Specialist, Manufacturing QA

Reposted 8 Hours Ago
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Sligo, IRL
In-Office
Mid level
Healthtech • Pharmaceutical
The Role
The QA Manufacturing Compliance Specialist ensures compliance with regulatory standards for drug products, oversees quality during manufacturing, and leads investigations into compliance issues.
Summary Generated by Built In
Company Description

About AbbVie

AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas including immunology, oncology and neuroscience - and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at www.abbvie.com. Follow @abbvie on LinkedIn, Facebook, Instagram, X and YouTube.

Job Description

In AbbVie Ballytivnan, we are recruiting for a QA Manufacturing Compliance Specialist to join our team. This position will report into the Quality Operations Lead and support the Quality Assurance team. The QA Manufacturing Specialist is responsible for documenting and establishing a quality system which ensures full compliance with all regulatory and AbbVie requirements.

The QA Manufacturing Compliance Specialist will have responsibility to assess and report on the effectiveness of the quality system to senior management. This role requires shift work.

What you will do:

  • Ensure that all products leaving AbbVie Biologics Ballytivnan meet the standards required for marketed and investigational drug products.
  • Ensure that products and aseptic process simulations manufactured at AbbVie Biologics Ballytivnan meet the requirements of the end users, regulatory authorities and of the company.
  • Provide quality and compliance oversight and assistance to the Operations function of the company to manufacture products in compliance with all site policies and procedures.
  • Provide quality oversight during the aseptic processing of products, including aseptic intervention observation.
  • Lead / Assist in investigations arising out of product or manufacturing processes non-compliance.
  • Review/Audit of completed Batch Records.
  • Review of Manufacturing Logs as required.
  • Completion of quality review of operations documentation (SOPs, JSTMs, Risk Assessments)
  • Completion of Line Clearance activities.
  • Completion of Incoming Raw Material checks, including product status maintenance (as required).
  • Provide Stability Program Support, e.g. sample pulls, weekly checks, protocol generation (as required).
  • Finished product status maintenance, including labelling as required.
  • Administration of Quality Logs, e.g. QA Hold, Sample Request.
  • Lead operations floor daily walk around of manufacturing areas.
  • Drive continuous improvements and simplify site processes and procedure, specifically relating to the Operations function to ensure compliance is always maintained.
  • Other support as deemed necessary.

Qualifications

What you will need:

  • A third level qualification in a science, quality or engineering discipline
  • Minimum 3 years’ Experience in a similar role in a Pharmaceutical or Sterile Manufacturing environment (Biologics desirable)
  • A strong knowledge of regulatory requirements is required.
  • Excellent written and verbal communication skills with a strong attention to detail

Additional Information

AbbVie is an equal opportunity employer and is committed to operating with integrity, driving innovation, transforming lives and serving our community.  Equal Opportunity Employer/Veterans/Disabled. 

US & Puerto Rico only - to learn more, visit https://www.abbvie.com/join-us/equal-employment-opportunity-employer.html

US & Puerto Rico applicants seeking a reasonable accommodation, click here to learn more:

https://www.abbvie.com/join-us/reasonable-accommodations.html

Skills Required

  • Third level qualification in a science, quality or engineering discipline
  • Minimum 3 years' experience in a similar role in a pharmaceutical or sterile manufacturing environment
  • Strong knowledge of regulatory requirements
  • Excellent written and verbal communication skills with attention to detail

AbbVie Compensation & Benefits Highlights

The following summarizes recurring compensation and benefits themes identified from responses generated by popular LLMs to common candidate questions about AbbVie and has not been reviewed or approved by AbbVie.

  • Retirement Support Retirement programs are portrayed as a standout, with a dollar‑for‑dollar 401(k) match up to 6% and an additional annual company contribution based on age and service. Feedback suggests this materially boosts perceived total compensation for many U.S. employees.
  • Parental & Family Support Paid parental and caregiver leave are emphasized, including up to 12 weeks of fully paid parental leave for all parents and 4 weeks of paid caregiver leave in the U.S. Feedback suggests these policies are a meaningful differentiator for employees balancing family needs.
  • Leave & Time Off Breadth Time off is described as extensive, with tiered vacation that scales with tenure, 17 company holidays, and two paid volunteer days in the U.S. Feedback suggests the breadth of leave contributes notably to overall benefits satisfaction.

AbbVie Insights

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The Company
HQ: North Chicago, IL
50,000 Employees
Year Founded: 2013

What We Do

AbbVie is a global biopharmaceutical company focused on creating medicines and solutions that put impact first — for patients, communities, and our world. We aim to address complex health issues and enhance people's lives through our core therapeutic areas: immunology, oncology, neuroscience, eye care, aesthetics and other areas of unmet need.

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