Manufacturing Quality Assurance Specialist II 2nd Shift

Our Work MattersAt Kindeva we make products that save lives ensuring better health and well-being for patients around the world. The Impact You Will Make: Responsible for on-shift support of manufacturing operations providing quality involvement and oversight during all stages of pharmaceutical development manufacturing and testing. Also responsible for review of controlled Current Good Manufacturing Practices (cGMP) documentation and manufacturing records including any deviations or Out-of-Specification (OOS) results that may have occurred during lot production. Participates in the release of raw materials intermediates and final products. Performs internal and external audits of facilities and products observes critical operations and procedures as they occur audits documentation records activities and keeps management informed on quality :Supports on-shift manufacturing operations and activities including but not limited to real-time auditing of production batch records sampling and Acceptable Quality Levels (AQLs) and line the development and maintenance of Quality Systems as appropriate. Leads continuous improvement objectives to assure compliance with Drug Enforcement Administration (DEA) and Food and Drug Administration (FDA) regulations. Advises senior management on findings and recommendations related to internal and external auditing. Manages deviation Out-of-Specification (OOS) Corrective and Preventive Action (CAPA) and Change Control Systems. Evaluates proposed changes to processes equipment materials or documentation to ensure compliance with regulatory and quality standards. Participates in investigations and root cause analyses for deviations OOS results and audit findings. Ensures timely implementation and effectiveness checks of CAPAs to prevent recurrence of quality issues. Reviews and approves cGMP documentation including but not limited to procedures batch records validation protocols development reports specifications raw data executed batch records material and batch disposition and other related and maintains metrics and trending reports for Compliance-related activities. Reviews and approves product complaint investigations and assists with investigations. Performs activities associated with various one-time or ongoing projects (from participation level to project manager). Collaborates with departments and external suppliers regarding quality concerns. Participates and/or coordinates Compliance Assessments of departments as necessary (Good Practice GxP 21 Code of Federal Regulations CFR Part 11 etc.). Supports regulatory inspections and customer audits. Assists the Manager with daily and project activities as other duties as :Bachelors degree in a scientific discipline. At least 3 years of Pharmaceutical/Medical Device cGMP quality of data integrity principles (Attributable Legible Contemporaneous Original Accurate Complete Consistent Enduring and Available ALCOA) and compliance with 21 CFR Part 11 for electronic records. Knowledge of High-Performance Liquid Chromatography (HPLC) principles and the ability to review data for accuracy and of microbiological testing principles and the ability to review data for accuracy and to assess problems to identify solutions to plan and implement necessary changes. Experience in quality systems auditing (internal and/or external) preferred. Familiarity with electronic Quality Management System (QMS) platforms (e.g. TrackWise MasterControl etc.). Experience in manufacturing aseptically filled sterile products preferred. Advanced knowledge of cGMP regulations and validation principles (e.g. FDA 21 CFR Part 820 International Organization for Standardization ISO 13485 etc.). Ability to work well in a team-oriented environment. Well-developed communication and technical writing to work with controlled substances. Experienced in leading and assisting in deviation investigations and implementation of appropriate Requirements:Specific vision requirements include close vision distance vision color vision and the ability to adjust and focus to read/understand/execute documentation as required by the positionEmployees are required to follow all cGMP and safety is required to regularly use their hands in order to handle materials and is required to regularly use their hands in order to handle materials and is required to effectively use communication by both telephone and electronic is required to regularly stand and walk for extended periods of time. The employee must wear all required safety equipment and safely perform assigned work. Employees must use proper lifting techniques and be conscious of hazards around him/her. Must follow all GMP and safety procedures within the employee must occasionally lift and/or move up to 25 pounds. # LI-OnsiteCalifornia residents should review our Notice for California Employees and Applicantsbefore applying. Kindeva does not accept unsolicited assistance from headhunters or recruitment firms for any of our job openings. Any resumes or candidate profiles submitted to Kindeva employeesregardless of formatwithout a valid signed agreement and an approved job order from an authorized signatory in Talent Acquisition will be considered the sole property of Kindeva. No fees will be paid in the event that a candidate is hired as a result of an unsolicited resume or Opportunity Employer:Kindeva Drug Delivery is an Equal Opportunity/Affirmative Action Employer and does not discriminate on the basis of race color religion gender age national origin disability Protected Veteran status sexual orientation or any other characteristic protected by federal state or local you see yourself as part of the Kindeva mission Click Apply Now Today!