pharmaceutical scientist

Ashland

<div>Ashland India Private Ltd
Role: Scientist II
Are you the kind of person who is always thinking, sketching, seeking, and adjusting? Who needs to understand how things work and then figure out how they can work better? Are you a passionate, tenacious solver who loves to work with others who share your drive? Are you positive, constructive, and ingenious?
Are you always solving?
Then we&rsquo;d like to meet you and bet you&rsquo;d like to meet us. 
 
Ashland has an exciting opportunity for a Scientist II to join our Pharma LAB &ndash; R&amp;D Team at our Hyderabad LAB office. This is a very visible, significant role within the Company and the Research &amp; Development function. This position will report to the Team Leader - Pharma R&amp;D . 
 
Area of Responsibility (business specifics):
<ul><li>Comply with company procedural guidelines, laboratory procedures, and safety programs.
</li><li>Provides technical and application development support to sales colleagues and pharmaceutical industry customers.
</li><li>Work with senior technical team in providing technical expertise regarding the development of pharmaceutical products.
</li><li>Designing, initiating and executing studies, and interpreting the study results
</li><li>Assimilating and analyzing data into reports, posters, and journal articles.
</li><li>Preparing technical presentations for internal and external customers at customer sites, scientific conferences and trade shows.
</li><li>Ability to handle multiple projects and work in high pressure environment.
</li><li>Maintaining lab notebooks and logbooks in accordance with company guidelines
</li></ul>Desired Candidate Skills/Experience:
<ul><li>Fundamental understanding on product development of solid dosage forms, injectables and polymer-based drug-delivery systems
</li><li>Proficient in technical understanding of customer end-use application.
</li><li>Hands-on experience with solubilization technologies such as spray drying and hot-melt extrusion.
</li><li>Hands-on experience with solid-oral pharmaceutical unit operations such as wet and dry granulation, tableting, tablet coating and fluid-bed processing/coating.
</li><li>Hands-on experience in formulation development of injectable dosage forms - PFS, Injections, depot injections and handling of machinery/equipment related to parenteral dosage forms.
</li><li>Working knowledge on formulation characterization and related analytical techniques
</li><li>Working knowledge of Design of Experiments (DOE), Microsoft Office Suite, and statistical analysis.
</li><li>Ability to organize and maintain lab area in a safe professional manner.
</li><li>Understanding of safety, housekeeping and good lab practices and good documentation practices.
</li><li>Strong written and oral presentation skills
</li><li>Strong organizational and problem-solving skills
</li><li>Time management
</li><li>Teamwork/interpersonal skill.
</li></ul>In more than 100 countries, the people of Ashland LLC. (NYSE: ASH) provide the specialty chemicals, technologies and insights to help customers create new and improved products for today and sustainable solutions for tomorrow. Our chemistry is at work every day in a wide variety of markets and applications, including architectural coatings, automotive, construction, energy, personal care and pharmaceutical. Visit www.ashland.com to see the innovations we offer.
 
 
At Ashland our vision is to be a leading, global specialty chemicals company whose inspired and engaged employees add value to all we touch. In fact our people, employees, customers and vendors define who we are. They are the driving force behind everything we do.
 
 
Not only do we value our customers but we value our employees, and we work to offer them a dynamic and challenging environment. We hold ourselves to high standards at Ashland, and we value integrity and honesty.
 
 
Ashland has a history of attracting the best people and keeping them. The reasons are simple: industry competitive salary and benefits, pay-for-performance incentive plans and a diverse work environment where employees feel challenged and valued. People come to Ashland and stay. As a growing Fortune 500 specialty chemicals company, we offer opportunities for development and advancement throughout our global organization. Our values define who we are and what we care about as a company. If you are looking for a relationship with a company instead of simply a job, this may be a great fit.
Ashland is proud to be an Equal Opportunity Employer Minorities/Women/Veterans/Disabled/Gender Identity/Sexual Orientation.
All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, gender identity, sexual orientation, national origin, or protected veteran status and will not be discriminated against on the basis of disability. NOTE: We do not accept resumes from external staffing agencies or independent recruiters for any of our openings unless we have a signed recruiting agreement in place to fill a specific position.</div>

SCIENTIST II - IND

Net2Source (N2S)

<div>
 
 Net2Source Inc. is an award-winning total workforce solutions company recognized by Staffing Industry Analysts for our accelerated growth of 300% in the last 3 years with over 5500+ employees globally, with over 30+ locations in the US and global operations in 32 countries. We believe in providing staffing solutions to address the current talent gap &ndash; Right Talent &ndash; Right Time &ndash; Right Place &ndash; Right Price and acting as a Career Coach to our consultants.
 
 
 
 
 Company: One of Our Clients
 
 
 
 
 
 
 
 
 
 
 Job Description:
 
 
 
 
 
 Title: Downstream Purification Scientist
 
 
 
 
 Duration: 12 months (Extendable)
 
 
 
 
 Location: Boston, MA 02210
 
 
 
 
 Pay Rate: $42.00-$45.40/hr on W2
 
 
 
 
 
 
 
 Description:
 
 
 
 We are seeking a highly motivated Contractor &ndash; Purification Scientist to join our Downstream Process Development team. The successful candidate will contribute to the purification and characterization of viral vectors, biologics, or recombinant proteins to support process development and manufacturing activities. The ideal candidate has hands-on experience in Cesium chloride (CsCl) density gradient ultracentrifugation, ion-exchange chromatography, affinity purification, and tangential flow filtration (TFF), with a strong understanding of purification principles and data analysis.
 
 
 
 
 
 
 Key Responsibilities
 
 
 
 &bull; Execute purification processes including CsCl density gradient ultracentrifugation, affinity chromatography (e.g., AVB, CaptureSelect), ion-exchange chromatography (AEX, CEX), and other polishing steps.
 
 
 &bull; Operate AKTA systems (Avant, Pure, or Pilot) for small- to large-scale purification runs.
 
 
 &bull; Perform TFF operations for buffer exchange and concentration of intermediate or final products.
 
 
 &bull; Support experimental design, data collection, and documentation following established procedures and GMP/GLP best practices.
 
 
 &bull; Assist in troubleshooting and optimization of purification processes.
 
 
 &bull; Analyze in-process and purified samples using relevant analytical methods (e.g., UV, SDS-PAGE, ddPCR, ELISA, or HPLC).
 
 
 &bull; Collaborate cross-functionally with upstream, analytical, and manufacturing teams.
 
 
 &bull; Maintain lab equipment, manage buffers and column inventory, and ensure compliance with safety and documentation standards.
 
 
 
 
 
 
 Qualifications
 
 
 
 &bull; Education: Master&rsquo;s degree in biology, biochemistry, chemical engineering, biotechnology, or related field.
 
 
 &bull; Experience: Minimum 2 years of hands-on purification experience in an academic or industry setting.
 
 
 
 
 
 
 Technical Skills:
 
 
 
 o Strong knowledge and practical experience with CsCl density gradient ultracentrifugation, ion-exchange, and affinity chromatography.
 
 
 o Familiarity with buffer preparation.
 
 
 o Understanding of basic analytical methods for product characterization.
 
 
 
 
 
 
 &bull; Soft Skills:
 
 
 
 o Strong attention to detail and excellent documentation habits.
 
 
 o Effective communication and teamwork skills.
 
 
 o Ability to manage multiple tasks and meet project timelines.
 
 
 
 
 
 
 Preferred Qualifications
 
 
 
 &bull; Experience in AAV or other viral vector CsCl density gradient and column purification.
 
 
 &bull; Experience with AKTA systems and Unicorn software.
 
 
 
 
 
 
 
 
 
 Regards,
 
 
 
 
 Prateek Pampattiwar
 
 
 
 
 Recruitment Specialist
 
 
 
 
 Net2Source Inc.
 
 
 
 
 Global HQ Address &ndash;270 Davidson Ave, Suite 704, Somerset, NJ 08873, USA
 
 
 
 
 Office: (201) 340-8700 x 324 | Cell: (551) 220 3007| Fax: (201) 221-8131| Email: Pampattiwar.Prateek@net2source.com
 
 
</div>

purification Scientist

Hikma

<div><div><div><div><div><div><div>Description:
<div>Job Summary:</div>
<div>
Operate more than one machine while ensuring compliance with the set guidelines to meet production targets. Jobs at this level also assist quality and plant management in investigations and prepare incident reports when the need rises. They also communicate internally with other departments such as quality and engineering and externally with technicians to ensure the progression of work and compliance with SOPs and GMPs.</div> 
<div></div>
<div>
Duties &amp; Responsibilities:</div>
<ul>
<li>Follows all relevant Manufacturing policies, processes and standard operating procedures so that work is carried out in a controlled and consistent manner.</li>
<li>Implements the day-to-day operations assigned for the function to ensure compliance with the established standards and procedures.</li>
<li>Supervises the day-to-day operations of line or machine to ensure that work processes are implemented as designed and in compliance with established standards and procedures.</li>
<li>Operates more than one machine while ensuring compliance with the set guidelines to meet production targets.</li>
<li>Coaches and trains lower level jobs on simple tasks to ensure compliance with set guidelines and SOPs.</li>
<li>Assists quality and plant management in investigations and prepares incident reports when the need rises.</li>
<li>Documents SAP and paper systems pertaining to manufacturing orders (MOs) and packaging standards (PSs) to ensure accurate and up-to-date information.</li>
<li>Troubleshoots and investigates more complex manufacturing issues, incidents and reliability problems on the production line to ensure continuity of operations.</li>
<li>Communicates internally with other departments such as quality and engineering to ensure the progression of work and compliance with SOPs and GMPs.</li>
<li>Complies with all relevant safety, quality, health and environmental procedures to ensure a healthy and safe work environment.</li></ul> 
<div></div>
<div>
Qualifications:</div>
<ul>
<li>B. Sc. in Pharmacy.</li>
<li>1-3 years of experience in a similar position.</li>
<li>Pharmaceutical manufacturing experience is required.</li>
<li>Strong Leadership, Planning and Organization capabilities</li>
<li>Very good command of English (spoken &amp; written)</li>
</ul></div></div></div></div><div><div><div><div>Location:
Giza, EG</div></div></div></div></div></div></div>

Production Pharmacist

Aria Systems India Pvt Ltd

<ul><li>Pharmaceutical &amp; Chemical Industry: Roles include Production Chemist, Quality Control (QC) Analyst, Analytical Chemist, and Drug Formulation Chemist.</li><li>Research &amp; Development (R&amp;D): Positions as Research Scientist or Lab Assistant in private firms or top government institutions like CSIR, DRDO, and BARC.</li><li>Quality Control &amp; Assurance: Ensuring product safety and regulatory compliance in food, beverages, cosmetics, and manufacturing industries.</li><li>Forensic &amp; Environmental Science: Working as a Forensic Scientist in crime labs or as a Toxicologist analyzing environmental samples.</li><li>Academia &amp; Education: Chemistry tutor, teacher, or lecturer (following NET/SET qualification).</li><li>Other Roles: Clinical Research Associate, Medical Coder, and Scientific Data Entry Specialist.</li></ul>Job Types: Full-time, Permanent, FresherPay: ₹18,086.00 - ₹32,445.44 per monthBenefits:<ul><li>Health insurance</li><li>Paid sick time</li><li>Paid time off</li><li>Provident Fund</li></ul>Work Location: In person

Bsc chemistry freshers

Robert Walters

<div>
 
 
 Job Title: AVP &ndash; Medicinal Chemistry
 
 
 
 
 Location: Hyderabad, India
 
 
 
 
 Perm/Contract/ Full-time/Part-time: Permanent
 
 
 
 
 On-site/Hybrid/Remote: On-site
 
 
 
 
 
 
 
 Who We Are
 
 
 
 Robert Walters is the world&rsquo;s most trusted talent solutions business. Across the globe, we deliver recruitment, outsourcing, and talent advisory services for businesses of all sizes, opening doors for people with diverse skills, ambitions, and backgrounds.
 
 
 
 
 
 Our Outsourcing service delivers recruitment for some of the world&rsquo;s top employers, and we are currently recruiting on behalf of one our client which is a biotechnology company that is learning from life&rsquo;s chemistry to create better medicines faster. It uses AI-powered tools to identify and characterize a wide range of molecules produced by living organisms&mdash;the vast majority of which have never been explored by science&mdash;creating a database of chemical biodiversity: the library of life. By growing, organizing, translating, and searching this unique library, it learns from life&rsquo;s evolved solutions to address today&rsquo;s pressing medical needs.
 
 
 
 
 
 
 The Role
 
 
 
 Our client is seeking a
 
 AVP - Medicinal Chemistry
 
 in the
 
 Pharmaceutical
 
 division.
 
 
 This role offers an exciting opportunity to join a global team, providing top-tier service to existing and prospective clients while expanding the business on a product and global level.
 
 
 
 
 
 The successful candidate will be responsible for acquiring new clients, managing existing relationships, and contributing to the company's mission of becoming a Top Clearer worldwide in commodity markets.
 
 
 
 
 
 
 Main purpose of the role:
 
 
 
 Asst. Vice President, Medicinal Chemistry with a demonstrated track record of delivery of hits, leads and clinical candidates for advancing them into human clinical trials. You will recruit PhD and M. Sc. synthetic chemists and mentor them as medicinal chemists and manage their performance and improve their productivity. You will collaborate with your peers in Medicinal Chemistry and work as a team to increase delivery of compounds to the Clinical Pipeline. You will also collaborate with Senior Leaders in other functional departments such as ADME, Analytical Sciences and Pharmacology and deliver high value molecules.
 
 
 
 
 
 
 You get to collaborate on
 
 
 <ul>
 <li>
 Medicinal Chemistry of Lead Generation and Lead Optimization of Pipeline Projects.
 </li>
 <li>
 Understand Structure Activity Relationships and Structure Property Relationships of various projects.
 </li>
 <li>
 Collaborate with Medicinal Chemistry, Pharmacology, Analytical, ADME and Site Leadership.
 </li>
 <li>
 Develop appropriate flow schemes of relevant in vitro and in vivo assays.
 </li>
 <li>
 Appropriate allocation of resources for maximum cost effectiveness.
 </li>
 <li>
 Work effectively with Project Management.
 </li>
 <li>
 You work with the site safety head and emphasize the importance of safe practices in the chemistry laboratories.
 </li>
 </ul>
 
 
 
 
 
 Who will thrive in this role?
 
 
 <ul>
 <li>
 Doctor of Philosophy in Synthetic Organic Chemistry.
 </li>
 <li>
 15-20 years of post-PhD experience in Medicinal Chemistry.
 </li>
 <li>
 Proven track record of delivery of hits, leads and clinical candidates to the pharmaceutical industry.
 </li>
 <li>
 Management and mentoring of synthetic chemists.
 </li>
 <li>
 Good understanding of intellectual property of medicinally valuable compounds with respect to composition of matter, method of use and chemical processes.
 </li>
 <li>
 Strong understanding of safety practices in organic synthesis laboratories.
 </li>
 </ul>
 
 
 
 
 This position is being recruited on behalf of our client through our Outsourcing service line. Resource Solutions Limited, trading as Robert Walters, acts as an employment business and agency, partnering with top organisations to help them find the best talent. We welcome applications from all candidates and are committed to providing equal opportunities.
 
 
 
 
 
 Client promotes collaboration and aims to provide a supportive and inclusive environment where all individuals can maximize their full potential.
 
 
 
 
 
 
 As we are continuously hiring for all our clients in the region, we will retain your CV in our database for any other positions that may fit your profile. Therefore, please let us know if you are not agreeable to that.
 
 
</div>

AVP - Medicinal Chemistry

SPECTRAFORCE

<div>
 
 
 Job title: Scientist I
 
 
 
 
 Location: Cambridge, MA 02141
 
 
 
 
 Duration: 1 year
 
 
 
 Work Schedule
 
 
 
 
 
 Generally, Monday to Friday 8 to 5 EST (slight flexibility in hours), potential weekends (max 40 hrs)
 
 
 
 
 
 
 HM Notes:
 
 
 
 Local candidates only
 
 
 Paid parking is required, it will be off site at the Museum of Science or Cambridge mall - Orange and green line subways
 
 
 No extension currently - References will be required for top candidates
 
 
 
 Must have experience: -
 
 
 
 Master&rsquo;s Degree plus a minimum of 2+ years of relevant research experience in a biopharmaceutical setting OR a bachelor&rsquo;s degree plus a minimum of 3 to 5 years of relevant research experience in a biopharmaceutical setting.
 
 
 In vivo pharmacology background, is a must-have - General dosing skills, sub, intranasal - Blood collection techniques, tissue collection - This role, dedication to COPD studies (4 hours per day) - Routing dosing
 
 
 
 Nice to have:
 
 - COPD studies - Experience with asthma, fibrosis, atopic dermatitis
 
 
 
 
 
 
 Description:
 
 
 
 &bull; Responsible for designing and performing in-vivo pharmacology experiments in support of project team goals. This includes study design, data collection and recording, communication of results, and report writing.
 
 
 &bull; Summarize and present study data to project teams within established timelines.
 
 
 &bull; Responsible for performing cigarette smoke induced COPD studies.
 
 
 &bull; Capacity to use established procedures and methodologies with the ability to transform novel approaches into routine practice.
 
 
 &bull; Must be a technical contributor.
 
 
 &bull; Ability to troubleshoot experiments.
 
 
 &bull; Support the development of disease relevant in-vivo models.
 
 
 &bull; Must be well organized and detail oriented.
 
 
 &bull; Must have meticulous record keeping skills according to Sanofi quality guidelines. Maintain a thorough and compliant laboratory notebook.
 
 
 &bull; Must adhere to all federal, local, and Sanofi animal welfare guidelines.
 
 
 &bull; Must be capable of working alone and in a team environment.
 
 
 
 
 
 
 Qualifications:
 
 
 
 &bull; Experience with in-vivo immunology models. Previous experience with models of respiratory disease, dermatitis models, and smoke-induced COPD models is a plus.
 
 
 &bull; Ability to apply technical skills to complete assigned work as a competent technical contributor.
 
 
 &bull; Ability to design and perform in-vivo pharmacology experiments.
 
 
 &bull; Experience in various dosing methods, blood collection techniques, and tissue harvest are required.
 
 
 &bull; Experience with compound or reagent preparation.
 
 
 &bull; Ability to work under moderate supervision with regular review of results and methods utilized.
 
 
 &bull; Ability to present study related results to project teams.
 
 
 &bull; Proven ability to work in a dynamic, customer-focused and results-oriented environment.
 
 
 
 
 
 
 Education and Experience:
 
 
 
 Master&rsquo;s Degree plus a minimum of 2 years of relevant research experience in a biopharmaceutical setting OR a Bachelor&rsquo;s Degree plus a minimum of 3 to 5 years of relevant research experience in a biopharmaceutical setting.
 
</div>

In-Vivo Pharmacology Scientist

Tabula Bioscience, Inc

About the role We&rsquo;re seeking a hands-on Scientist to support a fast-moving microbiology and molecular biology R&amp;D program focused on bacteriophages and gram-negative bacteria (including E. coli and Pseudomonas).What you'll doYou'll collaborate with the R&amp;D team to design and execute experiments related to our phage engineering. You will also work closely with our machine learning team to incorporate those results into the models we build.Core Responsibilities<ul><li>Design phage library assembly protocols for different phages in our bank and improve existing protocols</li><li>Analyze NGS data from our phage/bacteria screening</li><li>Perform routine molecular biology workflows, including PCR, agarose gels, basic molecular cloning, and DNA/RNA handling.</li><li>Conduct bacterial culture work with BSL-2 gram-negative organisms: picking colonies, streaking, culturing, preparing samples, and maintaining strain stocks.</li><li>Maintain excellent documentation in an R&amp;D environment (lab notebooking; Benchling experience is a plus).</li></ul>Required qualifications<ul><li>PhD in Microbiology, Virology, Molecular Biology, Bioengineering or a related field. Post-doctoral experience is a strong asset.</li><li>Experience with phage engineering or other relevant lab experience in either an industry or hands-on academic environment</li><li>Demonstrated track record of scientific productivity and publications</li><li>Familiarity with NGS techniques and bioinformatics analysis</li><li>Ability to work on-site in a BSL-2 lab and complete required safety training.</li></ul>About Tabula BioscienceTabula is developing a new class of phage therapies to address antibiotic resistant infections. We are a team of phage, machine learning, and genomics researchers from UW Madison, MIT, and Harvard.Pay: $75,000.00 - $100,000.00 per yearBenefits:<ul><li>401(k)</li><li>Dental insurance</li><li>Health insurance</li><li>Life insurance</li><li>Paid time off</li><li>Vision insurance</li></ul>Work Location: In person

Scientist I/II - Phage & Bacterial R&D

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