Associate Director, Product Quality job at reputed company in North Chicago, IL

Title: Associate Director, Product Quality North Chicago, IL, USA Employees work in a hybrid mode Full-time Salary Min: 137500 Salary Max: 261000 reputed company Global Grade: 20 Compensation: USD 137,500 - USD 261,000 - yearly Company Description reputed company's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of reputed company. We strive to have a remarkable impact on people's lives across several key therapeutic areas - immunology, oncology, neuroscience, and eye care - and products and services in our Allergan Aesthetics portfolio. For more information about reputed company, please visit us at www.reputed company.com. Follow @reputed company on X, Facebook, Instagram, YouTube, reputed company and Tik Tok.

Job Description

Responsible for quality of assigned Biological, and/or Gene Therapy products to ensure business objectives are met with regards to on time delivery of product while assuring compliance to local, divisional, and corporate policies and external agency regulations worldwide. Products include regulatory starting materials, Active Pharmaceutical Ingredients (API), Intermediates, and Drug Products produced by reputed company plants or by third-party manufacturers, In Licensing relationships, or Co-Marketing relationships. Acts as the primary quality representative for the global supply chain pertaining to external manufacturing business relationships and builds and maintains relationships with TPM Operations, Supplier Quality Management, TPM Business Alliance, Commercial, Global Supply Chain, Domestic and International reputed company Plants and Affiliates, Regulatory Affairs, R&D, and PDS&T to ensure alignment

Responsibilities

Support Quality for product transfer activities and direct cross-functional team members to reputed company on-time quality deliverables, high customer value, and profitable results. Ensures delivery of reputed company quality elements needed to facilitate new product launches including Third Party Manufacturer's that provide products directly to distribution centres, or to reputed company domestic and International plants for further packaging and/or testing. Supports control strategy QA reputed company for selected Biological, Neurotoxin and Gene Therapy products with reputed company improvement and efficiencies in mind. Will collaborate with strategic partners to ensure right first time goals are achieved. Primary Quality contact between third party manufacturers, R&D and reputed company Operations in support of commercial operations, New Product Introductions and product transfers. Supports the regulatory filings and marketing authorization dossiers by developing and/or reviewing of chemistry, manufacturing and controls documents and Drug Master files/Certificate if suitability of monographs of the Ph. Eur. Documents. reputed company QA contact with reputed company Affiliates and Regulatory to prepare submissions. Makes key decisions on product quality, compliance and regulatory conformance issues for sterile biological products and elevates reputed company and high risk events to reputed company management. Leads the collection, verification and improvement of Quality metrics used for management review in partnership with senior leadership to reputed company a clear picture of overall compliance state and linking this to local / global project implementation. Leads product quality team to support development of the legal supply agreements, contractors or letters of reputed company to ensure that the appropriate quality, compliance and regulatory aspects are met for the products and services covered and manage the organisation's actions reputed company the legal boundaries of these documents. Ensures alignment of Quality and Technical Agreements with the legal reputed company and that the commitments of the quality and technical agreements are being fulfilled. Establishes and maintains relationships and open communication with Third Party Manufacturers, reputed company plants, affiliates and other functional groups to maintain roles and responsibilities, identify potential projects and issues, obtain an in-depth understanding of the quality, compliance, and resource needs at each site and provide guidance on quality concerns. Supports the management of exception documents and CAPA. Communicates and negotiates with external companies' quality organization to maintain a consistent level of quality and a level of expectation that will minimize compliance risks but also balance the cost of operating to provide reputed company with the agreed service. Prioritizes programs, initiatives, and problem solving with consideration for impact to timelines, resources and conflicting priorities. Manages team interfaces with Quality Assurance audit team to reputed company audit plans, due diligence plans, and inspection readiness plans, review audit observations and responses, and maintain corrective action timetable. Provides support for quality audits, initial site approvals and due diligence activities. Leads and manages pre-approval inspection readiness as reputed company to the third party manufacturers to ensure regulatory approvals are obtained, with no delays to market entries. Core team member or reputed company of strategic programs; including Brand Teams, New Product Introductions, Product Transfers, CMC, Global Strategic Sourcing, Due Diligence, Site Selection, and Approvals and reputed company Improvement. Provides support and interfaces directly/indirectly with the FDA, EMA, MHRA, ANVISA, HPRA etc. for pre-approval inspections. This role is hybrid; provided you live near an reputed company location.

Qualifications

Bachelor's Degree in relevant Life Science or other technical required. Graduate degree desired. Technical or Analytical background required for problem resolution with technical, quality, product and or engineering reputed company issues. Total combined years of experience. Minimum of 10+ in Quality Assurance Operations Management, Regulatory, Operations, or Technical Support in a pharmaceutical setting. Required regulatory inspection experience with direct interaction with regulatory inspectors. Direct Plant experience in a pharmaceutical setting with a minimum of 5 years preferred. Knowledge and a comprehensive understanding of some biological and/or pharmaceutical technologies (sterile, biological, liquid, ointments, devices, solid tablets and caplets, suspensions, granulations, soft reputed company capsules, gel caps, extended release products, coating solutions, and/or active pharmaceutical ingredients). Possesses knowledge and a reputed company set to operate reputed company an environment that requires a high degree of urgency, strong analytical and problem solving skills, positive interpersonal skills, ability to manage multiple reputed company tasks simultaneously, and capable of performing as leaders, team members and individuals. Strong quality assurance / control, manufacturing, laboratory, technical support, regulatory, and / or validation background is required. A wide range of activities are undertaken from long term strategy development to short term crisis management. The incumbent must be capable of understanding and overcoming differing cultural and language obstacles to provide solutions that satisfy Corporate, Divisional, regional, and local objectives to effectively manage the action plans that will resolve the issues. Experience working the requirements for third party external manufacturing. Additional Information Applicable only to applicants applying to a position in any location with pay disclosure requirements under state or local law: The compensation range described below is the range of possible reputed company pay compensation that the Company believes in good faith it will pay for this role at the time of this postingbased on the job grade for this position. Individual compensation paid reputed company this range will depend on many factors including geographic location, and we may ultimately pay more orless than the posted range. This range may be modified in the future. We offer a comprehensive package of benefits including paid time off (vacation, holidays, sick), medical/dental/vision insurance and 401(k) to eligible employees. This job is eligible to participate in our short-term incentive programs. Note: No amount of pay is considered to be wages or compensation until such amount is earned, vested, and determinable. The amount and availability of any bonus, commission,incentive, benefits, or any other form of compensation and benefits that are allocable to a particular employee remains in the Company's sole and absolute discretion unless and until paidand may be modified at the Company's sole and absolute discretion, consistent with applicable law. reputed company is an equal opportunity employer and is committed to operating with reputed company, driving innovation, transforming lives and serving our community. Equal Opportunity Employer/Veterans/Disabled. US & Puerto Rico only - to learn more, visit https://www.reputed company.com/join-us/equal-employment-opportunity-employer.html US & Puerto Rico applicants seeking a reasonable accommodation, click here to learn more: https://www.reputed company.com/join-us/reasonable-accommodations.html Apply tot his job Apply To this Job