Patient Oriented Program Monitor

1.066.824. That’s the number of patients we reached in 2021. We want curious, courageous and collaborative people like you to join our inspiring environment. Here you’re given opportunities to make a genuine impact on our patient driven mission. Here you’re surrounded by people who share your determination to tackle the world’s toughest medical challenges. Did you ever imagine how many lives could be touched by your daily work?
The people we serve need you to achieve the extraordinary. That´s why at Novartis we empower you to bring your best self; we value your diversity of thought and trust your ability to make things happen.

**Your responsibilities**:
Your responsibilities include, but are not limited to:

- Planning and supporting PQR/APQR activities. Support site qualification and validation activities (planning, advising, review). Implementation of Quality Systems (incl. documentation management)
- Supplier management activities (agreements, oversight, audit)
- Preparation/support & coordination of CAPA/follow-up. Audit and inspection preparation and support
- Change control review/approval
- Ensure local DI and eCompliance oversight (training, inspections, plan, risk ID etc)
- Ensure process quality assurance acc. to regulations
- Reporting of technical complaints / adverse events / special case scenarios related to Novartis products within 24 hours of receipt
- Design and follow up of educational patient's material for assigned PSP/POP3 for Novartis IM Control of budget and monthly expenses Request and tracking of contracts, purchase orders and internal processes required for PSP/POP3 vendors

**Commitment to Diversity & Inclusion**:

- Novartis is committed to building an outstanding, inclusive work environment and diverse team’s representative of the patients and communities we serve._

**Minimum requirements**

**What you’ll bring to the role**:

- QC/ QA in pharmaceutical ind./ biotech with environmental monitoring & cleanliness zones
- Knowledge of GMP Knowledge of IT Applications & tools Knowledge of Core work processes
- Management of Quality Standards Quality Assurance
- Audit Planning, reporting and Risk Assessment; good Documentation Practice Knowledge of CAPA
- Medium to high English level is desired

**You’ll receive**:
Competitive salary, annual bonus, life insurance, home office policy, flexible working arrangements, birthday day-off, maternity and paternity leave, subsidized dining facilities, health and dental insurance, employee recognition scheme, Gympass, and virtual self-development tools.

**Why consider Novartis?**

21.000. That’s how many people Novartis hires globally every year, and while we’re proud of this, we know there is so much more we could do to help improve and extend people’s lives. We believe new insights, perspectives and ground-breaking solutions can be found at the intersection of medical science and digital innovation. That a diverse, equitable and inclusive environment inspires new ways of working. We believe our potential can thrive and grow in an unbossed culture underpinned by integrity, curiosity and flexibility. And we can reinvent what's possible, when we collaborate with courage to aggressively and ambitiously tackle the world’s toughest medical challenges. Because the greatest risk in life, is the risk of never trying

**Imagine what you could do at Novartis**

**Commitment to Diversity & Inclusion**:
Novartis is committed to building an outstanding, inclusive work environment and diverse team’s representative of the patients and communities we serve.

**Division**

PHARMA

**Business Unit**

LACAN PHARMA

**Country**

Colombia

**Work Location**

Bogotá D.C

**Company/Legal Entity**

NOV COL

**Functional Area**

Quality

**Job Type**

Full Time

**Employment Type**

Regular

**Shift Work**

No

**Early Talent**

No