The Operations Batch Review Specialist is responsible for reviewing batch documentation post execution to ensure that all work completed was carried out in accordance with regulatory requirements, Good Manufacturing Practices (cGMP) and Standard Operating Procedures (SOPs) while maintaining the highest possible quality standards.
Requirements
- Full batch documentation review of parenteral manufacturing Batch Records (Formulation, Filling, Inspection, & Packaging) for Media Fills and Drug Product.
- Identify correction, deviations and escalate found issues to Operations and Quality Supervisors.
- Provide training and feedback to Operators and Supervisors to improve on-the-floor Batch Record reviews during execution.
- Support Quality Systems with driving timely completion of batch impacting deviations to support on time batch release activities.
- Initiate deviations and participate in operations investigations for determining root cause and assessing mitigation for deviating events.
- Support authoring, reviewing and approving of various SOPs & Work Instructions.
- Prioritize and coordinate their record reviews within production timelines.
- Utilize various paper and automated systems (eDMS, SCADA, BMS, CMMS, LIMS, lab instrument software, etc.) to ensure data integrity in batch records.
- Ability to manage multiple projects in a fast-paced environment.
- Exemplify and take proactive approaches in terms of safety expectations, practice positive intervention, and enforce best practices that align to SOPs, compliance requirements, quality guidelines, and site goals.
Benefits
- Paid vacation days, amount based on tenure, and paid sick time
- 11 observed holidays
- 401(k) plan with company match up to 3.5% of salary, vested immediately.
- Choice of health & wellness plans.
- FSA and HSA programs.
- Dental & vision care.