Skip to content
CV Rocket
Get started
How it worksThe enginePricingBlogContactSign in

Open nowPosted today

Lead Tech, Operations

Merck813 open roles

Where
IRL - Meath - Dunboyne
Get the CV for this job

From $25 per CV, paid once. No subscription.

Your applicationOpen nowLead Tech, OperationsMerck · IRL - Meath - Dunboyne

  1. YouYes, apply to this one.

  2. CV RocketCV written for this posting.

  3. 25 readersRecruiter, hiring manager, skeptic. Round after round.

  4. CV RocketApplied on Merck's own form.

The reply lands in your private mailbox

3×more interviews than doing it yourself with ChatGPT.

The clock on this job

Early applications get read.

13.7% of postings close within 7 days. Measured by our own scanner across the market. Merck postings stay open a median of 16 days.

Share of postings closed within
  1. 2.3%1 day
  2. 4.8%3 days
  3. 13.7%7 days
  4. 22.1%14 days
  5. 37.6%30 days
  6. 59.1%60 days
This job: posted today

Merck median: 16 days open

The posting

Job Description

A fantastic opportunity has arisen for an Operations Lead Biotech Associate on the Cell Banking/Cell expansion team at our site in Dunboyne, Co. Meath.

Our facility in Dunboyne is a premier, state-of-the-art facility that enables and advances our best work. By integrating leading-edge technology with a dynamic, activity-based workspace, the facility supports seamless connection and collaboration within and across teams and functions. Our Dunboyne facility provides Biologics Drug Substance manufacturing for Clinical Supply, Registration, and Commercial Launch.

Job Purpose

The Operations Lead Biotech Associate is responsible for supporting end-to-end production operations within the specific Manufacturing IPT. This role involves taking ownership of activities within the assigned suite and unit operation, acting as a delegate for the shift lead when unavailable, and ensuring compliance with good manufacturing practices. The Operations Lead Biotech Associate will lead troubleshooting efforts, support continuous improvement projects, and maintain high standards of safety and GMP compliance.

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

  • Support end-to-end production operations within the specific Manufacturing IPT.
  • Act as a Unit Op Lead, take ownership of activities within the assigned suite and unit operation, and act as a delegate for the shift lead when unavailable.
  • Carry out and support assigned operations, delivering shift standard work through a team-based approach to batch progression.
  • Execute manufacturing processes according to established work instructions and Standard Operating Procedures (SOPs).
  • Run handover boards and provide key updates to shift leads for handover.
  • Act as the escalation point of contact (POC) for troubleshooting, task execution, problem solving, and continuous improvement (CI) projects. Support resolution of issues and delays and escalate unresolved issues to the shift manager or operations lead.
  • Document executed activities Right First Time (RFT), ensuring accountability and traceability of production records and compliance with good manufacturing practices.
  • Ensure Electronic Batch Record (EBR) and related documentation reviews are completed accurately. Confirm by the end of the shift that all activities are correctly completed, including real-time batch record, SAP Comet, and elogs reviews.
  • Author, review, and/or edit procedures and technical documents in accordance with cGMP requirements, including support for electronic batch records, sampling plans, work instructions, and SOPs.
  • Coach shift teams on RFT documentation and adherence to Right First-Time principles.
  • Maintain and support high standards of safety and Good Manufacturing Practice (GMP) compliance at all times. Identify and challenge opportunities to improve site safety and environmental programs.
  • Promote EHS leadership behaviours, engage employees at all levels on EHS issues, and visibly lead safety initiatives, including active involvement in safety forums.
  • Promote an environment where everyone speaks up for our culture of safety and looks out for one another.
  • Participate in safety walkdowns, internal audits, inspections, risk assessments, GEMBAs, and Go-Sees, and support implementation of agreed actions.
  • Support incident investigations and audits, including investigations arising from manufacturing documentation, and ensure improvement actions are implemented.
  • Coach and provide oversight on the shop floor to identify potential issues before they arise.
  • Lead by example through coaching, mentoring, and our company Production Systems (MPS) skill transfer.
  • Provide coaching on CAPAs, change actions, SOP updates, and training module development or revision for the assigned area or unit operation.
  • Actively participate in cross-functional manufacturing teams to advance projects, goals, and deliverables.
  • Lead approved projects and continuous improvement initiatives aligned with site strategies, and support site functional initiatives to improve compliance and operational efficiency.
  • Utilize real-time data analytics to inform decisions on value stream improvement initiatives.
  • Work as part of a multi-disciplined and dedicated process team where flexibility and teamwork are essential.
  • Maintain a high level of personal expertise and working knowledge of the manufacturing process and process equipment through continuous training and development.
  • Support maintenance, engineering, quality, or other colleagues as requested.
  • Use proactive recognition tools to recognize the teams and individuals you collaborate with.
  • Carry out other duties assigned by the Manager, including acting as a designee for the Operations Manager as required.

What skills you need

  • Bachelor’s degree in biotechnology, Chemistry, Biology, Pharmacy, or Process Engineering.
  • 5+ years’ experience in the biotech industry, including bulk manufacturing of pharmaceutical or biological components.
  • Familiarity with contamination control and batch release requirements.
  • Proficiency with Delta V, Pas X, and the use of automation in a manufacturing process.
  • Experience with various single-use technologies in a manufacturing environment.
  • Competence in troubleshooting and practical problem solving.
  • Ability to work independently and within a cross-functional team.

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. So, if you are ready to: Invent solutions to meet unmet healthcare needs, Impact the future by driving one of the world’s leading healthcare companies, and inspire your team to reach their full potential and push the boundaries of science and technology, please apply today.

This is site-based role and is 12/7 extended days (4 days on and 4 days off)

Additional location(s) Compensation Information:

Required Skills:

Autoclaving, Automation, Biotechnology, Biotechnology Manufacturing, Cell Culture Process Development, Good Manufacturing Practices (GMP), Liquid Chromatography (LC), Media Preparation, Production Management, Standard Operating Procedure (SOP)

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:

No relocation

VISA Sponsorship:

No

Travel Requirements:

No Travel Required

Flexible Work Arrangements:

Not Applicable

Shift:

1st - Day

Valid Driving License:

No

Hazardous Material(s):

na

Job Posting End Date:

11/26/2026

*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.

From $25, paid onceGet the CV for this job

What happens when you press

One press. We do the rest.

  1. A CV for this posting

    Written against Merck's own wording, from every piece of relevant proof in your profile.

  2. 25 readers review it

    Recruiter, hiring manager, skeptic and more read every draft, round after round. You get the best round.

    The review screen in CV Rocket: how each CV was read, round by round.

  3. We apply on Merck's form

    Our application engine gets through the hardest forms there are. Where a question needs you, AI suggests the best answer. Don't want us applying from our IP addresses? Use our Chrome extension: we apply straight from your own browser.

    An application in CV Rocket: every answer filled in on the employer's form.

  4. Every reply, sorted

    Merck's answer lands in your private mailbox, and we classify it on arrival: interview, question, rejection.

    The CV Rocket inbox: each employer reply classified as an interview, an action or a rejection.

  5. Reply with AI

    AI helps you write the email, checks it and sends it. We show you whether the recruiter read it.

  6. The interview in your calendar

    Full integration with your calendar. The invitation goes straight in.

    An interview invitation in the CV Rocket inbox, added to the candidate's calendar.
Get the CV for this job

From $25 per CV, paid once. No subscription.

Why it works

3×

more interviews than doing it yourself with ChatGPT.

ChatGPT writes a CV and never learns what happened to it. We see every reply. For each CV we know:

  • How it was written, and how the review scored it
  • When we applied, and how long after the posting went up
  • Which posting, which company, which city
  • Who got the interview, and who heard nothing

That is how we know which CVs get called.

Get the CV for this job

From $25 per CV, paid once. No subscription.

The numbers game

More applications. More interviews.

Every application goes out with its own CV, written for that posting and paid once. Send enough of them and the law of large numbers finds you the job.

Get the CV for this job
By hand5–10
With CV Rocket100
applications a day

Nearby

Live postings like this one

Same employer first, then the same role elsewhere.

Before you press

Straight answers

Get the CV for this job

From $25 per CV, paid once. No subscription.

What if my background isn't good enough?

We make the most of the background you have. The CV uses every piece of relevant proof your profile holds, and one of the 25 readers reads your whole profile and flags what the CV left out.

Do you really apply for me?

Yes, on the employer's own form, the hardest ones included. Where a question needs you, you answer it right there and AI suggests the best answer. Don't want us applying from our IP addresses? Use our Chrome extension: we apply straight from your own browser.

Is it a subscription?

No. You pay once per CV, from $25. Every application goes out with its own CV, written for that posting.

One job. One CV.
Paid once.

Pick the posting you want. We write for it, apply for you and catch the reply.

Get the CV for this job

From $25 per CV, paid once. No subscription.