The successful candidate will have a strong knowledge of GMP concepts regulatory requirements various process platforms and equipment technologies. They will have the ability to execute and lead projects through early phases of design including feasibility programming master planning concept and BOD. This position will require facilitating design workshops with clients key stakeholders and end users. This position will require a close collaboration with process engineers and architects as well as effective coordination with others within a team environment. Strong leadership interpersonal communication public speaking and technical writing skills will be necessary to be successful in this role.
Core Activities
- Works with clients and process engineers to define and document design basis.
- Works closely with process engineers to ensure coordination across process equipment regulatory compliance and facility design.
- Collaborates with architectural team to ensure cohesive design for the overall facility.
- Ability to conceptualize and communicate design ideas to clients in real time.
- Ability to facilitate design workshops with key stakeholders and end users as well as facilitating stakeholder consensus.
- Ability to execute high-level master plan and develop building- or site-level expansion strategies.
- Researches and applies cGMP regulatory and building codes and standards to facility design.
- Develops and generates studies presentations and reports.
- Ability to generate concept design plans and sections cleanroom classification plans GMP flow diagrams room summary list and other deliverables appropriate for feasibility programming or concept phases of design.
- Cultivates an industry presence through professional society memberships and activities speaking engagements and publication of blogs articles or white papers.
- Participates in proposal development and preparation and project interviews.
- Provides mentorship to Process Architects III and IV as well as Architectural Intern/Design staff.
Qualifications :
- Accredited Professional Degree in Architecture ( and/or ) or Canadian/International equivalent
- Architectural license in good standing within home state with ability for reciprocal licensure through NCARB
- 20 years of professional experience with minimum 15 years of focus on GMP facility design
Preferred Qualifications
- NCARB Certification
- Proficiency in Revit and Microsoft Office suite
- Relevant knowledge of International Building Code OSHA Regulations and ADA Standards
- Ability to interface with clients and external partners
- Flexibility for moderate travel in support of project-based or training activities
- Excellent verbal and written communications and presentation skills
- Experience with advanced technology industry projects including R&D labs biotechnology pharmaceutical food and nutrition and/or consumer products
- Experience with international clients and/or projects
- Expert-level knowledge of cGMP and regulatory concepts and requirements
- Entrepreneurial client focused and leadership skills
- Experience with Enscape Rhino or other 3D modeling/visualization software
- LEED Accreditation WELL Certification or similar sustainability credentials
#LI-JV1
Additional Information :
All your information will be kept confidential according to EEO guidelines.
CRB is committed to hiring and retaining a diverse workforce. We are proud to be an Equal Opportunity Employer and it is our policy to provide equal opportunity to all people without regard to race color religion national origin ancestry marital status veteran status age disability pregnancy genetic information citizenship status sex sexual orientation gender identity or any other legally protected category. Employment is contingent on background screening.
CRB does not accept unsolicited resumes from search firms or agencies. Any resume submitted to any employee of CRB without a prior written search agreement will be considered unsolicited and the property of CRB. Please no phone calls or emails.
CRB offers a complete and competitive benefit package designed to meet individual and family needs.
If you are unable to complete this application due to a disability contact this employer to ask for an accommodation or an alternative application process.
Remote Work :
No
Employment Type :
Full-time
The successful candidate will have a strong knowledge of GMP concepts regulatory requirements various process platforms and equipment technologies. They will have the ability to execute and lead projects through early phases of design including feasibility programming master planning concept and BOD...
The successful candidate will have a strong knowledge of GMP concepts regulatory requirements various process platforms and equipment technologies. They will have the ability to execute and lead projects through early phases of design including feasibility programming master planning concept and BOD. This position will require facilitating design workshops with clients key stakeholders and end users. This position will require a close collaboration with process engineers and architects as well as effective coordination with others within a team environment. Strong leadership interpersonal communication public speaking and technical writing skills will be necessary to be successful in this role.
Core Activities
- Works with clients and process engineers to define and document design basis.
- Works closely with process engineers to ensure coordination across process equipment regulatory compliance and facility design.
- Collaborates with architectural team to ensure cohesive design for the overall facility.
- Ability to conceptualize and communicate design ideas to clients in real time.
- Ability to facilitate design workshops with key stakeholders and end users as well as facilitating stakeholder consensus.
- Ability to execute high-level master plan and develop building- or site-level expansion strategies.
- Researches and applies cGMP regulatory and building codes and standards to facility design.
- Develops and generates studies presentations and reports.
- Ability to generate concept design plans and sections cleanroom classification plans GMP flow diagrams room summary list and other deliverables appropriate for feasibility programming or concept phases of design.
- Cultivates an industry presence through professional society memberships and activities speaking engagements and publication of blogs articles or white papers.
- Participates in proposal development and preparation and project interviews.
- Provides mentorship to Process Architects III and IV as well as Architectural Intern/Design staff.
Qualifications :
- Accredited Professional Degree in Architecture ( and/or ) or Canadian/International equivalent
- Architectural license in good standing within home state with ability for reciprocal licensure through NCARB
- 20 years of professional experience with minimum 15 years of focus on GMP facility design
Preferred Qualifications
- NCARB Certification
- Proficiency in Revit and Microsoft Office suite
- Relevant knowledge of International Building Code OSHA Regulations and ADA Standards
- Ability to interface with clients and external partners
- Flexibility for moderate travel in support of project-based or training activities
- Excellent verbal and written communications and presentation skills
- Experience with advanced technology industry projects including R&D labs biotechnology pharmaceutical food and nutrition and/or consumer products
- Experience with international clients and/or projects
- Expert-level knowledge of cGMP and regulatory concepts and requirements
- Entrepreneurial client focused and leadership skills
- Experience with Enscape Rhino or other 3D modeling/visualization software
- LEED Accreditation WELL Certification or similar sustainability credentials
#LI-JV1
Additional Information :
All your information will be kept confidential according to EEO guidelines.
CRB is committed to hiring and retaining a diverse workforce. We are proud to be an Equal Opportunity Employer and it is our policy to provide equal opportunity to all people without regard to race color religion national origin ancestry marital status veteran status age disability pregnancy genetic information citizenship status sex sexual orientation gender identity or any other legally protected category. Employment is contingent on background screening.
CRB does not accept unsolicited resumes from search firms or agencies. Any resume submitted to any employee of CRB without a prior written search agreement will be considered unsolicited and the property of CRB. Please no phone calls or emails.
CRB offers a complete and competitive benefit package designed to meet individual and family needs.
If you are unable to complete this application due to a disability contact this employer to ask for an accommodation or an alternative application process.
Remote Work :
No
Employment Type :
Full-time
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