Quality Assurance Document Controller

**Quality Assurance Document Controller**
- Great opportunity to join a global Biopharma
- Exciting Permanent role based in Upper Hutt, NZ
- Join a supportive & collaborative Quality team

Our Quality Assurance group ensures every single material inside our products is manufactured, processed, tested, packaged, stored and distributed aligned with our incredibly high standards of quality and meets all regulatory requirements. Partnering across our internal manufacturing facilities, external contract manufacturers and suppliers we create an interdependent global manufacturing network committed to deliver a compliant, reliable supply to customers and patients on time, every time, across the globe.

**THE OPPORTUNITY**

This role will see you will work as part of a team to ensure all core QA measures are achieved, such as:

- Responsibility for the timely, accurate and efficient management of documents & issuance of batch required documentation
- Reviewing / checking associated batch documentation
- Writing / reviewing SOPs and archiving
- Management of document control systems and administration of QA systems

**ABOUT YOU**

You will be a Documentation Officer with experience working in a regulated industry (eg. Pharma, Lab, Food, banking) who is looking for an opportunity to utilise & expand your record management skill set within Quality Assurance.

**You will have**:

- A degree in Records Management (or equivalent experience)
- Proven experience in a document management role in a highly regulated industry
- Knowledge of QA systems, GLP and GMP requirements (preferable)
- Proficiency as a user across the Microsoft suite (Word, Excel, Outlook) with experience in document control software
- A keen eye for detail with excellent organisation skills
- Ability to work well within a team and across departments
- Initiative & who works well with mínimal supervision
- Ability to work under pressure to meet deadlines
- Ability to make sound decisions on a day to day basis
- Ability to embrace a mindset of Networking, Empowering, Experimenting, Sharing & Learning, whilst maintaining focus on Purpose, High Integrity & Ethics, Patient-Focus and Diversity & Inclusiveness

Our Manufacturing & Supply Division is committed to be the most trusted supplier of bio-pharmaceuticals worldwide. Our facilities, along with our external contractors, suppliers, and partners, create an interdependent global manufacturing network that’s committed to delivering a high quality, reliable supply to customers and patients on time, every time.

**Who we are **

We are known as Merck & Co., Inc., Rahway, New Jersey, USA in the United States and Canada and MSD everywhere else. For more than a century, we have been inventing for life, bringing forward medicines and vaccines for many of the world's most challenging diseases. Today, our company continues to be at the forefront of research to deliver innovative health solutions and advance the prevention and treatment of diseases that threaten people and animals around the world.

**What we look for **

Imagine getting up in the morning for a job as important as helping to save and improve lives around the world. Here, you have that opportunity. You can put your empathy, creativity, digital mastery, or scientific genius to work in collaboration with a diverse group of colleagues who pursue and bring hope to countless people who are battling some of the most challenging diseases of our time. Our team is constantly evolving, so if you are among the intellectually curious, join us—and start making your impact today.

We are proud to be a company that embraces the value of bringing diverse, talented, and committed people together. The fastest way to breakthrough innovation is when diverse ideas come together in an inclusive environment. We encourage our colleagues to respectfully challenge one another’s thinking and approach problems collectively. We are an equal opportunity employer, committed to fostering an inclusive and diverse workplace.

**Search Firm Representatives Please Read Carefully**

**Employee Status**:
Regular

**Relocation**:
No relocation

**VISA Sponsorship**:
No

**Travel Requirements**:
**Flexible Work Arrangements**:
**Shift**:
**Valid Driving License**:
**Hazardous Material(s)**:
**Number of Openings**:
1
**Requisition ID**:R180179