Senior QA Compliance Specialist

3 days ago


Dublin, Ireland Regeneron Full time

Within this role you'll be responsible for maintaining the site's compliance of operations inclusive of but not limited to Manufacturing, Quality Systems, Quality Control, Quality Assurance, Facilities Maintenance, Materials Handling, and QA Validation in accordance with mandated regulatory requirements and site expectations.

Typical day might include, but is not limited to, the following:

Being responsible for ensuring compliance with all aspects of Quality for the Raheen site inclusive of manufacturing, quality systems, quality control, validation, facilities, and materials management.

Administrating and oversight of site quality systems including but not limited to:

Deviations

CAPA

Change Control

Audits

Customer Complaints

Quality Risk Management

Reviewing and approving the following types of documents, relating to area functions:

failure investigations

change control documents

corrective/preventative action documents

standard operating procedures

Maintaining electronic systems used for Change Control and Deviation Management

Reviewing procedures, policies and other instructional documents relating to quality systems to ensure compliance with company policy and local and international regulatory requirements

Monitoring and trending metrics associated with site quality systems

Participate in continuous improvement initiatives

Participating in regulatory and customer audits

Participating in quality risk assessments

Collaborating with functional departments to resolve issues and maintain compliance

Identifying gaps in systems and develop feasible plans for correction

Training of personnel on quality system processes

This role might be for you if you:

Have proven experience in conducting on-site investigations and analysis (GEMBA walks)

Have the ability to identify and address operational inefficiencies

Have a track record of implementing process improvements based on findings from direct workplace engagement

Can demonstrate respectful behaviour at all times

Have basic working knowledge of Microsoft Suite (Word, Excel, Powerpoint)

To be considered for this position you must hold:

Specialist: BS/BA in Engineering, Chemistry, or Life Sciences with 3+ years of relevant work experience in pharmaceutical or related industry

Senior Specialist: BS/BA in Engineering, Chemistry, or Life Sciences with 5+ years of relevant work experience in pharmaceutical or related industry

Does this sound like you? Apply now to take your first step towards living the Regeneron Way We have an inclusive and diverse culture that provides comprehensive benefits, which often include (depending on location) health and wellness programs, fitness centers, equity awards, annual bonuses, and paid time off for eligible employees at all levels

Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company's business.

For roles in which the hired candidate will be working in the U.S., the salary ranges provided are shown in accordance with U.S. law and apply to U.S.-based positions. For roles which will be based in Japan and/or Canada, the salary ranges are shown in accordance with the applicable local law and currency. If you are outside the U.S, Japan or Canada, please speak with your recruiter about salaries and benefits in your location.

Please note that certain background checks will form part of the recruitment process. Background checks will be conducted in accordance with the law of the country where the position is based, including the type of background checks conducted. The purpose of carrying out such checks is for Regeneron to verify certain information regarding a candidate prior to the commencement of employment such as identity, right to work, educational qualifications etc.

#J-18808-Ljbffr


  • Senior Qa

    3 weeks ago


    Dublin, Ireland Qa Full time

    at Archer - The IT Recruitment ConsultancyMid-Senior level Not disclosed Ireland Dublin, County Dublin, Ireland29 days agoJob Title: Senior QA Engineer (Manual Testing) – Contract €*******/DayLocation: DublinContract Length: 6 months (high potential for extension)Join a Global Leader in Insurance & TechnologyAn exciting opportunity awaits an experienced...

  • QA CQV Specialist

    1 week ago


    Dublin, Ireland PSC Biotech® Corporation Full time

    Overview Join to apply for the QA CQV Specialist role at PSC Biotech Corporation . PSC Biotech is a leading Biotech Consultancy firm founded in 1996, headquartered in Pomona, California, USA, with global operations in Ireland, India, Singapore, Australia and the US, serving 350 clients in more than 23 countries worldwide. We provide cloud-based software...


  • Dublin, Ireland Quanta part of QCS Staffing Full time

    QA Distribution Specialist - Life Science - Contract - Dublin Are you looking for the chance to join a life changing pharmaceutical organisation in their mission to continuously drive innovation? We are recruiting for a QA Distribution Specialist to support the QA Distribution Specialist function. Located 15 minutes from Dublin Airport and just a short...


  • Dublin, Ireland JobContax Full time

    Technical QA Specialist, Dun Laoghaire, DublinOffice/Project Location:Dun Laoghaire, DublinEmployment Type: ContractWork Location:  Hybrid Onsite requirement is 3 days per weekPay: €50 - €57 per hourExperience: 7+ yearsVisa: EU passport or Stamp 4 visa requiredOur client is a leading international Biotechnology company with a state of the art aseptic...

  • QA Lead Specialist

    3 weeks ago


    Dublin, Ireland Cpl Resources - TEG Full time

    QA Lead Specialist 12 months contract position Location: Swords Campus ABOUT US? SK pharmteco is a global Contract Development and Manufacturing organisation (CDMO) with state-of the-art facilities in Korea, US, France and Ireland. We are part of SK Inc., a Korea company with revenues of $99 billion in 2023. Our mission is to produce and deliver...


  • Dublin, Ireland Tandem Project Management Ltd. Full time

    Summary Our client, based in Louth, has an opportunity for a QA CQV Specialist to join their team. This role is responsible for providing quality oversight of all validation and qualification activities, ensuring compliance with current regulatory requirements, cGMP, and company SOPs. The position covers validation activities for facilities, utilities,...

  • QA Lead Specialist

    3 days ago


    Dublin, Ireland Cpl Full time

    Cpl, in partnership with SK pharmteco, is looking to hire a QA Lead Specialist on a 12 month contract, to join the team in the Swords Campus, North Dublin.ABOUT US? SK pharmteco is a global Contract Development and Manufacturing organisation (CDMO) with state-of-the-art facilities in Korea, US, France and Ireland. We are part of SK Inc., a Korea company...


  • Dublin, Ireland CPL Full time

    QA Lead Specialist 12 months contract position Location: Swords Campus ABOUT US? SK pharmteco is a global Contract Development and Manufacturing organisation (CDMO) with state-of the-art facilities in Korea, US, France and Ireland. We are part of SK Inc., a Korea company with revenues of $99 billion in 2023. Our mission is to ‘produce and deliver...


  • Dublin, Ireland CPL Full time

    QA Lead Specialist 12 months contract position Location: Swords Campus ABOUT US? SK pharmteco is a global Contract Development and Manufacturing organisation (CDMO) with state-of the-art facilities in Korea, US, France and Ireland. We are part of SK Inc., a Korea company with revenues of $99 billion in 2023. Our mission is to ‘produce and deliver...


  • Dublin, Ireland Cpl Resources Full time

    QA Lead Specialist 12 months contract position Location: Swords Campus ABOUT US? SK pharmteco is a global Contract Development and Manufacturing organisation (CDMO) with state-of the-art facilities in Korea, US, France and Ireland. We are part of SK Inc., a Korea company with revenues of $99 billion in 2023. Our mission is to produce and deliver...