Validation Supervisor Jobs

1. Membuat dan mengevaluasi protokol, formulir, dan laporan validasi.

2. Mengkoordinasikan pelaksanaan validasi dengan departemen lain yang bersangkutan.

3. Melaporkan segala bentuk penyimpangan selama proses validasi.

4. Merekap dan menyusun laporan pelaksanaan seluruh kegiatan validasi tiap bulan.

5. Memelihara inventaris dan dokumen terkait validasi.

Min. 3 years of professional experience in Finance & Accounting, especially in an account executive role

Strong familiarity with competency frameworks and their application in assessment development.

Review and validate the competencies' descriptions, proficiency levels, and mapping to various roles within the industry.

Create protocol document of process validation, packaging validation, cleaning validation, performance qualification or computerized system validation

Recording validation data in accordance with the validation protocol

Create report document of process validation

Perform physical testing checks during process validation, packaging validation or cleaning validation according to the validation protocol

Assist the QA Validation and Calibration Supervisor in providing training to other inspectors

Having minimum 5 years of working experiences in handling BoQ validation

Ensuring Program High Level cost addressed and proposed on cost and aligned with the agreed E2E design

Ensuring BoQ are validated and aligned with E2E High Level & Low Level design

Ensuring BoQ are price validated by Sourcing

Min Bachelor Degree with GPA min 3.00

Fluency in English is required

PT Digital Sawit Pro (

Pekerjaan yang akan kamu lakukan terkait pengecekan & pembersihan data (validating & cleansing). Segera kirimkan lamaran kamu!

- Fun facts about you

Mengembangkan dan memeligara program validasi, kalibrasi, dan kualifikasi yang komprehensif untuk peralatan, fasilitas, dan sistem yang digunakan dalam proses produksi farmasi

Memastikan bahwa semua aktivitas validasi, kalibrasi, dan kualifikasi dilakukan sesuai dengan peraturan cGMP, kebijakan internal, dan prosedur

Mengembangkan dan memehhara prosedur operas standar (SOP) untuk kegiatan validasi, kalibrasi, dan kualifikasi

Melakukan penilaian risiko dan menentukan strategi kalibrasi, dan kualifikasi yang sesuai

Bertanggung jawab atas penerapan sistem manajemen keamanan pangan, SJH dan SMK3

Bertanggung jawab terhadap hasil validasi produk cookies

Membuat laporan hasil validasi produk untuk disampaikan ke departemen terkait

Membuat schedule audit penerapan SMK3 di outlet dan factory sentul

Melakukan inspeksi dan pelaporan berkaitan dengan implementasi program SMK3

Membuat laporan ketidaksesuaian penerapan SMK3 di outlet dan factory sentul

·At least one year experience in the same position

·Have knowledge in the Serialization System, Track Wise System, LIMS system and Computer System Validation

·Bachelor Degree in Computer Science, Information Technology, Software Engineering or equivalent

·Familiarity with 21 CFR 11 and Annex 11 and Data Integrity

·Willing to be placed at Cikarang

·Evaluate proposed changes to validated computer systems and recommend level of validation activities required

Expertise:
Fluent in speaking English
Able to work in a team or individually Requirements:
1. Bachelor degree in pharmacy/ apotecary


Job Vacancy: Computerized System Validation Freelance Consultant

Support CSV and Data Integrity project such as testing and reporting.

Drop your CV to [email protected]

• At least 5 years of experience in validation, calibration, and qualification in a pharmaceutical manufacturing environment

• Experience in managing a team of validation, calibration, and qualification specialists

• Develop and maintain standard operating procedures (SOPs) for validation, calibration, and qualification activities