Career Conversion Programme - Quality Systems and Data Officer

GLAXO WELLCOME MANUFACTURING PTE LTD; Singapore; On-site; SGD 45,000 - 60,000; Full time

Job summary

A leading biopharmaceutical company is seeking a trainee in quality compliance to ensure standards are met in accordance with corporate and regulatory expectations. You will support quality management systems and compliance initiatives at one of their manufacturing sites in Singapore, suitable for candidates with a science degree eager to develop their skills in the industry.

Qualifications

• Graduated with an honours degree in a relevant science discipline.
• Experience in the pharmaceutical industry is advantageous.
• Preferably with experience in Quality functions.

Responsibilities

• Ensure quality compliance standards are maintained according to cGMP.
• Provide QA consultation and manage quality-related KPIs.
• Involved in compliance initiatives and standardization of quality systems.

Skills

Quality and manufacturing process

Interpersonal skills

Oral communication

Written communication

Project Management

Analytical thinking

Teamwork

Integrity

Attention to detail

Education

Honours degree in a relevant science discipline

Job description

Job Description

The Career Conversion Programme (CCP) (Train-and-Place with Commitment to Hire) for Advanced Biopharmaceuticals Manufacturing Executives/Professionals is a talent development programme aimed at building the next generation of skilled manpower for Singapore’s Biopharmaceuticals manufacturing industry in anticipation of hiring demand.

The training programme consists of 15 months of local attachment with GSK. Due to the nature of the programme, we can only consider Singapore Citizens and Singapore Permanent Residents. Due to the nature of this traineeship programme, kindly note that training allowances are CPF exempted.

For more information, please visit Career Conversion Programmes (CCP) for Individuals

Role Description:

The role has the accountability to ensure that quality compliance standards are defined, established and maintained on site in accordance with both internal (corporate) and external regulatory expectations on current Good Manufacturing Practices (cGMP).

Trainee to be involved in:

• Establish/maintain quality compliance standards consistent with Quality Management System (QMS) by providing support in areas such as

- Reviewing site policies, procedures and training materials related to quality system

- Providing advisory support to business on compliance area

• Provide QA consultation with stakeholders to resolve issues on Document and Data Management.
• Manage quality related Key Performance Indicator (KPI), including data collation, regular KPI metrics reporting and identification of issues and opportunities for improvements in site quality performance.
• Ensure the effective implementation of the GMP and Data Integrity training
• Steer and/or implement compliance initiatives, standardization of quality systems across key quality systems and quality improvement projects

Education / Requirements:

• Graduated with an honours degree in a relevant science discipline
• Relevant experience in the pharmaceutical industry (good to have)
• Preferably with experience in Quality functions

Competencies / Skills:

• Good knowledge of quality and manufacturing process
• Good interpersonal and influential skills
• Good oral and written communication skills
• Growth mindset
• Project Management skill
• Analytical thinking
• Teamwork
• Integrity
• Eye for details

Where will I be based?

You will be based at one of our manufacturing site in Singapore near Jurong.