senior 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>


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

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)

Altasciences

<div><p><b>Your New Company!
</b><br>
At Altasciences we all move in unison to assist and work in the discovery, development, and manufacturing of new drug therapies to get them faster to people who need them. No matter your role, we all play an important part and you will have a significant impact on the health and well-being of people across the globe. By living our values of Employee Development, Customer Focus, Quality and Excellence, Respect and Integrity, we look to foster a passionate and collaborative work environment and we are looking for talented and enthusiastic people, like you, to join our growing team! Whether you're a recent college graduate or seeking your next career opportunity, it's time to discover your future at Altasciences.
</p><p>We are better together and together We Are Altasciences.
</p><p></p><p><b>About the Role
</b><br>
As a Research Associate on the Formulations team, your primary responsibilities include performing test and control article formulation, dose preparation and dispensing. You will receive test and control article materials and maintain chain of custody documentation associated with test and control materials, including inventory. Additionally, maintaining accountability and reconciliation of test materials is required. Responsible for reviewing protocols and formulation instructions and calculations for accuracy and completeness.<br>
</p><p><br>
<b>What You&rsquo;ll Do Here
</b></p><ul><li><p>Perform dose preparation, sampling and dispensing of test and control article materials.
</p></li><li><p>Ensure appropriate review of data is completed in a timely manner.
</p></li><li><p>Demonstrate high quality documentation skills with few common documentation errors.
</p></li><li><p>Perform receipt, review and reconciliation of test material in a timely manner.
</p></li><li><p>Perform disposition of test materials when necessary.
</p></li><li><p>Evaluate as needed test article processes for adherence to GLP regulations.
</p></li><li><p>Coordinate and ensure the validation/calibration status of equipment used in the formulation laboratory with equipment group.
</p></li><li><p>Address audit findings and implement appropriate corrective actions.
</p></li><li><p>Review SOP's for laboratory procedures and equipment for completeness and accuracy.
</p></li><li><p>Participate in protocol review meetings, reviews protocols, formulation instructions and calculations for accuracy and correctness.
</p></li><li><p>Prepare and ship materials as needed.
</p></li><li><p>Cross train to support pharmacy operations, i.e. dispense controlled substances.
</p></li><li><p>Participate in reviewing training materials and SOPs.
</p></li></ul><p></p><p><b>What You&rsquo;ll Need to Succeed
</b></p><ul><li><p>BS in a scientific discipline (Chemistry is preferred) or relevant experience
</p></li><li><p>1+ years experience working in a regulated environment; combination of relevant experience and education considered
</p></li><li><p>Basic computer experience including Microsoft Office suite
</p></li><li><p>English proficiency required to read and interpret documents such as industry specific documents
</p></li><li><p>Solid reasoning abilities
</p></li><li><p>Able to operate laboratory equipment
</p></li><li><p>Work with a diverse group of people in a fast-paced environment
</p></li><li><p>Work cross functionally on process improvements
</p></li><li><p>Demonstrate attention to detail and ability to multi-task
</p></li><li><p>Maintain organization in a fast paced, changing environment.
</p></li><li><p>Able to manage change
</p></li><li><p>Readily adapt to new projects
</p></li><li><p>Positive attitude toward work and co-workers
</p></li><li><p>Comfortable communicating with all levels of management and employees
</p></li><li><p>Identify and resolve problems as they are encountered
</p></li><li><p>Understands work schedule and completes assignments on time
</p></li></ul><p></p><p><b>What We Offer
</b></p><p>The pay range estimated for this position is $23.00 - $29.00 per hour. Please note that hourly rates/salaries vary within the range based on factors including, but not limited to, prior relevant experience, skills, education, certification, location as well as internal equity and market data.
</p><p></p><p><b>Benefits
</b></p><p>Altasciences offers a wide variety of benefits to help our employees live healthy and fulfilling lives both at and outside of work.
</p><p></p><p><b>Altasciences&rsquo; Benefits Package Includes:
</b></p><ul><li><p>Health/Dental/Vision Insurance Plans
</p></li><li><p>401(k)/RRSP with Employer Match
</p></li><li><p>Paid Vacation and Holidays
</p></li><li><p>Paid Sick and Bereavement Leave
</p></li><li><p>Employee Assistance &amp; Telehealth Programs
</p></li><li><p>Telework when applicable.
</p></li></ul><p></p><p><b>Altasciences&rsquo; Incentive Programs Include:
</b></p><ul><li><p>Training &amp; Development Programs
</p></li><li><p>Employee Referral Bonus Program
</p></li></ul><p></p><p>#LI-ES1
</p><p></p><p><b>MOVING IN UNISON TO DELIVER A BIG IMPACT WITH A PERSONAL TOUCH
</b></p><p>Altasciences is an equal opportunity employer committed to diversity and inclusion. Our goal is to attract, develop and retain highly talented employees from diverse backgrounds, allowing us to benefit from a wide variety of experiences and perspectives. All qualified applicants will receive consideration for employment without regard to age, race, color, religion, creed, sex, sexual orientation, gender identity, national origin, disability or any other protected grounds under applicable legislation. Reasonable accommodations for persons with disabilities during the recruitment process are available upon request. Join us at Altasciences!</p></div>

Research Associate I, Formulations

<div><p><b>Your New Company!
</b><br>
At Altasciences we all move in unison to assist and work in the discovery, development, and manufacturing of new drug therapies to get them faster to people who need them. No matter your role, we all play an important part and you will have a significant impact on the health and well-being of people across the globe. By living our values of Employee Development, Customer Focus, Quality and Excellence, Respect and Integrity, we look to foster a passionate and collaborative work environment and we are looking for talented and enthusiastic people, like you, to join our growing team! Whether you're a recent college graduate or seeking your next career opportunity, it's time to discover your future at Altasciences.
</p><p>We are better together and together We Are Altasciences.
</p><p></p><p><b>About the Role
</b><br>
Primary responsibilities include performing basic test and control article formulation, dose preparation and dispensing. Also responsible for receiving test and control article materials and maintaining chain of custody documentation associated with test and control materials, including inventory control.
</p><p></p><p><b>What You&rsquo;ll Do Here
</b></p><ul><li>Prepare, sample, and dispense less complex dose formulations including solutions and suspensions
</li></ul><ul><li>Prepare, sample, and dispense more complex dose formulations including solutions and suspensions with guidance
</li></ul><ul><li>Receive test materials, reagents, review, and reconcile test material receipt
</li></ul><ul><li>Participate in disposition of formulation and test materials
</li></ul><ul><li>Document and review raw data accurately while preparing and maintaining study notebooks
</li></ul><ul><li>Reviews protocols and provides formulation comments
</li></ul><ul><li>Prepare and ship materials as needed
</li></ul><ul><li>Replenish supplies and maintains cleanliness of the laboratory and equipment
</li></ul><ul><li>May assist in study finalization and inventory of test materials in dispense
</li></ul><ul><li>May cross train to support pharmacy operations, i.e., dispense controlled substances
</li></ul><p></p><div><b>What You&rsquo;ll Need to Succeed
</b><br>
<ul><li>BS in a scientific discipline or relevant work experience
</li><li>Experience working in a regulated environment with animals in research or a regulated environment preferred
</li><li>Basic computer experience including Microsoft Office suite
</li><li>English proficiency required to read and interpret documents such as industry specific documents
</li><li>Basic math skills
</li><li>Solid reasoning abilities
</li><li>Able to operate laboratory equipment
</li><li>Work with a diverse group of people in a fast-paced environment
</li><li>Work cross functionally on process improvements
</li><li>Demonstrate attention to detail while multi-tasking and maintain organization in a fast paced, changing environment
</li><li>Able to manage change
</li><li>Readily adapts to new projects
</li><li>Positive attitude toward work and co-workers
</li><li>Comfortable communicating with all levels of management and employees
</li><li>Identify and resolve problems as they are encountered
</li></ul></div><p></p><p><b>What We Offer:
</b></p><p>Altasciences offers a wide variety of benefits to help our employees live healthy and fulfilling lives both at and outside of work.
</p><p><b>Altasciences' Benefits Package Includes:
</b></p><ul><li><p>Health/Dental/Vision Insurance Plans
</p></li><li><p>401(k)/RRSP with Employer Match
</p></li><li><p>Paid Vacation and Holidays
</p></li><li><p>Paid Sick and Bereavement Leave
</p></li><li><p>Employee Assistance &amp; Telehealth Programs
</p></li></ul><p><b>Altasciences' Incentive Programs Include:
</b></p><ul><li><p>Training &amp; Development Programs
</p></li><li><p>Employee Referral Bonus Program
</p></li><li><p>Annual Performance Review
</p></li></ul><p></p><p>#LI-TA1
</p><p></p><p><b>MOVING IN UNISON TO DELIVER A BIG IMPACT WITH A PERSONAL TOUCH
</b></p><p>Altasciences is an equal opportunity employer committed to diversity and inclusion. Our goal is to attract, develop and retain highly talented employees from diverse backgrounds, allowing us to benefit from a wide variety of experiences and perspectives. All qualified applicants will receive consideration for employment without regard to age, race, color, religion, creed, sex, sexual orientation, gender identity, national origin, disability or any other protected grounds under applicable legislation. Reasonable accommodations for persons with disabilities during the recruitment process are available upon request. Join us at Altasciences!</p></div>

Research Associate, Formulations

CPS, Inc.

<div>
 We are seeking an Associate Food Scientist to join our R&amp;D team. This is an entry-level to early career role designed for a recent graduate or someone with 0-2 years of industry experience who is excited to build hands-on technical skills and grow into owning product development projects.
 <br/>
 <br/>
 This role blends hands-on lab work with increasing responsibility in formulation, scale-up, and commercialization. You&rsquo;ll work closely with senior scientists, operations, and cross-functional partners to support product development activities.
 <br/>
 <br/>
 <strong>
  Key Responsibilities
  <br/>
  <br/>
 </strong>
 <ul>
  <li>
   Support formulation, bench-trials, and product development activities
  </li>
  <li>
   Prepare samples for internal evaluation, sensory testing, and external partners
  </li>
  <li>
   Execute lab, pilot, and plant trials, assist with setup, run and cleanup
  </li>
  <li>
   Accurately document formulas, trial results, and observations
  </li>
  <li>
   Maintain lab organization and follow food safety and GMP requirements
  </li>
  <li>
   Collaborate with R&amp;D, Operations, Quality, and Supply Chain teams
  </li>
  <li>
   Support troubleshooting during scale-up and production as needed
  </li>
  <li>
   Occasional travel to manufacturing or supplier locations as required
  </li>
  <li>
   If you&rsquo;d like to hear more about this opportunity and others we are currently working on, please contact Kristine O&rsquo;Sullivan at kosullivan@cps4jobs.com.
   <br/>
   <br/>
  </li>
 </ul>
 JO: 3.26KO
 <br/>
 <br/>
 Salary
 <br/>
 <br/>
 $50,000 - $80,000
 <br/>
 <br/>
 Benefits Available
 <br/>
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Associate Food Scientist

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