Project Engineer III (BioPharma)

SRG; Brookside Village (TX); On-site; USD 110,208 - 123,984; Full time

Job summary

An established industry player is seeking a dedicated Project Engineer III to enhance their Medical Device manufacturing team. In this pivotal role, you will provide technical leadership and manage capital projects, ensuring that equipment and facilities are optimized for production. Your expertise in biopharmaceutical manufacturing processes and strong communication skills will be essential as you collaborate with stakeholders and manage engineering contractors. This full-time, W2 contract position offers a unique opportunity to contribute to significant projects within a dynamic environment. If you're ready to take on challenges and make an impact, this role could be your next career step.

Qualifications

• 5-10 years of experience managing capital projects in biopharma.
• Strong knowledge of manufacturing processes and equipment.

Responsibilities

• Act as a technical resource to ensure equipment meets production needs.
• Implement engineering projects to support manufacturing requirements.
• Resolve major equipment breakdowns and quality issues.

Skills

Project Management

Technical Leadership

Communication Skills

Regulatory Knowledge (cGMP, FDA, EMA)

Problem Solving

Education

Bachelor’s degree in Engineering

Bachelor’s degree in Life Sciences

Job description

Salary: USD80 - USD90 per hour + W2 Contract only

SRG, the leader in the Life Sciences human capital industry, is looking for a full-time, contract Project Engineer III to join our client’s Medical Device manufacturing team in Cincinnati, OH. The Project Engineer role supports ongoing operations by providing technical leadership as it relates to manufacturing and process systems.

* W2 contract only.

MUST HAVES:

• Bachelor’s degree in Engineering, Life Sciences, or a related field
• Minimum of 5-10 years of experience managing capital projects, preferably in the biopharma or pharmaceutical industry
• Strong knowledge of biopharmaceutical manufacturing processes, manufacturing related equipment, and facility/utility equipment and processes
• Proven track record of managing large-scale CAPEX projects with budgets up to $5 million
• In-depth understanding of regulatory requirements, including cGMP, FDA, EMA, and other industry standards
• Effectively communicate progress and opportunities (i.e. roadblocks) to stakeholders
• Manage engineering contractors to augment Lonza engineering staff

JOB RESPONSIBILITIES:

• Act as a technical resource to operations customers to ensure that equipment and facilities are designed, operated, and maintained to meet production needs
• Implementation of engineering projects to support manufacturing requirements
• Responsible and accountable for resolution of all major equipment breakdowns and quality issues in the suites
• Provide SME support to Manufacturing and other departments for the design and operation of process equipment
• Modify/develop preventative maintenance plans and create spare parts
• Participates in audits and inspections as engineering SME

** Only candidates selected to be moved forward in the recruitment process will be contacted by SRG's Recruitment Team to schedule a conversation.

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