Find CMC Project Manage Jobs

Senior Technical Project Manager - CMC
Sia —Dublin, County Dublin
- Full-time
- Hybrid work
- Doctoral degree
- Engineering
- English
Quick apply
CMC Biopharma Regulatory Consultant — Ecolab Life Sciences
Ecolab Inc. —Dublin, County Dublin
- €7,425 a month
- Full-time
- Doctoral degree
- Sales
- English
9d
CMC Biopharma Regulatory Consultant — Ecolab Life Sciences
Ecolab —Dublin, County Dublin
- €7,425 a month
- Doctoral degree
- Sales
- English
9d
Project Scheduler - CMC
Sia —Dublin, County Dublin
- Full-time
- Hybrid work
- Engineering
- Project management
- Bachelor's degree
Quick apply
Director Regulatory CMC Sciences Project Management
Viatris —Northern Cross, County Dublin
- Full-time
- Microsoft Office
- Project management
- Mentoring
Senior Program Manager, PDS&T - Combination aesthetics & devices
AbbVie —Sligo, County Sligo
- Full-time
- Hybrid work
- Engineering
- Master's degree
- Project management
11d
Tech Transfer (Junior)
DPS Group —Dublin, County Dublin
- Full-time
- Engineering
- Master's degree
- Project management
10h
CMC Lead, Launch Product, Small Molecules
Takeda Pharmaceutical —Dublin, County Dublin
- €116,800–€160,600 a year
- Full-time
- Engineering
- Project management
- Bachelor's degree
Associate Director, Program & Alliance Management
Zymeworks Inc. —Swords, County Dublin
- €90,000–€138,000 a year
- Full-time
- Hybrid work
- Bachelor's degree
- Communication skills
- Annual leave
Quick apply
10d
Technical Manager (Biologics)
AbbVie —Sligo, County Sligo
- Full-time
- Management
- Master's degree
- Manufacturing
Senior Manager, Regulatory Affairs CMC
Viatris —Northern Cross, County Dublin
- Full-time
- Microsoft Office
- Project management
Director Regulatory Affairs Global CMC
Viatris —Northern Cross, County Dublin
- Full-time
- Project management
- Mentoring
- Manufacturing
Senior Manager, Quality Assurance - GxP
PTC Therapeutics International Limited —DUBLIN 2, County Dublin
- Full-time
- Microsoft Office
- Bachelor's degree
- Mentoring
Quick apply
Director, Regulatory Affairs Medical Devices & Combination Product
Takeda Pharmaceutical —Dublin, County Dublin
- €116,800–€160,600 a year
- Full-time
- English
- Bachelor's degree
- Communication skills
Director Respiratory Regulatory CMC
Viatris —Northern Cross, County Dublin
- Full-time
- Microsoft Office
- Project management
- Manufacturing
EHS Specialist 3
APC Ltd —Dublin, County Dublin
- Full-time
- Hybrid work
- Research
Quick apply

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CMC Biopharma Regulatory Consultant — Ecolab Life Sciences
Ecolab Inc. —Dublin, County Dublin
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Senior Technical Project Manager - CMC

Sia -
Dublin, County Dublin

Quick apply

Job details

Full-time

Qualifications

Doctoral degree
Chemical Engineering
Engineering
English
Master's degree
Project management
Bachelor's degree
Product development
Manufacturing
Leadership
Communication skills
Negotiation

Full job description

Company Description

Sia is a global management and AI-focused consulting firm with a strong presence in the energy and utilities sector. With €500m in annual revenue and 3,000 employees worldwide, around 20% of our business is focused on energy and utilities.

Founded in France over 25 years ago, Sia has grown rapidly and is now a recognised leader in energy transition, data science and AI solutions. In 2024, we announced a strategic partnership with Blackstone as our first external investor, supporting our continued growth.

Job Description

Provide consulting services for Sia/LBG’s clients including, but not limited to:

Routinely provide strategic oversight to maintain alignment of project milestones to day-to-day activities.
Responsible for content, quality, and distribution of project management deliverables (reports, dashboards, etc.) and routine updates (schedule, budget, risk), typically as the final reviewer.
Establish strong working relationships with leadership and project functional teams across all levels.
Serve as project spokesperson and facilitate communications with all internal and external stakeholders (meetings, reports, etc.).
Work with cross-functional teams (CMC, Med. Affairs/Clinical, Nonclinical, Quality, Regulatory, Finance, Legal, Contracts Management, etc.) to drive project activities against scheduled timelines, approved scope, and approved budget.
Manage project financials including vendor invoice review/approval, budget development, actuals tracking, maintenance of time-phased financial forecast, preparation of project financial reports for internal and external stakeholders.
Proactively manage strategic risks and issues, providing expertise in the identification and implementation of risk mitigation activities.
Demonstrate and foster excellent teamwork, with the ability to navigate within multidisciplinary teams.
Balance project demands to align/realign Budget, Quality, Timeline, and Scope, as needed.
Lead product development meetings, and ensure all Project Leaders, and/or subteam leaders, have all the information and support needed to implement the project.
Focus on customer service, with agility and clear communication.
Adhere to Sia/LBG quality standards regarding client deliverables.

Qualifications

Mandatory qualifications

8+ years of experience in the biopharmaceutical industry with a minimum of 5 years of project management experience.
BS, MS, or PhD in a scientific or engineering discipline
- E.g., Chemistry, Biochemistry, Chemical or Biomedical Engineering, Pharmaceutical Sciences.
Experience working with CDMOs to support outsourced development and manufacturing activities, including oversight of deliverables and timelines.
Ability to engage in technical and scientific discussions.
Strong communication and interpersonal skills, with the ability to influence, collaborate, and build alignment across diverse technical and leadership teams.
Proficiency in Planisware and principles to plan, manage, and track multiple parallel projects in a complex, matrixed environment.
Fluent and articulate communication in English (written and spoken).
Excellent written and oral communication, presentation, problem solving, and negotiation skills with an emphasis on building consensus.
Ability to work independently and in collaboration with others.
Flexibility and ability to deal with ambiguity, and sense of personal ownership of deliverables and results.
Works well with teams, often comprised of multiple disciplines.

Ideal candidates

Comprehensive understanding of CMC, including:
- Small molecule, biologics, or vaccine formulation, process development, analytical development, and GMP manufacturing across both early and late-stage development.
Formal project management training or certification (e.g., PMP).
Strong understanding of product development lifecycle and pharmaceutical manufacturing operations.
Strong understanding of cGXP guidelines and regulatory requirements.

Additional Information

Sia is an equal opportunity employer. All aspects of employment, including hiring, promotion, remuneration, or discipline, are based solely on performance, competence, conduct, or business needs.

Quick apply

Refine Your Search

CMC Project Manage jobs

Senior Technical Project Manager - CMC

CMC Biopharma Regulatory Consultant — Ecolab Life Sciences

CMC Biopharma Regulatory Consultant — Ecolab Life Sciences

Project Scheduler - CMC

Director Regulatory CMC Sciences Project Management

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Tech Transfer (Junior)

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Technical Manager (Biologics)

Senior Manager, Regulatory Affairs CMC

Director Regulatory Affairs Global CMC

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Director, Regulatory Affairs Medical Devices & Combination Product

Director Respiratory Regulatory CMC

EHS Specialist 3

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