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PCI Pharma Services

Pharmaceutical packaging and contract services

Manager, Drug Product Manufacturing - 2nd Shift

Bioprocess & BiomanufacturingConfirmed live in the last 24 hours
Full-timeSan Diego, CA, USA

About the Job

Requirements

  • A bachelor's degree in a scientific discipline or equivalent experience is required.
  • At least seven years of related technical experience is required.
  • At least three years of leadership or supervisory experience is required.
  • Understanding of current Good Manufacturing Practices (cGMP) is required.
  • Understanding of regulatory requirements is required.
  • A solid command of chemistry, including understanding of fillers and filling processes, is required.
  • Understanding of QAD, MasterControl, LIMS, and RAM is required.
  • The role requires the ability to sit, reach to use computers and other office equipment, stand for extended periods up to four hours at a time, lift up to 50 pounds, view objects at close and distant ranges with hand-eye coordination, and communicate with others.

Responsibilities

  • Manage day-to-day activities of fill-and-finish manufacturing.
  • Implement production and manufacturing equipment and procedures to optimize processes and meet regulatory requirements.
  • Coordinate with other departments to plan, schedule, and execute production operations in a validated cGMP environment.
  • Oversee daily operations including formulation, filtration, filling, and troubleshooting.
  • Review and generate batch records, and handle client calls and project-management interactions.
  • Plan drug product manufacturing, including defining schedules, coordinating preparation, and troubleshooting.
  • Participate in client calls, interactions, and meetings, including kickoff meetings, tours, and operational issue discussions.
  • Conduct internal investigations involving deviations, corrective and preventive actions, and product-quality reviews.
  • Plan facility shutdowns, maintenance, HEPA certifications, and media fills.
  • Respond to client, qualified-person, and regulatory audits and inspections, and revise standard operating procedures and batch records.
  • Manage quality interactions, including environmental monitoring, out-of-specification, and deviation investigations.
  • Maintain regular and reliable full-time attendance in accordance with the posted schedule.
  • Execute assignments properly, achieve desired outcomes on schedule, and meet quality standards.
  • Build working relationships with internal departments and external clients to support company goals.
  • Support and collaborate with others in difficult and high-pressure situations.
  • Ensure compliance with environmental, health, and safety policies and procedures to foster a safe and environmentally sustainable workplace.
  • Direct day-to-day drug product manufacturing activities and provide expert knowledge.
  • Identify, recruit, and retain employees.
  • Promote the company culture and empower employees to take responsibility for their jobs and goals.
  • Coach, mentor, engage, and develop the team; oversee new-employee onboarding and provide career-development planning and learning opportunities.
  • Set performance standards and encourage employee engagement and results through delegation, continuous feedback, goal setting, and performance management.
  • Communicate organization information through department and one-on-one meetings, email, and regular interpersonal communication.
  • Provide oversight and direction to employees in accordance with company policies and procedures.

About the Company

PCI Pharma Services

Pharmaceutical packaging and contract services

PCI Pharma Services provides end-to-end pharmaceutical packaging and related services, including folding cartons, labels, contract packaging, clinical services, and brand protection, acting as a one-stop source for healthcare product development and commercialization. It handles packaging operations from cartons and labels to contract packaging and labeling, plus clinical packaging and brand protection, with processes built on cGMP and ISO compliance, lean manufacturing, and ongoing R&D, supported by mandatory training and strict security, hygiene, and inspections. It differentiates itself with eight decades of experience and a broad, integrated service suite under one roof, reducing risk and handoffs for clients. Its goal is to be a trusted packaging partner that delivers reliable, compliant, and scalable solutions so healthcare brands stay protected and clients can focus on their core business.

Company size
1-10
Company stage
Debt Financing
Total funding
$4B
Headquarters
Burlington, Canada
Founded
1971

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