Pharmaceutical Consultant E.M.M.A. International Consulting Group Miami, FL Job Details Full-time 15 hours ago Qualifications Defect resolution root cause analysis Pharmaceutical regulatory compliance Defect analysis Drug regulation Technical writing experience within manufacturing Six Sigma methodology implementation Manufacturing facility experience ICH guidelines Bachelor's degree Pharmaceutical company experience Quality control problem-solving Technical troubleshooting support Quality improvement programs in engineering FDA regulations Failure analysis Pharmaceutical manufacturing facility experience Production troubleshooting Full Job Description Working for EMMA International means working in a fast-paced, team-centric environment. You will be a part of a hard-working, passionate, and motivated team who is dedicated to achieving collective goals. Being a successful part of the EMMA International team means being dependable, self-driven, and a team-player with a strong work-ethic. If you are a critical-thinker who is looking for an employer to grow with, EMMA International is the place for you! To apply for a job listed, please send a cover letter and resume to . Pharmaceutical Consultant Full-Time (On-Site)

Job Summary:

EMMA International, a leading consulting firm in the medical device, pharmaceutical, biotechnology, combination products, and diagnostics industries. We are seeking a highly motivated and experienced consultant to join our team. The successful candidate will be responsible for supporting our clients in the pharmaceutical manufacturing industry by providing technical expertise in areas such as microbiology, regulatory affairs, technical writing, Lean Six Sigma certification, and root cause analysis.

Essential Duties:

Provide technical expertise and support to clients in the pharmaceutical manufacturing industry. Perform root cause analysis and recommend corrective actions to address quality issues. Develop and review manufacturing procedures, including batch records, standard operating procedures, and protocols. Ensure compliance with relevant regulations and guidelines, including FDA, cGMP, and ICH. Conduct risk assessments and implement mitigation strategies. Support clients in the implementation of Lean Six Sigma methodologies to improve operational efficiency and reduce waste. Communicate effectively with clients and stakeholders, including presenting technical information in a clear and concise manner. Collaborate with cross-functional teams to drive projects to successful completion.

Qualifications :

3+ years of experience in pharmaceutical manufacturing, with a strong understanding of c

GMP, FDA

regulations, and ICH guidelines. Lean Six Sigma certification, with a proven track record of implementing process improvements. Strong technical writing and communication skills. Experience with root cause analysis and risk assessment. Ability to work independently and as part of a team. Strong analytical and problem-solving skills. Must have advanced experience with investigation Bio/Pharma industry experience preferred

Education:

Must have BA/BS in Biochemistry, Chemical Engineering, Biology or other relevant science discipline Must be willing to work additional various shifts as required Must be willing to work on-site at client facility Must have prior experience working in a manufacturing environment and troubleshooting manufacturing related issues If you have a passion for consulting and are looking for an opportunity to work with a dynamic team of experts, please apply today!