Jobs · Information Technology · New Jersey

Sr Manager, ECQ Delivery - Summit West NJ

VetJobs · New Jersey, United States · 1 wk ago
Information Technology$126k–$152k/yrFull-time

About the role

The Senior Manager, Equipment Commissioning & Qualification (ECQ) Delivery supports the successful operation of facility, laboratory and business functions at multi-use sites through interaction with internal team members, peer-level customers, and external service providers. The incumbent supervises entry, junior, and experienced-level professionals tasked with commissioning and qualifying new equipment, facilities, and utilities, and maintaining equipment systems in a qualified/validated state according to established policies and procedures.

Responsibilities

  • Directly manage Equipment Commissioning & Qualification equipment qualification and computerized system validation teams.
  • Manage and allocate resources responsible for teams performing validation activities of new equipment and standalone/enterprise laboratory computerized systems and/or changes to existing equipment and standalone/enterprise computerized systems.
  • Define the needs, benefits, and technical strategy within the project life-cycle and overall processes.
  • Manage project teams with emphasis on solutions to technical and compliance challenges in all phases of the System Lifecycle.
  • Oversee the Development/Review/Approval of SOPs, WPs, test protocols, validation deliverables, plans and policies as needed.
  • Maintain departmental commissioning and qualification procedures and policies.
  • Ensure site and project master plans comply with global policies and regulatory agency requirements.
  • Maintain resources performing validation activities are knowledgeable of and in tune with latest industry regulations and initiatives.
  • Provide input and guidance for change strategy, risk assessment, testing and compliance gaps.
  • Ensure compliance with Facilities Services Qualification Master Plan.
  • Oversee the site requalification activities and requalification programs.
  • Responsible for developing and managing budgets and resources for the program.
  • Create departmental metrics; understand, review, and deliver metrics to the team to determine areas for improvement.
  • Lead a larger team of up to 50 people across multiple areas, including 3 direct supervisors/manager-level personnel.
  • Interview and hire internal and/or external personnel to fill necessary roles.
  • Provide direction to internal and external team members.
  • Manage the workload of team members to ensure appropriate work-life balance.
  • Delegate, develop, and motivate direct and contract reports.
  • Set departmental and individual goals.
  • Deliver personnel performance reviews.
  • Ensure team members are appropriately trained for duties being performed.
  • Aid in the preparation of departmental operational expense and capital budgets; justify and work within approved headcount.
  • Promote and ensure the safety of all team members and adherence to site EHS procedures and guidelines.
  • Ensure the team is in full compliance with local, site and global BMS policies and procedures.
  • Manage staff workload of multiple complex projects and priorities across the many different departments that the ECQ organization serves.
  • Develop an effective mechanism for communicating the current status of all laboratory systems maintained by ECQ to all affected stakeholders.
  • Communicate effectively with peers and senior management to identify needs, justifications, and evaluate alternative business solutions when appropriate.
  • Regularly review, prioritize and promptly respond to customer equipment qualification and support requests.
  • Provide technical support and guidance on equipment and computer systems qualification and validation issues.
  • Interface with customers to ensure all expectations are being met.
  • Maintain a positive relationship with all members of the Equipment Commissioning & Qualification department and site customers while promoting a positive team environment.
  • Continually seek opportunities to increase internal client satisfaction and deepen client relationships.
  • Ensure equipment, facilities and programs are maintained in compliance.
  • Act as departmental lead and SME in both internal and regulatory audits.

    Qualifications

    • Expert knowledge of cGMP, GXP, GAMP, SDLC regulations, including 21CFR part 11, computer systems validation requirements and good documentation practices.
    • Expert knowledge of pharmaceutical, manufacturing and laboratory systems and equipment.
    • Ability to develop, delegate, and motivate others including direct and indirect reports.
    • Strong financial acumen.
    • Solid understanding of scheduling fundamentals, execution and cost control.
    • Advanced understanding of investigations, deviations and CAPA management in a regulated pharmaceutical industry.
    • Strong multi-tasking ability in conjunction with proven managing skills; ability to effectively manage multiple projects, initiatives and activities simultaneously.
    • Strong written and verbal communication skills.
    • Excellent interpersonal skills with experience dealing with a diverse workforce.
    • Strong presentation development and delivery skills.
    • Highly proficient computer skills in Microsoft Office Suite – Word, Excel, PowerPoint and Outlook with extensive background in database systems.
    • Innate ability to learn new software, such as corporate intranet and enterprise business tools.
    • Working knowledge of scheduling software and systems, and inventory management systems, mainly CMMS.
    • Experience with departmental capital and expense budget forecasting and management.

    Skills

    • Expert knowledge of cGMP, GXP, GAMP, SDLC regulations, including 21CFR part 11, computer systems validation requirements and good documentation practices.
    • Expert knowledge of pharmaceutical, manufacturing and laboratory systems and equipment.
    • Ability to develop, delegate, and motivate others including direct and indirect reports.
    • Strong financial acumen.
    • Solid understanding of scheduling fundamentals, execution and cost control.
    • Advanced understanding of investigations, deviations and CAPA management in a regulated pharmaceutical industry.
    • Strong multi-tasking ability in conjunction with proven managing skills; ability to effectively manage multiple projects, initiatives and activities simultaneously.
    • Strong written and verbal communication skills.
    • Excellent interpersonal skills with experience dealing with a diverse workforce.
    • Strong presentation development and delivery skills.
    • Highly proficient computer skills in Microsoft Office Suite – Word, Excel, PowerPoint and Outlook with extensive background in database systems.
    • Innate ability to learn new software, such as corporate intranet and enterprise business tools.
    • Working knowledge of scheduling software and systems, and inventory management systems, mainly CMMS.
    • Experience with departmental capital and expense budget forecasting and management.

    Benefits

    Not specified.

    Pay

    $125,740 - $152,368

    Schedule

    Mon-Fri: 8AM-5PM

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