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Before applying for this role, please read the following information about this opportunity found below. Get AI-powered advice on this job and more exclusive features. Dice is the leading career destination for tech experts at every stage of their careers. Our client, Tandym Tech, is seeking the following. Apply via Dice today! A pharmaceutical company in Massachusetts is currently seeking an experienced professional to join their growing team as their new Associate Director, Quality Assurance Operations. In this role, the Associate Director, Quality Assurance Operations will be responsible for the Quality oversite for a manufacturing area (such as Drug Substance) as well as provide on-the-floor oversite of downstream purification manufacturing activities. This is an onsite contract role in Bedford, MA Responsibilities Provide on the floor quality operations support for all areas and own the master batch record lifecycle processes including final review and approval Provide technical quality guidance as part of teams conducting investigations for complex manufacturing events Review and approve complex deviations and/or Investigations that are site specific Actively support and/or lead preparation activities for pre-approval Inspections and/or responses to observations Work with product release teams to support issuance of drug substance Certificates of Conformance and any other disposition required activities Manage CAPA records and may be required to function as a CAPA manager for minor or major CAPA as needed Serve as QA Reviewer or impact assessor for downstream purification change control records Support and/or review various reports from quality systems and ensure quality mindset is strong Own various Quality procedures and ensure the systems/processes are deployed effectively Qualifications 8+ years of leadership/management experience in an Operations, Manufacturing Technology or Technical Quality professional role Bachelor's Degree Excellent technical and regulatory understanding of the downstream drug substance purification processes Strong experience with various root cause analysis techniques such as 5-why, Kepner-Tregoe, force-field analysis, DMAIC, fault tree analysis Strong understanding of industry regulations such as CFR, USP, EP, JP, etc. Demonstrates strong quality judgement in various situation when making decision Desired Skills Master's Degree in Biological and/or Chemical Sciences Seniority level Director Employment type Contract Job function Quality Assurance Industries Software Development Referrals increase your chances of interviewing at Jobs via Dice by 2x Get notified about new Director of Quality Assurance jobs in Boston, MA . Note: This description retains the original job information and context while using only allowed HTML tags. It does not introduce new facts beyond the provided content.

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