pharmaceutical 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

BGIT India Private Limited

SUMMARY/JOB PURPOSE:On a day-to-day basis, scientist is expected to perform a variety of routine and complex analytical experiments using HPLC/UPLC, LC-MS, UV-Vis, FT-IR, Dissolution etc.<ul><li>Operate, maintain, and troubleshoot Agilent LC and MS instruments using Agilent OpenLab and EMPOWER softwares.</li></ul><ul><li>Ability to optimize methods, as well as analyze raw materials, intermediates, drug substance and drug product samples accurately in accordance with established methods.</li></ul>ESSENTIAL DUTIES AND RESPONSIBILITIES:<ul><li>Performing experiments to support drug substance and drug product development and release of finished products.</li></ul><ul><li>Analyze data acquired to draw conclusions based on statistical analysis and established quality control criteria.</li></ul><ul><li>Document work in ELN in compliance with company procedures and Good Documentation Practices.</li></ul><ul><li>Performing duties with commitment to laboratory safety and adherence to best practices is essential.</li></ul><ul><li>Occasionally, coordination with service engineers and company facilities team to schedule maintenance of analytical instrumentation is required.</li></ul>EDUCATION/EXPERIENCE/KNOWLEDGE &amp; SKILLS:<ul><li>Bachelor&rsquo;s or Master&rsquo;s degree in chemistry or related field with an emphasis in analytical chemistry.</li></ul><ul><li>One to five years of chromatography experience in pharmaceutical analytical field is required.</li></ul><ul><li>Knowledge and experience in developing and qualifying LC methods utilizing Agilent liquid chromatography instruments is desired.</li></ul>Pay: $65.00 - $70.00 per hourWork Location: In person

Scientist

SCA Pharma

<div>
 
 Description
 
 
 
 
 Company Description
 
 
 
 SCA Pharmaceuticals is a dynamic rapidly growing company consisting of passionate individuals who believe in our mission of providing high quality medications that are critical in saving and sustaining human life. SCA Pharma is an FDA 503B outsourcing facility providing customized medications for hospitals and healthcare facilities across the United States. We do this through unyielding quality, safety and integrity, our commitment to accountability and ownership, teamwork and problem solving.
 
 
 
 Summary:
 
 
 
 The Formulation Scientist is responsible for developing and optimizing sterile injectable formulations for 503B compounding operations. This role focuses on formulation design, scale-up, and technical support to ensure stability, manufacturability, and compliance with FDA and cGMP requirements. Key responsibilities include conducting compatibility and stability studies, preparing technical documentation for 503B compliance, and collaborating with cross-functional teams to support product development and scale-up. The Formulation Scientist provides formulation expertise during investigations and regulatory inspections as needed and contributes to new product initiatives and lifecycle management.
 
 
 
 Requirements
 
 
 
 
 Essential functions:
 
 
 
 <ul>
 <li>
 Lead the design and development of pharmaceutical formulations for sterile injectables in compliance with FDA and cGMP standards.
 </li>
 <li>
 Scale up lab formulations to commercial production, ensuring reproducibility and robust results. Support evaluation of technologies and processes to improve product performance.
 </li>
 <li>
 Conduct compatibility studies using stability testing and chromatographic techniques.
 </li>
 <li>
 Develop and optimize formulations to ensure stability and manufacturability.
 </li>
 <li>
 Evaluate and select appropriate pharmaceutical API and excipients based on functionality, compatibility, and regulatory status.
 </li>
 <li>
 Provide formulation support to troubleshoot manufacturing challenges.
 </li>
 <li>
 Prepare formulation development reports and technical documentation to support 503B compliance.
 </li>
 <li>
 Provide technical support during regulatory inspections as needed.
 </li>
 <li>
 Support investigations and provide formulation input for deviations and change controls.
 </li>
 <li>
 Collaborate with cross-functional teams to support product development and scale-up.
 </li>
 <li>
 Provide formulation input for new product development initiatives.
 </li>
 <li>
 Additional responsibilities as assigned.
 
 
 
 </li>
 </ul>
 
 Required Qualifications &amp; Experience:
 
 
 
 <ul>
 <li>
 Master&rsquo;s degree in biology, chemistry, engineering, or related field&mdash;or equivalent experience
 </li>
 <li>
 5+ years in pharmaceutical formulation development; experience in sterile compounding or aseptic manufacturing preferred
 </li>
 <li>
 Strong knowledge of formulation science and excipients for sterile injectables
 </li>
 <li>
 Experience with sterile and compounded dosage forms
 </li>
 <li>
 Working knowledge of cGMP compliant Quality Systems and FDA regulations including 21 CFR Part 503B, USP compounding standards (795, 797, 800), and 21 CFR Parts 210 and 211
 </li>
 <li>
 Proficiency with Quality by Design (QbD) principles and Design of Experiments (DOE) methodologies
 </li>
 <li>
 Strong project management, leadership and problem-solving abilities
 </li>
 <li>
 Proven ability to communicate and collaborate across teams
 </li>
 <li>
 Proficient in MS Office and statistical software
 
 
 
 </li>
 </ul>
 
 Desired Knowledge, Skills, and Abilities:
 
 
 
 <ul>
 <li>
 Experience with regulatory documentation and technical writing for 503B compliance.
 </li>
 <li>
 Understanding of risk management principles and failure mode effects analysis (FMEA).
 </li>
 <li>
 Ability to communicate complex scientific concepts to diverse audiences.
 </li>
 <li>
 Must be well organized and detail-oriented with proven initiative and self-starter skills.
 
 
 
 </li>
 </ul>
 SCA Pharma is an equal opportunity employer (Minorities/Females/Disabled/Veterans). We recruit, employ, train, compensate, and promote without regard to race, religion, creed, color, national origin, age, gender, sexual orientation, marital status, disability, veteran status, or any other basis protected by applicable federal, state or local law.
</div>

Formulation Scientist

DFE Pharma

<div>
 
 Did you know that you already know us? Almost every second tablet which is on the global market contains our products. This demands great entrepreneurial power so that we are always looking for people who take ownership and are not afraid of accountability.
 
 
 Now it is your chance to join!
 
 
 
 
 
 We are looking for laboratory based Formulation Scientist(s) with a solid pharmaceutical formulation background (API and excipients) to advise our customers on their formulation challenges. In this role you will formulate final dosage forms for customers with actual or model APIs to support them in their development programs. As part of a team of Formulation Scientists and with our Technical Managers in the market, you will translate customer formulation challenges into mechanistic based formulation protocols, execute the experiments, and report the results for sharing with the customer. You will be working in a new high end Technical Center of Excellence in Hyderabad, India. Do you have this combination of good pharmaceutical formulation knowledge and a drive to deliver relevant solutions for DFE Pharma&rsquo;s customers?
 
 
 
 
 
 
 What we ask
 
 
 <ul>
 <li>
 Experience in developing formulations for the regulated market, with a focus on oral solid dosage forms (like Tablets, Capsules, Granules, Powders, pellets etc.) showcasing strong pharmaceutical formulation development skills.
 </li>
 <li>
 A hands-on experience of handling equipments associated with OSD manufacturing is mandatory.
 </li>
 <li>
 Deriving product development strategy or customer solution based on targeted literature searches, including patent search is desirable.
 </li>
 <li>
 Having a good working knowledge of pharmaceutical process steps (Direct Compression, Wet Granulation, Dry granulation &amp; Wurster coating) and equipment to formulate oral solid dosage forms and execute relevant laboratory experiments.
 </li>
 <li>
 Scale up, Exhibit batches and technology transfer experience is mandatory.
 </li>
 <li>
 Ability to prepare consultative / mechanistic (powder technology) based formulation protocols. Knowledge of various excipients, their role in formulations, usage concentrations etc is a must.
 </li>
 <li>
 Review test results in alignment with the project goals, identify causes of variances and recommend solutions to achieve goals.
 </li>
 <li>
 Prepare/review master formulas, manufacturing procedures, SOPs, stability protocols/reports, Product Development Reports, QOS, QbR and other CMC documents for regulatory filings.
 </li>
 <li>
 Independent product development and stakeholder management skills to build strong connections with your team, the Technical Managers, and the Innovation &amp; Technical Solutions (ITS) team.
 </li>
 <li>
 Provide recommendations for continuous improvements in practices and systems to improve performance and enhance efficiency and quality.
 </li>
 <li>
 Striving for excellence in everything you do.
 </li>
 <li>
 Stakeholder management skills to build strong connections with colleagues in the team.
 </li>
 <li>
 High proficiency in English (spoken and written).
 </li>
 <li>
 Education qualification: M. Pharm or Ph.D.
 </li>
 <li>
 Min. 8 years of recent technical experience in the pharmaceutical industry, in formulation development of oral solid dosage forms.
 </li>
 </ul>
 
 
 
 
 
 What we offer
 
 
 <ul>
 <li>
 A very international work environment
 </li>
 <li>
 Working in a new high end laboratory facility in Hyderabad, India
 </li>
 <li>
 Continuous learning and development; your development is not only good for your career; we also benefit from it.
 </li>
 <li>
 Excellent remuneration package
 </li>
 <li>
 Short communication and short decision lines
 </li>
 </ul>
 
 
 
 
 
 Vacancy description
 
 
 <ul>
 <li>
 Translate the customer requirements into a solution/recommendation using a Design of Experiments (DoE) approach.
 </li>
 <li>
 Write the required protocols with agreed timelines &amp; outputs (what feasible, what not)
 </li>
 <li>
 Perform experiments with your colleagues in the formulation team and work out the solution within agreed timelines &amp; resources.
 </li>
 <li>
 Interact with internal stakeholders in a multidisciplinary &amp; multicultural set up.
 </li>
 <li>
 Write the required protocols with agreed timelines and outputs (what feasible, what not)
 </li>
 <li>
 Translate the experiment results into reports / presentations.
 </li>
 </ul>
 
 
 
 
 
 Team details
 
 
 <ul>
 <li>
 You will be part of a Formulation team.
 </li>
 <li>
 The formulation team, along with Analytical team, forms our newly established Technical Centre Excellence, led by the CoE Manager and Director.
 </li>
 <li>
 The Technical Centre of Excellence is part of the wider Innovation &amp; Technical Solutions Department of DFE Pharma.
 </li>
 </ul>
</div>

Formulation Development Scientist

Dr. Reddy's Laboratories

<div>
 
 Dr. Reddy&rsquo;s Laboratories Ltd. is a leading multinational pharmaceutical company based across global locations. Each of our 24,000 plus employees comes to work every day for one collective purpose: to accelerate access to affordable and innovative medicines because
 
 Good Health Can&rsquo;t Wait
 
 .
 
 
 
 
 We started in 1984 with a modest investment, 20 employees and a bold vision. Today, we have research and development centres, manufacturing facilities or a commercial presence in 66 countries.
 
 
 
 
 For nearly four decades, we have stood for access, affordability and innovation based on the bedrock of deep science, progressive people practices and robust corporate governance. As the pharmaceutical industry evolves and undergoes disruption, we see an opportunity &ndash; to strengthen our core further (the next steps) and to build the future (the new bets).
 
 
 
 
 &lsquo;The Next and the New&rsquo; is how we aim to continue to be the partner of choice &ndash; purpose-driven, future-ready and sustainable. Our aim is to reach over 1.5 Bn+ patients across the world by 2030 by growing our core businesses and building for the future with sustainability at the core of our purpose and strategy. Sustainability for us means operating in a manner that respects people, planet and purpose &ndash; helping us conserve precious resources, serve our patients, create value for stakeholders, give back to society, fulfil our potential and maintain our integrity and transparency
 
 
 
 
 Dr Reddy&rsquo;s maintains a work environment, free from discrimination and is an equal opportunity employer. We are committed to employ &amp; nurture all qualified diverse workforce without regard to race, colour religion, nationality, sex, age, disability status, genetics, sexual orientation, gender expression, citizenship or any other characteristic or classification protected by applicable law(s) of the country we operate in. We treasure every talent, and recognize merit and diversity in our organization.
 
 
 
 
 
 
 Job Description
 
 
 
 
 
 Job Summary
 
 
 
 We are seeking a dynamic and experienced Formulation Scientist in Injectable division for designing and development of formulation process, ensuring quality by design (QbD) implementation, scaling up for manufacturing of batches, coordinating manufacturing readiness, overseeing plant execution, and facilitating seamless technology transfer.
 
 
 
 
 
 Roles &amp; Responsibilities
 
 
 
 
 <ul>
 <li>
 You will be responsible for end to end Formulation development of Injectable including development, execution, filing and approval.
 </li>
 <li>
 You will be responsible to co-ordinate closely with analytical team to devise effective Proof of Concept (POC) for developing generic equivalent of Reference Listed Drug (RLD)/generic Injections.
 </li>
 <li>
 You will be responsible to support in scale-up to pilot/plant scales for Injectable Products.
 </li>
 <li>
 You will be responsible to monitor the development for robust, effective and bioequivalent drug product in timely manner adhering to safety and quality standards. Also provide support in documentation for regulatory submissions.
 </li>
 <li>
 You will be responsible for technology transfer and execution of the batches.
 </li>
 <li>
 You will be responsible for performing pre-formulation studies for material characterization, drug-excipient compatibility and Reference Listed Drug (RLD) characterization (including reverse engineering, formulation designing and optimization, processes designing and scale up).
 </li>
 <li>
 You will be responsible for preparation of risk evaluation and risk mitigation documents, Scale-up batch documents, and filing documents for drug product at every stage of development.
 </li>
 <li>
 You will be responsible to review data generated and participate in discussions with experts to conclude on prototype(s). Participate in strategizing the sourcing of Active Pharmaceutical Ingredient (API), raw materials and ensure development studies are performed related to regulatory and internal system requirements.
 
 
 </li>
 </ul>
 
 Qualifications
 
 
 
 
 
 Educational qualification:
 
 Masters in Pharmaceutical/M.Tech in Chemical Engineering
 
 
 
 
 
 Minimum work experience:
 
 5 to 8 years of experience in pharmaceutical company in Injectable products.
 
 
 
 
 
 Skills &amp; attributes:
 
 
 
 
 Technical Skills
 
 
 
 
 <ul>
 <li>
 Have work experience on Formulation Development and expertise in inhalation/injectable dosage form.
 </li>
 <li>
 Experience in areas of product development for Generic Injectable
 </li>
 <li>
 Experience in Quality by Design (QbD).
 </li>
 <li>
 Experience in Process Optimization and scale up.
 </li>
 <li>
 Experience in Operational Excellence.
 </li>
 <li>
 Knowledge on Good Manufacturing Practice and Good Laboratory Practice.
 </li>
 <li>
 Experience in Technology Transfer.
 </li>
 </ul>
 
 
 Behavioral
 
 
 Skills
 
 
 
 
 <ul>
 <li>
 Excellent communication and interpersonal skills.
 </li>
 <li>
 Strong analytical and problem-solving abilities.
 </li>
 <li>
 Ability to work collaboratively with own team and cross-functional teams.
 
 
 </li>
 </ul>
 
 Additional Information
 
 
 
 
 
 About the Department
 
 
 
 
 
 
 Integrated Product Development Organisation
 
 
 
 
 
 We integrate our deep science capabilities and cutting-edge technology to develop innovative, accessible and affordable therapies for patients worldwide. We are a science-driven, innovation-focused pharmaceutical company committed to accelerating access to healthcare solutions to patients around the world. We have End to end capabilities in API, Formulations, Clinical, Intellectual Property and Regulatory Affairs. We are serving 55+ markets including USA, Canada, Europe, China, LATAM, ASEAN and all Emerging Markets with innovative and generic products ranging from Active pharmaceutical ingredients (API), Oral formulations, Parenteral (Injectables, Opthalmics) &amp; Other dosages
 
 
 Our product development efforts drive a portfolio of more than 1,000 products Enabled by our robust R&amp;D team consisting of more 200 scientists and functional experts and more than 150 doctorates, we have filed 1,071 patents and also published over 1,000 papers for peer review over the years.
 
 
 
 
 
 Benefits Offered
 
 
 
 At Dr. Reddy&rsquo;s we actively help to catalyse your career growth and professional development through personalised learning programs.
 
 
 The benefits you will enjoy at Dr. Reddy&rsquo;s are on par with the best industry standards. They include, among other things and other essential equipment, joining &amp; relocation support, family support (Maternity &amp; Paternity benefits), learning and development opportunities, medical coverage for yourself and your family, life coverage for yourself.
 
 
 
 
 
 Our Work Culture
 
 
 
 Ask any employee at Dr. Reddy&rsquo;s why they come to work every day and they&rsquo;ll say, because Good Health Can&rsquo;t Wait. This is our credo as well as the guiding principle behind all our actions. We see healthcare solutions not only as scientific formulations, but as a means to help patients lead healthier lives, and we&rsquo;re always attuned to the new and the next to empower people to stay fit. And to do this, we foster a culture of empathy and dynamism. People are at the core of our journey over the last few decades. They have been supported by an enabling environment that buoys individual ability while fostering teamwork and shared success. We believe that when people with diverse skills are bound together by a common purpose and value system, they can make magic.
 
 
 For more details, please visit our career website at
 
 https://careers.drreddys.com/#!/
 
 
</div>

<div>
 
 
 1. Job Objective
 
 
 
 1.1 The main role of the R&amp;D Senior Formulation Scientist is to research, develop, and optimize product formulations, ensuring compliance with GCC and SFDA requirements for safety, efficacy, and quality.
 
 
 The Formulation Scientist will support research feasibility projects by conducting formulation evaluation and analytical characterization of products. Strict adherence to cGMP guidelines is required.
 
 
 
 2. Duties, Responsibilities, and Authorities
 
 
 
 2.1 Develop robust, stable, and effective formulations (solid oral and sterile) for in-house manufacturing based on the latest approaches such as QbD.
 
 
 2.2 Comply with GMPs, SOPs, and all regulatory documentation.
 
 
 2.3 Prepare manufacturing documentation for pilot/small production runs and scale-up operations.
 
 
 2.4 Collect scientific data and references, maintain research documentation in pharmaceutical manufacturing, and prepare reports on developments in drug manufacturing and products.
 
 
 2.5 Participate in the set-up and operation of pilot-scale equipment and instrumentation for small production runs in collaboration with the R&amp;D technician.
 
 
 2.6 Work with procurement and finance teams to select materials (excipients/medicinal ingredients) that meet financial goals and support cost-saving initiatives.
 
 
 2.7 Optimize processes to improve manufacturing efficiencies.
 
 
 2.8 Lead technology transfer and scale-up operations for in-house product manufacturing.
 
 
 2.9 Participate in investigations of product failures including quality, potency, visual characteristics, and other parameters. Ensure involvement in all troubleshooting activities.
 
 
 2.10 Develop and review Raw Material and Finished Product Specifications in collaboration with the Product Development Manager and QA/QC departments.
 
 
 2.11 Initiate accelerated and ongoing stability studies for new products and review/report results in collaboration with the Product Development Manager.
 
 
 2.12 Maintain the confidentiality of R&amp;D data and company documents.
 
 
 
 3. Education / Licensure
 
 
 <ul>
 <li>
 Bachelor&rsquo;s or Master&rsquo;s degree in Pharmacy.
 </li>
 </ul>
 
 
 4. Professional Experience
 
 
 
 4.1 Minimum of 7 years of experience in solid dosage forms (tablets, capsules, ODF) and sterile dosage forms (SVP and LVP) using BFS technology.
 
 
 
 5. Core Competencies
 
 
 
 5.1 Excellent organizational and planning skills. Strong written, verbal, and interpersonal communication skills. High attention to detail. Demonstrated analytical skills and the ability to work independently while managing multiple deadlines. Proficiency with Microsoft Office Suite and industry-related software.
 
 
 
 6. Job Frequency
 
 
 
 6.1 Everyday
 
 
 
 7. Conditions
 
 
 
 7.1 This job description becomes effective on the date of approval.
 
 
 7.2 This job description is subject to periodic review and may be revised at any time in consultation with the committee supervisor and the employee.
 
</div>

R&D Senior Formulation Scientist ALRAZI

Kelly Science, Engineering, Technology & Telecom

<div>
 
 Kelly&reg; Science &amp; Clinical is seeking a Senior Scientist for
 
 a Direct Dire
 
 position at
 
 a premier CDMO
 
 in
 
 Irvine, CA
 
 . If you&rsquo;re passionate about bringing the latest scientific discoveries to life and are ready to take the next step in your career, trust The Experts at Hiring Experts.
 
 
 
 
 
 
 Salary:
 
 
 
 $90k-95k
 
 
 
 
 
 
 Overview
 
 :
 
 
 In this role, you will focus on method development and validation using HPLC and GC for solid and semi-solid oral drug products, specifically in immediate-release and extended-release dosage forms. You will support regulatory documentation, mentor junior chemists, and maintain high standards of efficiency, quality, and compliance within a collaborative R&amp;D environment.
 
 
 
 
 
 
 Schedule:
 
 
 
 Monday-Friday, standard working hours
 
 
 
 
 
 
 
 
 
 Responsibilities:
 
 
 <ul>
 <li>
 Develop and validate analytical methods for solid and semi-solid oral drug products, focusing on immediate-release and extended-release dosage forms, utilizing techniques such as HPLC and GC.
 </li>
 <li>
 Perform a variety of analytical tests including wet chemistry, assay, impurity/degradant analysis, dissolution, and residual solvent testing on both raw materials and finished drug products, following USP or established in-house methods.
 </li>
 <li>
 Design stability-indicating methods and method validation protocols, carry out method verification activities, and prepare comprehensive scientific reports documenting findings.
 </li>
 <li>
 Support regulatory documentation needs, including CMC submissions for ANDA filings, by ensuring methods and results are accurately recorded and presented in accordance with FDA and cGMP requirements.
 </li>
 <li>
 Guide, mentor, and train junior chemists by facilitating knowledge transfer, overseeing peer reviews of lab notebooks and records, and helping maintain efficient laboratory operations.
 </li>
 <li>
 Foster a collaborative team environment, demonstrate strong leadership and communication skills, and provide technical guidance to maintain compliance and uphold quality standards in R&amp;D projects.
 </li>
 <li>
 Work closely with the Quality Control department to coordinate and transfer validated methods to QC chemists, ensuring proper communication and documentation.
 </li>
 <li>
 Troubleshoot analytical methods and laboratory instrumentation, interpret scientific literature and regulatory documents, apply advanced mathematical analyses, and contribute to process improvements for greater laboratory efficiency.
 </li>
 <li>
 Other duties as assigned.
 </li>
 </ul>
 
 
 
 
 
 Qualifications:
 
 
 <ul>
 <li>
 Bachelor&rsquo;s degree in Chemistry
 </li>
 <li>
 5+ years of relevant pharmaceutical industry experience focused on method development for solid oral dosage forms and semi solid oral dosage forms.
 </li>
 <li>
 Proven track record in developing and validating analytical methods using HPLC and GC for assay, impurities, residual solvents, and dissolution.
 </li>
 <li>
 Strong understanding of CMC regulations and drug product development, including support for ANDA filings, compliance with FDA guidelines, and participation in audits.
 </li>
 <li>
 Excellent communication, teamwork, and leadership skills, with the ability to mentor junior scientists, interpret regulatory documents, and perform advanced scientific and mathematical analyses.
 </li>
 </ul>
</div>

Senior Scientist

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1662 pharmaceutical scientist jobs NEAR_ME

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R&D Senior Formulation Scientist ALRAZI

Senior Scientist