Job description
Contact length: 12 months Fixed Term Contract
Location: Cambridge
Department: Quality Control
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 sits within the Quality Control team based in Cambridge responsible for Laboratory testing Pharmaceutical products that have been manufactured to ensure product quality.
Role and Responsibilities
The Stability Analyst will provide practical, analytical support within the Stability laboratory, which involves testing finished pack products manufactured at Cambridge and our contract manufacturers, for the shelf life monitoring program. Ensuring that all activities are undertaken in compliance with company standard operating procedures. Some of the responsibilities will include:
- Analysis and testing of the Company’s pharmaceutical finished products using a variety of analytical techniques. (HPLC, Dissolution, KF, UV vis, Titrimetric analysis, wet chemistry)
- Maintain accurate, clear and concise written records of all work undertaken, following the analytical methods and making sure all the correct documentation is reviewed and present within the analytical writeup.
- Routine shelf life /monitoring of the product
- Assisting in the management of stability samples from initialisation, sample pull through to destruction.
- Adhere to Good Laboratory and Manufacturing Practice (GxP) and Health and Safety in the workplace regulations.
- Use of key departmental software packages such as LIMS, Empower, Word and Excel.
- May involve individual working or working as part of a small team
What you’ll bring
- Previous Laboratory based experience
- Ideally graduated in Chemist related Degree but would be open to Biology and Pharmacology Degrees
- Knowledge of basic laboratory works - i.e. weighing / pipetting etc
- Knowledge of Good Laboratory and Manufacturing Practice (GxP) and Health and Safety in the workplace regulations.
- Ability to work individually or as part of a small team
- Experience in use of software packages such as LIMS, Empower, Word and Excel.
- Previous experience in handling of controlled drugs is beneficial
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.
Join our talent pool
If you’re not sure this role is right for you but you’re keen to hear about future opportunities at Mundipharma,
join our talent community
and be the first to hear about new roles.Additional Job Description:
Primary Location:
GB Cambridge
Job Posting Date:
REPLACEMENT_STRING09-07
Job Type:
Fixed Term Contract (Fixed Term)Mundipharma
https://www.mundipharma.com/homepage
Cambridge, United Kingdom
Marc Princen
Unknown / Non-Applicable
1001 to 5000 Employees
Company - Private
Biotech & Pharmaceuticals
1993