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  • Posted: Jul 26, 2017
    Deadline: Not specified
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    We are a science-led global healthcare company that researches and develops a broad range of innovative products in three primary areas of pharmaceuticals, vaccines and consumer healthcare. As one of the few healthcare companies researching both medicines and vaccines for the World Health Organization’s three priority diseases – HIV/AIDS, tube...
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    Peer Reviewer (30 months)

    Job description

    Basic Qualifications

    • School: Grade 12
    • Post School
    • Graduate qualification (or equivalent experience) in a scientific discipline.
    • B-Sc , Diploma in Analytical Chemistry or equivalent

    Experience

    • Pharmaceutical or related scientific discipline
    • A minimum of 3 years experience working in a Chemistry Laboratory in a pharmaceutical manufacturing environment.
    • A minimum of 3 years experience in validation of analytical methods for routine testing and cleaning.
    • Experience in operating HPLC and GC at least 3 years.

    Details

    Preferred qualifications:

    Job Purpose

    Provides proficient and supports technical investigations/monitoring and peer review of analytical data, utilising a range of analytical techniques including chromatography, pharmacopoeial and physical property tests.

    Scope

    The role directs corporate compliance by the interpretation of corporate standards, pharmacopoeial requirements, regulatory authority directives and commitments made to regulatory authorities relevant to the Site, and other GSK companies or third party contractors in respect to the testing of materials and products

    Quality Responsibilities

    • Read and understand all relevant Quality Management System documents and Operating Procedures relevant to your job role.
    • Perform duties in a compliant manner and behave in accordance with our Quality Management System requirements to ensure cGMP standards are maintained.
    • Participate fully in our quality initiatives and attend training and complete assessments as required.

    EHS Responsibilities

    • Read and understand the EHS Systems documents and Operating Procedures relevant to your job role.
    • Ensure risk assessments, risk communication and action planning are completed in accordance with our Risk Management System (RMS).
    • Ensure that all incidents and accidents are reported to determine root cause and that any subsequent CAPA’s are closed out in a timely manner.
    • Lead by example to demonstrate the right EHS behaviours and encourage others to improve our safety culture.

    Essential Job Responsibilities//Accountabilities

    • Prepares and checks analytical data accurately according to company, customer and regulatory requirements and site procedures.
    • Reviews ,Verifies the quality and accuracy of analytical results and determines if material meets pre-defined acceptance criteria.
    • Takes a lead role in batch/job approval process.
    • Is responsible for the safety of self and others within the laboratories
    • Ensures own work is right the first time (RFT). Shares best practices to aid others in improving RFT performance

    Customer

    • Ensures analytical records are accurate, clearly laid-out, legible, and recorded at the time of the task.
    • Communicates progress on tasks and may provide updates on project progress to team or cross-functional meetings
    • Approves batches/jobs, ensuring all documentation is complete, accurate and the material is suitable for intended use
    • Undertakes complex analytical tasks, such as the planning, execution and reporting of analytical studies.

    Compliance

    • Able to follow and have a detailed understanding of the specifications for sample analysis and be able to use Pharmacopoeias proficiently.
    • Checks analytical data/worksheets for accuracy and compliance and ensures correct methodology has been used.
    • Ensures training is provided where required.
    • Ensures that own training records are kept up to date to meet regulatory and company requirements.
    • Documentation is completed at all times accurately, clearly and in accordance with GMP requirements
    • Attends training courses and lectures that support the laboratory role.
    • To carry out Level 1 audits and support Level 2 audits, when required
    • Follow and apply principals of Data Integrity

    Continuous Improvement

    • Train, coach and mentor other team members. Act as a positive role model
    • Facilitates and promotes continuous improvement initiatives.
    • Encourages team to contribute ideas to new ways of working to improve systems in the laboratory.
    • Is required, to be involved in various audits and provide responses to auditors questions for Level 1,2,3 and 4 audits. Will lead internal audits. Completes all audit actions within agreed timelines
    • Seeks best practice and shares within the team and to a wider audience
    • Maintains continual on the job training for self and others
    • Maintains a development plan for self and others
    • Helps, encourages others to increase their skill base.

    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.

    Preference will be given to candidates in line with the GSK SA and GSK Consumer Healthcare Equity Plan.

    Method of Application

    Interested and qualified? Go to GlaxoSmithKline (GSK) on careers.peopleclick.com to apply

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