Senior Scientist

Merck & Co., Inc.

Rahway, NJ, USA
Base: $117,000.00 - $184,200.00; bonus/equity: ann...
Hybrid (3 days onsite, 1 day remote)
Phd in molecular biology or related field
Hands-on experience with mammalian cell culture
Expertise in molecular subcloning and vector design
Merck & Co., Inc. is seeking a Senior Scientist for their Process Cell Sciences team in Rahway, NJ, to develop and characterize mammalian production cell lines for biologics. The ideal candidate will have a strong background in molecular biology and cell line development, and possess excellent communication skills. This hybrid position offers competitive benefits and a supportive work environment

Job Summary

  • The role involves developing and characterizing mammalian production cell lines to support the company's innovative biologics pipeline.
  • Candidates will work independently on complex experimental protocols while serving as a technical lead on project teams.
  • The position offers a competitive salary range, annual bonuses, long-term incentives, and a comprehensive benefits package including medical and retirement plans.

Matching Summary

Match Score: 85

Merck & Co., Inc. is seeking a Senior Scientist for their Process Cell Sciences team in Rahway, NJ, to develop and characterize mammalian production cell lines for biologics. The ideal candidate will have a strong background in molecular biology and cell line development, and possess excellent communication skills. This hybrid position offers competitive benefits and a supportive work environment.

Salary

Base: $117,000.00 - $184,200.00; Bonus/Equity: Annual bonus and long-term incentive eligible; Benefits: Medical, dental, vision, 401(k), paid holidays, vacation

Skills & Requirements

Must-have

  • PhD in Molecular Biology or related field
  • Hands-on experience with mammalian cell culture
  • Expertise in molecular subcloning and vector design
  • Experience designing synthetic genetic circuits
  • Proficiency in integrating systems biology models

Nice-to-have

  • Experience with regulatory filing documentation
  • Knowledge of genomics and transcriptomics
  • Familiarity with genome editing technologies
  • Expertise in database software like JMP or Spotfire
  • Strong technical writing and communication skills

Key Requirements

  • PhD with 0-2 years industry experience OR MS with 4+ years OR BS with 7+ years
  • US and Puerto Rico residents only
  • Visa sponsorship available

Work Rights

US and Puerto Rico Residents Only

Sponsorship: available

Tailored Resume

Cover Letter