Job Engine: QA

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Showing posts with label QA. Show all posts
Showing posts with label QA. Show all posts

Monday, 14 October 2024

Hiring For Quality Assurance And Quality Control Department At Medley Pharmaceutical

October 14, 2024 0
Explore New Horizons with Medley

Medley Pharmaceuticals Ltd is one of the fastest growing amongst the top 40 pharmaceutical companies in the country as per IMS. Our manufacturing site is USFDA, UK-MHRA, WHO-GMP approved company beside approval by several other countries.

We are looking for competent and young professionals to be integral part of our team. We have requirement for below positions at manufacturing unit at Daman:

1. QC Officer: Raw Material, Finished Product and Stability Section (Experience 2-4 years)

Qualification: BSc/MSc/BPharm/MPharm.

Candidates must have experience in analysis of raw material, finished product and Stability. Should have hands on experience on HPLC (Chromeleon), GC etc.

2. QA Executive: QMS (Experience 4-8 years)

Qualification: BPharm /MPharm.

Candidate should have experience in Oral formulations (Solid and liquid) in QMS Section i.e. handling of Market complaint, Change Control, Deviation, CAPA, APQR and Quality Risk Management.

Preferred Male Candidate only

Interested candidates may attend Interview on 20th October 2024, Between 9 am to 2 pm at Medley Pharmaceuticals Ltd. Survey No. 378/7, 379/2 & 3, Zari Causeway Road, Kachigam, Daman (U.T): 396210.

Those who are unable to attend the interviews can send their CV at below mail id:

Contact No. 0260-7151400; 0260-7151408
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Sunday, 13 October 2024

Walk-in For Production,QA,QC,R&D, Purchase And ADL Departments At SIMPEX PHARMA

October 13, 2024 0
WALK-IN INTERVIEW

Production, QA, QC, R&D, Purchase & ADL

Simpex Pharma Pvt. Ltd. is a leading, international pharmaceutical company, producing a wide range of medicines, backed by constant research & innovation, which are trusted by health care professionals & patients across the globe.

Simpex Pharma is having following Regulatory Affairs approvals such as:

USFDA Certification

• Ukraine GMP

• Ethiopia GMP

DIGEMID Certification

• Philippines GMP

• Ivory Coast GMP

Yemen GMP

• Russia MОН

• WHO GMP

Documents Required: Please carry your Legible Documents Like Updated CV, Passport Size Photo, Copies of Education Documents, Aadhar & PAN, Latest CTC Documents, 3 Months Payslips, 3 Month bank Statement

Haridwar (Hotel Hyphen)

Job Location: Kotdwar

Date: 20th October 2024 (Sunday) Time- 10:00 Hrs To 16:00 Hrs
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Friday, 11 October 2024

Hiring For Microbiologist And Quality Control, Quality Assurance Departments At Choksi Laboratories Limited

October 11, 2024 0
Greetings from Choksi Laboratories Limited!!

We are looking for the following requirement for Indore HO.

(1).Position: - Microbiologist

Job Description:-
Performing Growth promotion test and Environmental monitoring, Performing the Internal calibrations of equipment's, Performing the equipment Maintenance, Maintaining records related to analysis, Media Preparation, Growth Promotion Test, MLT, and Water Testing.

Location: - Indore

Educational Qualification - M.Sc., B.Sc.

Experience: - 1-5 Year

(2).Position: - Quality Assurance Executive (Food & Agro)

Job Description:
Maintains operational responsibilities for the activities related to Food, Water and Agro Products.

Documents Issuance

Implement and proactively monitor for compliance with all applicable quality systems/regulations such as ISO 17025, NABL BIS AND FSSAI Review and authorization of the lab test reports. Archival and Restore

Must have faced the regulatory audits like N.A.B.L., EIC, APEDA, FSSAI, and SANTE. Educational Qualification - M.Sc., B.Sc.

Experience -1- 3 years

(3). Position: - Associate & Sr. Associate. (Quality Control)

Job Description:

Well Knowledge Handling of HPLC,GC,
UV, FT-IR and Wet Analysis,
Method Validation
Incoming sample analysis.
Daily and Monthly Calibration.
Documentation for Q.C

Educational Qualification - M.sc/B.sc/ B. Pharma / M.Pharma.

Experience - 1- 4 years

Only interested and relevant experienced candidates can share CV's to
Contact: 8815106847
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Monday, 7 October 2024

Hiring For Quality Assurance Department At Poland In ICON

October 07, 2024 0
Principal Auditor, Quality Assurance - Poland, Warsaw

ICON plc is a world-leading healthcare intelligence and clinical research organization. We’re proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development.

We are currently seeking a Principal Auditor Quality Assurance to join our diverse and dynamic team. As a Principal Auditor Quality Assurance at ICON, you will play a pivotal role in ensuring the quality and compliance of clinical trials, interpreting regulatory requirements, and contributing to the advancement of innovative treatments and therapies.
What You Will Be Doing:
  • Leading and conducting comprehensive audits of clinical trial processes, systems, and documentation to ensure compliance with regulatory standards and guidelines.
  • Collaborating with cross-functional teams to identify areas for improvement in quality assurance processes and practices.
  • Developing and implementing audit plans and strategies to assess the effectiveness of quality management systems.
  • Providing expert guidance and recommendations to stakeholders on quality assurance best practices and regulatory requirements.
  • Contributing to the continuous improvement of quality assurance programs and initiatives.

Your profile
  • Bachelor's degree in Life Sciences, Pharmacy, or related field; advanced degree preferred.
  • Minimum of 7 years of experience in quality assurance within the pharmaceutical, biotechnology, or CRO industry, with at least 3 years in a leadership role.
  • In-depth knowledge of regulatory requirements and guidelines governing clinical trials (e.g., ICH-GCP, FDA regulations).
  • Strong analytical and problem-solving skills, with the ability to identify and address complex quality issues.
  • Excellent communication and interpersonal skills, with the ability to effectively interact with internal and external stakeholders at all levels.
What ICON can offer you:
Our success depends on the quality of our people. That’s why we’ve made it a priority to build a diverse culture that rewards high performance and nurtures talent.

In addition to your competitive salary, ICON offers a range of additional benefits. Our benefits are designed to be competitive within each country and are focused on well-being and work life balance opportunities for you and your family.

Our benefits examples include:
  • Various annual leave entitlements
  • A range of health insurance offerings to suit you and your family’s needs.
  • Competitive retirement planning offerings to maximize savings and plan with confidence for the years ahead.
  • Global Employee Assistance Programme, LifeWorks, offering 24-hour access to a global network of over 80,000 independent specialized professionals who are there to support you and your family’s well-being.
  • Life assurance
  • Flexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidized travel passes, health assessments, among others.
Visit our to read more about the benefits ICON offers.

ICON, including subsidiaries, is an equal opportunity and inclusive employer and is committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, colour, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status.

If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or in order to perform the essential functions of a position, please let us know or submit a request 

Interested in the role, but unsure if you meet all of the requirements? We would encourage you to apply regardless - there’s every chance you’re exactly what we’re looking for here at ICON whether it is for this or other roles.

Are you a current ICON Employee? Please 
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Saturday, 28 September 2024

Opning For Freshers And Experience Candidates For Business Development,R&D And QA,QC Departments At Syngenesis Chemscience

September 28, 2024 0
HIRING OPEN POSITION

Business Development
Experience: Fresher

• R & D Department
• QA/QC Department
Experience: 1-2 year

Qualification: M,Sc/BSc/BPharm

Location: PUNE

APPLY NOW

Syngenesis Chemscience

SUBMIT YOUR RESUME
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Sunday, 22 September 2024

Job Opening For Production, Engineering,HR And Quality Assurance, Quality Control Department At Hester Biosciences

September 22, 2024 0
Certainly! Here’s a more detailed breakdown of each department in the pharmaceutical industry, including their roles, processes, and interactions.

 1. Production Department
Overview: The Production Department is central to the manufacturing of pharmaceutical products, ensuring that all processes align with regulatory requirements and company standards.

Key Responsibilities:
- Manufacturing Operations: Oversee the entire production process from raw material input to finished product output.
- Resource Management  Ensure that materials, personnel, and equipment are optimally utilized.
- Process Optimization Continuously improve production efficiency through lean manufacturing techniques and process re-engineering.

Key Functions*:
- Scheduling  Create and manage production schedules to meet demand while minimizing downtime.
- Compliance: Adhere to GMP guidelines to ensure product safety and efficacy.
- Documentation: Maintain accurate records of production activities, batch production records, and inventory levels.

 2. Engineering Department
Overview: The Engineering Department ensures that all equipment and facilities are maintained and operating efficiently, supporting the production process.

Key Responsibilities:
- Equipment Maintenance: Schedule and conduct preventive maintenance to minimize equipment failure.
- Process Engineering  Design and improve processes for better efficiency and quality.
- Facility Management: Ensure the facility meets safety and regulatory standards.

Key Functions:
- Calibration: Regularly calibrate equipment to ensure accurate performance.
- Technical Support: Provide troubleshooting and technical guidance during production.
- Project Management: Lead engineering projects for equipment upgrades or new technology implementations.

3. Human Resources (HR) Department
Overview: HR is crucial for managing the workforce, ensuring that the company attracts, retains, and develops talent in compliance with industry regulations.

Key Responsibilities:
- Recruitment: Identify staffing needs and source qualified candidates.
- Training and Development: Implement training programs focused on compliance, safety, and skills development.
- Employee Relations: Foster a positive workplace culture and manage conflict resolution.

Key Functions:
- Onboarding: Ensure new hires are integrated smoothly and trained on SOPs and safety protocols.
- Performance Management: Conduct evaluations and provide feedback to enhance employee performance.
- Compliance: Ensure that HR practices comply with labor laws and industry standards.

 4. Quality Assurance (QA) and Quality Control (QC) Departments
Overview: QA and QC ensure that all products meet the highest standards of quality and comply with regulatory requirements.

  Quality Assurance (QA)
Key Responsibilities:
- Quality Management Systems: Develop and maintain a robust QA system to ensure compliance with FDA and other regulatory agencies.
- Audits and Inspections: Conduct internal audits and prepare for external inspections to assess compliance.

Key Functions:
- Document Control: Manage SOPs, policies, and other documentation to ensure they are up to date and accessible.
- Training: Provide training on quality standards and procedures to all staff.
- Risk Management: Identify potential quality risks and implement corrective actions.
 
Quality Control (QC)
Key Responsibilities:
- Testing: Perform rigorous testing on raw materials, in-process samples, and finished products to ensure they meet specifications.
- Stability Studies: Conduct stability testing to ensure products maintain quality over their shelf life.

Key Functions:
- Laboratory Operations: Operate analytical laboratories equipped with the necessary instruments for testing.
- Data Analysis: Analyze test results and report findings to the production and QA departments.
- Non-Conformance Management: Manage deviations and implement corrective actions to resolve quality issues.

 Interdepartmental Collaboration
Effective collaboration among these departments is essential for a successful pharmaceutical operation. Here’s how they interact:

- Production and QA/QC: Regular communication to ensure production runs meet quality standards. QA conducts audits to ensure adherence to SOPs during production.
- Engineering and Production: Engineering supports production by resolving equipment issues and implementing improvements. They also collaborate on new technology deployments.
- HR and All Departments: HR ensures that all departments are staffed with qualified personnel, facilitates training programs, and manages compliance-related training.

In the pharmaceutical industry, the synergy between the Production, Engineering, HR, and QA/QC departments is vital for delivering safe, effective, and high-quality products. Each department has distinct roles but must work cohesively to meet regulatory requirements and industry standards. This collaboration not only enhances operational efficiency but also supports continuous improvement initiatives throughout the organization.
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