Associate Director – MSB LCMSHybrid
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Job Location:
Kansas City, KS - USA
Monthly Salary:
Not Disclosed
Posted on:
9 days ago
Vacancies:
1 Vacancy
Job Summary
Performing critical work that impacts our industry and our worlds health while problem solving and innovating in the field that is what an Associate Director at KCAS Bio get to do every day. If that gets you excited too then maybe working as an Associate Director at KCAS Bio is the role for you.
When you work as a Mass Spec Bioanalysis Associate Director at KCAS you get to further our mission as the core of KCAS carrying out and supervising all aspects of our studies by taking responsibility for the management and oversight of all assigned studies within the division assuring that assigned staff are productive and produce quality data and reports on time.
You will also ensure that all KCAS procedures and processes are understood and conducted by your addition you will serve as the primary scientific contact for key clients and manage on-site support for their programs as well as support for specialty studies.
Our Mass Spec Bioanalysis lab team delivers high-quality trace-level quantification using advanced LC-MS/MS and hybrid MS platforms to support small molecules large molecules and ADC programs. We develop and validate robust GLP-compliant bioanalytical methods and generate precise submission-ready data that drive confident decisions in drug development.
In this role we will rely on you in the following areas:
Leadership & Team Management
- Provide daily supervision and mentorship to departmental staff ensuring adherence to scientific and operational standards.
- Scheduling and prioritization of team workload to meet project timelines and quality expectations with operations and capacity planning support
- Conduct performance reviews and recommend development plans for direct reports.
Technical & Operational Execution
- Function as project manager (when required) for assigned studies including design validation interpretation and reporting.
- Serve as a technical lead for complex bioanalytical assays troubleshooting challenging scientific problems and ensuring robust validated methods.
- Oversee method validation and sample analysis for mass spectrometry with a focus on hybrid applications.
- Interpret complex data sets and provide scientific guidance to project teams for accurate conclusions and regulatory compliance.
- Collaborate with senior scientists to design innovative approaches for emerging client needs and novel assay formats.
- Ensure scientific integrity in all deliverables by reviewing protocols validation reports and final data packages.
- Function as a subject matter expert for internal teams and clients on specialized techniques and instrumentation.
- Ensure compliance with SOPs regulatory requirements and quality standards in all laboratory activities.
- Implement process improvements within the department to enhance efficiency and maintain best practices.
Client & Project Support
- Support client retention by delivering high-quality data and timely communication on assigned projects.
- Collaborate with business development teams to provide technical input for proposals and new service offerings.
Resource & Capacity Management
- Monitor departmental capacity and resource utilization; provide input to leadership on staffing and equipment needs.
Professional Development
- Stay current with scientific advancements relevant to departmental services and share knowledge with the team.
- Participate in internal meetings and contribute to cross-functional initiatives as needed.
To qualify specifically for this role you will have:
- Bachelors in a scientific related field required with a minimum of 7 years experience in CRO Pharma or Biotech industry conducting scientific research (MS or Ph.D. preferred).
- An equivalent combination of education and experience may be accepted as a satisfactory substitute for the specific education and experience listed below.
- Minimum 10 years experience in developing a wide variety of analytical and bioanalytical techniques for the quantitation of therapeutics.
- Excellent knowledge of the principles of bioanalysis for therapeutics by current state of
- the art technologies and methodologies including but not limited to LC-MS/MS HRMS UPLC-
- UV and UPLC-Fluorescence.
- Demonstrated proficiency in Watson LIMS Analyst SCIEX OS and Chromeleon software for bioanalytical data acquisition processing and reporting.
- Science and quantitation related to small molecules and metabolites mixed mode macro molecules proteins ADCs Oligonucleotides Peptides and other biotherapeutic target analytes through the utilization of diverse scientific procedures calculations and statistics.
- Working knowledge of state-of-the-art principles theories and regulatory updates for
- biopharmaceuticals and biotherapeutics.
- Good knowledge of MS Word Excel and technical writing.
- Familiar with current industry trends and expectations relating to biotherapeutic modalities.
(Please note this is a representative summary of responsibilities not a comprehensive or exclusive list of the duties to be performed in any position. Employees must follow instructions and perform additional duties as requested.)
WHO YOU ARE
You will thrive at KCAS Bio if you enjoy a relational environment are purpose- and values-driven embrace constant development and supportive leadership and enjoy being part of innovative work.
WHAT YOULL GET
Our benefits include and extend beyond the traditional package. At KCAS Bio you will enjoy company sponsored events like food trucks family days and spirit will grow in your career with KCAS will be able to connect with like-minded employees to further KCAS Bios approach to key areas such as wellness inclusion and community will engage as an owner in our stock ownership program. You will have access to the latest technology. And you will be able to invest in the community with paid time off to volunteer.
Learn more about the Benefits at KCAS Bio
WHO WE ARE
We are a fast-growing contract research organization (CRO) headquartered in Kansas City pioneering the latest drug development in both human and animal health for our expertise is growing and so is our need for great people to work in nimble empowered teams committed to one anothers growth. At KCAS Bio we advance both great science AND great people.
KCAS Bio is proud to be an Equal Opportunity Employer. Among other things we provide equal employment opportunities without regard to race color religion national origin ancestry marital status veteran status age disability pregnancy genetic information sex sexual orientation gender identity or any other legally protected category; we recruit qualified candidates without regard to citizenship status based on internal processes that enable us to hire the right candidates consistent with the appropriate U.S. Immigration framework; and (3) we work with and provide reasonable accommodations to individuals with disabilities and for sincerely held religious beliefs observances and practices. Anyone who needs reasonable accommodation may send an email to emailprotectedor call (for TTY assistance call 711) and ask for Human Resources.
IND123
We may use artificial intelligence (AI) tools to support parts of the hiring process such as reviewing applications analyzing resumes or assessing responses. These tools assist our recruitment team but do not replace human judgment. Final hiring decisions are ultimately made by humans. If you would like more information about how your data is processed please contact us.
Required Experience:
Director
Key Skills
- Program assessment
- FDA Regulations
- Manufacturing & Controls
- Program Evaluation
- budget forecast
- Research Experience
- Operations Management
- Research & Development
- Strategic Planning
- Contract Management
- Leadership Experience
- negotiation
About Company
As a full-service bioanalytical CRO and biomarker partner, KCAS Bio helps accelerate drug development in the pharma and biopharma industries with large and small molecule bioanalysis.
