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Jobs that require quality audit/management skill

Recruitexpress
27Dec
Executive, Clinical Quality - HEALTHCARE
Recruitexpress   via Recruitexpress

.

Identifies service discrepancies and works on process improvement.
Conducts internal audits and follow up measures.
Collates quality data for key performance indicators.
Collates feedbacks, conducts survey and data on quality improvement suggestions.
Maintains and updates the quality dashboard.
Participates in the planning, implementation and evaluation of new service initiatives and patient-centric work processes.
Plans, implements, facilitates and evaluates quality improvement initiatives/ activities.
Supports and coordinates the planning and organization of patient safety and quality events
Assists    Read more

in and supports quality improvement review panel meetings.
Collates, tracks and maintains records of incident reports.
Supports and facilitates the submission of quality improvement projects.
Assists in and supports the review of quality management, standards, guidelines, forms and policies.
Assists in the crafting of quality-related proposals and papers.

Requirements:

Min Degree in Nursing, Quality Management, Business Administration or equivalent.
Minimum of 2 years’ experience in a healthcare or related field preferred.
Proficient in MS Office, statistics and other trending tools.
Strong analytical and problem-solving skills.
Meticulous, proactive and able to work independently.
Good organisational, interpersonal and communication skills

For interested candidates, please send your most recent and updated resume to michelle.lee@recruitexpress.com.sg
Subject heading: Clinical Quality Exec

Michelle Lee Ser Min
> (R1440070)
> Recruit Express Pte Ltd
EA License No. 99C4599

Skills
Recruitexpress
26Dec
R&D Manager – Ref: NSJ
Recruitexpress   via Recruitexpress

R&D Manager  – Ref: NSJ
 
Responsibilities:

Responsible for development of new tests/capabilities, as well as management of R&D Projects / ad-hoc Projects
Responsible for the department's safety performance and awareness; spearheads and manages initiatives that drive a culture of safety first
Under the direction of the Operations Manager and / or General Manager, helps lead the efficient operation and growth of the assigned department
Plan, assign and schedule work for designated staff
Assists in    Read more

the engineering and coordination of projects from start to finish
Works to assure quality, timeliness, consistency and accuracy of test reports
Demonstrate knowledge of capabilities, processes and expertise to be able to clearly explain the benefits of Element testing services
Represents the highest levels of integrity and professionalism at all times
Responsible for promoting and ensuring the quality assurance and safety program initiatives are executed upon
Responsible and accountable to assigned staff decisions to include hiring, performance management, performance review decisions and execution, and approval of overtime and time cards
Work with assigned staff to ensure work schedules are maintained and balanced
Maintain an environment of respect and dignity within the department covering employee interactions and problem solving while ensuring work rules are known and followed
Manages a team with fairness and consistency and takes interest in the development of direct reports
Provide general administrative functions as required (invoicing, job list upkeep, supply report data for creation)
Review testing services and promote additional capacity and process improvement
Translate technical requirements of the client into providing pricing, timing and technical knowledge for quoting and commercial efforts

To apply, please email your detailed CV in MS Words format to: Sarah Jumain, sarahjumain@recruitexpress.com.sg
Sarah Binte Mohamed Jumain (CEI: R1981588)
Recruit Express Pte Ltd
EA license Number: 99C4599

Skills
Recruitexpress
24Dec
Medical Technologist (3 rotating shifts) - HEALTHCARE
Recruitexpress   via Recruitexpress

Perform a wide variety of diagnostic tests on patient specimens and report results of the tests accordingly to help clinicians diagnose, treat diseases and monitor therapy
Receiving and sorting of specimens, assessing suitability of specimens for testing, data entry of test requests and rejection of specimens that are not suitable for testing
Participate in quality assurance and quality control programmes 
Assist in phlebotomy for inpatients

 
Requirements

Min Degree in Biomedical Sciences or equivalent 
Good    Read more

interpersonal skills
Able to commit to 3 rotating shifts 

 
For interested candidates, please send your most recent and updated resume to michelle.lee@recruitexpress.com.sg
Subject heading: Med Tech 
Michelle Lee Ser Min
> Recruit Express Pte Ltd
> (R1440070)
> EA Licence No. 99C4599

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
20Dec
~PASIR PANJANG~ - FULL TIME FASHION WAREHOUSE ASSISTANT $1700++*
Recruitexpress   via Recruitexpress

Recruit Express Services Pte Ltd is hiring! 
(FASHION WAREHOUSE ASSISTANT)
Telegram channel: https://t.me/TempJobsNow
Location: Pasir Panjang

Pay:  $1.6k + $100 + $10(per night)

PERMANENT 

Working Hours:   (will be planned based on 44hrs per week) *Can choose between morning/night shift 

Morning Shift: 8am-6pm/10am-8pm (will be planned based on 44hrs per week)
Night Shift: 10pm-8am 

Responsibilities  (AIR-CON ENVIRONMENT)

Conduct quality check on apparels, bags (containing animal skin) for stains and defects.
Pack and sort out clothes into parcels/boxes for orders
Taking    Read more

of photographs (of clothes) 
Any other ad-hoc duties assigned *Must be proficient in usage of Smart Phones. 

Interested applicants whom meet above requirements, please kindly SMS/ Whatsapp your particulars to 9119^2824| Deneen in the following format:

Name
Location (Your residential area in short - eg Tampines)
Availability (When you can commence work and how long)
Indicate Job Title: Fashion Warehouse Assistant

Chia Xian Zhi, Deneen (R1985244)
Recruit Express Services Pte Ltd EA Licence: 13C6614 
*All information will be treated with strictest confidence. We regret that only short-listed applicants will be notified

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
20Dec
Medical Technologist (3 rotating shifts) - HEALTHCARE
Recruitexpress   via Recruitexpress

Perform a wide variety of diagnostic tests on patient specimens and report results of the tests accordingly to help clinicians diagnose, treat diseases and monitor therapy
Receiving and sorting of specimens, assessing suitability of specimens for testing, data entry of test requests and rejection of specimens that are not suitable for testing
Participate in quality assurance and quality control programmes 
Assist in phlebotomy for inpatients

 
Requirements

Min Degree in Biomedical Sciences or equivalent 
Good    Read more

interpersonal skills
Able to commit to 3 rotating shifts 

 
For interested candidates, please send your most recent and updated resume to michelle.lee@ recruitexpress.com.sg
Subject heading: Med Tech 
Michelle Lee Ser Min
> Recruit Express Pte Ltd
> (R1440070)
> 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
Technical Manager (Chemical)/East/ $10000 - $12000
Recruitexpress   via Recruitexpress

Overall Job Purpose
Research and development of new finishing and chemicals 
Job Responsibilities

Provide support and resolves issues pertaining to processes and finishing products in the domain of Quality, Product development, and operating procedures
Responsible for managing a technical testing laboratory and ensuring compliance with local regulations
Liaise with customers on technical requirements
Source and liaise with companies on new chemical development in the market to support product development/finishing
Provide technical support on new product    Read more

recipes, improvement on existing recipes, design processes for recipes production
Liaise with various department from testing to implementation of recipes
Projects as needed

Job Requirements

Bachelor of chemical engineering/chemistry with minimum 8 years’ of relevant experiences in chemical related industry especially in quality function
Strong in technical expertise, quality standards and processes
Possess technical knowledge and be adapt at all phases of the manufacturing process
Relevant experience in product development and quality control
Resourceful with strong problem-solving skills and leadership capabilities

Skills