Associate Director – Analytical Quality Control Jobs in Iowa

Excellent interpersonal skills with ability to work effectively with individuals at all levels (i.e. Management, CM, Development, etc.)

Apply software testing skills to ensure high quality software in multiple domains

Experience in developing comprehensive and accurate test designs and plans

Experience designing and executing black, white and gray box test conditions

Strong verbal and written communication skills

Experience with a comprehensive set of testing types, including unit, regression, integration, freestyle, and acceptance testing

EDUCATION, EXPERIENCE, KNOWLEDGE AND SKILLS:

Proven ability to function in multidisciplinary cross functional team environments using clear communication and matrix management skills.

Excellent self-management, organizational, and verbal/written communication skills.

PhD in chemistry, biochemistry, or closely related field, or equivalent experience applicable to the job responsibilities

Industry experience that includes transition of early-stage QC methods to late-stage programs including preparation of regulatory filings.

Experience with vaccine development and interactions with the Essential Regulatory Laboratories, desired

Perform other duties as needed or directed by direct manager/supervisor and/or the leadership team

Degree in ecology, biology, or marine related field or 1+ years of experience in aquaculture, lab, or other scientific setting

Ability to learn and use various digital systems (e.g. Excel, Google Suite, remote sensor monitoring systems)

Ability to use math skills in performing duties

Daily microscopy, documentation, and assessment reporting of algal cultures with respect to biosecurity and production targets.

Perform duties accurately and according to protocols, providing optimal care to the algae independently and with minimal supervision, once trained

Excellent written, oral communication skills, and experience with computer software such as WORD, EXCEL, etc.

Highly organized, detail-oriented, capable of multi-tasking, strong interpersonal skills in order to collaborate with individuals in a matrix environment.

Strong knowledge of QC testing of small molecule drugs in a compliant cGMP setting.

10+ years of relevant experience in a cGMP pharmaceutical QC environment, or 8+ years with a Master’s degree.

Experience in a commercial environment highly desirable.

Starts at $199,000 and is commensurate with experience