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Manager Aseptic Processing Jobs (NOW HIRING)

Aseptic Processing Technician

Mount Laurel, NJ · On-site

$22/hr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

... Manager. The successful candidate must be focused on achieving individual and team productivity ... aseptic processing, etc.) while maintaining cGMP records (e.g. batch record) * Ensure daily ...

Product Manager (Aseptic Packaging)

Greenville, SC · On-site

  • Medical

  • Dental

  • Life

  • Retirement

  • PTO

The Aseptic Product Manager is responsible for supporting the Regional Sales Managers (RSMs ... Maintain expert-level knowledge of aseptic filling and sterile processing product lines. * Maintain ...

Product Manager (Aseptic Packaging)

VA · Remote

  • Medical

  • Dental

  • Life

  • Retirement

  • PTO

The Aseptic Product Manager is responsible for supporting the Regional Sales Managers (RSMs ... Maintain expert-level knowledge of aseptic filling and sterile processing product lines. * Maintain ...

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Manager Aseptic Processing information

What is a manager aseptic processing?

A Manager of Aseptic Processing oversees the sterile production environments in pharmaceutical or biotechnology manufacturing. They are responsible for ensuring that products are processed and packaged without contamination, following strict regulatory and safety standards. Their role includes supervising staff, maintaining compliance with Good Manufacturing Practices (GMP), conducting risk assessments, and implementing process improvements. They also play a key part in training employees and managing documentation to ensure product quality and patient safety.

What are the key skills and qualifications needed to thrive as a manager aseptic processing?

To thrive as a Manager Aseptic Processing, you need a strong background in microbiology, pharmaceutical manufacturing, quality assurance, and regulatory compliance, often supported by a relevant degree and experience in sterile production environments. Familiarity with Good Manufacturing Practices (GMP), cleanroom management systems, and environmental monitoring tools is essential. Leadership, attention to detail, and effective communication are crucial soft skills for managing teams and ensuring strict adherence to protocols. These skills and qualities are vital to maintain product sterility, meet regulatory standards, and ensure patient safety in pharmaceutical operations.

What are some common challenges faced by a manager aseptic processing, and how can they be addressed?

Managers in Aseptic Processing often face challenges related to ensuring strict compliance with regulatory standards, maintaining a contamination-free environment, and leading cross-functional teams in high-pressure situations. Addressing these challenges requires staying updated on evolving industry guidelines, fostering a culture of continuous training, and implementing robust monitoring systems. Effective communication and collaboration with Quality Assurance, Maintenance, and Production teams are also crucial for swiftly resolving issues and upholding product safety.

What is the difference between Manager Aseptic Processing vs Aseptic Processing Technician?

AspectManager Aseptic ProcessingAseptic Processing Technician
CredentialsBachelor's degree in life sciences or related field, GMP training, leadership experienceHigh school diploma or associate degree, GMP training
Work EnvironmentSupervisory role overseeing aseptic processes in pharmaceutical manufacturingHands-on role operating aseptic equipment in cleanroom settings
ResponsibilitiesManaging teams, ensuring compliance, process optimizationPerforming aseptic procedures, equipment setup, documentation

The Manager Aseptic Processing oversees the aseptic manufacturing process, focusing on team management and compliance, while the Aseptic Processing Technician handles the direct operation of aseptic equipment. Both roles require GMP training and work in sterile environments, but the manager has additional leadership and oversight responsibilities.

More about Manager Aseptic Processing jobs

What cities are hiring for Manager Aseptic Processing jobs?

Cities with the most Manager Aseptic Processing job openings:

What are the most commonly searched types of Aseptic Processing jobs?

The most popular types of Aseptic Processing jobs are:

What states have the most Manager Aseptic Processing jobs?

States with the most job openings for Manager Aseptic Processing jobs include:

What job categories do people searching Manager Aseptic Processing jobs look for?

The top searched job categories for Manager Aseptic Processing jobs are:

Infographic showing various Manager Aseptic Processing job openings in the United States as of August 2026, with employment types broken down into 88% Full Time, 11% Part Time, and 1% Contract. Highlights an 85% Physical, 2% Hybrid, and 13% Remote job distribution.

QA Manager, Aseptic Manufacturing Oversight

AMERICAN REGENT

Shirley, NY

Full-time

Medical, Life, Retirement, PTO

Posted 9 days ago


American Regent rating

7.2

Company rating: 7.2 out of 10

Based on 12 frontline employees who took The Breakroom Quiz

70th of 86 rated pharmaceutical


Job description

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 jrossini@americanregent.com 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 hrtalentacquisition@americanregent.com.


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