- job summary: A current top partnership with a research-driven biopharmaceutical company is known as a powerhouse that aims to develop treatments for difficult-to-cure diseases. This renowned employer has created 32 products, that have highly impacted lives across the globe. If you're looking to stand out in your field and lead the way to innovative therapies, this position is for you! location: North Chicago, Illinois job type: Contract salary: &#xjob summary: A current top partnership with a research-driven biopharmaceutical company is known as a powerhouse that aims to develop treatments for difficult-to-cure diseases. This renowned employer has created 32 products, that have highly impacted lives across the globe. If you're looking to stand out in your field and lead the way to innovative therapies, this position is for you! location: North Chicago, Illinois job type: Contract salary: &#x
- job summary: Join our Parenteral Product Development Science and Technology - Analytical Development group and contribute to exciting programs transitioning from the development stage to optimization and commercialization. As a member of the team, you will support the development, optimization, and validation of analytical methods by ensuring that they are well documented. You'll gain experience in documentation of product control strategies, analytical mjob summary: Join our Parenteral Product Development Science and Technology - Analytical Development group and contribute to exciting programs transitioning from the development stage to optimization and commercialization. As a member of the team, you will support the development, optimization, and validation of analytical methods by ensuring that they are well documented. You'll gain experience in documentation of product control strategies, analytical m
- job summary: We are seeking a skilled Validation Engineer to lead validation efforts for a new drug delivery site. This role involves protocol development and execution, audit support, validation assessments, and analyst training, all under limited to no supervision. The ideal candidate will have a strong background in GMP compliance, regulatory standards, and validation processes within the pharmaceutical or medical device industry. Schedule/Shift: 1stjob summary: We are seeking a skilled Validation Engineer to lead validation efforts for a new drug delivery site. This role involves protocol development and execution, audit support, validation assessments, and analyst training, all under limited to no supervision. The ideal candidate will have a strong background in GMP compliance, regulatory standards, and validation processes within the pharmaceutical or medical device industry. Schedule/Shift: 1st
- job summary: As the world's largest staffing and recruitment agency, we are dedicated to helping you find the ideal role that offers growth and development opportunities within the life sciences sector. By working with a recruiter, you gain access to a vast network of leading employers and detailed insights into a wide range of positions. One of our premier partnerships is with a research-driven biopharmaceutical powerhouse focused on developing treatmentjob summary: As the world's largest staffing and recruitment agency, we are dedicated to helping you find the ideal role that offers growth and development opportunities within the life sciences sector. By working with a recruiter, you gain access to a vast network of leading employers and detailed insights into a wide range of positions. One of our premier partnerships is with a research-driven biopharmaceutical powerhouse focused on developing treatment
- job summary: The Analytical Development-Early Stage group within Biologics ARD is responsible for support of programs that are preparing for FIH clinical studies. The team leads Stage 1 method development, optimization, and validation. In collaboration with cross-functional partners, the team supports early phase formulation and process development studies. Key deliverables include product control strategies informed by analytical data and method understajob summary: The Analytical Development-Early Stage group within Biologics ARD is responsible for support of programs that are preparing for FIH clinical studies. The team leads Stage 1 method development, optimization, and validation. In collaboration with cross-functional partners, the team supports early phase formulation and process development studies. Key deliverables include product control strategies informed by analytical data and method understa
- job summary: As the largest staffing and recruitment agency in the world, we can commit to finding you the perfect role that gives you the opportunity to learn and grow in the life sciences arena. Utilizing a recruiter for your job search gives you access to a large network of top employers as well as detailed information about hundreds of positions. A current top partnership with a research-driven biopharmaceutical company is known as a powerhouse thatjob summary: As the largest staffing and recruitment agency in the world, we can commit to finding you the perfect role that gives you the opportunity to learn and grow in the life sciences arena. Utilizing a recruiter for your job search gives you access to a large network of top employers as well as detailed information about hundreds of positions. A current top partnership with a research-driven biopharmaceutical company is known as a powerhouse that
- The Manufacturing Technician I is responsible for executing processes in production at Takeda’s manufacturing facility in Round Lake, Illinois, while strictly adhering to cGMP, environmental health and safety guidelines and any other related regulations that apply. The incumbent will fully participate in both departmental projects and any quality working teams which may be applicable. Responsibilities include hands-on execution of all activities in tThe Manufacturing Technician I is responsible for executing processes in production at Takeda’s manufacturing facility in Round Lake, Illinois, while strictly adhering to cGMP, environmental health and safety guidelines and any other related regulations that apply. The incumbent will fully participate in both departmental projects and any quality working teams which may be applicable. Responsibilities include hands-on execution of all activities in t
- The Manufacturing Technician I is responsible for executing processes in production at Takeda’s manufacturing facility in Round Lake, Illinois, while strictly adhering to cGMP, environmental health and safety guidelines and any other related regulations that apply. The incumbent will fully participate in both departmental projects and any quality working teams which may be applicable. Responsibilities include hands-on execution of all activities in tThe Manufacturing Technician I is responsible for executing processes in production at Takeda’s manufacturing facility in Round Lake, Illinois, while strictly adhering to cGMP, environmental health and safety guidelines and any other related regulations that apply. The incumbent will fully participate in both departmental projects and any quality working teams which may be applicable. Responsibilities include hands-on execution of all activities in t
- job summary: Immediate opportunity for a Sr. Regulatory Affairs Associate, CMC to assist the technical team in preparing regulatory filing dossiers, assess changes for regulatory impact, and manage documentation systems. You will participate in Global Regulatory Product Team (GRPT) and Operations Brand Team meetings as needed. As a Senior Associate, RA CMC, you will work with internal and external partners in order to deliver products to patients. Preparejob summary: Immediate opportunity for a Sr. Regulatory Affairs Associate, CMC to assist the technical team in preparing regulatory filing dossiers, assess changes for regulatory impact, and manage documentation systems. You will participate in Global Regulatory Product Team (GRPT) and Operations Brand Team meetings as needed. As a Senior Associate, RA CMC, you will work with internal and external partners in order to deliver products to patients. Prepare
