Company Description: Synthena Pharmaceuticals is a science-driven biopharmaceutical company founded by internationally trained Vietnamese scientists and based in Hong Kong and Vietnam. The company focuses on advancing regenerative medicine by uncovering new molecular approaches to renewal and translating them into innovative therapies. Synthena is building a proprietary technology platform around polydeoxyribonucleotide (PDRN), an active ingredient used in tissue repair.
The organization is evolving toward a fully integrated biopharmaceutical company model, capable of developing, manufacturing, and commercializing active ingredients. Its therapeutic focus spans cardiovascular, musculoskeletal, gastrointestinal, neurological, and dermatological areas, offering talent the opportunity to contribute to impactful, cross-disciplinary research.
Role Description: This is a remote, contract role for an Analytical Chemist.
The Analytical
Chemist will perform routine and specialized chemical analyses on development and production samples, including method development, validation, and troubleshooting. Daily tasks include operating and maintaining laboratory equipment, preparing reagents and standards, documenting results in accordance with internal and regulatory requirements, and supporting quality control testing of active ingredients such as PDRN. The role also involves collaborating with research and development teams to interpret analytical data, optimize formulations, and improve manufacturing processes.
The Analytical
Chemist will contribute to technical reports, standard operating procedures, and continuous improvement initiatives while adhering to safety and good laboratory practice (GLP) standards.
Qualifications:
Candidates should possess strong Laboratory Skills, including sample preparation, handling of reagents, and adherence to GLP and safety protocols.
Candidates should possess robust Analytical Skills for method development, validation, data interpretation, and troubleshooting of chemical analyses.
Candidates should possess experience in Quality Control, including testing of raw materials and finished products, documentation, and compliance with relevant standards.
Candidates should possess proficiency with Laboratory Equipment such as HPLC, LC-MS, GC, UV-Vis spectrophotometers, and related analytical instruments.
Candidates should possess Research and Development (R&D) skills, including experimental design, problem-solving in a pharmaceutical context, and collaboration with cross-functional teams.
Bachelor's or Master's degree in Chemistry, Analytical Chemistry, Pharmaceutical Sciences, or a related field.
Familiarity with regulatory environments (e.g., ICH guidelines, GMP/GLP) and preparation of technical reports and documentation.
Strong written and verbal communication skills, attention to detail, and the ability to work independently in a remote setting.
Experience in biopharmaceuticals, regenerative medicine, or nucleic acid-based therapies is beneficial.
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