Moderna, Inc.

Engineer II, Drug Product Development

Moderna, Inc.$74K — $118K *
Pharmaceuticals & Biotech
Less than 5 years of experience
Job Overview by Ladders

Qualifications

  • Masters or Bachelor's Degree in Chemical Engineering, Biochemical or Biomedical Engineering, Pharmaceutical Sciences, or related fields.
  • 0-2 years post Master's Degree or 2+ years post Bachelor's Degree experience.
  • Exceptional laboratory skills for dynamic environments.
  • Knowledge of statistical design of experiments (DoE) and analysis.
  • Familiarity with nucleic acid chemistry and biology is a plus.
  • Preferred experience in BioPharma, BioPharmaceutical, Pharmaceutical or Biotechnology sector.
  • Knowledge of GMP compliance preferred.

Responsibilities

  • Conduct studies for scale-up of drug product manufacturing.
  • Develop protocols for evaluating drug product compatibility with materials.
  • Support drug product development with Pilot organization for toxicology fills and stability operations.
  • Plan and execute experiments, preparing protocols and summarizing results.
  • Collaborate with analytical development to compile experimental data.
  • Support manufacturing through troubleshooting studies and investigations.
  • Perform routine and non-routine characterization techniques.

Benefits

  • Competitive healthcare and voluntary benefit programs.
  • Holistic well-being approach with fitness, mindfulness, and mental health support.
  • Family planning benefits including fertility, adoption, and surrogacy support.
  • Generous paid time off and global recharge days.
  • Savings and investment plans for future planning.
  • Location-specific perks and extras.
Full Job Description
The Role

We are seeking a highly skilled and motivated Individual, to work in a team developing Moderna's sterile drug product processes and products that enable clinical and future commercial supply. The primary role for this position will be to support drug product development activities including: image development, process development and scale-up, container development and conditions of use studies. The incumbent will support the development of compositions, aseptic fill/finish unit operations through the development and use of scale-down models, process characterization studies etc. Applicants should have relevant pharmaceutical sciences related experience with various aspects of drug product development. The applicant should have exceptional ability to plan, execute and report, to communicate and collaborate, and requires strong attention to detail while working in a fast-paced, interdisciplinary environment.

Here's What You'll Do
  • Conduct studies to support scale-up of drug product manufacturing (e.g. freeze/thaw, mixing, filling, filtration, lyophilization, transport etc).
  • Develop protocols to evaluate the compatibility of the drug product with processing materials, container closure components, and sterilization processes.
  • Provide support to drug product development activities executed in collaboration with Moderna's Pilot organization, including toxicology fills stability fill operations.
  • Plan, organize and execute experiments (using DoE where possible) - prepare study protocols and summarize the development results with presentations and study reports.
  • Communicate and collaborate with various groups such as analytical development to execute experiments and compile data.
  • Support manufacturing with studies for process trouble-shooting and investigations.
  • Perform a range of routine and non-routine characterization techniques, including opacity testing, microscopy, particle sizing etc.
  • Develop processes suitable to ensure long-term stability of vialed drug product.
  • Maintain an up-to-date ELN with good documentation practices
  • Closely collaborate with multiple groups to generate innovative solutions to challenging formulation and process problems.


Here's What You'll Need (Basic Qualifications)
  • Education Qualifications - Masters or Bachelor's Degree in on one of the following fields: Chemical Engineering, Biochemical or Biomedical Engineering, Pharmaceutical Sciences, or any related or sub-disciplines of the above.
  • Relevant Experience: 0 - 2 years post Master's Degree or at least 2 years post Bachelor's Degree.
  • Exceptional laboratory skills with ability to work efficiently and productively in a highly dynamic environment
  • Knowledge of statistical design of experiments (DoE) and analysis
  • Knowledge of nucleic acid chemistry and biology is a plus
  • Preferred: Experience in BioPharma, BioPharmaceutical, Pharmaceutical, or Biotechnology industry
  • Preferred: Experience with nanoparticle formulation technology
  • Preferred: Knowledge of GMP compliance.
  • Ability to travel up to 20%.


Pay & Benefits

At Moderna, we believe that when you feel your best, you can do your best work. That's why our benefits and well-being resources are designed to support you-at work, at home, and everywhere in between.
  • Competitive healthcare, plus voluntary benefit programs to support your unique needs
  • A holistic approach to well-being, with access to fitness, mindfulness, and mental health support
  • Family planning benefits, including fertility, adoption, and surrogacy support
  • Generous paid time off, including vacation, volunteer days, sabbatical, global recharge days, and a discretionary year-end shutdown
  • Savings and investments to help you plan for the future
  • Location-specific perks and extras

The salary range for this role is $74,000.00 - $118,400.00. This is the lowest to highest salary we in good faith believe we would pay for this role at the time of this posting. An individual's position within the salary range will be based on several factors including, but not limited to, specific competencies, relevant education, qualifications, certifications, experience, skills, performance, and business or organizational needs.The successful candidate may be eligible for an annual discretionary bonus, other incentive compensation, or equity award, subject to company plan eligibility criteria and individual performance.

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