Lead Manufacturing Associate - Lyophilization

Alamar Biosciences • Fremont, CA

1d • Onsite

About The Position

At Alamar, we are passionate about enabling our customers to make scientific discoveries that translate into clinical outcomes and benefit patients. Our team is growing quickly as we develop innovative approaches to measure critical protein biomarkers from liquid samples that can enable the earliest possible detection of disease. We believe the next frontier in biology is enabled by measuring proteins at higher sensitivity in highly multiplexed assays at the push of a button, which is something only Alamar can do. As we build our team, we seek collaborative, driven, intellectually curious people committed to solving complex challenges. Our culture rewards accountability and cross functional teamwork because we believe this enables the kind of breakthrough thinking that will accelerate our mission. Description: We are seeking an experienced, detailed oriented, and results-driven candidate to join our Operations team as Lead Manufacturing Associate - Lyophilization. This position act 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.

Requirements

• Bachelor’s degree or above in biological sciences, chemical engineering or related discipline.
• 7+ years’ experience in pharmaceutical or biotechnology manufacturing or equivalent experience with minimum 4 years of hands-on experience in lyophilization.
• Knowledge of Good Manufacturing Practices.
• Experience in formulation and scale up.
• Good analytical skills to interpret manufacturing data and understand production problems.
• Excellent communications skills and good attention to detail.
• Ability to work in fast paced, dynamic, team environment.
• Ability to handle multiple projects at one time.
• Proficient in MS Office (Word, Excel, and PowerPoint).

Nice To Haves

• Experience with process development, transfer and optimization preferred.
• Mechanical aptitude on performing troubleshooting and PM on lyophilizers preferred.
• Hands‑on familiarity with process characterization, scale‑up, and validation readiness activities (e.g., support of IQ/OQ/PQ planning or execution).
• Practical experience driving or supporting continuous improvement initiatives within a manufacturing or operations organization.
• Demonstrated ability to lead cross‑functional teams by influence, aligning Manufacturing, Quality, Engineering, and Supply Chain toward shared objectives.

Responsibilities

• Lead, plan, and perform production activities for lyophilization
• Provide technical support for any lyophilization process-related issues
• Responsible for revising and originating production records, standard operating procedures, protocols and reports; initiates and closes out deviation reports and change requests
• Ensure lyophilization equipment is in controlled state to sustain manufacturing and ensure routine PM is executed on time
• Perform investigation and troubleshooting of technical issues in lyophilization with the identification and implementation of corrective actions.
• Collaborate with Product Development team to transfer new processes to manufacturing and generate production records and SOPs in compliance with ISO 13485
• Generate risk assessments and mitigation plans when processes are transferred to Manufacturing
• Facilitate continuous improvement of processes to increase efficiency, improve quality and promote sustainability
• Train new manufacturing staff on procedures, aseptic techniques, equipment and trouble-shooting skills
• Coordinate with Facilities, QC and R&D to complete all pre- and post-production activities
• Perform final review of manufacturing MPRs for accuracy and filing of records
• Adhere to best safety practices and documented procedures to ensure a safe working environment

Benefits

• bonus
• equity
• benefits

What This Job Offers

• Job Type: Full-time
• Career Level: Mid Level