Total 1,853 construction quality control job vacancies in The United States of America

Job Description

Responsibilities

• In-charge to perform quality assurance and quality checking processes.
• Inspect finished goods, follow through company’s procedure and ensure adherence to product quality standards.
• Identify Product Defects, record and report issues.
• Develops and implements inspection methods and procedures.
• Generates reports of conditions found during inspection activities, notifies operations and management of significant problems, and completes documentation necessary to attest to satisfactory completion of inspection or test activities.
• Attend to customer feedback on quality issues.
• To enhance quality improvement.
• Actively involved in improving factory operations.
• To complete, provide report and keep all related documentations.
• Ensure products meet corporate standards as well as all applicable government regulations.
• Upkeep ISO 9001 and other quality standard certifications.
• Any other ad-hoc task assigned.

Quality Control Analyst & Senior QC Analyst urgently required for our client in the Sandwich area.

These are exciting full-time permanent positions, 37.5 hours per week, 8am to 5pm, with an hour's lunch. Competitive salary of £27,000 per annum (£30,000 per annum for the senior role), plus a host of benefits, to include:

• 31 days annual leave, inclusive of Bank Holidays - increasing with length of service
• Auto enrolled pension scheme
• Healthcare, Death in Service, Private Medical insurance including dependants
• Annual bonus scheme
• Free parking
• Great working environment

* You must be committed to your role and have HPLC experience *

You will support the production and QA Departments in ensuring all aspects of the manufacture of products are performed in a controlled manner, meeting commitments to international regulatory bodies, as well as Good Manufacturing Practice. Ensure manufactured products are compliant and fit for purpose by performing physical and analytical testing and report accurate results. Duties to include:

• Being responsible for physical analytical testing.
• Follow internal methodologies.
• Adherence to GMP requirements.
• Accurately record microbiological results within data packages, as received.
• Execution of protocols.
• Ensure laboratory housekeeping standards are maintained and documented accurately.
• Ensure all equipment is suitable for use.

The ideal candidate will have the following:

• A relevant BSc degree, eg Chemistry, Analytical Chemistry, Pharmaceutical Sciences, Forensics, or equivalent.
• Be computer literate, with good working knowledge of MS Office.
• Experienced in QC testing of API, including HPLC and GC. Other wet chemistry techniques desirable.
• Good attention to detail, able to prioritise workload, positive and flexible approach.
• One to two years' experience in a similar role would be ideal, but not necessary.
• GMP experience would be desirable.

CVs in Word please.

New Appointments Group, Expertly Matching Employers and Jobseekers since 1975. Committed to diversity, equality and opportunity for all. s.mcdermott@newappointmentsgroup.co.uk

Responsibilities:

• Conduct inspections and quality checks on various components and products.
• Perform tests and measurements to ensure compliance with specifications and standards.
• Document test results and maintain detailed records.
• Identify and report any non-conformities or quality issues.
• Collaborate with cross-functional teams to address quality concerns and implement corrective actions.
• Ensure equipment used for inspections is properly calibrated and maintained.
• Other ad hoc duties as assigned.

Requirements:

• Diploma or equivalent in related field.
• Minimum 2 years of experience in related roles.
• Good understanding of quality control processes and techniques.
• Attention to detail and strong analytical skills.
• Ability to read technical specifications and drawings.

Interested candidates who wish to apply for the advertised position, please click on the APPLY button below to send in your resume to julie@talenttradersg.com

EA License No: 13C6305

Reg. No.: R1981808

For candidate who applied for the advertised position is deemed to have consented to us that we may collect, use or disclose your personal information for purpose in connection with the services provided by us.

Job Descriptions:

• Perform routine quality checks & inspections on all incoming products
• Conduct sensory evaluations for existing, re-formulated & new products
• Analyse possible reasons for defects and quality lapses
• Generate QC reports and maintaining quality assurance records
• Develop sampling plans for quality control purposes
• Implement plans and strategies to support provision of safe food products.
• Conduct regular on-site inspections to ensure meet company’s quality standards, food safety and hygiene compliances of FSMS, authority & customer requirement.
• Ensuring products adherence to Singapore food regulations
• Ensure production workers comply with GMP and hygiene practices, food safety standards and SOP at all times
• Report non-conformances to superior / person-in-charge for investigation & corrective action
• Resolve quality issues / customer feedbacks with the team
• Support R&D projects & assist in samples preparation
• Provide food quality & food safety related assistance to other departments (i.e. marketing)
• Assist in internal, external and regulatory audits
• Second point of contact for product certifications / documents request
• Involve in improvement project initiated by QA team
• Any other duties that the Company may assign from time to time

Job Requirements:

• Minimum Diploma in Food & Beverage Services Management / Food Technology or equivalent
• Minimum 2 year of QC experience in food manufacturing industry is preferred
• Equipped with basic cooking skills & sushi experience background will be an advantage
• Experience with managing food company factory will be an advantage
• Capable of working as part of a team as well as working independently with minimal supervision
• Possess good interpersonal skills, self-motivated & meticulous

• The preparation of the companies QA manual control and supervision of all amendments and revisions
• Control and the distribution of all the companies quality documentation
• Monitor all quality related activities on the project
• Perform all internal and external audits on behalf of the companies management
• Verify contractor quality requirements are specified to vendors and contractor documentation submittals.
• Attend all pre-bid meetings and coordinate all project requirements with the project bidders.
• Attend client quality management meetings
• The preparation and control of project quality system management documentation prior to project commencement.
• Review quality inspection personnel qualifications and training requirements
• Monitor the disposition of all issued nonconformance reports.

Job Description & Requirements

• 1. Approve or reject all procedures, specifications, methods, and results
• 2. Approve or reject all raw materials, packaging, materials, labelling and finished product
• 3. Review all production records for accuracy and completeness before approving for distribution
• 4. Establish procedures for revising procedures, formulas, and more
• 5. Approve changes to procedures, formulas, and more
• 6. Ensure that the latest version is being used at all times
• 7. Perform all the required tests to ensure identity, purity, potency and composition, and to ensure that products are not contaminated or adulterated
• 8. Investigation of customer complaints
• 9. Evaluation of new vendors/ materials
• 10. Internal audits to verify compliance to AVA regulations
• 11. Maintaining relationships with vendors and regulatory agencies
• 12. Maintain good personal hygiene as well as high work and safety standards in the workplace
• 13. Any ad-hoc duties as assigned

Qualifications & Skills

• Candidate must possess at least Diploma in Food Science/ Technology or in any field
• At least 1 years of working experience in the related field is required
• Proficient in MS Office (Excel, Powerpoint & Words)
• Strong communication skills
• Excellent time management and organisation
• Able to work in a fast-paced environment and within tight deadlines
• Is a team player with strong work ethics, great initiative with a positive and can-do attitude
• Familiar with HACCP and AVA standards

Working hours: 9am to 6pm Monday to Friday

Location: 10 Chin Bee Drive, level 3, Singapore 619861

Salary: S$2500 - $3200

Job Responsibilities:

• Perform regular quality assessments on all in-coming, in-process and out-going products.
• Inspects and approves incoming parts by confirming specifications as well rejecting and returning unacceptable materials.
• Developing and initiating quality standards for inspections, evaluations, and tests.
• Troubleshooting and resolving problems related to quality control.
• Coordinate corrective action for quality issues with the QA, Process, and Product teams.
• Generate report on the inspection results related to the production process and offer possible solutions.

Job Requirements:

• Good interpersonal and communication skills
• Prefer one with relevant working experience in Electronics Product Manufacturing environment.
• Knowledge of ISO 9001, 14001, 13485 & 45001, FDA requirement.
• Able to work independently as well as with a team.

AngelineMah
Reg No: R2096146
One Vogue Pte Ltd
EA License: 19C9629

Posted: 12/04/2024

Closing Date: 26/04/2024

Salary: $30.46 - $30.46

Job Type: Permanent - Full Time

Location: Rockhampton

Job Category: Warehouse


  Life at Vinnies
At Vinnies, we are what we do. We believe in making a difference. We are one of Queenslands most-loved charitable organisations and are committed to leading with our values and mission at heart. We work together to build a legacy that we can be proud of, supporting those in need within our communities. Our companions are why our journey started, striving to shape a more just and compassionate society. Our employees, members and volunteers are the reason our journey continues, and why we will succeed.
    What we can offer you

Work with a purpose not your average organisation and


... Click here to view more detail / apply for Quality Control Team Leader

The Opportunity: CSL Behring is a world class manufacturer of blood plasma proteins which are used to treat human immune deficiencies and severe autoimmune diseases. We are looking for an experienced Quality Control Biochemistry Analyst  to join Quality Control (QC) Biochemistry team at Broadmeadows site on a full-time permanent basis. In this varied role and a high-volume lab, you will ensure that all biochemistry tests are carried out safely, efficiently and following approved test procedures, standard operating procedures and the code of Good Manufacturing Practice.
The Role: Reporting to the Team Leader QC Biochemistry and based on site, you will:

Perform routine biochemistry testing including ELISA, electrophoresis, flow cytometry, nephelometry, auto-coagulation, haemagglutination and endotoxin testing;
Ensure equipment and facilities are maintained and calibrated following approved procedures, and perform troubleshooting in the case of equipment malfunction;
Ensure that all records are completed, signed off, entered onto LIMS, filed and archived;
Complete
... Click here to view more detail / apply for Quality Control Biochemistry Analyst

Job Description & Requirements

· Lead inspection teams (IQA & OQA), QA/QC Supervisor to undertake tasks assigned

· Manage Quality-related activities on the Project to ensure compliance to Project and applicable Regulatory requirement.

· Work with Project stakeholders to provide a consistent Quality framework for application across all project deliverables and promote the continual enhancement and consistent Quality Management System.

· Ensure timely closure of punch items to facilitate system handover to Client.

· Investigate and present Root-Cause Report for Resolution with Project Team as and when quality issues arise in the project.

· Implement and provide recommendations for improvements of Quality Management System.

· Implementation of systematic documentation turnover system for all Project Quality-related documentation.

· Implement quality plans & activities, ensure readiness of all sections for internal/external audits.

· Ensure Project SOP are appropriately authorized for implementation and adequate trainings are provided.

· Implement Audit Schedule for key work processes and design activities (Quality Reports, Engineering Drawings, Change Notices/Design Modifications, Quality Plans, Inspection Test Plans, etc).

· Perform all internal and external audits.

· Attend Qualification Review meetings with clients and project stakeholders.

· Take on role as Management Representative for ISO & OHSAS programs.

Experience & Certifications

· Diploma in Engineering related discipline.

· Minimum 5 years’ relevant experience in managing quality

· Candidates with senior experiences will be considered for a senior role.

• Prepare quality reports, perform process audit, develop & implements quality assurance standards, policies, processess & controls.
• Able to liaise & resolve with customers on quality related issues.
• Data compliation, co-ordination and facilitation of all internal and external audits, re-certification of ISO 9001.

To see the full detailed job description and main responsibilities of the job please refer to the job description attached.

ROLE: Responsible for GMP-compliant quality control tests of cell products

JOB SCOPE:

1. Performing quality control tests for clinical materials (cell therapy products) according to GMP standards.
2. Work with the Cell Manufacturing & Quality Assurance Team.
3. Ensuring GMP compliance is maintained at all times.
4. Be accountable for the highest level of execution of regulatory strategies, and standards of quality compliance.

EXPERIENCE REQUIREMENTS:

1. Experience in quality control tests of biologics or immune cell products, previous quality test experience of CAR-T/TCR-T/NK cell products is highly desired.
2. Experience in regulatory filing with FDA/HSA is desired.
3. Familiar with regular testing methods such as sterility/mycoplasma/endotoxin detection, flow cytometry analysis; Cytokine measurement assays; qPCR assays; etc.
4. Self-motivated, good interpersonal skills.
5. Project management experiences.

REQUIREMENTS:

• Bachelor & more advanced degree in cell biology /biomedical sciences or in a similar medical technology related field.
• Candidate who is bilingual in spoken English and Chinese will have an advantage for the role involving technical knowledge transfer and collaboration between China and Singapore.

Description:

• Work on construction site as developer representative.
• Monitor operations to ensure that they meet quality standards.
• Inspect, test, or measure materials being used.
• Report inspection and test data
• Operate electronic inspection equipment and software

Requirement:

• At least 5 Year(s) of working experience in the related field is required for this position.
• Require working on site experience
• Related safty course certificate
• Ability to use measuring devices like gauges, meters, calipers etc.

Goldfields Off Road Services is currently seeking an experienced and qualified Mechanical Engineer/Quality Control Engineer with a keen interest in the 4x4 industry and passion for quality workmanship.

Duties and Responsibilities:

* Plan and organize 4wd light commercial vehicle upgrade for our clients’ fleet of vehicles
* Organize and oversee the process of 4wd light commercial vehicle upgrade are getting according to Vehicle Standard Australian Design Rule
* Establish standards and policies for installation, modification, quality control, testing, inspection and maintenance according to engineering principles and safety regulations
* Design and optimizing mechanical systems integral to vehicles, such as engines, transmissions, and chassis components during the process of upgrade.
* Establish and oversee the quality of 4wd light commercial vehicle upgrades and maintenance.
* Inspect vehicle upgrades and ensure that optimum performance and integrity are maintained
* Design light commercial vehicle modified components, test and prepare for manufacturing depending on clients requirements
* Perform 4wd light commercial vehicle modification and upgrade for mining and government fleets and ensure that ready for registration
* Plan maintenance for both Government and Mining Light commercial vehicle upgrade as per manufacture specified interval.
* Oversee and control quality of workshop mechanical, electrical and modification standard

Qualifications and Requirements:

* Bachelor's degree in Mechanical Engineering/Production/Process Engineer
* Proven experience in mechanical design, preferably in [industry/sector].
* 4wd and light/commercial vehicle experience
* Strong analytical and problem-solving skills.
* Excellent communication and teamwork abilities.
* Ability to manage multiple projects simultaneously and prioritize tasks effectively.

Salary: $85,000 -$100,000 per year

About the Company

Goldfields Off Road is the leading mechanical and four-wheel drive modification and upgrade workshop in regional WA. Our professional service and wide variety of products and services truly make Goldfields Off Road a one stop shop for recreational, commercial, or mining vehicles. We service and repair many large fleets of Toyota and other vehicles in our extremely busy workshop. Everything we do is performed at or above the manufacturer and dealers’ standards.

Apply Now! The right candidates will secure this exciting and rewarding role.