Associate Scientist III - Pharma R&D & Tech Transfer Lead

ARx Pharma

Glen Rock (York County)

On-site

USD 85,000 - 110,000

Full time

11 days ago

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Job summary

ARx Pharma is seeking a Scientist to assist in preparation, testing, and analysis of pharmaceutical products in a GMP environment. The role supports R&D during tech transfer and manufacturing of validation and clinical batches, leading scale-up activities and formulation development.

The candidate will develop new products from material selection to process optimization, conduct dissolution and physical tests, and prepare SOPs. Strong English communication and knowledge of cGMP are essential.

Qualifications

  • Master’s degree or PhD with relevant experience in pharmaceutical product development.
  • Experience with transdermal/topical/oral/buccal delivery systems is a plus.
  • Familiarity with regulatory requirements (cGMP, 21 CFR Part 211) and quality standards.

Responsibilities

  • Assist in preparation, testing, and analysis of pharmaceutical products.
  • Support R&D and operations during tech transfer and manufacture of validation/clinical batches.
  • Lead scale up activities and process development.
  • Develop new formulations from raw material selection to process optimization.
  • Prepare test samples and carry out physical testing and dissolution studies.
  • Author and review SOPs for equipment and processes.

Skills

English communication
Quick learner
Chemical analysis techniques
cGMP knowledge
Oracle ERP
Microsoft Office

Education

MSc in Pharmaceutical / Medical Sciences / Chemistry
PhD in pharmaceutical / biomedical sciences

Tools

Oracle ERP systems
Microsoft Office

Job description

ARx Pharma is seeking a Scientist to assist in preparation, testing, and analysis of pharmaceutical products in a GMP environment. The role supports R&D during tech transfer and manufacturing of validation and clinical batches, leading scale-up activities and formulation development.

The candidate will develop new products from material selection to process optimization, conduct dissolution and physical tests, and prepare SOPs. Strong English communication and knowledge of cGMP are essential.

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