analytical development 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
 
 
 
 <ul>
 <li>
 Overall adherence to safe practices and procedures of oneself and the teams aligned
 </li>
 <li>
 Contributing to development of procedures, practices and systems that ensures safe operations and compliance to company&rsquo;s integrity &amp; quality standards
 </li>
 <li>
 Driving a corporate culture that promotes environment, health, and safety (EHS) mindset and operational discipline at the workplace at all times.
 </li>
 <li>
 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.
 </li>
 <li>
 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
 </li>
 <li>
 Compliance to Syngene&rsquo; s quality standards at all times
 </li>
 <li>
 Hold self and their teams accountable for the achievement of safety goals
 </li>
 <li>
 Govern and Review safety metrics from time to time
 
 
 </li>
 </ul>
 
 Core Purpose Of The Role
 
 
 
 <ul>
 <li>
 Analytical development supporting Formulation development
 </li>
 <li>
 Routine analysis of samples
 </li>
 <li>
 Method development
 </li>
 <li>
 Instrument calibrations
 </li>
 <li>
 Documentation
 </li>
 <li>
 Report preparation
 </li>
 <li>
 Miscellaneous lab responsibilities
 
 
 </li>
 </ul>
 
 Role Accountabilities
 
 
 
 <ul>
 <li>
 Candidate should have very good educational and theoretical background.
 </li>
 <li>
 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
 </li>
 <li>
 Knowledge of various regulatory guidelines w.r.t. method development, product development and documentation
 </li>
 <li>
 Knowledge of method development for oral dosage forms w.r.t. tests like assay, degradation products, dissolutions, blend uniformity, content uniformity, cleaning method, etc.
 </li>
 <li>
 Knowledge of specification setting for oral dosage forms, in-process specifications as well as product specifications
 </li>
 <li>
 Knowledge and operating of instruments like LC-MS, GC-MS will be added advantage
 </li>
 <li>
 Good understanding of Documentation as per GxP requirements
 </li>
 <li>
 Online Lab notebook writing
 </li>
 <li>
 Method development report preparation &ndash; Assay, Degradation products, Dissolution, cleaning method, etc.
 </li>
 <li>
 Method of Analysis, Test report, SOP preparation
 </li>
 <li>
 Calibration documentation
 </li>
 <li>
 Review of documents generated by peers or juniors
 </li>
 <li>
 Should be able to search scientific literature on-line
 </li>
 <li>
 Should be a team player and able to coach juniors technically
 
 
 </li>
 </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

City Therapeutics

<div>
 We are seeking a passionate Senior Scientist, CMC Analytical Development to join our growing team. You will lead method development, qualification, and transfer to support internal labs and external partners. The role is hands-on and highly cross-functional, partnering with CROs/CMOs to define impurity profiles and deliver comprehensive characterization of oligonucleotide drug substances, drug products, and process intermediates (e.g., siRNA and conjugates). You will report to the Director, CMC Analytical Development and contribute directly to City&rsquo;s next-generation siRNA programs.
 
 
 
 Please note this is a full-time onsite opportunity
 
 
 
 
 Responsibilities
 
 
 
 <ul>
 <li>
 Independently design and execute analytical methods for oligonucleotides and conjugates; drive continuous method improvement.
 </li>
 <li>
 Apply advanced scientific principles to solve complex analytical problems; propose innovative, phase-appropriate solutions.
 </li>
 <li>
 Lead method development, verification/qualification, validation (as needed), and transfer for existing and new programs.
 </li>
 <li>
 Develop and implement analytical technology such as HPLC-MS methods for impurity characterizations of oligonucleotides
 </li>
 <li>
 Conduct exploratory stability studies for raw materials, intermediates, DS, and DP; interpret trends and recommend actions.
 </li>
 <li>
 Generate high-quality data; analyze, interpret, and communicate results; propose data-driven next steps.
 </li>
 <li>
 Work both independently and with cross-functional teams to plan, prioritize, and meet project timelines
 </li>
 <li>
 Write CMC source documents such as, but not limited to, analytical methods, development reports, qualification/validation protocols and reports
 </li>
 <li>
 Operate, calibrate, maintain, and troubleshoot analytical instrumentation; ensure adherence to data integrity and safety practices.
 
 
 </li>
 </ul>
 
 Qualifications
 
 
 
 <ul>
 <li>
 Ph.D. in Analytical Chemistry or related field with 3+ years relevant industry experience; M.S. with 7+ years; or B.S. with 10+ years.
 </li>
 <li>
 Strong AX-HPLC and HPLC&ndash;MS technical background with hands-on oligonucleotide characterization experience.
 </li>
 <li>
 Proven understanding of analytical instrumentation theory and practice across DS/DP development and manufacturing processes.
 </li>
 <li>
 Demonstrated skills in handling, analyzing, and characterizing oligonucleotides and related organic molecules.
 </li>
 <li>
 Familiarity with cGxP expectations, analytical data systems, and data integrity principles.
 </li>
 <li>
 Knowledge of CMC regulatory requirements (e.g., IND/IMPD) is a plus.
 </li>
 <li>
 Understanding of basic theories and principles of synthetic organic chemistry is a plus
 </li>
 <li>
 Meticulous documentation, strong problem-solving, and the ability to operate with minimal supervision.
 </li>
 <li>
 Excellent communication, organization, and teamwork skills; comfortable in a fast-paced, multi-project environment with shifting priorities.
 
 
 </li>
 </ul>
 
 
 City Therapeutics is accepting resumes/CVs from direct applicants only. Recruitment Agency inquiries and submissions will not be accepted at this time.
 
 
 
 
 City Therapeutics is an Equal Opportunity and Affirmative Action employer committed to a culturally diverse workforce. All qualified applicants will receive consideration for employment without regard to race; color; creed; religion; national origin; age; ancestry; nationality; marital, domestic partnership or civil union status; sex, gender, gender identity or expression; affectional or sexual orientation; disability; veteran or military status or liability for military status; domestic violence victim status; atypical cellular or blood trait; genetic information (including the refusal to submit to genetic testing) or any other characteristic protected by law.
</div>

Sr. Scientist, CMC Analytical Development

Neurocrine Biosciences

<div>
 
 Who We Are
 
 
 
 At Neurocrine Biosciences, we pride ourselves on having a strong, inclusive, and positive culture based on our shared purpose and values. We know what it takes to be great, and we are as passionate about our people as we are about our purpose - to relieve suffering for people with great needs.
 
 
 
 What We Do
 
 
 
 Neurocrine Biosciences is a leading neuroscience-focused, biopharmaceutical company with a simple purpose: to relieve suffering for people with great needs. We are dedicated to discovering and developing life-changing treatments for patients with under-addressed neurological, neuroendocrine and neuropsychiatric disorders. The company's diverse portfolio includes FDA-approved treatments for tardive dyskinesia, chorea associated with Huntington's disease, classic congenital adrenal hyperplasia, endometriosis* and uterine fibroids,* as well as a robust pipeline including multiple compounds in mid- to late-phase clinical development across our core therapeutic areas. For three decades, we have applied our unique insight into neuroscience and the interconnections between brain and body systems to treat complex conditions. We relentlessly pursue medicines to ease the burden of debilitating diseases and disorders because you deserve brave science. For more information, visit neurocrine.com, and follow the company on LinkedIn, X and Facebook. (
 
 *in collaboration with AbbVie
 
 )
 
 
 
 About The Role
 
 
 
 Develops and executes instrumental methods of analysis for development compounds, drug substances, raw materials, intermediates, drug product, and packaging materials to develop assays based on new and existing methodologies. Responsible for coordinating and supporting day-to-day operations in an Analytical Development (AD) GMP lab. This role will focus mainly on GMP laboratory workflows. The person will also schedule all analytical instruments calibrations, maintenance and qualification activities. This role will ensure full compliance with GMP regulation and support continuous improvement of lab processes and equipment readiness.
 
 
 _
 
 
 
 Your Contributions (include, But Are Not Limited To)
 
 
 
 <ul>
 <li>
 Develops and executes instrumental methods (e.g. HPLC, GC, TGA, DSC, MS, FTIR) of analyses for development compounds, drug substances, raw materials, intermediates, drug product, and packaging materials
 </li>
 <li>
 Accurately follows established test methods, procedures, and pharmacopeia chapters (e.g. Dissolution) to generate data essential for strategic decision making
 </li>
 <li>
 Serve as the primary point of contact for all instrument-related activities and maintain equipment inventory, calibration and service records in compliance with GMP regulations
 </li>
 <li>
 Coordinates vendors service calls for repair and maintenance of laboratory instruments, with training perform routine maintenance of laboratory instrumentation, maintains complete and accurate records of instrument service and repairs in conformance with company SOPs and policies
 </li>
 <li>
 With supervision and as appropriate, assists investigations for out of specification, out of trend, and/or anomalous results
 </li>
 <li>
 Participates in internal and external audits as SME for lab instrumentation
 </li>
 <li>
 Support training of GMP lab staff on procedures, GMP requirements and safety protocols
 </li>
 <li>
 Coordinate daily lab operations
 </li>
 <li>
 Maintains complete and accurate records of laboratory work in conformance with company standard operating procedures (SOPs) and training
 </li>
 <li>
 Provides detailed reviews of peer generated data as well as that generated from contracted service providers
 </li>
 <li>
 Maintains the inventory of GMP laboratory consumables and clean glassware
 </li>
 <li>
 Performs other duties as assigned
 
 
 </li>
 </ul>
 
 Requirements
 
 
 
 <ul>
 <li>
 BS/BA degree in chemistry or closely related field and 2+ years of pharmaceutical industry experience in an R&amp;D/QC setting, including conducting HPLC analysis and troubleshooting, evaluating analytical data and drawing meaningful conclusions
 </li>
 <li>
 MS/MA degree in chemistry or closely related field preferred and some similar industry experience noted above
 </li>
 <li>
 PhD in chemistry or closely related field and some industry or relevant experience a plus
 </li>
 <li>
 Proficient in using MS-Excel, MS-Word as well as data systems for computer-controlled instrumentation
 </li>
 <li>
 Practical working knowledge of conducting HPLC analysis and troubleshooting
 </li>
 <li>
 Some expertise in evaluating analytical data and drawing meaningful conclusions
 </li>
 <li>
 Knowledge of cGMP expectations for laboratory records and quality systems
 </li>
 <li>
 Ability to provide ideas for process improvements
 </li>
 <li>
 Recognizes fundamental anomalies in data points and identifies issues in experiments / processes
 </li>
 <li>
 Begins to understand how to think outside of the technical process and consider the impact decisions will have on the broader scientific goals
 </li>
 <li>
 Strong knowledge of one scientific discipline
 </li>
 <li>
 Good knowledge of scientific principles, methods and techniques
 </li>
 <li>
 Good knowledge and demonstrated ability working with a variety of laboratory equipment/tools
 </li>
 <li>
 Ability to work as part of a team of individuals to meet goals, tasks in a timeline driven setting
 </li>
 <li>
 Strong computer skills
 </li>
 <li>
 Good communications, problem-solving, analytical thinking skills
 </li>
 <li>
 Detail oriented
 </li>
 <li>
 Ability to meet deadlines
 </li>
 <li>
 Good project management skills
 
 
 </li>
 </ul>
 Neurocrine Biosciences is an EEO/Disability/Vets employer.
 
 
 We are committed to building a workplace of belonging, respect, and empowerment, and we recognize there are a variety of ways to meet our requirements. We are looking for the best candidate for the job and encourage you to apply even if your experience or qualifications don&rsquo;t line up to exactly what we have outlined in the job description.
 
 
 _
 
 
 The annual base salary we reasonably expect to pay is $88,000.00-$127,550.00. Individual pay decisions depend on various factors, such as primary work location, complexity and responsibility of role, job duties/requirements, and relevant experience and skills. In addition, this position offers an annual bonus with a target of 20% of the earned base salary and eligibility to participate in our equity based long term incentive program. Benefits offered include a retirement savings plan (with company match), paid vacation, holiday and personal days, paid caregiver/parental and medical leave, and health benefits to include medical, prescription drug, dental and vision coverage in accordance with the terms and conditions of the applicable plans.
 
 
</div>

Scientist / Sr. Scientist, Analytical Chemistry

Eli Lilly and Company

<div>
 At Lilly, we unite caring with discovery to make life better for people around the world. We are a global healthcare leader headquartered in Indianapolis, Indiana. Our employees around the world work to discover and bring life-changing medicines to those who need them, improve the understanding and management of disease, and give back to our communities through philanthropy and volunteerism. We give our best effort to our work, and we put people first. We&rsquo;re looking for people who are determined to make life better for people around the world.
 
 
 
 Overview
 
 
 
 At Lilly, we unite caring with discovery to make life better for people around the world. We are a global healthcare leader headquartered in Indianapolis, Indiana. Our employees around the world work to discover and bring life-changing medicines to those who need them, improve the understanding and management of disease, and give back to our communities through philanthropy and volunteerism. We give our best effort to our work, and we put people first. We&rsquo;re looking for motivated individuals who are determined to make life better for people around the world.
 
 
 The Bioproduct Research and Development (BR&amp;D) organization delivers new medicines to patients through the development and commercialization of insulins, peptides, oligonucleotides, monoclonal antibodies, novel therapeutic proteins, and gene therapy systems. BR&amp;D is a multidisciplinary group with deep technical expertise that works collaboratively with our discovery and manufacturing colleagues. Located in Indianapolis, IN, scientists have full access to Lilly&rsquo;s deep pharmaceutical development expertise and engineering capabilities. In this role, you will be part of a diverse team of analytical chemists, pharmaceutical scientists, and engineers delivering product and process understanding for assets in Lilly&rsquo;s clinical development portfolio. Ideal candidates will possess experience across multiple analytical techniques, demonstrate an aptitude in technical problem solving, and be motivated to work both independently and collaboratively in a dynamic environment.
 
 
 
 Responsibilities
 
 
 
 <ul>
 <li>
 Evaluate and/or implement new analytical technologies/methods to advance Lilly's current analytical capabilities for bioproduct testing with a focus on state-of-the-art separation sciences capabilities.
 </li>
 <li>
 Generate key data and information applying HPLC, UHPLC, capillary electrophoresis, LCMS and/or other instrumental analysis techniques.
 </li>
 <li>
 The ideal candidate will demonstrate learning agility and be able to work with cross-functional teams.
 </li>
 <li>
 Engage with scientists across Lilly&rsquo;s Development and Manufacturing organizations to develop and validate robust analytical methods
 </li>
 <li>
 Identify and exploit new scientific concepts, strong problem-solving skills, and be self-motivated to contribute across multiple projects
 </li>
 <li>
 Strong written and verbal communication to speak to both technical and business-related implications of your work.
 
 
 
 </li>
 </ul>
 
 Basic Requirements
 
 
 
 <ul>
 <li>
 MS in Analytical Chemistry, Biochemistry, Chemistry, or a related field; or,
 </li>
 <li>
 BS in Analytical Chemistry, Biochemistry, Chemistry, or a related field with a minimum of 2 years of relevant experience
 
 
 
 </li>
 </ul>
 
 Additional Preferences
 
 
 
 <ul>
 <li>
 Experience with chromatographic separations and/or spectroscopic methods and methods for the analysis of oligonucleotides, LNPs, peptides, therapeutic recombinant proteins, synthetic/pegylated peptide/proteins, monoclonal antibodies, and/or cell-gene therapy systems.
 </li>
 <li>
 Experience with method validation and transfer.
 </li>
 <li>
 Demonstration of scientific and people leadership skills.
 </li>
 <li>
 Effective oral and written communication skills.
 </li>
 <li>
 The ability to work productively in an interdisciplinary team environment
 </li>
 <li>
 Ability to balance multiple activities, prioritize and handle ambiguity
 
 
 
 </li>
 </ul>
 
 Additional Information
 
 
 
 <ul>
 <li>
 Potential exposure to chemicals, allergens, and loud noises
 </li>
 <li>
 Travel: 0 to 10%
 </li>
 <li>
 Position Local: Indianapolis, IN; Lilly Technology Center-North (LTC-N)
 
 
 
 </li>
 </ul>
 Lilly is dedicated to helping individuals with disabilities to actively engage in the workforce, ensuring equal opportunities when vying for positions. If you require accommodation to submit a resume for a position at Lilly, please complete the accommodation request form (https://careers.lilly.com/us/en/workplace-accommodation) for further assistance. Please note this is for individuals to request an accommodation as part of the application process and any other correspondence will not receive a response.
 
 
 Lilly is proud to be an EEO Employer and does not discriminate on the basis of age, race, color, religion, gender identity, sex, gender expression, sexual orientation, genetic information, ancestry, national origin, protected veteran status, disability, or any other legally protected status.
 
 
 Our employee resource groups (ERGs) offer strong support networks for their members and are open to all employees. Our current groups include: Africa, Middle East, Central Asia Network, Black Employees at Lilly, Chinese Culture Network, Japanese International Leadership Network (JILN), Lilly India Network, Organization of Latinx at Lilly (OLA), PRIDE (LGBTQ+ Allies), Veterans Leadership Network (VLN), Women&rsquo;s Initiative for Leading at Lilly (WILL), enAble (for people with disabilities). Learn more about all of our groups.
 
 
 Actual compensation will depend on a candidate&rsquo;s education, experience, skills, and geographic location. The anticipated wage for this position is
 
 
 $65,250 - $169,400
 
 
 Full-time equivalent employees also will be eligible for a company bonus (depending, in part, on company and individual performance). In addition, Lilly offers a comprehensive benefit program to eligible employees, including eligibility to participate in a company-sponsored 401(k); pension; vacation benefits; eligibility for medical, dental, vision and prescription drug benefits; flexible benefits (e.g., healthcare and/or dependent day care flexible spending accounts); life insurance and death benefits; certain time off and leave of absence benefits; and well-being benefits (e.g., employee assistance program, fitness benefits, and employee clubs and activities).Lilly reserves the right to amend, modify, or terminate its compensation and benefit programs in its sole discretion and Lilly&rsquo;s compensation practices and guidelines will apply regarding the details of any promotion or transfer of Lilly employees.
 
 
 #WeAreLilly
</div>

Analytical Chemist, Cell & Gene Therapy Products – Bioproduct Research and Development

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

Tap Growth ai

<div>
 
 🌟 We're Hiring: Scientist! 🌟
 
 
 
 We are seeking a dedicated and analytical Scientist to join our research team and contribute to groundbreaking scientific discoveries. The ideal candidate will have a strong foundation in scientific methodology, data analysis, and research techniques to support our innovative projects and drive scientific excellence.
 
 
 
 📍 Location:
 
 Durham, United States
 
 
 
 ⏰ Work Mode:
 
 Work From Office
 
 
 
 💼 Role:
 
 Scientist
 
 
 
 Pay Scale:
 
 Up to $98, 404.80 (Dependent on Experience)
 
 
 
 What You'll Do
 
 
 
 Laboratory Data Review:
 
 
 <ul>
 <li>
 Scientific data review of laboratory documentation and data to appropriate standards (GMPs, SOPs, protocols, methods).
 </li>
 <li>
 Good understanding of data integrity and ALCOA+ (Attributable, Legible, Contemporaneous, Original, and Accurate) principles.
 </li>
 <li>
 Peer review of results and documentation of product development studies including statistical data reports (JMP).
 </li>
 <li>
 Peer review of method validations and analytical technical transfers.
 </li>
 <li>
 Transcription checking of regulatory submissions, reports, and / or JMP tables / plots.
 
 
 </li>
 </ul>
 
 What We're Looking For
 
 
 
 <ul>
 <li>
 BS or MS in Chemistry, Pharmaceutical Sciences, or a similar applicable discipline.
 </li>
 <li>
 Experience with HPLC in a GMP / QC setting, Empower software preferred.
 </li>
 <li>
 Experience with Inhalation testing products, large and small molecule preferred.
 </li>
 <li>
 Strong understanding of GMP and FDA guidelines for pharmaceutical manufacturing and validation.
 </li>
 <li>
 Strong organizational skills for managing multiple priorities.
 </li>
 <li>
 Effective communication and interpersonal skills for coordination with lab personnel, and management.
 
 
 </li>
 </ul>
 
 
 Ready to advance science? 🚀 Apply now and let's innovate together!
 
 
</div>

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>
 <li>
 Design and carry out experiments to investigate Chemical/Material/Biological properties of candidate materials for use in applications in Orthopedics and General Surgery
 </li>
 <li>
 Develop prototypes and processes at the lab-scale.
 </li>
 <li>
 Develop Analytical methods as necessary for product testing and process development.
 </li>
 <li>
 Provide technical support for manufacturing, marketing, and regulatory as needed.
 </li>
 <li>
 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>
 <li>
 Experience with Polymer-based Biomaterials.
 </li>
 <li>
 Experience in Formulation of gels and emulsions.
 </li>
 <li>
 Knowledge of Hyaluronic Acid and/or Polysaccharide chemistry.
 </li>
 <li>
 Experience with Formulation of active ingredients in pharmaceutical applications.
 </li>
 <li>
 Experience with Chemical Synthesis, Analytical Chemistry methods, Physical/Rheological characterization, or Cell-based Biological assays.
 </li>
 <li>
 Experience with Quality System requirements for Class III Medical Devices.
 </li>
 </ul>
</div>

Scientist I

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