Quality Program Manager- Packaging Supplier Quality Events
Columbus, Ohio, United States · On-site
$99k–$199k/yr
Senior+$20B raised
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Cardiovascular Disease Specialist – Columbus, OH District
Columbus, Ohio, United States · Remote OK
$79k–$125k/yr
Mid level
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Poison Info Specialist (Non Certified) - Poison Control Center (Evening Shift)
Columbus, Ohio, United States · On-site
Entry level$4M raised
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Other, Full-time
bachelor degree, postgraduate degree
Posted 4d ago
~40 hrs/week
Responsibilities
The Sr. Project Manager leads cross-functional teams to manage generic commercialization, site transfers, and lifecycle changes for pharmaceutical products. They are responsible for project planning, risk mitigation, and ensuring all technical and commercial milestones are met within established timelines and budgets.
Requirements
Candidates must hold a B.S. or M.S. degree in a scientific or operations discipline with at least 7-9 years of relevant pharmaceutical industry experience. An active PMP certification is required, along with expert knowledge of cGMP, FDA regulations, and pharmaceutical supply chain processes.
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 Sr. Project Manager, Technical Services to join our team.
In this role, you will be responsible for will lead and manage cross-functional project teams for products produced or distributed from Columbus either via launch, transfer and/or lifecycle.
This position is responsible to provide all necessary project management skills/tools for the successful, timely completion of all assigned projects in order to achieve the site’s goals for each year with key performance indicators being timing, cost and process robustness.
This role has full accountability for the planning and execution of Generic commercialization, Site Transfers, Buy-ins, Third Party, Alternate API, process changes (Quality & Product Robustness driven) and changes to Active Pharmaceutical Ingredients, Excipient, Packaging and Raw Material items.
Key Responsibilities:
Manages and delivers organizational and project leadership for Generic commercialization, Site Transfers, Buy-ins, Third Party, Alternate API, process changes (Quality & Product Robustness driven) and changes to Active Pharmaceutical Ingredients, Excipient, Packaging and Raw Material items. Proactively identifies & manages risk which could adversely affect successful project completion.
Lead & facilitate multiple cross-functional team by managing and directing project team resources / experts to identify relevant issues and effectively manage progress and change. Ensures integration of technical/commercial information and activities necessary to develop and support the success of the plan by utilizing project management skills/tools, including but not limited to, to successfully drive the project to meet established timelines:
Project Plan
Meeting Minutes/Agendas
RAID log
Costing assessments
Meeting facilitation (Core & relevant sub-teams)
Assesses critical data and contributes information to identify / facilitate critical “Go / No Go” project decisions. Provide proactive communication to all stakeholders, regarding issues, risks, contingency plans and potential negative impacts to the established milestones and timelines.
Be change leaders ensuring change management requirements are being facilitated i.e.
Management of Tactical and Strategic change meetings
Creation of required Protocols (Change & Master Change)
Creation of Qualification Technical Reports
Management of CC’s in appropriate system
Stage/Que/Monitor work in-progress
Develop/Manage implementation plan
Ensure Document review prior to final implementation
Assess completed projects for lessons learned to drive improvement in project performance/execution and capture data to drive/refine resource allocation/costing for future projects.
Mentor and develop other members of the Technical Services department. Act as a subject matter expert on core technologies and/or project management topics (e.g. meeting facilitation, influence, risk management, etc.).
Lead knowledge sharing, individual skill development, and career development within the department, through sharing and implementation of best practices in both individual and group settings (e.g. 1:1 mentoring regarding a specific product/process challenge, and in PC meetings/staff meetings, respectively).
Identify and proactively create opportunities to mentor/job shadow with Junior Project Managers on specific equipment and process technologies (e.g. bringing Junior Project Managers to the shop floor during production and/or troubleshooting support), and on project problem solving (e.g. risk mitigation of various end to end supply chain trends of potential concern during peer review of a Junior Project Manager’s project, provide mentoring on recommend approaches for analysis and remediation, if needed).
Lead skill development of Junior Project Managers in the competency of Planning/Organizing, Critical Thinking, Problem Solving/Resolution, and Influence.
Qualifications:
We value the skills and experiences candidates bring to the table. While we have listed some qualifications below, we encourage candidates to apply even if they do not meet all of them:
B.S. degree in a scientific and/or related operations discipline plus a minimum of 9 years’ experience in pharmaceutical (multi-disciplinary experience: change management, analytical and/or drug regulatory affairs preferred) and/or project management.
Alternatively, a M.S. degree in a scientific and/or related operations discipline plus a minimum of 7 years’ experience in pharmaceutical (multi-disciplinary experience: change management, analytical and/or drug regulatory affairs preferred) and/or project management.
Minimum 9 years of industrial multi-disciplinary experience managing multiple, complex projects and/or implementing continuous improvement.
Expert knowledge and understanding of applicable regulations pertaining to the development and manufacturing of pharmaceuticals including cGMP, DEA, and FDA, EMEA.
Must possess knowledge of SOP’s, production processes and equipment and have strong understanding of pharmaceutical supply chain operations, business analysis, and pharmaceutical technology. In addition, demonstrated knowledge of pharmaceutical development, scale-up and validation, and lifecycle processes.
Expert knowledge and understanding of project management methodology with an active PMP certification with the ability to effectively manage and partner with subordinates, peers, suppliers and contractors.
Demonstrated ability to deliver on results to meet determined business objectives/targets.
Demonstrated ability to communicate effectively (oral and written) both internally and externally at various levels locally, regionally & globally
Demonstrated knowledge in continuous improvement methodologies and implementation with an active six-sigma certification preferred.
Competencies:
Critical Thinking: Ability to work in uncharted areas; capable of integrating large amounts of information to address complex issues. Challenges conventional wisdom when required. Intellectually aggressive with a strong end-product orientation.
Complex Problem Solving: Expert knowledge and ability to apply investigative techniques to uncover problem areas, determine root causes, and drive corrective actions at both the individual and cross-functional team level. Uses problem solving abilities requiring attention to detail, accuracy, and scientific judgment. Develops solutions to a variety of problems of high scope and complexity, as defined in Accountabilities section.
Project Management: Experience managing and leading projects and/or process improvements teams of high scope and complexity.
Initiative: Works independently on activities ranging from strategic decisions to tactical execution of tasks with high complexity. Exercises latitude in determining objectives and approaches to assignments.
Organizational Skills - Able to operate independently. Manages time well, follows through on commitments and pays attention to details. Able to work on several projects simultaneously.
Teamwork: Demonstrated ability to be influence team members and senior leaders on topics of high complexity, and to lead/facilitate teams on tasks of high complexity.
Coaching/ Mentoring/Influencing: Strong ability to coach and/or mentor/influence both in and out of reporting structure. Foster the professional development by willing sharing of personal knowledge and experience enabling individuals and teams to higher levels of performance.
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.
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
710,968
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
How many Healthcare jobs are open in Columbus, OH right now?
There are currently 2,674 open healthcare positions in Columbus, OH listed on Clera. New openings are added daily as companies post roles.
Which companies are hiring for Healthcare roles in Columbus, OH?
Companies currently hiring include Nationwide Children's Hospital, OhioHealth, Department of Animal Sciences at The Ohio State University, St. Peter's Health Partners, Ohio State University Physicians, among others. Browse the listings above to see every active employer.
Are there remote or hybrid Healthcare jobs in Columbus, OH?
Yes — 266 of the 2674 open healthcare positions offer remote or hybrid work (102 remote, 164 hybrid).
How do I apply for Healthcare jobs in Columbus, OH?
Each listing links directly to the employer's application page. Apply early — fresh listings get the most recruiter attention in the first two weeks.