Engineering Coordinator - Texas, College Station

The announced job offer is made public by the firm: FUJIFILM Diosynth Biotechnologies and it was included in jobs list the date of: 2022-10-22 in the website greenenergyjobsonline.com.

It is announced that they have a job offer at the category of Engineering and the jobs location is in the state of Texas at the city College Station, in the country US - at this current ZipCode: 77840

The information residing in this page is not directly announced by our websites, we help users in the intent of finding the jobs they want and redirect them back to jobs8 for apropriate applying to any of the jobs listed on www.greenenergyjobsonline.com.

The Engineering Coordinator, under the supervision of the Director of Engineering, will be responsible for performing engineering coordination activities on behalf of the different facilities at Fujifilm Diosynth Biotechnology Texas (FDBT) and the projects implementation under the engineering department responsibility. These activities include but are not limited to tracking and review projects and engineering documentation, coordinating construction activities and/or equipment installations, coordinating with impacted areas for activities implementation, performing asset inductions, support work order generation and documentation and preparing project updates, status and/or metrics. This position will work closely with project/process engineers, CAPEX team, manufacturing resources, validation and contractors to help coordinate engineering activities in support of project's implementation and/or utility/process equipment complex operational issues. This position will also support P&ID development/redlining, and maintenance strategies development.

External US

Essential Functions:

• Tracking projects and engineering documentation (eTOPs, FAT/SATs, equipment manuals, submittals, ) and delivery them to the engineering documentation room.
• Asset inductions creation for utilities and process equipment related to projects implementation.
• Gathering documentation for change controls implementation and closure.
• Gathering service and materials quotes required to support engineering activities implementation.
• Work directly with contractors to coordinate and monitor construction and installation of new equipment.
• Attend planning/scheduling meetings to coordinate windows with impacted areas for activities implementation.
• Support work order generation and documentation for scheduled work.
• Support development and/or redlining of drawings (P&IDs, electrical, ...) as a result of engineering activities execution.
• Support maintenance strategies (PMs) development/updates related to new equipment and/or systems.
• Support project and process engineering tasks.
• Support equipment IQ/OQ/PQ or any other validation/commissioning startup activity as required.
• Assist in preparing project updates, status and/or metrics on an established frequency.
• Communicate efficiently with Contractors, Suppliers, OEM providers as well as internal equipment owners and operators for a successful execution of engineering activities.
• Able to work with other contractors, manufacturing, validations and quality control personnel regarding changes or improvements to new equipment and/or systems.
• Ensure compliance, as set forth in internal quality protocols and SOPs including cGMP and FDA regulatory guidelines, within the areas of responsibility, and document out of specification conditions with deviations, CAPAs and Change Controls as appropriate.
• Continuously stay current with assigned SOPs and keep up to date training file ensuring compliance with all applicable Standard Operating Procedures.
• Ensure a safe work environment is maintained through adherence and compliance with safety guidelines, policies, site procedures and job performance qualifications.
• Demonstrate continuous personal pursuit to increasing job knowledge, proficiency in technical understanding, and problem solving abilities.
• Maintain a positive, professional, and customer oriented attitude.
• All other duties as assigned.

Required Skills & Abilities:

• Ability to coordinate, facilitate and organize resources.
• Possess the skills and capability to plan ahead and comply with timelines and milestones.
• Must be flexible and able to manage multiple priorities and tasks.
• Knowledge and understanding using P&IDs, equipment manuals, specifications, SOPs, and be able to use proper judgment when working with engineering tasks.
• Must be able to develop, and draft operational procedures and maintenance procedures for (utilities/process) equipment using the OEM manuals and feedback from owners/technicians.
• Possess or have the ability to gain knowledge of FDA, OSHA, EH&S, EPA, and state of Texas requirements.
• Must be able to use project management software such as Microsoft Project. Proficient with MS Office products (Word, Excel, Outlook, PowerPoint).
• Must be results driven and goal oriented.
• Self-starter and detail oriented.
• Strong written and verbal communications skills, be self-motivated and possess interpersonal skills.
• Ability to learn quickly and work effectively with little supervision when needed.
• Desire to work in a fast paced, state of the art, alternately research and customized manufacturing facility.
• Ability to effectively communicate requirements to vendors and manufacturers.
• Support and supervise activities outside normal business hours as needed, during night-time and weekends.
• Knowledge of bio-medical, bio-technical equipment, both upstream and downstream highly desirable.
• All other duties as assigned.

Working Conditions & Physical Requirements:

The physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. While performing the duties of this job, the employee is regularly required to:

• Experience prolonged sitting, standing, walking, bending, stooping and stretching.
• Use hand-eye coordination and manual dexterity sufficient to operate portable tools, test instruments, as well as a computer keyboard, telephone, calculator, and other office equipment is required.
• Have a normal range of vision.
• The ability to regularly lift and/or move up to 50 pounds.
• Climb ladders and stairs of various heights.
• Be exposed to wet or humid conditions.
• This position may require off shifts, weekends and/or holidays support.
• Be exposed to outdoor weather conditions.
• Be exposed to noisy environments.
• Attendance is Mandatory

Minimum Qualifications:

• Bachelor's Degree in Engineering, technology disciple or related field, OR
• Associate degree in Engineering, technology discipline or related field with two (2) years of qualified experience in an FDA regulated research or manufacturing facility or any other regulated engineering role, OR
• High School Diploma/GED with at least one year of education or training in a technical school, university or trade with four (4) years of qualified experience in an FDA regulated research or manufacturing facility or any other regulated engineering role.

Preferred Qualifications:

• cGMP experience
• Engineering documentation management
• Knowledge of bio-processing equipment, clean utilities, and single use equipment
• Experience with project management software specifically Revu Bluebeam and SmartSheets

Salary: Starting salary will be commensurate with education and experience.

We are an equal opportunity and affirmative action employer. All qualified applicants will receive consideration without regard to race, color, national origin, sex, gender identity, sexual orientation, religion, disability, protected veteran status or any other characteristic protected by applicable federal, state or local law.

If an accommodation to the application process is needed, please e-mail or call .