Director, Manufacturing

PCI Pharma Services•Bedford, NH

About The Position

The Director of Manufacturing for our Bedford site is responsible for the manufacturing of aseptic and non-aseptic pharmaceuticals in accordance with the most stringent quality, regulatory, and safety standards. The Director provides support to Manufacturing Managers, Supervisors, and Associates and strives for excellence and continuous improvement to further enhance site performance and client satisfaction. In conjunction with the Senior Director of Operations, provides direction as well as develops and implements medium and long-term plans for multiple manufacturing buildings within the Bedford site.

Requirements

10+ years direct management experience with demonstrated leadership of increasing responsibility, team management, and coaching skills.
10+ years of experience in cGMP pharmaceutical and/or medical device manufacturing, experience in aseptic fill/finish is preferred.
Prior experience and knowledge of a CDMO or working with CDMOs strongly preferred.
Previous experience with lyophilized products preferred.
Working knowledge of FDA, ICH, and EU pharmaceutical preferred.
Bachelors in a STEM field is required.
Excellent written, verbal, and interpersonal communication skills.
Ability to work in a fast-paced environment and handle multiple tasks simultaneously.
The ability to develop solutions to complex problems, which require a high degree of ingenuity, reactivity, and innovativeness.
Ability to lead other leaders in a dynamic, fast-paced work environment.
Honesty, integrity, respect, and courtesy with all colleagues.
Ability to work with minimal supervision, utilizing creative and balanced independent thinking.
Resilient through operational and organizational change.

Nice To Haves

experience in aseptic fill/finish is preferred
Prior experience and knowledge of a CDMO or working with CDMOs strongly preferred
Previous experience with lyophilized products preferred
Working knowledge of FDA, ICH, and EU pharmaceutical preferred

Responsibilities

Acts as a technical expert and an escalation point for complex/high impact manufacturing issues/decisions.
Oversees daily manufacturing of pharmaceuticals, in compliance with all corporate and regulatory requirements.
Responsible for maintaining cGMP compliance and accuracy of all documentation related to manufacturing.
Ensures that all production teams operate in accordance with department SOPs, which meet regulatory and cGMP standards.
Instill a strong culture of Lean and Continuous Improvement using the site maturity index.
Implements changes to procedures and documentation to ensure all regulatory requirements are being met.
Responsible for management of production operations in accordance with all relevant health, safety and environmental legislation.
Ensures safety policies and procedures are always adhered to and recommends safety improvements, as needed.
Participates in regulatory inspections and client quality audits.
Demonstrates substantial knowledge of industry best practices and trends of aseptic manufacturing.
Identifies root causes of production problems and designs improvements while working within cGMP regulatory requirements.
Leads project (client and internal) teams to represent the Operations organization.
Accountable for identification of gaps, remediation, and developing action plans for the implementation of systems to meet short and long-term manufacturing goals.
Makes key decisions and formulates policies that impact strategic objectives of the department.
Provides leadership and guidance to direct reports and project team members to develop strong leaders and support the vision of the organization.
Writes performance reviews and oversees team development and communication by providing training, development opportunities, and guidance to staff.
Works with direct reports to ensure adequate staffing levels are maintained.
Other tasks as assigned by management.