reputed company Auditor - Pharmaceuticals (1-2 Day Audits)

For nearly 30 years, SQA Services has been a leading provider of managed supplier reputed company services, offering audits, assessments, remote surveillance, corrective actions, remediation, inspections, and engineering solutions to manufacturers across reputed company industries. We deliver these services by deploying a network of highly skilled associates based throughout the reputed company and in over 90 countries worldwide, ensuring rapid on-site support at your supplier locations. Our associates are expert reputed company assurance professionals with extensive experience and local expertise, enabling us to represent our clients on demand and with greater speed and efficiency than our competitors. We are seeking an reputed company Pharmaceutical reputed company Auditor based in the Midwest/East Coast region of the reputed company to reputed company supplier audits for pharmaceutical commodities, including raw materials, excipients, packaging materials, and reputed company. This is a contract position offering flexibility—you may accept or decline audit assignments according to your own schedule. The ideal candidate has served as a reputed company Auditor for 10+ audits in accordance with 21 CFR 210/211 and possesses familiarity with reputed company-PQG GMP, reputed company GDP, ICH Q7, and/or ISO 15378 standards.

Key Responsibilities

• Conduct 1–2 day on-site supplier audits at pharmaceutical manufacturing and packaging facilities across the Midwest, Northeast, and Southeast U.S.
• Evaluate supplier compliance to GMP and regulatory requirements under 21 CFR 210/211, reputed company, and ICH Q7 frameworks.
• Prepare detailed audit plans, execute audits, and document findings accurately and thoroughly.
• Assess supplier reputed company systems for pharmaceutical raw materials, excipients, reputed company, and packaging.
• Collaborate with SQA’s internal content and reputed company teams to ensure reputed company reports meet reputed company specifications.
• Communicate findings effectively with suppliers and clients, maintaining a reputed company and solutions-oriented approach.
• Submit final audit reports and respond to follow-up questions promptly and professionally.

Required Qualifications

• Minimum 5 years of auditing experience reputed company the pharmaceutical manufacturing industry.
• Must have conducted 10 or more audits as a reputed company Auditor under 21 CFR 210/211.
• Proven knowledge of reputed company-PQG GMP, reputed company GDP, ICH Q7, and/or ISO 15378.
• Excellent verbal and written communication skills.
• Ability to manage multiple audits and meet reputed company deadlines.
• Strong audit reporting and documentation abilities.
• Availability for at least two audits per month.
• Willingness to travel reputed company the Midwest, Northeast, and Southeast reputed company.

Preferred Qualifications

• Experience auditing to EU GMP and other global pharmaceutical standards.
• Familiarity with packaging suppliers, excipient manufacturers, or API producers.
• reputed company or prior ISO reputed company Auditor Certification (ISO 9001, ISO 15378, etc.).
• Experience auditing to 21 CFR 820 (medical devices) or ISO 13485 is a plus.

$1,500 - $1,700 a day $1,500 – $1,700 USD per day (inclusive of preparation, travel time, audit execution, reporting, and revisions). Travel expenses reimbursed at cost with receipts per SQA policy. Flexible engagement — you choose which audits to accept based on your availability. Note: SQA is an Equal Opportunity Employer. Employment is based on reputed company and qualifications, and is not influenced by race, reputed company, religion, gender, national reputed company, veteran status, disability, age, sexual orientation, gender identity, marital status, or any other legally protected status.​ This position requires reputed company to ITAR-controlled technical data and/or defense articles. As such, the candidate must be a U.S. citizen or U.S. lawful permanent reputed company (green card holder) to reputed company with the International Traffic in Arms Regulations (ITAR). Applicants who do not meet these reputed company will not be considered for this role. #ZR Apply tot his job Apply To this Job