Manufacturing Technician

Allergan; Lincoln (NE); On-site; USD 50,000 - 65,000; Full time

Job summary

A leading company in the biopharmaceutical sector is seeking Manufacturing Technicians to join their Biologics team in Westport on a fixed-term contract. The role involves ensuring safety compliance, working within quality assurance systems, and performing aseptic manufacturing tasks. Ideal candidates will have relevant education and experience in GMP environments, with strong team collaboration skills.

Qualifications

• 1-2 years GMP experience, preferably Aseptic/Sterile Manufacturing.
• Strong communication, documentation, and IT skills.
• Ability to multitask and adapt in a fast-paced environment.

Responsibilities

• Carry out daily tasks according to GMP and quality systems.
• Perform compounding, filling and capping of aseptic processes.
• Accurately complete documentation and maintain cleanliness.

Skills

Communication

Documentation

IT skills

Organization

Flexibility

Attention to detail

Multitasking

Education

Leaving cert or equivalent qualification

3rd level qualification in Science/Engineering

Tools

SAP

Job description

Company Description

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. For more information about AbbVie, please visit us at www.abbvie.com. Follow @abbvie on X, Facebook, Instagram, YouTube, LinkedIn and Tik Tok.

Job Description

There are many ways to be a difference maker. Find yours.

We are now recruiting forManufacturing Techniciansto join our diverseBiologicsteam inWestport, on a fixed-term contract basis. As our newest technician, you will ensure the highest quality and safety compliance standards while gaining exposure to new and advanced technology in our quality assurance systems. You will also ensure the continued success of our business unit by taking ownership of duties such as compounding, filling and capping of an aseptic product, preparing autoclave loads, testing filters, preparing components, documenting batch related activities, housekeeping and environmental monitoring.

PLEASE NOTE:The following role is a 12 hour monthly rotational shift pattern, covering days, nights, weekdays and weekends.

If great benefits, a defined career path, and work-life balance are important in your next career move, then read on to find out more.

Your Key Activities will include, but are not limited to:

• Carry out daily tasks as assigned by the Production Manager according to GMP and the quality system
• Perform activities associated with the compounding, filling and capping of an aseptic process.
• Prepare components and equipment for processing into a Grade A environment.
• Accurately completing documentation on time, accurately and legibly.
• Keeping the Manufacturing area tidy and clean.
• Review and update documentation as requested by the Production Manager
• Participating in root cause analysis and problem-solving.
• Completing compliant investigations and environmental excursions.
• Adhering to all company standards in the area of safety, housekeeping and quality, notifying management of any discrepancies.
• Follow gowning procedures on entry to areas
• Report any machine issues to the Production Manager and the maintenance department.
• Set-up, clean and maintain equipment
• Transfer of waste material out of the cleanroom areas
• Perform environmental monitoring
• Participate in media runs
• Adhere to and support all EHS & E standards, procedures, and policies.

Qualifications

Education and Experience:

• Leaving cert or equivalent qualification required,3rd level qualification in a Science/Engineering or related discipline is preferred
• 1-2 years GMP experience, preferably Aseptic/Sterile Manufacturing in a cleanroom environment
• Experience working with SAP within a similar industry is preferable.
• Strong communication, documentation, and IT skills.
• Ability to multitask and adapt in a fast-paced environment.
• Outstanding organization, flexibility, and time management skills
• High attention to detail and methodical in approach
• Ability to build strong relationships and work within cross-functional teams.
• Adaptability to work in a fast, dynamic environment whilst adjusting readily to meet unexpected constraints.
• Drive, high energy, maturity, and ability to work under pressure, deliver results, and overcome obstacles.
• Team player who can collaborate with others to achieve organizational targets and goals.

So, does this all sound like the right role for you?

Then apply now and join AbbVie today!

#Monster

Additional Information

Multiple times, we have been globally recognized as a "Great Place to Work" and we are proud to provide our employees with the flexibility to maintain a healthy work-life balance. We take our impact on the environment and our communities seriously and therefore focus on giving something back on a regular basis. We are committed to equality, equity, diversity and inclusion (EED&I) – a commitment that is fundamental to us. This includes appreciating different perspectives, creating an inclusive culture and treating all employees with dignity and respect.

At AbbVie, your individual contributions count – help us move mountains together. Be a part of our success, grow with us and accomplish more than you could have imagined. Sounds like the perfect career opportunity for you? We look forward to receiving your application! All you need is a complete CV – we will discuss everything else with you in person.

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, visithttps://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