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Pharmaceutical Production Specialist
2 weeks ago
Job Description:
">As a key member of the production team, you will be responsible for ensuring the efficient and high-quality production of pharmaceuticals. Your duties will include generation and ordering for manufacturing to support production batches, as well as assisting with writing Standard Operating Procedures (SOPs) and forms.
">You will also be responsible for recording data and logging activities according to Current Good Manufacturing Practice (cGMP) standards, which involves accurate documentation and adherence to regulatory requirements.
">In addition, you will be required to calibrate, set up, and operate production equipment, including autoclaves, balances, pH and conductivity meters, osmometers, Blood Gas Analyzers, and peristaltic pumps.
">You will also prepare solutions, including buffers, reagents, and cell culture media, as well as perform tasks such as pH titration, osmolality adjustment, sterile filtration techniques, and sampling.
">Furthermore, you will assist in setting up GMP areas for batch production, including receiving materials, stock counts, and performing cleaning tasks.
">Sanitization of the Water for Injection (WFI) loop is another critical aspect of your role, as is routine WFI sampling for Production and logging production samples to Quality Control.
">Requirements:
">To be successful in this role, you must have a Leaving Cert or equivalent qualification, with Higher Certificates or Bachelor's degrees in science-related fields being desirable.
">Experience in a GMP environment is essential, as well as proficiency in computer skills and familiarity with Microsoft Office.
">Randstad encourages applications from individuals of all ages and backgrounds.
">Candidates must be able to prove their right to work in the UK or Republic of Ireland, as relevant.
">Randstad acts as an employment agency for permanent recruitment and an employment business for temporary recruitment, as defined by the Conduct of Employment Agencies and Employment Business Regulations 2003.
">Skills and Qualifications:
">- ">
- Quality assurance">
- GMP pharmaceuticals production">
- Production management">
- Standard operating procedures">
- Regulatory compliance">
- Equipment operation and maintenance">
- Solution preparation and testing">
- Data recording and analysis">
- Cleaning and sanitization">
- Sampling and quality control">