Compliance Specialist

PCI Pharma Services•Bedford, NH

12h•Onsite

About The Position

As the Engineering Compliance Specialist, you will play a pivotal role in ensuring the effective management and implementation of change controls, deviations, CAPA plans, and SOP updates within our sterile fill finish operations. You will collaborate with various departments to drive continuous improvement, maintain regulatory compliance, and enhance overall operational efficiency.

Requirements

2+ years’ experience with GMP, ISO, and/or an FDA-regulated environment is required.
Strong technical writer and SME in writing all Quality system documents (CAPAs, Deviations, Change Controls, SOPs, Reports, etc.)
SME in investigation, root cause, and risk analysis in a cGMP environment for complex issues within the production environment
Strong understanding of regulatory requirements, and industry best practices

Nice To Haves

Bachelor’s Degree in a Science or Engineering related field preferred
Detail oriented with strong analytical and problem-solving capabilities
Project management skills and the ability to drive initiatives to completion
Excellent communication and interpersonal skills with the ability to work collaboratively across departments
Assertive, self-directed, and results-oriented
Honesty, integrity, respect, and courtesy with leadership and peers
Strong commitment to conducting PCI PHARMA SERVICES business according to the highest legal and ethical standards and to continually pursue excellence in the manufacturing and delivery of PCI PHARMA SERVICES products and services.

Responsibilities

Initiate, review, and manage change control documentation related to equipment, processes, and systems.
Facilitate cross-functional communication to ensure alignment with stakeholders and timely resolution of change requests.
Conduct impact assessments to evaluate the potential effects of proposed changes on product quality, safety, and efficacy.
Lead investigations into deviations, identifying root causes and implementing corrective and preventive actions.
Collaborate with Quality Assurance, Manufacturing, and other relevant departments to develop comprehensive deviation reports.
Ensure timely closure of deviations while maintaining compliance with regulatory requirements.
Develop and execute robust CAPA plans in response to identified issues or areas for improvement.
Coordinate with cross-functional teams to implement corrective actions and preventive measures.
Monitor and track CAPA effectiveness, making adjustments as necessary to enhance long-term performance.
Act as a liaison between engineering, quality, manufacturing, and other relevant departments to ensure seamless communication and collaboration.
Provide regular updates on change control, deviations, and CAPA status to management and relevant stakeholders.
Foster a culture of proactive problem-solving and continuous improvement.