Quality Assurance Director

Lampire Biological Laboratories, Inc.Pennsylvania, United StatesOn-siteFull-timeSenior, 5–8 yearsListed 1 month ago

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About this role

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.