Senior Manufacturing Technician

Alamar Biosciences•Fremont, CA

1d•$30 - $35

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. We are seeking a result-driven Senior Manufacturing Technician to join our Manufacturing team for a special second shift. The qualified candidate will be responsible for the manufacturing of intermediates and finished products in a controlled GMP environment. Experience in reagent filling and packaging of reagent kits under Good Manufacturing Practice (GMP) in a regulated industry is highly preferred. Work Schedule: This position is for the following schedule: 10 am to 6:30 pm Thursday, Friday, Saturday, Sunday, and Monday. Second Shift Expectations: Minimal supervision is provided over the weekend; candidates must demonstrate extensive experience working independently and making sound decisions in a manufacturing environment. Ability to troubleshoot and resolve complex technical issues autonomously, escalating only when necessary. Provide guidance to junior staff as needed. Strong organizational skills and self-motivation are essential to maintain productivity and quality standards during off-hours. Effective communication skills to provide regular updates and document activities for review by weekday supervisors. Commitment to safety, quality, and continuous improvement, even when working independently.

Requirements

Associate degree or bachelor’s degree in biology, chemistry, or a related field.
Minimum 4 years of relevant experience in GMP-regulated manufacturing, preferably in biotech, pharma, or diagnostics.
Demonstrated ability in following established procedures and maintaining detailed and accurate manufacturing records
Demonstrated experience working independently with minimal supervision, especially during weekend or off-hour shifts. Ability to communicate effectively with remote or off-site supervisors.
Proven ability to make sound decisions and solve problems autonomously
Proficiency in troubleshooting process and equipment.
Effective verbal and written communication skills. Ability to communicate effectively with remote or off-site supervisors.
Good time management skills
Strong team player, self-motivated, and willing to learn new techniques and concepts in a fast-paced environment
Able to lift up to 25 lbs. Position requires working in a standing position for long periods of time on a daily basis.

Nice To Haves

Previous experience with inventory management system preferred
Experience in ISO 13485 and GMP environment a plus.

Responsibilities

Operate, maintain, and troubleshoot manufacturing equipment and systems (manual, semi-automated and automated).
Perform reagent filling, packaging, and labeling under ISO and GMP standards.
Support other manufacturing activities as required, such as simple buffers and reagents formulation.
Conduct quality checks and ensure products meet specifications.
Maintain organized production areas and labs, ensure safety and compliance with all laboratory practices are followed.
Participate in laboratory maintenance, including general cleaning of facility, cleaning of labware, and routine laboratory housekeeping.
Track manufacturing supplies and consumables inventory.
Document production data, maintenance activities, and quality control results in compliance with company protocols.
Train junior technicians: act as lead when supervisor is unavailable.
Participate in internal and external safety and quality inspections.
Collaborate cross-functionally with QC, Engineering, and Supply Chain teams.
Initiate and participate in continuous improvement initiatives (Lean, Six Sigma, Kaizen).
Adhere to laboratory safe practices and maintain a safe working environment.
Support quarterly Cycle Count to ensure inventory accuracy