Sr. Technical Project Manager

haemonetics; Boston (MA); On-site; USD 90,000 - 153,000; Full time

Benefits offered by this job

401(k) match

Employee stock purchase plan

Flexible time off

Vacation accrual for hourly employees

Paid sick time

Holidays

Parental leave

Disability insurance

Tuition reimbursement

Health benefits

Job summary

Haemonetics is seeking a Sr. Project Manager in Boston to plan, execute, and commercialize NPI and large sustaining projects on strict deadlines and budgets.

You will lead cross-functional teams, manage risks, and maintain governance to ensure alignment of costs, schedules, and scope across projects. Strong experience in medical device development and regulatory standards is required.

Qualifications

• 5+ years of project management experience leading medical device development.

Responsibilities

• Analyze project risks and identify impact while developing mitigation strategies.
• Identify and manage critical path across projects.
• Ensure project definition aligns with stakeholders and drive from concept to commercialization.
• Create and execute detailed project plans and revise as needed to meet changing requirements.
• Manage day-to-day operational aspects and project scope.
• Ensure compliance with Stage Gate and SOPs; enforce quality systems.
• Escalate issues and resolve team conflicts to maintain momentum.
• Establish governance for clear objectives and accountability.
• Ensure product compliance with design history file, regulatory standards, and QMS.

Skills

Project management

Medical device development

Regulatory compliance

Job description

Pay Transparency:

The pay range for this role is:

$90,100.00-$153,300.00/Annual

The base pay actually offered to the successful candidate will take into account, without limitation, the candidate's location, education, job-knowledge, skills, and experience in prior relevant roles.

Incentives may also be provided as part of Haemonetics' employee compensation. For sales roles , employees will be eligible for sales incentive (i.e., commission) under the applicable plan terms. For non-sales roles , employees will be eligible for a discretionary annual bonus, the target amount of which varies based on the applicable role, to be governed by the applicable plan terms. Employees may also be eligible to participate in the Company's long-term incentive plan, with eligibility and target amount dependent on the role.

• a 401(k) with up to a 6% employer match and no vesting period
• an employee stock purchase plan
• "flexible time off" for salaried employees
• for hourly employees, accrual of three to five weeks' vacation annually (based on tenure)
• accrual of up to 64 hours (annually) of paid sick time
• paid and/or floating holidays
• parental leave
• short- and long-term disability insurance
• tuition reimbursement
• and/or health and welfare benefits

Depending on your location, you may be eligible for more detailed information related to the compensation and benefits related to this job posting. If you believe you may be entitled to such information by law, you may contact 1-781-348-7777, Monday through Friday, 7:30 a.m. - 5 p.m. ET or email [e-mail] .

We are constantly looking to add to our core talent. If you are seeking a career that is challenging and rewarding, a work environment that is diverse and dynamic, look no further - Haemonetics is your employer of choice.

Job Details

The Sr. Project Manager is responsible to plan, execute, manage risk, manage critical path and commercialize NPI and large sustaining projects according to strict deadlines and within budget. This includes engaging resources and coordinating the efforts of team members, third-party organizations and the client in order to deliver projects according to plan.

Accountable to create project team governance to engage cross functional accountability of costs, schedules, scope, and track risks of projects. Duties are listed in order of greatest importance.

The incumbent may be asked to perform other function-related activities in addition to the below mentioned responsibilities as reasonably required by business needs.

Responsibilities/Essential Duties :

• Analyze project risks and identify their impact while developing mitigation strategies,
• Identify and manage critical path,
• Ensure appropriate project level definition across all stake holders and manage the project from concept to commercialization
• Creates and executes project work plans and revises as appropriate to meet changing needs and requirements.
• Manages day-to-day operational aspects of a project and scope.
• Complies with the Stage Gate Process quality system and helps to enforce standard operating procedures (SOPs).
• Escalates appropriately when required. Mitigates team conflict and communication problems.
• Escalates appropriately when required. Motivates team to work together in the most efficient manner. Leverages project management tools to assist in the development of and adherence to a schedule and reporting status.
• Own and create appropriate levels of governance to ensure alignment and clear objectives
• Accountable for product compliance to design history file, regulatory standards, and QMS procedures
• Keeps track of lessons learned and shares those lessons with team members

Experience Details:

• 5 plus yrs in project management leading medical device development.
• Experience with medical device development under FDA Quality Systems Regulations, CE Marking, and ISO Quality Systems
• Technical project management in software, Medical Disposables and hardware product development

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