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Sr. Analyst- CZ
Ver: 141
Dia de atualização: 05-11-2024
Localização: Xindian District New Taipei City
Categoria: Vendas
Indústria: Consumer Services
Tipo de empregos: Full-time
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Conteúdo do emprego
Pobočka: HsinchuDatum zveřejnění: Apr 18 2022
Are you looking for a new challenge to drive and improve quality control testing, with a chance to broaden your leadership skills? If so, this Senior Quality Control Chemist role could be a great opportunity to consider.
As a Senior Quality Control Chemist, you will play an integral role in the continued success of our analytical laboratories. You will have responsibility to train new chemists/microbiologist in the laboratory and thus set the tone for the way in which a new analyst generates data for the release of products and materials.
This role will provide YOU the opportunity to lead key activities to progress YOUR career, these responsibilities include some of the following…
- Conduct routine analytical/microbiological testing of raw materials, packaging materials, finished products and environmental samples using approved methods and various instrumentation while adhering to cGMP and established policies.
- Assist in analytical/microbiological method development, validation, revision and transfer including automated methods.
- Interpret validity of own test data and generate accurate results.
- Evaluation and interpret results of analytical/microbiological testing performed by others.
- Support all aspects of laboratory investigations.
- Assist in basic technical writing such as specifications, laboratory work sheets, standard operating procedures and technical reports.
- Troubleshoot test methods and laboratory instrumentation.
- Provide technical support by executing protocols and evaluating results for non-routine testing.
- Independently organize daily work activities and those of other staff, as needed.
- Conduct training of laboratory personnel on methods, instrumentation and computer systems.
- Clear understanding and application of data integration and calculation of results.
- Participate in interdepartmental project teams or committees.
Basic Qualifications:
We are looking for professionals with these required skills to achieve our goals:
- Bachelor’s Degree or equivalent
- 2 or more years of industry experience
- Proven experience working in teams to improve processes or resolve problems using organizational effectiveness tools.
- Experience providing Quality Control (QC) testing support to at least one value stream.
If you have the following characteristics, it would be a plus:
- Developing knowledge and application of the QMS (Quality Management System).
- Knowledge of company products and quality impact as it relates to those products.
Our values and expectationsare at the heart of everything we do and form an important part of our culture.
These include Patient focus, Transparency, Respect, Integrity along with Courage, Accountability, Development, and Teamwork.As GSK focuses on our values and expectations and a culture of innovation, performance, and trust, the successful candidate will demonstrate the following capabilities:
- Operating at pace and agile decision-making – using evidence and applying judgement to balance pace, rigour and risk.
- Committed to delivering high quality results, overcoming challenges, focusing on what matters, execution.
- Continuously looking for opportunities to learn, build skills and share learning.
- Sustaining energy and well-being.
- Building strong relationships and collaboration, honest and open conversations.
- Budgeting and cost-consciousness.
- This is a job description to aide in the job posting, but does not include all job evaluation details.
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.
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Data limite: 20-12-2024
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