Manufacturing Biotech Associate

Job Description

A great opportunity has arisen for a Manufacturing Biotech Associate within our new state of the art single use multi-product biotech facility.

The Manufacturing Biotech Associate will work in a manufacturing self-directed shift team to deliver batch operations successfully, identify and resolve issues in order to allow the site to deliver for our patients in a culture that supports Quality, EHS, Learning and Continuous improvement. The biotech associate will drive to optimise and improve the processing activities through use of standard work and lean processing techniques while supporting operations team to consistently deliver on specific Key Performance Indicators (KPIs).

You will also be involved in setting up the single use equipment between runs, carrying out the production process according to world class GMP and EHS principles. At all times this role is focused on delivery to the patient through living the Dunboyne culture including a commitment to safety, focusing on right first time in everything we do and a concentrating on the engagement and development of self and peers.

What you will do:

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

• Complete COMMIT cards to highlight ways of working within our SDWT’s and Hubs and across our site that support our COMMIT culture.
• Provide immediate feedback to others at any time to reinforce good safety and improvement behaviours and acts.
• Execute commercial manufacturing processes according to established work instructions and Standard Operating Procedures (SOPs).
• Ensures that all assigned task related to manufacturing documentation support is in accordance with good manufacturing practices.
• Routinely talk about any safety issues you are concerned about.
• Work as part of a dedicated proess team where flexibility and teamwork are a key requirement.
• Generate SOPs/ Work Instructions (WIs) to ensure compliance with regulatory standards.
• Adhere to Right First-Time principles.
• Provide assistance and/or support maintenance, engineering, quality or other colleagues as requested.
• Escalate issues as appropriate to manager/designee.
• Maintain a high level of personal expertise and working knowledge of all aspects of the manufacturing process and process equipment through continuous training and development.
• Liaise with other groups and individuals to ensure planning of tasks is effective and linked into the manufacturing process plan and site schedule.
• Challenge and identify improvements to the safety and environmental programmes on site.
• Celebrate with use of proactive recognition tools that inspire teams and individuals you collaborate with.
• Take part in shift handovers and tier 1 meetings, raising concerns or issues promptly and providing options for resolutions.
• Act as an ERT during emergency situation if trained.

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

• Level 7 qualification in a science/engineering or equivalent work experience.
• 1 to 3 years’ experience in the biotechnology and/or pharmaceutical industry or equivalent.
• Experience in a highly regulated pharmaceutical manufacturing environment would be desirable.
• Downstream or Chromatography experience is preferred.
• Ability to work as part of a shift team and on own initiative in a constructive manner.
•  Ability to think logically and be proactive under pressure.
• Flexible and self-motivated.

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.

So, if you are ready to:

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

Required Skills:

Accountability, Accountability, Analytical Problem Solving, Cell Cultures, Communication, Computer Literacy, Corporate Productions, Data Entry, Equipment Maintenance, GMP Compliance, GMP Documentation, Good Manufacturing Practices (GMP), Key Performance Indicators (KPI), Lean Management, Mammalian Cell Culture, Manufacturing Compliance, Manufacturing Documentation, Manufacturing Operations, Manufacturing Processes, Manufacturing Quality Control, Media Preparation, Operations Management, Process Improvements, Production Processes, Regulatory Compliance {+ 3 more}

Preferred Skills:

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):

Job Posting End Date:

11/24/2025

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