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Quality Control jobs in Mexico

Quality Control Analyst - Contract

Pfizer, S.A. de C.V

Saudi Arabia
On-site
SAR 168,000 - 244,000
Today
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Quality Control Manager

Client of New Alfa International

Saudi Arabia
On-site
SAR 150,000 - 200,000
Today
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Quality Control Analyst - Contract

Pfizer

Makkah Region
On-site
SAR 150,000 - 200,000
Yesterday
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Executive - Quality Control

Jamjoom Pharma

Jeddah
On-site
SAR 120,000 - 150,000
Yesterday
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Executive - Quality Control

jamjoompharma/careers

Jeddah
On-site
SAR 149,000 - 225,000
2 days ago
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QC Supervisor Welding

UnisuS

Saudi Arabia
On-site
SAR 150,000 - 200,000
Today
Be an early applicant

PRN Core Banking QA Engineer

Saudi Networkers Services

Riyadh
On-site
SAR 200,000 - 300,000
Today
Be an early applicant

Coating QC Supervisor JIS116332

KHIAR CONTRACTING COMPANY

Dammam
On-site
SAR 150,000 - 200,000
Today
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Welding QC Supervisor

Global Projects Services

Dammam
On-site
SAR 150,000 - 200,000
Today
Be an early applicant

QC Engineer - Civil

Premium Solutions Consultancy

Saudi Arabia
On-site
SAR 150,000 - 200,000
Yesterday
Be an early applicant

Senior QA Test Engineer

Master-Works

Riyadh
On-site
SAR 60,000 - 80,000
Yesterday
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QA Inspector & Document Controller

TTC International

Riyadh
On-site
SAR 150,000 - 200,000
2 days ago
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Continuous Improvement Coordinator

Afaq - Logistics Branch - J05

Al-Kharj
On-site
SAR 150,000 - 200,000
2 days ago
Be an early applicant

Quality Inspector, Product QC

Baker Hughes

Dammam
On-site
SAR 150,000 - 200,000
2 days ago
Be an early applicant

Quality Control Inspector

Domo Ventures W.L.L.

Jeddah
On-site
SAR 150,000 - 200,000
3 days ago
Be an early applicant

QC Engineer - Quality Control

Domo Ventures W.L.L.

Dammam
On-site
SAR 120,000 - 150,000
3 days ago
Be an early applicant

Quality Control Inspector

SupportFinity™

Sayhat
On-site
SAR 150,000 - 200,000
5 days ago
Be an early applicant

Quality Control Inspector – MRO

Strance HR Solutions India Pvt Ltd

Riyadh
On-site
SAR 150,000 - 200,000
5 days ago
Be an early applicant

Career Opportunities: Quality Control Lab Technician (21736)

Sadara Chemical Company

Al Jubayl
On-site
SAR 60,000 - 80,000
6 days ago
Be an early applicant

Senior QA

PradeepIT Consulting Services Pvt Ltd

Riyad Al Khabra
On-site
SAR 60,000 - 80,000
3 days ago
Be an early applicant

Welding QC Supervisor

Global Projects Services AG

Dammam
On-site
SAR 187,000 - 263,000
3 days ago
Be an early applicant

Quality Assurance Section Head

Hill International

Riyadh
On-site
SAR 300,000 - 400,000
3 days ago
Be an early applicant

Procurement QC Supervisor

Client of Premium Solutions Consultancy

Saudi Arabia
On-site
SAR 200,000 - 300,000
4 days ago
Be an early applicant

QA Inspector

Electrical Industries Company

Dammam
On-site
SAR 60,000 - 80,000
4 days ago
Be an early applicant

QC Inspectors

Banyai Consulting India

Saudi Arabia
On-site
SAR 150,000 - 200,000
4 days ago
Be an early applicant

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Similar jobs:

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Quality Control Analyst - Contract
Pfizer, S.A. de C.V
Saudi Arabia
On-site
SAR 168,000 - 244,000
Full time
Today
Be an early applicant

Job summary

A global pharmaceutical company in Saudi Arabia is seeking a qualified candidate to assist in media preparation and carry out microbiological tests. This role requires strong technical skills and the ability to multi-task in a fast-paced environment. Ideal candidates should have a Bachelor's degree or equivalent experience and be proficient with Quality Control instruments. Join our commitment to delivering high-quality products to patients worldwide.

Benefits

Competitive compensation and benefits
Innovative work environment

Qualifications

  • Ability to understand compendial methods and governmental regulations.
  • Proficiency with Quality Control instruments for sample management.
  • Knowledge of Good Manufacturing Practices and their application.

Responsibilities

  • Assist in preparation and maintenance of media stocks.
  • Perform microbiological tests and ensure compliance with Good Manufacturing Practices.
  • Conduct analyses on finished products and maintain quality records.

Skills

Technical skills in method validation and testing
Strong written and verbal communication skills
Excellent organizational skills
Ability to multi-task

Education

Bachelor's degree
Associate's degree with 4 years experience
High school diploma with 6 years experience

Tools

Analytical HPLC techniques
Quality Control instruments
Job description
Overview

We’re in relentless pursuit of breakthroughs that change patients’ lives. We innovate every day to make the world a healthier place.

To fully realize Pfizer’s purpose – Breakthroughs that change patients’ lives – we have established a clear set of expectations regarding “what” we need to achieve for patients and “how” we will go about achieving those goals.

Pfizer Global Supply proudly shoulders the responsibility of manufacturing and distributing our wide-ranging pharmaceutical products.

Pfizer offers competitive compensation and benefits programs designed to meet the diverse needs of our colleagues.

Transforming Delivery of high quality products

Pfizer, We are one

PGS - Manufacture the Future

Every day, our unwavering commitment to quality ensures the delivery of safe and effective products to patients. Our flexible, innovative, and customer-oriented culture is rooted in science and risk-based compliance. Whether you are engaged in development, maintenance, compliance, or research analysis, your contributions have a direct impact on patient care. By being part of our team, you help uphold a quality culture that adapts and evolves to meet the needs of patients, ensuring that every product we deliver is of the highest standard.

Responsibilities

What You Will Achieve

  • Assist in the preparation and maintenance of media stocks, including sterilization of accessories by autoclave cycles.
  • Manage receipt, storage, and handling of Bio ball cultures, and assist in the maintenance of Master cultures and preparation of Cryo vials.
  • Perform various microbiological tests such as water analysis, Microbial Limit Test, Sterility tests, Bacterial Endotoxin Test, CCIT, and micro challenge studies.
  • Ensure training records are updated and correctly filed to reflect current testing capabilities.
  • Perform sampling and labeling of materials as per defined procedures and verify all equipment and instruments.
  • Interpret and evaluate data for accuracy, precision, trends, and potential cGMP impact, recommending appropriate corrective actions.
  • Ensure all documentation and quality records comply with Good Manufacturing Practices and Good Laboratory Practices and are filed according to existing policies.
  • Review and revise Standard Operating Procedures, analytical methods, and related documents to keep them current.
  • Conduct analyses on finished products, raw materials, and components, including data entry, review, and approval in a computerized database, and generate EMS reports.
  • Contribute to the completion of complex projects, manage time effectively to meet targets, and develop plans for work activities within a team, while exercising judgment with reliance on supervisor and working under their direction.
Minimum Requirements
  • Bachelor's degree with any years of experience, or an Associate's degree with 4 years of relevant experience, or a high school diploma (or equivalent) and 6 years of relevant experience
  • Demonstrated technical skills in method validation and testing
  • Ability to read and understand applicable compendial methods, Standard Operating Procedures, technical procedures, and governmental regulations
  • Knowledge of Good Manufacturing Practices and its application standards, processes, and policies.
  • Excellent organizational skills and strong ability to multi-task
  • Strong written and verbal communication skills
  • Proficiency with unique Quality Control instruments to meet accuracy specifications for sample management, retains management, interpretation, and evaluation
Preferred Qualifications
  • Experience with laboratory work, particularly using analytical HPLC (High Pressure Liquid Chromatography) techniques
  • Proven track record in leading continuous improvement projects
  • Strong knowledge of lean manufacturing principles, six sigma methodologies, and statistical analysis
  • Strong problem-solving skills and attention to detail
  • Ability to manage multiple priorities and meet deadlines.
  • Excellent interpersonal skills and the ability to communicate effectively with colleagues at all levels
  • Adaptability and willingness to learn new techniques and procedures

Pfizer is an equal opportunity employer and complies with all applicable equal employment opportunity legislation in each jurisdiction in which it operates.

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* The salary benchmark is based on the target salaries of market leaders in their relevant sectors. It is intended to serve as a guide to help Premium Members assess open positions and to help in salary negotiations. The salary benchmark is not provided directly by the company, which could be significantly higher or lower.

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