Project Management Group Leader
Our Business
Adare Pharma Solutions is a global Contract Development and Manufacturing Organization (CDMO) with locations across North America and Italy. We offer a wide range of manufacturing, packaging, and research and development services. Our clients range from growing biotech firms advancing groundbreaking clinical trials to established pharmaceutical companies producing high volumes of approved, widely used medicines.
By combining top talent from the life sciences industry with modern research and manufacturing technologies, Adare enables clients to deliver potentially lifesaving medicines in more easily consumable formats - particularly for patients such as infants or the elderly. This is the meaning behind “Transforming Drug Delivery – Transforming Lives.”
Our Culture
When it comes to being an employee of Adare, although we are located across multiple countries and come from diverse backgrounds, we work together toward a common purpose. Supported by leadership that is experienced and highly regarded in the industry, we are paving the way for a brighter and better future by attracting top talent from both within and beyond the CDMO space.
In addition to delivering high-quality results for our external clients, we foster a collaborative, client-centric culture internally - one where employees support one another, share knowledge, and encourage each other to bring their best selves to work each day.
Why Come to Adare?
Adare is Private Equity owned and poised for growth. Employees are provided with internal development opportunities to progress within the organization, enhancing their professional skills and industry knowledge through Adare’s investment in their growth.
We offer a variety of fields to embark in, including manufacturing, engineering, quality, chemistry, formulations, analytical research and development, finance, supply chain, sales, marketing, project management, human resources, and environmental health and safety. Our benefits package is highly competitive, offering medical, dental, and vision coverage; a retirement plan with company match, paid time off and company holidays, tuition reimbursement with no waiting period, life insurance, pet insurance, Flexible Spending Accounts (medical and dependent care), and disability coverage.
Position
Project Management Group Leader
Summary
The Project Management Group Leader is responsible for managing and delivering complex customer programs for oral solid dosage pharmaceutical products, as well as leading the Italy PM team. Reporting directly to the Vice President of Global Project Management, this role combines direct people management with ownership of selected strategic projects, site portfolio oversight, and cross-functional leadership.
The successful candidate will be the primary local PM leadership contact; working closely with the General Manger, Pharmaceutical Development, Quality/Regulatory, Industrialization, Operations, and global stakeholders.
Responsibilities:
People leadership and team performance: Directly supervise, coach and develop a small team of PMs; establish objectives and individual development plans; hold regular one-to-ones; provide timely feedback; conduct performance evaluations; support recruitment and onboarding; manage workload, coverage and capability gaps.
Project and program delivery: Personally lead selected high-complexity customer projects from development and technical transfer through scale-up, process validation/PPQ and commercial launch; establish scope, deliverables, integrated schedules, dependencies, critical paths and decision logs; drive timely execution and issue resolution.
Manufacturing, packaging and analytical coordination: Integrate plans for API/excipient readiness, equipment and production slots, granulation, blending, compression, encapsulation, coating, packaging, QC testing, method transfer/validation, stability and batch release; coordinate interfaces when manufacturing and packaging/testing occur at different sites.
GMP, quality and validation interface: Partner with Pharmaceutical Development, QA, QC, Industrialization and Manufacturing to track readiness, deviations, change controls, validation protocols/reports and batch disposition. Escalate GMP risks promptly while respecting Quality Unit independence and technical ownership.
Financial stewardship: Monitor project budgets, forecast milestones and revenue timing; identify scope creep and change-order opportunities; work with the Proposal team to request and approve change order opportunities.
Client Engagement and Communication: Leads customer meetings, completes agendas, meeting minutes and project timelines using Microsoft Project and Adare’s Project Management System. Manages customers expectation and critical development timelines. Model best practices in all client interactions.
Required Skills, Qualifications, and Experience:
Education: Bachelor’s degree or higher in pharmacy, chemistry, pharmaceutical sciences, chemical engineering, engineering, or related scientific/technical discipline; equivalent relevant experience may be considered.
Industry background: 10+ years of relevant pharmaceutical experience, including at least 5 years leading projects in GMP manufacturing, technical operations or CDMO environments; substantial oral solid dosage exposure required.
Leadership: Demonstrated ability to supervise or lead others, coach PMs, allocate work, provide constructive feedback and manage cross-functional accountability; prior direct line management strongly preferred.
Technical knowledge: Working knowledge of OSD unit operations, pharmaceutical development, technology transfer, analytical methods, GMP manufacturing, packaging, process validation/PPQ, stability and regulatory-driven milestones.
Delivery capability: Proven experience managing multiple concurrent projects, integrated timelines, risks, deviation related schedule impacts, resource conflicts and customer commitments.
Communication: Professional fluency in Italian and English, written and spoken; confident presentation and escalation skills with customers and senior leadership.
Systems: Strong MS Project or equivalent scheduling tools, Excel, PowerPoint and project reporting/dashboard capabilities; comfort with document management systems.
Attention Job Seekers and Applicants: Please be aware of attempted recruiting scams. While Adare does conduct virtual interviews for some positions, we do NOT use Skype or Google Meet. If you are contacted by someone regarding a job opportunity, please be vigilant in reviewing the details of any and all correspondence. Here are some things to look out for: bad grammar; font inconsistencies or formatting irregularity: logos not properly sized, stretched out, blurred; numerous different font styles and sizes within the content of an email or letter; company impersonators (postings that mirror a reputable company, but there’s no link to the business) mismatched email or website domains, or there is difficulty with locating an address, business phone number, and/or email address, financial requests: Do not provide payment or account credentials as part of the application process. Legitimate companies should not require transfers, checks, gift cards or the wiring of funds as a condition of the application process. Additionally, equipment purchases: be cautious if a company asks you to purchase your own equipment (computers, iPads, mobile phones) and requests you to mail it to their IT department. Applicant Follow-up Questions: Proceed with caution if you receive an application follow-up request that requires you to click on a link to answer additional questions; especially if the questions request personal information such as a social security number. General anonymity: proceed with caution if you can’t quickly verify the identity of the poster.
Adare Pharma Solutions is a global Contract Development and Manufacturing Organization (CDMO) with locations across North America and Italy. We offer a wide range of manufacturing, packaging, and research and development services. Our clients range from growing biotech firms advancing groundbreaking clinical trials to established pharmaceutical companies producing high volumes of approved, widely used medicines.
By combining top talent from the life sciences industry with modern research and manufacturing technologies, Adare enables clients to deliver potentially lifesaving medicines in more easily consumable formats - particularly for patients such as infants or the elderly. This is the meaning behind “Transforming Drug Delivery – Transforming Lives.”
Our Culture
When it comes to being an employee of Adare, although we are located across multiple countries and come from diverse backgrounds, we work together toward a common purpose. Supported by leadership that is experienced and highly regarded in the industry, we are paving the way for a brighter and better future by attracting top talent from both within and beyond the CDMO space.
In addition to delivering high-quality results for our external clients, we foster a collaborative, client-centric culture internally - one where employees support one another, share knowledge, and encourage each other to bring their best selves to work each day.
Why Come to Adare?
Adare is Private Equity owned and poised for growth. Employees are provided with internal development opportunities to progress within the organization, enhancing their professional skills and industry knowledge through Adare’s investment in their growth.
We offer a variety of fields to embark in, including manufacturing, engineering, quality, chemistry, formulations, analytical research and development, finance, supply chain, sales, marketing, project management, human resources, and environmental health and safety. Our benefits package is highly competitive, offering medical, dental, and vision coverage; a retirement plan with company match, paid time off and company holidays, tuition reimbursement with no waiting period, life insurance, pet insurance, Flexible Spending Accounts (medical and dependent care), and disability coverage.
Position
Project Management Group Leader
Summary
The Project Management Group Leader is responsible for managing and delivering complex customer programs for oral solid dosage pharmaceutical products, as well as leading the Italy PM team. Reporting directly to the Vice President of Global Project Management, this role combines direct people management with ownership of selected strategic projects, site portfolio oversight, and cross-functional leadership.
The successful candidate will be the primary local PM leadership contact; working closely with the General Manger, Pharmaceutical Development, Quality/Regulatory, Industrialization, Operations, and global stakeholders.
Responsibilities:
People leadership and team performance: Directly supervise, coach and develop a small team of PMs; establish objectives and individual development plans; hold regular one-to-ones; provide timely feedback; conduct performance evaluations; support recruitment and onboarding; manage workload, coverage and capability gaps.
Project and program delivery: Personally lead selected high-complexity customer projects from development and technical transfer through scale-up, process validation/PPQ and commercial launch; establish scope, deliverables, integrated schedules, dependencies, critical paths and decision logs; drive timely execution and issue resolution.
Manufacturing, packaging and analytical coordination: Integrate plans for API/excipient readiness, equipment and production slots, granulation, blending, compression, encapsulation, coating, packaging, QC testing, method transfer/validation, stability and batch release; coordinate interfaces when manufacturing and packaging/testing occur at different sites.
GMP, quality and validation interface: Partner with Pharmaceutical Development, QA, QC, Industrialization and Manufacturing to track readiness, deviations, change controls, validation protocols/reports and batch disposition. Escalate GMP risks promptly while respecting Quality Unit independence and technical ownership.
Financial stewardship: Monitor project budgets, forecast milestones and revenue timing; identify scope creep and change-order opportunities; work with the Proposal team to request and approve change order opportunities.
Client Engagement and Communication: Leads customer meetings, completes agendas, meeting minutes and project timelines using Microsoft Project and Adare’s Project Management System. Manages customers expectation and critical development timelines. Model best practices in all client interactions.
Required Skills, Qualifications, and Experience:
Education: Bachelor’s degree or higher in pharmacy, chemistry, pharmaceutical sciences, chemical engineering, engineering, or related scientific/technical discipline; equivalent relevant experience may be considered.
Industry background: 10+ years of relevant pharmaceutical experience, including at least 5 years leading projects in GMP manufacturing, technical operations or CDMO environments; substantial oral solid dosage exposure required.
Leadership: Demonstrated ability to supervise or lead others, coach PMs, allocate work, provide constructive feedback and manage cross-functional accountability; prior direct line management strongly preferred.
Technical knowledge: Working knowledge of OSD unit operations, pharmaceutical development, technology transfer, analytical methods, GMP manufacturing, packaging, process validation/PPQ, stability and regulatory-driven milestones.
Delivery capability: Proven experience managing multiple concurrent projects, integrated timelines, risks, deviation related schedule impacts, resource conflicts and customer commitments.
Communication: Professional fluency in Italian and English, written and spoken; confident presentation and escalation skills with customers and senior leadership.
Systems: Strong MS Project or equivalent scheduling tools, Excel, PowerPoint and project reporting/dashboard capabilities; comfort with document management systems.
Attention Job Seekers and Applicants: Please be aware of attempted recruiting scams. While Adare does conduct virtual interviews for some positions, we do NOT use Skype or Google Meet. If you are contacted by someone regarding a job opportunity, please be vigilant in reviewing the details of any and all correspondence. Here are some things to look out for: bad grammar; font inconsistencies or formatting irregularity: logos not properly sized, stretched out, blurred; numerous different font styles and sizes within the content of an email or letter; company impersonators (postings that mirror a reputable company, but there’s no link to the business) mismatched email or website domains, or there is difficulty with locating an address, business phone number, and/or email address, financial requests: Do not provide payment or account credentials as part of the application process. Legitimate companies should not require transfers, checks, gift cards or the wiring of funds as a condition of the application process. Additionally, equipment purchases: be cautious if a company asks you to purchase your own equipment (computers, iPads, mobile phones) and requests you to mail it to their IT department. Applicant Follow-up Questions: Proceed with caution if you receive an application follow-up request that requires you to click on a link to answer additional questions; especially if the questions request personal information such as a social security number. General anonymity: proceed with caution if you can’t quickly verify the identity of the poster.