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Role Summary
Senior Scientist, Production Operations will lead and provide technical support for departmental projects, change controls, risk assessments, deviations, CAPAs and audits. The role will drive and/or coordinate process improvements, utilizing the quality system as required. Generate and analyze trend reports on production processes (both in-process and FIN) as needed and track effectiveness of changes. Support a strong cGMP environment.
Responsibilities
- Develop subject matter expertise in biologic protein fractionation, purification, and fill finish technologies to support Production Operations.
- Technical lead for all departmental projects, change controls, risk assessments, deviations, CAPAs, and audit support.
- As needed provide data/analysis to support groups including: MQA, PD, Regulatory Affairs, Microbiology, Engineering and Validation.
- Utilize project management skills to track progress of projects to ensure milestones are met.
- Drive process improvements. Take charge of assigned projects and be able to work with other departments to ensure completion by the deadline set and communicate status on a routine basis.
- As needed analyzes quality indicators, including yields, microbial data, environmental monitoring, deviations, etc., evaluates information relating to process conditions and assesses their state of control.
- Support the development of training strategies and materials for manufacturing and support teams as needed.
- Work closely with department leaders and peers and interfaces to fill in for leaders and peers as required.
- Partner with support functions to continuously improve safety and quality to meet ADMA goals.
- Stay current on industry trends.
Qualifications
- Education Requirements: Bachelor’s degree in science, engineering, or another related technical field preferred
- Experience Requirements:
- 10+ years of experience in Plasma Fractionation or Purification or Fill Finish Operations
- Experience in all aspects of Manufacturing preferred
- Knowledge of world-class manufacturing methods (QLP, Lean, Six Sigma), DMAIC, Good Manufacturing Practices, Food and Drug Administration regulations
- Must have demonstrated interpersonal and leadership skills with the ability to interface well with personnel at all levels.
- Must be able to work and facilitate a team-orientated environment.
- Must have demonstrated project management skills and/or project delivery skills.
Skills
- cGMP adherence
- Strong organizational, interpersonal and collaborative skills
- Data analysis and interpretation
- Project management and cross-functional collaboration
Education
- Bachelor’s degree in science, engineering, or another related technical field (preferred)