Sr cGMP Pharmaceutical Manager

Fresenius Medical Care; New Orleans (LA); On-site; USD 150,000 - 190,000; Full time

Benefits offered by this job

Medical Insurance

401(k) with company match

Paid time off

Parental leave

Performance bonuses

Job summary

Fresenius Medical Care in the United States seeks a Quality Manager for cGMP Pharmaceutical Products to lead QA activities across sites, ensure 21 CFR compliance, and partner with Manufacturing, Regulatory Affairs, Supply Chain and R&D to embed a culture of quality.

The role covers batch disposition, CAPA, validation, supplier quality, regulatory inspections, and management reviews, with a focus on continuous improvement and staying audit-ready across the organization.

Qualifications

• Minimum 10+ years of quality assurance in drug product manufacturing.
• Minimum 5+ years in a senior QA leadership role with people management.
• Hands-on experience with FDA inspections and Form 483 remediation.
• Demonstrated experience leading Management Reviews and executive presentations.
• Deep knowledge of 21 CFR Parts 4, 210, 211 and ICH Q7–Q11.

Responsibilities

• Oversee cGMP QA responsibilities across sites and processes.
• Lead CAPA management, change control and regulatory readiness.
• Prepare for FDA inspections and respond to 483 observations with Regulatory Affairs.
• Collaborate with Manufacturing, Regulatory Affairs, Supply Chain, and R&D.
• Drive continuous quality improvement and resource planning.

Skills

QA leadership

Regulatory inspections

CAPA management

Quality systems

Data analysis

Cross-functional collaboration

Training and development

Problem solving

Education

Bachelor’s degree in chemistry or related field

Master’s degree preferred

Tools

eQMS platforms (SAP)

QMS

qTrack

Agile

Job description

PURPOSE AND SCOPE:

The Quality Manager, cGMP Pharmaceutical Products is responsible for overseeing and supporting quality assurance responsibilities at pharmaceutical / drug manufacturing sites, ensuring full compliance with 21 CFR Parts 4, 210, 211, and applicable ICH guidelines for drug product manufacturing. This role provides cGMP strategic and operational quality leadership and guidance across systems and processes including batch disposition, CAPA management, validation, supplier quality, regulatory inspections, management reviews and others. The Quality Manager provides solutions by partnering closely with Manufacturing, Regulatory Affairs, Supply Chain, and R&D to embed a culture of quality and ensure uninterrupted, compliant supply of pharmaceutical / drug products.

PRINCIPAL DUTIES AND RESPONSIBILITIES:

• - Leads and demonstrates cGMP knowledge and expertise including its application of cGMP requirements as well as training.
• - Provides solutions and resolutions on how best to deploy systems and processes.
• - Actively participates in FDA inspections and other regulatory audits.
• - Actively engages and supports all pharma/drug sites to ensure cGMP requirements are met.
• - Provides guidance on all pharma/drug related processes and system improvements and changes.
• - Ensures by working with manufacturing sites and site quality personnel that all pharma/drug requirements are in place, procedures are compliant and being followed.
• - Assesses effectiveness of pharma/drug requirements at sites.
• - Provides independent inputs into in-process and finished product results, as appropriate.
• - Performs analysis of deviations, OOS results, complaints, and audit findings to identify systemic quality issues.
• - Escalates critical quality issues to senior leadership and regulatory affairs in a timely manner.
• - Provides inputs into Management Reviews in accordance with ICH Q10 and site QMS requirements.
• - Compiles and presents comprehensive Management Review input data including CAPA trends, deviation metrics, audit outcomes, product quality reviews, regulatory intelligence, and resource assessments.
• - Maintains compliant, audit-ready Management Review records with appropriate retention. Use Management Review outcomes to drive continuous improvement priorities and resource allocation decisions.
• - Analyzes product and process data trends to assess the state of control and identify improvement opportunities.
• - Manages the change control program where appropriate.
• - Serve as a quality representative during FDA pre-approval inspections (PAIs), surveillance inspections, and for-cause inspections.
• - Prepare site and personnel for regulatory inspections. Develop and manage responses to FDA Form 483 observations and Warning Letters in collaboration with Regulatory Affairs.
• - Other duties as assigned.

PHYSICAL DEMANDS AND WORKING CONDITIONS :

• - The physical demands and work environment characteristics described here are representative of those an employee encounters while performing the essential functions of this job. Reasonable accommodation may be made to enable individuals with disabilities to perform the essential functions.
• - Ability to work across time zones for North American multi-site coordination.
• - May require response to urgent regulatory or quality events outside of standard hours.
• - Travel up to 15% as required.

EDUCATION :

• - Bachelor’s degree in chemistry, Pharmaceutical Sciences, Chemical Engineering, Biology, or related scientific discipline (required).
• - Master's degree or advanced technical degree preferred.

EXPERIENCE AND REQUIRED TECHNICAL SKILLS :

• - Minimum 10+ years of quality assurance experience in pharmaceutical drug product manufacturing.
• - Minimum 5+ years in a senior QA leadership role with direct people management responsibility.
• - Hands-on experience with FDA inspections including Form 483 responses and remediation.
• - Demonstrated experience leading Management Reviews and presenting to site and executive leadership.
• - Familiarity with contract manufacturing organization (CMO) oversight is a plus.
• - Deep expertise in 21 CFR Parts 4, 210 and 211.
• - Strong working knowledge of ICH guidelines: Q7, Q8, Q9, Q10, Q11.
• - Experience with statistical process control (SPC), process capability analysis, and quality risk management (ICH Q9) is a plus.
• - Familiarity with FDA guidance documents on process validation, data integrity (21 CFR Part 11), and pharmaceutical quality systems is a plus.
• - Knowledge of EU GMP Annex requirements is advantageous for global supply programs is a plus.
• - Proficiency in eQMS platforms (e.g., SAP, QMS, qTrack, Agile etc).

The rate of pay for this position will depend on the successful candidate’s work location and qualifications, including relevant education, work experience, skills, and competencies.

Benefit Overview: This position offers a comprehensive benefits package including medical, dental, and vision insurance, a 401(k) with company match, paid time off, parental leave and potential for performance-based bonuses depending on company and individual performance.

Fresenius Medical Care maintains a drug-free workplace in accordance with applicable federal and state laws.
Fresenius Medical Care is an equal opportunity employer and does not discriminate on the basis of race, color, religion, sexual orientation, gender identity, parental status, national origin, age, disability, military service, or other non-merit-based factors