Senior Biopharma Project Engineer

Initial Therapeutics, Inc.; Boca Raton (FL); On-site; USD 90,000 - 120,000; Full time

Benefits offered by this job

401K plan with employer match and immediate vesting

Medical, Vision, Life and Dental Insurance

Pet Insurance

Company paid STD and LTD

Company Paid Holidays

3 Weeks’ Paid Time Off

Tuition Assistance

Free shuttle to the Boca Tri-Rail station

Job summary

ADMA Biologics in Boca Raton, FL is looking for a Senior Project Engineer to provide engineering and project management support at their GMP manufacturing site. The ideal candidate will have a minimum of 10 years of experience in a cGMP environment and strong abilities in project management and communication. Responsibilities include managing engineering projects, developing and reviewing technical documents, and ensuring compliance with regulatory requirements. The position offers various benefits including a 401K plan and paid time off.

Qualifications

• Minimum of 10 years of engineering experience in a cGMP Pharmaceutical/Biological manufacturing environment.
• Ability to follow cGMP regulations and procedures with great attention to detail.
• Must have excellent writing and oral skills.

Responsibilities

• Managing mid-to-large sized engineering projects and tracking activities.
• Developing and reviewing process flow diagrams and piping and instrumentation drawings.
• Leading investigations of process systems and documenting root causes.

Skills

Project management

Troubleshooting

Technical writing

Communication skills

Problem-solving

Interpersonal skills

Education

Bachelor's degree in Engineering

Tools

Microsoft Office

Job description

ADMA Biologics in Boca Raton, FL is looking for a Senior Project Engineer to provide engineering and project management support at their GMP manufacturing site. The ideal candidate will have a minimum of 10 years of experience in a cGMP environment and strong abilities in project management and communication. Responsibilities include managing engineering projects, developing and reviewing technical documents, and ensuring compliance with regulatory requirements. The position offers various benefits including a 401K plan and paid time off.