About Us
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 – immunology, oncology, neuroscience, and eye care – and products and services in our Allergan Aesthetics portfolio.
We are seeking a dynamic Biologics Manufacturing Manager to lead our biologics manufacturing team at our Ballytivnan Site in Co. Sligo. This role is crucial in ensuring safe, efficient, and compliant manufacturing operations.
The ideal candidate will apply their extensive expertise and leadership skills to drive operational excellence and foster team development.
Award-winning AbbVie Ballytivnan site is a hub of innovation and excellence in the pharmaceutical industry located in the scenic County Sligo, Ireland.
Why Choose Our Location?
* State-of-the-Art Facilities: Our site is equipped with cutting-edge technology and advanced manufacturing capabilities.
* Skilled Professionals: At Ballytivnan, we boast a team of highly skilled professionals who are dedicated to pushing the boundaries of science.
* Commitment to Quality: Quality is at the heart of everything we do. Our rigorous quality control processes ensure that we consistently deliver products that patients and healthcare providers can trust.
* Community and Sustainability: We take pride in our commitment to sustainability and community engagement.
* Strategic Presence: As part of AbbVie's global network, the Ballytivnan site plays a crucial role in connecting our European operations with a broader international landscape.
Key Responsibilities:
* Lead and facilitate safe and effective operations of the biologics manufacturing team.
* Supervise and execute pharmaceutical processing activities to achieve operational objectives.
* Provide leadership and motivation to maximize team effectiveness.
* Plan and coordinate resources to ensure sufficient personnel for safe, efficient manufacturing operations.
* Coordinate training requirements and train new team members.
* Measure, report, and manage key performance metrics.
* Oversee manufacturing control system transactions for accuracy and timeliness.
* Ensure compliance with safety, environmental, and quality SOPs.
* Develop team members through appropriate training, task assignments, and performance reviews.
* Serve as a subject matter expert in interactions with QA department, regulatory bodies, and during internal audits.
* Collaborate with cross-functional teams to forecast and procure necessary raw materials.
* Provide technical guidance on SOPs and batch records required for manufacturing.
* Manage compliance with applicable policies and ensure quality results through sound design and risk mitigation.
Qualifications:
* Bachelor's Degree in engineering, science, or a closely related discipline.
* Master's Degree preferred.
Experience and Skills:
* 10+ years of experience in a pharma/biopharma manufacturing facility, with expertise in supply chain management, engineering, quality, and/or drug development.
* At least 3 years of direct management experience.
* Strong technical knowledge and application of industry practices and procedures.
* Proficiency in financial systems and fiscal control.
* Excellent interpersonal and communication skills, with the ability to work collaboratively in a diverse environment.
Reporting:
* The role operates with a high degree of autonomy, reporting to the Operations Manager.
* Manages 10-16 direct reports and provides leadership in a collaborative, fast-paced environment.
EHS Responsibilities:
* Adhere to EHS policies and best practices in all activities.
* Report EHS incidents and near misses promptly and support a culture of EHS excellence.
* Participate in EHS training and wear required PPE.