Formulation Scientist at Ajulia Executive Search
Rock Hill, SC 29730, USA -
Full Time


Start Date

Immediate

Expiry Date

19 Oct, 25

Salary

110000.0

Posted On

20 Jul, 25

Experience

0 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

No

Skills

Manufacturing Processes, Drug Discovery, Regulatory Requirements, Root, Technology Transfer, Raw Materials, Microsoft Office, Biochemistry, Chemistry, Biotechnology, Communication Skills, Design Techniques, Training, Regulatory Documentation

Industry

Pharmaceuticals

Description

FORMULATION SCIENTIST

(Pharmaceutical Manufacturing Industry)

  • Previous work experience in formulation development department with good experience in formulation development, process development.
  • Previous work experience in formulation technology and development in dietary supplements, nutraceuticals, or medical foods.
  • Collaborate with Product Development (PD) staff to plan and execute pilot and scale-up batches.

Are you looking to make a career change to a stable company? This exciting opportunity offers a competitive salary plus an excellent benefits package including medical insurance, dental insurance, vision insurance and paid PTO.Does this position match your future career goals? Then this opportunity could be the right fit for you.

Responsibilities
  • Bachelor’s degree in Chemistry ,Biochemistry, Biotechnology or related field.
  • Previous 3 plus years of in a pharmaceutical manufacturing industry.
  • Formulation/process development
  • Collaborate with Product Development (PD) staff to plan and execute pilot and scale-up batches.
  • Collect and analyze in-process data to support manufacturing parameters and final product specifications.
  • Provide technical support during initial production runs of new and reformulated products.
  • Formulation/process development, commercial support, and/or technology transfer.
  • Comply with GMP’s, SOP’s and all regulatory documentation.
  • Understanding of pharmaceutical manufacturing concepts. Knowledge of pharmaceutical GMPs and regulatory requirements.
  • Perform root cause analysis to troubleshoot formulation issues and ensure compliance with FDA regulations and GMP standards.
  • Collaborate with cross-functional teams in drug discovery and manufacturing processes.
  • Follow applicable cGMP processes.
  • Provide training to manufacturing associates on new processes and process modifications/improvements.
  • Assist in developing new formulations for new active raw materials.
  • Compile and provide summaries of stability data.
  • Possesses applied knowledge of root cause analysis and troubleshooting techniques. Able to apply statistical analyses and experimental design techniques.
  • Must have knowledge of cGMPs, Quality Concepts, and Microsoft Office.
  • Excellent written and verbal communication skills.
  • Proficiency in MS Office.
  • Strong attention to detail.
    Job Type: Full-time
    Pay: $100,000.00 - $110,000.00 per year
    Work Location: In perso
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