Project Manager (Manufacturing Engineering)

Tegra Medical; Country View Estates (MA); On-site; USD 96,000 - 120,000; Full time

Benefits offered by this job

On-the-job training and advancement

Health, dental, vision, life, and/disb

401K

Paid time off

Sick time

Holiday pay

Tuition Reimbursement

Job summary

Tegra Medical in Franklin, MA seeks a Project Manager (Manufacturing Engineering) to lead cross-functional projects from initiation to closure in a regulated medical-device setting.

The role emphasizes scheduling, risk management, root-cause analysis and continuous-improvement initiatives with Engineering, Quality and Operations. Bachelor's in engineering and 3–5 years in manufacturing are preferred.

Qualifications

• Strong project-planning, organization and follow-through skills.
• Ability to lead cross-functional teams without direct authority.
• Strong meeting-facilitation, action-management and reporting skills.
• Working knowledge of root-cause and corrective-action methods.
• Knowledge of manufacturing processes, process validation and quality-system requirements.
• Proficiency with MS Project, Excel and PowerPoint.

Responsibilities

• Lead projects from authorization through implementation and closure with sponsors and stakeholders.
• Develop and maintain project schedules, set review cadence based on complexity.
• Track actions and open issues to completion with accountable team members.
• Coordinate schedule delays and resource constraints with site leadership.
• Provide status reports on milestones, risks and decisions.
• Coordinate cross-functional activities across Engineering, Quality, Operations and Purchasing.
• Support validation and production-readiness activities with Engineering and Operations.

Skills

Project management

Cross-functional leadership

Meeting facilitation

Root-cause analysis

Schedule management

Communication

Education

Bachelor's degree in engineering

Tools

Microsoft Project

Microsoft Excel

PowerPoint

Job description

If you are unable to complete this application due to a disability, contact this employer to ask for an accommodation or an alternative application process.

Project Manager (Manufacturing Engineering)

FT Salary Full Time Franklin, MA, US

Salary Range: $96,000.00 To $120,000.00 Annually

Join Our Team at Tegra Medical!

We’re a trusted contract manufacturer for some of the biggest names in the medical device industry. Known for taking on complex projects that others can’t, we pride ourselves on precision and innovation. Headquartered in Franklin, MA, Tegra Medical is part of the global SFS Group, based in Heerbrugg, Switzerland. Together, we’re shaping the future of healthcare.

Job Summary

The Project Manager – Engineering leads and coordinates cross-functional engineering and manufacturing projects from initiation through closure, including root-cause investigations, corrective-action and continuous-improvement initiatives, cost-reduction and supplier projects, equipment implementation and other manufacturing-support efforts.

The role owns project execution—schedules, milestone tracking, action follow-up, status reporting and issue escalation—and coordinates the resources, meetings, supplier activities and cross-functional dependencies that keep projects on objective and on time. The Project Manager may lead structured problem-solving but does not replace the technical authority of Engineering, Quality, Operations or other subject‑matter experts; technical, process‑development, Quality and commercial decisions remain with the responsible functional owners.

Role and Responsibilities

Project planning and execution

• Lead assigned projects from authorization through implementation and formal closure, defining scope, objectives, deliverables, milestones and completion criteria with sponsors and stakeholders.
• Develop and maintain project schedules identifying activities, dependencies, owners and due dates, and set a review cadence based on complexity, urgency and business impact.
• Track actions, decisions, deliverables and open issues to completion, holding team members accountable for agreed commitments and dates.
• Identify and escalate schedule delays, resource constraints and unresolved dependencies to the appropriate functional or site leadership.
• Provide regular status reports on progress, milestones, open actions and risks; verify deliverables are accepted before closure and document lessons learned.

Root‑cause analysis and corrective‑action projects

• Lead structured root‑cause and corrective‑action projects, facilitating problem‑solving with methods such as 8D, DMAIC, 5 Whys, cause‑and‑effect or fault‑tree analysis.
• Ensure the team establishes a clear problem statement, containment plan, investigation strategy and measurable success criteria.
• Coordinate data collection, testing and technical analysis, ensuring actions are assigned to qualified subject‑matter experts.
• Drive timely containment, root‑cause analysis, corrective‑action implementation and effectiveness verification supported by objective evidence.
• Escalate stalled investigations or unresolved disagreements and support investigation summaries, reports and presentations; technical experts remain responsible for technical conclusions.

Cross‑functional coordination

• Coordinate activities and resource needs across Engineering, Quality, Operations, Materials, Maintenance, Purchasing, Customer Service and other functions.
• Run project meetings—agendas, decisions and action items—and manage dependencies so one group’s work does not unnecessarily delay another’s.
• Coordinate supplier schedules, technical reviews, quotations, deliverables, installations and open actions.
• Coordinate customer and external communication through the appropriate Program Management, Customer Service, Quality or commercial representative, and document decisions and scope or timing changes.

Validation and implementation support

• Support validation and qualification planning by coordinating schedules, resources, prerequisites and required deliverables.
• Track equipment qualification, process validation, inspection, documentation, training and production‑readiness activities, and coordinate implementation with Engineering, Quality and Operations.
• Identify and elevate open items affecting production release, and support transition of completed projects to the responsible owner once documentation and training are complete.

Qualifications

• Strong project‑planning, organization and follow‑through skills, with the ability to manage multiple projects and competing priorities.
• Ability to lead cross‑functional teams without direct authority; experience leading cross‑functional technical or operational projects required.
• Strong meeting‑facilitation, action‑management and written and verbal communication skills, including clear reporting of status, risks and decisions to management.
• Working knowledge of structured root‑cause and corrective‑action methods; experience with root‑cause analysis, corrective action or continuous improvement required.
• Working knowledge of manufacturing processes, process validation, equipment qualification, change control and quality‑system requirements preferred.
• Ability to challenge assumptions respectfully and maintain accountability.
• Proficiency with Microsoft Project or comparable scheduling software.
• Proficiency with Microsoft Excel, PowerPoint and other project‑reporting tools; project‑management, Lean, Six Sigma or structured problem‑solving training preferred.

Education Requirements

A bachelor's degree in engineering or a related technical discipline and a minimum of three to five years’ engineering experience in a manufacturing environment is required. Experience in a medical‑device, pharmaceutical or another regulated manufacturing environment is strongly preferred.

Physical Requirements

• Frequent performing repetitive work
• Occasional lifting (max. 40 lbs.)
• Occasional carrying (max. 40 lbs.)
• Subject to physical hazards from moving equipment and machine parts
• Constant safety glasses
• Constant full PPE
• Frequent standing
• Occasional sitting, walking, pushing, pulling, reaching
• Regular attendance in the office is required

What We Offer:

• On‑the‑job training and advancement opportunities
• Competitive hourly wage + shift differentials(2nd& 3rdShift)
• Great benefits like health, dental, vision, life, and disability insurance; 401K and much more.
• Paid time off, sick time and holiday pay
• Employee Assistance Program/ Tuition Reimbursement

Join Our Team at Tegra Medical!

We’re a trusted contract manufacturer for some of the biggest names in the medical device industry. Known for taking on complex projects that others can’t, we pride ourselves on precision and innovation. Headquartered in Franklin, MA, Tegra Medical is part of the global SFS Group, based in Heerbrugg, Switzerland. Together, we’re shaping the future of healthcare.

Job Summary

The Project Manager – Engineering leads and coordinates cross‑functional engineering and manufacturing projects from initiation through closure, including root‑cause investigations, corrective‑action and continuous‑improvement initiatives, cost‑reduction and supplier projects, equipment implementation and other manufacturing‑support efforts.

The role owns project execution—schedules, milestone tracking, action follow‑up, status reporting and issue escalation—and coordinates the resources, meetings, supplier activities and cross‑functional dependencies that keep projects on objective and on time. The Project Manager may lead structured problem‑solving but does not replace the technical authority of Engineering, Quality, Operations or other subject‑matter experts; technical, process‑development, Quality and commercial decisions remain with the responsible functional owners.

Role and Responsibilities

Project planning and execution

• Lead assigned projects from authorization through implementation and formal closure, defining scope, objectives, deliverables, milestones and completion criteria with sponsors and stakeholders.
• Develop and maintain project schedules identifying activities, dependencies, owners and due dates, and set a review cadence based on complexity, urgency and business impact.
• Track actions, decisions, deliverables and open issues to completion, holding team members accountable for agreed commitments and dates.
• Identify and elevate schedule delays, resource constraints and unresolved dependencies to the appropriate functional or site leadership.
• Provide regular status reports on progress, milestones, open actions and risks; verify deliverables are accepted before closure and document lessons learned.

Root‑cause analysis and corrective‑action projects

• Lead structured root‑cause and corrective‑action projects, facilitating problem‑solving with methods such as 8D, DMAIC, 5 Whys, cause‑and‑effect or fault‑tree analysis.
• Ensure the team establishes a clear problem statement, containment plan, investigation strategy and measurable success criteria.
• Coordinate data collection, testing and technical analysis, ensuring actions are assigned to qualified subject‑matter experts.
• Drive timely containment, root‑cause analysis, corrective‑action implementation and effectiveness verification supported by objective evidence.
• Escalate stalled investigations or unresolved disagreements and support investigation summaries, reports and presentations; technical experts remain responsible for technical conclusions.

Cross‑functional coordination

• Coordinate activities and resource needs across Engineering, Quality, Operations, Materials, Maintenance, Purchasing, Customer Service and other functions.
• Run project meetings—agendas, decisions and action items—and manage dependencies so one group’s work does not unnecessarily delay another’s.
• Coordinate supplier schedules, technical reviews, quotations, deliverables, installations and open actions.
• Coordinate customer and external communication through the appropriate Program Management, Customer Service, Quality or commercial representative, and document decisions and scope or timing changes.

Validation and implementation support

• Support validation and qualification planning by coordinating schedules, resources, prerequisites and required deliverables.
• Track equipment qualification, process validation, inspection, documentation, training and production‑readiness activities, and coordinate implementation with Engineering, Quality and Operations.
• Identify and escalation open items affecting production release, and support transition of completed projects to the responsible owner once documentation and training are complete.

Qualifications

• Strong project‑planning, organization and follow‑through skills, with the ability to manage multiple projects and competing priorities.
• Ability to lead cross‑functional teams without direct authority; experience leading cross‑functional technical or operational projects required.
• Strong meeting‑facilitation, action‑management and written and verbal communication skills, including clear reporting of status, risks and decisions to management.
• Working knowledge of structured root‑cause and corrective‑action methods; experience with root‑cause analysis, corrective action or continuous improvement required.
• Working knowledge of manufacturing processes, process validation, equipment qualification, change control and quality‑system requirements preferred.
• Ability to challenge assumptions respectfully and maintain accountability.
• Proficiency with Microsoft Project or comparable scheduling software.
• Proficiency with Microsoft Excel, PowerPoint and other project‑reporting tools; project‑management, Lean, Six Sigma or structured problem‑solving training preferred.

Education Requirements

A bachelor's degree in engineering or a related technical discipline and a minimum of three to five years’ engineering experience in a manufacturing environment is required. Experience in a medical‑device, pharmaceutical or another regulated manufacturing environment is strongly preferred.

Physical Requirements

• Frequent performing repetitive work
• Occasional lifting (max. 40 lbs.)
• Occasional carrying (max. 40 lbs.)
• Subject to physical hazards from moving equipment and machine parts
• Constant safety glasses
• Constant full PPE
• Frequent standing
• Occasional sitting, walking, pushing, pulling, reaching
• Regular attendance in the office is required

What We Offer:

• On‑the‑job training and advancement opportunities
• Competitive hourly wage + shift differentials(2nd& 3rdShift)
• Great benefits like health, dental, vision, life, and disability insurance; 401K and much more.
• Paid time off, sick time and holiday pay
• Employee Assistance Program/ Tuition Reimbursement

Monday to Friday, Standard Working Hours