Commercial Manufacturing Project Manager

Publiceringsdatum: 2025-03-20

Är du intresserad av att jobba inom industriell tillverkning? Letar du efter en chans att arbeta som arbetsledare, tillverkning kemiska produkter på Magle Chemoswed AB? Nu är det möjligt. Vill du arbeta heltid hos Magle Chemoswed AB? Just nu letar de efter någon som vill ha en tjänst tills vidare.

För detta jobb är Malmö den angivna tjänsteorten. Magle Chemoswed AB söker efter fler duktiga individer som vill arbeta som arbetsledare, tillverkning kemiska produkter. De har just nu ett ledigt jobb som arbetsledare, tillverkning kemiska produkter som kan vara av intresse för dig. Bli en del av Magle Chemoswed AB genom att ansöka till jobbet som arbetsledare, tillverkning kemiska produkter senast lördag den sjätte september 2025.

Jobbannons

Magle Group is growing and we are looking for a Commercial Manufacturing Project Manager who is ready for a new challenge and who wants to be part of a small but dynamic project team.

Magle Group is supporting other Life Science Companies by providing CDMO services as well developing and manufacturing our own products with DSM technology.

As a Commercial Manufacturing Project Manager, you will play a crucial role in ensuring the successful coordination and timely release of commercial production batches. Serving as the key link between multiple teams, you will oversee all critical activities, from production start-up through to final product release.

In this position, you will also provide critical support in Tech Transfer, ensuring smooth transitions from development to commercial manufacturing. A solid understanding of release processes, deviation investigations, and production coordination within regulated industries such as pharmaceuticals or medical devices is essential. Your ability to drive cross-functional collaboration, manage timelines, mitigate risks, and optimize resources will be key to ensuring the seamless execution of projects.

This newly created role offers you the opportunity to influence processes, enhance efficiencies, and contribute to the overall success of both production and commercial operations. If you excel in fast-paced environments, enjoy problem-solving, and are passionate about project management, this is an exciting opportunity to make a significant impact.

Key Responsibilities:

• Collaborate with teams in QC, QA, Production, R&D, Supply Chain, and Engineering to ensure operational readiness.

• Effectively manage project timelines, risks, and resources to achieve on-time and on-budget delivery.

• Lead and coordinate commercial production projects, ensuring timely product release through effective cross-functional alignment.

• Provide support in Tech Transfer, managing the smooth transition from development to production, ensuring operational continuity and compliance.

• Ensure adherence to regulatory and quality standards, especially GMP and medical device regulations.

• Serve as a liaison between internal teams and external stakeholders, facilitating clear communication and alignment.

• Handle customer communication regarding deliveries for commercial batches, ensuring customers are informed of timelines, potential delays, and any changes.

• Drive and optimize processes for batch coordination, release, and product quality improvement.

• Generate and maintain comprehensive project documentation, including status reports, timelines, and compliance records.

• Take on additional commercial production projects as needed to support business objectives and enhance operational efficiency.

• Perform other duties as assigned to support the project management team.

Qualifications:

• Bachelor’s degree in a scientific or related field; advanced degree or relevant industry experience preferred.

What we are looking for:

• Proven project leadership experience in regulated industries such as pharmaceuticals, biotech, medical devices, or related fields.

• Strong background in operational QA, production engineering, or similar roles within the medical device or pharmaceutical industry, with additional experience in supply chain, manufacturing, or production coordination considered a plus.

• Extensive knowledge of medical device regulations, GMP, quality systems, release processes, deviation management, and production workflows.

• Experience working with customers or acting as a liaison to ensure clear communication and alignment on project goals and deliverables.

• Demonstrated ability to manage multiple stakeholders and work cross-functionally.

• Strong organizational, leadership, and project management skills.

• Excellent communication and problem-solving abilities.

• Proven track record of delivering impactful results

If this position aligns with your experience and you’re excited about joining a company with a promising future, we’d love to hear from you.

We are a value-driven organization, and we seek individuals who share our passion for making a meaningful impact and improving lives. We’re looking for someone who not only meets the qualifications but also embraces our values and fits within our organizational culture.

This is an ongoing recruitment process. Please submit your CV along with a brief cover letter explaining why you’re interested in this position. The role is based at our office in Malmö, with collaboration at our sites in Lund and Denmark. It’s a full-time position.