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Quality Assurance Officer

Contact length: Permanent

Location: Cambridge

Department: Quality Assurance

Job type: Full Time

Join us and make a difference when it matters most!

At Mundipharma, we are proud of the work we do to bring innovative treatments to patients. We challenge ourselves constantly to deliver more for patients, healthcare professionals, our partners, and our employees.

The Team

This role will sit in the Quality Assurance team at the Cambridge Science Park, acting as a key point of contact in providing front-line QA support to Bard manufacturing operations. Previous experience in Quality Assurance operations, Pharmaceutical/Medical Device industries and GMP are essential to the role.

This is a double day shift role so will work on a weekly rotational shift basis: Monday - Friday: 6am - 2pm / 1:30pm - 9pm.

Role and Responsibilities

The Quality Assurance Officer will be providing front line QA support in the manufacturing operations at Bard. Other responsibilities of the role include: Proactively carrying out walkabouts within the operational areas, ensuring continuous compliance of Bard operations to GMP and company requirements and providing QA guidance as required

Advising in the event of deviations, including with regards to containment actions and product disposition, liaising with senior members of the QA team and/or QA Manager and Qualified Person, and overseeing and reviewing investigations and the design and implementation of appropriate corrective / preventive actions and associated effectiveness checks

Leading/facilitating Quality investigations for the identification of root causes and continuous improvements as a result of Deviations and/or Customer Complaints in conjunction with the relevant functional areas, communicating and monitoring the implementation of appropriate corrective / preventive actions

Contributing to ensure compliance is maintained in all aspects of QA processes in support of the company's inspection readiness and compliance programs

Leading or supporting internal audits in support of the company self-inspection programme

Supporting the business in managing the risk to quality including risk assessments and the identification of risk control measures as appropriate.

What you'll bring Scientific degree in Pharmacy, Chemistry, Biology, Engineering or similar, or aligned working experience

Practical experience in QA roles within the Pharmaceutical and/or Medical Devices Industry

Knowledge and application of GMP and Pharmaceutical regulatory requirements, including solid knowledge of Eudralex Vol. 4 Chapters and Annexes, Orange Guide and key EU Directives, and solid knowledge of the regulatory framework for pharmaceuticals i.e. MIA, GMP cert, MA, types of regulatory variations

Broad knowledge and experience of various manufacturing process and equipment for various dosage forms

Previous oral solid dose experience or experience with tablets and capsules would be beneficial

Knowledge of Critical Quality Attributes of solid dose products and what can impact those (e.g. friability, harness, content uniformity, assay, dissolution profile)

Technical report writing skills and strong ability to communicate and interact at all levels of the business and externally

Ability to provide independently front-line support to operations and make decisions on complex failure modes.

What we offer in return flexible benefits package

opportunities for learning & development through our varied programme

collaborative, inclusive work environment

Diversity and inclusion

Building an inclusive environment where people can thrive, grow and achieve their full potential is a priority. We believe this isn't just the right thing, but also the smart thing to do, as we focus on making a positive difference for our customers and their patients.

About Mundipharma

Mundipharma is a global healthcare company with a presence across Africa, Asia Pacific, Canada, Europe, Latin America, and the Middle East. Mundipharma is dedicated to bringing innovative treatments to patients in the areas of Pain Management, Infectious Disease and Consumer Healthcare as well as other severe debilitating disease areas. Our guiding principles, centered around Integrity and Patients-Centricity, are at the heart of everything we do.

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Additional Job Description:

Primary Location:
GB Cambridge
Job Posting Date:
2024-11-19
Job Type:
Permanent