Supervisor, Biorepository Operations

Posted 12 Days Ago
Be an Early Applicant
Indianapolis, IN, USA
In-Office
65K-88K Annually
Junior
Biotech
The Role
Manage day-to-day biorepository operations, supervise and develop staff, ensure quality and compliance (GMP/GLP), oversee sample receipt/accessioning/storage, resolve client issues, and drive process improvements.
Summary Generated by Built In
Azenta Inc.

At Azenta, new ideas, new technologies and new ways of thinking are driving our future. Our customer focused culture encourages employees to embrace innovation and challenge the status quo with novel thinking and collaborative work relationships.
All we accomplish is grounded in our core values of Customer Focus, Achievement, Accountability, Teamwork, Employee Value and Integrity

Job TitleSupervisor, Biorepository Operations

Job Description

How You’ll Add Value:

This Biorepository Supervisor serves as the point of contact for all sample service requests and deliveries, is responsible for both operational and quality excellence, and provides technical and managerial guidance to of the team. 

What You’ll Do:

  • Set, maintain, track and communicate all goals and objectives- including individual learning plans, individual/team/department goals, and daily work assignments

  • Promote collaboration across all shifts, teams and departments

  • Manage all aspects of Biobank team including personnel, productivity, general inventory, team metrics, and resources in support of department objectives

  • Enforce all policies and procedures with attention to Quality compliance

  • Effectively communicate all team affairs as needed and provide data, reports, and documentation as requested to support Lead Supervisor/Director.

  • Work with PMO to ensure customer expectations are met

  • Oversee and participate in the receipt of packages, sample data entry, accessioning of samples, labeling samples, and assigning storage locations to samples as needed

  • Proactively manage and drive the resolution of assigned clients’ issues

  • Recognize, escalate, and ensure resolution of operational, quality, or financial concerns of the team/department

  • Write and present semi-annual and annual performance reviews for assigned staff including the initiation of commendation or disciplinary action as applicable

  • Coach and assist staff in their career development efforts

  • Promote culture of continuous process improvement by leading, participating, and implementing improvements

  • Facilitate or participate in identification and execution of effective corrective and preventative actions. Document and follow through with root cause analysis for departmental errors

  • Generate change control requests and initiate/investigate Nonconformance’s as necessary

  • Review QRs identified by team members and send initial notification to PM and client

  • Perform or facilitate the creation of client specific SOPs, job aids and other customer documents

  • Ensure all service/process failures are identified, investigated and appropriately resolved

  • Ensure equipment and facility are maintained in good working order. Maintain a safe work environment by following all established safety and universal precautions guidelines and procedures

  • Direct and effectively plan daily activities of Biobank technicians, assigning work accordingly

Your Management Responsibilities:          

Hiring & Staffing

  • Skills assessment

  • Resource planning

  • Competency based, quality hiring

  • Effective on-boarding

Collaboration

  • Constructive conflict

  • Appropriate follow-up

  • Holds self and other accountable

  • Builds relationships & partners across-functions

  • Considers and communicates cross-functionally

Communication to Inspire & Empower

  • Regular meaningful communications

  • Connection of department & individual purpose to strategic direction

  • Follow-up to address obstacles

Performance Management

  • Reinforce behaviors that drive results

  • Assess -right person in the right job

  • Feedback/coaching

  • Raising the bar; increasing contribution

  • Address misaligned or misplaced talent

Develop People

  • Dialogue about skills & behaviors for success at Azenta

  • Understanding employee aspirations

  • Opportunities for experiential learning & growth

  • Experience planning & delegate to develop

What You Will Bring:

  • Bachelor’s Degree + 2 years of people and functional experience

  • OR Associate Degree + 4 years of experience, 2 years must be in a people and functional experience

  • OR HS Diploma + 5 years of experience, 2 years must be people and functional experience

  • OR one year experience as a Team Coordinator at Azenta with no correction action of any type (documented warnings/PIP) within the last 6 months

  • Experience in FDA regulated industry (GMP or GLP) preferred

  • Previous sample and/or data management experience preferred

Physical Requirements:

  • Able to lift 50 lbs

Your Working Conditions: 

  • Employee will be working in an area with potentially infectious materials

  • Employee will be responsible for maintaining a clean work environment and enforce and follow Universal Precautions for bloodborne pathogens when working in an area considered to be potentially contaminated

If any applicant is unable to complete an application or respond to a job opening because of a disability, please email at [email protected] for assistance. 

Azenta is an Equal Opportunity Employer. This company considers candidates regardless of race, color, age, religion, gender, sexual orientation, gender identity, national origin, disability or veteran status.

United States Base Compensation: $65,000.00 - $88,000.00

The posted pay range for this position is an estimate based on current market data and internal pay structure. Final compensation may vary above or below this range depending on factors such as experience, education (including licensure and certifications),  qualifications, performance, and geographic location, among other relevant business or organizational needs.

Skills Required

  • Bachelor's Degree and 2 years of people and functional experience
  • Associate Degree and 4 years of experience, 2 years must be people and functional experience
  • High School Diploma and 5 years of experience, 2 years must be people and functional experience
  • One year experience as a Team Coordinator at Azenta with no corrective action within the last 6 months
  • Experience in FDA regulated industry (GMP or GLP)
  • Previous sample and/or data management experience
  • Able to lift 50 lbs
  • Ability to work in areas with potentially infectious materials and follow Universal Precautions for bloodborne pathogens

Azenta Life Sciences Compensation & Benefits Highlights

The following summarizes recurring compensation and benefits themes identified from responses generated by popular LLMs to common candidate questions about Azenta Life Sciences and has not been reviewed or approved by Azenta Life Sciences.

  • Equity Value & Accessibility An employee stock purchase plan with a discounted share price and a lookback feature, plus equity and bonus eligibility, provides additional upside beyond base pay.
  • Retirement Support A 401(k) program with company match is highlighted in official materials, indicating meaningful support for long‑term savings.
  • Leave & Time Off Breadth Flexible or unlimited PTO is available for many salaried roles, and paid holidays are included in the package.

Azenta Life Sciences Insights

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The Company
HQ: Burlington, MA
1,095 Employees
Year Founded: 2011

What We Do

Azenta (Nasdaq: AZTA) is a leading provider of life sciences solutions worldwide, enabling impactful breakthroughs and therapies to market faster. Azenta provides a full suite of reliable cold-chain sample management solutions and genomic services across areas such as drug development, clinical research and advanced cell therapies for the industry's top pharmaceutical, biotech, academic and healthcare institutions globally. Azenta is headquartered in Chelmsford, MA, with operations in North America, Europe and Asia. For more information, please visit www.azenta.com.

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