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- Equipment Preparation: Perform Cleaning-In-Place (CIP) operations on mobile tanks, reactors, and hoses.
- Conduct Steam-In-Place (SIP) procedures on clean bulk tanks.
- Daily Checks & Equipment Setup: Execute daily inspections of analytical equipment and room pressures.
- Perform filter integrity testing.
- Equipment & Parts Handling: Set up clarification filters for the purification process.
- Conduct manual cleaning and verification sampling of small parts.
- Operate autoclave runs and part washer runs.
- Assemble and prepare equipment.
- Compliance & Safety: Adhere to departmental, corporate, industrial, health & safety, and regulatory requirements.
- Maintain a safe and clean work environment in accordance with cGMP and standard operating procedures.
- Inventory Management: Perform regular stock checks of all materials.
- Transfer materials from non-classified areas to Grade C/D areas.
- Conduct pasteurisation cycles for filled albumin bags.
- Clean pasteuriser baths.
- Transfer pasteurised bags to drying and caging areas.
- Coordinate handover of pasteurised bags to the warehouse team for incubation.
- Albumin Purification: Set up ultrafilters for diafiltration and concentration.
- Perform sterile filtration of formulated products.
- Prepare buffers and stabilizers.
- Work independently to maintain production targets.
- Utilize MRP systems for batch-specific transactions and documentation.
- Equipment Setup & Operation: Responsible for equipment setup and operation in a biologics processing environment for plasma-derived pharmaceuticals.
- Class A/B gowning qualified.
- Operate support fill equipment.
- Perform filter integrity testing.
- Prepare chemical solutions for production use.
- Facility Housekeeping: Perform minor cleaning, keep work and production areas neat and free from clutter.
- Conduct sanitization per procedures, document sanitization, mop, disinfect floors, walls, and equipment.
- Documentation: Maintain real-time documentation during production runs and accurate records/logs.
- Monitor and operate various computer control systems for production activities (e.g., SCADA).
- Validation Protocols & Reports: Write, review, and execute validation protocols and reports for equipment, utilities, processes, cleaning, temperature mapping, and equipment software.
- Ensure compliance with global and local quality and validation procedures/standards.
- Project Documentation: Generate and review project documentation (User Requirement Specifications, validation protocols, reports, etc.) and Standard Operating Procedures.
- Validation Activities: Support validation activities, including documentation review and hands-on execution (FAT, SAT, IQ, OQ, PQ) to ensure equipment meets current GMP requirements and industry standards.
- SITE VALIDATION MASTER PLAN: Maintain the SITE VALIDATION MASTER PLAN (VMP) and associated Project VMPs.
- Define the validation approach for each piece of equipment, system, process, and requalification requirements.
- Execute/coordinate re-validation activities as required.
Manufacturing Graduate Program - Dublin - Grifols, S.A

Description
**Grifols Manufacturing Graduate Rotation Program**
About Us:
Grifols is a global healthcare company that has been working to improve the health and well-being of people around the world since 1909. We are leaders in plasma-derived medicines and transfusion medicine, and we develop, produce, and market innovative medicines, solutions, and services in more than 110 countries and regions.
About the Role:
We are seeking highly motivated and talented individuals to join our 24-month Manufacturing Graduate Rotation Program at Grifols Worldwide Operations (GWWO). This program offers a wide variety of experiences across different areas within manufacturing, giving you the skills and knowledge to excel in your career.
The Program:
The program consists of three rotations, each lasting six months:
Rotation 1: Purification
Rotation 2: Filling
Rotation 3: Validation
What We Are Looking For:
We are looking for highly motivated and talented individuals who possess:
Qualifications:
Minimum BSc/BA/BEng in Science or Engineering Discipline.
Knowledge and Skills:
Excellent verbal and written communication skills in English.
Good analytical skills/mindset.
Strong technical writing skills.
Strong interpersonal skills with the ability to interact professionally at all levels.
Good organizational skills.
Flexibility and adaptability.
Task and results-focused mindset.
Why Join Our Program?
Participating in Grifols' 24-month Manufacturing Graduate Program offers numerous benefits, including:
Competitive Compensation:
Enjoy a competitive salary and benefits package that rewards your hard work and dedication.
Group Pension Scheme:
Contribution rates are (1.5% / 3%/ 5%/ 7%) and the company will match.
Comprehensive coverage for the employee.
Hands-On Experience:
Dive into real-world manufacturing tasks and projects, gaining practical skills that will set you apart.
Skill Development:
Continuously enhance your technical and professional abilities through structured rotations and training.
Mentorship:
Benefit from the guidance of experienced professionals who are committed to your growth and success.
Networking:
Build a robust professional network by collaborating with colleagues and industry experts.
Career Advancement:
Unlock future career opportunities within Grifols and the broader biotechnology industry.
Innovation:
Be part of a forward-thinking team that values innovative ideas and creative solutions.
Global Exposure:
Work in a diverse, global environment, gaining insights into different cultures and business practices.
Wellness Activities:
Engage in wellness programs to maintain a healthy work-life balance.
Social Activities:
Participate in social events specifically tailored for the graduate group.
Work-Life Balance:
Thrive in a supportive work environment that prioritizes your well-being and work-life balance.
Impact:
Contribute to meaningful projects that make a difference in the healthcare industry.
We understand that self-doubt can hold talented individuals back from applying for opportunities.
We encourage everyone who meets the qualifications to apply – we're excited to hear from you!
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