What Jobs are available for Production in Dublin?

Rottapharm Limited

At VIATRIS, we see healthcare not as it is but as it should be. We act courageously and are uniquely positioned to be a source of stability in a world of evolving healthcare needs.

Viatris empowers people worldwide to live healthier at every stage of life.

We do so via:

Access – Providing high quality trusted medicines regardless of geography or circumstance;

Leadership – Advancing sustainable operations and innovative solutions to improve patient health; and

Partnership – Leveraging our collective expertise to connect people to products and services.

Our global portfolio includes best-in-class, iconic brand-name products as well as global key brands; generics, including branded and complex generics; and other offerings across a wide range of therapeutic areas. We are committed to helping create healthier communities worldwide through education, outreach and better access to treatment.

For those driven to live their lives with purpose, Viatris helps employees realise their full potential by creating a collaborative culture that fosters courage and resilience. Viatris is more than just a place to work. This is a place to make a difference in the world.

The Role & What You Will Be Doing

Every day, we rise to the challenge to make a difference and here's how the Production Operator role will make an impact:

• To safely carry out production duties as directed in the assigned packaging area.
• To carry out all production operations in the assigned area in accordance with Standard Operating Procedures (SOPs) or as directed by the relevant Batch Manufacturing or Packaging instructions.
• To assist, as a member of the Production team, towards the delivery of production output targets and quality levels on schedule.
• To carry out all production operations in the designated area in accordance with current Good Manufacturing Practices (cGMPs).
• To complete all documentation and/or electrical batch records relating to production activities as required in a timely fashion.
• To immediately notify the Supervisor or Line/Process Lead of any deviation from SOPs and/or deviations in the standard production process.
• To actively take part in Continuous Improvement on site – e.g. 6S and TPM.
• To ask, if in doubt, about any particular practice or unusual finding.

About Your Skills & Experience

For this role, we're looking for a candidate who has an effective combination of the following qualifications, skills and experiences:

• A third level education is desirable.
• Experience in high speed packaging experience in the Pharmaceutical industry, Medical devices or Food industry will be advantageous.
• Experience with one or more of the following operations would be advantageous: high speed packaging lines and/or working in a GMP Environment).

At Viatris, we are dedicated to building a truly diverse, inclusive and authentic workplace, so if you're excited about this role but your past experience doesn't fully align with every requirement, we still encourage you to apply. You may just be the right candidate for this or other roles.

Diversity & Inclusion at Viatris

At Viatris, diversity and inclusion are essential to our mission. The diversity we foster in all aspects of our business can be one of our greatest strengths in redefining healthcare not as it is, but as it should be. If you would like to know more about what diversity, equity and inclusion means to us, please visit

Sustainability at Viatris

Corporate social responsibility is fundamental to the Viatris mission. We work to advance responsible and sustainable operations and leverage our collective expertise to empower people to live healthier at every stage of life, recognizing that our actions affect the stakeholders and communities we serve. To learn more about our efforts, please visit

At Viatris, we offer competitive salaries, benefits and an inclusive environment where you can use your experiences, perspectives and skills to help make an impact on the lives of others.

Viatris is an Equal Opportunity Employer.

The Blink Group is now seeking to recruit a Seasonal Production & Event Crew for their premises, in in Kylemore Road, Inchicore, Dublin 10:

Seasonal Production & Event Crew

Contract:Seasonal Temporary

Start date: Oct 1st

Salary: €15.00 per hour

Hours of work: varied hours per week (Band E-F possible 30 hrs) including evenings and weekends

The role

The Seasonal Production & Event crew will provide support across both warehouse operations and live events. This is a varied, hands-on role, working collaboratively within a team to deliver high-quality brand experiences.

This role offers excellent opportunities for growth and development, with the potential to progress into a permanent full-time position.

Main Duties and Responsibilities

Prepare and manage props and kit in the warehouse.

Drive vans to deliver props to venues and clients nationwide.

Assist with on-site event build, set-up, and de-rig.

Support stock control, prop tracking, and basic maintenance.

Adhere to health & safety procedures at all times.

Work evenings and weekends as required during peak event periods.

Essential Criteria

Full clean EU driving license.

Van driving experience

Manual handling experience.

Strong teamwork skills with a reliable, "can-do" attitude.

Flexibility to work up to 30 hours per week, evenings and weekends.

Hands on approach and willingness to get involved

Desirable Criteria

Forklift certification

Manual handling certification

How to apply

To apply for this position, please send your (CV/Cover letter) to Indeed portal or clearly outlining how you meet the criteria before Sept 26th 2025

Job Type: Fixed term

Contract length: 3 months

Pay: €15.00 per hour

Expected hours: 25 – 30 per week

Work Location: In person

1. JOB PURPOSE

Responsible for maintaining quality control processes, analyzing the results, and giving feedback and guidance to the product development and production team. In addition to overseeing stringent quality control measures, the QC Manager will also act as an integral part of the purchasing team, ensuring that purchased materials align with approved supplier lists and quality criteria while maintaining the highest standards of product quality and reliability.

1. DUTIES AND RESPONSIBILITIES

2. Liaises with Director of Operations, Head of Quality and Regulatory Affairs, Production Manager,

Project Managers, Process Scientist and Quality Assurance.

• Responsible for ensuring raw materials, intermediates, and manufactured products meet standard standards of quality, reliability, and performance.
• Ensure proper maintenance of detailed records encompassing quality tests, procedures, and established standards, facilitating a comprehensive repository that guarantees traceability and compliance within the quality control framework.
• Establish procedures and processes for sampling, recording, and reporting of quality data.
• Request quotes from suppliers for product specific materials or services.
• Carry out research to identify ways to reduce waste and maximize resources.
• Ensures that all production materials are purchased from suppliers that are listed on the Approved

Supplier List.

• Ensure manufacturing processes are in compliance with both national and international standards of production.
• Oversee and execute comprehensive quality control protocols to guarantee adherence to established standards and procedures within the organization.
• Provide strategic recommendations to company management aimed at enhancing and optimizing existing quality control processes for heightened efficiency and superior output quality.
• Supervise QC technicians to ensure they perform their duties in line with established quality

procedures.

• oversee and analyze the product development processes to promptly identify and address any

deviations or variances from established quality policies and standards.

• Approve compliant products and reject defective ones.
• Compile and present reports detailing quality control activities and findings to upper management

to provide transparent updates on the organization's adherence to quality standards and initiatives.

• Maintain proper records of quality test, procedures and standards.
• Develops and implements an electronic Quality Management System in compliance with

ISO13485, IVDR 2017/746 and FDA 21CFR820.

• Act as a Functional Manager.

• Other duties as defined by your manager a from time to time.

• QUALIFICATIONS

• A bachelor's degree in a related field; a graduate degree is recommended for advancement.

• 3 years experience within a similar role within a regulated industry
• Good communication skills for effective liaison and teamwork.
• Problem-solving skills, analytical skills, and attention to detail.
• Excellent organisational skills and the ability to work on several tasks or projects concurrently.
• Commercial acumen and an awareness of the business value of work undertaken.
• Presentation skills - for presenting ideas and findings to colleagues and customers.
• The ability to work well independently, with minimum supervision.

• Drive, enthusiasm, and self-motivation.

• WORKING CONDITIONS

• The work environment characteristics described here are representative of those an employee encounters while performing the essential functions of this job.

• Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.

• The noise level in the work environment is usually moderate.

• PHYSICAL REQUIREMENTS

• The physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of this job.

• The employee must occasionally lift and/or move up to 10 pounds. Specific vision abilities required

by this job include close vision, distance vision, peripheral vision, depth perception and ability to adjust focus.

The above job description is not intended to be an all-inclusive list of duties and standards of the position. Incumbents will follow any other instructions, and perform any other related duties, as assigned by their manager.

Job Type: Full-time

Pay: €55,000.00-€60,000.00 per year

Benefits:

• Bike to work scheme
• Company pension
• Employee assistance program
• On-site parking

Work authorisation:

• Ireland (required)

Work Location: In person

This job operates on a 16/5 cycle shift pattern. This job specification outlines the general responsibilities associated with the role of Manager QC Microbiology on the Amgen Manufacturing site. This role will be responsible for managing the QC Microbiology team and owning, facilitating, and undertaking activities pertaining to Microbiology within QC and Manufacturing. The successful candidate will focus on compliance, continuous improvement and implementing a lean culture and Right First Time (RFT) for QC Microbiology duties and testing, including release of commercial and global release testing. The role also represents the QC unit by liaising with internal and external stake holders.

The site is focused on continuous improvement of all work processes and practices and all colleagues are required to be flexible in this regard. This means that they may be asked to carry out additional work functions that are not described in this specification but are associated with their role. This role will be responsible for oversight of some analytical in-process methods and may require shift work depending on company needs.

Key Responsibilities:

• Supervision/Management of QC Microbiology team.
• Ensure the QC Microbiology area is operated in a safe manner.
• Overall responsibility for QC In process, Environmental Monitoring, Release and Stability testing and the associated test and laboratory documentation.
• Develop and maintain quality systems within the QC laboratories to ensure ongoing compliance to cGLP Compliance with Standard Operating Procedures and Registered specifications.
• Provide an effective and efficient QC service to operations by supervising, developing and coaching the QC team.
• Ensure timely completion of Laboratory Investigation Reports and deviations through the Deviation procedures.
• Issue trend reports on investigations, non-conformances and Environmental Monitoring and identify laboratory practices and procedures for further development/improvement.
• Keeps abreast of current Corporate and industry requirements and compliance trends as they pertain to laboratory operations and aseptic manufacturing.
• Approval of SOP's, trend data, investigations, non-conformances, validation protocols, reports, method validation/verifications and equipment qualifications.
• Participate in regulatory agency inspections as required.
• Plan and implement procedures and systems to maximise operating efficiency.
• Manage and contribute to the achievements of department productivity and quality goals.

Primary knowledge, skills, competencies and relevant experience Knowledge:

Broad technical knowledge within Microbiology and expanding knowledge of related disciplinary areas Recognizes and understands the cross-dependencies of the role and understands the impacts on the organization Enhances own knowledge through understanding business trends and objectives Knowledge of industry and business principles Understands the core business process and purpose of the functional area in Amgen's commercialization process Developing own project management techniques

Problem Solving:

Applies analytical skills to evaluate and interpret complex situations/ problems using multiple sources of information Creates new procedures and processes to drive desired results Handles diverse scope of issues that require evaluation of a variety of factors including current business trends

Autonomy:

Managerial/Supervisory experience with a proven record in a Supervisor/ Team Lead role Experience leading cross-functional teams is desirable Work is guided by operational and project objectives Manages multiple assignments and processes Independently determines approach to project May be responsible for specific programs and/or projects Independently develops solutions that are thorough, practical, and consistent with functional objectives

Contribution:

Contributes to work group/team by ensuring quality of tasks/services provided by self and others with a strong focus on RFT and Lean Provides training and guidance to others Extends capabilities by working closely with senior staff/experts within and outside the internal organization

Skills:

Lead with initiatives to identify and drive improvements Communication skills (verbal and written) at all levels Strong Technical writing skills for GMP documentation (e.g. investigations, procedures, change controls) Presentation skills Escalate issues professionally and in a timely basis and know when to escalate Decision Making skills – will be require to make decisions independently Teamwork, Coaching and motivating others Negotiation and Influence skills, Planning and organisation skills Investigation skills Demonstrated ability to interact with regulatory agencies Experience working with interdepartmental and cross functional teams and influencing decisions

Relevant experience:

Bachelor's degree in a Science related field is required. 6+ years of biopharmaceutical QC experience or related quality control or GMP laboratory experience in the pharmaceutical or medical device industry, with 2 – 3 years of specific Microbiology management experience desirable. Experience with regulatory compliance in cGMP manufacturing and testing of pharmaceutical products. Some analytical experience for oversight of analytical in-process methods would be an advantage. Possess key competencies to include planning/organisation, problem solving, communication, teamwork, flexibility, coaching and motivating. Proven experience of leading teams.