Start Date
Immediate
Expiry Date
25 Jun, 25
Salary
0.0
Posted On
19 May, 25
Experience
0 year(s) or above
Remote Job
Yes
Telecommute
Yes
Sponsor Visa
No
Skills
Good communication skills
Industry
Pharmaceuticals
QUALITY ASSURANCE OFFICER - OPERATIONS
· Role: Full-time, 12-month Fixed Term Contract
· Location: Barnstaple, Devon
· Salary: Competitive + bonus + benefits
A BIT ABOUT US
Accord Healthcare Europe is one of the fastest growing pharmaceutical companies in Europe. Accord has one of the largest market footprints of any European generic and biosimilars companies selling generic medicines in over 80 countries around the world. This global footprint enables us to deliver vital, affordable medicines to national health systems supporting healthcare professionals to transform patient lives worldwide. The approach of Accord is agile and inventive, always seeking to improve products and patients’ access to them. Accord are driven to think differently and deliver more for the benefit of patients worldwide.
To continue our growth, we’re looking for the best and brightest technical minds and forward-thinking business professionals. Keeping our people at the heart of all we do, we offer rewarding opportunities for those looking for continued personal and professional growth, investing in training and development tailored to each individual’s focus. So, if you’re looking for an inclusive company to take your career to the next level, you’re certainly in the right place; come and join us to make it better.
Job Types: Full-time, Fixed term contract
Contract length: 12 months
Additional pay:
Benefits:
Schedule:
Ability to commute/relocate:
Work Location: In person
Application deadline: 26/05/202
We’re seeking a meticulous and customer-focused QA Officer to support our QA Operations Manager with a range of QA tasks to ensure all Quality and Regulatory requirements are met and our products remain safe, compliant and of a high standard for release. Partnering with our Operations department, you’ll provide support across a range of tasks assigned by our quality management system (QMS) – from generating Product Quality Reviews and approving change controls, to reviewing batch records and approving technical and validation documents. In this varied role, you’ll spend time in our Production department providing real-time support to the team – this might include attending functional meetings, resolving any quality issues and assessing the compliance of our new and existing active pharmaceutical ingredients (APIs), raw materials and packaging components against their original specification for use. In addition, you’ll conduct and support our investigation and audit activities: assessing anomaly impacts on product quality, identifying root cause issues and establishing corrective and preventative actions (CAPAs) and contributing to customer complaint investigations or site visits. To support the smooth running of the department, you’ll proactively identify improvements to our Pharmaceutical Quality System, rollout relevant training across the business and have the opportunity to support cross-functional projects, as required.