Supervisor, Reagent Manufacturing - 2nd Shift

Element Biosciences · San Diego - Headquarters

  • Junior
  • Full-time
  • $102,000 – $125,000
  • Posted 2026-09-21
  • Confirmed live on 25 September 2026

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Job description

At Element Biosciences, we are passionate about our mission to empower the scientific community with more freedom and flexibility to accelerate our collective impact on humanity. We have built a highly efficient product-driven organization where employees can learn, grow, and thrive in a challenging but encouraging environment. We are committed to scientific integrity, collegiality, honesty, objectivity, and openness.

We are looking for a dynamic, driven, and passionate Manufacturing Supervisor to build, grow, and run a manufacturing team in a fast-paced and fun environment. We need an individual comfortable developing an organization and processes to support the unique needs of the genomics industry. We are building a fully integrated Operations team to work closely with our technology and product development teams to empower the scientific community and accelerate our collective impact on humanity. We look for flexible candidates eager to build an amazing company and launch amazing products!

Our Reagent Manufacturing Supervisor will be leading a team of full-time and contractor technicians responsible for production execution across the entire Reagent Manufacturing value stream.

This role will report to our Manager, Reagent Manufacturing and will be a 2nd Shift San Diego based role.

If you possess the following and want to make a meaningful impact, we invite you to explore this role.

Essential Functions and Responsibilities:

• As a PEOPLE LEADER: Professional and servant leader who removes roadblocks from the team, motivates them to victory, and supports their professional development

• As a SUPERVISOR: A team player when it comes to solving problems and achieving production goals

• As a CONTRIBUTOR: An innovative and proactive problem solver and can be fully entrusted to deliver exceptional results on any project, task, or duty

• Directs manufacturing leads and team members to ensure day-to-day production goals and schedule commitments are met

• Accountable for the shift's key performance indicators and the team's completion of the daily production schedule; ensures the team meets or exceeds manager expectations

• Establishes production schedules and priorities with manager oversight and ensures execution of the schedule is efficient and optimized

• Contributes to technology transfer and new product introduction as the voice of Manufacturing. Responsible for successful pilot/development runs and consults the manager on decisions impacting the broader team

• Partners with Process Engineering and other support groups to enable troubleshooting and continuous improvement. Focuses on resource management, impact analysis, and improvements to safety, quality, efficiency, and throughput

• Collaborates with the Quality team to maintain adherence to quality systems, procedures, operating standards, and applicable compliance requirements

• Partners with the Manager and Human Resources on hiring, performance, promotion, and termination decisions. Provides major input on FTE decisions, is responsible for contractor hiring, and executes the approved hiring plan

• Accountable and responsible for the team's training program, including on-time completion of training assignments, accurate training plans, a robust OJT program, and appropriate ad-hoc, awareness, and remedial training

• Responsible for tactical coaching and development of team members and contributes to strategic team development in consultation with the manager. Provides leadership to a diverse workforce and supports ancillary production activities as needed

• Ensures team adherence to the Employee Handbook, company policies, environmental health and safety requirements, and safe work practices across formulating, filling, and kitting operations

• Key contributor to ECO/DCO/NCR documentation. Authors selected technical documentation, owns area-specific WI/BR/SOP redlines, and contributes to higher-level Manufacturing documentation

Education and Experience:

• Bachelors in science, engineering, or a related discipline is preferred with 2+ years of relevant manufacturing/engineering experience in life sciences, biotechnology, pharmaceutical, or diagnostic manufacturing

• An equivalent combination of experience and education, including a high school diploma plus equivalent progressive experience, may be considered

• Prior experience leading or supervising manufacturing personnel is required

• Relevant experience in the life science industry is preferred

• Knowledge of ISO 13485 is preferred

• Advanced understanding of Lean Manufacturing principles and Six Sigma methodologies; Green Belt training

• Strong verbal, written, and presentation skills; able to lead shift start-up/Tier I meetings and small-to-medium meetings

• Proficiency in people skills with sufficient emotional intelligence; collaborates effectively across teams and delivers tactful constructive feedback to direct reports

• Demonstrated competency in critical thinking an

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