Sr Engineer Details

Sr Engineer

Biopharma Consulting Services - Juncos, PR

Employment Type : Full-Time

Independently provides and/or directs the characterization of process optimization strategies and/or troubleshooting of operational issues in the operations, manufacturing, pilot plant or capital projects environment. Applies advanced and diverse engineering principles to the design and implementation of major system modifications, experiments, process and/or capital projects. Develops, organizes, analyzes and presents interpretation of results for operational issues or engineering projects of significant scope and complexity

FUNCTIONS
General:
1. Complete complex or novel assignments requiring development of new and/or improved engineering techniques and procedures.
2. Develop engineering policies and procedures that affect multiple organizational units.
3. Supervise, coordinate and review work of a small staff of engineers, associates and/or technicians on an ongoing basis as well as on a project basis.
4. Employ advanced engineering techniques and/or modifications of advanced techniques within area of engineering expertise.
5. Apply knowledge of engineering principles and practices outside of area of discipline expertise to broad variety of assignments in related fields.
6. Serves as a peer-recognized engineering technology specialist in at least one area, with overall responsibility for determining methodologies in that area.
7. Application of mature engineering knowledge in planning and conducting projects. * Other functions may be assigned

Design Engineering:
1. Develop technical solutions to complex problems requiring the regular use of ingenuity and creativity.
2. Work with research, manufacturing, process development, utilities, facilities, quality assurance and validation departments in developing requirements and recommendations for large and/or highly complex system/facility modifications.
3. Work with project managers to complete design and engineering projects within schedule, budget and quality constraints.
4. Coordinate the work of consultants, architects and engineering firms on development of standard design documents.
5. Develop departmental budgets or project budgets encompassing multiple disciplines for area within project or entirety of smaller project

EDUCATION
Doctorate degree or Master’s degree and 3 years of Engineering experience or Bachelor’s degree in Engineering and 5 years of Engineering experience.

PREFERRED QUALIFICATIONS:

• Working knowledge of pharmaceutical/biotech processes
• Familiarity with validation processes
• Familiarity with documentation in a highly regulated environment
• Ability to operate specialized laboratory equipment and computers as appropriate.
• Ability to interpret and apply GLPs and GMPs.
• Ability to apply engineering science to production.
• Able to develop solutions to routine technical problems of limited scope
• Demonstrated skills in the following areas:

o Problem solving and applied engineering.
o Basic technical report writing
o Verbal communication

• Comprehensive understanding of validation protocol execution requirements.
• Demonstrated Skills in the following areas:

o Basic technical presentations
o Personal Organization
o Validation Protocol Writing
o Dealing with and managing change
o Technical (Equipment Specific)
o Analytical Problem Solving
o Computer Literacy

• Specialized equipment/process expertise
• In-depth knowledge of validation processes and requirements as applied to new equipment installations
• Interacts effectively with variety of communication and working styles
• Ability to independently determine when additional internal resources are required to solve problems
• Ability to handle multiple projects at one time
• Demonstrated Skills in the following areas:

o Schedule development
o Facilitation
o Collaboration
o Basic project management
o Completion and follow-up

• Established expertise in at least 3 separate areas of engineering technology.
• Ability to independently determine when additional external resources are required to solve problems
• Ability to provide solutions to a large variety of technical problems of moderate to large complexity and scope
• Problem solving skills requiring the application of scientific and engineering theory and calculations and creative skills in the development of hypotheses and approach
• Working knowledge of financial analysis tools
• Ability to delegate and manage the project work of others
• Demonstrated Skills in the following areas:

o Negotiation, persuasion and facilitation
o Collaboration
o Project cost development
o Conflict Resolution
o Leadership and teambuilding

• Management of contractors and vendors

Working experience with bioprocessing equipment such as bioreactors, centrifuges, homogenizers, chromatography skids, filtration skids, clean in place systems, and their associated instrumentation.
Comprehensive knowledge of standard maintenance practices, preferably using Maximo maintenance management system.
Knowledge of standard calibration practices. Ability to interpret calibration documentation and define calibration criteria based on equipment and process requirements.
Working experience supporting routine manufacturing operations in a biotech or pharmaceutical environment.
Ability to lead troubleshooting initiatives for equipment and operational issues.
Experience defining, managing and implementing equipment related change records (change controls).
Excellent interpersonal and time management skills to work with changing priorities from multiple stakeholders.
Experience managing deviation records
Experience managing and implementing corrective and preventive actions.
Experience managing or supporting Environmental, health and safety programs of not required but will be considered favorably.

Job Types: Full-time, Contract

Pay: $0.00 per hour

Schedule:

• 10 hour shift
• 8 hour shift

Education:

• Bachelor's (Required)

Experience:

• bioreactors: 5 years (Required)
• centrifuges: 5 years (Required)
• homogenizers: 5 years (Required)
• chromatography skids: 5 years (Required)
• filtration skids: 5 years (Required)
• clean in place systems: 5 years (Required)
• Maximo maintenance management system: 5 years (Required)
• change records: 5 years (Required)
• deviation records: 5 years (Required)
• Engineering: 5 years (Required)
• Validation Protocol Writing: 5 years (Required)

Language:

• Spanish/ English (Required)

Contract Length:

• More than 1 year

Work Remotely:

• Temporarily due to COVID-19

COVID-19 Precaution(s):

• Remote interview process
• Personal protective equipment provided or required
• Temperature screenings
• Social distancing guidelines in place
• Virtual meetings
• Sanitizing, disinfecting, or cleaning procedures in place