Supports formulation and aseptic filling through process optimization, investigations, data analysis, GMP compliance, and technical writing.
30th June, 2026
SUMMARY
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.
FUNCTIONS
Conceives and designs, executes or evaluates, and interprets experimental strategies.
Provides input to new processes to generate robust and reliable data.
Ensures that studies are conducted in compliance with the respective protocol and applicable guidelines and regulations.
Designs, monitors or conducts experimental strategies with general guidance from supervisor.
Provides data analysis and interpretation, and assesses impact of the data on the project.
Keeps current in field of scientific expertise and areas relevant to their function.
Monitors field of expertise, including literature and technology development, and communicates relevant observations.
May introduce advanced scientific methods.
Develops and implements new and novel protocols to address specific issues.
May represent the department on project teams under 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.
May assume lead role in department-wide support efforts such as safety, recruiting and committees.
May develop supervisory and mentoring skills.
Develops and follows timelines for completing project team work.
REQUIREMENTS
Doctorate OR Master’s + 2 years of Scientific experience OR Bachelors + 4 years of Scientific experience.Preferred: Educational background in Life Sciences or Engineering (Biochemistry, Chemical Engineering, etc.).
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.
The routine work schedule is 8:00 am to 5:00 pm (admin shift). However, staff will support a 24/7 formulation and filling operations, and irregular shifts, including extended hours (12 hrs), nights, weekends, or holidays may be required based on business needs.