Manager, Quality Validation

Manager, Quality Validation

私たちがしていること

Kenvueで、日常のケアの並外れた力を実感します。100年以上にわたる伝統を基盤に、科学に根ざした当ホテルは、ニュートロジーナ®、アヴェーノ®、タイレノール®、リステリン®、ジョンソンズ®、バンドエイド®など、すでにお馴染みのアイコニックなブランドを展開しています。科学は私たちの情熱です。ケアは私たちの才能です.

Who We Are

私たちのグローバルチームは~22,000人の優秀な人々で、すべての声が重要で、すべての貢献が評価される職場文化を持っています。 私たちは洞察に情熱を注いでいます。 革新とお客様に最高の製品を提供することに取り組んでいます。専門知識と共感力を持つKenvuerであることは、毎日何百万人もの人々に影響を与える力を持つことを意味します。私たちは人を第一に考え、熱心に気を配り、科学で信頼を勝ち取り、勇気を持って解決します。そして、素晴らしい機会があなたを待っています!私たちと一緒に、私たちの、そしてあなたの未来を形作りましょう。詳細についてはをクリックしてくださいhere.

Role reports to:

Site Quality Director

Location:

North America, United States, Pennsylvania, Fort Washington

勤務地:

フルオンサイト

あなたがすること

The Manager, QA Validation is responsible for managing daily operations of the QA validation department, designing and developing validation policies and procedures, and ensuring continuous improvement in line with regulatory requirements:

Key Responsibilities

• Lead a team of QA professionals to ensure compliance with industry standards for Commissioning & Qualification (C&Q), cleaning validation, manufacturing process qualification, packaging line trials (PLT) process performance validation (PPQ), and computer system validation (CSV)
• Collaborate with cross-functional teams to achieve site and company objectives
• Lead cross-functional teams to drive continuous improvement in validation processes and strategies, as necessary
• Stay updated on industry trends and regulatory requirements to provide expert guidance on validation activities
• Collaborate with senior management to address critical business issues and identify growth opportunities
• Ensure strict adherence to Health, Safety, and Environmental guidelines in all validation practices
• Represent FWP QA at VRC and TRF
• Provide quality support and oversight to the criticality assessment process
• Support New Product Introduction (NPI), Technical Transfer (TT) and continuous improvement projects
• Support in house deviation processes, providing insights and validation input.
• Interact with Regulatory Health Authority representatives during inspections as an SME.  Support responses to Regulatory Health Authorities.
• Responsible for accurate preparation, review and approval of protocols and reports.
• Responsible for ensuring adherence to protocol sampling plans
• Responsible for collecting and providing required APR/PQR quality attribute data and analysis of the data
• QA Validation SME with responsibility for understanding the critical aspect of products, components and labeling requirements.
• Must understand product familiies, product size and put-up and product characteristics associated with active ingredients and excipients.  Must understand the link between Critical Quality Attributes (CQAs) and Critical Processing Parameters (CPPs)
• Coordinate with regional and global teams to standardize the validation process and communicate trends in audit findings and actions

What we are looking for

Required Qualifications

• Bachelors Degree in Engineering, Chemistry, Microbiology or a related field
• Minimum 8-10 years of experience in quality validation, preferably within the drug industry
• Strong leadership skills with the ability to mentor and motivate team members
• In-depth knowledge of regulatory requirements and quality standards, especially in the areas of equipment commissioning and qualification, cleaning validation, computer system validation, and process performance qualification
• Strong organization skills and ability to manage multiple competing priorities

Desired Qualifications

• Proven track record of leading key enabling functions
• Exceptional analytical skills to interpret complex business data and make informed decisions
• Ability to influence decision-making at plant leadership level
• Effective leadership in navigating ambiguity, conflict, and complexity
• Demonstrated alignment with Leadership Imperatives through behaviors and actions
• Excellent communication skills, both verbal and written

それは何ですか

$124,100.00 - $175,200.00

これは、勤務地、候補者のスキル、経験、教育レベルなど、多くの要素を考慮に入れています。その他の仕事関連の要因.

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