Pharmaceutical Jobs in Maryland
Pharmaceutical jobs in Maryland are concentrated in biotech research, drug manufacturing, and clinical development, anchored by the state's dense corridor of life sciences companies stretching from Rockville and Gaithersburg to Baltimore. Maryland is among the most active markets in the country for pharmaceutical professionals at every level, from entry-level research associates to senior regulatory affairs and clinical operations directors. Major employers with lasting presences in the state include AstraZeneca, Emergent BioSolutions, and the U.S. Food and Drug Administration, which draws a large supporting ecosystem of contractors and CROs across Montgomery and Baltimore counties. See the openings below and apply to the ones that match your experience.
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Showing 5 of 19+ Pharmaceutical jobs
Build your best future with the Johnson Controls team!
As a global leader in smart, healthy, and sustainable buildings, our mission is to reimagine the performance of buildings to serve people, places, and the planet. Join a winning team that enables you to build your best future!
Our teams are uniquely positioned to support a multitude of industries across the globe. You will have the opportunity to develop yourself through meaningful work projects and learning opportunities. We strive to provide our employees with an experience focused on supporting their physical, financial, and emotional wellbeing.
Become a member of the Johnson Controls family and thrive in an empowering company culture where your voice and ideas will be heard – your next great opportunity is just a few clicks away!
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 the Life at JCI!
What will you do:
Provide executive-level leadership for a portfolio of validated environment and laboratory construction programs (including cleanrooms, BSCs, containment suites, biocontainment labs, and associated utilities) across a campus.
Act as the domain authority for programs requiring rigorous validation lifecycles (IQ/OQ/PQ), equipment qualification, and compliant deployment of regulated systems, ensuring alignment with corporate validation strategy and regulatory expectations.
Set strategic direction and governance for the validated program portfolio, partnering with QA/Validation, Project Development, Delivery, Sponsors, and regional leadership to achieve objective outcomes within a validated-state framework.
Lead the campus Project Management Office for validated environments, ensuring compliance with contract requirements, validation plans, and data integrity standards while coordinating with enterprise systems for performance reporting.
Anticipate, escalate, and mitigate risks that could impact validation deliverables, schedules, budgets, data integrity, or regulatory compliance; drive issues to resolution with executive-level visibility.
Oversee risk management of the campus portfolio, directing recovery and remediation plans that preserve validated status and impact metrics (scope, schedule, cost, quality).
Ensure accurate, timely, and actionable reporting of portfolio performance to Executive Management, including financial performance, validation milestones, compliance status, and risk controls, using validated data sources and enterprise systems.
Drive client relationship management and business development within the validated-environment sector, identifying opportunities to expand scope, deepen partnerships, and improve customer satisfaction through compliant, high-quality delivery.
Lead strategic vendor and subcontractor relationships, selecting qualified partners experienced in validated environments and aligning them to project goals and timelines.
Govern program financials at the campus level, including budgeting, forecasting, progress billings, and payables, ensuring alignment with validated project baselines.
Ensure program documentation controls meet contract, regulatory, and QA requirements (validation protocols, IQ/OQ/PQ records, SOP alignment, QA approvals) and support regulatory inspections/audits.
Continually seek opportunities to improve client satisfaction, streamline validation workflows, and enhance the competitive position through compliant, high-quality delivery.
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.
15+ years of direct Project/Program Management experience, including large, capital projects in regulated or validated settings (minimum $10M per project; portfolio-level responsibility preferred).
Demonstrated success delivering complex, multi-site programs in validated environments (GMP/GLP/ISO 17025) within labs, biopharma, pharmaceutical manufacturing, medical devices, healthcare, or related sectors.
Deep understanding of contract language, project accounting, and portfolio management as they apply to validated environments.
Strong executive communication skills, with proven ability to present to senior leadership and diverse stakeholder groups; capable of influencing across functional boundaries.
Proven ability to lead and align diverse, 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 leading programs in datacenter-adjacent facilities requiring stringent validation regimes.
Demonstrated ability to develop and implement continuous improvement programs for validation processes and data integrity across a portfolio.
HIRING SALARY RANGE: $130,000.00 - 165,000.00 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 the Johnson Controls team!
As a global leader in smart, healthy, and sustainable buildings, our mission is to reimagine the performance of buildings to serve people, places, and the planet. Join a winning team that enables you to build your best future!
Our teams are uniquely positioned to support a multitude of industries across the globe. You will have the opportunity to develop yourself through meaningful work projects and learning opportunities. We strive to provide our employees with an experience focused on supporting their physical, financial, and emotional wellbeing.
Become a member of the Johnson Controls family and thrive in an empowering company culture where your voice and ideas will be heard – your next great opportunity is just a few clicks away!
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 the Life at JCI!
What will you do:
Provide executive-level leadership for a portfolio of validated environment and laboratory construction programs (including cleanrooms, BSCs, containment suites, biocontainment labs, and associated utilities) across a campus.
Act as the domain authority for programs requiring rigorous validation lifecycles (IQ/OQ/PQ), equipment qualification, and compliant deployment of regulated systems, ensuring alignment with corporate validation strategy and regulatory expectations.
Set strategic direction and governance for the validated program portfolio, partnering with QA/Validation, Project Development, Delivery, Sponsors, and regional leadership to achieve objective outcomes within a validated-state framework.
Lead the campus Project Management Office for validated environments, ensuring compliance with contract requirements, validation plans, and data integrity standards while coordinating with enterprise systems for performance reporting.
Anticipate, escalate, and mitigate risks that could impact validation deliverables, schedules, budgets, data integrity, or regulatory compliance; drive issues to resolution with executive-level visibility.
Oversee risk management of the campus portfolio, directing recovery and remediation plans that preserve validated status and impact metrics (scope, schedule, cost, quality).
Ensure accurate, timely, and actionable reporting of portfolio performance to Executive Management, including financial performance, validation milestones, compliance status, and risk controls, using validated data sources and enterprise systems.
Drive client relationship management and business development within the validated-environment sector, identifying opportunities to expand scope, deepen partnerships, and improve customer satisfaction through compliant, high-quality delivery.
Lead strategic vendor and subcontractor relationships, selecting qualified partners experienced in validated environments and aligning them to project goals and timelines.
Govern program financials at the campus level, including budgeting, forecasting, progress billings, and payables, ensuring alignment with validated project baselines.
Ensure program documentation controls meet contract, regulatory, and QA requirements (validation protocols, IQ/OQ/PQ records, SOP alignment, QA approvals) and support regulatory inspections/audits.
Continually seek opportunities to improve client satisfaction, streamline validation workflows, and enhance the competitive position through compliant, high-quality delivery.
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.
15+ years of direct Project/Program Management experience, including large, capital projects in regulated or validated settings (minimum $10M per project; portfolio-level responsibility preferred).
Demonstrated success delivering complex, multi-site programs in validated environments (GMP/GLP/ISO 17025) within labs, biopharma, pharmaceutical manufacturing, medical devices, healthcare, or related sectors.
Deep understanding of contract language, project accounting, and portfolio management as they apply to validated environments.
Strong executive communication skills, with proven ability to present to senior leadership and diverse stakeholder groups; capable of influencing across functional boundaries.
Proven ability to lead and align diverse, 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 leading programs in datacenter-adjacent facilities requiring stringent validation regimes.
Demonstrated ability to develop and implement continuous improvement programs for validation processes and data integrity across a portfolio.
HIRING SALARY RANGE: $130,000.00 - 165,000.00 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 19 Pharmaceutical Jobs in Maryland
Find roles in Maryland that match your experience and apply in just a few clicks.
Find Pharmaceutical JobsPharmaceutical Jobs by City in Maryland
Where Maryland roles are concentrated, by current openings.
Pharmaceutical Job Market in Maryland
A snapshot from current Maryland openings, updated as new roles post.
Who's Hiring
What Maryland Employers Look For
The qualifications that appear most often in pharmaceutical jobs across Maryland.
- Active Maryland pharmacist license issued by the Maryland Board of Pharmacy required
- Bachelor's or advanced degree in pharmacy, chemistry, biology, or a related life sciences field
- Experience with FDA regulatory submissions, GMP compliance, or clinical trial documentation
- Proficiency with laboratory information management systems or pharmaceutical data software
- Strong knowledge of cGMP, cGLP, or cGCP guidelines relevant to the specific role
- Excellent written communication skills for regulatory documents, SOPs, and scientific reports
Pharmaceutical Jobs in Maryland: Frequently Asked Questions
How do you become a pharmaceutical in Maryland?
Pharmacists in Maryland must earn a Doctor of Pharmacy degree from an accredited program, pass both the NAPLEX and MPJE licensing exams, and obtain licensure through the Maryland Board of Pharmacy before practicing. For non-pharmacist pharmaceutical roles such as research associates, regulatory specialists, or manufacturing technicians, employers typically require a relevant bachelor's or master's degree and may prefer candidates with laboratory or compliance experience gained through Maryland's many university and industry internship programs.
Which companies hire pharmaceuticals in Maryland?
Companies currently hiring pharmaceuticals in Maryland include サイネオス・ヘルス, Syneos Health Commercial Solutions, and Inizio Engage, per current listings on Migrate Mate as of August 2026. Maryland's concentration of federal health agencies and biotech firms in the I-270 technology corridor creates steady, year-round demand across research, regulatory, and manufacturing roles.
Which Maryland cities have the most pharmaceutical jobs?
The Maryland cities with the most pharmaceutical openings are Baltimore, Bowie, and Oxon Hill. Rockville and Gaithersburg lead because they sit at the center of the I-270 biotech corridor, home to major drug developers and federal agencies including the FDA and NIH, while Baltimore draws significant volume from its hospital-affiliated research institutions and established manufacturing facilities.
Are there remote pharmaceutical jobs in Maryland?
Yes, but they are less common than in purely desk-based fields because many pharmaceutical roles require on-site lab access, GMP manufacturing oversight, or in-person regulatory work. About 100% of pharmaceutical openings tied to Maryland are remote or hybrid as of August 2026, reflecting availability across the broader role category. Regulatory affairs, medical writing, pharmacovigilance, and clinical data management positions are the sub-areas most likely to offer remote or hybrid arrangements.
How can I get hired as a pharmaceutical in Maryland with little or no experience?
The most realistic entry path is targeting research associate, pharmacy technician, or quality control analyst positions at Maryland's large biotech and CRO employers, where structured new-hire training programs are common. Institutions like the University of Maryland and Johns Hopkins maintain partnerships with area companies that offer internships and post-graduate fellowships specifically for candidates without direct industry experience. Obtaining Maryland Board of Pharmacy registration as a pharmacy technician, or earning a relevant certification such as CPHT, gives applicants a concrete credential that moves applications forward at manufacturing and retail pharmacy employers across the state.
Where can I find and apply to pharmaceutical jobs in Maryland?
You can find and apply to pharmaceutical jobs in Maryland on Migrate Mate, which lists current openings across the state. Search for roles that fit your background, experience level, and preferred location, then apply directly to the ones that match. No signup is required to view the listings.
See All 19 Pharmaceutical Jobs in Maryland
Find roles in Maryland that match your experience and apply in just a few clicks.
Find Pharmaceutical Jobs