WHAT WE'RE LOOKING FOR:
- Education: Bachelor’s degree in a technical field, preferably life science, chemistry, and/or engineering discipline, or equivalent experience required.
- Experiences: Minimum 5 years of progressive manufacturing experience with responsibilities, including at least 1 year in a supervisory capacity; or an equivalent combination of education and experience.
- Experience in life sciences, chemistry, chemical engineering, or chemical production is required.
- Experience in cGMP manufacturing is a plus.
- Preferred Qualifications:
- Familiarity with chemical and/or aseptic production processes within a similar industry is preferred.
- Highly organized and self-motivated individual capable of working independently with minimal supervision.
- Strong leadership and problem-solving skills are essential.
- Excellent oral and written communication skills.
- Ability to perform risk assessments on products and processes, and develop corrective measures.
- Capable of managing multiple tasks and priorities, with adaptability to changing situations.
- Proficient in computer applications related to scheduling, procedure updates, and data management.
- Initiative-driven, deadline-oriented, and able to lead team efforts.
- Proven track record of reducing costs through process improvements and efficiencies.
- Hands-on, team-oriented, and committed to business improvement processes.
- Experience with SAP system is advantageous.
- Meticulous in work and proficient in multitasking.
- Ability to work effectively in high-paced and high-pressure environments, leading teams to drive results.
HOW YOU WILL THRIVE AND CREATE AN IMPACT:
- Supervise manufacturing employees and potentially other departments such as production, maintenance, and shipping.
- Plan, schedule, and coordinate departmental activities, including staffing, to fulfill sales orders, meet inventory requirements, and ensure timely delivery of products following established procedures and processes.
- Responsible for site security, safety, and proper shutdown procedures at shift end.
- Participate in production operations supervision and execution.
- Monitor and improve manufacturing efficiency, output, and safety through observations, measurements, and data analysis.
- Ensure compliance with manufacturing processes according to documentation such as Batch Records, cGMPs, SOPs, and Work Instructions.
- Maintain and update procedures related to production processes to ensure quality and consistency.
- Create, edit, and maintain necessary documentation including SOPs and Work Instructions.
- Implement and uphold all safety policies and procedures.
- Identify and eliminate departmental non-conformities using root cause analysis and corrective actions.
- Design lean manufacturing cells to optimize space, equipment, materials, and personnel, increasing capacity.
- Participate in internal and external audits, ISO certifications, and ongoing compliance activities.
- Collaborate with internal departments to meet customer commitments efficiently.
- Ensure calibration and maintenance of production equipment are performed timely with records kept up-to-date.
- Perform other duties as assigned.