d) otherwise protected by law.</div><div><br>
Our environment respects individual differences and recognizes each employee as an integral member of our company. Our workforce reflects these values and celebrates the individuals who make up our growing team.</div><div><br>
Gilead provides a work environment free of harassment and prohibited conduct. We promote and support individual differences and diversity of thoughts and opinion.</div><div><br>
For Current Gilead Employees and Contractors:</div><div>
Please apply via the Internal Career Opportunities portal in Workday.</div></div>

Senior Scientist, Stability

Pfizer

<div><div>Why Patients Need You</div><div></div><div>
Pfizer&rsquo;s purpose is to deliver breakthroughs that change patients&rsquo; lives. Research and Development is at the heart of fulfilling Pfizer&rsquo;s purpose as we work to translate advanced science and technologies into the therapies and vaccines that matter most. Whether you are in the discovery sciences, ensuring drug safety and efficacy, or supporting clinical trials; you will apply cutting edge design and process development capabilities to accelerate and bring the best-in-class medicines to patients around the world.</div><div></div><div>
What You Will Achieve</div><div></div><div>
As an Associate Scientist, you will be at the center of our operations and you&rsquo;ll find that everything we do, every day, is in line with an unwavering commitment to quality. Your work in the Analytical R&amp;D Microbiology Strategy &amp; Testing organization helps enable development of biological therapeutics at Pfizer. Your responsibilities will be applying GMP microbiological methods (bioburden, endotoxin, PCR, etc.) in the assessment of product quality and detection of impurities. Your contributions are part of a group performing microbiology identification, testing, and method qualifications to support multiple sites in the Pfizer network. You will be responsible for Environmental Monitoring (EM) of manufacturing facilities, waters, and compressed gases at the site. The Associate Scientist is responsible for utilizing established microbiological methodologies to support GMP in-process and research &amp; development testing of clinical supplies. You will become proficient in aseptic lab technique and facility gowning to thrive in this fast-paced environment. Your strong foundation in general scientific practice, its principles and concepts will help in meeting critical deadlines. You will be relied on as a technical contributor to assess the assigned tasks and make decisions that involve direct application of your knowledge. It is your focus and commitment that will help in making Pfizer ready to achieve new milestones and help patients across the globe.</div><div></div><div><br>
How You Will Achieve It</div><ul><li><div>
Exercise and build basic team effectiveness skills {e.g., commitment, feedback, consensus management) within the work group.</div></li><li><div>
Review and contribute to technical documents, including validation protocols and reports, analytical test procedures, investigation reports, monitoring trend reports, and change controls.</div></li><li><div>
Directly interact with multiple department team members, including presentation of data.</div></li><li><div>
Complete all Good Manufacturing Practice {part of G<i>x</i>P} and safety training in compliance with departmental requirements and follow appropriate safety practices in the workplace.</div></li><li><div>
Perform various experiments for microbial analysis, qualification/validation, and characterization of biological therapeutics.</div></li><li><div>
Perform and document environmental monitoring of manufacturing areas and related Microbiological activities.</div></li><li><div>
Conduct all work according to appropriate Standard Operating Procedures following Good Manufacturing Practices/Good Laboratory Practices (GMP/GLP) requirements and ensure integrity of all data generated and documented.</div></li><li><div>
Independently analyze and provide conclusions regarding data generated.</div></li><li><div>
Plan and prioritize assigned testing activities.</div></li><li><div>
Present problems and propose solutions in discussions with group members.</div></li></ul><div></div><div><br>
Qualifications</div><div>
Must-Have</div><ul><li><div>
Bachelor's degree in microbiology, biochemistry, biology, or related field with 0 to 2 years of experience</div></li><li><div>
Excellent documentation skills with high attention to detail</div></li><li><div>
Strong organizational skills and effective interpersonal and written communication skills</div></li><li><div>
Self-motivated and highly effective in a team-based environment</div></li><li><div>
Ability to follow established procedures under minimal supervision</div></li></ul><div></div><div>
Nice-to-Have</div><ul><li><div>
1+ years&rsquo; experience with Quality Systems in a Good Manufacturing Practices (GMP) environment</div></li><li><div>
Experience with laboratory data systems such as Laboratory Information Management Systems (LIMS)</div></li><li><div>
Hands on experience or working knowledge in pharmaceutical industry and handling of analytical instruments</div></li><li><div>
Some knowledge of drug development process for progression of biological candidates</div></li></ul><div></div><div>
PHYSICAL/MENTAL REQUIREMENTS</div><div></div><div>
Position requires occasional light lifting and periods of standing, sitting or walking. Laboratory testing involves repetitive operations using hand-held instruments (micropipettes).</div><div></div><div>
NON-STANDARD WORK SCHEDULE, TRAVEL OR ENVIRONMENT REQUIREMENTS</div><div></div><ul><li><div>
This is typically a Monday-Friday schedule, first shift. Occasional weekend work or off-shift hours work is required per business need.</div></li><li><div>
Candidate must be able to qualify on cleanroom gowning to conduct weekly monitoring of the manufacturing areas.</div></li></ul><div><br>
Work Location Assignment: On Premise</div><br>
<div></div>
The annual base salary for this position ranges from $60,200.00 to $97,500.00. In addition, this position is eligible for participation in Pfizer&rsquo;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&rsquo;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 &ndash; 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.<div></div><div>
Relocation assistance may be available based on business needs and/or eligibility.</div><div></div><div><div><div><div><div><div><div><div><div>
Sunshine Act</div><div>
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&rsquo;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.</div></div></div></div></div></div></div></div></div><div></div><div><div><div><div><div><div><div><div><div>
EEO &amp; Employment Eligibility</div><div>
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.</div><div></div><div>
Pfizer endeavors to make <div>www.pfizer.com/careers</div> accessible to all users. If you would like to contact us regarding the accessibility of our website or need assistance completing the application process and/or interviewing, please email <div>disabilityrecruitment@pfizer.com</div>. This is to be used solely for accommodation requests with respect to the accessibility of our website, online application process and/or interviewing. Requests for any other reason will not be returned.</div></div></div></div></div></div></div></div></div><div></div>
Research and Development</div><div></div>

Associate Scientist, Microbiology

Actalent

<div>
 <strong>
  Associate Scientist/Chemist
  <br/>
  <br/>
 </strong>
 <strong>
  Job Description
  <br/>
  <br/>
 </strong>
 We are seeking dedicated Chemists to perform routine tests on various samples, including finished products, stability samples, raw materials, and more using techniques such as UV and HPLC in a regulated laboratory environment. The role involves evaluating test results, maintaining accurate lab documentation, and ensuring compliance with SOPs and cGMP standards.
 <br/>
 <br/>
 <strong>
  Responsibilities
  <br/>
  <br/>
 </strong>
 <ul>
  <li>
   Conduct routine tests of finished products, stability samples, raw materials, and CV samples using techniques such as assays, chromatographic purity, and particle size distribution.
  </li>
  <li>
   Evaluate test results and determine the acceptability of samples based on the results.
  </li>
  <li>
   Maintain accurate lab notebooks and complete all related analytical reports and documentation in compliance with SOPs.
  </li>
  <li>
   Ensure laboratories are maintained with good housekeeping practices and in compliance with cGMP standards.
  </li>
  <li>
   Review notebooks promptly and ensure compliance with SOPs.
  </li>
  <li>
   Analyze and interpret results in both written and oral formats.
  </li>
  <li>
   Assist in training new analysts.
  </li>
  <li>
   Conduct laboratory investigations and initiate Quality Events, CAPA, and Change Controls as needed.
  </li>
  <li>
   Follow all SOPs and safety guidelines to ensure compliance with a cGMP environment.
   <br/>
   <br/>
  </li>
 </ul>
 <strong>
  Essential Skills
  <br/>
  <br/>
 </strong>
 <ul>
  <li>
   Proficiency in HPLC, UPLC, and UV-Vis techniques.
  </li>
  <li>
   Strong analytical Experience in chemistry.
  </li>
  <li>
   Familiarity with FDA and GMP regulations.
  </li>
  <li>
   Ability to analyze and interpret complex data.
   <br/>
   <br/>
  </li>
 </ul>
 <strong>
  Additional Skills &amp; Qualifications
  <br/>
  <br/>
 </strong>
 <ul>
  <li>
   Bachelor&rsquo;s degree in Chemistry or related scientific field with 1-2 years of related experience in pharmaceutical analysis, or a Master&rsquo;s degree with 1 year of experience.
  </li>
  <li>
   Problem-solving skills involving several concrete variables in standardized situations.
  </li>
  <li>
   Ability to perform necessary computations and interpret graphs.
  </li>
  <li>
   Working knowledge of instrumentation software used in laboratories.
   <br/>
   <br/>
  </li>
 </ul>
 <strong>
  Work Environment
  <br/>
  <br/>
 </strong>
 This position is based in a lab environment regulated by FDA and GMP standards.
 <br/>
 <br/>
 <strong>
  Job Type &amp; Location
  <br/>
  <br/>
 </strong>
 This is a Contract to Hire position based out of Fort Lauderdale, FL.
 <br/>
 <br/>
 <strong>
  Pay And Benefits
  <br/>
  <br/>
 </strong>
 The pay range for this position is $29.00 - $35.00/hr.
 <br/>
 <br/>
 Eligibility requirements apply to some benefits and may depend on your job classification and length of employment. Benefits are subject to change and may be subject to specific elections, plan, or program terms. If eligible, the benefits available for this temporary role may include the following:
 <br/>
 <br/>
 <ul>
  <li>
   Medical, dental &amp; vision
  </li>
  <li>
   Critical Illness, Accident, and Hospital
  </li>
  <li>
   401(k) Retirement Plan &ndash; Pre-tax and Roth post-tax contributions available
  </li>
  <li>
   Life Insurance (Voluntary Life &amp; AD&amp;D for the employee and dependents)
  </li>
  <li>
   Short and long-term disability
  </li>
  <li>
   Health Spending Account (HSA)
  </li>
  <li>
   Transportation benefits
  </li>
  <li>
   Employee Assistance Program
  </li>
  <li>
   Time Off/Leave (PTO, Vacation or Sick Leave) Workplace Type This is a fully onsite position in Fort Lauderdale,FL. Application Deadline This position is anticipated to close on Feb 23, 2026.
   <br/>
   <br/>
  </li>
 </ul>
 <strong>
  About Actalent
  <br/>
  <br/>
 </strong>
 Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.
 <br/>
 <br/>
 The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.
 <br/>
 <br/>
 If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing due to a disability, please email actalentaccommodation@actalentservices.com for other accommodation options.
</div>


Scientist/chemist/ QC/Associate Scientist

AbbVie

<div>
 <strong>
  Company Description
  <br/>
  <br/>
 </strong>
 AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas &ndash; immunology, oncology, neuroscience, and eye care &ndash; and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at www.abbvie.com. Follow @abbvie on X, Facebook, Instagram, YouTube, LinkedIn and Tik Tok.
 <br/>
 <br/>
 <strong>
  Job Description
  <br/>
  <br/>
 </strong>
 <strong>
  Purpose:
  <br/>
  <br/>
 </strong>
 The Associate QC Scientist performs laboratory testing within a fast paced GMP environment in support of one or more of the following areas; raw materials, in-process product, final Bulk product, stability, and/or validation. Analyzes test data and evaluates results. Writes procedures with guidance. Works under the guidance of a supervisor but is able to manage time efficiently in achieving timely completion of assigned duties. Assists in trending data to support assay performance. Assists in writing lab Investigation reports.
 <br/>
 <br/>
 <strong>
  Responsibilities
  <br/>
  <br/>
 </strong>
 <ul>
  <li>
   Perform routine tasks competently and independently, and generate reliable and consistent results.
  </li>
  <li>
   Analyze and critique results, noting significant deviations.
  </li>
  <li>
   Troubleshoot experiments and instrumentation.
  </li>
  <li>
   Learn and understand new experimental techniques.
  </li>
  <li>
   Demonstrate skill in multiple techniques and appropriately modify protocols, as required, to suit the changing needs of research or development sciences.
  </li>
  <li>
   Place data in proper scientific context by consulting and citing relevant literature.
  </li>
  <li>
   Demonstrate technical proficiency in his/her field.
  </li>
  <li>
   Impact projects predominantly through lab and/or pilot plant based activities.
  </li>
  <li>
   Understand and adhere to corporate standards regarding code of conduct, safety, appropriate handling of materials, controlled drug and radioactive compounds, GxP compliance, and animal care where applicable.
   <br/>
   <br/>
  </li>
 </ul>
 <strong>
  Qualifications
  <br/>
  <br/>
 </strong>
 <ul>
  <li>
   BA/BS in Chemistry, Biochemistry, Medical Technology, Biology or equivalent science degree.
  </li>
  <li>
   2+ years of related work experience
  </li>
  <li>
   Maintains their certifications as needed for assigned job tasks.
   <br/>
   <br/>
  </li>
 </ul>
 Additional Information
 <br/>
 <br/>
 Applicable only to applicants applying to a position in any location with pay disclosure requirements under state or local law:
 <br/>
 <br/>
 <ul>
  <li>
   The compensation range described below is the range of possible base pay compensation that the Company believes in good faith it will pay for this role at the time of this posting based on the job grade for this position. Individual compensation paid within this range will depend on many factors including geographic location, and we may ultimately pay more or less than the posted range. This range may be modified in the future.
  </li>
  <li>
   We offer a comprehensive package of benefits including paid time off (vacation, holidays, sick), medical/dental/vision insurance and 401(k) to eligible employees.
  </li>
  <li>
   This job is eligible to participate in our short-term incentive programs.
   <br/>
   <br/>
  </li>
 </ul>
 Note: No amount of pay is considered to be wages or compensation until such amount is earned, vested, and determinable. The amount and availability of any bonus, commission, incentive, benefits, or any other form of compensation and benefits that are allocable to a particular employee remains in the Company's sole and absolute discretion unless and until paid and may be modified at the Company&rsquo;s sole and absolute discretion, consistent with applicable law.
 <br/>
 <br/>
 AbbVie is an equal opportunity employer and is committed to operating with integrity, driving innovation, transforming lives and serving our community.  Equal Opportunity Employer/Veterans/Disabled.
 <br/>
 <br/>
 US &amp; Puerto Rico only - to learn more, visit https://www.abbvie.com/join-us/equal-employment-opportunity-employer.html
 <br/>
 <br/>
 US &amp; Puerto Rico applicants seeking a reasonable accommodation, click here to learn more:
 <br/>
 <br/>
 https://www.abbvie.com/join-us/reasonable-accommodations.html
</div>


Associate Scientist, Quality Control

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