Sr Engineer at BioPharma Consulting JAD Group

Juncos, , Puerto Rico -

Full Time

Start Date

Immediate

Expiry Date

01 Aug, 26

Salary

0.0

Posted On

03 May, 26

Experience

2 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

Skills

Process optimization, Troubleshooting, Engineering project management, GMP compliance, GLP regulations, Validation, Technical writing, Cross-functional collaboration, Budget management, Capital projects, Subject matter expertise, System modification, Analytical skills, Problem-solving, Leadership, Asset management

Industry

Biotechnology Research

Description

Independently provides leadership in process optimization, troubleshooting, and execution of engineering projects within manufacturing, pilot plant, or capital project environments. The Senior Engineer applies advanced engineering principles to design and implement complex system modifications, drive continuous improvement, and lead projects of significant scope and complexity across cross-functional teams. Key Responsibilities Execute complex and novel engineering assignments, developing new or improved techniques and procedures Develop and implement engineering policies and procedures impacting multiple departments Supervise, coordinate, and review work of engineers, associates, and technicians Apply advanced and cross-disciplinary engineering principles to diverse technical challenges Serve as a subject matter expert (SME) in a specialized engineering area Lead planning and execution of engineering projects and initiatives Develop innovative technical solutions for complex engineering problems Collaborate with Manufacturing, Quality, Validation, Facilities, Utilities, and Process Development teams on system and facility modifications Partner with project managers to ensure projects are delivered on time, within scope, and within budget Coordinate work with consultants, architects, and external engineering firms Develop and manage project and departmental budgets Support capital projects, including scope development, execution, and closure Required Skills & Competencies Strong knowledge of pharmaceutical/biotech manufacturing processes Expertise in GMP/GLP regulations and highly regulated environments Advanced understanding of validation processes and protocol execution Ability to apply engineering principles to production systems and equipment Strong analytical and problem-solving skills, including development of technical hypotheses Proven ability to manage multiple projects and priorities simultaneously Strong technical writing, reporting, and presentation skills Effective communication and collaboration across diverse teams and stakeholders Experience with specialized equipment and process systems Ability to delegate, lead, and manage team performance Working knowledge of financial analysis and project cost management Education & Experience Doctorate degree OR Master’s degree + 2 years of Engineering experience OR Bachelor’s degree in Engineering + 4 years of Engineering experience Preferred Qualifications Strong experience with cGMP engineering practices in pharmaceutical/biotech environments Experience with Quality Systems (e.g., Change Control, Non-Conformance, CAPA, Risk Assessments) Experience with validation of new equipment and system installations Familiarity with Maximo or similar asset management systems Experience managing vendors, contractors, and purchase orders (POs) Ability to work in fast-paced, multi-project environments with shifting priorities Strong leadership, negotiation, and conflict resolution skills Demonstrated ability to influence and drive cross-functional alignment Work Schedule Shift: 1st Shift Flexibility required to support 24/7 operations, including occasional after-hours support

Responsibilities

The Senior Engineer will lead complex engineering projects, drive process optimization, and serve as a subject matter expert across manufacturing and capital project environments. They are responsible for supervising engineering teams, managing budgets, and ensuring compliance with GMP/GLP regulations.