Pharma Production Supervisor | GMP & Quality Focus

PL Developments Careers; Lynwood (CA); On-site; USD 90,000 - 120,000; Full time

Benefits offered by this job

Medical and Dental Benefits

401K with employer match

Paid Time Off and Paid Holidays

Opportunities to Flourish Within the公司

Job summary

PL Developments seeks a Production Supervisor to oversee daily manufacturing operations at its Lynwood, CA facility, ensuring efficient production, strict quality adherence, and regulatory compliance for OTC products.

You will direct supervisors and team leads, plan material flow, monitor performance metrics, collaborate with QA and Planning, and promote a safe, productive work environment. Some overtime may be required to meet deadlines.

Qualifications

• 5+ years in a manufacturing environment with OTC production experience.
• Strong verbal and written communication skills.
• FDA – GMP and GDP knowledge.
• Proven supervisory experience (min 3 years).
• Proficient in MS Office (Word, Excel, PowerPoint).
• Ability to plan production start and completion times.
• University degree or college diploma or equivalent.

Responsibilities

• Provides support by directing and coaching supervisors and team leads to achieve production goals.
• Plan flow of materials through departments and communicate to ensure deadlines are met.
• Monitors key performance indicators to drive improvements.
• Collaborates with QA to resolve quality issues related to filling/production components.
• Identifies and facilitates continuous improvement activities.
• Collaborates with Planning to resolve scheduling issues and line productivity.
• Supervises personnel and maintains a safe, organized work environment.

Skills

Strong verbal and written沟通?

Education

University degree or college diploma

3+ years supervisor experience

Tools

Microsoft Office

Word

Excel

PowerPoint

Job description

PL Developments seeks a Production Supervisor to oversee daily manufacturing operations at its Lynwood, CA facility, ensuring efficient production, strict quality adherence, and regulatory compliance for OTC products.

You will direct supervisors and team leads, plan material flow, monitor performance metrics, collaborate with QA and Planning, and promote a safe, productive work environment. Some overtime may be required to meet deadlines.