Senior Process Engineer - Camurus (Lund)

TOBLOR Consulting; Lunds kommun; On-site; SEK 558,000 - 781,200; Full time

Benefits offered by this job

International work environment

Opportunities for individual development

Dynamic corporate culture

Job summary

TOBLOR Consulting is seeking an experienced Senior Process Engineer in Lund, Sweden. You will lead technology transfer activities for injectable pharmaceutical products, ensuring compliance with GMP regulations.

The ideal candidate has at least 7 years of experience in pharmaceutical manufacturing, a Master's degree in a relevant field, and a collaborative spirit. This role offers opportunities for professional development within an international work environment.

Qualifications

• At least 7 years of experience in pharmaceutical manufacturing operations.
• Hands-on experience in manufacturing process development and technology transfer.
• Fluency in spoken and written English.

Responsibilities

• Lead technology transfers of injectable pharmaceutical products.
• Partner with R&D for successful scale-up and manufacturability.
• Provide technical support for process development and validation.

Skills

Pharmaceutical manufacturing experience

Technology transfer expertise

GMP compliance

Problem-solving skills

Collaboration

Education

Master's degree in Engineering, Life Sciences, or related discipline

Job description

Senior Process Engineer - Camurus (Lund)

We are looking for an experienced Senior Process Engineer to join our Manufacturing Operations team. In this role, you will be responsible for leading technology transfer activities for manufacturing processes for injectable pharmaceutical products, from development into manufacturing environments at Contract Manufacturing Organizations (CMOs). You will support products from clinical development through to commercial supply.

As Senior Process Engineer, you will act as a subject matter expert in pharmaceutical manufacturing processes, working closely with internal stakeholders and external partners to ensure robust, scalable, and GMP‑compliant manufacturing operations. You will report to the Director Manufacturing Operations.

Main responsibilities

• Lead technology transfers of injectable pharmaceutical products from development into commercial manufacturing at CMOs.
• Partner with R&D to ensure that formulation and process development activities support successful scale-up, manufacturability, and long‑term process robustness.
• Provide technical support for process development, scale‑up, validation, and commercial manufacturing activities at CMOs.
• Act as technical lead for investigations and troubleshooting of process deviations, OOS results, manufacturing failures, and other complex technical challenges.
• Contribute to CMC documentation in support of global regulatory submissions and product lifecycle management.
• Ensure that manufacturing processes are executed in accordance with applicable GMP requirements and regulatory expectations.

Candidate profile

We are looking for a professional with at least 7 years of experience from pharmaceutical manufacturing operations. You hold a Master’s degree in Engineering, Life Sciences, or a related scientific discipline.

You have hands‑on experience from manufacturing process development, technology transfer, and GMP‑regulated pharmaceutical manufacturing, preferably within sterile or injectable products. Experience from fill‑finish operations and combination products development is considered a strong merit.

As a person, you are collaborative, responsible, and driven by solving problems. You enjoy getting to the bottom of complex technical challenges and you are a pragmatic team player who takes ownership and follows through on commitments. At the same time, you are humble and low‑prestige, always willing to support colleagues and contribute wherever needed. You thrive in a dynamic environment where technical expertise, collaboration, and problem‑solving go hand in hand. Fluency in spoken and written English is required.

Benefits

This is a great opportunity to join a highly dynamic company during a very exciting phase of growth. The position offers an international work environment and corporate culture, with the possibility for individual development and growth. You will have great opportunities to influence, and you will work together with highly competent colleagues, caring for each other.