Program Manager, Technical Operations

BMA Group Global; Guayama (PR); On-site; USD 110,000 - 160,000; Full time

Job summary

BMA Group Global is seeking an experienced Innovation and Program Manager, Technical Operations to drive commercialization, technical transfer, and execution of new product initiatives in an FDA-regulated manufacturing environment. The role requires close partnership with Operations, Quality, Engineering, R&D, and Finance to meet quality, cost, timing, and capability requirements.

You will lead cross-functional teams, manage site assessments, and ensure robust processes for NPI and

Qualifications

• Bachelor’s degree in Science, Engineering, Business Administration, or related field.
• Minimum 5 years of experience in FDA-regulated manufacturing or NPI.
• Experience leading technology transfer and manufacturing/process improvements.
• Proven ability to manage cross-functional projects and risk assessments.
• Experience in pharmaceutical or FMCG industries.

Responsibilities

• Lead cross-functional partnerships to drive project execution and transfers.
• Oversee commercialization and introduction of new products and line extensions.
• Manage risk assessments and ensure cost-effective manufacturing.
• Coordinate Site Impact Assessments and investment planning.
• Ensure products meet quality, process capability, and business criteria.
• Provide resource management and oversight to project managers.

Skills

Cross-functional

Project management

NPI

Tech transfer

Risk assessment

Education

Bachelor's degree (Science/Engineering/Business)

Job description

We are seeking an experienced Innovation and Program Manager, Technical Operations to drive the successful commercialization, technical transfer, and execution of new product initiatives within an FDA-regulated manufacturing environment. This role will partner closely with Operations, Technical, Quality, Logistics, Finance, Engineering, R&D, and other key stakeholders to ensure projects are delivered successfully while meeting quality, cost, timing, and manufacturing capability requirements.

Responsibilities

• Lead cross-functional partnerships across Operations, Technical, Quality, Logistics, Finance, Engineering, and R&D to ensure successful project execution and technical transfers.
• Lead the commercialization and introduction of new products, line extensions, geographic expansions, and other innovation initiatives.
• Manage project and technical risk assessments, ensuring robust and cost-effective manufacturing processes.
• Conduct and coordinate Site Impact Assessments (SIA) to evaluate site capabilities, required investments, estimated costs, resources, and timelines for potential product transfers.
• Ensure new and transferred products meet established quality, process capability, design specification, and business acceptance criteria.
• Provide resource management and oversight to Project Managers executing NPI, VE/PPV, line extensions, and complex site projects.
• Develop project plans, secure appropriate resources, monitor execution against established timelines, and implement contingency plans when necessary.
• Ensure appropriate risk mitigation plans are established and aligned with Site and Regional Quality Councils.
• Establish effective project teams and maintain clear communication with senior leadership and key stakeholders.
• Ensure project risks and issues are appropriately escalated and communicated throughout the organization.

Qualifications

Education

• Bachelor’s degree in Science, Engineering, Business Administration, or a related field.

Experience

• Minimum of 5 years of relevant experience in one or more of the following areas:
• FDA-regulated manufacturing or processes
• New Product Introduction (NPI)
• Manufacturing or product introduction project management
• Technology transfer
• Demonstrated experience within the pharmaceutical or FMCG industry.
• Experience leading the technical aspects of: