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QA Sr Associate (Senior)
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QA Sr Associate (Sen....
Independent Solutions
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QA Sr Associate (Senior)

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1 Vacancy
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Jobs by Experience

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3-5 years

Job Location

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Lagos - Nigeria

Monthly Salary

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Not Disclosed

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Salary Not Disclosed

Vacancy

1 Vacancy

Job Description

Req ID : 1173908
Job Title:QA Sr Associate (Senior) A31852

About the Company:
Our client is a Multinational Biopharmaceutical company with more than 20,000 employees worldwide and approximately 500 workers in its D n Laoghaire (co. Dublin) facility, which is a 37,000-square-metre aseptic operations facility with freeze-dry product (lyophilization) and liquid vial-filling capabilities.
Its Irish site specializes in secondary manufacturing activities formulation, fill, and packaging, and also includes a bioprocessing suite and laboratories. The local team is currently engaged in one of the largest and fastest technology transfer programs in the company s history. Make a difference in the lives of others, working at the forefront of biotechnology with the top minds in the field.

Duration of Job:12months

Job summary:
The Sr. Associate in Quality Assurance (QA) will be an active member of the ADL QA team and will be assigned to the IQA Quality functional area, which is responsible for the inspection and release of primary packaging components. The Sr. Associate in Quality Assurance will report to a QA Senior Manager and will serve as Quality point of contact for Incoming Inspection of Primary and packaging components.
The site is focused on continuous improvement of all work processes and practices, therefore in addition to routine Quality Assurance duties, IQA Snr. Associates may be asked to carry out additional work functions to support site continuous improvement activities.

Job Duties:
Testing of primary and secondary components for use in the manufacture of aseptic products.
Sampling of Excipients and Drug Substance under Grade C conditions.
Review/approve documentation associated with component testing in preparation for QA Specialist or Qualified Person disposition activities
Compiling, Review and approval of minor NC and CAPAs for closure ensuring compliance with appropriate documentation, whilst ensuring that CAPA actions address root cause and implementation plan dates are achievable
Provide training and advice to staff in relation to testing of components and packaging.
Actively participate in audits and their preparation.
Review cGMP records (e.g., WO, JP, GDMS, NC, CAPA, protocols, reports, SOP, etc.) ensuring compliance with appropriate documentation
Write, review and approve Standard Operating Procedures in accordance with company Policies.
Perform all activities in compliance with company safety standards and SOPs
Support continuous improvement and Operational Excellence initiatives
Any other tasks/projects assigned as per manager s request.

Requirements

Basic Qualifications & Experience:
Must Pass Eye-Tests required for Visual Inspection
University degree. Engineering or Science related discipline preferred.
Relevant experience (4 yrs. +) working in the pharmaceutical or biotechnology industry or other combination of experience and educational background that may otherwise satisfy the requirements of the role.

Preferred Qualifications & Experience:
Excellent written and verbal communication skills
Experience working with dynamic cross-functional teams and proven abilities in decision making
Strong organizational skills, including ability to follow assignments through to completion
Demonstrated ability in problem solving and experience in managing Root Cause Analysis / Non-Conformance /Deviation investigations
Experience working in aseptic operations, protein formulation, vial and syringe filling.

*** No Visa Process ***

Benefits

  • Benefit from Independent Solutions ethical principles!

  • We look after our team, we know the business, we have been working in the sector >20 years. We are not a recruitment agency

  • While placed on client sites you will be an integral part of our team, gaining support and access to the knowledge and experience of our cross functional LifeScience team

  • We offer attractive rates - competitive margins compared to our competitors

  • Payment on time and in full

  • We continue to partner and grow our client base and thereby ensure that we have a continuous supply of High-Value Projects

  • We work for you!



Basic Qualifications & Experience: Must Pass Eye-Tests required for Visual Inspection University degree. Engineering or Science related discipline preferred. Relevant experience (4 yrs. +) working in the pharmaceutical or biotechnology industry or other combination of experience and educational background that may otherwise satisfy the requirements of the role. Preferred Qualifications & Experience: Excellent written and verbal communication skills Experience working with dynamic cross-functional teams and proven abilities in decision making Strong organizational skills, including ability to follow assignments through to completion Demonstrated ability in problem solving and experience in managing Root Cause Analysis / Non-Conformance /Deviation investigations Experience working in aseptic operations, protein formulation, vial and syringe filling. *** No Visa Process ***

Employment Type

Full Time

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