Position: Entry level

Job type: Full-time

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  • The Senior Quality Control Analyst is an experienced analyst who is competent in a broad range of analytical techniques, providing practical, analytical support within the relevant laboratory teams (QC, Stability and Analytical services). This involves testing incoming raw materials as well as intermediate and finished products manufactured at Cambridge and other contract manufacturers with reference to product release testing, shelf life monitoring, process and method validation. Regarded as an expert in a number of analytical techniques. They will undertake extra responsibilities in addition to those of the normal job role. This may include development and implementation of new equipment, systems, new procedures, method transfers and assist in the review and validation of old procedures and methodologies. . Senior QC Analyst Contact length: 12 months FTC Location: Cambridge Department: Quality 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 The Senior Quality Control Analyst will join the quality team based in Cambridge on a 12 month FTC. You will be an experienced analyst who is competent in a broad range of analytical techniques, providing practical, analytical support within the relevant laboratory teams (QC, Stability and Analytical services). This involves testing incoming raw materials as well as intermediate and finished products manufactured at Cambridge and other contract manufacturers with reference to product release testing, shelf life monitoring, process and method validation. Role and responsibilities To carry out the analysis and testing of the Company’s pharmaceutical products and incoming raw materials using a variety of analytical techniques (HPLC, Dissolution, Karl Fischer, wet chemistry techniques, Robotic sample prep systems, automated dilutors) and software packages (LIMS, Empower, Tiamo, Vison, LabX, minitab). Carry’s out peer to peer data review of analytical data on appropriate LIMS and documentation systems where applicable 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 write up, to ensure compliance against registered methodologies and adherence to data integrity. Will Identify OOS results and assist in investigations and take appropriate courses of action. Be a point of reference for analytical problems, a "go to person". Will take appropriate action where unexpected results are obtained. What you’ll bring Graduate with a Degree in Chemistry, Pharmacy, Biology or similar scientific area or equivalent knowledge through experience. Solid experience working in an Analytical Pharma laboratory. Previous HPLC experience is essential and Dissolution experience is advantageous. Ideally be an experienced Analytical Chemist, with a strong background in all or some of the following activities. Method development/validation, method transfer, routine QC and stability processes. A good level of knowledge for the manufacture of the products tested and the key attributes of the raw materials in the formulations. Systems expert - Is considered an expert in a variety of key analytical techniques and software packages. Previous working knowledge of LIMS system and Empower is ideal Report writing, Statistical analysis and data presentation. A comprehensive understanding of GMP, Health and Safety, laboratory instrumentation, laboratory practices and plant procedures 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, centred 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: 2024-01-29 Job Type: Fixed Term Contract (Fixed Term)
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Deadline: 28-06-2024

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