Manager, Master Data Governance

Hiring By - Biostaffic



Job Highlights

Not Disclosed

Mid-Senior level

Posted 4 months ago
Job details

About OmniaBio:

OmniaBio Inc. is a subsidiary of Toronto-based CCRM (, a leader in developing and commercializing regenerative medicine-based technologies and cell and gene therapies. OmniaBio’s facility will be Canada’s first commercial-scale contract development and manufacturing organization (CDMO) dedicated to cell and gene therapies and is expected to be the largest facility of its kind in Canada.

Based at McMaster Innovation Park in Hamilton, Ontario, OmniaBio will anchor a biomanufacturing centre of excellence and open in three phases between 2024 and 2026. OmniaBio has built a substantial team and continues to grow to prepare for this expansion. Benefitting from CCRM’s existing expertise and business practices, OmniaBio currently has established process and analytical development teams and contract manufacturing capabilities. OmniaBio is built upon leadership in induced pluripotent stem cells (iPSCs), immunotherapy and lentiviral vectors (LVVs). The vision is to provide focused support for clients with late clinical-stage manufacturing and commercial supply needs, in addition to early-stage development and first in-human clinical trial material services. Please visit us at to learn more.

Role Summary:

Reporting to the Senior Director, IT-GMP Systems, the Manager, Master Data Governance is responsible for managing and governing all enterprise master data and associated processes; and ensuring data accuracy, completeness and compliance with corporate policies and regulatory requirements (privacy, security and Good Manufacturing Practices (GMP)).


  • Develops, implements and maintains master data governance policies and procedures to ensure the accuracy, completeness and timely availability of data across the organization.
  • Collaborates with cross-functional teams to identify and prioritize data management and analytics initiatives.
  • Owns and drives mobile device management (MDM) roadmap items spanning systems (e.g. ERP, LIMS, MES), governance, process, people and data culture.
  • Assesses and proposes solutions for specific MDM challenges.
  • Ensures compliance with applicable data privacy, security and GMP regulations, and corporate policies.
  • Develops and implements a data governance organization, including identification and training of data stewards.
  • Provides leadership and mentorship to the extended master data management team (i.e, data stewards).
  • Builds organizational capability in data management best practices by preparing and delivering training sessions.


  • Bachelor’s degree, or equivalent academic qualification, in computer science/engineering, information systems, data management or related field.
  • At least five years of work experience with extensive knowledge of master data governance.
  • At least three years of work experience in a leadership role.
  • Extensive knowledge of enterprise data architectures and MDM tools and best practices.
  • Experience working with SAP ERP (S4/HANA preferred).
  • Excellent communication, interpersonal and leadership skills.
  • Experience leading cross-functional teams and developing data-driven solutions. Candidates should be comfortable working in a fast-paced environment and possess excellent communication and leadership skills.

Desired Competencies:

  • Experience with master data governance within a pharmaceutical manufacturing environment (e.g. ERP, LIMS, MES).
  • Experience in a pharmaceutical manufacturing (clinical and/or commercial) environment.
  • Understanding of GxP regulatory requirements (e.g. 21 CFR Part 11, Annex 11, GMP).
  • Analytical skills and strong organizational abilities.
  • Attention to detail and problem-solving aptitude.
  • Ability to work within a matrix organizational structure.
  • Experience working with cloud-based architectures (e.g. Azure, AWS) and SaaS applications.
  • Experience implementing cloud-based analytics platforms (e.g. SAP Analytics Cloud, Power BI).

OmniaBio is a developing organization and represents a fluid working environment. Flexibility and adaptability are essential, and duties will be influenced by the needs of the organization.

Applicants must be legally eligible to work in Canada.

OmniaBio is committed to accessibility, diversity, and equal opportunity. Requests for accommodation can be made at any stage of the recruitment process, providing the applicant has met the bona fide requirements for the open position. Applicants should make their requirements known once contacted to schedule an interview, or when the job offer has been made.

Benefits Offered?

  • No

Bonus Offered?

  • No

Travel Required?

  • No


  • Canada


  • Mid-Senior level

Global Experience Needed?

  • No

Specialized Experience Needed?

  • No

Apply before:

  • Apr 13, 2024
Company Overview

Current Openings: 0

OmniaBio Inc., a subsidiary of CCRM, launched July 1, 2022. OmniaBio is a contract development and manufacturing organization (CDMO) conducting process development and producing gene-modified cells and viral vectors for Phase I clinical trials to commercial-scale manufacturing. OmniaBio is bringing life-saving cell and gene therapies to patients in Canada and around the world.
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