formulation scientist

Life Extension

<div>
 
 📍
 
 Hybrid &ndash; 2 Onsite Days/Week | Full-Time
 
 
 
 
 
 
 Are you passionate about innovation in the health and wellness space? Do you thrive at the intersection of science, formulation, and market-ready product development?
 
 
 
 
 
 We&rsquo;re seeking a
 
 Formulation Scientist
 
 to join our forward-thinking team and help bring high-quality dietary supplements from concept to launch. This critical role involves developing new products, qualifying cutting-edge ingredients, and collaborating across teams to shape the future of nutraceutical wellness.
 
 
 
 
 
 
 What You'll Do
 
 
 
 You&rsquo;ll be at the heart of our product innovation pipeline&mdash;evaluating new ingredients, formulating breakthrough products, and ensuring manufacturability, stability, and regulatory compliance.
 
 
 
 
 
 
 Core Responsibilities Include:
 
 
 <ul>
 <li>
 Lead ingredient qualification with suppliers and manufacturers
 </li>
 <li>
 Partner with Discovery Research to ensure timely approvals of ingredients
 </li>
 <li>
 Develop novel nutraceutical formulations, delivery systems, and technologies
 </li>
 <li>
 Analyze clinical/lab research to guide product efficacy and safety
 </li>
 <li>
 Conduct competitive product and pricing analyses to guide innovation
 </li>
 <li>
 Evaluate product opportunities for scientific merit and regulatory compliance
 </li>
 <li>
 Collaborate with QA/QC and Purchasing to source high-quality ingredients
 </li>
 <li>
 Assess manufacturability and stability of ingredients and formulas
 </li>
 <li>
 Manage product launches from initial concept through successful rollout
 </li>
 <li>
 Draft technical documentation and marketing support materials
 </li>
 <li>
 Respond to advanced customer and internal product inquiries
 </li>
 <li>
 Present product concepts to executives and cross-functional teams
 </li>
 <li>
 Contribute to article reviews for marketing, publication, and product launches
 </li>
 </ul>
 
 
 
 
 
 What You Bring
 
 
 <ul>
 <li>
 Bachelor&rsquo;s
 
 
 degree in Chemistry, Biochemistry, Pharmaceutical Sciences, or related field
 
 (Master&rsquo;s or PhD strongly preferred)
 
 </li>
 <li>
 3+ years experience in the dietary supplement industry
 </li>
 <li>
 2+ years experience in product development or formulation
 </li>
 <li>
 Deep understanding of nutraceutical ingredients, regulatory guidelines, and delivery technologies
 </li>
 <li>
 Exceptional verbal and written communication skills
 </li>
 <li>
 Strong analytical and research evaluation skills
 </li>
 <li>
 Proficiency in Microsoft Office Suite
 </li>
 </ul>
 
 
 
 
 Ready to develop the next generation of cutting-edge wellness products?
 
 Apply now
 
 and bring your scientific expertise to a company that values curiosity, innovation, and integrity. Visit https://lifeextension.com/careers the full job description.
 
</div>

Formulation Scientist

AMVAC U.S.

<div>
 
 AMVAC, an American Vanguard company is a leading manufacturer and marketer of innovative solutions for the Ag industry in the areas of crop protection and nutrition, turf and ornamental management, and commercial pest control.
 
 
 We are looking for a Formulation Development Scientist with a passion for learning and creating value through unwavering customer focus, collaborative innovation, and responsible stewardship.
 
 
 
 
 
 
 Job Duties &amp; Responsibilities:
 
 
 <ul>
 <li>
 Lead the design, prototyping, and advancement of innovative formulation strategies and delivery system technologies for active ingredients
 </li>
 <li>
 Collaborate cross-functionally with internal and external teams, including analytical sciences, process engineering, field product development, biological sciences, regulatory affairs, manufacturing, and commercial operations&mdash;to ensure seamless integration and success of formulation initiatives
 </li>
 <li>
 Staying abreast of new discoveries and technologies in the area of formulation and delivery system technologies
 </li>
 <li>
 Contribute to the generation of intellectual property, and prepare comprehensive technical documentation, including research reports and presentations
 </li>
 <li>
 Ensure compliance with laboratory safety procedures and best practices in experimental design and execution
 </li>
 </ul>
 
 
 
 
 
 Skills &amp; Qualifications:
 
 
 <ul>
 <li>
 Solid background in formulation science with hands-on experience in areas such as colloidal systems, interfacial science, rheology, and material processing
 </li>
 <li>
 Prior hands-on experience in R&amp;D
 </li>
 <li>
 Ability to work independently and drive projects to completion
 </li>
 <li>
 Strong collaborative and interpersonal skills with the ability to build effective working relationships across diverse teams
 </li>
 <li>
 Skilled in cross-functional collaboration, engaging with colleagues and stakeholders from various technical and business backgrounds
 </li>
 <li>
 Excellent verbal and written communication skills; specifically, the ability to persuade/influence others of the value of AMVAC technology and to clearly articulate the value of technology when talking with customers
 </li>
 <li>
 Working knowledge of formulation design &amp; development and global regulatory product registration process
 </li>
 </ul>
 
 
 
 
 
 Education Requirements:
 
 
 <ul>
 <li>
 PhD Chemistry Preferred
 </li>
 <li>
 Bachelors Degree in Chemistry, Chemical Engineering, Material Science, or related fields required;
 </li>
 <li>
 Master's Degree MS ChE / Material Science preferred
 </li>
 </ul>
 
 
 
 
 
 Experience Requirements:
 
 
 <ul>
 <li>
 7+ yrs. industry experience
 </li>
 <li>
 Colloid &amp; Surface science,
 </li>
 <li>
 Surfactant chemistry, rheology expertise
 </li>
 <li>
 Raman microscopy, granular formulation development, encapsulation techniques
 </li>
 <li>
 Manufacturing scale-up experience in the chemicals or related industry
 </li>
 </ul>
 
 
 
 
 
 Benefits &amp; more:
 
 
 
 We offer a work environment that values diversity and inclusion, promotes continuous learning and professional growth, and supports a healthy work-life balance to empower team members
 
 
 
 
 <ul>
 <li>
 Exceptional Health insurance including Medical, Dental, and Vision offered at low cost to employees and their families
 </li>
 <li>
 Life; AD&amp;D insurance for employees and their families
 </li>
 <li>
 401(k) Retirement Savings Plan with employer matching
 </li>
 <li>
 Employee Stock Purchasing Plan (ESPP) with employee discount [AMVAC is an American Vanguard Company (NYSE: AVD)]
 </li>
 <li>
 Health Savings Account (HSA) / Flexible Spending Account (FSA) available
 </li>
 <li>
 Salary range : $120K - $150K - not including bonus and other compensation
 </li>
 <li>
 Wellness program; tuition reimbursement and other benefits
 </li>
 </ul>
 
 
 
 
 We are an Equal Opportunity Employer and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or veteran status, or any other characteristic protected by law. AMVAC is proud to be an EEO/AA employer M/F/D/V. We maintain a drug-free workplace and perform pre-employment background checks and substance abuse testing. We participate in the E-Verify Federal Identification System.
 
 
 
 AMVAC, An American Vanguard Company, (NYSE: AVD)
 
 
</div>

Somafina

<div>Why Somafina? 
 
Somafina is an industry leader in contract manufacturing of dietary supplements. Our commitment to our customers and our aggressive growth strategy provide opportunities to manage uniquely complex projects with a team of dedicated and expert collaborators. We pride ourselves in our superior commitment to maintaining the highest quality standards while fostering a company culture that is collaborative and supportive.
Job Summary: This position will be responsible for developing new gummy dietary supplement products. The Gummy Formulation Scientist will work with sales representatives and customers to develop efficacious gummy dietary supplement formulas to meet expected price points. They will make recommendations for in process formula adjustments to improve efficiencies in manufacturing and provide relevant information to marketing department to write supplement/nutritional facts panels. This is an exciting opportunity with growth potential to combine science and creativity to develop gummy products that enhance customer health and wellness. 
Job Duties &amp; Responsibilities:<ul><li>New formula development of gummies that meet cost targets.</li><li>Compile and store all relevant ingredient and packaging documentation (COA&rsquo;s Specifications, Certifications, Clinical Studies, etc.)</li><li>Assist with allowable product claims, and ensure they are formulated to meet certification requirements as needed (Kosher, Halal, Non-GMO, Certified Organic, Gluten Free, etc.)</li><li>Assist with Supplement Facts Panels</li><li>Provide samples and documentation to quality to qualify new suppliers and materials.</li><li>Suggest changes to existing formulas to assist manufacturing efficiency improvement efforts.</li><li>Establish testing requirements (methods &amp; frequency) for new ingredients and products.</li><li>Develop finished product specifications for new and existing products.</li><li>Develop raw material specifications for new ingredients and packaging.</li><li>Create samples for customer approval and to initiate stability testing.</li><li>Provide Certificates of Analysis on new product samples.</li><li>Assists production of scale up for new gummy formulas.</li><li>Troubleshooting for gummy production batches.</li><li>Support Sales Inquiries about Products/Ingredients</li><li>Other duties as assigned &ndash; Please note this job description is not designed to cover or contain a comprehensive listing of activities, duties or responsibilities that are required of the employee for this job. Duties, responsibilities, and activities may change at any time with or without notice.</li></ul> 
Job Education &amp; Experience:<ul><li>Minimum of 5 years&rsquo; experience developing gummy formulas for dietary supplements, OTC drugs or food production.</li><li>In-depth theoretical and hands on experience in gummy technologies and equipment for various dosage formulas including sustained release (MR/DR) formulations.</li><li>May handle hazardous materials and may require wearing personal protective equipment as needed.</li><li>Must be able to move about the laboratory and the facility.</li><li>Extensive knowledge of the handling of gummy production materials as well as the compounding process, acquired either through experience or education.</li><li>Continuously demonstrate a strong and efficient performance in all aspects of formulation activities; including but not limited to, minimizing and/or eliminating errors in your performance, assist with support tasks (stocking, cleaning, filter testing, etc.) without additional prompting, and help others with their formulations when available.</li><li>Strong attention to detail, math skills, and knowledge of the metric system</li><li>Ability and willingness to change direction and focus promptly to meet shifting organizational and business demands.</li><li>Ability to work individually and as part of a team to create and contribute to an environment that values people and encourages trust, teamwork, and open communication.</li><li>Ability to effectively manage oneself, demonstrate integrity, be productive under pressure, and achieve developmental goals.</li><li>Ability to communicate effectively to team members and superiors.</li></ul> 
 Job Competencies:<ul><li>Adaptability - Adapts to changes in the work environment; Manages competing demands; Changes approach or method to best fit the situation; Able to deal with frequent change, delays, or unexpected events.</li><li>Analytical - Synthesizes complex or diverse information; Collects and researches data; Uses intuition and experience to complement data; Designs workflows and procedures.</li><li>Business Acumen - Understands business implications of decisions; Displays orientation to profitability; Demonstrates knowledge of market and competition; Aligns work with strategic goals.</li><li>Change Management - Develops workable implementation plans; Communicates changes effectively; Builds commitment and overcomes resistance; Prepares and supports those affected by change; Monitors transition and evaluates results.</li><li>Cost Consciousness - Works within approved budget; Develops and implements cost saving measures; Contributes to profits and revenue; Conserves organizational resources.</li><li>Design - Generates creative solutions; Translates concepts and information into images; Uses feedback to modify designs; Applies design principles; Demonstrates attention to detail.</li><li>Innovation - Displays original thinking and creativity; Meets challenges with resourcefulness; Generates suggestions for improving work; Develops innovative approaches and ideas; Presents ideas and information in a manner that gets others' attention.</li><li>Judgement - Displays willingness to make decisions; Exhibits sound and accurate judgment; Supports and explains reasoning for decisions; Includes appropriate people in decision-making process; Makes timely decisions.</li><li>Leadership - Exhibits confidence in self and others; Inspires and motivates others to perform well; Effectively influences actions and opinions of others; Accepts feedback from others; Gives appropriate recognition to others.</li><li>Motivation - Sets and achieves challenging goals; Demonstrates persistence and overcomes obstacles; Measures self against standard of excellence; Takes calculated risks to accomplish goals.</li><li>Planning/Organizing - Prioritizes and plans work activities; Uses time efficiently; Plans for additional resources; Sets goals and objectives; Organizes or schedules other people and their tasks; Develops realistic action plans.</li><li>Problem Solving - Identifies and resolves problems in a timely manner; Gathers and analyzes information skillfully; Develops alternative solutions; Works well in group problem solving situations; Uses reason even when dealing with emotional topics.</li><li>Professionalism - Approaches others in a tactful manner; Reacts well under pressure; Treats others with respect and consideration regardless of their status or position; Accepts responsibility for own actions; Follows through on commitments.</li><li>Project Management - Develops project plans; Coordinates projects; Communicates changes and progress; Completes projects on time and budget; Manages project team activities.</li><li>Quality - Demonstrates accuracy and thoroughness; Looks for ways to improve and promote quality; Applies feedback to improve performance; Monitors own work to ensure quality.</li><li>Quality Management - Looks for ways to improve and promote quality; Demonstrates accuracy and thoroughness.</li><li>Quantity - Meets productivity standards; Completes work in timely manner; Strives to increase productivity; Works quickly.</li><li>Safety and Security - Observes safety and security procedures; Determines appropriate action beyond guidelines; Reports potentially unsafe conditions; Uses equipment and materials properly.</li><li>Strategic Thinking - Develops strategies to achieve organizational goals; Understands organization's strengths &amp; weaknesses; Analyzes market and competition; Identifies external threats and opportunities; Adapts strategy to changing conditions.</li><li>Technical Skills - Assesses own strengths and weaknesses; Pursues training and development opportunities; Strives to continuously build knowledge and skills; Shares expertise with others.</li><li>Visionary Leadership - Displays passion and optimism; Inspires respect and trust; Mobilizes others to fulfill the vision; Provides vision and inspiration to peers and subordinates.</li><li>Written Communication - Writes clearly and informatively; Edits work for spelling and grammar; Varies writing style to meet needs; Presents numerical data effectively; Able to read and interpret written information.</li></ul> 
PHYSICAL DEMANDS AND WORK ENVIRONMENT: Work is performed in an office setting, sitting in front of a computer approximately 75% of the time. Must be able to lift to 10 lbs., push and pull up to 10 lbs., have proper hearing, vision, and speech capabilities.
The above is intended to describe the general content of and requirements for the performance of this job. It is not to be construed as an exhaustive statement of duties, responsibilities, or physical requirements. Nothing in this job description restricts management&rsquo;s right to assign or reassign duties and responsibilities to this job at any time. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.</div>

Gummy Formulation 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

Formulated Solutions

<div>
 
 
 
 THE COMPANY:
 
 
 
 
 Formulated Solutions is redefining the Pharmaceutical and Self-Directed Consumer Healthcare CDMO experience through creativity and invention; delivering our world class Marketing Partners unmatched formulations, innovative packaging and cost effective, reliable supply.
 
 
 Formulated Solutions is and shall always be a company of people with the knowledge and dedication to provide our Marketing Partners with a single source solution for delivering quality and innovative products to market. We shall embrace changes and new opportunities as a vehicle to continually develop and grow sustainable relationships. As a company we shall never accept anything less than a culture that fosters creativity, growth, and profitability for both our Partners and the company.
 
 
 
 
 
 
 PRIMARY PURPOSE:
 
 
 
 The I&amp;D Formulator III will have responsibilities for the design, development, testing and implementation of new formulations from initial concept through production; troubleshooting/resolving, adjusting or reformulating existing formulas as needed. This individual must have extensive cGMP experience and FDA and ICH Guidance experience. Must be able to provide leadership and mentoring to I&amp;D Interns, Associates, and Formulator I(s).
 
 
 
 
 
 
 MAJOR DUTIES AND RESPONSIBILITIES:
 
 
 <ul>
 <li>
 Supports efforts to brainstorm new customer concepts based on personal experience, market insights, competitive position, online research, technology/market trends, etc.
 </li>
 <li>
 Develops new products to meet customer requirements per assigned projects.
 </li>
 <li>
 Works to proactively prioritize multiple projects/workload, effectively anticipate/manage resource gaps, and deliver on agreed-to timelines.
 </li>
 <li>
 Develops new product ideas for presentation to Marketing for future consideration in customer innovation events.
 </li>
 <li>
 Prepares samples for customer evaluation or for use by Marketing, Project Management, Engineering, QC/QA.
 </li>
 <li>
 Actively assists in the troubleshooting of off-target batches in the I&amp;D Lab.
 </li>
 <li>
 Prepares protocols for both formal and informal stability testing.
 </li>
 <li>
 Accurately records raw data and analyzes, as well as calculates and interprets the results. Ensures all documentation produced is in compliance with cGMP standards.
 </li>
 <li>
 Communicates effectively in verbal and written form on research results and plans.
 </li>
 <li>
 Demonstrates initiative in handling responsibilities.
 </li>
 <li>
 Attends project meetings and prepares project updates.
 </li>
 <li>
 Develops working relationships with vendors and attends vendor meetings.
 </li>
 <li>
 Maintains raw material supply in I&amp;D laboratory including but not limited to: vendor sample inventory, in-house sample inventory.
 </li>
 <li>
 Promotes cGMP and safety practices throughout the facility.
 </li>
 <li>
 Promotes continuous improvement and customer satisfaction.
 </li>
 <li>
 Recognizes OOS or out of trend results and assists in the completion of lab investigations.
 </li>
 <li>
 Reads and understands SDSs for all raw materials they will be working with.
 </li>
 <li>
 Responsible and accountable for compliance with all aspects of the company's Health and Safety policies, and Safe Work Procedures.
 </li>
 <li>
 Works to identify more efficient ways of working and shares ideas with management.
 </li>
 <li>
 Prepare and present technical presentations
 </li>
 <li>
 Participates in other activities as assigned by the I&amp;D Manager or VP of I&amp;D.
 </li>
 </ul>
 
 
 
 
 
 QUALIFICATION:
 
 
 
 Required
 
 <ul>
 <li>
 Responsible for contributing to audit readiness and for assisting in quality audits with FDA, other Regulatory Agencies, and customers, as needed.
 </li>
 <li>
 Working knowledge of FDA regulation for drug/device especially for the lab.
 </li>
 <li>
 Ability to use a personal computer and peripheral equipment to accurately enter an analyze data and produce reports.
 </li>
 <li>
 Knowledge of chemical safety and personal protective equipment.
 </li>
 <li>
 Proficient in approaches to aerosol and/or emulsion blending, chemistry and troubleshooting.
 </li>
 <li>
 Advanced knowledge of various analytical equipment and techniques utilized in an analytical laboratory including but not limited to pH, viscosity, specific gravity, infrared spectroscopy, HPLC, GC, atomic absorption.
 </li>
 <li>
 Demonstrated ability to represent the I&amp;D technical function in cross functional team meetings.
 </li>
 <li>
 Ability to establish priorities, work independently, productively and proceed with objectives without supervision.
 </li>
 <li>
 Ability to handle and resolve recurring problems.
 </li>
 <li>
 Communicates effectively in verbal and written form on projects and research results.
 </li>
 <li>
 Ability to work in a dynamic fast paced-sometimes rapidly shifting environment and quickly establish priorities. Ability to concentrate in such an environment and perform quality work.
 </li>
 <li>
 Contributes to for overall lab safety, organization, cleanliness, calibration, and maintenance.
 </li>
 <li>
 Strong leadership and mentoring skills.
 </li>
 <li>
 Must be able to lift up to 15 pounds.
 </li>
 </ul>
 
 
 
 
 
 Preferred Additional
 
 
 <ul>
 <li>
 Aerosol formulation experience strongly preferred.
 </li>
 <li>
 Regulated products formulation experience strongly preferred.
 </li>
 </ul>
 
 
 
 
 
 CRITICAL SKILLS AND ABILITIES:
 
 
 <ul>
 <li>
 Advanced knowledge of benchtop and production scale emulsion chemistry
 </li>
 <li>
 Familiarity with aerosol chemistry and delivery systems
 </li>
 <li>
 Ability to independently generate formulas for experimental blending
 </li>
 <li>
 Demonstrated ability to work both independently and in a team environment
 </li>
 </ul>
 
 
 
 
 
 COMPUTER SKILLS:
 
 
 <ul>
 <li>
 Familiarity with the use of MS Word, MS Excel, MS Access.
 </li>
 </ul>
 
 
 
 
 
 EDUCATION AND/OR TRAINING
 
 
 <ul>
 <li>
 Bachelor&rsquo;s degree in Chemistry or appropriate discipline with 5+ years related experience in the personal care or pharmaceutical industry.
 </li>
 <li>
 OR MS in Analytical Chemistry or equivalent with 3+ years related experience in a pharmaceutical industry a strong plus.
 </li>
 </ul>
 
 
 
 
 
 Environmental Demands
 
 
 <ul>
 <li>
 Exposure to chemicals and/or other potential hazards.
 </li>
 <li>
 Exposure to loud noises.
 </li>
 <li>
 Moving machines and robots.
 </li>
 <li>
 Self-starting machinery.
 </li>
 </ul>
 
 
</div>

Formulation Scientist III

Azurity Pharmaceuticals

<div>
 Azurity Pharmaceuticals is a privately held, specialty pharmaceutical company that focuses on innovative products that meet the needs of underserved patients. As an industry leader in providing unique, accessible, and high-quality medications, Azurity leverages its integrated capabilities and vast partner network to continually expand its broad commercial product portfolio and robust late-stage pipeline. The company&rsquo;s patient-centric products span the cardiovascular, neurology, endocrinology, gastro-intestinal, institutional, and orphan markets, and have benefited millions of patients. For more information, visit www.azurity.com.
 
 
 Azurity Pharmaceuticals is proud to be an inclusive workplace and an Equal Opportunity Employer. Azurity's success is attributable to our incredibly talented, dedicated team that focuses on benefiting the lives of patients by bringing the best science and commitment to quality into everything that we do. We seek highly motivated individuals with the dedication, integrity, and creative spirit needed to thrive in our organization.
 
 
 
 Job Responsibilities
 
 
 
 <ul>
 <li>
 Design, conduct and or supervise formulation development, process development, process optimization, scale up and manufacturing of product.
 </li>
 <li>
 Prepare and review documents such as batch records, Batch Packaging Records, Product Development reports, SOPs, Stability protocols, Raw material specifications, Packaging material specifications and In-process/ Finished product specifications, labelling and stability loading.
 </li>
 <li>
 Review of test results in alignment with the project goals, identify causes of variances and recommend solutions to achieve goals.
 </li>
 <li>
 Schedule experiments and prioritize assignments to meet project objectives and deadline.
 </li>
 <li>
 Maintain laboratory equipment and follow company safety standards.
 </li>
 <li>
 Conduct laboratory experiments and prepare reports with conclusions and recommendations.
 </li>
 <li>
 Follow current laboratory procedure and develop new laboratory procedures or improvise existing procedures to meet project objectives.
 </li>
 <li>
 Identify and manage the potential risks within complex projects in a timely fashion.
 </li>
 <li>
 Record accurate and complete experimental methods and results in compliance with good documentation practices.
 </li>
 <li>
 Act as primary scientific contact to external collaborators.
 </li>
 <li>
 Check and manage inventories of supplies and raw materials.
 </li>
 <li>
 Ensure completion of all the training on time.
 
 
 </li>
 </ul>
 
 Qualifications And Education Requirements
 
 
 
 <ul>
 <li>
 M. Pharm or Ph.D. in Pharmacy with minimum industrial experience of 3 to 6years in pharmaceutical development and scale-up of products.
 </li>
 <li>
 Preferred area of expertise is oral dosage forms precisely in Modified Release/ extended release/ targeted release/immediate release solid/Suspensions/Solutions.
 </li>
 <li>
 Global Product Development Experience with markets like US/EU/China/ROW.
 </li>
 <li>
 Experience of developing branded and differentiated products &ndash; 505(b)(2) category would be preferred.
 </li>
 <li>
 Experience of working with CROs/CDMOs would be preferred.
 </li>
 <li>
 Should be well versed with Microsoft office applications.
 
 
 </li>
 </ul>
 By applying for this role, you confirm that you are mentally and physically capable of fulfilling the job responsibilities detailed in the job description without any restrictions. If you have any concerns or even the slightest disability that may affect your ability to perform the job, please inform HR in advance.
</div>

Formulation Development Scientist

Medasource

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

Associate Scientist

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