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Quality Assurance Director

Lampire Biological Laboratories, Inc.

Job Description

Job Description

Are you looking to increase your impact on life sciences? Lampire Biological Labs is a premier biotech life science company dedicated to providing biological reagents to the pharmaceutical, diagnostic, and biotech industries and is seeking a motivated Quality Assurance Director to lead quality compliance and drive quality improvement. If you thrive in a fast-paced environment, take pride in running a compliant facility, and love developing talented teams, this is your opportunity to make a mark.

 
Why Join Us? Lampire offers competitive compensation, comprehensive health and retirement benefits, and an environment where operational initiative is recognized and rewarded.

Scope of Responsibility:

Planning, implementation and surveillance of entire QMS; ensure compliance with ISO, FDA, EU and USDA regulations (6 facilities across state of PA).

Supervisory Responsibilities:

Supervise and manage all QA and Document Control staff.

Position Requirements:

Note: Qualifications are based upon education, resume and/or work experience.

  • Minimum 5 years of experience in quality assurance management role.
  • Experience with ISO 9001, ISO 13485 and/or 21CFR820.
  • Experience with client and regulatory audits/inspections.
  • Experience with cGMP (21CFR820) quality systems and manufacturing operations, experience with 21CFR211 and/or 21CFR58 is a plus.
  • Experience with USDA Requirements for shipping animal blood products is preferred.
  • Well-organized and detailed oriented professional, with strong written communication skills.
  • Good computer skills with working knowledge of MS office such as Word and Excel
  • MS Access knowledge would be a plus.
  • Must be self-motivated with ability to handle, organize and prioritize multiple tasks and meet deadlines.
  • Ability to perform all work, and interact with others, in a safe and responsible manner.

Responsibilities include (but are not limited to):

  • Responsible for all QA and Document Control staff.
  • Establish and monitor performance of company Quality Policy and Objectives
  • Preparation, hosting, execution, and responses for client, regulatory and internal audits
  • Maintain and evaluate effectiveness of company-wide training program.
  • Perform staff and all company training.
  • Serves as Management Representative
  • Preparation, Coordination, Reporting and Follow up on all Management Review meetings
  • Document, review and approval of Quality Technical, Supply and Distribution Agreements
  • In charge of all investigations, corrections and CAPAs for customer complaints, NCRs and audit findings
  • Supplier Management program, involving ranking, auditing and surveillance of all suppliers.
  • Review and Approval of all controlled documents, customer specifications, change controls and validations, including software validation.
  • Production and Process Controls which include, material receiving, calibration and equipment maintenance, environmental monitoring and pest management, identification and traceability, record review, labeling, packaging and shipping activities.
  • Assists QA Specialists in release of finished goods, Material Receiving and Quarantine and disposition of nonconforming materials.
  • Completes client requested documentation such as supplier questionnaires and health certificates.
  • In charge of all facility record retention and archival program.
  • Ability to perform all work and interact with others in a safe and responsible manner.
  • Other duties as assigned

 

Education:

  • BS Degree in scientific discipline preferred
  • Minimum 5 years of experience in quality assurance management role
  • Physical Requirements:
  • Prolonged periods of sitting at a desk and working on a computer.
  • Must be able to lift and move up to 25 pounds at a time.
  • Must be able to access and navigate each department at the organization’s facilities.

 

Working Conditions:

  • Conditions inside the office are generally quiet, periodically there may be mid-level noise from various equipment when traveling to other facilities.
  • While performing the duties of this job, the employee is frequently standing, walking, and sitting.

Vacancy posted 5 days ago
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