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Jobs that require manufacturing skill

Recruitexpress
23Dec
Production Planner (up to S$3.8K/1 yr contract)
Recruitexpress   via Recruitexpress

Job Scope

Planning & scheduling of production operations
Ensure production and shipment schedule are met
Handle daily documentation and other administrative duties
Plan & update material plans according to latest production schedule, as well as to maintain stock levels within responsible areas to meet stock goals for manufacturing plant
Manage all inventory planning, sourcing and expediting for appointed part
Follow up on delivery and manage inventory to prevent over or under stocking situation

DO NOT    Read more

CLICK QUICK APPLY
Interested applicants, please kindly forward a copy of your updated resume in MS Word format to
Adriana.koh@recruitexpress.com.sg
Attn: Ms. Adriana Koh Xue Ting (CEI Reg No.: R1104499)
EA License No.: 99C4599
*We regret that only shortlisted candidates will be notified.

Skills
Recruitexpress
23Dec
Buyer/Planner (1 year contract/up to S$3.8K)(Ref:JBB)
Recruitexpress   via Recruitexpress

Job Scope

To source and negotiate for direct/indirect materials
Process purchase orders and liaise with suppliers and end-users
Handle daily and monthly planning reports
Responsible for production scheduling, and related manufacturing isses
Optimize manufacturing runs and inventory control
Other duties as required

To apply, please email your resume to 
adriana.koh@recruitexpress.com.sg
Attn: Ms. Adriana Koh Xue Ting (CEI Reg No.: R1104499)
*Only shortlisted candidates will be notified. 
EA License No.: 99C4599

Skills
Recruitexpress
22Dec
Contract Senior Supply Planning Executive (Immediate / WEST / Pharma MNC / up to $5500) - HSJ
Recruitexpress   via Recruitexpress

Job scope:

Responsible for Supply Assurance 
Continuously monitor and ensure product supply
Escalate and resolve risks and issues with various stakeholders
Analyze inventory performance versus budget and develop action plans to achieve targets
Perform root cause analysis and comparison of inventory deviations and  targets to produce improvement plans
Monitor and manage inventory shelf-life 
Proactively and continuously support Product Change Management activities securing achievement of business objectives, service levels, costs and working capital requirements
Liaise with manufacturing    Read more

sites on queries relating to assigned product portfolio
Any other ad-hoc duties assigned

Job Requirements:

Bachelor Degree in Supply Chain / Logistics / Operations Management or equivalent
Min 3 years of relevant experience in Supply and Logistics planning ideally in pharmaceutical industry or healthcare industry
Knowledge of principles and strategy for Sales Forecasting / Demand and Supply Planning is advantageous
Experience in APO Planning
Excellent communication skills (both oral and written) and analytical skills
Able to commence work immediately / short notice

All Interested candidates are invited to email your resume in MS Word format to:
jen.ooi@recruitexpress.com.sg
>
>Jenalyn Ooi Huai Sian (R1765551)
> Recruit Express Pte Ltd Company Reg. No. 199601303W | EA License Number: 99C4599
We regret to inform that only suitable candidates will be shortlisted for an interview.

Skills
Recruitexpress
21Dec
Process Engineer / Validation Engineer (Office Hrs 5D, cGMP, Pharma MNC)
Recruitexpress   via Recruitexpress

Overview:

Under general supervision, reviews specifications and determines the critical aspects of facilities, utilities, computer systems and manufacturing equipment with regard to product and process quality, writes qualification protocols for operating systems and records related test results. prepares final reports that identify the results of protocol testing and the conditions of release.

Essential Job Functions:

• Carries out responsibilities in accordance with the organization's policies, procedures, and state, federal and local    Read more

laws.
> • Writes protocols that challenge the critical parameters related to installation, operation, and performance of the related facility, utilities, computer systems, or equipment.
> • Assures that protocols are approved through proper channels; writes and revises validation protocols.
> • Executes validation and qualification protocols per related SOPs and assures that acceptance criterion related to validation and qualification protocols are met.
> • Analyzes new and existing equipment, recommends equipment modifications as needed for validation optimization.
> • Assures that all test data is gathered and recorded in accordance with cGMP requirements.
> • Analyzes data to ascertain if it meets related protocol acceptance criteria; writes deviation reports as required upon failures to meet protocol acceptance criteria.
> • Writes final reports and assures that they are approved through proper channels.
> • Performs necessary equipment and system IQ, OQ, and PQ's to assure compliance in all manufacturing and support areas.
> • Develops and communicates project timelines and status.
> • Complies with all GMP and safety requirements, SOP's and Company policies and procedures.
> • Performs related duties as assigned.
> • Work in self-directed manner and must be able to work on problems of a complex scope where analysis of data requires and in-depth evaluation of various factors
> • Ability to exercise judgment within broadly defined practices and policies in selecting methods, techniques and evaluation criteria for obtaining results
> • Demonstrated understanding and use of statistical methods in experiment design, data analysis, validation, and process monitoring

Process Engineer 

• Coordinates all work related to Process Engineering deliverables on scheduled projects needed to meet the deadlines developed by Plant Capital Plan, New Product Introductions, and New Process Technology Developments.
> • Responsible for manufacturing engineering support, the development of new process technologies, and the support of new product introductions/tech transfers.
> • Organizes testing associated with the development of new process technologies and the support of new product introductions/tech transfers and works closely with the overall Tech Transfer team.
> • Works closely with technical services to develop and confirm Critical and Key Process Parameters needed for Equipment and Process Validation. Develops and delivers presentations to communicate project timelines and milestone completions.
> • Serve as the Subject Matter Expert for equipment and processes within area of responsibility and thereby serving as the SME for investigations, design reviews, equipment/process troubleshooting , Capital Project planning , change control and other related activities for the site.
> • Able to work well in cross functional TEAMS, good communication and presentation skills, strong technical understanding, general automation knowledge, multi-tasking and time management
> • Work effectively with others from diverse backgrounds and demonstrate capability to adapt to new, different, or changing requirements. Display strong moral principles and work ethics while demonstrating initiative. Maintain a professional presence and display responsible behaviors.
> • Develops conceptual strategies, processing schemes, feasibility studies, PFD’s, and detailed scopes of work.
> • Identify and execute projects to increase safety, reduce product cost, improve product quality, improve yield, and reduce material usage.
> • Work on several different projects and be able to prioritize these projects.
> • Assists in developing control strategy and instrument process design, including emergency and shutdown procedures, instrument specification sheets, control ranges, alarm points, and automation strategy.
> • Authors, updates, reviews, and approves area procedures and master batch records to ensure correct content and compliance with Good Manufacturing Practices.
> • Designs studies, executes experiments and perform data analysis.
> • Writes study proposals, progress reports, development reports, and various technical memo’s.
> • Evaluates new technologies to improve the commercial production process.
> • Supports scale up activities from R&D to production.
> • Provides miscellaneous overhead support of facility.
> • Supports the assurance of a robust manufacturing process for the current registered process as experience is gained post launch.
> • Sets up robust process for trouble shooting.
> • Acts as an effective change agent.
> • Acts as a key player for the expansion of projects as needed to increase scale of manufacture.
> • Investigate deviations from standards of manufacturing process using effective root cause analysis tools. Recommending and implementing effective corrective and preventative actions.
> • Generating, evaluating, and implementing innovative and creative solutions.
> • Assist as subject matter expert for technical projects.
> • Capable of generating a project scope and cost plan to effectively draft a capital request.
> • Develops product and process knowledge in multiple process train areas.
> • Contributes to equipment URS development and retrofit. Participates in equipment FAT’s, SAT’s, etc.
> • Participate in Quality Risk Assessments and process hazards analysis activities.

Job skills & knowledge:

• Current Good Manufacturing Practices (cGMP), Food and Drug Administration (FDA), and other regulatory requirements.
> • Pharmaceutical principles, practices and applications.
> • Principles of mathematical and statistical computations.
> • Interpreting software and ladder logic diagrams and flowcharts.
> • Interpreting electrical and mechanical blue prints and specifications including HVAC systems and. construction plans.
> • Solving practical problems and considering a variety of concrete variables in situations where only limited standardization exists.

Basic Qualifications

• Min 5 years experience working in a regulated environment
> • Working knowledge of Standard Operating Procedures and Protocols/Reports
> • Understanding of validation/qualification strategies
> • Knowledge of applicable quality regulations and standards
> • Quality or quality support experience in a regulated environment (GLP, cGMP, ISO)
> • 3 years quality assurance or quality control experience in cGMP pharmaceutical or drug development organization
> • Working knowledge of facility equipment commissioning and qualification
> • Working knowledge of process and cleaning validation
> • Working knowledge of Computer System Validation
> • Quality assurance or quality control experience in a cGMP pharmaceutical setting
> • Education: B.S. in an Engineering discipline, or Life Science degree
> • Required: 3-5 years quality or quality support experience in a cGMP pharmaceutical setting
> • Desired: 4-7 years facility, equipment, and/or cleaning validation experience in a cGMP manufacturing setting
> • Sound working knowledge of processing equipment used to manufacture APIs
> • Knowledge of clean room standards

Professional Skills, Qualifications and Experience:
• Strong ability to manage multiple priorities, self-starter attitude, good oral and writing skills and the ability to work independently and as a team in an efficient manner.
> • Ability to utilize GDP during document creation and review.
> • Working knowledge of current regulatory guidelines and standards.
> • Ability to apply and incorporate pharmaceutical standards, rules and guidances. (e.g. FDA, EU, ISO, ICH, ISPE, etc.)
> • Comfortable in a fast-paced environment with the ability to adjust to changing priorities.
> • Flexible and accountable.
> • Detailed oriented work standards.
> • Office Hours 5 Days

Interested candidates please send a copy of your resume to leonleong@recruitexpress.com.sgEmail Subject: Validation / Process Engineer – Leon

Leon Leong De Cong
R1551708
Recruit Express Pte Ltd (Healthcare & Lifesciences Division)
EA License: 99C4599

Skills
Recruitexpress
21Dec
Contract Senior Supply Planning Executive (Immediate / WEST / Pharma MNC / up to $5500) - HSJ
Recruitexpress   via Recruitexpress

Job scope:

Responsible for Supply Assurance 
Continuously monitor and ensure product supply
Escalate and resolve risks and issues with various stakeholders
Analyze inventory performance versus budget and develop action plans to achieve targets
Perform root cause analysis and comparison of inventory deviations and  targets to produce improvement plans
Monitor and manage inventory shelf-life 
Proactively and continuously support Product Change Management activities securing achievement of business objectives, service levels, costs and working capital requirements
Liaise with manufacturing    Read more

sites on queries relating to assigned product portfolio
Any other ad-hoc duties assigned

Job Requirements:

Bachelor Degree in Supply Chain / Logistics / Operations Management or equivalent
Min 3 years of relevant experience in Supply and Logistics planning ideally in pharmaceutical industry or healthcare industry
Knowledge of principles and strategy for Sales Forecasting / Demand and Supply Planning is advantageous
Experience in APO Planning
Excellent communication skills (both oral and written) and analytical skills
Able to commence work immediately / short notice

All Interested candidates are invited to email your resume in MS Word format to:
jen.ooi@recruitexpress.com.sg
>
>Jenalyn Ooi Huai Sian (R1765551)
> Recruit Express Pte Ltd Company Reg. No. 199601303W | EA License Number: 99C4599
We regret to inform that only suitable candidates will be shortlisted for an interview.

Skills
Recruitexpress
20Dec
QA Technician / $2400 / North
Recruitexpress   via Recruitexpress

Job Scope:
First Article Inspection

 Main Duty: Perform First Article inspection as per procedure, drawings and BOM. Able to use basic measuring instrument, like caliper, micrometer, and high gauge.
 For any rejected parts at FAI, follow-up disposition by PPS/ICS/Regulatory Engineer and ensure NCR disposition is done correctly.
To change receipt routing from “New” to “Approval” for approval part. 
Transact the FA sample in to system.
Perform NCR verification for rework parts from supplier on    Read more

FA related issue. Feedback any rejected NCR verification parts for next course of action.
Quality Issues
Support any co-relation First Article quality issue with supplier on the dimension problem or visual inspection criteria.
Administrative - Provide FAI and FAAS performance data to relevant stake holders
Other duties/ ad hoc tasks as assigned.

 
Qualification

Min. Diploma in Mechanical Engineering
Min 1 year experience in an instrument / equipment manufacturing environment in a quality function
Proficient in the Microsoft Office applications (Excel, Word, Powerpoint, etc)

Skills
Recruitexpress
19Dec
(6 mths) Contract Accounts Assistant (Manufacturing Industry/ West)
Recruitexpress   via Recruitexpress

(To & Fro Transportation provided at Boonlay & Yewtee)
Working hours: Monday to Friday, 8.30am to 5.30pm
Job Scope:

Process petty cash claims.
Handle Accounts Payable and Accounts Receivable.
Record bank receipt/ payment in accounting software.
Monthly bank reconciliation.
Liaise with customer on payment status and other enquiries.
Issue monthly Statement of Accounts to customers.
Any other ad-hoc duties as assigned by Accountant. 

Requirements:

Able to start work immediately/ on short notice.
Minimum Diploma in Accounts/ Finance or related field.
On-job    Read more

training is provided.

Interested applicants, please email your resume in MS Word Format to Ms Winnie Lui Wing Lam (CEI: R1871406)
Email: winnielui@recruitexpress.com.sg
Whatsapp: 9386-6178
(EA Licence No.: 99C4599)

Skills
Recruitexpress
18Dec
Validation Engineer (Pharmaceutical, Office hours 5 days, Manufacturing)
Recruitexpress   via Recruitexpress

Overview:
 
Under general supervision, reviews specifications and determines the critical aspects of facilities, utilities, computer systems and manufacturing equipment with regard to product and process quality, writes qualification protocols for operating systems and records related test results. prepares final reports that identify the results of protocol testing and the conditions of release.
>
>Essential Job Functions:

Carries out responsibilities in accordance with the organization's policies, procedures, and state, federal and local laws. 
Writes    Read more

protocols that challenge the critical parameters related to installation, operation, and performance of the related facility, utilities, computer systems, or equipment. 
Assures that protocols are approved through proper channels; writes and revises validation protocols. 
Executes validation and qualification protocols per related SOPs and assures that acceptance criterion related to validation and qualification protocols are met. 
Analyzes new and existing equipment, recommends equipment modifications as needed for validation optimization. 
Assures that all test data is gathered and recorded in accordance with cGMP requirements. 
Analyzes data to ascertain if it meets related protocol acceptance criteria; writes deviation reports as required upon failures to meet protocol acceptance criteria. 
Writes final reports and assures that they are approved through proper channels. 
Performs necessary equipment and system IQ, OQ, and PQ's to assure compliance in all manufacturing and support areas. 
Develops and communicates project timelines and status. 
Complies with all GMP and safety requirements, SOP's and Company policies and procedures. 
Performs related duties as assigned. 
Work in self-directed manner and must be able to work on problems of a complex scope where analysis of data requires and in-depth evaluation of various factors 
Ability to exercise judgment within broadly defined practices and policies in selecting methods, techniques and evaluation criteria for obtaining results 
Demonstrated understanding and use of statistical methods in experiment design, data analysis, validation, and process monitoring
>  

Job skills & knowledge:

Current Good Manufacturing Practices (cGMP), Food and Drug Administration (FDA), and other regulatory requirements. 
Pharmaceutical principles, practices and applications. 
Principles of mathematical and statistical computations. 
Interpreting software and ladder logic diagrams and flowcharts. 
Interpreting electrical and mechanical blue prints and specifications including HVAC systems and. construction plans. 
Solving practical problems and considering a variety of concrete variables in situations where only limited standardization exists. 

 
Basic Qualifications

Min 5 years experience working in a regulated environment
Working knowledge of Standard Operating Procedures and Protocols/Reports
Understanding of validation/qualification strategies
Knowledge of applicable quality regulations and standards
Quality or quality support experience in a regulated environment (GLP, cGMP, ISO)
3 years quality assurance or quality control experience in cGMP pharmaceutical or drug development organization
Working knowledge of facility equipment commissioning and qualification
Working knowledge of process and cleaning validation
Working knowledge of Computer System Validation
Quality assurance or quality control experience in a cGMP pharmaceutical setting
Education: B.S. in an Engineering discipline, or Life Science degree
Required: 3-5 years quality or quality support experience in a cGMP pharmaceutical setting
Desired: 4-7 years facility, equipment, and/or cleaning validation experience in a cGMP manufacturing setting
Sound working knowledge of processing equipment used to manufacture APIs
Knowledge of clean room standards

Professional Skills, Qualifications and Experience:

Strong ability to manage multiple priorities, self-starter attitude, good oral and writing skills and the ability to work independently and as a team in an efficient manner.
Ability to utilize GDP during document creation and review.
Working knowledge of current regulatory guidelines and standards.
Ability to apply and incorporate pharmaceutical standards, rules and guidances. (e.g. FDA, EU, ISO, ICH, ISPE, etc.)
Comfortable in a fast-paced environment with the ability to adjust to changing priorities.
Flexible and accountable.
Detailed oriented work standards.
Office Hours 5 Days

 
 
Interested candidates please send a copy of your resume to leonleong@recruitexpress.com.sg
Email Subject: Validation Engineer – Leon
 
Leon Leong De Cong
> R1551708
Recruit Express Pte Ltd (Healthcare & Lifesciences Division)
> EA License: 99C4599

Skills
Recruitexpress
17Dec
QA Technician/ $2400/ North
Recruitexpress   via Recruitexpress

Scope:

Main Duty: Perform First Article inspection as per procedure, drawings and BOM. Able to use basic measuring instrument, like caliper, micrometer, and high gauge.
Candidate who able to operate accurate measurement instrument (Smart scope / CMM) will be a plus.
For any rejected parts at FAI, follow-up disposition by PPS/ICS/Regulatory Engineer and ensure NCR disposition is done correctly.
Perform NCR verification for rework parts from supplier on FA related issue. Feedback    Read more

any rejected NCR verification parts for next course of action.
Quality Issues : Support any co-relation First Article quality issue with supplier on the dimension problem or visual inspection criteria.
Other duties/ ad hoc tasks as assigned.

Qualification

Min. Diploma in Mechanical Engineering
Min 1 year experience in an instrument / equipment manufacturing environment in a quality function.
Proficient in the Microsoft Office applications (Excel, Word, Powerpoint, etc)

Skills
Recruitexpress
17Dec
Biotechnologist ( West Area / MNC ) / 6 months
Recruitexpress   via Recruitexpress

Key Responsibilities:

To perform functions associated with cGMP manufacturing operations within the biologics production facility, including working with engineers in set-up and calibration tasks, as well as performing rework and quality testing related to the production of parts, components and final materials
Use sophisticated programs (such as LIMS, SAP, automated control systems, etc.) to collect and evaluate operating data, which can be used to conduct on-line adjustments to products, instruments    Read more

or equipment and determine and may assist in developing methods and procedures to control or modify the manufacturing process
Responsible for Cell culture (from vial thaw to production scale).
Work on shifts or be on call to ensure quick resolution of any issues that surface during campaigns, if required

Requirements:

Degree/ Diploma in Science, Engineering or equivalent
Minimum 2 years of relevant experience working in Biologics Production facility
Proven problem-solving skills and the ability to adapt to new requirements
Strong working knowledge of Microsoft and other software packages, SAP, LIMS, Atlas systems are preferred

Skills