Alamar Biosciences
Senior Manufacturing Associate
Fremont, California · Senior
Sponsorship not specifiedDetected 12 days ago
GMPMedical DevicesCommunicationMentoringOrganizational SkillsGxP
About the role
- 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
Responsibilities
- Perform processing and conjugation of antibodies and lyophilization of critical components for downstream manufacturing.
- Assist in other manufacturing activities deemed high priority such as filling and packaging, label printing, and special builds, etc.
- Perform batch records review and sign off to ensure completeness and compliance to Quality System standards.
- Support production scheduling and assignment of job duties to team members.
Requirements
- Ability to troubleshoot and resolve complex technical issues autonomously, escalating only when necessary.
Nice to have
- 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.
- Senior Manufacturing Associate handles various Manufacturing assignments ranging from routine to complex, requiring sound judgment to solve issues, identify areas for enhancement, and suggest improvements.
- Capable of prioritizing tasks independently and apply their experience to effectively plan and achieve objectives.
- Experience working under ISO 13485 and/or current Good Manufacturing Practice (cGMP) in a biotechnology or pharmaceutical industry is highly preferred.
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