An established manufacturing facility seeks an Assistant Production Manager to help lead daily operations in a regulated, cGMP-compliant environment. This role supports 1st and 2nd shift teams and is key in promoting safety, maintaining quality, ensuring on-time delivery, and managing production costs. The ideal candidate brings a blend of leadership, cross-functional collaboration, and hands-on production management expertise.
Responsibilities
Safety :
- Promote a safety culture and ensure compliance with local, state, and federal safety regulations.
- Conducted safety training, risk assessments, and audits and supported the resolution of action items.
- Lead or support safety-related programs and initiatives across shifts.
Quality :
- Support quality systems in compliance with regulatory requirements and internal standards.
- Participate in internal / external audits, root cause analysis, and corrective / preventive action planning.
- Review and approve production documentation, including SOPs, batch records, and work instructions.
- Mentor team members on maintaining high standards of quality and compliance.
Delivery :
- Help lead daily production meetings and alignment efforts across shifts.
- Assist in executing the production schedule and resolving operational bottlenecks.
- Collaborate with departments on new product introductions and continuous improvement efforts.
- Conduct Gemba walks and 5S audits and support cross-shift communication.
- Assist in executing cost reduction initiatives and tracking key performance indicators (KPIs).
- Monitor productivity metrics and identify opportunities for process improvements.
- Support budget adherence and the annual capital planning process.
Team Development :
- Support staffing, training, and development efforts to build a high-performing production team.
- Provide coaching and guidance in partnership with HR as needed.
- Encourage professional growth and cross-functional collaboration.
Qualifications
- 5+ years of experience in manufacturing operations (production, quality, engineering, or supply chain).
- Bilingual in English and Spanish is a plus.
- Willing to work across shifts as needed.
- Familiarity with FDA and cGMP standards is a must.
- Proven leadership, problem-solving, and organizational skills.
- Experience with Lean / Six Sigma principles and ERP systems preferred.
- Strong communication and technical skills (Microsoft Office proficiency required).
Education
- A bachelors degree in engineering, business, manufacturing, or a related field is preferred.
- An associate degree with equivalent experience will be considered.
LI-DNI
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