QA Manager, Aseptic Manufacturing Oversight

Posted Yesterday
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Shirley, NY, USA
In-Office
118K-137K Annually
Senior level
Pharmaceutical • Manufacturing
The Role
Lead QA oversight for aseptic processing areas, including sterility assurance and video monitoring staff. Manage media fills, environmental and personnel monitoring, airflow visualization, risk assessments, deviations/CAPAs, change control, and cGMP compliance. Provide training, competency qualification, quality metrics, cross-functional collaboration, regulatory inspection support, and people management for aseptic manufacturing quality.
Summary Generated by Built In

Nature and Scope

The QA Manager, Aseptic Manufacturing Oversight ensures that American Regent operates in compliance with all applicable procedures and regulations. The role is responsible for providing oversight for Aseptic Processing Area (APA) in relation to aseptic practices and behaviors, including direct managerial responsibility for the Sterility Assurance function and video monitoring staff. The role has full signatory authority and accountability for quality/compliance matters within the scope of responsibility.

Essential Duties and Responsibilities

Nothing in this job description restricts management’s right to assign or reassign duties and responsibilities to this job at any time.

  • Oversee qualification and periodic requalification of new employees and current APA personnel to ensure continued aseptic processing competency and compliance with applicable procedures and regulatory expectations.

  • Provide oversight of video monitoring programs for aseptic operations, including review, escalation, and follow-up of observations to support contamination control and operator behavior expectations.

  • Provide quality oversight of media fill planning, execution, documentation, exception management, and post-execution assessment to verify aseptic process control.

  • Oversee Environmental Monitoring and Personnel Monitoring events, including review of results, assessment of adverse trends, escalation of excursions, guiding risk assessment and confirmation of appropriate investigation and corrective action.

  • Lead and support lifecycle risk assessments for aseptic processing activities, contamination control strategies, facility/equipment changes, and process improvements, ensuring risks are identified, evaluated, mitigated, and periodically reassessed.

  • Provide quality oversight of airflow visualization studies, including protocol review, execution support, observation assessment, documentation review, and evaluation of findings for impact to aseptic operations.

  • Direct responsibility and oversight of the Sterility Assurance staff and video monitoring staff.

  • Review and approval of cGMP documentation including protocols, procedures, policies, and change controls.

  • Review and approval of deviation investigations and CAPAs.

  • Oversee manufacturing activities to ensure adherence to procedures. This includes direct observation, video review and frequent contact and alignment with operations, engineering and maintenance stakeholders.

  • Develop and improve quality systems to ensure quality compliance and adherence to cGMPs.

  • Develop and manage quality metrics related to aseptic behaviors / practices and state of microbial control for the APA, identify trends, and take action as appropriate.

  • Lead risk management activities and develop mitigation plans as appropriate.

  • Actively Participate in cross-functional project teams.

  • Collaborate with colleagues to achieve desired outcomes.

  • Make recommendations for improvement and procedure and processes.

  • Support, coordinate, and interface with regulatory agencies as required in support of regulatory agency inspections.

  • Support and maintain Quality programs, policies, processes, procedures and controls ensuring compliance with current Good Manufacturing Practices (cGMP) expectations and established agency requirements/guidelines.

  • Provide expectations, goals, coaching, and annual performance reviews for subordinates.

  • Keep informed about current good industry practices and suggest areas of improvement.

  • Consistently perform all duties in accordance with American Regent and Daiichi Sankyo Business Principles, corporate directives, SOPs, policies, and government and industry regulatory guidelines.

  • Perform any other tasks/duties as assigned by management.

Education Requirements and Qualifications

To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. The requirements listed below are representative of the knowledge, skill and/or ability required.

  • Bachelor’s degree, required. 

  • 5+ years of relevant experience providing oversight in a GMP setting with 1-3 years of people management experience, required.

  • Minimum of 5 years of sterility assurance or microbiology experience within the pharmaceutical industry aseptic manufacturing, required.

  • Demonstrate critical thinking, initiative to identify opportunities and drive to implement projects independently.

  • Demonstrate ability to become and remain gown qualified for APA presence.

  • Strong knowledge of appropriate Quality Systems and current Good Manufacturing Practice (cGMP) requirements (FDA, EU, ICH) with the ability to assess compliance risks.

  • Isolator technology experience, preferred.

  • Demonstrate ability to perform detail-oriented work with a high degree of accuracy.

  • Excellent verbal, written, and interpersonal communication skills.

  • Effective time management and collaboration skills.

  • Strong organizational skills, planning skills and must work effectively within teams.

  • Demonstrates good stress management skills and analytical problem-solving skills.

  • Ability to resolve conflicts and disagreements on regulatory compliance issues.

  • Ability to occasionally travel both domestically and internationally – 10% at maximum.

Physical Environment and Requirements

  • May have to wear protective clothing in the laboratories and manufacturing areas for access as required for safety and product controls.

Expected Salary Range:

$117,900 - $137,000

The salary range, displayed is the  minimum and maximum annual salary range of compensation for the role that the employer in good faith believes to be accurate at the time of the posting of an advertisement for the role.  Actual compensation for the role will be based on a number of different factors including but not limited to the candidate’s qualifications, education, knowledge, skills and experience.

American Regent also offers a competitive total rewards package which includes healthcare, life insurance, profit sharing, paid time off, matching 401k as well as a wide range of other benefits.

American Regent celebrates diversity and we are committed to creating an inclusive environment for all employees. We are an Equal Opportunity Employer and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability status, or protected veteran status.

Applicants have rights under Federal Employment Laws.

  • FMLA poster: https://www.dol.gov/whd/regs/compliance/posters/fmlaen.pdf

  • Know Your Rights: Know Your Rights: Workplace discrimination is illegal (eeoc.gov)

  • Employee Polygraph Protection Act: https://www.dol.gov/whd/regs/compliance/posters/eppac.pdf

Alert: We’re aware of individuals impersonating our staff to target job seekers. Please note:

·         All legitimate communication will come directly from a verified ARI recruiter either by phone or via an americanregent.com email address.

·         Our recruiting process includes multiple in person and/or video interviews and assessments.

·         If you are unsure about the legitimacy of a message, contact John Rossini at [email protected]  before responding.

·         We never request payment, bank information, or personal financial details during our offer process.

Your security is important to us, and we encourage you to stay vigilant when job searching.

American Regent Inc. endeavors to make https://careers.americanregent.com/ accessible to any and all users.  If you would like to contact us regarding the accessibility of our website or need assistance completing the application process, please email [email protected].

Skills Required

  • Bachelor's degree
  • 5+ years relevant experience providing oversight in a GMP setting
  • 1-3 years people management experience
  • Minimum of 5 years sterility assurance or microbiology experience in pharmaceutical aseptic manufacturing
  • Ability to become and remain gown qualified for APA presence
  • Strong knowledge of Quality Systems and current Good Manufacturing Practice (cGMP) requirements (FDA, EU, ICH)
  • Experience with media fill planning, execution, and assessment
  • Experience overseeing environmental monitoring and personnel monitoring programs
  • Ability to review and approve cGMP documentation, deviations, and CAPAs
  • Excellent verbal, written, and interpersonal communication skills
  • Effective time management, organizational, planning, and collaboration skills
  • Ability to occasionally travel domestically and internationally (up to 10%)
  • Isolator technology experience
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The Company
1,130 Employees

What We Do

American Regent, Inc., a Daiichi Sankyo Group Company, is a leading manufacturer of generic and branded specialty sterile injectable products. Dedicated to improving human and animal health, the company develops, manufactures, and supplies high-quality injectables for healthcare providers, clinics, and hospitals across the United States and Canada. Their expansive portfolio includes a strong focus on IV iron therapy and other critical specialty injectable medications.

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