pharmaceutical scientist

Tap Growth ai

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 🌟 We're Hiring: Scientist! 🌟
 
 
 
 We are seeking a dedicated and analytical Scientist to join our research team and contribute to groundbreaking scientific discoveries. The ideal candidate will have a strong foundation in scientific methodology, data analysis, and research techniques to support our innovative projects and drive scientific excellence.
 
 
 
 📍 Location:
 
 Durham, United States
 
 
 
 ⏰ Work Mode:
 
 Work From Office
 
 
 
 💼 Role:
 
 Scientist
 
 
 
 Pay Scale:
 
 Up to $98, 404.80 (Dependent on Experience)
 
 
 
 What You'll Do
 
 
 
 Laboratory Data Review:
 
 
 <ul>
 <li>
 Scientific data review of laboratory documentation and data to appropriate standards (GMPs, SOPs, protocols, methods).
 </li>
 <li>
 Good understanding of data integrity and ALCOA+ (Attributable, Legible, Contemporaneous, Original, and Accurate) principles.
 </li>
 <li>
 Peer review of results and documentation of product development studies including statistical data reports (JMP).
 </li>
 <li>
 Peer review of method validations and analytical technical transfers.
 </li>
 <li>
 Transcription checking of regulatory submissions, reports, and / or JMP tables / plots.
 
 
 </li>
 </ul>
 
 What We're Looking For
 
 
 
 <ul>
 <li>
 BS or MS in Chemistry, Pharmaceutical Sciences, or a similar applicable discipline.
 </li>
 <li>
 Experience with HPLC in a GMP / QC setting, Empower software preferred.
 </li>
 <li>
 Experience with Inhalation testing products, large and small molecule preferred.
 </li>
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 Strong understanding of GMP and FDA guidelines for pharmaceutical manufacturing and validation.
 </li>
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 Strong organizational skills for managing multiple priorities.
 </li>
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 Effective communication and interpersonal skills for coordination with lab personnel, and management.
 
 
 </li>
 </ul>
 
 
 Ready to advance science? 🚀 Apply now and let's innovate together!
 
 
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Scientist

Anika

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 Position Scope:
 
 
 
 The Scientist is responsible for providing support to R&amp;D and Manufacturing teams under the supervision of the Director of R&amp;D. We are seeking a candidate who is energetic and can carry out development projects with minimal supervision. A hands-on scientist that is a problem-solver, who can provide imaginative solutions to issues as they arise.
 
 
 
 Specific Tactical Responsibilities:
 
 
 
 <ul>
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 Design and carry out experiments to investigate Chemical/Material/Biological properties of candidate materials for use in applications in Orthopedics and General Surgery
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 Develop prototypes and processes at the lab-scale.
 </li>
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 Develop Analytical methods as necessary for product testing and process development.
 </li>
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 Provide technical support for manufacturing, marketing, and regulatory as needed.
 </li>
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 Prepare R&amp;D Reports and file Patent Applications for any inventions.
 
 
 </li>
 </ul>
 
 Supervisory Responsibilities:
 
 
 
 None
 
 
 
 Required Qualifications:
 
 
 
 <ul>
 <li>
 Ph.D. in Biomaterials Science, Polymer Science, Pharmaceutical Science, Materials Science, Chemistry, or related field.
 
 
 </li>
 </ul>
 
 Desired Experience, Knowledge, and Skills:
 
 
 
 <ul>
 <li>
 Experience with Polymer-based Biomaterials.
 </li>
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 Experience in Formulation of gels and emulsions.
 </li>
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 Knowledge of Hyaluronic Acid and/or Polysaccharide chemistry.
 </li>
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 Experience with Formulation of active ingredients in pharmaceutical applications.
 </li>
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 Experience with Chemical Synthesis, Analytical Chemistry methods, Physical/Rheological characterization, or Cell-based Biological assays.
 </li>
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 Experience with Quality System requirements for Class III Medical Devices.
 </li>
 </ul>
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Scientist I

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
 
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Associate Scientist

Deciphera Pharmaceuticals

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 Job Description
 
 
 
 The Pharmacovigilance Scientist serves an integral role in safety data analyses for assigned investigational and/or marketed product(s) in partnership with the Safety Physician. The Pharmacovigilance Scientist is expected to be equally effective working collaboratively and independently. She/he will support activities such as signal management, aggregate reports, RMP development, ad hoc safety query responses, literature surveillance, and other safety analyses; and must ensure deliverables are of high quality and are completed according to required timelines. For investigational products, this role will contribute to safety review and analysis for clinical trial documents. The Pharmacovigilance Scientist will also support the maintenance of relevant SOPs, Work Instructions, and other documents.
 
 
 The successful candidate will have demonstrated adequate prior experience of the above responsibilities. Key indicators of success in this role include accountability, attention to detail, appropriate prioritization, management of assigned projects with quality and timeliness, and effective communication.
 
 
 This position will report to the Sr. Pharmacovigilance Scientist and will be located in the Waltham, MA office/Remote.
 
 
 
 What You&rsquo;ll Do
 
 
 
 <ul>
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 Coordinate and document signal management activities with the product Safety Physician. This includes performing signal evaluations and drafting signal evaluation reports.
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 Prepare aggregate safety reports (e.g. DSURs, PADERs, PBRERs), including project management, database requests, data analysis, report authoring, assimilating information from other groups, review coordination, and quality checks.
 </li>
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 Support RMP updates and REMS reports as appropriate.
 </li>
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 Perform literature surveillance for marketed and investigational products .
 </li>
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 Prepare materials for Safety Committee meetings in conjunction with the product Safety Physician and document/archive meeting minutes and materials.
 </li>
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 Coordinate responses for ad hoc safety queries in conjunction with the Safety Physician and other cross-functional experts, including data analysis and authoring, as applicable.
 </li>
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 Support review and analysis of safety content for study protocols, CRFs, IB/RSIs, ICFs, SMPs, CSRs, DMC meetings, and coding reviews, as applicable.
 </li>
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 Demonstrate knowledge and stay up to date to ensure compliance with current and applicable global PV regulations and guidelines (e.g., CIOMS, EMA, FDA, ICH, etc.)
 </li>
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 Contribute to process improvement and consistency of cross-product processes.
 </li>
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 Maintain inspection readiness.
 </li>
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 Perform other tasks as assigned or required.
 
 
 </li>
 </ul>
 
 Qualifications
 
 
 
 
 What You&rsquo;ll Bring:
 
 
 
 <ul>
 <li>
 1+ years relevant medical, scientific/clinical, or pharmaceutical experience, including experience in drug safety serving in a PV Scientist or similar role.
 </li>
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 Advanced degree (PharmD, RN, MD, PhD, MPH, NP, MS).
 </li>
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 Demonstrated experience in analysis and interpretation of medical and scientific data.
 </li>
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 Excellent oral and written communication skills.
 </li>
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 Demonstrated ability to work effectively in a team environment (including Safety, Clinical Development, Medical Affairs, Clinical Operations, Regulatory, Biostatistics, etc.) as well as independently.
 </li>
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 Ability to apply clinical judgment to interpret case information.
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 Knowledge of pharmacovigilance and drug development, including knowledge of applicable clinical trial and post-marketing safety regulations.
 </li>
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 Familiarity with case processing, expedited reporting rules, and safety database concepts.
 </li>
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 Proficiency with Microsoft Office Suite and Argus Safety systems.
 
 
 </li>
 </ul>
 
 Additional Information
 
 
 
 Deciphera is committed to fair and equitable compensation practices. The base salary pay range for this role is $135,000 - $189,000. Actual compensation packages will depend on various factors, including, but not limited to depth of experience, education, skillset, overall performance and/or location.
 
 
 Deciphera believes in providing a competitive compensation and benefits package to all employees. Our base salary is just one component of Deciphera&rsquo;s competitive total rewards strategy that also includes annual performance bonus, a long-term incentive plan, full range of benefits and other incentive compensation plans (if applicable)
 
 
 
 Benefits
 
 
 
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 Competitive salary and annual bonus.
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 Comprehensive benefits package including medical, dental, vision insurance, 401(k) retirement plan with company match, and more.
 </li>
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 Generous parental leave and family planning benefits.
 </li>
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 Outstanding culture and opportunities for personal and professional growth.
 
 
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 </ul>
 
 Apply Now:
 
 Join us in our mission to improve the lives of people with cancer. Apply today to become a part of our dynamic team!
 
 
 
 EQUAL EMPLOYMENT OPPORTUNITY INFORMATION
 
 
 
 Deciphera is committed to equal employment opportunity and values diversity. To ensure that we comply with reporting requirements, we invite you complete the confidential survey at the end of this application. Providing this information is optional. It will not be accessible or used in the hiring process, and has no effect on your opportunity for employment. This information will also be treated confidentially. We are committed to make all hiring decisions and other employment decisions on a non-discriminatory basis.
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Pharmacovigilance Scientist

Quotient Sciences Limited

Posted Thursday 4 September 2025 at 05:00Quotient Sciences: Molecule to Cure. Fast. We accelerate drug development by integrating formulation development, clinical testing, data sciences, and manufacturing into one seamless process. Our proprietary platform,Translational Pharmaceutics, shortens timelines by 9-12 months on average.Arcinova, our specialist arm in Reading and Alnwick, UK, delivers end-to-end drug substance and early drug product services, including bioanalysis and radiolabeling-streamlining early development from candidate selection to proof of concept.Why join us? Because every day counts when bringing new medicines to patients. Our 1,000+ experts across the US, UK, and beyond are united by science, agility, and a culture that turns ideas into impact-fast. The Role Are you passionate about formulation science and ready to make a real impact in clinical development? We're looking for aSenior Formulation Scientist Ito support the delivery of cutting-edge aseptic and non-sterile pharmaceutical projects at our in Alnwick. This is a fantastic opportunity to work in a fast-paced, GMP-regulated environment where your expertise will help bring life-changing therapies to patients. What You'll Be Doing <ul><li>Supporting the development of innovative formulations for aseptic and non-sterile products.</li><li>Ensuring all work complies with cGMP and cEHS standards.</li><li>Collaborating on the resolution of quality events and deviations.</li><li>Driving continuous improvement across formulation processes.</li><li>Contributing to the technical transfer of products into clinical trial manufacturing.</li><li>Participating in internal, client, and regulatory audits.</li><li>Engaging in customer meetings and providing expert technical input.</li><li>Managing project timelines to ensure successful and timely delivery.</li></ul> What You'll Bring <ul><li>A BSc (Hons) or equivalent in a relevant scientific discipline.</li><li>Extensive experience in pharmaceutical aseptic and/or non-sterile manufacturing.</li><li>Good awareness of the current GMP regulatory environment.</li><li>Solid knowledge of sterile formulation development.</li></ul> Who You Are <ul><li>A clear and confident communicator, both written and verbal.</li><li>Flexible, adaptable, and comfortable working in a dynamic setting.</li><li>Detail-oriented with a strong commitment to quality.</li><li>Willing to go the extra mile, including occasional work outside standard hours.</li></ul> Application Requirements When applying for a position with Quotient Sciences to be able to work in our organization you must be aged 18 years or over and not have been debarred by the FDA. If you indicate you are under the age of 18 or have been debarred then your application will be automatically declined. Our Commitment to Diversity, Equity and Inclusion Quotient Sciences are advocates for positive change and conscious inclusion. We strive to create a diverse Quotient workforce and develop a workplace culture that provides a sense of acceptance for every person within our organization. As a global employer, we recognize the value in having an organization that is a true reflection and representation of our society today.Specifically we will not discriminate on the basis of race, color, creed, religion, gender, gender identity, pregnancy, marital status, partnership status, domestic violence victim status, sexual orientation, age, national origin, alienage or citizenship status, veteran or military status, disability, medical condition, genetic information, caregiver status, unemployment status or any other characteristic prohibited by federal, state and/or local laws.This applies to all aspects of employment, including hiring, promotion, demotion, compensation, training, working conditions, transfer, job assignments, benefits, layoff, and termination.<img src="https://www.jobg8.com/Tracking.aspx?Z3TFjo9onGkbATCuQol2AYFgZox3vGiSk" width="0" height="0" />

Senior Formulation Scientist I

1100 Mylan Pharmaceuticals Inc.

Undergraduate Industrial Placement Material Scientist (12 months fixed term contract) page is loaded Undergraduate Industrial Placement Material Scientist (12 months fixed term contract)locations: Sandwich, England, United Kingdomtime type: Vollzeitposted on: Vor 14 Tagen ausgeschriebenjob requisition id: RMylan Pharma UK LimitedBei VIATRIS, sehen wir das Gesundheitswesen nicht so, wie es ist, sondern so, wie es sein sollte. Wir handeln entschlossen, und unsere einzigartige Positionierung sorgt für Stabilität in einer Welt, in der sich die Bedarfe im Gesundheitswesen stets verändern. Viatris befähigt Menschen in allen Teilen der Welt, in jeder Lebensphase gesünder zu leben. Dies erreichen wir durch: Zugang - Zugang zu hochwertigen, bewährten Arzneimitteln und Impfstoffen sowie auch neu entwickelten Biosimilars für Patienten in allen Lebensumständen weltweit Führungsverantwortung - Verbesserung der Patientengesundheit durch zukunftsgerichtete nachhaltige Unternehmensführung und innovative Lösungen Partnerschaft - Optimaler Einsatz unserer Kompetenzen, um Menschen den Zugang zu Produkten und Dienstleistungen zu ermöglichen.Our global portfolio includes best-in-class, iconic brand-name products as well as global key brands; generics, including branded and complex generics; and other offerings across a wide range of therapeutic areas. We are committed to helping create healthier communities worldwide through education, outreach and better access to treatment.For those driven to live their lives with purpose, Viatris helps employees realise their full potential by creating a collaborative culture that fosters courage and resilience. Viatris is more than just a place to work. This is a place to make a difference in the world. The Role & What You Will Be Doing Every day, we rise to the challenge to make a difference and here's how the Undergraduate Industrial Placement Material Scientist (12 months fixed term contract) role will make an impact: Perform analyses related to clinical supplies, formulation development, stability and process scale up using a variety of analytical and material characterisation techniques. Process data and report to team. Interpret test results and contribute to team discussions with formulation and device development teams. Maintain relevant documentation according to cGMP documentation practices. Troubleshoot instrumentation and investigate aberrant sample results. Adherence to all applicable policies and procedures, including those relating to EHS, GMP, GCP, Quality and Compliance, consistent with the role and any associated responsibilities. Perform other duties as assigned consistent with the grade of the role. About Your Skills & Experience For this role, we're looking for a candidate who has an effective combination of the following qualifications, skills and experiences: A-level or equivalent qualifications in science subjects. Must be registered on an undergraduate chemistry or pharmaceutical sciences related degree program, must have completed at least 2 years of study and must not have graduated at the start of the placement. Foundation skills in analytical chemistry. Has knowledge and/or experience of modern instrumental methods of analysis, e.g., particle sizing, surface area, amorphous content, FT-IR, SEM and thermal analysis techniques. Ability to work autonomously and be familiar with basic concepts of calculations in Analytical Chemistry. Ability to work flexibly across multidisciplinary lines (formulation, pharm sci and device) and within a team environment. Organises tasks allocated by his/her supervisor and planning his/her own work to consistently achieve output of high-quality results in a timely manner. Effective verbal and written communication skills.At Viatris, we are dedicated to building a truly diverse, inclusive and authentic workplace, so if you're excited about this role but your past experience doesn't fully align with every requirement, we still encourage you to apply. You may just be the right candidate for this or other roles. What we offer: Top Employer Accreditation, demonstrating that we provide excellent people policies and practices Competitive compensation package inclusive of annual discretionary bonus Focus on career progression with growth and development opportunities Hybrid work model Emphasis on Health and Wellness programmes 100% paid medical insurance and Employee Assistance Programme Life cover Excellent employer-matched pension scheme with Viatris contributing up to 11% 2 paid volunteer days per year Diversity & Inclusion at Viatris At Viatris, diversity and inclusion are essential to our mission. The diversity we foster in all aspects of our business can be one of our greatest strengths in redefining healthcare not as it is, but as it should be. If you would like to know more about what diversity, equity and inclusion means to us, please visit Sustainability at Viatris Corporate social responsibility is fundamental to the Viatris mission. We work to advance responsible and sustainable operations and leverage our collective expertise to empower people to live healthier at every stage of life, recognizing that our actions affect the stakeholders and communities we serve. To learn more about our efforts, please visitBei Viatris, bieten wir wettbewerbsfähige Gehälter, Sozialleistungen und ein integratives Umfeld, in dem Sie Ihre Erfahrungen, Perspektiven und Fähigkeiten einsetzen können, um das Leben anderer zu beeinflussen.<img src="https://www.jobg8.com/Tracking.aspx?BrmZWvLiuv772n0YDYqIb3Pa3HO3XRI1s" width="0" height="0" />

Undergraduate Industrial Placement Material Scientist (12 months fixed term contract)

Novartis India

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 Summary
 
 
 
 Plan and perform scientific experiments (or pilot plant processes) for the preparation and timely delivery of drug substances (DS), drug products (DP), processes and procedures in collaboration within a multifunctional project team coordinated by a Project leader. Contribute to maintenance of lab instruments/infrastructure.
 
 
 
 About The Role
 
 
 
 
 Your responsibilities include, but are not limited to:
 
 
 
 <ul>
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 Meet quality, quantity and timelines in all assigned projects; Perform and document scientific experiments; Plan &amp; organize scientific experiments under minimal guidance from more experienced team members. Seeks proactively for support and coaching from Project Leader, Scientific Expert or other team members during the whole process if necessary.
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 Provide documentation of raw data. Evaluate and Contribute to interpretation and report results under minimal guidance from more experienced team members. Propose and provide input for the design of next experiments. Optimize existing methods (lab or plant) or contribute to new method development and reproduce published methods and develop more efficient ones.
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 Generate lab procedures, reports and/or instructions and/or SOP&rsquo;s. Actively transfer procedures/instructions to pilot plant or production, including troubleshooting, process steering controls etc. Communicate and address problems, perform safety and literature searches under moderate guidance from more experienced team member.
 </li>
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 Keep record of and manage chemicals, intermediates, excipients and solvents within own area of responsibility.
 </li>
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 Collaborate with other team members to facilitate deliveries of DS and/or DP. Act as mentors for new joinees.
 </li>
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 Utilize special tools/equipment&rsquo;s and/or specialized facilities e.g., containment/sterile labs. Evaluate new lab equipment. Schedule and perform routine maintenance and calibration of lab instruments/equipment &amp; contribute to maintenance of infrastructure/equipment.
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 Actively participate in project teams/meetings/networks. Actively contributes to team goals.
 </li>
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 Ensure all own activities are aligned with overall drug development process. Work according to appropriate SOPs, GMP, GLP, QM, HSE, ISEC &amp; Novartis Guidelines ;Strategic and scientific contribution to Networks, target achievements according to net-work charter and annual objectives
 
 
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 </ul>
 
 What You&rsquo;ll Bring To The Role
 
 
 
 <ul>
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 PhD on technical subject with relevant experience. or Master of Science with 4+ years of relevant experience Fluency in English language.
 </li>
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 Awareness for safe handling of chemicals, potentially dangerous materials and equipment. Broad theoretical and scientific knowledge in the relevant area (e.g. manufacturing, analytical, pharmaceutical).
 </li>
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 Skilled scientist with expertise in trace level quantification of GTI/ Nitrosamines/Nitrites or similar impurities using LC-UV/FID, Ion chromatography and LCMS.
 </li>
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 Experience on dealing OOS/OOE and deviations involving above mentioned analytical techniques.
 </li>
 <li>
 Proficient with laboratory and/or technical tools. Good knowledge of software and computer tools.
 </li>
 <li>
 Good documentation skills.
 
 
 </li>
 </ul>
 
 Why Novartis:
 
 Helping people with disease and their families takes more than innovative science. It takes a community of smart, passionate people like you. Collaborating, supporting and inspiring each other. Combining to achieve breakthroughs that change patients&rsquo; lives. Ready to create a brighter future together? https://www.novartis.com/about/strategy/people-and-culture
 
 
 
 Join our Novartis Network:
 
 Not the right Novartis role for you? Sign up to our talent community to stay connected and learn about suitable career opportunities as soon as they come up: https://talentnetwork.novartis.com/network
 
 
 
 Benefits and Rewards:
 
 Read our handbook to learn about all the ways we&rsquo;ll help you thrive personally and professionally: https://www.novartis.com/careers/benefits-rewards
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Expert Science and Technology (Nitrosamine/Nitrite)

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