Job Title

Client: Leading Pharmaceutical Company Location: Multiple Sites (with 50% travel) Role Overview We are seeking highly experienced Subject Matter Experts (SMEs) across key manufacturing domains: Compression Operations . Each SME will be responsible for providing deep technical expertise, process optimization, and compliance oversight in their respective area. The role requires extensive travel (~50%) to support multiple facilities, audits, and technology transfers. Key Responsibilities (per area) SME – Compression Lead process design, scale-up, and troubleshooting for tablet compression. Provide expertise on different makes/models of compression equipment, including OEM systems. Develop SOPs, batch records, and validation protocols. Train operators and ensure compliance with cGMP and regulatory standards.     Common Responsibilities Travel (~50%) to our facilities for audits, training, troubleshooting, and technology transfer. Collaborate with R&D, QA, and manufacturing teams to ensure process excellence. Author and review technical documentation, validation protocols, and reports. Ensure compliance with global regulatory standards (FDA, EMA, WHO). Mentor and train operators and technical staff. Qualifications Bachelor’s/Master’s in Pharmacy, Biotechnology, Chemical/Mechanical Engineering, or related discipline. 8–12 years of hands-on experience in the respective domain (Compression, Granulation, ). Proven expertise working with different makes/models of equipment or directly with OEMs . Strong knowledge of cGMP, regulatory requirements, and validation practices. Excellent communication, analytical, and cross-functional collaboration skills. Willingness to travel up to 50% of the time. . Skillset Required: Engineering, Projects, Compression, Granulation