pharmaceutical scientist

Medasource

<div>
 
 
 Title:
 
 Associate Scientist I
 
 
 
 Duration:
 
 Contract through June 2026
 
 
 
 Schedule:
 
 M-F 8-5 Onsite
 
 
 
 Occupational Summary
 
 
 
 The Associate Scientist I will support the development, qualification, and execution of analytical methods to
 
 
 enable optimization of processes, formulations and characterization of vaccine products. This incumbent in this
 
 
 position will be involved in pharmaceutical and analytical development for GMP production of vaccine products
 
 
 and therapeutics.
 
 
 
 Work Performed
 
 
 
 &bull; Perform pharmaceutical development and successful GMP release including:
 
 
 o Analytical development
 
 
 o Develop product specific release and characterization methods
 
 
 &bull; Quality methods for product release and complete comprehensive characterization of clinical lots
 
 
 &bull; Complete GMP testing in line with OCH and regulatory guidance
 
 
 &bull; Formulation development - developing formulations to stabilize vaccine products
 
 
 &bull; Employ analytical characterization tools to inform product formulation design
 
 
 &bull; Lead formulation &amp; filling of vaccine products including tech transfer &amp; production under GMP
 
 
 conditions
 
 
 &bull; Execute and document development and GMP actitivites in compliance with regulatory requirements
 
 
 &bull; Collaborate closely with other development teams to provide support for development activities and will
 
 
 work diligently with other development functions to understand how the production process changes
 
 
 impact product quality
 
 
 &bull; Compile data and perform analysis and interpretation and draw conclusions regarding progress and
 
 
 results of work, utilizing the data in appropriate decision making; summarize date, present results and
 
 
 propose next steps to advance development
 
 
 &bull; Write and review development reports; writes procols for tech transfer and SOPs for GMP production,
 
 
 and present data to project teams and larger settings
 
 
 
 Required Qualifications
 
 
 
 &bull; Knowledge and hands on classwork with analytical methods and/or product formulation
 
 
 &bull; Hands on experience with specific analytical methods (HPLC, immunoassays, biochemical methods),
 
 
 molecular or pharmaceutical product formulation (buffer &amp; excipient screening, thermal stability
 
 
 evaluation, biophysical methods) is preferred.
 
 
 &bull; GMP experience huge plus
 
 
 &bull; Must have the ability to work independently with guidance from senior scientists/managers
 
 
 &bull; Demonstrated ability in solving moderately complex analytical problems with guidance from senior
 
 
 development scientists
 
 
 &bull; Strong oral and written communication skills
 
</div>

Associate Scientist

HEOR Scientist - Pneumococcal Vaccines Location: RemoteContract Type: TemporaryRate: £650-800 per day approx. (Umbrella) SRG are supporting a leading global pharmaceutical company with their search for an HEOR Scientist supporting Pneumococcal Vaccines. This will be an initial 9 month contract and the role is predominantly remote based. Reporting to the Global RWE & Health Outcomes Research Lead, you'll play a key role in designing and delivering impactful real-world evidence (RWE) studies that inform strategic decisions and support global market access. Key Responsibilities <ul> <li>Design and execute multiple RWE studies, managing timelines, deliverables, and budgets.</li><li>Ensure quality and compliance across study documentation including protocols, analysis plans, and publications.</li><li>Translate strategic evidence needs into innovative study concepts and protocols.</li><li>Advise internal and external stakeholders on scientific design and data sources.</li><li>Build strong cross-functional relationships across medical, market access, and commercial teams.</li><li>Engage with external thought leaders to ensure robust and credible research approaches.</li></ul> Requirements & Experience <ul> <li>MSc or equivalent in health economics, epidemiology, pharmacy, or life sciences.</li><li>1-3 years' experience in the pharmaceutical industry, ideally within a multinational setting.</li><li>Proven ability to manage projects and budgets in a matrix environment.</li><li>Experience with RWE study designs and HTA/reimbursement evidence generation.</li><li>Experience with Pneumococcal Vaccines would be a major advantage - Vaccines in general or Immunology also useful experience</li><li>Strong communication skills to translate complex data for diverse audiences.</li><li>Knowledge of global healthcare systems and payer decision-making processes.</li></ul> Preferred: PhD/PharmD, launch experience, and direct payer engagement. To Apply If you are interested and want to find out more about this role, please click to apply or contact Theo Charles to discuss further. Carbon60, Lorien & SRG - The Impellam Group STEM Portfolio are acting as an Employment Business in relation to this vacancy.

HEOR Scientist - Vaccines

CPS, Inc.

<div>
 The Formulation Scientist will join the R&amp;D Group in Utah, reporting to the Director of R&amp;D. The role focuses on application development of Nutraceutical oral dosage forms including hands on experience in product development, physical properties, analytical testing, technical support, and primarily for the pharmaceutical and nutraceutical markets.
 
 
 The Formulation Scientist applies formulation science knowledge to oral solid dosage forms, collaborating with marketing, sales, manufacturing, supply chain, quality, analytical labs, and other R&amp;D groups. Responsibilities include generating scientific data across lab, pilot plant, and commercial scales, becoming an in-house expert on customer usage of company products. The role involves project management, report writing, and data presentation, balancing customer-facing and laboratory-focused tasks. Travel to customer locations for visits and scale-up trials is required. The working environment spans office, laboratory, pilot production, and manufacturing setting, with occasional domestic and international travel.
 
 
 
 Essential Functions
 
 
 
 <ul>
 <li>
 Execute application development projects for customers in the nutraceutical market.
 </li>
 <li>
 Identify gaps in the company product line and generate new product ideas.
 </li>
 <li>
 Collaborate with R&amp;D team members on new product development.
 </li>
 <li>
 Validate company products through qualitative and analytical evaluations.
 </li>
 <li>
 Contribute to customer formula development programs, showcasing company ingredients in various product categories.
 </li>
 <li>
 Assess competitive product lines.
 </li>
 <li>
 Stay current with new technologies and developments.
 </li>
 <li>
 Perform tests on new samples produced in the pilot plant, comparing actual results to predictions.
 </li>
 <li>
 Source equipment and ingredients for laboratory projects.
 </li>
 <li>
 Maintain accurate R&amp;D files, project files, and lab notebooks.
 </li>
 <li>
 Perform other duties as assigned.
 </li>
 <li>
 If you&rsquo;d like to hear more about this opportunity and others we are currently working on, please contact Sam Kovacevic at skova@cps4jobs.com.
 
 
 </li>
 </ul>
 JO: 135.25KK
 
 
 Salary
 
 
 $110,000
 
 
 Benefits Available
 
 
</div>

Formulation Scientist (Nutraceuticals)

Curia

<div>Research Scientist I; Medicinal Chemistry in Buffalo, NY
Build your future at Curia, where our work has the power to save lives.
The Research Scientist I is an integral part of the Curia team, contributing to our success by the synthesis, purification and identification of intermediates and target compounds. The Research Scientist is expected to demonstrate expertise in both the theoretical and practical aspects of organic chemistry.
Curia is a global contract development and manufacturing organization (CDMO) with over 30 years of experience partnering with pharmaceutical and biotech companies to provide life-saving treatments to patients. At Curia, we are on a mission to advance our customers&rsquo; therapies from curiosity to cure and ultimately to improve patients&rsquo; lives.
We proudly offer
<ul><li>Generous benefit options (eligible first day of employment)
</li><li>Paid training, vacation and holidays (vacation accrual begins on first day of employment)
</li><li>Career advancement opportunities
</li><li>Education reimbursement
</li><li>401K program with matching contributions
</li><li>Learning platform
</li><li>And more!
</li></ul>Responsibilities
<ul><li>Synthesize compounds efficiently using literature or in-house notebook procedures.
</li><li>Purify synthesized chemicals to an appropriate degree. The scientist will be able to use the full range of chromatographic, crystallization, and distillation techniques.
</li><li>Analyze and identify compounds using a good range of modern separation and spectroscopic techniques. This will include interpretation of TLC, HPLC, polarimetry, IR, and NMR spectra of moderate complexity.
</li><li>Organize work time so that several reactions are run concurrently. Use time efficiently to produce target compounds and perform other tasks.
</li><li>Manage workload and time to enable the incumbent to perform multiple projects effectively, and ensure all necessary paperwork is completed on a timely basis.
</li><li>Conduct laboratory operations in a safe manner. Maintain familiarity with the Chemical Hygiene Plan. Exhibit safety awareness and safe work practices.
</li></ul>Qualifications
<ul><li>Bachelor&rsquo;s or Master&rsquo;s Degree with major in chemistry or equivalent industrial/scientific experience
</li><li>0-5 years of industry experience in the medicinal chemistry field
</li></ul>Preferred
<ul><li>The capability to modify reaction conditions in order to improve yields (design of new or alternate reaction sequences is not a normal expectation, but will enhance the performance evaluation of the scientist).
</li><li>The ability to conduct literature searches for specific target compounds, structures related to the target compound, or to determine specific conditions for compounds and reactions.
</li></ul>Pay Range : $60,046/yr.
Education, experience, location and tenure may be considered along with internal equity when job offers are extended.
We do not accept unsolicited assistance from any headhunters or recruitment firms for any of our job openings. All resumes or profiles submitted by search firms to any employee at Curia, in any form without a valid, signed search agreement by an authorized signatory in place for the specific position, approved by Talent Acquisition, will be deemed the sole property of Curia. No fee will be paid in the event the candidate is hired by Curia because of the unsolicited referral.
All interested applicants must apply online. Please be aware of scammers. Curia will only send offer letters and requests for sensitive personal information from a curiaglobal.com email address. Curia is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, or protected veteran status and will not be discriminated against on the basis of disability. Curia is an E-Verify employer.
#LI-KD1</div>

Research Scientist I, Medicinal Chemistry

Julphar

<div></div><div><div><div><div><div>At Julphar, we are on a journey of culture transformation &amp; our mission is to provide a better quality of life for the entire family by delivering best in class solutions and real value with compassion and professionalism.
Our core values: Respect, Collaboration, innovation, Integrity and Compassion - Combined with a focus on diversity, inclusion, and equal opportunities - are key drivers in our aim to make a positive impact on the lives of the patients we serve, enable Talents , create a healthy work environment, and accomplish our goals through world-class research and with the compassion and commitment of our employees.
<h3 class="jobSectionHeader">
Job Overview</h3>

The Senior Research Scientist 2 will play a key role in the formulation development of pharmaceutical products for regulated markets. This position involves hands-on R&amp;D activities, cross-functional collaboration, and end-to-end project management from literature review to technology transfer.

<h3 class="jobSectionHeader">Key Responsibilities</h3>
<ul>
<li>Conduct comprehensive literature surveys and patent searches; prepare Prototype Formulation Reports.
</li>
<li>Identify reference products and coordinate procurement activities.
</li>
<li>Develop Quality Target Product Profiles (QTPP) based on literature and reference product characterization.
</li>
<li>Finalize API and excipient sources for new product development.
</li>
<li>Execute pre-formulation studies and drug&ndash;excipient compatibility assessments.
</li>
<li>Drive process optimization and reformulation activities with thorough documentation and closure.
</li>
<li>Prepare regulatory dossiers and support CTD documentation for submissions.
</li>
<li>Design and execute pharmaceutical experiments using Quality by Design (QbD) principles.
</li>
<li>Review analytical development data and compile comprehensive product development reports.
</li>
<li>Support batch manufacturing for process optimization, regulatory submissions, and bioequivalence (BE) studies.
</li>
<li>Assist with pilot and scale-up batches, including documentation and technology transfer to production.
</li>
<li>Develop and maintain R&amp;D SOPs in line with cGMP and GDP standards.
</li>
<li>Submit periodic project reports to management for review and alignment.
</li>
<li>Collaborate with departments including Analytical R&amp;D, Supply Chain, Production, QC, QA, Regulatory Affairs, and Medical Affairs to ensure project timelines are met.
</li>
<li>Handle Technology Transfer Out and Contract Manufacturing for assigned projects.
</li>
<li>Oversee and manage eQMS activities related to R&amp;D.
</li>
</ul><h3 class="jobSectionHeader">Core Competencies</h3>
<ul>
<li>Strong result and process orientation with a proactive, responsible approach.
</li>
<li>High level of accountability, ownership, and attention to detail.
</li>
<li>Demonstrated cost-consciousness in R&amp;D operations.
</li>
<li>Effective team collaboration, time, and task management.
</li>
<li>Excellent written and verbal communication in English.
</li>
<li>Highly disciplined, motivated, and organized.
</li>
</ul><h3 class="jobSectionHeader">Educational Qualifications</h3>
<ul>
<li>Master&rsquo;s degree in Pharmacy (preferred) or Bachelor&rsquo;s degree in Pharmacy.
</li>
</ul><h3 class="jobSectionHeader">Experience &amp; Functional Knowledge</h3>
<ul>
<li>Minimum 8 years of hands-on experience in Formulation Development for regulated markets.
</li>
<li>Proven experience in addressing regulatory queries for agencies such as US-FDA, EU, Canada, UAE, Jordan, and KSA.
</li>
<li>Strong background in developing and handling multiple dosage forms, particularly Biosimilars and Injectables.
</li>
<li>Expertise in Technology Transfer and Contract Manufacturing processes.
</li>
</ul>We value people from different backgrounds. Could this be your story? Apply today or visit www.Julphar.net to read more about us and the journey of Julphar</div></div></div></div></div>

Senior Research Scientist 1- Formulation

Baxter International Inc.

<div>
 
 
 This is where&nbsp;
 
 your work makes a difference.
 
 
 At Baxter, we believe every person&mdash;regardless of who they are or where they are from&mdash;deserves a chance to live a healthy life. It was our founding belief in 1931 and continues to be our guiding principle. We are redefining healthcare delivery to make a greater impact today, tomorrow, and beyond.
 
 
 Our Baxter colleagues are united by our Mission to Save and Sustain Lives. Together, our community is driven by a culture of courage, trust, and collaboration. Every individual is empowered to take ownership and make a meaningful impact. We strive for efficient and effective operations, and we hold each other accountable for delivering exceptional results.
 
 
 Here, you will find more than just a job&mdash;you will find purpose and pride.&nbsp;
 
 
 
 Baxter Pharmaceuticals R&amp;D is seeking a highly motivated scientist with proven expertise in liquid chromatography and mass spectrometry to join its Characterization team.&nbsp; As a key contributor within the Pharmaceuticals Global Business Unit, the successful candidate will oversee and apply state-of-the-art technologies in LC-MS and GC-MS in support of new and existing pharmaceutical products.&nbsp; The scientist in this role will support Nitrosamine studies using mass spectrometry-based approaches to identify nitrosamines, potential leachables nitrosamines from container extracts and develop and validate LC/MS methods to quantify nitrosamines in finished drug product solutions.&nbsp; The candidate is expected to work independently in the laboratory, to direct studies, conduct independent experiments, and generate and interpret data to solve challenging analytical problems.
 
 
 
 
 &nbsp;
 
 
 
 What you'll be doing
 
 <ul>
 <li>
 Perform chemical extractions of container closure systems and drug product solutions in the laboratory.
 
 </li>
 <li>
 Apply state-of-the-art mass spectrometry-based approaches to solve challenging problems.&nbsp; Develop and validate novel mass spectrometry-based analytical methods.
 
 </li>
 <li>
 Independently plan, execute, and manage projects/programs that both span multiple disciplines and utilize established methods, techniques, or approaches.
 
 </li>
 <li>
 Approve technical feasibility of complex design concepts within area of expertise; advise management regarding appropriate action.
 
 </li>
 <li>
 Interpret data, evaluate analytical results, identify trends/exceptions relative to product requirements, definitions, and/or project goals.
 
 </li>
 <li>
 Reach conclusions based on research analysis and incorporate recommendations into larger projects. &nbsp;
 
 </li>
 <li>
 Share research outcomes and methodology with team members and other divisional personnel.
 
 </li>
 <li>
 Maintain current knowledge of relevant Quality System Regulations and other regulatory requirements related to research and development to ensure compliance in all research, data collection, and reporting activities.
 
 </li>
 <li>
 Maintain an in-depth knowledge and understanding of GxP and related regulations and guidance.&nbsp; Be able to provide expert insights into such regulations so as to facilitate efficient product registration.&nbsp; Be an active participant in the generation, review, adoption, and interpretation of such regulations.
 
 
 
 </li>
 </ul>
 &nbsp;
 
 
 What you'll bring
 
 <ul>
 <li>
 Master's degree with at least 10-14 years, or PhD with 6-7 years in relevant discipline required.
 
 </li>
 <li>
 Must have formal training in mass spectrometry.&nbsp; Must be skilled in carrying out sophisticated mass spectrometric experiments, such as accurate mass and MS/MS, and in the interpretation of mass spectrometric data.
 
 </li>
 <li>
 Must have good knowledge of organic chemistry and other analytical disciplines, such as chromatography, NMR, IR, etc. Possess skills or demonstrated scientific background for the development of the necessary skills, for the elucidation of unknown compound structure using a multidisciplinary approach.
 
 </li>
 <li>
 Experience in Nitrosamine (must), E&amp;L testing (optional) /study design, environmental chemistry testing, and/or trace organic analysis preferred.
 
 </li>
 <li>
 Experience with complex method development and validation, particularly for quantitative LC/MS methods, preferred.
 
 </li>
 <li>
 Must be able to able to carry out strategy and vision set by upper management and be able to communicate the vision to more junior associates.
 
 </li>
 <li>
 Ability to make routine, and some less routine, decisions independently.
 
 </li>
 <li>
 Can effectively communicate with internal and external partners.
 
 </li>
 <li>
 Experience working in a regulated pharmaceutical environment (e.g., cGXP) preferred.
 
 </li>
 <li>
 Ability to learn quickly and to tackle problems in a timely manner using analytical chemistry skills.
 
 
 
 </li>
 </ul>
 
 Equal Employment Opportunity
 
 
 
 Baxter is an equal opportunity employer. Baxter evaluates qualified applicants without regard to race, color, religion, gender, national origin, age, sexual orientation, gender identity or expression, protected veteran status, disability/handicap status or any other legally protected characteristic.
 
 
 
 Reasonable Accommodations
 
 
 
 Baxter is committed to working with and providing reasonable accommodations to individuals with disabilities globally. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application or interview process, please click on the link here and let us know the nature of your request along with your contact information.
 
 
 
 Recruitment Fraud Notice
 
 
 
 
 Baxter has discovered incidents of employment scams, where fraudulent parties pose as Baxter employees, recruiters, or other agents, and engage with online job seekers in an attempt to steal personal and/or financial information. To learn how you can protect yourself, review our Recruitment Fraud Notice.
 
 
</div>

Research Scientist I, R&D - CRT

US Pharmacopeia

<div>
 
 Description
 
 
 
 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.
 
 
 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.
 
 
 
 Brief Job Overview
 
 
 
 This is a non-supervisory position in the Compendial Development Laboratory (CDL) within Global Laboratory Operations. The incumbent will be responsible for performing analytical method development and validations for USP/NF monographs/General Chapters and maintaining safety and GLP environment in the lab. This position is a component of USP&rsquo;s core business, and the incumbent is expected to support monograph modernization initiatives.
 
 
 
 How will YOU create impact here at USP?
 
 
 
 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.
 
 
 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.
 
 
 
 The Scientist IV Has The Following Responsibilities
 
 
 
 <ul>
 <li>
 Engage in project planning, execution, method development and validation of projects according to set standards as USP general chapters, guidelines, SOPs and protocols.
 </li>
 <li>
 Apply technical and scientific expertise in analytical method development and validation of pharmaceuticals.
 </li>
 <li>
 Prepare and review the project plans, reports, laboratory notebook/ Laboratory management system (LMS) and compile project data as per requirement.
 </li>
 <li>
 Adhere to GLP and safety practices while working in the Lab.
 </li>
 <li>
 Practice Diversity, Equity, Inclusion, and Belonging principles at USP India.
 
 
 </li>
 </ul>
 
 Who is USP Looking For?
 
 
 
 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
 
 
 <ul>
 <li>
 Master&rsquo;s Degree in Chemistry (Analytical/Organic) or Pharmaceutical Sciences with 8-10 years of experience.
 </li>
 <li>
 Strong knowledge in designing, executing, and interpreting extractables and leachables studies for packaging systems, medical devices, and drug products.
 </li>
 <li>
 Familiarity with regulatory requirements for E&amp;L in pharmaceutical and medical device sectors.
 </li>
 <li>
 Must have hands on experience in working with chemical methods and handling instruments like LC-MS, GC-MS.
 </li>
 <li>
 Strong expertise in mass spectrometry, including hands-on experience with HRMS, is required.
 </li>
 <li>
 Proficient in interpreting data using advanced mass spectrometry software tools.
 </li>
 <li>
 Understanding of USP/NF monographs/general chapters/general notices.
 </li>
 <li>
 Exposure to GMP/GLP/QMS environment and documentation procedures and champions the data integrity.
 </li>
 <li>
 Should be capable of performing analytical method developments and method validations using modern techniques and protocols.
 </li>
 <li>
 Good analytical skills in handling method development and Validations for Drug substances and Drug products.
 </li>
 <li>
 Should have exposure to GMP/GLP environment and documentation procedures.
 </li>
 <li>
 Awareness of ISO/IEC 17025 is desirable.
 
 
 </li>
 </ul>
 
 Additional Desired Preferences
 
 
 
 Desired preferences are to showcase any additional preferred levels of expertise to perform the role. Reminder: any items listed in this section are not requirements nor disqualifies for candidate consideration.
 
 
 <ul>
 <li>
 Exceptional breadth of pharmaceutical industry experience.
 </li>
 <li>
 Excellent technical writing and oral communication skills required.
 </li>
 <li>
 Must be able to communicate effectively with diplomacy and enthusiasm.
 </li>
 <li>
 Hands on experience in working with chemical methods and handling instruments like HPLC, GC, FTIR, UV-Visible.
 </li>
 <li>
 Technical and analytical skills required including the ability to interpret technical information.
 </li>
 <li>
 Should have good understanding of GLP regulations and exposed to external regulatory audits.
 
 
 </li>
 </ul>
 
 Supervisory Responsibilities
 
 
 
 None, this is an individual contributor role.
 
 
 
 Benefits
 
 
 
 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.
 
 
 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.
 
 
 
 Job Category
 
 Chemistry &amp; Scientific Standards
 
 
 
 Job Type
 
 Full-Time
</div>

Scientist IV, Compendial Development Laboratory (Extractables and Leachables)

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