formulation development scientist

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>
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 Design, conduct and or supervise formulation development, process development, process optimization, scale up and manufacturing of product.
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 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.
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 Review of test results in alignment with the project goals, identify causes of variances and recommend solutions to achieve goals.
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 Schedule experiments and prioritize assignments to meet project objectives and deadline.
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 Maintain laboratory equipment and follow company safety standards.
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 Conduct laboratory experiments and prepare reports with conclusions and recommendations.
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 Follow current laboratory procedure and develop new laboratory procedures or improvise existing procedures to meet project objectives.
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 Identify and manage the potential risks within complex projects in a timely fashion.
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 Record accurate and complete experimental methods and results in compliance with good documentation practices.
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 Act as primary scientific contact to external collaborators.
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 Check and manage inventories of supplies and raw materials.
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 Ensure completion of all the training on time.
 
 
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 </ul>
 
 Qualifications And Education Requirements
 
 
 
 <ul>
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 M. Pharm or Ph.D. in Pharmacy with minimum industrial experience of 3 to 6years in pharmaceutical development and scale-up of products.
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 Preferred area of expertise is oral dosage forms precisely in Modified Release/ extended release/ targeted release/immediate release solid/Suspensions/Solutions.
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 Global Product Development Experience with markets like US/EU/China/ROW.
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 Experience of developing branded and differentiated products &ndash; 505(b)(2) category would be preferred.
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 Experience of working with CROs/CDMOs would be preferred.
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 Should be well versed with Microsoft office applications.
 
 
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 </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

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
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 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
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 Staying abreast of new discoveries and technologies in the area of formulation and delivery system technologies
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 Contribute to the generation of intellectual property, and prepare comprehensive technical documentation, including research reports and presentations
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 Ensure compliance with laboratory safety procedures and best practices in experimental design and execution
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 </ul>
 
 
 
 
 
 Skills &amp; Qualifications:
 
 
 <ul>
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 Solid background in formulation science with hands-on experience in areas such as colloidal systems, interfacial science, rheology, and material processing
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 Prior hands-on experience in R&amp;D
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 Ability to work independently and drive projects to completion
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 Strong collaborative and interpersonal skills with the ability to build effective working relationships across diverse teams
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 Skilled in cross-functional collaboration, engaging with colleagues and stakeholders from various technical and business backgrounds
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 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
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 Working knowledge of formulation design &amp; development and global regulatory product registration process
 </li>
 </ul>
 
 
 
 
 
 Education Requirements:
 
 
 <ul>
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 PhD Chemistry Preferred
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 Bachelors Degree in Chemistry, Chemical Engineering, Material Science, or related fields required;
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 Master's Degree MS ChE / Material Science preferred
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 </ul>
 
 
 
 
 
 Experience Requirements:
 
 
 <ul>
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 7+ yrs. industry experience
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 Colloid &amp; Surface science,
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 Surfactant chemistry, rheology expertise
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 Raman microscopy, granular formulation development, encapsulation techniques
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 Manufacturing scale-up experience in the chemicals or related industry
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 </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
 
 
 
 
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 Exceptional Health insurance including Medical, Dental, and Vision offered at low cost to employees and their families
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 Life; AD&amp;D insurance for employees and their families
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 401(k) Retirement Savings Plan with employer matching
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 Employee Stock Purchasing Plan (ESPP) with employee discount [AMVAC is an American Vanguard Company (NYSE: AVD)]
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 Health Savings Account (HSA) / Flexible Spending Account (FSA) available
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 Salary range : $120K - $150K - not including bonus and other compensation
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 Wellness program; tuition reimbursement and other benefits
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 </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>

Formulation Scientist

Syngene International Limited

<div>
 Date: 14 Oct 2025
 
 
 Location:
 
 
 IN
 
 
 Division: Discovery Services
 
 
 
 Job Title: Junior Analytical Development Scientist - OSD
 
 
 
 
 Job Location: Bengaluru
 
 
 
 
 Department: DPA &ndash; FD
 
 
 
 
 About Syngene :
 
 Syngene (www.syngeneintl.com) is an innovation-led contract research, development and manufacturing organization offering integrated scientific services from early discovery to commercial supply.
 
 
 At Syngene, safety is at the heart of everything we do personally and professionally. Syngene has placed safety at par with business performance with shared responsibility and accountability, including following safety guidelines, procedures and SOPs, in letter and spirit
 
 
 
 Mandatory expectation for all roles as per Syngene safety guidelines
 
 
 
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 Overall adherence to safe practices and procedures of oneself and the teams aligned
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 Contributing to development of procedures, practices and systems that ensures safe operations and compliance to company&rsquo;s integrity &amp; quality standards
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 Driving a corporate culture that promotes environment, health, and safety (EHS) mindset and operational discipline at the workplace at all times.
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 Ensuring safety of self, teams and lab/plant by adhering to safety protocols and following environment, health, and safety (EHS) requirements at all times in the workplace.
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 Ensure all assigned mandatory trainings related to data integrity, health, and safety measures are completed on time by all members of the team including self
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 Compliance to Syngene&rsquo; s quality standards at all times
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 Hold self and their teams accountable for the achievement of safety goals
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 Govern and Review safety metrics from time to time
 
 
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 </ul>
 
 Core Purpose Of The Role
 
 
 
 <ul>
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 Analytical development supporting Formulation development
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 Routine analysis of samples
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 Method development
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 Instrument calibrations
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 Documentation
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 Report preparation
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 Miscellaneous lab responsibilities
 
 
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 Role Accountabilities
 
 
 
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 Candidate should have very good educational and theoretical background.
 </li>
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 Candidate should have knowledge of calibration, method development and troubleshooting using various instruments like KF auto titrator, dissolution (I, II &amp; IV), spectroscopic instruments e.g. UV spectrometer, IR and Chromatographic instruments e.g. HPLC, GC
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 Knowledge of various regulatory guidelines w.r.t. method development, product development and documentation
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 Knowledge of method development for oral dosage forms w.r.t. tests like assay, degradation products, dissolutions, blend uniformity, content uniformity, cleaning method, etc.
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 Knowledge of specification setting for oral dosage forms, in-process specifications as well as product specifications
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 Knowledge and operating of instruments like LC-MS, GC-MS will be added advantage
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 Good understanding of Documentation as per GxP requirements
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 Online Lab notebook writing
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 Method development report preparation &ndash; Assay, Degradation products, Dissolution, cleaning method, etc.
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 Method of Analysis, Test report, SOP preparation
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 Calibration documentation
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 Review of documents generated by peers or juniors
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 Should be able to search scientific literature on-line
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 Should be a team player and able to coach juniors technically
 
 
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 </ul>
 
 Syngene Values
 
 
 
 All employees will consistently demonstrate alignment with our core values
 
 
 Excellence
 
 
 Integrity
 
 
 Professionalism
 
 
 
 Experience:
 
 More than 5 years up to 8 years
 
 
 
 Skills And Capabilities
 
 
 
 Candidate should have good proficiency for MS-office tools
 
 
 Should be able to search scientific literature on-line
 
 
 
 Behavioral Skills
 
 
 
 Strong commitment towards work, and a high level of dedication, enthusiasm, motivation, and persuasive ability in a team.
 
 
 Good speaking-listening-writing skills, attention to details, proactive self-starter.
 
 
 Ability to work successfully in a dynamic, ambiguous environment.
 
 
 Ability to meet tight deadlines and prioritize workloads.
 
 
 Ability to develop new ideas and creative solutions.
 
 
 Should be able to work in team and flexible for working in shifts.
 
 
 Should be a focused employee.
 
 
 
 Education:
 
 M.Pharm / M.Sc
 
 
 
 Equal Opportunity Employer
 
 
 
 It is the policy of Syngene to provide equal employment opportunity (EEO) to all persons regardless of age, color, national origin, citizenship status, physical or mental disability, race, religion, creed, gender, sex, sexual orientation, gender identity and/or expression, genetic information, marital status, status with regard to public assistance, veteran status, or any other characteristic protected by applicable legislation or local law. In addition, Syngene will provide reasonable accommodations for qualified individuals with disabilities.
</div>

Junior Analytical Development Scientist - OSD

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

Anika

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

Scientist I

Pacer Group

<div>
 
 
 Job Title: Scientist
 
 
 
 
 Duration:
 
 
 12 Months
 
 
 
 
 Location: West Point, PA 19486
 
 
 
 
 Shift Hours: M-F 8:00 AM To 5:00 PM
 
 
 
 
 
 
 
 
 Minimum Education Requirement:
 
 
 
 
 &bull; B.S. in Chemistry, Biology, Biochemistry, Biophysics, Chemical/Biochemical engineering, Virology, or related discipline with 3-5 years of relevant experience
 
 
 -or-
 
 
 &bull; M.S. in Chemistry, Biology, Biochemistry, Biophysics, Chemical/Biochemical engineering, Virology, or related discipline with 1-2 years of relevant experience
 
 
 
 
 
 
 
 Required Skills and Experience:
 
 
 
 
 &bull; Hands-on laboratory experience (academic or industry) designing, driving, and interpreting results from experiments
 
 
 &bull; Excellent communication, writing and collaboration skills
 
 
 &bull; Excellent organizational and technical problem-solving abilities
 
 
 &bull; Comfortable working in a fast-paced environment and adapting to change
 
 
 &bull; Ability to provide critical input into experimental plans
 
 
 &bull; Team-oriented, motivated to learn, and able to manage multiple priorities under technical supervision
 
 
 
 
 
 
 
 Desired Skills and Experience:
 
 
 
 
 &bull; Experience with analytical characterization of biotherapeutics including protein biochemistry and analytical characterization (e.g., particle size analysis and other biophysical methodologies)
 
 
 &bull; Formulation development experience with biotherapeutics including RNA, carbohydrate, protein and/or live viral vaccines as well as adjuvants for parenteral administration
 
 
 &bull; Demonstrated proficiency in aseptic technique
 
 
 &bull; Understanding of the drug product manufacturing process and scale-up considerations
 
 
 &bull; Experience with preparation and/or manufacturing of safety assessment or clinical supplies
 
 
 &bull; Experience authoring source documents used in regulatory filings
 
 
 &bull; General knowledge and/or experience with lyophilization, including techniques to examine residual moisture and the physical properties of lyophilized formulations
 
 
 
 
 
 Preferred candidates will have experience in drug product development techniques (e.g. formulation, filtration, analytical/biochemical/biophysical characterization, and process development).
 
 
 
 
 
 
 
 Responsibilities:
 
 
 
 
 Vaccine Drug Product Development, a part of Client's Research Laboratories in West Point, PA, is seeking a Contract Scientist or Engineer to join our department for one year. The selected candidate will work as part of a team responsible for the design and development of vaccine drug products from preclinical through Phase III with a line of sight to commercialization. The successful candidate will work hands-on in a fast-paced laboratory and collaborate closely with cross-functional teams to develop the next generation of vaccine drug products.
 
 
 
 
 
 Primary responsibilities include the design, execution, and documentation of laboratory activities supporting formulation of novel vaccine antigens (e.g., RNA, live virus vaccines, subunit, conjugate etc.), adjuvants, and delivery systems.
 
 
 
 
 
 
 
 Responsibilities:
 
 
 
 
 &bull; Design and perform hypothesis-driven formulation and process development experiments for sterile vaccine drug products (buffers, stabilizers, antigen/adjuvant, vials, syringes) across multiple vaccine modalities (subunit, conjugate, live-attenuated, etc.).
 
 
 &bull; Prepare formulations and fill vials/syringes for characterization &amp; animal studies using aseptic technique and Good Laboratory Practices (GLP); support transfer to GMP manufacturing.
 
 
 &bull; Conduct stability and forced-degradation studies; analyze data, summarize findings, and author technical reports and electronic notebook entries.
 
 
 
 &bull; Operate and troubleshoot benchtop unit operations (mixing, filtration, pumping, lyophilization), common lab instruments (pH, scales, pipettes), and analytical tools (DLS, SLS, KF, DSC, DSF)
 
 
 
 &bull; Collaborate with cross-functional teams (discovery, analytical, manufacturing, regulatory) to meet project timelines and deliverables.
 
 
 &bull; Continuously learn and apply current literature, methods, and technologies to improve formulations and processes.
 
 
 &bull; Support selected analytical studies on formulated products such as osmolality, viscosity, pH, and dynamic light scattering.
 
 
 &bull; Follow safe laboratory practices and maintain the work area in a clean orderly and safe manner.
 
 
 &bull; Draft, review and execute protocols for batch manufacture.
 
</div>

Analytical Chemist

DataAnnotation

<div>
 We are looking for a Research Scientist (Chemistry) to join our team to train AI models. You will measure the progress of these AI chatbots, evaluate their logic, and solve problems to improve the quality of each model.
 
 
 In this role you will need to hold an expert level understanding of chemistry. Other related fields include, but are not limited to: Research and Development Chemist, Formulation Scientist, Development Chemist, Analytical Chemist, Chemical Engineer, Medicinal Chemist, Biochemist, Process Development Chemist.
 
 
 
 Benefits
 
 
 
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 This is a full-time or part-time REMOTE position
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 You&rsquo;ll be able to choose which projects you want to work on
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 You can work on your own schedule
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 Projects are paid hourly starting at $40+ USD per hour, with bonuses on high-quality and high-volume work
 
 
 </li>
 </ul>
 
 Responsibilities
 
 
 
 <ul>
 <li>
 Give AI chatbots complex chemistry questions and evaluate their outputs
 </li>
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 Evaluate the quality produced by AI models for correctness and performance
 
 
 </li>
 </ul>
 
 Qualifications
 
 
 
 <ul>
 <li>
 Fluency in English (native or bilingual level)
 </li>
 <li>
 Detail-oriented
 </li>
 <li>
 Solid knowledge of general, organic, and physical chemistry concepts
 </li>
 <li>
 A current, in progress, or completed Masters and/or PhD is preferred but not required
 
 
 </li>
 </ul>
 
 Notes
 
 
 
 Payment is made via PayPal. We will never ask for any money from you. PayPal will handle any currency conversions from USD. Only applicants in the United States will be considered for this role. This is an independent contract position.
 
 
 #chem
</div>

Research Scientist (Chemistry)

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