Project Supervisor – Drug Product Manufacturing

Techfirm Industrial Services
is looking for an experienced and motivated
Project Supervisor – Drug Product Manufacturing (m/w/d)
to join the team

About the Role:

Join the team as a Project Supervisor to steer technical expansion and capacity enhancement projects in Drug Product manufacturing. You will ensure projects are delivered efficiently, meeting quality, compliance, and operational standards in a dynamic GMP production environment. This role demands strong project coordination skills, regulatory insight, and a hands-on leadership approach to support production ramp-up and continuous improvement initiatives.

Key Responsibilities:

• Supervise and lead technical projects focused on expanding drug product manufacturing capacity.
• Provide technical expertise and ensure project alignment with operational and regulatory requirements such as EU GMP Annex 1.
• Coordinate cross-functional teams and external vendors, overseeing project timelines, governance, and delivery within scope and budget.
• Develop, implement, and maintain operational procedures in collaboration with manufacturing and quality functions.
• Manage change control processes, troubleshoot project-related issues, and handle deviations effectively.
• Foster continuous process improvements and best practices aligned with current industry standards.

Key Requirements:

• Minimum 4 years of experience in GMP pharmaceutical manufacturing, preferably in
  drug product environments.
• Proven track record in
  project supervision or coordination
  within pharmaceutical or biopharmaceutical manufacturing.
• Experience with
  CAPEX projects and equipment qualification
  is a distinct advantage.
• Solid knowledge of cGMP and Annex 1 compliance requirements.
• Fluent in English
  ; proficiency in German is a plus.
• Excellent interpersonal and communication skills with a collaborative, results-driven mindset.
• Agile and adaptable to changing priorities in a fast-paced production setting.
• Must be willing to work on-site; remote work is not available for this position.

Why Join:

• Play a pivotal role in driving scalable manufacturing projects that support critical drug product supply.
• Collaborate with multidisciplinary teams and contribute to state-of-the-art pharmaceutical production.
• Develop your professional skills within a respected company committed to quality, innovation, and compliance.
• Engage in a hands-on role with meaningful impact on production efficiency and product quality.

If you are an experienced project supervisor ready to take on challenging manufacturing projects and deliver high-quality results, we welcome your application.