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Unicon Pharma Inc

QCS-CQV Project Director

Unicon Pharma Inc, Charlotte, North Carolina, United States, 28269

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2 weeks ago Be among the first 25 applicants

Is this your next job Read the full description below to find out, and do not hesitate to make an application. This range is provided by Unicon Pharma Inc. Your actual pay will be based on your skills and experience — talk with your recruiter to learn more. Base pay range $70.00/hr - $80.00/hr Direct message the job poster from Unicon Pharma Inc Recruiter at Unicon Pharma | Quality & Compliance | Validation

Position:

QCS–CQV Project Director Location:

NC (Onsite) Start:

ASAP Duration:

6 months to start (possibility of extension based) Hours:

40 hrs/week *Skills, experience, and other compensable factors will be taken into account when determining pay rate. The pay range provided in this posting is a reflection of a W2 hourly rate; other employment options may be available that may result in pay outside of the provided range. *Due to client requirement, applicants must be willing and able to work on a w2 basis Overview We are seeking an accomplished

QCS–CQV Project Director

to lead the commissioning, qualification, and start-up of a large-scale biologics drug substance facility. This senior leadership role will oversee all phases of the project — from design through operational handover — ensuring delivery of complex, high-value equipment packages and facility systems that meet cGMP and regulatory requirements. Key Responsibilities Direct the end-to-end delivery of a greenfield CQV project, including planning, execution, risk management, and operational readiness. Oversee the procurement, installation, commissioning, and qualification of equipment packages valued at

$100–200M . Lead and inspire multidisciplinary teams of up to

60 personnel , including internal staff, contractors, and vendor partners. Ensure alignment between CQV activities, process engineering deliverables, and overall project timelines and budgets. Drive adherence to quality, safety, and compliance standards across all project phases. Collaborate closely with operations teams to ensure smooth transition from project delivery to commercial manufacturing, including facility acceptance and ramp-up. Provide executive-level reporting and stakeholder engagement to maintain alignment on scope, progress, and risk mitigation. Qualifications 15+ years

of experience in process engineering, CQV, or project management within the biologics drug substance space. Candidates with

10+ years

and an exceptional track record will also be considered. Proven leadership in delivering full lifecycle projects from concept through operational start-up. Demonstrated success managing complex equipment packages in the

$100–200M

range. Experience overseeing large, diverse teams (up to 60 people) on major capital projects. Greenfield project experience

is essential. Operational leadership experience, particularly in accepting facilities from a project team into GMP operations, is highly beneficial. Seniority level

Seniority levelDirector Employment type

Employment typeContract Job function

Job functionConsulting IndustriesBiotechnology Research and Pharmaceutical Manufacturing Referrals increase your chances of interviewing at Unicon Pharma Inc by 2x Get notified about new Project Director jobs in

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