Quality Relationship Manager, QA Tech Service

Summary of Position The QRM (Quality Relationship Manager) Technical Services is a member of the US Quality department. In this position, the QRM will be interacting primarily with Alvogen's external business partners/CMOs. The incumbent will have responsibility for mainly managing products from development to product launch and commercial phase as assigned. QRM is responsible for supporting the technical aspects of the products as well as the adherence to Alvogen's Quality Management System. The position will require in depth knowledge of Quality Systems including activities such as development, validation, troubleshooting/ investigation support, complaint handling, change control, product release, inspection support, etc. The individual will also support the technical transfer of products to/from various CMO's. The individual serves as a critical link to Alvogen's external partners. Being able to effectively communicate and transmit information to/from partners is essential to ensure compliance and optimal performance. Organization Structure The QRM Tech. Services reports directly to the Director Quality, Commercial and Technical Services, Third Party Quality US. There are no reports. Responsibilities Primary responsibilities of this role include, but are not limited to, the following: Documentation Review & Approval: Review and approve documentation such as Method Validations, Manufacturing Records, SOPs, Investigations, Change Controls, Validation Reports, Technical reports required for regulatory filing, including but not limited to Extractables/ Leachable studies, Nitrosamine Reports etc, Equipment Qualifications and similar documents as directed by Quality Management. Inspections and Audits: Prepare / Support preparation activities for regulatory inspections Evaluate regulatory agency findings from inspections conducted at CMOs/CPOs/analytical Laboratories, etc. Support the design and implementation of system / process improvements where opportunities are identified (Commercial & Development), including associated CAPA's. Support technical transfer / validation activities with external business partners / CMOs. Manage the Finished Product / Bulk Drug Product ANDA/NDA, Launch Release System: Execute the Alvogen Inc. and Almatica Pharma Inc. material release procedure(s). Manage ANDA/NDA, launch release priorities per business deadlines. Work directly with CMOs and partners to resolve related questions/issues. File, retrieve, and maintain organized records Communicate with external business partners / CMOs regarding quality related issues and Quality Agreements. Provide investigation/trouble-shooting support as needed. Review and approve investigations, unexplained discrepancies, failures, and out-of-specification results. Evaluate if there is any quality impact to process/product and take appropriate action. Track metrics for external business partners / CMOs on change controls, deviations, complaints, audits, product releases and rejections and other Third-Party Quality Key Performance Indicators. Change Management Program: Process change controls for all systems requiring change control support (e.g. specifications for raw materials, drug product intermediates and finished drug products, validation protocols and reports, master production and packaging records, cleaning records, and analytical methods). Maintain change control electronic records in EQMS. Review, assess, and approve change controls as required by SOP's. Support training of company personnel on change control system. Support the corporate Training Program, when / if needed. Support the corporate audit program as needed / required. Keeps abreast of industry regulations and cGMP trends. Stays informed of FDA and ICH Guidelines related to GMP (Commercial & Development). Qualifications Position requires the following education and qualification prerequisites: Good leadership skills in all areas of communication, influencing, collaboration and decision-making. BS in Pharmacy, Chemistry, Microbiology or Biology with a minimum of 10 years' experience in the Pharmaceutical Industry preferred. Other degrees will be considered based on extensive industry experience. Experience in GxP laboratory practices. Release of materials and products supporting both development and commercial activities. Has knowledge of GxP quality systems, US FDA regulations and ICH guidance documents. Experience with various manufacturing / filling processes associated with non-sterile drug products. Demonstrated experience supporting deviations, investigations especially, OOS investigations. Experience in conducting, writing/reviewing deviations and investigations, root cause analyses, and identifying corrective actions. Must have strong technical knowledge of FDA and other regulatory guidance and be able to critically review complex investigations, interpret results and able to evaluate technical input against compliance requirements in line with CFR requirements and other regulatory requirements and Alvogen procedures/policies. Must hold strong interpersonal and communication skills. Must have the ability to work well with diverse groups including the ability to work in a team environment. Must also display strong organizational skills with the ability to lead team meetings and to manage multiple projects at one time. Strong technical writing and computer skills are also required. Must display the ability to work independently with little or no supervision and plan and accomplish set goals. Physical Demand Factors While performing the duties of this job, the QRM Tech. Services is required to sit and work at a computer for extended periods of time. Is regularly required to talk, listen, and attend meetings / teleconference calls. Approximately 20% business travel required to external Contract Manufacturing Organization (CMO) / Business Partner sites, or to attend professional development training seminars - as needed / directed. GMP Decision-Making Authority Independent decision-making activities will be performed by the QRM Tech. Services for all the quality management system elements outlined in the Responsibilities section of this Job Description. An equal opportunity employer statement is included below as part of the description: An Equal Opportunity Employer, including disability/vets. Note: The anticipated base salary range for this position is $100,000-$135,000. This position is eligible for Alvogen's annual discretionary bonus and comprehensive benefits package, consisting of medical and prescription drug coverage, dental, vision, flexible spending accounts, a retirement savings program, long-term care coverage, paid time off (176 hours per year, prorated to hire date) inclusive of sick time, disability benefits, life insurance, a wellness program, and 13 company recognized paid holidays per year. We anticipate this position will be posted on March 19, 2026 and remain open for at least 30 days. To apply, select the apply button and submit your application. EOE statement: An Equal Opportunity Employer, including disability/vets. #J-18808-Ljbffr Alvogen