Scientific Laboratory Professional

Scientist III will be responsible for performing complex laboratory analysis of pharmaceutical products and proficiently using analytical instrumentation.

• The ideal candidate will independently perform method validations, method transfers and analytical testing of pharmaceutical and biopharmaceutical compounds in a variety of formulations and/or delivery systems. Understands and conforms to methods and protocols applicable to assigned tasks. Designs and drives experiments with minimal supervision.

Our team is dedicated to providing the highest quality results and ensuring the accuracy of our data. As a Scientist III, you will play a crucial role in this process by reviewing, interpreting, and analyzing data for technical, quality, and compliance to protocols, methods, SOPs, client criteria, and GMP or GLP. You will also perform self and peer review of the data for accuracy and compliance with reporting requirements prior to submission to QA and issuance to customers.

• Perform complex laboratory analysis of pharmaceutical products and proficiently use analytical instrumentation.
• Independently perform method validations, method transfers, and analytical testing of pharmaceutical and biopharmaceutical compounds.
• Design and drive experiments with minimal supervision.
• Review, interpret, and analyze data for technical, quality, and compliance to protocols, methods, SOPs, client criteria, and GMP or GLP.
• Perform self and peer review of the data for accuracy and compliance with reporting requirements.
• Prepare study protocols, project status reports, final study reports, and other project-related technical documents.
• Communicate data and technical issues to the client and respond to client needs and questions.
• Mentor, train, and coordinate laboratory activities of other team members and assist in troubleshooting instrument and analytical problems.
• Assist with quality systems and new equipment.
• Assist in designing method validation or method transfer protocols and establish project timelines.

As a key member of our team, you will have the opportunity to work on a variety of projects and collaborate with colleagues from different backgrounds and disciplines. Our company values innovation, excellence, and teamwork, and we are committed to providing our employees with the resources and support they need to succeed.

• Bachelor's degree in a relevant area, i.e., chemistry, biochemistry.
• 5+ years' relevant industry experience within a GMP laboratory (with experience in the following lab testing areas HPLC, UPLC, Electrophoresis (CE, iCE, SDS-PAGE), ELISA, spectrophotometry).
• Experience in Method Validation, Method Transfer, and Analytical testing.
• Detailed knowledge of method validation; method development would be an advantage.
• Ability to plan, schedule, and carry out work for successful project completion.
• Positive attitude and ability to work well with others.
• Excellent attention to detail.

• Competitive salary and benefits package.
• Opportunity to work on a variety of projects and collaborate with colleagues from different backgrounds and disciplines.
• Professional development and training opportunities.
• A dynamic and supportive work environment.

Our company values the health and wellbeing of our employees. We support and encourage individuals to create a healthy and balanced environment where they can thrive. Below are listed the working environment/requirements for this role:

• Ability to communicate, receive, and understand information and ideas with diverse groups of people in a comprehensible and reasonable manner.
• Ability to work upright and stationary and/or standing for typical working hours.
• Ability to lift and move objects up to 25 pounds.
• Ability to work in non-traditional work environments.
• Ability to use and learn standard office equipment and technology with proficiency.
• May have exposure to potentially hazardous elements, including infectious agents, typically found in healthcare or laboratory environments.
• Ability to perform successfully under pressure while prioritizing and handling multiple projects or activities.