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Clark Associates

Packaging Engineer

Lancaster, PA · On-site +1

$70K - $110K/yr

Ensure compliance with GMP, FDA, ISO, ASTM, and ISTA standards * Partner with cross-functional ... Remote Work Qualifications * Access to a reliable and secure high-speed internet connection. Cable ...

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How much do remote gmp auditor jobs pay per hour?

As of Sep 10, 2026, the average hourly pay for remote gmp auditor in the United States is $19.21, according to ZipRecruiter salary data. Most workers in this role earn between $14.42 and $19.23 per hour, depending on experience, location, and employer.

What is a remote GMP auditor?

A Remote GMP Auditor is a professional who evaluates a company's compliance with Good Manufacturing Practice (GMP) standards through virtual assessments, rather than on-site visits. Using digital tools, they review documentation, conduct virtual tours, and interview staff to ensure products are made safely and meet regulatory requirements. Remote GMP auditing is increasingly common due to advancements in technology and the need for flexibility. This role is essential for maintaining product quality and regulatory compliance in industries like pharmaceuticals, food, and cosmetics.

What are the key skills and qualifications needed to thrive as a remote GMP auditor?

To thrive as a Remote GMP Auditor, you need a strong background in Good Manufacturing Practices, regulatory compliance, and quality assurance, typically supported by a degree in life sciences or related fields and auditing certifications. Proficiency with audit management software, virtual meeting platforms, and document control systems is commonly required. Attention to detail, analytical thinking, and clear communication are vital soft skills that help auditors identify issues and collaborate with clients remotely. These skills ensure thorough, effective audits that uphold regulatory standards and maintain product quality across remote operations.

What are some common challenges faced by remote GMP auditors, and how can they be effectively managed?

Remote GMP Auditors often encounter challenges such as limited on-site access, time zone differences, and ensuring data integrity during virtual audits. To overcome these, auditors should leverage robust digital tools, establish clear communication protocols with auditees, and schedule meetings in advance to accommodate different time zones. It's also important to request comprehensive documentation ahead of time and conduct thorough pre-audit planning to ensure a smooth and effective remote audit process.

What is the difference between Remote Gmp Auditor vs Remote Quality Assurance Specialist?

AspectRemote Gmp AuditorRemote Quality Assurance Specialist
CertificationsGMP certifications, auditor credentialsQA certifications, such as CQE or ASQ
Work EnvironmentAudit sites, review documentation remotelyDevelop and review quality processes remotely
Industry UsagePharmaceutical, biotech, medical devicesPharmaceutical, biotech, manufacturing

Remote Gmp Auditors focus on conducting compliance audits of facilities and documentation, often traveling or reviewing remotely, while Remote Quality Assurance Specialists develop, implement, and monitor quality systems. Both roles require GMP knowledge and certifications, but their core functions differ in scope and daily tasks.

How to become a remote GMP auditor?

To become a remote GMP auditor, candidates typically need a background in life sciences, pharmacy, or related fields, along with experience in quality assurance or regulatory compliance. Certification such as RAC or ASQ Certified Quality Auditor can enhance prospects, and familiarity with auditing tools and regulations like FDA or EMA standards is essential. Strong communication skills and the ability to conduct thorough document reviews remotely are also important.
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Remote Gmp Auditor jobs near you
Infographic showing various Remote Gmp Auditor job openings in the United States as of September 2026, with employment types broken down into 88% Full Time, 1% Part Time, 1% Temporary, 4% Contract, and 6% Nights. Highlights an 97% Physical, 1% Hybrid, and 2% Remote job distribution, with an average salary of $39,947 per year, or $19.2 per hour.

Associate Director, Quality Assurance (Drug Substance/Drug Product)

Remote

NewAmsterdam Pharma Company N.V.
See more jobs at NewAmsterdam Pharma Company N.V.external

Full-time

Medical, Dental, Vision, Life, Retirement

Re-posted 4 days ago

Job description

Job Description:

Associate Director, Quality Assurance (Drug Substance/Drug Product)

Associate Director, Quality Assurance to assist in the overall management of end-to-end GxP quality activities for NAP manufacturing programs specifically focusing on Drug Substance and Drug Product. Primary responsibilities will be to ensure quality and compliance of NAP's development and commercial programs with respect to QMS management, controlled documents, and applicable regulatory requirements (FDA/ICH/EMEA, and current industry standards and practices) are conducted in a compliant manner. The team operates in a highly collaborative, resultsoriented, and fastpaced environment, requiring a handson mindset and strong crossfunctional engagement. This is a remote position and will report to the Senior Director, QA/QC.

Key Responsibilities:

Manufacturing Quality

  • Responsible for GxP (GMP, GCP, GLP, GVP) quality and guidance to cross functional teams for late stage through commercial drug lifecycle development.

  • Ensure compliance with all applicable global GxP regulations and guidelines

  • Ensure CMO quality systems, processes, specifications, and SOPs are appropriate for clinical and commercial manufacturing, release and distribution of quality product meeting relevant regulatory requirements, applicable standards and guidance

  • Serve as the primary QA point of contact for external manufacturing sites, contract labs, and suppliers.

  • Conduct Quality review and approval of vendor master and executed batch records, stability protocols, validation protocols/reports and analytical protocols, methods and reports

  • Conduct product release of drug substance, drug product, packaged and labeled product

  • Assist in evaluation and escalation (as appropriate) of product quality issues. Ensure timely and effective follow-up of all identified or assigned quality issues

  • Drive quality activities for internal and external Change Controls assessing product quality and regulatory impact

  • Provide Quality review and approval for deviations, complaint investigations, and OOS/OOTs, assessing for product quality and program impact. Partner with internal and external stakeholders to drive issue resolution, CAPA identification and ensure timely closure

  • Review and verify data to ensure compliance with data integrity and regulatory requirements, as appropriate

  • Support preparation of CMC investigational and commercial regulatory submissions by reviewing and approving relevant documents per program timelines and associated Health Authority (HA) information requests, as required

  • Assist in generation, tracking and trending of manufacturing quality compliance metrics and compile metrics and information for Quality Management Team reports

  • For the EU, work with the selected EU Designated Person to ensure Good Distribution Practices.

Quality Systems:

  • Develop, review and approve GxP controlled documents, such as: Policies, Standard Operating Procedures (SOPs), Work Instructions, and supporting documents related to GxP activities

  • Assist in phase appropriate oversight of systems and optimize systems as they move from clinical to commercial phases

  • Assist in coordination and conduct of routine and non-routine quality assurance audits including: CROs/vendors, process, system, and document reviews to assure quality assurance compliance with regard to all internal procedures as well as regulatory guidelines; this will include conducting audits

  • Participate in internal audits to identify areas of improvement and collaborate with stakeholders to implement effective and sustainable corrective measures

  • Support related activities in preparation for HA inspections and support interactions during HA inspections

  • Continuously improve and maintain Quality Systems related to GxP activities, maintain documentation for compliance with quality and regulatory standards

Requirements:

  • Bachelor's degree in scientific discipline, advanced degree a plus

  • 6-8 years in the pharmaceutical industry, with a minimum of 6 years in Quality

  • Solid understanding of GxP standards, policies, and procedures (domestic and international)

  • Demonstrated experience and understanding of small molecule drug substance and non-sterile oral solid dosage drug product manufacturing

  • GMP vendor auditing experience a strong plus

  • Experience in commercial launch and product is preferred.

  • Experience working with CMOs

  • Excellent verbal and written communication skills

  • Collaborative problem-solver, ability to analyze complex issues to develop relevant and realistic plans, programs, and recommendations

  • Ability to continuously re-prioritize and work independently, as a member of a cross-functional team, and with external vendors with minimal supervision

  • Ability to travel domestically and internationally, approx. 20% of the time

Salary and Benefits:
We offer a competitive base salary, annual bonus, and long-term incentives. In addition, we provide a comprehensive benefits package, including health insurance, dental and vision coverage, term life and disability coverage, and retirement plans.
NewAmsterdam Pharma is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to sex, gender identity or expression, sexual orientation, marital status, race, color, national origin, ancestry, ethnicity, religion, age, veteran status, disability, genetic information, or any other basis protected by federal, state or local law.

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