Job Description

No Deviation is a provider of patient-centric solutions for the pharmaceutical industry, and we are currently seeking individuals who are passionate about joining our team. Our areas of expertise include engineering consultancy, Commissioning Qualification Validation (CQV), as well as Quality, Compliance, and Regulatory services.

We strongly uphold our core values of Empathy, Integrity, and Transparency, and we strive to create a collaborative, innovative, and inclusive work environment that fosters personal growth and development.

By joining our team, you will have the opportunity to make a meaningful impact in the pharmaceutical industry while advancing your career.

Scope and Responsibilities:

• Operate and monitor the chemical processes assigned.
• Record all operational and analytical data on the appropriate documents.
• Maintain material segregation and label appropriately and accurately all containers, bags, and vessels.
• Carry out routine checks and scheduled cleaning procedures.
• Obtain and verify materials necessary for processing, monitor materials stock.
• Notify Shift Production Lead of any process/ supply abnormalities, and of requirement for maintenance. Prepare equipment before maintenance work.
• Perform material handling duties.
• Meet eligibility requirements for the Emergency Response Team.
• Assist in troubleshooting and resolving problems that arise during the processing.
• Participate in pre-commissioning and chemical commissioning activities as required under the direction of the Senior Manager, Operations and Shift Production Lead.
• Participate in SHE, Business Compliance, cGMP and all other compliance-related matters, where applicable.
• Adhere to and comply with the company and departmental procedures, health & safety rules and regulations, and comply with current Good Manufacturing Practice and Good Housekeeping at all times.

• NTC/ITC/Diploma in Chemical, Pharmaceutical, or related disciplines
• 0 - 3 years of experience in the Pharmaceutical, Chemical, or related industries.
• Good understanding of safe working practices, cGMP and good documentation practice.

No deviation