Brand new opportunity for an experienced Process Engineer or skilled chemist to join a leading pharmaceutical organisation and assist in the manufacture of drug substances for a "big pharma" company.
You will inform process development activities, conduct risk assessments and generally support the overall delivery of safe and efficient medicines.
In this role, you will apply subject matter expertise in production plant equipment and operations as a part of a multidisciplinary team to ensure successful technology transfer, pilot plant scale-up, and manufacturing of active pharmaceutical ingredients (API).
I am currently recruiting for a Pharmacist to work at a Pharmaceutical distribution centre based in Northampton.
You will be required to physically check Renal and TPN prescriptions and orders Prescription Only Medicines & Pharmacy medicines, along with ancillary items before their dispatch to patients.
Our Client develops and distributes innovative, high-value specialty pharmaceutical products.
They are now seeking a Technical Specialist - Pharmaceutical QC & Manufacturing.
This position is a full-time permanent role which will be office based in Surrey with blended (hybrid) working arrangements currently in place and expected to continue on a non-contractual basis in future.
Our Client develops and distributes innovative, high-value specialty pharmaceutical products.
This position is a full-time permanent role which will be office based in Surrey with blended (hybrid) working arrangements currently in place and expected to continue on a non-contractual basis in future.
Job Purpose
Take day-to-day responsibility for managing Tech Transfers, trouble-shooting activities, and project management to secure existing manufacturing processes and active ingredients supplies and support new product development within the group.
Join our global quality team where you will be responsible for providing active ingredients that meet the highest pharmaceutical regulatory and compliance standards.
The duration of the contract will be 23 months.
This opportunity is for a Senior QC Analyst to join the QC Technical Services Team on a contract basis.
As a Responsible Person you will be an integral part of the Quality Team; approving Pharmaceutical products for release as per Good Distribution Practice of Medicinal Products of Human Use (2013/C 343/01) legislation while also leading GDP QA strategy and activities across the company.
Science Solutions are currently working with a pharmaceutical company in the North East to recruit a Responsible Person.
Key Responsibilities
Implement, maintain and deliver Quality Management Systems and GDP Compliance Programs and quality strategies.
Aerosols, specialising in the pharmaceutical and cosmetic industries.
The majority of our business is the design and assembly of filling and packaging lines for
Technical Author / Validation Engineer required based in Laindon, Essex in a purpose-built design, engineering and headquarters building with 70 employees at this site.