Internship Intern, QA - Documentation Jobs, salary up to MYR 1,000 in Novugen Pharma Sdn Bhd Bandar Baru Bangi - Maukerja

About us

Novugen is a wholly owned subsidiary of SciTech International, a UAE-based group with over 30 years of experience in the healthcare industry. We specialize in venturing into strategic healthcare businesses and developing world-class healthcare facilities across the globe. With operations in multiple countries across continents, our global presence and expertise empower us to meet the complex challenges of delivering hard-to-source, technology-intensive pharmaceutical products to market.

Our manufacturing facilities in Bandar Enstek, Negeri Sembilan, are the first USFDA-approved pharmaceutical manufacturing facilities in Malaysia and Southeast Asia. We are also the first pharmaceutical company in the region to be vertically integrated from R&D to manufacturing, giving us greater control over the supply chain and reflecting our commitment to meeting a wide range of stringent regulatory standards.

At Novugen, we are united by a shared vision, with a team of talented individuals from diverse backgrounds and nationalities working together towards one common goal. We are driven by a passion for science and innovation, striving to accelerate the launch of pharmaceuticals that lack robust generic alternatives due to their complexity. Our continued investment in R&D and dedication to excellence aim to provide early access to affordable, high-quality medicines, impact lives across the world.

Together, we are shaping the future of healthcare and changing lives everywhere.

About Role

What will you gain experience in:

The Intern, Quality Assurance is responsible for performing following key responsibilities:

• Assist in document control activities including filing, indexing, scanning, and archiving QA records
• To prepare controlled copy, forms, logbook, and control the distribution.
• Support the issuance, tracking and retrieval of controlled documents.
• Ensure controlled document (SOPs, forms, logbooks, batch records are :-

i - Properly formatted

ii- Version - controlled

• Verify completeness of records before filing
• To maintain master list of documents and ensure updates are current.
• To maintain availability of hardcopy and softcopy of document.
• To follow up document status for preparation, review and approval.
• Archival of GMP/quality documents.
• To assist QA personnel during trainings on SOPs and other current Good Manufacturing Practices (cGMP) topics with respect to continuous quality improvement programs.
• To provide support during external and regulatory authority inspection.

About you

Job Requirements:

• Must be a final year Degree student in Pharmaceutical Technology, Biotechnology, or relevant field.
• Able to attend minimum of 6 months period of internship
• Must be willing to work in Bandar Enstek, Nilai

Job Type: Internship

Pay: RM1,000.00 per month

Ability to commute/relocate:

• Bandar Baru Enstek: Reliably commute or planning to relocate before starting work (Preferred)

Application Question(s):

• If selected, would you be able to begin your internship on 10 August 2026?
• Our minimum period for internship is 6 months. Are you able to stay for 6 months internship period?

Work Location: In person