Full Time GMP Pharma Consultant Jobs, in WORK ANYWHERE Malaysia Selangor - Maukerja

Company Description A Malaysian-owned, technology-based company founded in December 2016 to deliver innovative products and services to the nation. The organization began with a focus on engineering and project management consulting and then expanded into product innovation through collaboration with reputable research and development centers. Recove aims to create solutions that improve quality of life and maximize time-value for customers. With a strong foundation in engineering expertise and proprietary technology, the company is working toward establishing its own brand of products. Recove receives support from well-established Malaysian government technology development centers, reinforcing its commitment to growth and innovation.

Role Description The GMP Pharma Consultant is a full-time, on-site role based in Bandar Baru Bangi. This role is responsible for providing expert guidance on Good Manufacturing Practice (GMP) compliance for pharmaceutical operations, including facility design, equipment qualification, and process validation. The consultant will review and develop standard operating procedures, quality documentation, and regulatory submissions, ensuring alignment with local and international standards. Daily tasks include conducting GMP audits, identifying gaps, recommending corrective and preventive actions, and training internal teams on compliance requirements. The GMP Pharma Consultant will also collaborate with engineering, quality, and project management teams to support technology-based solutions and continuous improvement initiatives within pharmaceutical manufacturing environments.

Qualifications

• Strong knowledge of pharmaceutical GMP regulations, quality systems, and regulatory guidelines, with experience applying them in manufacturing or consulting environments.
• Experience in process validation, qualification of equipment and utilities, and preparation of GMP documentation and standard operating procedures.
• Ability to conduct compliance audits, risk assessments, and root cause analyses, and to recommend effective corrective and preventive actions.
• Background in engineering, pharmaceutical sciences, or related technical field, preferably with exposure to technology-driven projects and product development.
• Excellent analytical, problem-solving, and report-writing skills, with attention to detail and a structured approach to documentation.
• Strong communication and training skills, with the ability to present complex regulatory requirements clearly to diverse internal and external stakeholders.
• Ability to work on-site in Bandar Baru Bangi, collaborate within multidisciplinary teams, and manage multiple projects and deadlines.
• Bachelor’s degree in Pharmacy, Chemical Engineering, Biotechnology, or a related discipline; professional GMP or quality certifications are an advantage.
• Prior experience in pharmaceutical manufacturing, quality assurance, or regulatory affairs is highly beneficial.