Senior Scientist, Preclinical Sterile Biologics Formulation

Merck; Rahway (NJ); Sur place; USD 117 000 - 184 000; Plein temps

Avantages offerts par ce poste

Medical Insurance

Dental Insurance

Vision Insurance

401(k)

Résumé du poste

Merck in Rahway, NJ is seeking a lab-based scientist to design and develop sterile drug products for biologics, including injectables and ophthalmic formulations. You will support both early and late-stage assets, build mechanistic insight into degradation and process space, and document results for regulatory filings.

Responsibilities include developing robust drug product compositions, scalable processing, and primary packaging concepts while leading formulation development activities and

Qualifications

• Masters or Ph.D. in a relevant field for sterile product development (chemistry/biochemistry/biomedical engineering).
• Experience with formulation development, stability, and process understanding is preferred.
• Strong analytical and communication skills with a collaborative mindset.

Responsabilités

• Design and develop sterile products for biologics across injectable and ophthalmic routes.
• Support early and late-stage assets; build mechanistic understanding of degradation and process space.
• Document findings in formulation development reports and regulatory filings; lead cross-functional teams.

Connaissances

Biochemisty

Bioconjugation

Biologics

Biomolecular Chemistry

Bioprocessing

Design of Experiments (DOE)

Drug Delivery Technology

Drug Formulations

Medicinal Chemistry

Molecular Biology Techniques

Preclinical Research

Process Optimization

Formation

Masters with four years or Ph.D. Degree in Chemical/ Biochemical/ Biomedical Engineering, Pharmaceutics, Pharmaceutical Chemistry, Pharmaceutical Sciences, Chemistry, Biochemistry or related field

Description du poste

Merck in Rahway, NJ is seeking a lab-based scientist to design and develop sterile drug products for biologics, including injectables and ophthalmic formulations. You will support both early and late-stage assets, build mechanistic insight into degradation and process space, and document results for regulatory filings.

Responsibilities include developing robust drug product compositions, scalable processing, and primary packaging concepts while leading formulation development activities and