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$182k–$331k/yr
Other, Full-time
professional certificate
Annual performance bonus, 401(k) program, Paid time off, Personal days, Company paid holidays, Health insurance
Posted 2d ago
~40 hrs/week
Responsibilities
The AVP of North America Engineering provides executive leadership for engineering and capital projects across the manufacturing network to support business growth and operational excellence. This role is responsible for managing large-scale capital investments, ensuring regulatory compliance, and driving innovation in a highly regulated pharmaceutical environment.
Requirements
Candidates must have 15+ years of progressive leadership experience within pharmaceutical manufacturing, including expertise in both injectable and solid-dose operations. A strong background in leading large-scale capital projects, facility modernization, and managing high-performing engineering organizations is required.
Full job description
Location: Columbus OH, Bedford, OH or Cherry Hill, NJ
Job Type: Full-Time
About Us:
As a developer, manufacturer, and supplier of essential medicines, Hikma Pharmaceuticals USA Inc. and its affiliates’ purpose is to put better health within reach, every day for millions of patients around the world. We are a trusted, reliable partner and dependable source of over 760 high-quality generic, specialty and branded pharmaceutical products that hospitals, physicians and pharmacists need to treat their patients across North America, the Middle East, North Africa and Europe. Through our global footprint of 30+ manufacturing plants, 8+ R&D centers, and 9,000+ empowered employees, we are committed to making high-quality medicines accessible to the people who need them.
Description:
We are committed to building a diverse and inclusive team and encourage applications from candidates of all backgrounds. We are seeking a talented and motivated AVP, North America Engineering to join our team. In this role you will be providing executive leadership for Engineering and Capital Projects across the North America manufacturing network. Responsible for developing and executing engineering and technical operations strategies that support business growth, uninterrupted product supply, regulatory compliance, operational excellence, and cost competitiveness across injectable and solid-dose manufacturing operations.
The role leads large-scale capital investments with a multi-million dollar operating and capital responsible for an annual CAPEX exceeding US$ 75M (with significantly higher investment levels during expansion and growth periods), facility and equipment lifecycle management, process optimization initiatives, and engineering organizations while driving innovation, reliability, and continuous improvement in a highly regulated pharmaceutical environment, ensuring on-going and continuous collaboration and coordination across the North American engineering teams.
Responsibilities:
Strategic Leadership
Develop and execute North America engineering and technical operations strategies aligned with business objectives, manufacturing priorities, and global initiatives
Provide both short-term and long-term strategic direction for engineering infrastructure, manufacturing technologies, asset reliability, CAPEX, and facility expansion
Serve as a key member of a North American Operations Leadership Team and as a strategic advisor to executive leadership
Engineering & Capital Programs
Lead engineering strategy and execution across all North America manufacturing sites
Manage large-scale capital investment programs, including facility expansions, equipment upgrades, automation initiatives, and capacity enhancement projects
Ensure projects are delivered safely, on time, within budget, and in compliance with quality and regulatory requirements
Establish long-range capital plans supporting growth, productivity, compliance, and business continuity
Ensure all engineering, validation, maintenance, and technical operations activities comply with FDA, DEA, OSHA, environmental, applicable laws, and Hikma group requirements, policies, and expectations
Commercialization & Technology Transfer
Lead engineering and technical support for new product introductions, site transfers, technology transfers, and third-party manufacturing initiatives
Partner with R&D, Operations, Supply Chain, Procurement, and Commercial teams to ensure successful product launches and lifecycle management activities
Provide technical due diligence support for business development opportunities, acquisitions, partnerships, and external manufacturing relationships
Talent & Organizational Leadership
Build and develop high-performing engineering and technical organizations
Mentor and coach leaders across Engineering and associated projects functions
Drive succession planning, organizational effectiveness, and employee engagement initiatives
Collaboration and Communications
Partner with global engineering, technical operations, procurement, supply chain, and quality organizations to ensure alignment of standards, priorities, and strategic initiatives
Collaborate with multiple site leaders and global Engineering functions
Interact with various external contacts such as regulatory agencies, contract manufacturing organizations (CMO’s), engineering service providers, equipment manufacturers, construction contractors, suppliers, strategic partners, industry associations, and consultants
General
Perform other duties as assigned
Maintain regular, predictable onsite attendance and punctuality
Professional Engineering (PE), Lean Six Sigma, PMP, or equivalent certifications preferred.
Qualifications:
To perform this job successfully, an individual must be able to perform each essential duty satisfactorily:
15+ years of progressive leadership within pharmaceutical manufacturing, including the following:
Managing others both internally and externally
Demonstrated experience supporting both injectable and oral, including solid dose, manufacturing operations
Establishing strategies and leading Engineering organizations, technical operations.
Experience leading large-scale capital projects and facility modernization programs.
Strong understanding of generic pharmaceutical manufacturing environments and cost-competitive operations.
Experience with combination products
Preferred experience in:
IV bag manufacturing.
Multi-site and global leadership.
Supporting acquisitions, network optimization, or major capacity expansion initiatives.
Proven experience and process knowledge in pharmaceutical manufacturing / packaging technology, engineering, maintenance and technical operations.
Strong knowledge of cGMP requirements, validation principles, human factors, quality systems, regulatory expectations and industrial safety.
Proven leadership in high-volume manufacturing, driving operational excellence through Lean Manufacturing, Six Sigma, reliability engineering and continuous improvement methodologies.
Understanding and planning for scaled operations from R&D to commercialization.
Demonstrated success improving throughput, asset utilization, overall equipment effectiveness (OEE), quality, cost efficiency, and material control.
Proven ability to influence and collaborate with stakeholders at all levels, including executive leadership, regulatory agencies, suppliers, customers, and global teams.
Exceptional leadership, coaching, mentoring, and talent development skills, including guiding senior-level professionals and leading organizational transformation initiatives.
Results-oriented leader with a strong focus on safety, quality, compliance, delivery, and cost performance.
Expertise in capital project management, facility engineering, asset lifecycle management, and engineering program execution.
Strong strategic planning, portfolio management, budgeting, capital planning, and resource allocation capabilities.
Strong analytical, problem-solving, and data-driven decision-making abilities.
Excellent project management skills with a track record of delivering complex initiatives across cross-functional and global organizations.
Highly effective communicator with exceptional verbal, written, presentation, and executive communication skills; able to translate complex technical and financial information for diverse audiences.
Self-motivated, detail-oriented team player with the ability to work effectively in domestic and international environments.
Significant travel expected to support operational needs
What We Offer:
Annual performance bonus, commission, and share potential
Auto enrollment in a Hikma-sponsored 401(k) program at a pre-tax contribution rate of 3% of eligible pay. Hikma will match 100% of the first 6% of eligible pay that you contribute
A generous paid time off (PTO) bank starting with 20 days (prorated based on hire date). Additional days granted upon reaching work milestone anniversaries
3 personal days (prorated based on hire date)
11 company paid holidays
Comprehensive benefits including health, dental, vision, mental health, disability, life insurance, prescription drug coverage, and a variety of voluntary benefits
Employee discount program
Wellbeing rewards program
Safety and Quality is a top organizational priority
Career advancement and growth opportunities
Tuition reimbursement
Paid maternity and parental leave
Eligibility requirements apply to some benefits and depend on the job classification, role, and length of employment. Benefits are subject to change as well as specific plan or program terms.
Compensation:
Base Salary: $182,000 to $331,250 annually. The compensation for this position will be determined during the interview process and will vary based on multiple factors, including, but not limited to, work location, prior experience and job-related knowledge, relevant skills and expertise, current business needs, and market factors. The Talent Acquisition team can provide more details about the specific salary range for the job location during the hiring process.
Equal Opportunity Employer:
Hikma Pharmaceuticals USA Inc. is an Equal Opportunity Employer. Employment decisions are made without regard to race, color, religion, national or ethnic origin, sex, sexual orientation, gender identity or expression, age, disability, protected veteran status, or other characteristics protected by law.
Agency Notice:
Please note that Hikma has a set roster of approved recruiters for specific roles agreed to in advance and does not accept unsolicited resumes or calls from third-party recruiters or employment agencies regarding open positions. In the absence of a signed agreement and approval from Hikma’s Human Resources department to submit resumes for a specific
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Related keywords
Pharmaceutical manufacturingEngineeringCapital projectsCAPEXInjectablesSolid-doseFDADEAOSHAcGMPLean Six SigmaPMPProfessional EngineeringAutomationTechnology transferAsset lifecycle management
At Hikma, we help put better health, within reach, every day.
Industry
Pharmaceutical Manufacturing
Company size
5,001-10,000 employees
Founded
1978
Headquarters
London, London
LinkedIn followers
711,316
Total funding
$250M
For almost 50 years, we’ve been creating high-quality medicines and making them accessible to the people who need them. We are a trusted, reliable partner and dependable source of over 825* high-quality generic, specialty and branded pharmaceutical products that hospitals, physicians and pharmacists need to treat their patients across North America, MENA and Europe. We have 29 manufacturing plants, 3 R&D hubs and c9,400 employees worldwide.
*As of March 2026
Subscribe to our channel on YouTube https://youtube.com/@hikmapharmaceuticals5668
For all product information and enquiries, please contact us at [email protected]
Offices: 1 New Burlington Place, London, London W1S 2HR, GB · 1809 Wilson Road, Columbus, Ohio 43228, US · 9 N. Olney Avenue, Cherry Hill, New Jersey 08003, US · 159 N Sangamon St, Suite 327, Chicago, Illinois 60607, US · 200 Connell Drive, 4th Floor, Berkeley Heights, New Jersey 07922, US