Compliance Specialist III

Job Description

Job Description

Description :

Title: Compliance Specialist III

Work Arrangement: Fully on-site

Schedule: Monday Friday, 8:00 a.m. 5:00 p.m.

Assignment Duration: Two years

Interview Process: Two Step Interview Process. First interview will be virtual via Microsoft Teams. Second interview will be in person, on-site, including a facility tour.

Core Essential Skills Minimum 5 years of experience:

1. Bachelor's Degree, preferably in a scientific or engineering discipline, or equivalent education/experience with a minimum of 7 years relevant progressive experience in the pharmaceutical or related industry.
2. GMP Quality Systems and Regulatory Compliance Experience
3. Internal & External Auditing and Inspection Readiness
4. CAPA, Investigations, and Compliance Issue Resolution
5. Quality Documentation Review and Quality Technical Agreements
6. Independent Problem-Solving, Sound Judgment, and Cross-Functional Communication
7. Candidates should be senior-level, independent, motivated, and comfortable making higher-level decisions
8. Experience with compliance or quality systems, documentation review and approval, and strong technical writing skills. Management experience is not required.

POSITION SUMMARY

This position will be responsible for Quality Compliance Oversight, Quality Council Management Review, Site Compliance Metrics, Knowledge Management, Site Inspection Readiness program, Internal Audit program, Partner Management activities, and Supplier Qualification and Vendor Management program. The position is responsible for the development and monitoring of corrective action plans related to trends identified from inspection and audit observations.

ESSENTIAL AREAS OF RESPONSIBILITY

All areas of responsibility listed below are essential to the satisfactory performance of this position by any incumbents with reasonable accommodation if necessary. Any non-essential functions are assumed to be included in other related duties or assignments.

• Prepare and support communication of site quality system status through management review forums.
• Manage Quality Technical Agreements (QTA) with internal and external partners to ensure compliance.
• Lead and execute internal audits to verify adherence to pharmaceutical manufacturing regulations.
• Coordinate and manage external audits/inspections, including timely responses and CAPA tracking.
• Oversee Inspection Readiness program to maintain site preparedness.
• Collaborate with Site Operations and Quality Management to resolve compliance issues promptly.
• Conduct Knowledge Management activities, including regulatory review and gap assessments.
• Support investigation reviews and corrective action plans, ensuring proper documentation and notification.
• Manage vendor/supplier qualification and related compliance activities.
• Ensure periodic document reviews and gap assessments for department and site compliance.
• Own and update procedures for assigned responsibilities.
• Lead special cross-functional projects and present findings to senior management.
• Complete required training and maintain compliance with all assignments.
• Maintain work areas and perform duties safely and efficiently in accordance with company policies, cGMPs, SOPs, and Batch Records.
• Responsible for performing additional related duties as assigned.

POSITION REQUIREMENTS

Any equivalent combination of education, training and/or experience that fulfills the requirements of the position will be considered.

Education/Certification/Experience:

• Bachelor's Degree, preferably in a scientific or engineering discipline, or equivalent education/experience with a minimum of 7 years relevant progressive experience in the pharmaceutical or related industry.
• Strongly prefer a minimum of 3 years performing audits and measurements of GMP Quality Systems, preferably in the pharmaceutical industry.
• Requires experience and knowledge of cGMP and other applicable industry regulatory requirements as they relate to the production of pharmaceutical products and associated quality systems.
• Working knowledge of FDA, EMA, DEA, EPA and other regulatory requirements for a research and commercial environment.
• Experience providing support for regulatory agency inspections preferred.
• Experience with writing and negotiating Quality Technical Agreements preferred.
• Experience in a pharmaceutical manufacturing environment preferred.
• Experience with internal/external auditing is preferred.
• ASQ CQE/CQA Certification (or equivalent) is preferred.

Skills/Knowledge/Abilities:

• Computer proficiency with comprehensive working knowledge of MS Office products, Learning Management Systems (LMS), ERP systems such as SAP or Oracle and manufacturing/quality systems such as LIMS, TrackWise, Veeva, and Qdocs.
• Ability to manage multiple priorities and reporting requirements.
• Ability to motivate and influence others with and/or without direct supervisory authority.
• Ability to communicate effectively with excellent written and oral communication skills.
• Ability to interact positively and collaborate with co-workers, management and internal/external partners.
• Detail oriented with ability to analyze information, develop possible solutions, create metrics and articulate the link to business needs/objectives.
• Project management and advanced presentation skills.
• Self-directed with ability to organize and prioritize work.

Problem Solving:

• Proactively works on problems of a moderate to complex scope where evaluation of contributing factors requires the analysis of situations or data and an in-depth knowledge and evaluation of various known and unknown factors.
• Seeks out all resources when selecting methods and techniques for obtaining results.
• Acts independently and proactively to recommend and administer methods and procedures for problem resolution.