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:
• Support day-to-day Quality Assurance activities in accordance with approved
SOPs / Policies for a multi-product, cGxP contract manufacturing facility
• A good understanding of cGxPs and compliance in a GxP manufacturing
setting performing both supervised and unsupervised tasks
• Receive minimal supervision and able to perform independently on routine
assignments
• Revise, review and approve SOPs, protocols, reports or records
• Make real-time decisions on process events on the floor based on knowledge
of defined SOPs & policies
• Demonstrate appropriate interpersonal skills which encourage collaboration
of individuals or teams to meet objectives
Qualifications:
- Bachelor's Degree in a Science or technical field
- Minimum 5 years’ experience in the biopharmaceutical or biologics industry
- Hands-on prior QA Batch Release and SAP experience
- Understand GMP documentation with a high level of proficiency
- Ability to interpret and evaluate data and summarize results independently