Executive, Quality Control

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 the role

The Executive, Quality Control will oversee Quality control activities such as calibration, verification and standardization and comply with GMP, GLP procedures and other regulatory requirements within Chemical testing (In-Proces & Finished Products/Raw Material & Finished Goods) section.

Key Responsibilities: -

• Assist QC Manager in the management and administration of the QC Laboratory.
• Ensure the cleanliness of working area, verification of calibration status, maintenance of workspaces and preventive maintenance status of the instruments.
• Responsible to management of chemicals, HPLC and GC Column, reference standard and working standard as per the SOP.
• Responsible to perform the daily verification, calibration, and maintenance of instruments/equipment's activities as per the schedule.
• Responsible to perform the analysis for working standard, raw materials, in-process, finished product and stability samples as per predefined procedures.
• Responsible to review and verified logbook in QC Lab.
• Responsible to calibration, and maintenance of stability chamber
• Responsible to prepare of the new and revision of SOPs for improvement of GLP compliance and revisions.
• Responsible to ensure good documentation practices in all QC documents and ensure real-time documentation completion.
• Responsible to initiate purchase requisition through SAP system.

Perform other related duties as assigned from time to time based on company needs

About you

• Candidate must possess at least a Bachelor's Degree, in Science (Chemistry, Pharmaceutical Technology, Biotechnology).
• Minimum 3 year of working experience preferably in Pharmaceutical Manufacturing/ Medical Device industry.
• Hands on exposure in HPLC, GC, FTIR , UV-Vis, Stability and IP/FP will be an added advantage.
• Fresh Graduate with relevant internship experience are welcome to apply.
• Proficient in Microsoft Office Suite.
• Must be willing to work at Bandar Baru Enstek, Negeri Sembilan.

Job Type: Permanent

Pay: From RM2,500.00 per month

Application Question(s):

• How long is your notice period?
• What is your salary expectation?

Experience:

• Pharmaceutical Manufacturing: 2 years (Preferred)
• Pharmaceutical Laboratory: 3 years (Required)

Work Location: In person