Laboratory Analyst

Job description

Details:

The Laboratory Analyst role is within Ware's Global Manufacturing and Supply (GMS) Laboratories. The laboratory organisation consists of Quality Assurance Laboratories for the Chemical and Microbiological testing of incoming materials and finished products (Respiratory and Oral Solid Dose products) and Analytical Support Teams supporting the introduction of new products and equipment. The role currently available is within the Analytical Support Team.
The Laboratory Analyst responsibilities include:
• Providing a proficient service in the analysis of samples and supports technical investigations/monitoring, utilising a range of analytical techniques.
• Takes a lead role in batch/job approval process. Releasing batch/jobs to customer requirements.
• Planning and prioritisation of tasks within team and with other departments
• Is responsible for assigned items of Laboratory equipment and instrumentation or 5S standards.
• Is an expert user, resolving issues and promoting best practices.
• Provides training and coaching in areas of expertise, sharing knowledge and agreed best practices.
• Is responsible for the safety of self and others within the Laboratory.
• Is an analytical expert in multi-functional work parties providing expertise in Laboratory practices and GMP
• Having a sound knowledge of the production processes. Uses this knowledge and experience to support resolution of manufacturing, laboratory investigations or project/equipment design.
• Leads and authorises Investigations (e.g. laboratory investigations and deviations). Oversees the design of root causing experiments and retest plans, ensuring investigations are completed in a timely manner and that sound scientific rationale is employed at all stages. Liaises with OQ for final approval where required.
• Acts as laboratory signatory on cross-functional protocols/reports.
• Assists in the development and execution of short and long-term work plans and coordinates laboratory activities
• Participates in audit of Laboratory systems, in inspection readiness activities and preparation for external audits for both quality and safety
• Participate in method transfers and new product introduction exercise
• Maintenance of own training and development plan

Basic Education Required

• Completed HNC or equivalent qualification in a relevant scientific discipline or have significant practical experience

Basic Experience Required
• High level of technical competence
• Good understanding of key analytical techniques
• Understanding of all relevant techniques for dosage form
• Is proficient in problem solving and has expertise in troubleshooting analytical equipment
• Has understanding of method transfer and new product introduction
• Is required to demonstrate competence in current Good Manufacturing Practice (cGMP), understands its impact on their own role and implications of not following cGMP
• Understands and can apply company and site procedures and standards
• Understands and can support the wider business vision and objectives
• Is computer literate, competent in Microsoft packages
• Is proficient in the use of basic Lean Sigma tools (e.g. 5S and standard work)
• Has understanding of regulatory requirements, and registration process
• Plan and prioritise tasks within team and with other departments
• Demonstrates excellent team working skills. Supports or Leads when required. Assumes additional responsibility in the absence of other team members.

The closing date for applications is Friday 26th August

Please apply using the online application system only.

Contact information:

You may apply for this position online by selecting the Apply now button.

Important notice to Employment businesses/ Agencies

GSK does not accept referrals from employment businesses and/or employment agencies in respect of the vacancies posted on this site. All employment businesses/agencies are required to contact GSK's commercial and general procurement/human resources department to obtain prior written authorization before referring any candidates to GSK. The obtaining of prior written authorization is a condition precedent to any agreement (verbal or written) between the employment business/ agency and GSK. In the absence of such written authorization being obtained any actions undertaken by the employment business/agency shall be deemed to have been performed without the consent or contractual agreement of GSK. GSK shall therefore not be liable for any fees arising from such actions or any fees arising from any referrals by employment businesses/agencies in respect of the vacancies posted on this site.

Desired profile

Basic qualifications:

• High level of technical competence
• Good understanding of key analytical techniques
• Understanding of all relevant techniques for dosage form
• Is proficient in problem solving and has expertise in troubleshooting analytical equipment
• Has understanding of method transfer and new product introduction
• Is required to demonstrate competence in current Good Manufacturing Practice (cGMP), understands its impact on their own role and implications of not following cGMP
• Understands and can apply company and site procedures and standards
• Understands and can support the wider business vision and objectives
• Is computer literate, competent in Microsoft packages
• Is proficient in the use of basic Lean Sigma tools (e.g. 5S and standard work)
• Has understanding of regulatory requirements, and registration process
• Plan and prioritise tasks within team and with other departments
• Demonstrates excellent team working skills. Supports or Leads when required. Assumes additional responsibility in the absence of other team members.
• Completed HNC or equivalent qualification in a relevant scientific discipline or have significant practical experience

Preferred qualifications:

See Basic Qualifications