Experienced Scientist, Upstream Development

At Johnson & Johnsonwe believe health is everything. Our strength in healthcare innovation empowers us to build aworld where complex diseases are prevented treated and curedwhere treatments are smarter and less invasive andsolutions are our expertise in Innovative Medicine and MedTech we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow and profoundly impact health for more at

Job Function :

Discovery & Pre-Clinical / Clinical Development

Job Sub Function : Biotherapeutics R&D

Job Category :

Scientific / Technology

All Job Posting Locations :

Malvern Pennsylvania United States of America

Job Description :

About Innovative Medicine

Our expertise in Innovative Medicine is informed and inspired by patients whose insights fuel our science-based advancements. Visionaries like you work on teams that save lives by developing the medicines of tomorrow.

Join us in developing treatments finding cures and pioneering the path from lab to life while championing patients every step of the way.

Learn more at & Johnson Innovative Medicine R&D is recruiting for an Experienced Scientist Upstream Development. This position is a hybrid role and will be located in Malvern PA.

The Experienced Scientist Upstream Development will contribute to upstream process development within the therapeutic protein process development group. This individual will be responsible for performing upstream process development studies.

Additional Responsibilities :

Participate in design of experiments.

Perform routine upstream laboratory operations to support execution of mammalian bioprocess experiments.

Record and analyze data.

Participate in scientific investigations and trouble-shoot process issues that arise during development technology transfer or scale-up.

Participate in control strategy development.

Participate in tech transfer facility fit and process scale up / scale down.

Author technical reports and contribute to regulatory filings

Work effectively in a team environment as well as contributing individually to meet project objectives and timelines.

Other duties will be assigned as necessary.

Qualifications :

A minimum of a Bachelors degree in Chemical Engineering or Biological Sciences or Biochemistry or a related discipline field is required. Masters degree in Chemical Engineering or Biological Sciences or Biochemistry or related discipline is preferred.

A minimum of 3 years of relevant industry experience with a Bachelors degree or a Masters degree (0-2 years of relevant industry experience) is required.

Knowledge of and hands-on experience performing large molecule drug substance (API) upstream manufacturing process development is required.

Experience in maintaining written records of work in the form of laboratory notebooks (paper or electronic) is required.

Experience with team-based collaborations and direct management of daily laboratory responsibilities is required.

Must have excellent written and verbal communication and interpersonal skills.

Must be highly organized with acute attention to details.

The ability to manage / pursue multiple projects with some supervision is required.

The ability to report data present findings to management is required

This position will require occasional weekend work.

Johnson & Johnson is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race color religion sex sexual orientation gender identity age national origin disability protected veteran status or other characteristics protected by federal state or local law. We actively seek qualified candidates who are protected veterans and individuals with disabilities as defined under VEVRAA and Section 503 of the Rehabilitation Act.

Johnson and Johnson is committed to providing an interview process that is inclusive of our applicants needs. If you are an individual with a disability and would like to request an accommodation please email the Employee Health Support Center () or contact AskGS to be directed to your accommodation resource.

#LI-Hybrid

Required Skills : Preferred Skills :

Analytical Reasoning Biochemistry Chemistry Manufacturing and Control (CMC) Coaching Collaborating Conducting Experiments Data Quality Drug Discovery Development Molecular Diagnostics Patent Applications Pharmacogenetics Report Writing Research Documents Scientific Research Technologically Savvy Written Expression

Required Experience :

Senior IC

Key Skills

Fire Protection,Attorney At Law,Cost Estimation,Cloud Services,Art & Design

Employment Type : Full-Time

Experience : years

Vacancy : 1