Skip to main content
Post your CV and find your next job on Indeed!

Scientific, Medical, Clinical Smc jobs

Sort by: -
    • Bachelors Degree in a scientific/technical discipline required.
    • This position is responsible for carrying out tasks and projects related to management of…
    • Or another relevant scientific or engineering discipline.
    • Experience planning and executing scientific experiments independently.
    • View all AbbVie jobs - Westport jobs - Senior Scientist jobs in Westport, County Mayo
    • Salary Search: Scientist, II PDS&T (24 month Contract) salaries
    • See popular questions & answers about AbbVie
    • Pharmaceutical processing activities in our manufacturing building and support locations.
    • Cross training within the team and training of new team members.
    • Demonstrated scientific communication and presentation skills by presenting at leading scientific conferences.
    • Present at leading scientific conferences.
    • The Sterility Assurance Lead will play a critical role in the design, qualification, and operational compliance of sterile manufacturing at AbbVie Cork.
  • View similar jobs with this employer
    • Waters collaborates with analytical laboratories around the world to advance the release of effective, high-quality medicines, assure the safety of food and…
    • Provide scientific justification and technical conclusions arising from study outcomes.
    • The Visual Inspection Subject Matter Expert (SME) is responsible for…
    • Full training will be provided by ALS.
    • To perform work as allocated by Shift Supervisor to the high standards of quality required and to inform Shift Supervisor…
    • Perform microbiological testing including confirmation and identification tests for a variety of enumeration and detection methods.
    • Bachelor's degree in Chemistry, Analytical Chemistry, Food Science, or a related scientific discipline.
    • The Laboratory Technician will support the Central…
    • A third level qualification in a scientific/technical discipline required.
    • This position is responsible for carrying out tasks and projects related to equipment…
    • Understanding of GMP, compliance, validation practices, system development life cycle principles and regulatory expectations relevant to a medical-device…
    • Medical Dictation: Complete medical reporting after consultations in a timely manner.
    • Financial Competency: Proven ability to manage medical finances and…
    • The Training Coordinator is responsible for the coordination and implementation of learning.
    • Solutions across the site, including administration of site…
    • Coordinate operational activities across clinical, administrative, and technical teams to ensure seamless service delivery.
QA Specialist
J&J
·
4.2
Cork, County Cork
Full-time
Apply on company site

Job details

Pay information not provided
Full-time
Cork, County Cork

Full job description

QA Specialist


Location: Cork

Duration: 12 Months

Hours: 39 months


This position is responsible for carrying out tasks and projects related to management of Quality Assurance activities at Johnson & Johnson Innovative Medicine (JJIM) as required by Good Manufacturing Practice (GMP).

These activities include change control, nonconformance investigation, quality systems auditing, supplier qualification, documentation management, incoming materials release, batch release, annual product review and validation compliance activities at JJIM.


Roles and Responsibilities

  • Provides support and direction to all departments in respect of specific quality system elements to ensure business, quality and compliance goals are met following the J&J Standard of Leadership behavior model. Partners with other Departments to ensure that compliance systems are implemented in an efficient manner.

  • Supports the development and management of GMP compliance systems by developing and implementing processes, procedures, forms, work instructions and tools related to the implementation of compliance systems at the site.

  • Carries out tasks related to the administration of site nonconformance management systems

  • Carries out tasks related to the management of site change control systems

  • Supports system qualification and process validation activities

  • Carries out administration of the Supplier Assessment, Auditing and Inspection Readiness Systems at the site

  • Supports GMP training activities

  • Carries out tasks related to the administration of site supplier approval systems

  • Carries out tasks related to the management of batch records design and release systems

  • Supports system process support validation and process validation activities

  • Carries out administration of the SAP Quality Management Module for JJIM

  • Reviews and approves SOPs/work instructions/forms/validation plans from other departments on behalf of Quality Assurance.

  • Deputises for the Quality Assurance as appropriate.


How to Succeed

  • Bachelors Degree in a scientific/technical discipline required

  • A minimum of 2 years experience in a quality, manufacturing, validation or compliance role within the biological and/or pharmaceutical industry.

  • Knowledgeable of FDA/EMEA regulatory requirements applicable to biologics and/or pharmaceuticals. Ability to apply GMP regulations and other FDA and international guidelines to all aspects of the position.

  • Demonstrated knowledge and application of industry regulations as they apply to quality, including those of FDA, HPRA, EMEA and other authorities.


Desirable

  • Experience in auditing of external suppliers, contractors and vendors.

  • Experience in development/and or evolution of GMP systems and/or start up experience highly desirable.


Benefits

This role offers a very competitive hourly rate. This contract will run for 12 months.


about Johnson & Johnson Innovative Medicine

Patients inform and inspire our science-based innovations, which continue to change and save lives. Applying rigorous science and compassion, we confidently address some of the most complex diseases of our time and unlock the potential medicines of tomorrow.


Our diverse portfolio spans multiple therapeutic areas — Oncology, Immunology, Neuroscience, Cardiovascular, Pulmonary Hypertension, and Retina.

We are continuously working to develop treatments, aspiring to find cures, pioneering the path from lab to life, and championing patients every step of the way.


Janssen UK: https://www.janssen.com/uk/

Janssen Ireland: https://www.janssen.com/ireland/


Application Process

We are looking to process the first round of applications within the next 2 working days.

We do not accept applications via email. The pay rate for this role will depend on how you are paid. PAYE, LTD & Umbrella options are available.

Diversity, Equity & Inclusion

For more than 130 years, diversity, equity & inclusion (DEI) have been part of our cultural fabric at Johnson & Johnson and woven into how we do business every day. Our commitment to respect the dignity and diversity of all is embedded in our Credo.

We know that the success of our business depends on having the best talent in a workforce that reflects the diverse markets we serve around the world and an inclusive culture that values different perspectives and life experiences. That is why we are working to create an inclusive environment where diverse backgrounds, perspectives and experiences are valued and each one of our people feels that they belong and can reach their potential. No matter who they are. Diversity, Equity & Inclusion at Johnson & Johnson means “You Belong”.

Let Employers Find YouUpload Your Resume