Quality Assurance Manager - 172475

ZP Group

Elkridge (MD)

On-site

USD 115,000 - 135,000

Full time

14 days+
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Benefits offered by this job

Comprehensive benefits package

Job summary

Piper Companies is seeking a Quality Assurance Manager in Elkridge, Maryland, to lead QA within a GMP environment for a growing pharmaceutical company. The role emphasizes leadership, regulatory compliance, and document control excellence.

The position requires extensive experience in cGMP, US/EU regulatory knowledge, and a scientific Bachelor's degree. A comprehensive benefits package and on-site work are provided.

Qualifications

  • Minimum 8+ years in FDA/GMP manufacturing environments.
  • Hands-on leadership experience in pharmaceutical QA.
  • In-depth knowledge of cGMP and US/EU regulations.
  • Bachelor's or higher degree in a scientific field.

Responsibilities

  • Manage a team of QA professionals in a GDA/GMP pharmaceutical environment.
  • Follow SOPs to support document approvals, training workflows, and archiving.
  • Serve as eDMS administrator and coordinate change control documentation.
  • Resolve document control issues with originators and stakeholders.
  • Organize and maintain controlled document files for retrievability.
  • Ensure compliance with FDA and international regulatory guidelines.
  • Maintain training records, master files, and authorized signatures.
  • Familiarize operations with site processes and cGMP Health Authority regulations.
  • Review and approve qualification activities, deviations, complaints, investigations, and procedures.

Skills

Leadership
Regulatory knowledge
GMP experience
Quality Assurance

Education

Bachelor's degree in Scientific field

Tools

eDMS

Job description

Piper Companies is currently looking for an experienced Quality Assurance Manager in Elkridge, Maryland (MD) to work for an innovative and growing pharmaceutical company.

Responsibilities for the Quality Assurance Manager include:
  • Manage a team of quality assurance professionals within a GDA/GMP Pharmaceutical manufacturing environment.
  • Follow Policies and SOPs to support the document approval process, assign effective dates and training workflows, and archive documents and document change requests.
  • Serves as the Electronic Document Management System (eDMS) administrator, maintains and implements eDMS processes; partners with Validation to manage/maintain change control and validation documentation for eDMS.
  • Coordinate with document originators and/or stakeholders to resolve document control issues to obtain final approval/ensure smooth operation of all functions.
  • Manage the organization of controlled document files within the Document Control center and ensure that records are readily retrievable.
  • Ensure all controlled documents follow regulatory requirements, including FDA and international guidelines.
  • Maintain employee training records, document master files, authorized signature forms according to company procedures, industry best practices, and government regulations.
  • Carry out a variety of activities to support manufacturing operations becoming familiar with site processes, procedures, and policies as individual develops knowledge aligned with cGMPs and Health Authority regulations.
  • Review and approval of qualification activities, quality records like deviations OOS, complaints, auxiliary forms, investigations, procedures and other quality related documentation.
Qualifications for the Quality Assurance Manager Include:
  • A minimum of 8+ years of work experience within FDA/GMP regulated manufacturing environments
  • Hands on leadership experience within pharmaceutical quality assurance
  • In-depth knowledge of cGMP and regulatory requirements (US and EU) applicable to the pharmaceutical, biotechnology, or related industries.
  • Bachelor's or higher degree within in Scientific field
Compensation for the Quality Assurance Manager include:
  • Salary Range is $115,000 - $135,000 dependent upon experience
  • Comprehensive benefits package
Keywords

Pharmaceutical Manufacturing, QA, Quality Assurance, Manager, Leadership, FDA, Science, comprehensive benefits package, Health, Vision, Dental #LI-ONSITE #LI-DF1

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