Process Development Scientist ID 35470

PR·Juncosmid

OtherDevelopment

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Quick Summary

Key Responsibilities

Designs, monitors, or conducts strategies with general guidance from the supervisor. Provides data analysis and interpretation and assesses the impact of the data on the project.

Requirements Summary

Relevant experience in a commercial biopharmaceutical manufacturing environment, preferably supporting formulation and aseptic filling operations. Understanding of protein science,

Technical Tools

OtherDevelopment

To conceive, design, implement and execute specific scientific experiments, which contribute to the successful completion of goals and/or projects under general guidance of supervisor.

Responsibilities

~1 min read

→Designs, monitors, or conducts strategies with general guidance from the supervisor.
→Provides data analysis and interpretation and assesses the impact of the data on the project. Keeps current in technical expertise and areas relevant to their function.
→Monitors field of expertise, including literature and technology development, and communicates relevant observations.
→Develop and implement new and novel protocols to address specific issues.
→May represent the department on project teams under the supervision of a senior scientific staff member.
→May initiate productive collaborations within and outside of the department or company.
→Advises or assists others in experimental design and/or interpretation/diagnosis of data and implementing innovative remedies.
→Able to develop solutions to routine technical problems of limited scope.
→Comprehensive understanding of validation protocol execution requirements. In-depth knowledge of validation processes as applied to new equipment installations.

Requirements

~1 min read

Relevant experience in a commercial biopharmaceutical manufacturing environment, preferably supporting formulation and aseptic filling operations.
Understanding of protein science, formulation and filling processes.
Experience with process monitoring, data trending, and statistical analysis tools (e.g., JMP)
Experience supporting deviations, investigations, root cause analysis, and product impact assessments.
Ability to provide manufacturing floor support in a fast-paced, 24/7 operation.
Bilingual proficiency in Spanish and English (written and verbal).
Strong technical writing skills with experience preparing documentation for regulatory audits.
Excellent communication, presentation, problem-solving, project management skills and cross-functional collaboration skills.

Doctorate OR Masters + 2 years of Scientific experience OR Bachelors + 4 years of Scientific experience.
Preferred: Educational background in Life Sciences or Engineering (Biochemistry, Chemical Engineering, etc.).