我們做什麼

在 Kenvue，我們意識到日常護理的非凡力量。我們以一個多世紀的傳統為基礎，植根於科學，是標誌性品牌的品牌 - 包括您已經熟悉和喜愛的 NEUTRGENA®、AVEENO、TYLENOL®®、LISTERINE®、JOHNSON'S® 和 BAND-AID®。科學是我們的熱情所在;關心就是我們的才能。

我們是誰

我們的全球團隊由 ~ 22,000 名才華橫溢的員工組成，他們的職場文化中，每個聲音都很重要，每一個貢獻都受到讚賞。 我們熱衷於洞察， 創新並致力於為我們的客戶提供最好的產品。憑藉專業知識和同理心，成為 Kenvuer 意味著每天有能力影響數百萬人。我們以人為本，熱切關懷，以科學贏得信任，以勇氣解決——有絕佳的機會等著您！加入我們，塑造我們和您的未來。有關更多資訊，請按兩下 here.

Role reports to：

位置：

工作地點：

你會做什麼

The position is responsible for providing daily Quality Assurance support to the manufacturing site to ensure internal and regulatory cGMP and CFR requirements are met. Quality Assurance support areas include but are not limited to Batch Record Review, Product Release, Standard Operating Procedures, Investigations, CAPA, Change Control, Shop Floor Audits. The position will interact with other departments including Manufacturing, Packaging, Quality Laboratories, Quality Systems, Validation, Engineering, Maintenance and other departments as it relates to site Quality Assurance responsibilities.

As a QA Associate I, you will:

• Provides daily ‘Shop Floor” QA support to warehouse, bulk manufacturing and packaging lines.

• Provides leadership support to QA Shop Floor activities including communication of quality events to management.

• Performs or supports activities related to Batch Record Review, Raw Material, Bulk, and Finished Product Releases.

• Provides support to Investigations and/or Investigation Protocols, responsibilities include conducting, writing, reviewing and approvals.

• Performs or supports activities related Line Audits, Line or Area Cleaning Verifications

• Participates in design of quality processes and creation/modification/approval of Standard Operating Procedures (SOP’s).

• Provides support to Consumer Complaint investigations.

• Provide QA support to various project teams, as needed.

• Actively supports Site metrics, compliance improvement and training initiatives.

• Provide support to capturing of site metrics and promote improvement opportunities.

• Facilitate resolution of issues to improve site metrics.

• Represents Quality Assurance in positive manner

• Performs other related duties as required.

Qualifications

Required:

• Minimum of B.S. / B.A. Degree is required, a Science or technical field is preferred

• Minimum of 0-3 years of pharmaceutical industry quality experience, with shop floor experience

• Proven success in quality systems/compliance improvement

• Active cGMP interpretation and application experience

• Batch Record Review experience

• Problem solving/investigation experience

• Expertise in handling multiple priorities

• Strong organizational, communication/interpersonal and facilitation Skills (verbal, written and presentation)

• Requires up to 10% travel required based on business demands

• Ability to be based in Fort Washington, PA and requires up to ten percent (10%) of travel

• Ability to work (2) 12 hour shifts on weekend and (2) 8 hour shifts during the week

Preferred

• Process and Systems Experience, especially with MBRs, Change Controls, and Non-Conformance Investigation Documentation required

• Experience with Liquid Dose processing and packaging technology

對您有什麼好處

這考慮了許多因素，包括工作地點、候選人的技能、經驗、教育水準和其他與工作相關的因素

Kenvue 很自豪能成為一個機會均等的雇主。所有合格的申請人都將根據業績獲得就業考慮，不分種族、膚色、宗教、性別、性取向、性別認同、年齡、國籍或受保護的退伍軍人身份，並且不會因殘疾而受到歧視。