Associate Director, LBA
Apply NowCompany: Altasciences
Location: Columbia, MO 65203
Description:
Your New Company!
At Altasciences we all move in unison to assist and work in the discovery, development, and manufacturing of new drug therapies to get them faster to people who need them. No matter your role, we all play an important part and you will have a significant impact on the health and well-being of people across the globe. By living our values of Employee Development, Customer Focus, Quality and Excellence, Respect and Integrity, we look to foster a passionate and collaborative work environment and we are looking for talented and enthusiastic people, like you, to join our growing team! Whether you're a recent college graduate or seeking your next career opportunity, it's time to discover your future at Altasciences.
We are better together and together We Are Altasciences.
About The Role
The Associate Director, LBA will coordinate the operations of the Ligand binding assay department to ensure the performance, productivity and efficiency of the group's operations and logistics. The Associate Director is responsible for processes and policies in support of organizational goals. Monitor adherence to procedures. Generates all updates and forecasts for the department (daily, weekly, monthly). Stays appraised of the status of all projects and recommends resource adjustment based on deliverable schedules. Monitors schedules and timelines. Advise of delays and impact for projects. Provide operational guidance and efficiency initiatives that have impact on improving productivity and profitability.
What You'll Do Here
Responsible for personnel management activities of assigned staff such as: scheduling projects, training and development, providing regular direction and feedback on performance, disciplinary actions, preparing and delivering annual performance and salary reviews.
Responsible for scientific review of driving documents and reports and raising any pertinent issues to Senior Director LBA.
Contribute to financial success in their areas of expertise, as demonstrated by revenue and GM targets and client satisfaction achieved.
Responsible for ensuring quality and regulatory requirements are met by scientific staff in their team and that any quality issues, KPI issues are promptly resolved.
Responsible for ensuring continued operational improvements for efficiency and cost control in their areas of expertise.
Provide Scientific support to assigned Bioanalytical Principle Investigator within the area of expertise and ensure project timelines are respected and any delays communicated in a prompt fashion to all key internal and external stakeholders; Recommends resource adjustment when required based on deliverable schedules.
Responsible for set up and implementation of training for technical and scientific LBA staff.
Responsible for improved efficiency initiatives in the laboratory, including scheduling assays, operations and improving workflows.
Review costing assessments and scheduling projects with business development and Operations.
Contributes to the growth and development of Altasciences ligand binding assay services, as well as participate in strategic planning; Responsible for working closely with other management members and serve as back-up when any of them is out of office.
Contribute in professional internal/external presentations, scientific out-reach, and conferences.
Respect Health and Safety standards in terms of personal protection, laboratory maintenance, and work procedures.
May act as the Test Site Management for applicable validation and sample analysis studies as well as method SOP approval.
What You'll Need to Succeed
Ph.D. with 5+ years of relevant experience; or M.Sc. with 7+ years of relevant experience; or B.Sc. with 10+ years of relevant experience in bioanalysis or other pertinent laboratory-based qualifications in a CRO or Pharma.
Supervisory experience in a multidisciplinary environment is essential.
Previous work experience in a GLP regulated environment is a plus.
Good leadership and people skills, teamwork experience, demonstrated conflict handling and resolution ability.
Good achievement record in scientific research and technical development evidenced by research paper and conference presentation.
MOVING IN UNISON TO DELIVER A BIG IMPACT WITH A PERSONAL TOUCH
Altasciences is an equal opportunity employer committed to diversity and inclusion. Our goal is to attract, develop and retain highly talented employees from diverse backgrounds, allowing us to benefit from a wide variety of experiences and perspectives. All qualified applicants will receive consideration for employment without regard to age, race, color, religion, creed, sex, sexual orientation, gender identity, national origin, disability or any other protected grounds under applicable legislation. Reasonable accommodations for persons with disabilities during the recruitment process are available upon request. Join us at Altasciences!
At Altasciences we all move in unison to assist and work in the discovery, development, and manufacturing of new drug therapies to get them faster to people who need them. No matter your role, we all play an important part and you will have a significant impact on the health and well-being of people across the globe. By living our values of Employee Development, Customer Focus, Quality and Excellence, Respect and Integrity, we look to foster a passionate and collaborative work environment and we are looking for talented and enthusiastic people, like you, to join our growing team! Whether you're a recent college graduate or seeking your next career opportunity, it's time to discover your future at Altasciences.
We are better together and together We Are Altasciences.
About The Role
The Associate Director, LBA will coordinate the operations of the Ligand binding assay department to ensure the performance, productivity and efficiency of the group's operations and logistics. The Associate Director is responsible for processes and policies in support of organizational goals. Monitor adherence to procedures. Generates all updates and forecasts for the department (daily, weekly, monthly). Stays appraised of the status of all projects and recommends resource adjustment based on deliverable schedules. Monitors schedules and timelines. Advise of delays and impact for projects. Provide operational guidance and efficiency initiatives that have impact on improving productivity and profitability.
What You'll Do Here
Responsible for personnel management activities of assigned staff such as: scheduling projects, training and development, providing regular direction and feedback on performance, disciplinary actions, preparing and delivering annual performance and salary reviews.
Responsible for scientific review of driving documents and reports and raising any pertinent issues to Senior Director LBA.
Contribute to financial success in their areas of expertise, as demonstrated by revenue and GM targets and client satisfaction achieved.
Responsible for ensuring quality and regulatory requirements are met by scientific staff in their team and that any quality issues, KPI issues are promptly resolved.
Responsible for ensuring continued operational improvements for efficiency and cost control in their areas of expertise.
Provide Scientific support to assigned Bioanalytical Principle Investigator within the area of expertise and ensure project timelines are respected and any delays communicated in a prompt fashion to all key internal and external stakeholders; Recommends resource adjustment when required based on deliverable schedules.
Responsible for set up and implementation of training for technical and scientific LBA staff.
Responsible for improved efficiency initiatives in the laboratory, including scheduling assays, operations and improving workflows.
Review costing assessments and scheduling projects with business development and Operations.
Contributes to the growth and development of Altasciences ligand binding assay services, as well as participate in strategic planning; Responsible for working closely with other management members and serve as back-up when any of them is out of office.
Contribute in professional internal/external presentations, scientific out-reach, and conferences.
Respect Health and Safety standards in terms of personal protection, laboratory maintenance, and work procedures.
May act as the Test Site Management for applicable validation and sample analysis studies as well as method SOP approval.
What You'll Need to Succeed
Ph.D. with 5+ years of relevant experience; or M.Sc. with 7+ years of relevant experience; or B.Sc. with 10+ years of relevant experience in bioanalysis or other pertinent laboratory-based qualifications in a CRO or Pharma.
Supervisory experience in a multidisciplinary environment is essential.
Previous work experience in a GLP regulated environment is a plus.
Good leadership and people skills, teamwork experience, demonstrated conflict handling and resolution ability.
Good achievement record in scientific research and technical development evidenced by research paper and conference presentation.
MOVING IN UNISON TO DELIVER A BIG IMPACT WITH A PERSONAL TOUCH
Altasciences is an equal opportunity employer committed to diversity and inclusion. Our goal is to attract, develop and retain highly talented employees from diverse backgrounds, allowing us to benefit from a wide variety of experiences and perspectives. All qualified applicants will receive consideration for employment without regard to age, race, color, religion, creed, sex, sexual orientation, gender identity, national origin, disability or any other protected grounds under applicable legislation. Reasonable accommodations for persons with disabilities during the recruitment process are available upon request. Join us at Altasciences!