REQUIREMENTS

• HS Diploma/GED required; Bachelor’s degree in Biology, Chemistry, Engineering, or related field preferred.
• 5-9 years of relevant work experience, with at least 2 years in a supervisory role, preferably in the pharmaceutical industry.
• Proven knowledge of cGMP practices, aseptic techniques, and chemical concepts.
• Strong critical thinking, problem-solving capabilities, and effective communication skills.
• Ability to multi-task, work independently, and collaborate within a team.
• Physical capability to adhere to cleanroom gowning requirements and lift a minimum of 25 lbs independently.

• Supervise and lead night shift operations in the formulation manufacturing department, ensuring adherence to cGMP standards.
• Coordinate flawless execution of manufacturing batch records, work instructions, and SOPs.
• Strictly monitor and maintain suite, supplies, equipment, logbooks, and data integrity.
• Proactively identify and resolve supply and raw material deficiencies, scheduling conflicts, and process deviations.
• Conduct root cause analysis and drive continuous improvement initiatives.
• Lead and facilitate daily huddles and shift exchanges, acting as a liaison and Subject Matter Expert.
• Provide mentorship and training to team members, encouraging a collaborative and high-performance culture.
• Ensure compliance with all safety regulations and promote safe work habits.