Drug Product Manufacturing Manager - Weekend Ops

PCI TRGR Penn Pharmaceutical Services Ltd; San Diego (CA); On-site; USD 107,000 - 120,000; Full time

Benefits offered by this job

Paid time off

Health insurance (dental & vision)

Flexible spending account

401(k) plan

Job summary

PCI Pharma Services seeks a senior manufacturing leader to manage day-to-day Drug Product Manufacturing in a cGMP environment in California. You will oversee fill/finish activities, batch records, and cross-functional scheduling, including weekend operations.

This role stresses leadership, regulatory compliance, and continuous productivity improvements. You will mentor staff, drive CAPA investigations, and ensure quality standards while coordinating with internal and client teams to meet project

Qualifications

• Bachelor’s degree in scientific discipline or equivalent experience.
• 7+ years of related technical experience.
• 3+ years of leadership/supervisory experience.
• Solid understanding of cGMPs.
• Understanding of regulatory requirements.
• Strong knowledge of fillers and filling processes.
• Experience with QAD, MasterControl, LIMS, RAM.

Responsibilities

• Oversee daily fill-finish operations in a validated cGMP environment.
• Coordinate batch records and project management interactions with clients.
• Lead cross-functional planning with DP manufacturing to meet schedules and resolve issues.
• Manage investigations (Deviations, CAPA, PQRs) and quality events.
• Ensure facility planning, shutdowns, HEPA certifications, and media fill planning.
• Provide coaching and development for team and uphold PCI culture.

Skills

Leadership experience

cGMP knowledge

Regulatory understanding

Filling processes

Quality systems familiarity

Team coordination

Education

Bachelor’s degree in scientific discipline

Tools

QAD

MasterControl

LIMS

RAM

Job description

PCI Pharma Services seeks a senior manufacturing leader to manage day-to-day Drug Product Manufacturing in a cGMP environment in California. You will oversee fill/finish activities, batch records, and cross-functional scheduling, including weekend operations.

This role stresses leadership, regulatory compliance, and continuous productivity improvements. You will mentor staff, drive CAPA investigations, and ensure quality standards while coordinating with internal and client teams to meet project