What are the responsibilities and job description for the Pharmaceutical Process Development Scientist position at Orion Group?
Job Summary
At Orion Group, we are seeking a skilled Pharmaceutical Process Development Scientist to join our Product Development Science and Technology team in North Chicago. This role is responsible for designing and executing lab studies to develop robust manufacturing processes for clinical phase and commercial products.
About the Role
This position will be an integral part of the product development and CMC teams. The candidate will work independently or under the direction of a more senior scientific leader to generate and analyze precise, reliable, and reproducible data in a timely manner.
Key Responsibilities:
- Support the process development of parenteral drug products with a focus on antibody drug conjugates (ADCs)
- Design and execute studies evaluating the stability (chemical & physical) of biologics against solution conditions (pH, ionic strength, temperature, light, moisture, etc.) and physical stresses arising from manufacturing process conditions (freeze thaw, mixing, filtration, filling, and lyophilization), to develop robust dosage forms
- Interpret results and draw conclusions from own multistage experiments, note significant deviations, then suggest, design, and pursue relevant experiments
Requirements:
- Bachelor's Degree, or equivalent education, with typically 7 or more years' experience or Master's degree or equivalent education with 3 years' experience in Chemistry, Chemical Engineering, Pharmaceutical Sciences, or similar area
- Demonstrated scientific writing skills and strong verbal communication skills
- Proven experience with process development of parenteral drug products with a focus on antibody drug conjugates (ADCs)
- Ability to design and execute studies evaluating the stability (chemical & physical) of biologics against solution conditions (pH, ionic strength, temperature, light, moisture, etc.) and physical stresses arising from manufacturing process conditions (freeze thaw, mixing, filtration, filling, and lyophilization), to develop robust dosage forms
- Ability to interpret results and draw conclusions from own multistage experiments, note significant deviations, then suggest, design, and pursue relevant experiments
What We Offer
- Competitive hourly pay rate: $53-57/hr (individual medical benefits available at a cost)
- Opportunity to work with a global pharmaceutical client's Product Development Science and Technology team in North Chicago, IL
At Orion Group, we are seeking a skilled Pharmaceutical Process Development Scientist to join our Product Development Science and Technology team in North Chicago. This role is responsible for designing and executing lab studies to develop robust manufacturing processes for clinical phase and commercial products.
About the Role
This position will be an integral part of the product development and CMC teams. The candidate will work independently or under the direction of a more senior scientific leader to generate and analyze precise, reliable, and reproducible data in a timely manner.
Key Responsibilities:
- Support the process development of parenteral drug products with a focus on antibody drug conjugates (ADCs)
- Design and execute studies evaluating the stability (chemical & physical) of biologics against solution conditions (pH, ionic strength, temperature, light, moisture, etc.) and physical stresses arising from manufacturing process conditions (freeze thaw, mixing, filtration, filling, and lyophilization), to develop robust dosage forms
- Interpret results and draw conclusions from own multistage experiments, note significant deviations, then suggest, design, and pursue relevant experiments
Requirements:
- Bachelor's Degree, or equivalent education, with typically 7 or more years' experience or Master's degree or equivalent education with 3 years' experience in Chemistry, Chemical Engineering, Pharmaceutical Sciences, or similar area
- Demonstrated scientific writing skills and strong verbal communication skills
- Proven experience with process development of parenteral drug products with a focus on antibody drug conjugates (ADCs)
- Ability to design and execute studies evaluating the stability (chemical & physical) of biologics against solution conditions (pH, ionic strength, temperature, light, moisture, etc.) and physical stresses arising from manufacturing process conditions (freeze thaw, mixing, filtration, filling, and lyophilization), to develop robust dosage forms
- Ability to interpret results and draw conclusions from own multistage experiments, note significant deviations, then suggest, design, and pursue relevant experiments
What We Offer
- Competitive hourly pay rate: $53-57/hr (individual medical benefits available at a cost)
- Opportunity to work with a global pharmaceutical client's Product Development Science and Technology team in North Chicago, IL
Salary : $53 - $57
