Scientist II

FULLTIME/PARTTIME: 12-Month Assignment
LOCATION: Maple Grove MN
SCHEDULE: Business Needs
PAY RANGE: $45/HR
(Exact compensation may vary based on skills experience and location. Base pay information is based on market location.)

JOB DESCRIPTION:
This Scientist II supports the development and optimization of drug delivery systems for combination products used in preclinical and clinical studies. Working as part of a multidisciplinary R&D team this role conducts laboratory experiments characterizes physicochemical properties of drug substances (including physical form stability solubility and drug-excipient interactions) analyzes experimental data and documents scientist collaborates with senior team members to execute formulation development activities while building technical expertise in drug delivery combination products and pharmaceutical development.

Our products and technologies are used to diagnose or treat a wide range of medical conditions. We continue to innovate in key areas and are extending our innovations into new geographies and high-growth adjacency markets. Our R&D teams design develop and produce technologies for diagnosing and treating coronary artery disease peripheral artery disease heart failure and other cardiovascular conditions through products such as Drug-Eluting Stents Bare-Metal Stents Catheters Balloons Guide Wires Atherectomy and Intravascular Ultrasound. As a member of this team you will contribute to the development of innovative interventional therapies that improve patient outcomes while working in a collaborative cross-functional environment focused on advancing patient care.

Apply established scientific methods and assist in evaluating technical approaches under the guidance of senior team members

Plan and execute laboratory experiments including analytical testing including drug assay degradants and other physicochemical characterization using established methods; assist with method development qualification and validation activities as needed

Support release and stability testing activities by coordinating with internal and external laboratories and documenting results

Prepare technical documentation and data packages to support regulatory submissions design history files and other product development documentation

Participate on cross-functional product development teams collaborating with formulation scientists analytical scientists manufacturing quality regulatory and other functional groups to achieve project objectives

Identify opportunities for laboratory experimental or process improvements and contribute ideas that enhance efficiency quality and technical capability

Communicate technical findings clearly through written reports presentations and team discussions

Maintain laboratory activities and documentation in compliance with applicable quality system requirements laboratory procedures and safety practices.

Quality System Requirements
In all actions demonstrates a primary commitment to patient safety and product quality by maintaining compliance to the Quality Policy and all other documented quality processes and procedures.

Qualifications:
Bachelors degree or higher in Chemical Engineering Biomedical Engineering Pharmaceutical Sciences Chemistry Materials Science or related technical field

Minimum of 2 years of relevant experience with a Bachelors degree or 1 year of relevant experience with a Masters degree in pharmaceutical medical device biotechnology or a related product development environment

Understanding of pharmaceutics physical chemistry and drug delivery systems

Strong written and verbal communication skills including the ability to prepare technical documentation and present scientific findings


Preferred Qualifications :
Masters degree in Pharmaceutical Sciences Chemistry Chemical Engineering Biomedical Engineering Materials Science or related technical field

Familiarity with analytical techniques such as HPLC UPLC GC LC/MS GC/MS UV-Vis DSC TGA or NMR

Understanding of analytical method development qualification or validation especially for drug release stability testing or physicochemical characterization.

Experience working within a regulated environment (FDA ISO GMP or GLP) through academic or industry research

Knowledge of controlled drug delivery systems

Exposure to pharmacokinetic/pharmacodynamic (PK/PD) studies or preclinical model development is desirable

Strong organizational analytical and problem-solving skills with attention to detail

WORKING CONDITIONS:

• May on occasion be exposed to loud sounds and distracting noise levels such as from office equipment.
• The ability to lift up to 30lbs
• Use of computers and technology

Here at Canon Recruiting People are our priority and we are committed to Include Diversity in every segment of who we are. It is only through our Diversity we are made a stronger organization and increase our ability to provide top tier candidates that our clients have come to know Canon for. We have an inclusive environment all employees are celebrated for their unique differences. The different perspectives and experiences of our workforce give us the competitive advantage that is essential for success in an ever-changing market. By promoting inclusion with the same enthusiasm we devote to quality and competency and using the experience from a diverse assortment of backgrounds and experiences Canon is able to improve the services and value we deliver to clients employees and customers. At Canon Diversification and Inclusiveness are much more than a corporate ambition; they are a critical component in our daily corporate life.

Canon Recruiting is committed to a diverse and inclusive workplace. Canon Recruiting is an equal opportunity employer and does not discriminate on the basis of race national origin gender gender identity sexual orientation protected veteran status disability age or other legally protected status.

The pay range for this position is listed above. Base pay information is based on market location.
We will consider for employment qualified applicants with arrest and conviction records. Our range of benefits may include health care and 401(k) savings plans.
For individuals with disabilities who would like to request an accommodation please email our HR team.

Required Experience:

IC