Eurofins CDMO Alphora Inc. is a leading contract development and manufacturing organization specializing in complex active pharmaceutical ingredients (APIs). We are looking for a driven Process Specialist to join our Technology Transfer team and play a key role in bringing innovative chemical processes from development to full-scale GMP manufacturing.
This is an exciting opportunity for an early-career professional who is passionate about pharmaceutical manufacturing, thrives in a fast-paced technical environment, and loves collaborating across diverse scientific and operational teams.
About the Role
As a Process Specialist, you will serve as a critical bridge between our R&D teams, Operations, and our clients. Working under the guidance of senior team members, you will help design, implement, and support safe, scalable, and compliant manufacturing processes within our cGMP facilities.
This client-facing, cross-functional role offers hands-on exposure to every stage of the manufacturing lifecycleâfrom process design and batch record generation to on-the-floor support and production troubleshooting. Itâs the perfect entry point for someone eager to grow into a technical operations, technology transfer, or manufacturing leadership path.
What Youâll Do
Be a Key Contributor to Process Scale-Up & Technology Transfer
- Collaborate with stakeholders across R&D, QC, QA, Operations, Supply Chain, and Engineering to design safe, scalable processes from gram to multiâkilogram scale.
- Support the generation, review, and execution of Master Batch Records (MBRs), Production Batch Records (PBRs), and Executed Batch Records (EBRs).
- Provide technical support during manufacturing campaigns, spending required time âon the floorâ to guide batch execution.
Drive Operational Readiness & Project Success
- Participate in batch scheduling, readiness checks, material availability reviews, and daily Operations activities.
- Support Material Readiness by coordinating bills of materials (BOMs) and maintaining tracking tools.
- Contribute to Campaign Summary Reports and process data trending to support continuous improvement.
Serve as the Operations Point of Contact
- Represent Operations in internal and external project meetings.
- Provide timely production updates to clients and help maintain strong communication throughout each project.
- Assist in managing process deviations, amendments, SOP updates, and other quality-related activities.
Contribute to a Culture of Safety & Compliance
- Uphold cGMP, Environmental Health & Safety (EHS), Good Documentation Practices, and internal procedures.
- Ensure accurate, timely documentation and escalate any incidents or concerns.
Participate in On-Call Support (as per rotation)
- Provide after-hours support to resolve processing issues, report IPCs, and collaborate with QA, R&D, and Ops leadership when needed.
What You Bring
- A degree in chemistry, chemical engineering, life sciences, or a related discipline.
- Strong attention to detail and commitment to safety and compliance.
- Excellent communication and collaboration skills.
- An eagerness to learn, ask questions, and grow within a high-performing technical environment.
- A passion for solving problems and supporting complex chemical manufacturing processes.
Why Join Eurofins CDMO Alphora?
- Work at the intersection of science, manufacturing, and client engagement.
- Gain hands-on experience with cGMP manufacturing and technical transfer.
- Collaborate with industry experts and contribute to impactful pharmaceutical projects.
- Grow your career within the global Eurofins networkâhome to more than 61,000 employees worldwide.