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QC Associate 29620

  • Job reference: 930794
  • Location: Dublin South, Dublin
  • Salary: Negotiable
  • Job type: Contract
  • Sector: Life Sciences, Quality, Compliance, Regulatory Affairs
  • Date posted: 20/04/2020

Orion Group Life Sciences have an exciting opportunity for a QC Associate for our Multinational Pharmaceutical client based in the South of Dublin area on a 12-month contract.


Job Purpose

Under minimal supervision, responsible for one or more of the following activities in QC including: Reagent management / HPLC mobile phase preparation, GMP document review and management, sample and data management and some analytical testing.

  • Contributes to team by ensuring the quality of the tasks/services provided by self
  • Contributes to the completion of milestones associated with specific projects or activities within team

This role will support manufacturing operations, as such some extended hours and weekend work flexibility may be necessary as required.

Main Responsibilities of the role

  • Understanding and application of principles, concepts, theories and standards of GMP QC analytical laboratories. Deepens technical knowledge through exposure and continuous learning
    * Knowledge of related regulatory/industry considerations, compliance issues and/or scientific discovery
    * Some / limited experience in a wide variety of analytical techniques including but not limited to Capillary Electrophoresis, Gels or HPLC.
    Skills:
    * Take initiative to identify and drive improvements
    * Excellent verbal and written communication skills
    . Strong Technical writing skills for GMP documentation (e.g. investigations, procedures, change controls)
    . Presentation skills
    . Escalate issues professionally and on a timely basis
    * Decision Making skills
    * Teamwork and Coaching others
    * Negotiation and Influence skills
    * Project Management and organizational skills, including ability to follow assignments through to completion
    Competencies:
    * Demonstrated ability to work independently and deliver right first time results
    . Works under minimal direction
    . Work is guided by objectives of the department or assignment
    . Follows procedures
    . Refers to technical standards, principles, theories and precedents as needed
    . May set project timeframes and priorities based on project objectives and ongoing assignments. Recognizes and escalates problems
    * Demonstrated communication skills
    * Auditing documentation and operation process
    * Demonstrated ability to interact with regulatory agencies

Desired Experience and Background of the successful candidate

  • 1-2 years of biopharmaceutical QC experience or related quality control or GMP laboratory experience in the pharmaceutical or medical device industry.
  • Experience with regulatory compliance in cGMP manufacturing and testing of pharmaceutical products.

For more information on this role, call Kate O' Sullivan on +353 (0) 212063412 or email Kate.OSullivan@orioneng.com for a completely confidential chat about this role and other opportunities using the reference number: 930794

#pharmaceutical #pharma #multinational #QC #GMP


Our role in supporting diversity and inclusion
As an international workforce business, we are committed to sourcing personnel that reflects the diversity and values of our client base but also that of Orion Group. We welcome the wide range of experiences and viewpoints that potential workers bring to our business and our clients, including those based on nationality, gender, culture, educational and professional backgrounds, race, ethnicity, sexual orientation, gender identity and expression, disability, and age differences, job classification and religion. In our inclusive workplace, regardless of your employment status as staff or contract, everyone is assured the right of equitable, fair and respectful treatment.

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