Formulation Development Associate Scientist

at  PHARMAGEND GLOBAL MEDICAL SERVICES PTE LTD

Singapore, Southeast, Singapore -

Start DateExpiry DateSalaryPosted OnExperienceSkillsTelecommuteSponsor Visa
Immediate06 Oct, 2024USD 8000 Monthly06 Jul, 2024N/ASoftware,Spectroscopy,Statistical Tools,Gmp,Jmp,Ema,Experimental Design,Analytical Techniques,Minitab,Regulatory Guidelines,Pharmaceutical Sciences,Chemistry,Chemical Engineering,Data AnalysisNoNo
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Description:

Job Summary:
We are seeking a highly motivated and skilled Laboratory Formulation Development Associate Scientist/Scientist to join our dynamic Technology Transfer team. The successful candidate will play a key role in the formulation and process development of pharmaceutical products, contributing to the innovation and improvement of drug delivery systems. This position involves hands-on laboratory work, including the design, development, and optimization of pharmaceutical formulations, as well as analytical method development and validation.

Key Responsibilities:

  • Design and develop innovative pharmaceutical formulations (solid, liquid, semi-solid, etc.) in accordance with project objectives and timelines.
  • Optimize and scale-up formulation processes from lab-scale to pilot and commercial-scale manufacturing.
  • Plan, execute, and analyze experiments to support formulation development and process optimization, ensuring reproducibility and robustness of results.
  • Prepare and review technical documents, including formulation protocols, batch records, development reports, and regulatory submission documents.
  • Work closely with cross-functional teams, including Analytical Development, Quality Assurance, Regulatory Affairs, Manufacturing, Engineering and Supply chain to ensure project success.
  • Ensure all laboratory activities comply with regulatory requirements, Good Laboratory Practices (GLP), and Good Manufacturing Practices (GMP).
  • Stay current with industry trends, scientific literature, and technological advancements to drive innovation in formulation development.
  • Troubleshoot and resolve technical issues related to formulation and process development.
  • Any other duties as assigned by supervisor.

Educations and qualifications:

  • Bachelor’s degree/ Master’s or Ph.D. in Pharmaceutical Sciences, Chemistry, Chemical Engineering, or related field.
  • 2- 5 years of experience in pharmaceutical formulation development or related field.

Technical Skills

  • Hands-on experience with formulation and process development for various dosage forms (e.g., tablets, capsules, injectables, topical formulations).
  • Proficiency in analytical techniques such as HPLC, GC, spectroscopy, and microscopy.
  • Familiarity with regulatory guidelines (e.g., FDA, EMA) and quality systems (e.g., GLP, GMP).
  • Prefer have experience with advanced drug delivery systems (e.g., nanoparticles, liposomes)
  • Prefer have knowledge of statistical tools and software for experimental design and data analysis (e.g., Design of Experiments (DOE), Minitab, JMP).
  • Previous experience in preparing regulatory submission documents (e.g., IND, NDA, ANDA).

Working Conditions:

  • This position involves working in a laboratory setting with potential exposure to chemicals and biological materials.
  • Must adhere to safety protocols and wear appropriate personal protective equipment (PPE).

How To Apply:

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Responsibilities:

  • Design and develop innovative pharmaceutical formulations (solid, liquid, semi-solid, etc.) in accordance with project objectives and timelines.
  • Optimize and scale-up formulation processes from lab-scale to pilot and commercial-scale manufacturing.
  • Plan, execute, and analyze experiments to support formulation development and process optimization, ensuring reproducibility and robustness of results.
  • Prepare and review technical documents, including formulation protocols, batch records, development reports, and regulatory submission documents.
  • Work closely with cross-functional teams, including Analytical Development, Quality Assurance, Regulatory Affairs, Manufacturing, Engineering and Supply chain to ensure project success.
  • Ensure all laboratory activities comply with regulatory requirements, Good Laboratory Practices (GLP), and Good Manufacturing Practices (GMP).
  • Stay current with industry trends, scientific literature, and technological advancements to drive innovation in formulation development.
  • Troubleshoot and resolve technical issues related to formulation and process development.
  • Any other duties as assigned by supervisor


REQUIREMENT SUMMARY

Min:N/AMax:5.0 year(s)

Pharmaceuticals

Pharma / Biotech / Healthcare / Medical / R&D

Clinical Pharmacy

Graduate

Chemical, Chemistry, Engineering

Proficient

1

Singapore, Singapore