formulation scientist

Dot & Key Skincare

<div>
 <p>
  <strong>
   Job Summary
  </strong>
  : We at Dot &amp; Key are seeking a meticulous and experienced formulation scientist to join our formulation team.
 </p>
 <p>
  <br/>
 </p>
 <p>
  <strong>
   Key Responsibilities
  </strong>
  :
 </p>
 <p>
  <br/>
 </p>
 <ul>
  <li>
   End to end responsible for developing skincare and cosmetic products. Should be able to develop the products independently.
  </li>
  <li>
   Interface on all project activities starting with formulation development, sensory evaluation, manufacturing process and stability.
  </li>
  <li>
   In depth knowledge in suncare moisturizer, serum, rinse off and lip care products formulation. Should have knowledge in the latest formats and technologies in technology space.
  </li>
  <li>
   Manage the product development process from formulation to final approval.
  </li>
  <li>
   Oversee the product processing and manufacturing to maximize output.
  </li>
  <li>
   Generate and maintain a product database for substantiating claims regarding the safety and efficacy of produced products for both the national and international market.
  </li>
  <li>
   Effectively document all findings, writeups, protocols and other authorization regarding products, publication.
  </li>
  <li>
   Express a high degree of flexibility and availability.
  </li>
 </ul>
 <p>
  <br/>
 </p>
 <p>
  <strong>
   Required candidate profile:
  </strong>
 </p>
 <p>
  <br/>
 </p>
 <ul>
  <li>
   Bachelor&rsquo;s degree/Master&rsquo;s degree in Chemistry/Cosmetic Technology/Chemical Engineering/ Oil technology/Pharmacology/Pharmaceutics.
  </li>
  <li>
   Experience: 4-5 years&rsquo; experience in formulation development of personal care products for e.g. sunscreen, moisturizer, lip care, serums etc.
  </li>
 </ul>
 <p>
 </p>
</div>


Formulation Scientist

Kelly Science, Engineering, Technology & Telecom

<div>
 <p>
  <strong>
   Formulations Scientist
  </strong>
 </p>
 <p>
  Kelly Sciene and Clinical has an opportunity for a
  <strong>
   Formulation Scientist
  </strong>
  for our client a leading medical device company in Raritan, NJ. 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. This role is a full-time, fully benefited position. As a Kelly employee, you will be eligible for Medical, Dental, 401K and paid time off, including holiday, vacation and sick/personal time.
 </p>
 <p>
  Length of assignment one year
 </p>
 <p>
  Must provide your own laptop
 </p>
 <p>
  Day shift
 </p>
 <p>
  Hybrid &ndash; 3 days on site
 </p>
 <p>
  Pay $50-55 an hour depending on experience
 </p>
 <ul>
  <li>
   <strong>
    Responsibilities:
   </strong>
   Leads formulation design efforts from concept through to prototyping phases, Design Reviews and Validation
  </li>
  <li>
   Collaborate with external suppliers and internal partners to develop products
  </li>
  <li>
   Drive product characterization to ensure rigorous technical understanding and relationships to pre-clinical/clinical outcomes
  </li>
  <li>
   Lead raw material suppliers through raw material iterations, correlating to product design window
  </li>
  <li>
   Drive execution of Learning Plans
  </li>
  <li>
   Participate in multi-functional discussions and design reviews, including product creation at multiple scales (modeling, lab, pilot and manufacturing)
  </li>
  <li>
   Participate in clinical procedures and activities, translating learning into viable prototypes
  </li>
  <li>
   Proven problem-solving skills using analytical technologies is preferred\
  </li>
  <li>
   Experience with respect to PMA preferred Proven problem-solving skills using analytical technologies is preferred
  </li>
  <li>
   Experience Design of Experiments (DOE) is preferred.
  </li>
  <li>
   Experience in developing protocols and writing completion reports is preferred.
  </li>
  <li>
   Experience developing combination (drug/device) medical devices products is preferred
  </li>
  <li>
   Working knowledge of basic statistics is required.
  </li>
  <li>
   Experience in vitro and ex vivo methods for characterizing prototypes and products is preferred
  </li>
  <li>
   Experience in developing and validating biochemical test methods for finished products and raw materials is preferred
  </li>
  <li>
   Excellent communication, collaboration and influencing skills
  </li>
  <li>
   Demonstrated ability to deliver project outcomes in an ambiguous environment
  </li>
  <li>
   Requires experience managing self-directed work teams
  </li>
  <li>
   Travel up to 20% may be required (domestic and international)
  </li>
  <li>
   <strong>
    Qualifications
   </strong>
   Education:
  </li>
  <li>
   Minimum Bachelor's degree required; advanced degree (Ph D) in Chemistry, Chemical Engineering, Pharmaceutical Sciences, Polymer Science, Polymer Engineering, strongly preferred
  </li>
  <li>
   Experience in
   <strong>
    medical device development is required
   </strong>
   5 -10 years ideally
  </li>
  <li>
   Successful experiences in launching new products &amp; formulations to market is required. Experience in biomaterials and material development highly preferred
  </li>
 </ul>
 <p>
  <strong>
   What happens next
  </strong>
 </p>
 <p>
  Once you apply, you&rsquo;ll proceed to the next steps if your skills and experience look like a good fit. But don&rsquo;t worry&mdash;even if this position doesn&rsquo;t work out, you&rsquo;re still in our network. That means all our recruiters will have access to your profile, expanding your opportunities even more.
 </p>
 <p>
  Helping you discover
  <strong>
   what&rsquo;s next
  </strong>
  in your career is what we&rsquo;re all about,
 </p>
 <p>
  #P1
 </p>
</div>


Tata Consultancy Services

<div>
 <strong>
  Job Description
  <br/>
  <br/>
 </strong>
 Must Have Technical/Functional Skills
 <br/>
 <br/>
 <ul>
  <li>
   Product formulation and launch experience.
  </li>
  <li>
   Biomaterials and material development.
  </li>
  <li>
   Medical device and combination product design and development; PMA familiarity.
  </li>
  <li>
   Problem solving using Analytical tools.
  </li>
  <li>
   Design of Experiments (DOE) and applied statistics.
  </li>
  <li>
   Protocol development, reporting, and documentation.
  </li>
  <li>
   In-vitro/ex-vivo characterization of prototypes.
  </li>
  <li>
   Biochemical test method development and validation.
  </li>
  <li>
   Strong communication and collaboration across teams.
  </li>
  <li>
   Ability to work in ambiguous environments and deliver outcomes.
  </li>
  <li>
   Experience with self-directed teams and multitasking.
  </li>
  <li>
   Effective prioritization and decision-making.
  </li>
  <li>
   Travel up to 20% may be required (domestic and international)
   <br/>
   <br/>
  </li>
 </ul>
 Salary Range $135,000-$150,000year
 <br/>
 <br/>
 <strong>
  TCS Employee Benefits Summary
  <br/>
  <br/>
 </strong>
 Discretionary Annual Incentive.
 <br/>
 <br/>
 Comprehensive Medical Coverage: Medical &amp; Health, Dental &amp; Vision, Disability Planning &amp; Insurance, Pet Insurance Plans.
 <br/>
 <br/>
 Family Support: Maternal &amp; Parental Leaves.
 <br/>
 <br/>
 Insurance Options: Auto &amp; Home Insurance, Identity Theft Protection.
 <br/>
 <br/>
 Convenience &amp; Professional Growth: Commuter Benefits &amp; Certification &amp; amp; Training Reimbursement.
 <br/>
 <br/>
 Time Off: Vacation, Time Off, Sick Leave &amp; Holidays.
 <br/>
 <br/>
 Legal &amp; Financial Assistance: Legal Assistance, 401K Plan, Performance Bonus, College Fund, Student Loan Refinancing.
 <br/>
 <br/>
 <strong>
  Qualifications:
 </strong>
 BACHELOR OF COMPUTER SCIENCE
 <br/>
 <br/>
</div>


Nutramax Laboratories

<div>
 <p>
  <strong>
   Nutramax desires to provide a drug-free, healthful, and safe workplace. We hold a zero-tolerance policy for drug use. Employment is contingent upon successfully passing a preemployment background check and drug screen (subject to applicable law).
  </strong>
 </p>
 <p>
  <br/>
 </p>
 <p>
  <strong>
   The hours for this position are Monday - Friday 8:30am - 5:00pm.
  </strong>
 </p>
 <p>
  <br/>
 </p>
 <p>
  <strong>
   <u>
    Summary of the Position:
   </u>
  </strong>
  The Formulation Scientist will provide new product development, product reformulation and process improvement support to a wide range of growth/quality/cost savings projects from ideation through commercialization under direction of the Formulations/Tech Transfer Director. Additionally, this position will work with operations, quality, business teams, and other functional partners; acting as product and process development/improvement support on cross-functional new product development and quality improvement/cost savings teams.
 </p>
 <p>
  <strong>
   <u>
    Roles and Responsibilities:
   </u>
  </strong>
 </p>
 <ul>
  <li>
   Capable of formulating moderately complex new products for soft chews, powders, tablets, capsules, pellets, and liquids.
  </li>
  <li>
   Perform bench trials, physical evaluations, and collect data to support new product development.
  </li>
  <li>
   Cooperate with PD staff in preparation/execution of pilot batches and product scale up batches and gather data to support in-process parameters and finished product specifications.
  </li>
  <li>
   Able to direct product development technicians in data collection and processing.
  </li>
  <li>
   Assist in developing new formulations for early-stage development and clinical batches.
  </li>
  <li>
   Work with new equipment/develop studies with equipment that could improve soft chew manufacturing process and/or formulation.
  </li>
  <li>
   Prepare and approve Master Batch Records, Change Control Requests for all scale up or production batches.
  </li>
  <li>
   Follow applicable cGMP processes.
  </li>
  <li>
   Compile and provide summaries of stability data.
  </li>
  <li>
   Provide Technical support to Manufacturing and Operations teams, monitor initial production batches for new and reformulated products.
  </li>
  <li>
   Provide training to manufacturing associates on new processes and process modifications/improvements.
  </li>
  <li>
   Continue education by attending expos and conferences and applying knowledge gained
  </li>
  <li>
   Communicate effectively with other departments within the organization and function within a team environment
  </li>
  <li>
   Regular attendance is required
  </li>
  <li>
   Perform other assigned duties as may be required in meeting company objectives
  </li>
 </ul>
 <p>
  <strong>
   <u>
    Minimum Requirements:
   </u>
  </strong>
 </p>
 <p>
  &middot; Experience working with soft chew (or similar) dosage forms
 </p>
 <p>
  &middot; Excellent interpersonal, communication, and organizational skills
 </p>
 <p>
  &middot; Basic ability to define problems, collect data, establish facts, draw valid conclusions, and offer solutions.
 </p>
 <p>
  <strong>
   <u>
    Education and Experience
   </u>
  </strong>
 </p>
 <p>
  &middot; BS/BA in chemistry, food science, life sciences, engineering, or a related discipline, or equivalent experience.
 </p>
 <p>
  &middot; Must have &gt;5 years of hands-on experience in product development of food, dietary supplements or related products, including dough, confectionery, or pet treats (animal feed/animal health a plus).
 </p>
 <p>
  &middot; Experience in a cGMP environment with understanding of cGMP principles and requirements.
 </p>
 <p>
  &middot; Experience working as part of a cross functional team.
 </p>
 <p>
  &middot; Knowledge of animal feed regulations a plus
 </p>
 <p>
  <br/>
 </p>
 <p>
  <strong>
   <u>
    Supervisory Responsibilities:
   </u>
  </strong>
  None
 </p>
</div>


Formulation Scientist of Product Development

Astellas Pharma

<div>
 Do you want to be part of an inclusive team that works to develop innovative therapies for patients? Every day, we are driven to develop and deliver innovative and effective new medicines to patients and physicians. If you want to be part of this exciting work, you belong at Astellas!
 <br/>
 <br/>
 Astellas Pharma Inc. is a pharmaceutical company conducting business in more than 70 countries around the world. We are committed to turning innovative science into medical solutions that bring value and hope to patients and their families. Keeping our focus on addressing unmet medical needs and conducting our business with ethics and integrity enables us to improve the health of people throughout the world. For more information on Astellas, please visit our website at
 <strong>
  www.astellas.com
 </strong>
 .
 <br/>
 <br/>
 <strong>
  The Role
  <br/>
  <br/>
 </strong>
 The primary purposes of the Scientist I, in Formulation &amp; Analytical Development, are to design, evaluate and develop suitable formulations and manufacturing processes for rAAV drug product under development, supporting the growing and diversifying portfolio of programs within AGT&rsquo;s pipeline.
 <br/>
 <br/>
 <strong>
  Responsibilities
  <br/>
  <br/>
 </strong>
 <ul>
  <li>
   Evaluate and understand the properties of new rAAV and propose formulations with sufficient stability during storage and suitability for clinical use.
  </li>
  <li>
   Conduct in-use stability and delivery device compatibility studies to ensurethe quality of drug products during administration at clinical sites.
  </li>
  <li>
   Author regulatory documents such as IND and briefing documents for meetings with health authorities.; prepare responses to Information Requests from agencies.
  </li>
  <li>
   Join the technical discussion cross-functional/divisional to align and enable efficient drug development work
  </li>
  <li>
   Evaluate and understand analytical tools and methods to develop rAAV formulation appropriately.
   <br/>
   <br/>
  </li>
 </ul>
 <strong>
  Required Qualifications
  <br/>
  <br/>
 </strong>
 <ul>
  <li>
   Advanced degree in biology or engineering with 5+ years of relevant experience in the biopharmaceutical industry
  </li>
  <li>
   Experience in formulation development for biopharmaceutical products
  </li>
  <li>
   Positive, professional attitude with a passion for science
  </li>
  <li>
   Business-level proficiency in English
   <br/>
   <br/>
  </li>
 </ul>
 <strong>
  Preferred Qualifications
  <br/>
  <br/>
 </strong>
 <ul>
  <li>
   Experience in authoring IND, BLA or other related regulatory filings, and responding to agency feedback/inquiries
  </li>
  <li>
   Experience with process development and technology transfer to GMP facilities for drug product manufacturing process
  </li>
  <li>
   Experience in operating basic analytical tools, such as chromatography and electrophoresis
  </li>
  <li>
   Experience working with external vendors, institutions, and other collaborators to develop new and innovative technologies
   <br/>
   <br/>
  </li>
 </ul>
 <strong>
  Working Environment
  <br/>
  <br/>
 </strong>
 <ul>
  <li>
   This position is based in Japan or US and will require on-site work.
   <br/>
   <br/>
  </li>
 </ul>
 <strong>
  Salary Range
 </strong>
 : $91,000 - $143,000 (Final compensation will be determined based on a variety of factors, including but not limited to skills, experience and organizational equity considerations)
 <br/>
 <br/>
 <strong>
  Benefits
  <br/>
  <br/>
 </strong>
 <ul>
  <li>
   Medical, Dental and Vision Insurance
  </li>
  <li>
   Generous Paid Time Off options, including Vacation and Sick time, plus national holidays including year-end shut down
  </li>
  <li>
   401(k) match and annual company contribution
  </li>
  <li>
   Company paid life insurance
  </li>
  <li>
   Annual Corporate Bonus and Quarterly Sales Incentive for eligible positions
  </li>
  <li>
   Long Term Incentive Plan for eligible positions
  </li>
  <li>
   Company-paid fleet vehicle for eligible positions
  </li>
  <li>
   Referral bonus program
   <br/>
   <br/>
  </li>
 </ul>
 \
 <br/>
 <br/>
 Category Gene Therapy Technical Dev
 <br/>
 <br/>
 Astellas is committed to equality of opportunity in all aspects of employment.
 <br/>
 <br/>
 EOE including Disability/Protected Veterans
 <br/>
 <br/>
</div>


Scientist I (Formulation Development)

Medical Group Care

<div><div><div><b>Benefits:</b></div>
<ul><li>401(k) matching</li>
<li>Bonus based on performance</li>
<li>Health insurance</li>
<li>Paid time off</li>
</ul></div><div><div><b>About the Role</b></div>
<div>We are seeking a highly skilled and experienced <b>Senior Formulation &amp; Quality Assurance</b>
</div><div><b>Scientist</b> to join our growing team. In this dual-focus role, you will be responsible for developing innovative,</div>
<div>safe, and effective formulations across FDA-regulated categories in cosmetics and health while ensuring that all products meet rigorous quality, regulatory, and</div>
<div>safety standards. The ideal candidate brings a deep passion for cosmetic science, a sharp analytical mindset,</div>
<div>and a proven track record in both the lab and in quality systems.<br>
<br>
<b>Key Responsibilities</b><br>
<b>Ideation, Strategy &amp; Market Opportunity</b><br>
<ul><li>lead white space research and competitive landscape analysis to identify consumer needs and market share growth opportunities across cosmetics, OTC, and medical device categories to grow (own merit) category for both retail and cobtorl brands.</li><li>benchmark formulations, claims, performance, and cost structures against national brands and category leaders to infomr innovation and positioning strategies.</li></ul>
translate cosnumer insights, clinical needs, and regulatory constraints into clear technical and commercialization roadmaps.<br>
</div><div><b>Product Formulation &amp; Technical Ownership</b><br>
<ul><li>own the development and formulation specifications as the subject-matter-expert (SME)</li></ul></div>
<ul><li>design, develop, and optimize skincare formulations across Cosmetic skincare and personal care assortments, OTC drug products (e.g. acne, dandruff, skin protectants, suncreens, cold/cough remedies, digestive health) and Medical devices and combination products, where applicable</li><li>take full ownership of formulations, including composition, processing parameters, stabilty, performance, and cost optimization.</li></ul>
<ul><li>source and evaluate raw materials and active ingredients in collaboration with key stakeholders and maintain clear communication in driving cost-effective startegy(ies) while maintaining competitive in market share.</li><li>guide and parter with contract manufacturers (co-mans) and their technical teams, providing direction on formulation refinement, process optimization, and scale-up readiness.</li><li>lead formulation advacement from bench prototype &gt;&gt;pilot &gt;&gt; full-scale commercial production, resolving scale-related challenges proactively.</li><li>evaluate, qualify, and approve rwa materials, actives, excipients, and packaging components in alignments with regulatory and quality requirements.</li></ul>
<ul><li>conduct and interpret stability, compatibility, and efficacy testing to validate new formulations.</li></ul>
<ul><li>stay current with emerging ingredients, technologies, and consumer trends to drive product innovation.</li></ul>
<ul><li>work cross-functionally with marketing, packaging, and regulatory teams to bring products from concept</li></ul>
<div>to commercialization.<br>
</div><div><b>Commercilization &amp; Scale-Up</b><br>
<ul><li>own technical readiness for launch, nsuring formulations are robust, reproducible, and commercially viable.</li><li>support road map transfer to manufacturing sites, processing instructions and specifications, and critical quality attributes.</li><li>ensure seamless collaborationacross to meet launch timelines.</li><li>identify and mitigate technical, quality, and regulatory risks prior to commercialization.</li></ul><br>
</div>
<div><b>Quality Assurance</b></div>
<ul><li>maintain data-driven quality management systems (QMS) in accordance with GMP, relevant ISO standardsand regulatory frameworks.</li><li>develop and implement streamlined, standardized processes across contract manufacturing parters to improve operational efficiency, reduce cycle times, and ensure consistent, on-time delivery of development and commercialization milestones.</li></ul>
<ul><li>establish and oversee SOPs for raw material testing, in-process checks, and finished product release.</li></ul>
<ul><li>investigate and resolve product quality complaints, non-conformances, and deviations using root cause</li></ul>
<div>analysis (e.g., CAPA, 8D).</div>
<ul><li>ensure all products comply with applicable cosmetic regulations (FDA, EU Cosmetics Regulation, or relevant regional standards).</li></ul>
<ul><li>maintain and review safety data sheets (SDS), product safety assessments, and documentation for</li></ul>
<div>regulatory submissions.<br>
</div><div><b>Qualifications</b></div>
<div><b>Education</b></div>
<div>Bachelor's degree (minimum) in Cosmetic Science, Chemistry, Biochemistry, Pharmaceutical Sciences,</div>
<div>or a related field.</div>
<div>Master's degree or PhD is a strong advantage.</div>
<div><b>Experience</b></div>
<div>5+ years of hands-on experience in skincare product formulation.</div>
<div>5+ years of experience in a quality assurance or regulatory compliance role within the cosmetics or</div>
<div>personal care industry.</div>
<div>Demonstrated experience working with a wide range of cosmetic raw materials, emulsion systems,</div>
<div>actives, and preservative systems.<br>
</div><div><b>Skills &amp; Knowledge</b></div>
<div>Deep knowledge of cosmetic chemistry, skin biology, and ingredient interactions.</div>
<div>Proficiency with formulation software and laboratory equipment (rheometers, pH meters,</div>
<div>spectrophotometers, etc.).</div>
<div>Strong understanding of global cosmetic regulatory requirements (FDA 21 CFR, EU No. 1223/2009, ISO</div>
<div>22716, etc.).</div>
<div>Experience with stability testing protocols (ICH guidelines or equivalent).</div>
<div>Excellent analytical, problem-solving, and documentation skills.</div>
<div>Strong project management and cross-functional collaboration abilities.</div>
<div>Familiarity with ERP and QMS software is a plus.<br>
<br>
<b>Soft Skills &amp; Leadership Competencies</b><br>
<ul><li>self-starter with high initiative; thrives in fast-paced, ambiguous environments</li><li>innovative and forward-thinking mindset, with ability to seek forward towards continuous improvement.</li><li>results-oriented problem solver who delivers practical, scalable solutions.</li><li>strong ownership mentality with accountability of outcomes.</li><li>effective communicator capable of influencing without authority.</li><li>able to work independently while collaborating seamlessly across teams.</li></ul></div></div></div><div></div>

Senior Formulation and Quality Assurance Scientist

EPM Scientific

<div>
 <p>
  <strong>
   Principal Scientist: Idaho
  </strong>
 </p>
 <p>
  <strong>
   Position Summary
  </strong>
 </p>
 <p>
 </p>
 <p>
  As the Principal Scientist for Skin, Sun &amp; Lip Care, you will serve as the internal subject-matter expert responsible for driving technical execution, advancing new technologies, and elevating product performance. You'll own formulations from concept through commercialization and play a key role in shaping the innovation pipeline.
 </p>
 <p>
  You'll collaborate closely with R&amp;D leadership, product development, regulatory, operations, and marketing teams to deliver high‑performing products that meet consumer expectations, regulatory standards, and business objectives.
 </p>
 <p>
  <strong>
   Key Responsibilities
  </strong>
 </p>
 <p>
 </p>
 <ul>
  <li>
   Lead innovation by identifying new technologies, ingredients, and formulation opportunities across Skin, Sun, and Lip Care categories
  </li>
  <li>
   Develop and optimize formulations from concept through launch, ensuring efficacy, safety, stability, and sensory performance
  </li>
  <li>
   Design and oversee testing programs, including stability, performance, safety, and clinical evaluation to support claims
  </li>
  <li>
   Conduct competitive benchmarking and technology assessments to inform category strategy and innovation pipelines
  </li>
  <li>
   Partner with Regulatory, Legal, Quality, and Marketing to ensure claims substantiation and global compliance
  </li>
  <li>
   Collaborate cross‑functionally with R&amp;D, Operations, and Marketing to ensure seamless project execution
  </li>
  <li>
   Contribute to intellectual property strategy by supporting patent development and driving scientific excellence
  </li>
  <li>
   Stay up to date on scientific literature, raw material innovations, regulatory changes, and market trends
  </li>
 </ul>
 <p>
  <strong>
   Qualifications
  </strong>
 </p>
 <p>
 </p>
 <ul>
  <li>
   Bachelor's, Master's, or Ph.D. in Chemistry or related scientific field
  </li>
  <li>
   5+ years of experience in personal care, skincare, sun care, beauty, bath &amp; body, OTC, or similar FMCG categories
  </li>
  <li>
   Strong formulation chemistry expertise with experience in in vitro/in vivo/clinical testing
  </li>
  <li>
   Understanding of global cosmetic regulations, labeling compliance, and GMP/GLP practices
  </li>
  <li>
   Proven ability to develop new formulations, evaluate emerging technologies, and improve existing products
  </li>
  <li>
   Strong analytical skills, including experimental design, data interpretation, and scientific documentation
  </li>
  <li>
   Excellent written and verbal communication, with experience preparing technical reports and supporting IP activities
  </li>
  <li>
   Demonstrated collaboration and leadership capabilities, including mentoring or guiding scientific staff
  </li>
  <li>
   Ability to relocate to the Idaho region and work onsite five days per week
  </li>
 </ul>
</div>


Principal Scientist

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Formulation Scientist

Formulation Scientist

Formulation Scientist

Formulation Scientist of Product Development

Scientist I (Formulation Development)

Senior Formulation and Quality Assurance Scientist

Principal Scientist