Manufacturing Site Manager
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Job Location:
Monthly Salary:
Posted on:
21 hours ago
Vacancies:
1 Vacancy
Job Summary
Purpose
To plan schedule organize manage and control the production and engineering activities of bulk drug substances in Production Building to achieve targeted production levels cost effectively efficiently and reliably within the framework of current Good Manufacturing practices (cGMP) quality safety occupational hygiene responsible environmental protection and in cognizance of the dynamic business environment.
Responsibilities
Focus on the routine manufacture activities to ensure that production of bulk drug substances meets stipulated quality time and cost specifications and in full compliance with the relevant internal and external requirements regulations and standards.
Manage a group of professionals e.g. Manufacturing Engineer/Chemist etc. to trouble shoot all process manufacturing and customer related issue and implement remedial actions to minimize impact to production.
Monitor and ensure compliance by sections staff with the various operating procedures documentation GMP safety occupational hygiene environmental and regulatory requirements.
Develop review and approve all relevant manufacturing documents in accordance to site procedures.
Support the generation of the capital expenditure (CAPEX) proposal list for budgeting. Work closely with the Technical Operations Team to establish windows for New Production Introduction (NPI) and capital projects implementation.
Generate operating budget for own section and manage expenditure to ensure achievement of operational targets and drive cost reduction initiatives.
Ensure information related to routine production activities are actively tracked & captured for consolidation at the departmental level & submitted to management for decision. Perform various tier reviews and ensure visuals for various metrics are updated.
Manage develop and motivate staff to help realize their maximum potential so as to contribute towards achieving the objectives of the department.
Fulfill the role of Value Stream Embedded GSK Production System (GPS) Practitioner to drive reduction in accidents defects and waste including continuous improvement within the Value Stream.
Knowledge Skills & Experience
A degree in Chemistry or Chemical Engineering or any relevant field.
At least 8 years of relevant experience in the pharmaceutical chemical or petrol chemical industry.
At least 2 years management experience of managing teams of shift workers (4 shifts at 5-8 people per shift)
Experience commissioning and operational experience in pharmaceuticals plants.
Strong knowledge and experience of pharma product production processes and plant.
Good engineering maintenance knowledge
Good statistical knowledge.
Good troubleshooting skills.
Good knowledge of GMP safety hygiene and environment regulations.
Good knowledge of NDA registration procedures.
Good presentation communication and project management (Lean Six Sigma) skills
Proven experience in successfully interacting with other department stakeholders
Good understanding of the business processes and MERPS
To learn more about Singapore GSK and our people please click on this link: GSK
Uniting science technology and talent to get ahead of disease together.
GSK is a global biopharma company with a purpose to unite science technology and talent to get ahead of disease together. We aim to positively impact the health of 2.5 billion people by the end of the decade as a successful growing company where people can thrive. We get ahead of disease by preventing and treating it with innovation in specialty medicines and vaccines. We focus on four therapeutic areas: respiratory immunology and inflammation; oncology; HIV; and infectious diseases to impact health at scale.
People and patients around the world count on the medicines and vaccines we make so were committed to creating an environment where our people can thrive and focus on what matters most. Our culture of being ambitious for patients accountable for impact and doing the right thing is the foundation for how together we deliver for patients shareholders and our people.
We are committed to creating an inclusive workplace and providing equal opportunities for all applicants. We embrace an agile working culture across our roles so if flexibility is important to you please discuss opportunities with our hiring team. If you need any adjustments to the recruitment process to help you demonstrate your strengths and capabilities contact . Please note this email is for adjustment requests only; for other enquiries please use our standard contact channels.
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 GSKs 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 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.
Required Experience:
Manager
Key Skills
- Lean Manufacturing
- Six Sigma
- Continuous Improvement
- ISO 9001
- Lean Six Sigma
- Management Experience
- Manufacturing & Controls
- 5S
- Manufacturing Management
- Kaizen
- Chemistry
- Manufacturing
About Company
About us We are a science-led global healthcare company with a special purpose: to help people do more, feel better, live longer. We have 3 global businesses that research, develop and manufacture innovative pharmaceutical medicines, vaccines and consumer healthcare products.
