Associate Director, Quality Assurance
PPL Healthcare LLC
Be the First to Apply Division Piramal Pharma Solutions Piramal Pharma Solutions is a contract development and manufacturing organization (CDMO), offering end-to-end development and manufacturing solutions across the drug life cycle. We serve our clients through a globally integrated network of facilities in North America, Europe and Asia. This enables us to offer a comprehensive range of services including Drug Discovery Solutions, Process & Pharmaceutical Development services, Clinical Trial Supplies, Commercial supply of APIs and Finished dosage forms. We also offer specialized services like development and manufacture of Highly Potent APIs and Antibody Drug Conjugation. Our capability as an integrated service provider & experience with various technologies enables us to serve Innovator and Generic companies worldwide. For more details, please visit : Job Title Associate Director, Quality Assurance Job Description The Associate Director, Quality Assurance provides leadership and oversight of Quality Operations supporting both Clinical and Commercial manufacturing activities at the Sellersville site. The role ensures compliance with cGMP requirements, data integrity standards, computer system validation requirements, and client and regulatory expectations. Lead Quality Operations, Clinical Operations, Commercial Operations, Data Auditing and QA IT support. Provide oversight of deviations, CAPAs and change controls. Review and approve GMP documentation including batch records, SOPs, protocols and validation documents. Serve as primary quality contact for clients and support project meetings. Develop and monitor operational quality metrics and KPIs. Support audits and inspections by customers and regulatory agencies. Oversee staffing, capacity planning, cross-training and talent development. Manage supplier quality activities, annual product reviews and departmental budgets. Ensure compliance with 21 CFR Part 11, Annex 11 and GAMP 5 requirements. Act as designee for Quality leadership as needed. Key Stakeholders Internal: Technical Operations, Supply Chain, Quality Control, Quality Systems, Engineering, Facilities, R&D, Project Management and Business Units. External: Commercial and Clinical Clients, FDA, EU and other regulatory agencies. Qualifications Bachelor’s degree in a scientific discipline preferred. Minimum 10 years of progressive Quality experience in a regulated cGMP environment. Minimum 3 years of people leadership experience. Experience in oral solid dosage manufacturing required. CDMO experience preferred. Other duties as deemed necessary. Knowledge & Skills Strong leadership, communication and interpersonal skills. Expertise in QA, QC, Compliance and Quality Systems. Experience with SAP, TrackWise, Ensur and other GxP systems. Knowledge of regulatory requirements and inspection readiness. Strong attention to detail and problem-solving skills. Piramal Pharma Limited, offers a portfolio of differentiated products and services through its 17 global development and manufacturing facilities and a global distribution network in over 100 countries. PPL includes Piramal Pharma Solutions (PPS), an integrated Contract Development and Manufacturing Organization; Piramal Critical Care (PCC), a Complex Hospital Generics business; and the India Consumer Healthcare business, selling over-the- counter products. In addition, one of PPL’s associate companies, AbbVie Therapeutics India Private Limited is a JV with AbbVie Inc. and has emerged as one of the market leaders in the ophthalmology therapy area. Further, PPL has a minority investment in Yapan Bio Private Limited. In October 2020, PPL received a 20% strategic growth investment from the Carlyle Group. PPL provides equal employment opportunities to all employees and applicants for employment. It prohibits discrimination and harassment based on race, color, age, sex, religion, national origin or ethnicity, disability status, genetics, protected veteran status, sexual orientation, gender identity, or expression, or any other characteristic protected by applicable law. Our employment decisions are based on merit considering qualifications, skills, performance, and achievements. Equal employment opportunity applies to all terms and conditions of employment, including recruitment, selection, training, social programs, placement, promotion, demotion, compensation and benefits, transfers, terminations, and working conditions. #J-18808-Ljbffr PPL Healthcare LLC
$129k - $203.1k
Job DescriptionSummary:The Associate Director within Quality is responsible for providing quality direction and oversight to one of our sites according to our quality systems, including Training, Documentation (including but not limited to Standard Operating Procedures...SuggestedFull timeFor contractorsLocal areaFlexible hours$137k - $235.75k
...& Johnson Innovative Medicine (IM) is recruiting for an Associate Director of AI Quality and Governance - R&D Data Science & Digital Health.This... ...risks.Develop, implement, and drive adoption of quality assurance processes for AI/ML and GenAI development, integrate those...SuggestedFull timeLocal areaImmediate start$142.4k - $224.1k
Job DescriptionThe West Point Quality organization ensures our products are manufactured,... ...and meets all regulatory requirements. The Associate Director, Inspections lead will be a core member of the West Point Quality Assurance Leadership Team and serves as a quality...SuggestedPermanent employmentFull timeFor contractorsWork experience placementLocal areaFlexible hours- Job Description The mission of Quality Assurance is to: safeguard the rights and well-being of patients; the welfare of animals; comply with... ...review and approval of contractor-initiated investigations associated with deviations, negotiation of site and global Technical...SuggestedFor contractors
$129k - $203.1k
Job Description The mission of Quality Assurance is to: safeguard the rights and well-being of patients; the welfare of animals; comply with... ...review and approval of contractor-initiated investigations associated with deviations, negotiation of site and global Technical...SuggestedFor contractorsLocal areaRelocationVisa sponsorshipFlexible hoursShift work- Merck & Co. is seeking a senior professional to lead quality oversight for external entities (CMOs) in the Clinical Finished Goods platform. The role involves acting as the quality representative to ensure GMP compliance, coordinating with R&D, and driving strategic quality...For contractors
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- ...Merck, a global healthcare science company, seeks an experienced ServiceNow Quality Engineering leader to guide testing across ITSM, ITOM, ITIL/IRM processes in a hybrid West Point setting. You will drive automation, data validation, and QA strategy with cross-functional...
- ...Merck & Co. in Rahway/West Point area is seeking an experienced ServiceNow Quality Engineering leader. You will drive testing strategy for ITSM, ITOM, IRM/GRC, HRSD, and more, delivering automated and manual test artifacts to validate requirements and OOTB behavior....
- Merck is seeking an experienced Quality Assurance professional to oversee external entities and CMOs for clinical finished goods. You will lead investigations, drive data-driven quality improvements, and ensure regulatory compliance across the vendor network. In this role...For contractors
- ...Job Description Job Description We are seeking an experienced and detail-oriented Quality Control Supervisor to lead and oversee all quality assurance and quality control functions within our food container manufacturing facility. This role ensures that all products...Contract workWork at office
- ...with various technologies enables us to serve Innovator and Generic companies worldwide. For more details, please visit : Job Title Quality Control Supervisor Job Description Piramal Pharma Solutions is seeking an experienced and motivated QC Supervisor to lead a team of...Contract workWork at officeWorldwide
$134.67k - $188.53k
Director, Manufacturing Quality, GIS Location: Aizu Manufacturing Location, Japan (relocation required) Responsibilities Manage and lead the site Quality organization supporting NPD, procurement, manufacturing, servicing, and returns. Ensure Quality System compliance...Local areaRelocation- Job Title Quality Control Supervisor Company Overview Piramal Pharma Solutions is a contract development and manufacturing organization... ..., selling over‑the‑counter products. In addition, one of PPL’s associate companies, AbbVie Therapeutics India Private Limited is a JV...Contract workWork at officeWorldwide
- ...facility. The role involves supervising laboratory operations, ensuring GMP compliance, and driving operational excellence within Quality Control. You will review data from HPLC, UPLC, GC, and ICP-MS and coordinate testing with production. Responsibilities include OOS/...
- ...manufacturing organization that provides end-to-end development and manufacturing services across the drug life cycle. This role leads Quality Operations for both Clinical and Commercial manufacturing at the Sellersville site, ensuring cGMP compliance, data integrity, and...Contract work
- ...Customer Accountability Hold overall accountability for portfolio delivery performance, ensuring commitments on scope, timeline, cost, quality, and compliance are met through effective PM execution. Act as the escalation point for high-risk, cross-project, or unresolved...
- Piramal Pharma Solutions is seeking a Senior Project Management leader to own portfolio delivery and governance at the site level. You will drive customer satisfaction, manage escalations, and partner with Finance on forecasts while coordinating with global PMO for standardized...
$156.9k - $247k
Job DescriptionGlobal Quality Program Integration ManagerAt our company, we aspire to be the premier research-intensive biopharmaceutical... ..., Negotiation, Pharmaceutical Projects, Pharmaceutical Quality Assurance, Presentation Delivery, Project Construction Management,...Full timeTemporary workFor contractorsLocal areaFlexible hours$110k
...quickly to change, and continually raise the bar for the speed and quality of clinical research. We are expanding our team and seeking... ...environment focused on making a meaningful impact through quality assurance, process optimization, and regulatory compliance. With diverse...Full timeWork at officeLocal areaWorldwide- ...various technologies enables us to serve Innovator and Generic companies worldwide. For more details, please visit : Job Title Associate Director, Human Resources Job Description The Associate Director, Human Resources will play a critical role in developing and...Contract workLocal areaWorldwide
- ## Director, Human ResourcesApplylocations: Sellersvilletime type: Full timeposted on: Posted Todayjob requisition id: R00002421***Be the... ...and future vacancies with focus on key metrics such as TAT, Quality of Hire* Work with Central and Regional Learning and Development...Contract workWork at officeWorldwide
$70k - $80k
...yourself and your team accountable - Motivated by developing people and getting things done the right way—not the easy way Associate Director of Construction Project Coordination $70,000 - $80,000 per year We are seeking a highly organized, strategic, and...For subcontractorLocal area$90k - $110k
...Job Description Job Description Job Title: Quality Control Manager Job Description The Quality Control Manager leads the Quality... ...environment. Hands-on experience in quality control and quality assurance within cGMP and cGLP manufacturing settings. Strong...Permanent employment- ...Manufacturing, a growing defense contractor located in North Wales, PA, is a state-of-the-art manufacturing facility dedicated to producing quality products for the U.S. Department of Defense and various U.S. Federal Law Enforcement Agencies. As an innovative company offering a...For contractors
- ...include aerospace and defense, factory automation, air and water quality environmental monitoring, electronics design and development,... ...role provides strategic and operational leadership for Quality Assurance, Supplier Quality, and Compliance, ensuring adherence to AS9100...Work at office
- Gwynedd Manufacturing Inc. seeks a Quality Manager to lead the QMS, oversee metrology, and ensure products meet military, ISO, and customer requirements. The role directs testing, inspection, and continuous improvement across cross‑functional teams in a defense/aerospace...
- Role: A well-established and growing manufacturing organization is seeking an experienced Quality Manager to lead all aspects of quality operations across a multi-site manufacturing environment. This individual will oversee the Quality Management System, drive continuous...Full timeWork at office
- ...Job Description Job Description Quality Manager Full-Time | Onsite *This position is not eligible for relocation assistance... ...technical discipline. ~8+ years of progressive experience in Quality Assurance, Quality Engineering, or Quality Systems within the medical...Full timeWorldwideRelocation packageFlexible hours
- ...way.Learn more at We are searching for the best talent for an Associate Director, Laboratory Automation Systems to be located in Spring House... ...IT/data teams, AI teams, scientific users, facilities, EHS, quality, procurement, and external partners. It does not replace...Full timeLocal area
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