Deskripsi Pekerjaan:
Info Terbaru Seputar Pekerjaan dari Perusahaan Kenvue sebagai posisi In Process Control Officer. Jika Lowongan Kerja In Process Control Officer di Jakarta ini sesuai dengan kriteria anda silahkan langsung mengirimkan lamaran / CV Terbaru anda melalui situs loker terkini dan terupdate Lokerindo.ID.
Setiap pekerjaan mungkin tidaklah mudah untuk dilamar, karena sebagai kandidat baru / calon pegawai harus memenuhi beberapa kualifikasi dan persyaratan sesuai dengan kriteria yang dicari dari Perusahaan tersebut. Semoga info karir dari Kenvue sebagai posisi In Process Control Officer dibawah ini sesuai dengan Kualifikasi anda.
Description
Kenvue is currently recruiting for:
In Process Control Officer
This position reports to Production Lead/ Production Supervisor and is based in Jakarta Raya
Who We Are
At Kenvue, we realize the extraordinary power of everyday care. Built on over a century of heritage and rooted in science, we're the house of iconic brands - including NEUTROGENA®, AVEENO®, TYLENOL®, LISTERINE®, JOHNSON'S® and BAND-AID® that you already know and love. Science is our passion; care is our talent. Our global team is made up with 22,000 diverse and brilliant people, passionate about insights, innovation and committed to deliver the best products to our customers. With expertise and empathy, being a Kenvuer means to have the power to impact life of millions of people every day. We put people first, care fiercely, earn trust with science and solve with courage - and have brilliant opportunities waiting for you! Join us in shaping our future-and yours.
Job Summary:
The In-Process Control Officer is responsible for ensuring manufacturing compliance with GMP and SOP standards through active quality oversight, including batch record review, SOP revision, and on-the-floor monitoring. The role supports issue resolution, process improvement, training, and audit readiness, working closely with cross-functional teams to drive quality and operational excellence.
Key Responsibilities
- Promote and drive HSE and Quality culture
- In case of technical issues, mobilize the Operators to identify and set up quick remediation solutions, or notify the Supervisor/ Manager or the on-call Expert after having performed a first level investigation and propose solutions to be validated by the responsible person.
- Facilitate / Coordinate, in collaboration with Quality Assurance and Technical Operations, the upgrading, and the improvement of production/ packaging procedure by verifying the practical application on the shop floor
- Be responsible for the compliance to the principles and practices described in the "SOP and WI" and their implementation on the site for his area.
- Ensure completion of all production operations in accordance with the documentation and in compliance with GMP and approved SOP and batch records.
- Revise and Review SOPs (Standard Operating Procedures): Review and update existing SOPs to ensure they are aligned with current regulatory requirements, industry standards, and Global SOPs. Collaborate with cross-functional teams to assess the relevance of existing procedures and recommend necessary revisions or improvements. Ensure that all SOPs are thoroughly reviewed, approved, and communicated to the relevant teams.
- Review Executed MBR/EBR (Master Batch Records/Equipment Batch Records): Perform detailed reviews of executed MBRs and EBRs to ensure that all steps and activities have been completed per specifications and compliance requirements.
Identify and document any discrepancies or non-conformances and work with the manufacturing team to resolve them promptly.
- Provide feedback and support for improving the execution process to ensure quality compliance.
- Provide Quality Oversight (GEMBA Walks, GMP Walks): Actively participate in GEMBA walks and GMP walks to observe and assess current manufacturing practices, identify areas for improvement, and ensure compliance with quality standards. Monitor and report on the execution of manufacturing processes, ensuring adherence to established quality protocols. Provide on-the-spot quality guidance and corrective actions when necessary to ensure adherence to GMP.
- Perform verification of Operators for On-the-Job Training qualification
- Assist in the preparation of documents for audits and inspections as required by internal and external regulatory bodies.
- Provide training and guidance to production Operators on new SOP, new batch records, processes, and equipment to ensure successful implementation and operation.
- Manage / participate in continuous improvement projects in line with strategic objectives and ensure communication and involvement of Operators, technicians and support functions
Qualifications
What We Are Looking For
Required Qualifications
- Bachelor's degree in Pharmacy or equivalent
- Knowledge and experience in coated tablet, non sterile Liquid, suspension, and packaging process
- Min. 1-2 years experience in a coordination role in GMP environment in a pharmaceutical or consumer healthcare manufacturing
- Strong knowledge of GxP, GMP requirements, BPOM and PIC(s) requirements, process qualification/ validation
- Excellent problem-solving and analytical skills with the ability to identify and resolve issues and keen attention to detail
- Effective communication skills to collaborate with cross-functional teams and stakeholders
- Proficiency for speaking and writing in English
Desired Qualifications
- Minimum 1-2 years of relevant work experience
- Experience in Manufacturing and Quality for OTC pharmaceutical products
- Experience with production/ packaging machines, solid and liquid process technology
- Proficiency with Microsoft Office tools (Word, Excel, PowerPoint, and Outlook)
- Technical writing skills in English
- Operations experience within a cGMP environment in the pharmaceutical
- Ability to work in shifts and during weekend working schedule, when required
What's In It For You
- Competitive Benefit Package
- Learning & Development Opportunities
Kenvue is proud to be an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, age, national origin, or protected veteran status and will not be discriminated against on the basis of disability.
Primary Location Asia Pacific-Indonesia-Jawa-Jakarta Raya Job Function Production
Info Pekerjaan:
- Perusahaan: Kenvue
- Posisi: In Process Control Officer
- Lokasi Kerja: Jakarta
- Negara: ID
Cara Mengirimkan Lamaran:
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