pharmaceutical scientist

SOKOL GxP Services

<div><p>SOKOL GxP Services is seeking an Associate Scientist/Engineer to join our on-site team in Summit, NJ. This role is integral to supporting oral solid formulation studies, working hands-on in laboratory and pilot plant settings. You will collaborate with cross-functional teams and travel between Summit and New Brunswick sites as needed to access specialized equipment and facilities.<br>
<br>
Key responsibilities include:</p><ul><li>
Executing laboratory and pilot plant work to establish oral solid formulations;</li><li>
Designing and conducting experimental formulation studies;</li><li>
Performing material characterization and formulation testing;</li><li>
Developing and optimizing oral formulations using a design of experiments approach;</li><li>
Utilizing HPLC and dissolution testing techniques for oral formulations;</li><li>
Tracking and trending data for formulation development projects;</li><li>
Communicating effectively and transparently with peers and cross-functional partners;</li><li>
Traveling between NJ sites (Summit and New Brunswick) as required to access labs and equipment.</li></ul><br>
<b>
Requirements</b><br>
<br>
Required Qualifications:<ul><li>
Bachelor&rsquo;s degree in a science or engineering field;</li><li>
0&ndash;3 years of relevant experience in pharmaceutical formulation, laboratory, or pilot-plant work (internship experience acceptable);</li><li>
Hands-on experience performing HPLC and dissolution testing for oral formulations;</li><li>
Experience working in cGMP/FDA-regulated pharmaceutical manufacturing environments (internship experience acceptable);</li><li>
Ability to travel between Summit, NJ and New Brunswick, NJ sites as needed.</li></ul>
Preferred Qualifications:<ul><li>
Advanced degree in a science or engineering field;</li><li>
Experience with oral solid formulation development;</li><li>
Experience with material characterization techniques such as DSC and/or TGA;</li><li>
Experience using Design of Experiments (DoE) to design and optimize formulation studies;</li><li>
Data trending and statistical analysis skills.</li></ul><br>
<b>
Benefits</b><p><br>
Competitive hourly rate: <b>$28 &ndash; $35.56/hr (W-2 only, no C2C)</b>
</p><p>Working Hours: Monday - Friday, regular business hours</p><p>
8-month contract with possible extension
</p><p>Health insurance, holiday pay, 401(k) program, and other benefits</p><p>
Employee referral bonus program</p></div>

Assistant Scientist - Oral Solid Formulation

United Therapeutics

<div><div>California, US residents <div></div>.</div><div></div><div>
The job details are as follows:</div><div></div><div>
Who We Are</div><div></div><div>
We are the first publicly-traded biotech or pharmaceutical company to take the form of a public benefit corporation. Our public benefit purpose is to provide a brighter future for patients through the development of novel pharmaceutical therapies; and technologies that expand the availability of transplantable organs.</div><div><br>
United Therapeutics (Nasdaq: UTHR) seeks to travel down the corridors of indifference to develop treatments for rare, deadly diseases. We were founded in 1996 by a family seeking a cure for their daughter&rsquo;s pulmonary arterial hypertension (PAH). Today, we have six FDA-approved therapies that treat PAH, pulmonary hypertension associated with interstitial lung disease (PH-ILD) and neuroblastoma, a rare pediatric cancer. Our near-term pipeline seeks to develop additional therapies for PAH and pulmonary fibrosis (PF).</div><div><br>
The cure for end-stage life-threatening diseases like PAH, PH-ILD, PF, and many others is an organ transplant, but only a small percentage of donated organs are available to address the vast need. For this reason, we are working to create manufactured organs to address the shortage of kidneys, hearts, lungs, and livers available for transplant. We believe an unlimited supply of tolerable, transplantable organs will eliminate the transplant waiting list and cure end-stage organ diseases for which transplant is not currently an option.<br>
<br>
Who You Are</div><div>
As an Associate/Research Scientist, Analytical Chemistry, you&rsquo;ll be a critical scientific partner at the intersection of discovery, development, and scale‑up&mdash;helping transform complex chemistry into therapies that can change lives. In this role, you&rsquo;ll work side‑by‑side with synthetic chemists to develop and execute advanced analytical methods, generate high‑quality data, and solve real‑world challenges tied to route selection, impurity control, and process understanding. You&rsquo;ll bring clarity to complexity by interpreting chromatographic data, supporting tech transfer and GMP readiness, and ensuring analytical rigor from early research through manufacturing. If you enjoy being hands‑on in the lab, thinking deeply about data, and collaborating across teams to move innovative science forward, you&rsquo;ll find both purpose and momentum here</div><div></div><div>
The Associate/Research Scientist, Analytical Chemistry supports a team of synthetic chemists by developing and executing various analytical (LC, GC, SFC, KF etc.) methods to solve complex research problems such as route scouting, process understanding, scale-up and impurity isolation/purification. This role also partners with QC, and external vendors to develop robust analytical methods, generate high-quality data, to ensure analytical readiness for scale-up, tech transfer and GMP manufacturing.</div><ul><li>
Collaborate with synthetic chemists to support isolation and characterization of API, impurities, intermediates, and markers using preparative techniques such as prep‑HPLC and SFC while meeting assigned project timelines</li><li>
Execute established analytical methods for chromatographic techniques including LC, GC, and SFC using appropriate detection such as UV, ELSD, CAD, MS, and FID</li><li>
Trend and interpret chromatography data to provide actionable insights including reaction completion, chiral selectivity, impurity profiles, and purge trends, and communicate results clearly to synthetic chemists</li><li>
Analyze samples or materials from vendors according to established or transferred analytical procedures</li><li>
Operate, calibrate, and maintain laboratory instruments and associated computer systems by coordinating with groups such as IT and OT for basic troubleshooting</li><li>
Coordinate vendor service activities including preventive maintenance, repairs, and column selection, and assist with obtaining quotes or making purchases for columns, consumables, and chemicals</li><li>
Author and review technical documentation such as analytical reports, method SOPs, method development summaries, investigations, and data packages for method transfer</li><li>
Contribute to technical documentation such as development summaries, experiment records, method notes, and invention disclosures as needed</li><li>
Ensure data quality and adherence to internal policies and scientific standards</li><li>
Review data packages such as method development reports and protocols from other departments and vendors</li><li>
Utilize scientific literature to support execution of research assignment objectives</li><li>
Drive improvements in analytical throughput and lab efficiency</li><li>
Support safety practices, chemical hygiene, and waste management while applying principles of sustainability</li></ul><div></div><div>
Minimum Requirements</div><div>
Associate Research Scientist, Analytical Chemistry R&amp;D</div><ul><li>
5+ years of relevant chemistry experience in pharmaceutical industry with a Bachelor's degree or 3+ years of relevant chemistry experience in pharmaceutical industry with a Master's degree or 0+ years of relevant chemistry experience in pharmaceutical industry with a PhD</li><li>
Foundational understanding of chromatographic techniques (LC, GC, SFC) and associated detection technologies (UV, ELSD, CAD, MS, FID), sufficient to execute established analytical methods independently</li><li>
Ability to trend and interpret chromatography data to provide actionable insights (reaction completion, chiral selectivity, impurity profiles, purge trends) and communicate results clearly to synthetic chemists</li><li>
Ability to operate, calibrate and maintain various laboratory instruments and related computers by interacting with other departments IT/OT for basic troubleshooting</li><li>
Ability to coordinate vendor service activities (PM visits, repairs, column selection) and assist with obtaining quotes/purchase for columns, consumables, and chemicals</li><li>
Ability to contribute to technical documentation such as development summaries, experiment records, and method notes; contribute to invention disclosures as needed</li><li>
Ability to utilize scientific literature for accomplishing research assignment objectives</li></ul><div></div><div>
Preferred Qualifications</div><ul><li>
Ability to analyze materials from external vendors/CDMOs using transferred procedures; confirm compliance with method requirements and report deviations</li><li>
Ability to ensure data quality and adherence to internal policies and scientific standards</li><li>
Proficient with MS Office, ChemDraw, and SciFinder</li></ul><div></div><div>
Minimum Requirements</div><div>
Research Scientist, Analytical Chemistry R&amp;D</div><ul><li>
8+ years of relevant chemistry experience in pharmaceutical industry with a Bachelor's degree or 6+ years of relevant chemistry experience in pharmaceutical industry with a Master's degree or 2+ years of relevant chemistry experience in pharmaceutical industry with a PhD</li><li>
Experience in independently leading analytical investigations, hands-on experience with HPLC/UPLC/GC method development, troubleshooting and common sample prep techniques</li><li>
Working knowledge of LC&ndash;MS (TOF) for mass-based compound characterization</li><li>
Ability to interpret analytical data in the context of chemical process development</li><li>
Sound knowledge of chromatography software: Waters Empower, Agilent MassHunter, Thermo Scientific Chromeleon and Waters ChromScope</li><li>
Clear technical writing and data storytelling (chromatogram stacking, overlays, etc.)</li><li>
Comfortable in fast-paced R&amp;D environments with shifting priorities</li><li>
Experience with chiral analysis/method development (chiral HPLC and/or SFC) is highly preferred</li></ul><div></div><div>
Preferred Qualifications</div><ul><li>
Doctor of Philosophy (PhD) in chemistry or related discipline</li><li>
Sound knowledge of MS Office, ChemDraw, and SciFinder</li><li>
Experience supporting API process development (route scouting and kilo lab)</li><li>
Experience with CAD detectors and SFC</li><li>
Experience working with external CDMOs and reviewing vendor analytical packages</li><li>
Familiarity with KF, NMR, FTIR</li><li>
Familiarity with regulatory expectations for early to late-stage development (ICH concepts, specs setting and CMC support)</li></ul><div></div><div>
Job Location</div><div>
United Therapeutics requires this candidate to be 100% on-site at our Silver Spring, Maryland location.</div><div></div><div>
The salary range for the Associate Research Scientist position is $96,500 - $130,000 per year and the salary range for the Research Scientist is $111,000 - $150,000 per year. These ranges reflect our good-faith estimate of the compensation for this role at the time of posting. An employee&rsquo;s position within the salary range will be based on factors such as education, qualifications, experience, skills, geographic location, and business needs, as well as other factors permitted by law at the time of posting. This range may be modified in the future based on company and market factors.</div><div></div><div>
At United Therapeutics, our mission and vision are one. We use our enthusiasm, creativity, and persistence to innovate for the unmet medical needs of our patients and to benefit our other stakeholders. We are bold and unconventional. We have fun, we do good.</div><div></div><div>
Eligible employees may participate in the Company&rsquo;s comprehensive benefits suite of programs, including medical / dental / vision / prescription coverage, employee wellness resources, savings plans (401k and ESPP), paid time off &amp; paid parental leave benefits, disability benefits, and more. For additional information on Company benefits, please visit <div>https://www.unither.com/careers/benefits-and-amenities</div></div><div></div><div>
United Therapeutics Corporation is an Equal Opportunity Employer, including veterans and individuals with disabilities.</div></div><div></div>

Associate Research Scientist/Research Scientist, Analytical Chemistry R&D

ATCONNECTS

<p>Job Description: BioPharma Research Lead (Females Only)</p><p><b>Position Title:</b> BioPharma Research Lead<br/><b>Location:</b> Atconnects Head Office<br/><b>Industry:</b> B2B Event Management (Pharmaceutical/Biotech Focus)</p><p><b>About Us:</b></p><p>We are a B2B event management company specializing in organizing scientific conferences across Europe and the USA, exclusively working with international pharmaceutical and biotech companies. As pharma management consultants, we assist our clients in the drug development process by connecting them with decision-makers and deal-makers in the industry.</p><p>For information visit our website</p><p>Nexus-conference.com</p><p><b>Key Responsibilities:</b></p><ul><li><b>Conference Engagement:</b></li><li>Identify, research, and connect with international pharmaceutical and biotech dealmakers.</li><li>Persuade industry leaders and decision-makers to attend our conferences.</li><li>Build and maintain strong professional relationships with clients.</li><li><b>Client Research and Communication:</b></li><li>Conduct in-depth research on potential attendees, their areas of expertise, and market trends.</li><li>Effectively communicate our conference value propositions to clients.</li><li><b>Problem Solving:</b></li><li>Address client concerns or queries with a proactive and positive approach.</li><li>Collaborate with internal teams to resolve issues promptly and efficiently.</li><li><b>Learning and Growth:</b></li><li>Stay updated on industry developments, market trends, and competitor activities.</li><li>Leverage industry knowledge to add value to client interactions.</li><li><b>Goal-Oriented Execution:</b></li><li>Meet or exceed targets for conference attendance and client engagement.</li><li>Maximize opportunities to achieve bonuses and commissions under the structured incentive plan.</li></ul><p><b>Key Skills and Qualifications:</b></p><ul><li><b>Education:</b> Bachelor&rsquo;s degree in life sciences, healthcare, business administration, or a related field.</li><li><b>Experience:</b> Preferably 1-2 years in a similar role, though motivated fresh graduates with strong communication skills are encouraged to apply.</li><li><b>Communication Skills:</b> Excellent written and verbal English communication skills are essential.</li><li><b>Personality Traits:</b></li><li>Energetic and motivated with a hunger for learning.</li><li>Positive thinker and problem solver with a client-focused mindset.</li><li><b>Interpersonal Skills:</b> Strong ability to build rapport and maintain professional relationships.</li><li><b>Adaptability:</b> Ability to work in a dynamic, fast-paced environment.</li></ul><p><b>Why Join Us?</b></p><ul><li><b>Career Growth:</b> Opportunity to work with top-tier pharma and biotech companies on a global scale.</li><li><b>Exciting Incentives:</b> Lucrative bonus and commission structure.</li><li><b>Supportive Environment:</b> Stable career path with a positive and collaborative workplace culture.</li><li><b>Impactful Role:</b> Contribute to the drug development process by connecting industry leaders.</li></ul><p><b>Note:</b></p><p>This role is open exclusively for female candidates. We are NOT a call center or software house. We operate as trusted pharma management consultants.</p><p><b>Interview &amp; Joining Location:</b><br/>Interviews will be conducted at our Millat Road office. Selected candidates will join at our new office: <b>Plot 29A, Amir Town, East Canal Expressway, near Marhaba 2, Faisalabad.</b></p><p><b>Application Deadline: 23rd March 2026</b></p><p>Job Type: Full-time</p><p>Location:</p><ul><li>Faisalabad (Required)</li></ul><p>Work Location: In person</p><p>Application Deadline: 23/3/2026</p><p>Expected Start Date: 1/4/2026</p><p>Job Type: Full-time</p><p>Work Location: In person</p><p>Job Type: Full-time</p><p>Pay: Rs40,000.00 - Rs45,000.00 per month</p><p>Work Location: In person</p>

BioPharma Research Lead

Get Offers

<div>
 <ul>
  <li>
   <strong>
    Title:
   </strong>
   Mass Spectomery Scientist (Remote)
  </li>
  <li>
   <strong>
    Engagement:
   </strong>
   Hourly contract (independent contractor)
  </li>
  <li>
   <strong>
    Location:
   </strong>
   Remote
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  <li>
   <strong>
    Compensation:
   </strong>
   $100 &ndash; $300 per hour
  </li>
 </ul>
 <p>
  <br/>
 </p>
 <p>
  <br/>
 </p>
 <p>
  <strong>
   Job Summary
  </strong>
 </p>
 <p>
  Join our customer&rsquo;s innovative team as a
  <strong>
   Mass Spectrometry Scientist
  </strong>
  , where you will drive scientific discovery through advanced mass spectrometry techniques in a flexible remote setting. This role offers the opportunity to contribute deep analytical expertise in a collaborative environment while advancing high-impact research initiatives. You will translate complex analytical data into clear, actionable insights for multidisciplinary stakeholders.
 </p>
 <p>
  <br/>
 </p>
 <p>
  <strong>
   Key Responsibilities
  </strong>
 </p>
 <ul>
  <li>
   Develop, optimize, and validate mass spectrometry (MS) methods for qualitative and quantitative analysis of complex biological, chemical, or environmental samples.
  </li>
  <li>
   Operate, maintain, calibrate, and troubleshoot mass spectrometry instrumentation and associated laboratory systems.
  </li>
  <li>
   Perform rigorous data interpretation and statistical analysis to ensure scientific accuracy and reproducibility.
  </li>
  <li>
   Collaborate with R&amp;D, quality, regulatory, and cross-functional teams to support project objectives and timelines.
  </li>
  <li>
   Prepare detailed technical documentation, experimental protocols, validation reports, and scientific summaries.
  </li>
  <li>
   Stay current with advancements in MS technologies, ionization techniques, and analytical workflows.
  </li>
  <li>
   Present findings clearly through written reports, publications, and stakeholder presentations.
  </li>
 </ul>
 <p>
  <br/>
 </p>
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  <strong>
   Required Skills and Qualifications
  </strong>
 </p>
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  <li>
   Advanced hands-on expertise in mass spectrometry techniques (e.g., LC-MS/MS, GC-MS, MALDI-TOF, HRMS).
  </li>
  <li>
   Strong background in analytical method development, validation, and troubleshooting.
  </li>
  <li>
   Ability to interpret complex datasets with high scientific rigor.
  </li>
  <li>
   Proficiency in MS data processing and analysis software.
  </li>
  <li>
   Excellent written and verbal communication skills with strong attention to detail.
  </li>
  <li>
   Experience working collaboratively in multidisciplinary scientific environments.
  </li>
  <li>
   Ability to manage multiple priorities effectively in a remote work setting.
  </li>
  <li>
   MS or PhD in Chemistry, Biochemistry, Analytical Science, Pharmaceutical Sciences, or a related field.
  </li>
 </ul>
 <p>
  <br/>
 </p>
 <p>
  <strong>
   Preferred Qualifications
  </strong>
 </p>
 <ul>
  <li>
   Experience with industry-standard MS software (e.g., Xcalibur, MassLynx, Analyst, or similar platforms).
  </li>
  <li>
   Experience in regulated environments (GLP, GMP, ISO standards).
  </li>
  <li>
   Publication record or conference presentation experience.
  </li>
  <li>
   Background in pharmaceutical, biotech, proteomics, metabolomics, or environmental analysis applications.
  </li>
 </ul>
 <p>
  <br/>
 </p>
 <p>
  <strong>
   APPLY NOW !
  </strong>
 </p>
</div>


Mass Spectomery Scientist (Remote)

The Fountain Group

<div>
 <strong>
  Contractor - Research Analyst II - Global Material and Parenteral Packaging Sciences
  <br/>
  <br/>
 </strong>
 <strong>
  Pay: $39 per hour
  <br/>
  <br/>
  Duration:2 years
  <br/>
  <br/>
 </strong>
 The candidate will help drive the development of Container Closure Systems (CCS) for Client parenteral and biotechnological products (NBEs), supporting the advancement of some of Client's most strategic pipeline assets, including monoclonal antibodies, antibody-drug conjugates, and therapeutic toxins.
 <br/>
 <br/>
 In this role, you will leverage your expertise in characterizing CCS&mdash;encompassing vials, prefilled syringes, and prefilled cartridges&mdash;with a strong focus on Container Closure Integrity (CCI) and process capability. Your responsibilities will include conducting performance analyses using force analyzers, developing and validating analytical methods, providing technical support for CCS and process qualification in pharmaceutical manufacturing, and evaluating and implementing cutting-edge techniques.
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 <strong>
  Responsibility:
  <br/>
  <br/>
 </strong>
 <ul>
  <li>
   Preparation, execution and evaluation of experiments for development of container closure systems of new parenteral drug products, namely drug preparations of biotechnological drugs in vials, pre-filled syringes and cartridges as well as lyophilizates.
  </li>
  <li>
   Technical evaluation and implementation of CCI and process methods as well as continuous improvement based on a holistic CCI strategy and current regulatory requirements.
  </li>
  <li>
   Responsibility for maintaining lab equipment. Ensure required maintenance schedule, proper documentation, and training.
  </li>
  <li>
   Technical support of the landscaping programs for innovative CCS, including implementation and characterization based on various CCI techniques.
  </li>
  <li>
   Collaborations with Client partner labs and/or external labs and manufacturing sites.
  </li>
  <li>
   Coordination of suppliers for materials, equipment, and services needed to perform work.
  </li>
  <li>
   Documentation of all work according to applicable GxP and internal procedural requirements.
  </li>
  <li>
   Authoring comprehensive, scientifically sound reports, e.g. lab reports, development reports or risk assessments that could serve as source documents for authority submissions.
  </li>
  <li>
   Compliance with all relevant work safety requirements.
   <br/>
   <br/>
  </li>
 </ul>
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  Qualifications:
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 </strong>
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  <li>
   Degree from an accredited University in pharmacy/biology/biotechnology/chemistry/process engineering/material sciences/physics or related areas.
  </li>
  <li>
   Bachelor's Degree or equivalent education with typically 2 or more years of experience, or Master's Degree
  </li>
  <li>
   Good technical and scientific understanding of parenteral drug product development and CCI test methods.
  </li>
  <li>
   Understanding of relevant scientific literature and ability to apply theoretical framework to solving problems within their scientific discipline in a timely manner.
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   Ability to work concurrently on multiple projects, work in teams, and manage priority conflicts.
  </li>
  <li>
   Good verbal and written communication skills.
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  <li>
   Ability to establish comprehensive scientific and project related documentation.
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  <li>
   Strong motivation and proactive approach to lab responsibilities
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  </li>
 </ul>
 <strong>
  #ZIP
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 </strong>
</div>


Research Analyst II

izil Beauty

<div>
 <p>
  We are looking for a talented and analytical
  <strong>
   NPD Senior Scientist
  </strong>
  to join our growing team. As the NPD Senior Scientist, you will work with autonomy and be guided by the NPD manager to develop products, perform cost improvement projects, lead product troubleshooting, improve product performance and stability, and develop innovative products. The successful candidate will have in-depth knowledge of cosmetic formulations and product lifecycle knowledge, Microsoft tools and AI to assist in the product development phase, lab experiment tools (DOE), a deep understanding of project management, scale-up knowledge, and chemical understanding of raw materials and functions.
 </p>
 <p>
  <br/>
 </p>
 <p>
  <strong>
   Job Description:
  </strong>
 </p>
 <p>
  1. Lead formulation development activities with up-to-date knowledge of emerging market trends, diverse product aesthetics and textures, advanced technologies, and innovative cosmetic ingredients, ensuring compliance with Halal, COSMOS, and GSO regulations.
 </p>
 <p>
  2. Demonstrate strong formulation expertise and ingredient selection knowledge in accordance with Halal, COSMOS, and GSO guidelines, balancing performance, safety, sustainability, and cost.
 </p>
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  3. Formulate and develop cosmetic and personal care products across skincare, haircare, makeup, and toiletries, including research, evaluation, and selection of raw materials and actives based on efficacy, safety, and cost-effectiveness.
 </p>
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  4. Drive product innovation by supporting marketing claims, conducting product safety assessments, substantiating claims, developing differentiated concepts, and executing cost-effective formulation optimization and reformulation strategies.
 </p>
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  5. Possess in-depth knowledge of stability studies, product performance evaluation, consumer study and protocol preparation and compliance requirements under GSO cosmetic regulations.
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  6. Lead formulation scale-up activities from laboratory to pilot and full-scale manufacturing, ensuring product quality and consistency.
 </p>
 <p>
  <br/>
 </p>
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  <strong>
   Requirements:
  </strong>
 </p>
 <p>
  ● Bachelor's degree in chemistry, Cosmetics, Pharmaceutical, or a related area (to be evaluated during CV selection).
 </p>
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  ● A minimum of 6 to 8 years&rsquo; experience in a similar role in beauty care.
 </p>
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  ● Advanced knowledge in statistics and lab experiment methodologies (DOE).
 </p>
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  ● Good analytical view, verbal and written communication skills, discipline, and customer focus.
 </p>
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  ● Advanced knowledge in project management tools.
 </p>
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  ● Effective communication and teamwork skills.
 </p>
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  ● Advance understanding of Microsoft tools.
 </p>
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  ● Deep chemical understanding of products, raw materials, specifications
 </p>
</div>


NPD Senior Scientist

Julphar

<div></div><div><div><div><div><div><p>At Julphar, we are on a journey of culture transformation &amp; our mission is to provide a better quality of life for the entire family by delivering best in class solutions and real value with compassion and professionalism.</p>
<p>Our core values: Respect, Collaboration, innovation, Integrity and Compassion - Combined with a focus on diversity, inclusion, and equal opportunities - are key drivers in our aim to make a positive impact on the lives of the patients we serve, enable Talents , create a healthy work environment, and accomplish our goals through world-class research and with the compassion and commitment of our employees.</p>
<p><b>
Roles and Responsibilities</b></p><br>
<ul>
<li>Conduct literature surveys, patent searches, and prepare Prototype Formulation Reports.</li>
<li>Identify reference products and initiate procurement processes.</li>
<li>Develop <b>Quality Target Product Profiles (QTPP)</b> based on literature insights and reference product characterization.</li>
<li>Development of Injectable dosage forms; Biologics/Biosimilar products- upstream &amp; downstream, for regulated markets.</li>
<li>Identify and finalize API and excipient sources for new product development.</li>
<li>Perform and conclude pre-formulation and drug&ndash;excipient compatibility studies for assigned projects.</li>
<li>Contribute to product process optimization and reformulation activities, including report preparation and closure.</li>
<li>Prepare registration dossiers for submission and support <b>CTD/dossier documentation</b> requirements.</li>
<li>Plan, design, and execute pharmaceutical experiments using the <b>QbD (Quality by Design)</b> approach.</li>
<li>Review analytical development data and systematically compile product-related data.</li>
<li>Support manufacturing of batches for process optimization, submission, and bioequivalence (BE) studies.</li>
<li>Assist in pilot and scale-up batch manufacturing, with necessary documentation, and facilitate technology transfer to production.</li>
<li>Develop and maintain R&amp;D-related <b>SOPs</b> in compliance with cGMP and GDP principles.</li>
<li>Prepare and submit periodic project reports to management.</li>
<li>Collaborate cross-functionally with <b>Analytical R&amp;D, Supply Chain, Production, QC, QA, Regulatory Affairs, and Medical Affairs</b> to ensure timely project completion.</li>
<li>Handle Technology Transfer out/Contract Manufacturing activities for assigned projects</li>
<li>Experience in packaging development and life cycle management</li>
</ul>
<p><b>Qualification/Functional Knowledge</b></p>
<p><b>
Education: </b>Master&rsquo;s degree in Pharmacy/ Master&rsquo;s degree in Biotechnology</p>
<p><b>
Experience:</b></p>
<ul>
<li>Minimum 8 years of extensive experience of working in Formulation Development of Injectable dosage forms; Biologics/Biosimilar products- upstream &amp; downstream, for regulated markets.</li>
<li>Significant exposure in addressing regulatory queries for US-FDA, EU, Canada, UAE, KSA and other stringent regulatory markets.</li>
<li>Past experience of handling different dosage forms in R&amp;D i.e. injectables, Biosimilars, Biologics etc.</li></ul><p></p><p><br>
We value people from different backgrounds. Could this be your story? Apply today or visit www.Julphar.net to read more about us and the journey of Julphar</p></div></div></div></div></div><p></p>

Sr. Research Scientist 2

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