Pharmaceutical Jobs in Virginia
Pharmaceutical jobs in Virginia are concentrated in the Richmond corridor, Northern Virginia, and the Hampton Roads area, where life sciences research, contract manufacturing, and clinical operations drive steady hiring at every level from lab technician to regulatory affairs director. Pfizer, Booz Allen Hamilton's health sciences division, and Cardinal Health maintain significant operations in the state, alongside a dense network of biotech and specialty pharma firms clustered near the National Capital Region. The most in-demand roles lean toward regulatory affairs, quality assurance, and clinical research, reflecting Virginia's strong federal health agency proximity and growing CRO presence. See the openings below and apply to the ones that match your experience.
Find Pharmaceutical JobsOverview
Showing 5 of 13+ Pharmaceutical jobs
Build Your Best Future with Johnson Controls
Join a global leader in smart, healthy, and sustainable buildings.
At Johnson Controls, you'll work on meaningful projects, grow your career through ongoing development opportunities, and make an impact on communities around the world.
We support your physical, financial, and emotional wellbeing while fostering an inclusive culture where your ideas matter.
Join us and build what's next.
What we offer
- Competitive base salary and a comprehensive bonus program.
- Three weeks paid vacation in a calendar year/holidays/sick time/three PTO days in a calendar year.
- Comprehensive benefits package including 401K, medical, dental, and vision care - Available day one.
- Extensive product and on the job/cross training opportunities
- Encouraging and collaborative team environment
- Dedication to safety through our Zero Harm policy
- Providing Scheduling and management support.
- JCI Employee discount programs (The Loop by Perk Spot)
Check us Out: A Day in Life at JCI!
This role is the day-to-day project lead for validated environment and laboratory construction projects (e.g., cleanrooms, biosafety cabinets, containment suites, biocontainment labs, and related utilities) across a campus.
The Senior Project Manager will report to the Project Executive and partner with Engineering, QA/Validation, Delivery, Sponsors, and regional leadership to deliver projects within a validated-state framework, focusing on operational excellence, compliance, and both tactical and financial performance.
What will you do:
- Plan, execute, monitor, and close validated environment projects across multiple sites, ensuring IQ/OQ/PQ, equipment qualification, data integrity, and regulatory expectations are met.
- Serve as the on-site/day-to-day on-site project lead, coordinating Owners, Architects, Engineers, QA/Validation, Contractors, and Vendors to achieve project objectives within validated-state constraints.
- Collaborate with the Project Executive to define and maintain project scope, schedule, and budget baselines; monitor progress and report deviations.
- Develop and implement validation strategies and documentation (validation plans, commissioning/qualification activities, and related records) aligned with corporate validation policy.
- Identify, assess, and mitigate project-level risks that could impact deliverables, schedules, budgets, data integrity, or compliance; escalate as needed with proposed remedies.
- Track and report project performance to the Project Executive, including schedule status, budget, risk, QA/validation progress, and regulatory readiness.
- Manage and appropriately change orders, project delays, procurement, and contract administration for assigned projects; ensure alignment with validated baselines and contract requirements.
- Update all logs on at least a weekly basis. Manage all documentation as per standards in Solution Navigator.
- Ensure robust documentation controls that meet contract, QA, and regulatory standards (validation protocols, IQ/OQ/PQ records, SOP alignment, QA approvals) and support regulatory inspections.
- Seek opportunities to improve validation workflows, data integrity practices, and delivery quality to enhance client satisfaction.
- Maintain relationships with sponsors and stakeholders; act as a trusted advisor on validated-environment delivery and compliance at the project level.
- Manage vendor and subcontractor performance for assigned projects, selecting qualified partners and ensuring alignment with timelines and objectives.
- Manage project finances at the assignment level, including budgeting, forecasting, progress billings, and payables, ensuring alignment with project baselines.
- Prepare the project team for regulatory inspections and audits through thorough documentation and traceability.
- Encourage a safe, compliant, and collaborative project environment; provide guidance to junior team members as needed.
What you will need to be successful (Required):
- Bachelor’s degree in construction, Civil, Mechanical, Electrical Engineering, Construction Management, Business Management, Architecture, or a related field.
- 5–10 years of direct project management experience on large capital projects, including regulated or validated settings (typical project sizes in the $5–$20M range; portfolio responsibility not required).
- Demonstrated success delivering complex, multi-site projects in validated environments (GMP/GLP/ISO 17025) within labs, biopharma, pharmaceutical manufacturing, medical devices, healthcare, or related sectors.
- Understanding of contract language, project accounting, and basic portfolio management as they apply to validated environments.
- Strong executive communication skills; ability to present to senior leadership and diverse stakeholder groups; capable of influencing across functional boundaries.
- Ability to lead and coordinate cross-functional teams (Owners, Architects, Engineers, QA/Validation, Contractors) in regulated contexts.
- Proficiency with standard project management tools (Primavera P6, MS Project) and reporting platforms; advanced skills in MS Office with the ability to create executive-level dashboards and presentations.
- Working knowledge of validation concepts, commissioning/qualification processes, data integrity best practices, and regulatory expectations for validated facilities.
- Ability to establish and maintain professional relationships with key stakeholders and subcontractors in validated environments.
- Willingness to travel and operate across multiple sites as needed.
Preferred:
- Master’s degree.
- PMI certification (PMP) or equivalent.
- Certifications or hands-on experience in CQV; CSV awareness; familiarity with FDA 21 CFR Part 11, EU Annex 11, and related regulatory frameworks.
- Specific experience delivering validated environments: GMP/GLP labs, ISO 14644 cleanrooms, ISO 17025 laboratories, or similar.
- Experience working on programs in datacenter-adjacent facilities requiring stringent validation regimes.
- Demonstrated ability to contribute to continuous improvement programs for validation processes and data integrity across a project portfolio.
Reporting line:
- This position reports to the Project Executive. May supervise project coordinators or junior project team members as part of the assigned project team.
HIRING SALARY RANGE: $95,000.00 – 130,000.00 USD Annual. Salary to be determined by the education, experience, knowledge, skills, and abilities of the applicant, internal equity, and alignment with market data. This position includes a competitive benefits package.
For details, please visit the About Us tab on the Johnson Controls Careers site.
https://jobs.johnsoncontrols.com/about-us
Build Your Best Future with Johnson Controls
Join a global leader in smart, healthy, and sustainable buildings.
At Johnson Controls, you'll work on meaningful projects, grow your career through ongoing development opportunities, and make an impact on communities around the world.
We support your physical, financial, and emotional wellbeing while fostering an inclusive culture where your ideas matter.
Join us and build what's next.
What we offer
- Competitive base salary and a comprehensive bonus program.
- Three weeks paid vacation in a calendar year/holidays/sick time/three PTO days in a calendar year.
- Comprehensive benefits package including 401K, medical, dental, and vision care - Available day one.
- Extensive product and on the job/cross training opportunities
- Encouraging and collaborative team environment
- Dedication to safety through our Zero Harm policy
- Providing Scheduling and management support.
- JCI Employee discount programs (The Loop by Perk Spot)
Check us Out: A Day in Life at JCI!
This role is the day-to-day project lead for validated environment and laboratory construction projects (e.g., cleanrooms, biosafety cabinets, containment suites, biocontainment labs, and related utilities) across a campus.
The Senior Project Manager will report to the Project Executive and partner with Engineering, QA/Validation, Delivery, Sponsors, and regional leadership to deliver projects within a validated-state framework, focusing on operational excellence, compliance, and both tactical and financial performance.
What will you do:
- Plan, execute, monitor, and close validated environment projects across multiple sites, ensuring IQ/OQ/PQ, equipment qualification, data integrity, and regulatory expectations are met.
- Serve as the on-site/day-to-day on-site project lead, coordinating Owners, Architects, Engineers, QA/Validation, Contractors, and Vendors to achieve project objectives within validated-state constraints.
- Collaborate with the Project Executive to define and maintain project scope, schedule, and budget baselines; monitor progress and report deviations.
- Develop and implement validation strategies and documentation (validation plans, commissioning/qualification activities, and related records) aligned with corporate validation policy.
- Identify, assess, and mitigate project-level risks that could impact deliverables, schedules, budgets, data integrity, or compliance; escalate as needed with proposed remedies.
- Track and report project performance to the Project Executive, including schedule status, budget, risk, QA/validation progress, and regulatory readiness.
- Manage and appropriately change orders, project delays, procurement, and contract administration for assigned projects; ensure alignment with validated baselines and contract requirements.
- Update all logs on at least a weekly basis. Manage all documentation as per standards in Solution Navigator.
- Ensure robust documentation controls that meet contract, QA, and regulatory standards (validation protocols, IQ/OQ/PQ records, SOP alignment, QA approvals) and support regulatory inspections.
- Seek opportunities to improve validation workflows, data integrity practices, and delivery quality to enhance client satisfaction.
- Maintain relationships with sponsors and stakeholders; act as a trusted advisor on validated-environment delivery and compliance at the project level.
- Manage vendor and subcontractor performance for assigned projects, selecting qualified partners and ensuring alignment with timelines and objectives.
- Manage project finances at the assignment level, including budgeting, forecasting, progress billings, and payables, ensuring alignment with project baselines.
- Prepare the project team for regulatory inspections and audits through thorough documentation and traceability.
- Encourage a safe, compliant, and collaborative project environment; provide guidance to junior team members as needed.
What you will need to be successful (Required):
- Bachelor’s degree in construction, Civil, Mechanical, Electrical Engineering, Construction Management, Business Management, Architecture, or a related field.
- 5–10 years of direct project management experience on large capital projects, including regulated or validated settings (typical project sizes in the $5–$20M range; portfolio responsibility not required).
- Demonstrated success delivering complex, multi-site projects in validated environments (GMP/GLP/ISO 17025) within labs, biopharma, pharmaceutical manufacturing, medical devices, healthcare, or related sectors.
- Understanding of contract language, project accounting, and basic portfolio management as they apply to validated environments.
- Strong executive communication skills; ability to present to senior leadership and diverse stakeholder groups; capable of influencing across functional boundaries.
- Ability to lead and coordinate cross-functional teams (Owners, Architects, Engineers, QA/Validation, Contractors) in regulated contexts.
- Proficiency with standard project management tools (Primavera P6, MS Project) and reporting platforms; advanced skills in MS Office with the ability to create executive-level dashboards and presentations.
- Working knowledge of validation concepts, commissioning/qualification processes, data integrity best practices, and regulatory expectations for validated facilities.
- Ability to establish and maintain professional relationships with key stakeholders and subcontractors in validated environments.
- Willingness to travel and operate across multiple sites as needed.
Preferred:
- Master’s degree.
- PMI certification (PMP) or equivalent.
- Certifications or hands-on experience in CQV; CSV awareness; familiarity with FDA 21 CFR Part 11, EU Annex 11, and related regulatory frameworks.
- Specific experience delivering validated environments: GMP/GLP labs, ISO 14644 cleanrooms, ISO 17025 laboratories, or similar.
- Experience working on programs in datacenter-adjacent facilities requiring stringent validation regimes.
- Demonstrated ability to contribute to continuous improvement programs for validation processes and data integrity across a project portfolio.
Reporting line:
- This position reports to the Project Executive. May supervise project coordinators or junior project team members as part of the assigned project team.
HIRING SALARY RANGE: $95,000.00 – 130,000.00 USD Annual. Salary to be determined by the education, experience, knowledge, skills, and abilities of the applicant, internal equity, and alignment with market data. This position includes a competitive benefits package.
For details, please visit the About Us tab on the Johnson Controls Careers site.
https://jobs.johnsoncontrols.com/about-us
See All 13 Pharmaceutical Jobs in Virginia
Find roles in Virginia that match your experience and apply in just a few clicks.
Find Pharmaceutical JobsPharmaceutical Jobs by City in Virginia
Where Virginia roles are concentrated, by current openings.
Pharmaceutical Job Market in Virginia
A snapshot from current Virginia openings, updated as new roles post.
Who's Hiring
Top Industries Hiring
- Biotechnology & Pharmaceuticals
What Virginia Employers Look For
The qualifications that appear most often in pharmaceutical jobs across Virginia.
- Active Virginia Board of Pharmacy registration or a license recognized through reciprocity
- Bachelor's degree in pharmaceutical sciences, chemistry, or a closely related field
- Experience with FDA regulatory submissions, GMP compliance, or quality systems
- Proficiency with clinical data management platforms or laboratory information systems
- Strong familiarity with 21 CFR Part 11 electronic records requirements
- Demonstrated ability to work cross-functionally with regulatory, clinical, and manufacturing teams
Pharmaceutical Jobs in Virginia: Frequently Asked Questions
How do you become a pharmaceutical in Virginia?
The path depends on your specific role within the field. Pharmacists must pass the NAPLEX and MPJE and obtain a license through the Virginia Board of Pharmacy before practicing. Pharmaceutical scientists, regulatory affairs specialists, and quality professionals typically need at minimum a bachelor's degree in a relevant science discipline, with many Virginia employers expecting prior GMP or FDA regulatory experience for mid-level positions. Graduate degrees strengthen candidacy for clinical and research roles.
Which companies hire pharmaceuticals in Virginia?
Employers hiring pharmaceuticals in Virginia right now include Eli Lilly, Phlow, and Johnson Controls, based on current listings on Migrate Mate as of October 2026. Virginia's proximity to federal health agencies in the National Capital Region also makes it a hub for consulting firms and contract research organizations with active pharmaceutical teams.
Which Virginia cities have the most pharmaceutical jobs?
Charlottesville, Richmond, and Arlington account for the largest share of pharmaceutical openings in Virginia. Richmond anchors the state's life sciences manufacturing base, Northern Virginia benefits from proximity to FDA headquarters and federal health contracting activity, and Hampton Roads supports clinical and healthcare operations tied to its large medical center network.
Are there remote pharmaceutical jobs in Virginia?
Yes, but they're selective. About 80% of pharmaceutical openings tied to Virginia are remote or hybrid as of October 2026, reflecting that many roles require on-site lab, manufacturing, or clinical work. The positions most likely to offer remote flexibility are regulatory affairs, medical writing, pharmacovigilance, and certain clinical data roles that do not require physical presence in a facility.
How can I get hired as a pharmaceutical in Virginia with little or no experience?
The most realistic entry point is applying to associate or technician-level roles at Virginia's large health systems and contract manufacturers, such as those operating in the Richmond and Northern Virginia corridors. VCU Health, Inova, and several regional CROs run structured new-graduate and rotational programs in pharmacy operations and clinical research. Candidates moving from adjacent roles in medical device quality, laboratory science, or hospital pharmacy technician positions also find these openings accessible. Earning your Virginia Board of Pharmacy technician registration before applying gives you a concrete credential that separates your application.
Where can I find and apply to pharmaceutical jobs in Virginia?
You can find and apply to pharmaceutical jobs in Virginia on Migrate Mate, which lists current openings from employers actively hiring across the state. Search the listings for roles that match your experience level and specialty, then apply directly through each posting.
See All 13 Pharmaceutical Jobs in Virginia
Find roles in Virginia that match your experience and apply in just a few clicks.
Find Pharmaceutical Jobs