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About Alamar Biosciences, Inc.
At Alamar Biosciences, we're on a mission to transform the field of proteomics for the early detection of cancer and other diseases. We are creating the world's most sensitive proteomics platform to unmask the deepest secrets of our proteome. Our fully automated, high throughput platform will empower new biomarker discoveries for early detection and prevention of common diseases. We provide exceptional opportunities for those who have the entrepreneurial spirit, enjoy developing novel technologies and products, and aspire to grow together with the company.
Description
We are seeking an experienced, detail-oriented, and results-driven candidate to join our Operations team as Lead Manufacturing Specialist - Lyophilization. This position acts as the subject matter expert to commission new lyophilizers, train Manufacturing staff, drive continuous improvements for processes and equipment related to lyophilization, and transfer of new products/processes into routine manufacturing. In addition, this position is also responsible for planning and executing lyophilization to meet production demand and overseeing other Manufacturing Associates in lyophilization. Experience in production planning and working under ISO 13485 and/or current Good Manufacturing Practice (cGMP) in a biotechnology or pharmaceutical industry is highly preferred.
Responsibilities
Lead, plan, and perform production activities for lyophilizationProvide technical support for any lyophilization process-related issuesResponsible for revising and originating production records, standard operating procedures, protocols and reports; initiates and closes out deviation reports and change requestsEnsure lyophilization equipment is in controlled state to sustain manufacturing and ensure routine PM is executed on timePerform investigation and troubleshooting of technical issues in lyophilization with the identification and implementation of corrective actionsCollaborate with Product Development team to transfer new processes to manufacturing and generate production records and SOPs in compliance with ISO 13485Generate risk assessments and mitigation plans when processes are transferred to ManufacturingFacilitate continuous improvement of processes to increase efficiency, improve quality, and promote sustainabilityTrain new manufacturing staff on procedures, aseptic techniques, equipment, and trouble-shooting skillsCoordinate with Facilities, QC and R&D to complete all pre- and post-production activitiesPerform final review of manufacturing MPRs for accuracy and filing of recordsAdhere to best safety practices and documented procedures to ensure a safe working environmentRequired Qualifications
Bachelor's degree or above in biological sciences, chemical engineering or related discipline7+ years' experience in pharmaceutical or biotechnology manufacturing or equivalent experience, with 4+ years of hands-on experience in lyophilizationKnowledge of Good Manufacturing PracticesCan follow/interpret SOPs and train manufacturing staff in lyophilizationGood analytical skills to interpret manufacturing data and understand production problemsExperience with process development, transfer and optimization preferredMechanical aptitude on performing troubleshooting and PM on lyophilizers preferredExperience with execution of validation protocols is a plusExcellent communication skills and good attention to detailAbility to work in a fast-paced, dynamic team environmentAbility to handle multiple projects at one timeThe base salary range for this full-time position is $110,000 - $130,000 + bonus + equity + benefits. Our salary ranges are determined by work location, job-related skills, experience, and relevant education or training. The ranges displayed on each job posting reflect the minimum and maximum target for new hire salaries but are subject to change if the leveling of the role is adjusted. Your recruiter can share more about the specific salary range during the hiring process.
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