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Lead Engineer- Pharmaceutical manufacturing

I am working with a pharmaceutical manufacturing site based in St Albans, currently looking for a Lead Engineer, to perform Maintenance, Repairs and Troubleshoot, packaging and manufacturing equipment.

Key responsibilities for the Lead Engineer- Pharmaceutical manufacturing

Lead hands on engineering activities for machinery, both equipment and plant.Lead and supervise a team of both Engineers and technicians for daily, weekly and monthly schedules.Responsible for planning scheduled maintenance for both routine and preventive maintenance, conducting troubleshooting for production equipment to reduce downtime.Communicate with external suppliers and agreed contractors for the most effective service level agreements

Requirements for the Lead Engineer- Pharmaceutical manufacturing

NVQ or equivalent qualification within Engineering 5 years' experience within the FMCG or pharmaceutical industryExperience leading Engineering teams.

Benefits for the Lead Engineer- Pharmaceutical manufacturing

Free on-site parking.Private healthcare schemeNo weekends.25+ 8 bank holidays.

To apply for the Lead Engineer or here more information, please contact Liam Shannon at Smart4Sciences on 01925 239723.

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Smart4Sciences - Head of Quality - Pharmaceuticals

Smart4Sciences are currently working with a Pharmaceutical Manufacturing company in Hertfordshire to recruit an experienced Head of Quality to lead and the develop an experienced Quality team and ensure all products are manufactured inline with GMP and MHRA Regulations.

As the Head of Quality you will be part of the SLT; essential in driving the business forward, developing current processes and delivering continuous improvement throughout the Quality function.

Key Responsibilities

Verify and ensure that all processes and procedures to include effective data management systems, policies, processes and programmes to provide assurances of ongoing statutory, regulatory and MA compliance.As a key member of the SLT escalate any quality issues that are detected during batch review.Host MHRA inspections, writing the responses and liaising with the MHRA Inspectorate.Provide effective oversight of all remediation projects from a quality perspective.Responsible for the review and closure of Deviations, OOS, CAPA and Change control

Key Requirements

BSc or above in a suitable Scientific/Pharmaceutical DisciplineSignificant experience in a Quality Management/Leadership position within the Pharmaceutical IndustryIn-depth working knowledge of EU GMP guidelines and other regulatory requirementAbility to act as a Qualified Person is desirable but not essential.

This Head of Quality position is an immediate need to please apply now or contact Gareth Gooley at Smart4Sciences for more information

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Smart4 Sciences are currently working with a GMP regulated Pharmaceutical Manufacturer to recruit a Validation Officer to their site in Hertfordshire

As a Validation Officer you be part of a small team responsible for maintaining the site Validation Master Plan and will be required to lead, author and perform IQ, OQ, PQ protocols including Process, Cleaning, Equipment and Computer Systems; completing all associated documentation in accordance with ICH guidelines and GMP standards.

Key Responsibilities

Lead, author and execute IQ, OQ, PQ protocols on specific projects including Process Validation, Cleaning Validation, Computer System Validation and Facilities ValidationManage all validation documentation including commissioning test scripts, qualification/validation protocols, summary reports and risk assessmentsPerform qualification reviews, identifying and implementing any remedial work required.

Key Requirements

BSc or equivalent in a relevant life science or engineering disciplineDemonstrable experience of validation and qualification within the Life Science sector including working knowledge of GMP requirements for validation in the UK and/or EU.Strong communication and project management skills including the ability to collaborate with colleagues at all levels.

If you have prior experience in Validation and would be interested this position please apply to day or contact Gareth at Smart4 Sciences for more information

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QC Analyst - Pharmaceuticals

Smart4Sciences are currently recruiting for a QC Analyst based in North London, working with one of North London's leading contract manufacturers of pharmaceutical products.

This QC Analyst position is a great opportunity for a candidate with GMP experience to further develop their career and gain experience with QA activities and non-routine analysis

Key responsibilities

Routine testing on finished products, via HPLC, GC, FTIR, UV-vis and Wet ChemistryAssist with continuous improvement and work with the QC Team Leader/Manager to implement this.Write technical/scientific reports.Assist with analytical testing for the NPD team and provide input how to improve this.Leadership within the laboratory for the analyst within the team.Assist with CAPAs and Deviations (When required)

Requirements

BSc or equivalent in a relevant subject matter ( Chemistry, Pharmaceutical Science etc)Prior experience in Pharmaceutical QCStrong written and verbal communication skills.

Interviews for this QC Analyst position are imminent so please apply today or contact Gareth Gooley at Smart4Sciences for more information

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Smart4Sciences - Head of Quality - Pharmaceuticals

Smart4Sciences are currently working with a Pharmaceutical Manufacturing company in Hertfordshire to recruit an experienced Head of Quality to lead and the develop an experienced Quality team and ensure all products are manufactured inline with GMP and MHRA Regulations.

As the Head of Quality you will be part of the SLT; essential in driving the business forward, developing current processes and delivering continuous improvement throughout the Quality function.

Key Responsibilities

Verify and ensure that all processes and procedures to include effective data management systems, policies, processes and programmes to provide assurances of ongoing statutory, regulatory and MA compliance.As a key member of the SLT escalate any quality issues that are detected during batch review.Host MHRA inspections, writing the responses and liaising with the MHRA Inspectorate.Provide effective oversight of all remediation projects from a quality perspective.Responsible for the review and closure of Deviations, OOS, CAPA and Change control

Key Requirements

BSc or above in a suitable Scientific/Pharmaceutical DisciplineSignificant experience in a Quality Management/Leadership position within the Pharmaceutical IndustryIn-depth working knowledge of EU GMP guidelines and other regulatory requirementAbility to act as a Qualified Person is desirable but not essential.

This Head of Quality position is an immediate need to please apply now or contact Gareth Gooley at Smart4Sciences for more information

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