Manufacuring Operative - Pharmaceutical GMP
- Recruiter
- Anonymous
- Location
- Nottingham
- Salary
- 19000.00 - 23000.00 GBP Annual
- Posted
- 21 Sep 2018
- Closes
- 19 Oct 2018
- Sectors
- Scientific & Pharmaceutical
- Contract Type
- Permanent
- Hours
- Full Time
Sinceratis are recruiting for a GMP Manufacturing Operator for a growing Contract Development and Manufacturing company based in the Nottingham they specialise in formulation development, analytical services and clinical manufacturing for pharmaceutical clients globally.
This is an exciting time for their rapidly growing business and we are looking for a new member to join their team.
The role:
Working within the Clinical Manufacturing function the role will involve:
• The preparation of development, technical and clinical trial products to a high standard of quality in accordance with current Good Manufacturing Practice (cGMP) across a full range of dosage forms.
• Carrying out GMP Manufacturing activities according to clearly defined documentation and cleaning validation processes.
• Ensuring that the recording of tasks and events on the batch manufacturing documentation is carried out both timely and accurately in accordance with GMP.
• cGMP compliance activities related to manufacturing equipment, documentation and facilities
• Ensuring that the Production area is maintained to the level of cleanliness and tidiness required under GMP.
The ideal candidate will have:
• 2 - 3 years of experience in GMP pharmaceutical manufacturing facility
• GMP Compliance • Equipment setup, maintenance and validation
• Excellent organisational, interpersonal and communication skills
• Enthusiastic and passionate about pharmaceutical manufacture
• Ideally experience of tablet pressing and wet granulation.
• Excellent numerical skills
Please apply now enclosing you up to date cv and salary expectations for Sinceratis now
This is an exciting time for their rapidly growing business and we are looking for a new member to join their team.
The role:
Working within the Clinical Manufacturing function the role will involve:
• The preparation of development, technical and clinical trial products to a high standard of quality in accordance with current Good Manufacturing Practice (cGMP) across a full range of dosage forms.
• Carrying out GMP Manufacturing activities according to clearly defined documentation and cleaning validation processes.
• Ensuring that the recording of tasks and events on the batch manufacturing documentation is carried out both timely and accurately in accordance with GMP.
• cGMP compliance activities related to manufacturing equipment, documentation and facilities
• Ensuring that the Production area is maintained to the level of cleanliness and tidiness required under GMP.
The ideal candidate will have:
• 2 - 3 years of experience in GMP pharmaceutical manufacturing facility
• GMP Compliance • Equipment setup, maintenance and validation
• Excellent organisational, interpersonal and communication skills
• Enthusiastic and passionate about pharmaceutical manufacture
• Ideally experience of tablet pressing and wet granulation.
• Excellent numerical skills
Please apply now enclosing you up to date cv and salary expectations for Sinceratis now