Job Title: Commissioning and Qualification Program Lead
Location: Richmond VA
Work Type: Hybrid (will likely start remote)
Job Type: Contract (multi-year project)
Rate: $110/hr on 1099
Notes:
- 3 openings
- LinkedIn needed
- US Citizen or Green Card ONLY
- Interviews are virtual
- It is normal for candidates to relocate for this kind of role
- On-site part of this role is in Virginia
MUST:
- 15 years developing and delivering CQ programs for greenfield sites
- Managing scope budget schedule hiring performance of CQ teams
- Connecting cross-functionally with different groups (quality EPCM firms subcontractors)
- Coming from a pharmaceutical build background
Job description
Primary Responsibilities
- Provide strategic leadership for all C&Q activities ensuring scope timelines and budgets are consistently met.
- Direct day to day performance of the C&Q team and offer technical guidance to support successful project delivery.
- Develop and oversee FAT planning test case creation and all field execution logistics.
- Partner closely with construction automation QA project management and end user groups to maintain alignment on system requirements and delivery expectations.
- Maintain adherence to GMPs regulatory standards internal procedures and overall project safety practices.
- Lead training sessions for internal teams and external vendors on C&Q methodology ASTM E2500 processes and Kneat system usage.
- Coordinate the sourcing readiness and deployment of test equipment and field support resources.
- Communicate progress risks and performance metrics to project leadership with clarity and consistency.
- Drive timely escalation and resolution of technical issues to keep projects moving efficiently.
Qualifications
- Bachelors degree in Engineering or equivalent practical experience.
- 15 years of experience delivering C&Q efforts for large pharmaceutical programs.
- Proven track record supporting full lifecycle delivery of both Greenfield and Brownfield facilities.
- Strong team building leadership and communication skills.
- Expertise in GMPs regulatory frameworks commissioning qualification and ASTM E2500 practices.
- Hands on proficiency with Kneat or similar electronic C&Q/validation platforms.
Job Title: Commissioning and Qualification Program Lead Location: Richmond VA Work Type: Hybrid (will likely start remote) Job Type: Contract (multi-year project) Rate: $110/hr on 1099 Notes: 3 openings LinkedIn needed US Citizen or Green Card ONLY Interviews are virtual It is normal for candida...
Job Title: Commissioning and Qualification Program Lead
Location: Richmond VA
Work Type: Hybrid (will likely start remote)
Job Type: Contract (multi-year project)
Rate: $110/hr on 1099
Notes:
- 3 openings
- LinkedIn needed
- US Citizen or Green Card ONLY
- Interviews are virtual
- It is normal for candidates to relocate for this kind of role
- On-site part of this role is in Virginia
MUST:
- 15 years developing and delivering CQ programs for greenfield sites
- Managing scope budget schedule hiring performance of CQ teams
- Connecting cross-functionally with different groups (quality EPCM firms subcontractors)
- Coming from a pharmaceutical build background
Job description
Primary Responsibilities
- Provide strategic leadership for all C&Q activities ensuring scope timelines and budgets are consistently met.
- Direct day to day performance of the C&Q team and offer technical guidance to support successful project delivery.
- Develop and oversee FAT planning test case creation and all field execution logistics.
- Partner closely with construction automation QA project management and end user groups to maintain alignment on system requirements and delivery expectations.
- Maintain adherence to GMPs regulatory standards internal procedures and overall project safety practices.
- Lead training sessions for internal teams and external vendors on C&Q methodology ASTM E2500 processes and Kneat system usage.
- Coordinate the sourcing readiness and deployment of test equipment and field support resources.
- Communicate progress risks and performance metrics to project leadership with clarity and consistency.
- Drive timely escalation and resolution of technical issues to keep projects moving efficiently.
Qualifications
- Bachelors degree in Engineering or equivalent practical experience.
- 15 years of experience delivering C&Q efforts for large pharmaceutical programs.
- Proven track record supporting full lifecycle delivery of both Greenfield and Brownfield facilities.
- Strong team building leadership and communication skills.
- Expertise in GMPs regulatory frameworks commissioning qualification and ASTM E2500 practices.
- Hands on proficiency with Kneat or similar electronic C&Q/validation platforms.
View more
View less