Senior Bioprocess Associate

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Senior Bioprocess AssociateApply remote type Not Applicable locations IRL - Dublin - Swords (Biotech) time type Full time posted on Posted 7 Days Ago time left to apply End Date: August 25, 2025 (5 days left to apply) job requisition id R359755

Job Description

An amazing opportunity has arisen for a Senior Bioprocess Associateto join our dynamic Upstream Operations team at Dublin Biotech Swords. In this pivotal role, you will oversee the entire manufacturing process of large-scale drug substances at our innovative facility.

As a Bioprocess Associate, you will be at the forefront of operations, responsible for preparing, operating, and monitoring state-of-the-art equipment. Your expertise will ensure that all tasks—ranging from but not limited to cleaning and validation to in-process testing and essential maintenance—are executed in strict accordance with current Good Manufacturing Practices (cGMP

What you will do:

Bring energy, knowledge, innovation, and leadership to carry out the following:

• Foster a safety-focused culture and always ensure a compliant cGMP work environment.
• Support Operations team to consistently deliver on specific area Key Performance Indicators (KPI), e.g. Health & Safety metrics, Production Plan, Operational Improvements and Efficiency compliance and team training.
• Execute commercial manufacturing processes according to established work instructions and Standard Operating Procedures.
• Generate SOPS/Electronic Batch Records.
• Embed Lean tools and principles throughout all areas of work.
• Assist maintenance, engineering, quality, and other teams as needed.
• Coordinate with various teams to ensure effective task planning aligned with the manufacturing process.
• Escalate issues when necessary.
• This is a shift-based role (24/7 Operations). 12-hour shift on a 4- cycle schedule (7am-7pm/7pm-7am)

Qualifications

In order to excel in this role, you will more than likely have:

• Minimum of a Level 7 qualification in a science or engineering discipline.
• A level 6 with a minimum of 3 years' experience in a GMP Manufacturing requirement shall be deemed equivalent.
• Euthanistic team-player capable of working both independently and collaboratively within an energetic, fast-paced environment that demands flexibility and initiative.
• Able to collaboratively across divergent functions and with diverse stakeholders.
• Proficiency in troubleshooting and strong critical thinking skills.
• Excellent communication skills.
• Experience in the biopharmaceutical sector or related manufacturing industries.
• Experience with manufacturing control systems, including Delta V, MES, SAP, LIMs.
• Capable of handling multiple tasks simultaneously.
• Applicants must be legally eligible to work in Ireland

As a company, we are committed to 'Inventing for Life' in all that we do. We keep the patient at the very heart of all that we do and strive to find solutions and treatments for some of the world's most challenging healthcare needs.

As an equal opportunity employer, we are proud to be a company that embraces the value of bringing diverse, talented, and committed people together. Please don't hesitate to contact the Talent Acquisition Advisor assigned to this role should you need any support during our recruitment process.

We are committed to flexible working where possible, and this is why our Company has introduced a new hybrid working model for office-based colleagues around the world.

Please feel free to speak to us about what flexibility means to you during your application or click on the link to find out more about our hybrid working model

So, if you are ready to:

Invent solutions to meet unmet healthcare needs, please apply today.

Current Employees apply HERE

Current Contingent Workers apply HERE

Search Firm Representatives Please Read Carefully
Merck & Co., Inc., Rahway, NJ, USA, also known as Merck Sharp & Dohme LLC, Rahway, NJ, USA, does not accept unsolicited assistance from search firms for employment opportunities. All CVs / resumes submitted by search firms to any employee at our company without a valid written search agreement in place for this position will be deemed the sole property of our company. No fee will be paid in the event a candidate is hired by our company as a result of an agency referral where no pre-existing agreement is in place. Where agency agreements are in place, introductions are position specific. Please, no phone calls or emails.

Employee Status:

Regular

Relocation:

VISA Sponsorship:

Travel Requirements:

Flexible Work Arrangements:

Not Applicable

Shift:

Valid Driving License:

Hazardous Material(s):

Required Skills:

Applied Engineering, Applied Engineering, Aseptic Operations, Biological Sciences, Bioprocess Engineering, Cleanroom Operations, Data Entry, Equipment Maintenance, GMP Compliance, Good Manufacturing Practices (GMP), Internal Auditing, Key Performance Indicators (KPI), Laboratory Processes, Liquid Chromatography (LC), Maintenance Processes, Manufacturing Processes, Mechatronics, Media Preparation, Physical Abilities, Process Control, Process Improvements, Production Operations, Production Planning, Production Scheduling, Regulatory Compliance Consulting {+ 5 more}

Preferred Skills:

Job Posting End Date:

08/25/2025

*A job posting is effective until 11:59:59PM on the day BEFOREthe listed job posting end date. Please ensure you apply to a job posting no later than the day BEFORE the job posting end date.

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