3 Manufacturing jobs in Mallow

Lecturer Manufacturing Engineering

Tralee, Munster Munster Technological University

Posted 2 days ago

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Job Description

This post will be filled on a two year fixed term contract basis and will be filled in accordance with the requirements of the Technological Universities Act 2018. Lecturer Manufacturing Engineering (Kerry Campus) Appropriate honours primary degree(s) (second class or higher) in an Engineering related discipline or equivalent. and (b)Three years relevant post qualification experience in the manufacturing sector i.e. three years relevant experience having gained the qualifications at 1(a) above Desirable Skills: Significant experience in programme design and development with/in industry. Significant experience in working in/with industry on collaborative projects. Significant experience in/with academic Industrial engagement. Experience in lean six sigma industrial process. Experience in a leadership capacity. Evidence of Continuing Professional Development. Appropriate post-graduate qualification (Masters/Phd). 2. Duties The Lecturer will play an active role in the academic direction of courses including teaching, research, academic assessment and academic administration. The appointee should carry out such duties as are assigned by management including but not limited to:- teaching such assigned classes as deemed appropriate by management of the University, day or evening, up to 560 hours per annum including supervision of post-graduate students where appropriate; carrying out assessment, monitoring and evaluation of examinations work and providing an academic and consultative support to students in their learning activities; providing academic input on existing and new courses and course development; engaging in research, consultancy and development work as appropriate; participating in committees appropriate to courses and meetings convened by management; maintaining appropriate records and making available information as required by management; engaging in promotion including student recruitment as appropriate; participating in development, implementation and maintenance of academic quality assurance arrangements; participating in appropriate activities necessary to the development of their department / school and the University; directing and supervising the work of Tutor/Demonstrator and taking academic responsibility for the academic standards of this work. The appointee shall carry out the lawful instructions of the President or Authorized Officer and comply with the requirements and regulations of the Minister for Further and Higher Education, Research, Innovation and Science. The performance of these duties will require attendance in addition to class contact hours during the normal working week. 3.Salary The salary scale as at 01/8/2025 for Lecturer per annum is: €68,253 - €105,605 4.Citizenship Requirement Candidates should note that eligibility to compete for posts is open to citizens of the European Economic Area (EEA) or to non-EEA nationals with a valid work permit. The EEA consists of the Member States of the European Union, United Kingdom along with Iceland, Liechtenstein and Norway. Swiss citizens under EU agreements may also apply. It is an offence under the Employment Permits Acts 2003 and 2006 for both an employer and an employee if a non-EEA National is in employment without an appropriate employment permit. Employment permit holders can only work for the employer named on the permit. . 5.The Interview Process If invited to interview, applicants will be assessed at the interview under the following criteria Qualifications Experience/Achievements to date Communications & Pedagogical Skills Professional & Personal Development/Potential Knowledge of and interest in Higher Education Sector Team Working and Organisational Skills In addition, candidates will be invited to make a short presentation the topic below: The development of industrial and Manufacturing Engineering engagement opportunities in MTU over the next 5 years 6.IMPORTANT NOTES Application Form: Please ensure that full information is given on qualifications etc and that the information is accurate and corresponds to the original transcript of qualifications. Please note that any misstatement will result in disqualification. Note the declaration to be ticked at the end of the application form. Screening and short-listing takes place only on the basis of information submitted on the official application form. There is an appeals process in place whereby applicants can appeal the decision of the screening process within 10 days of the letter advising them of the decision at the screening stage. Please ensure that those you nominate as referees are contacted by you and will be able to supply a reference without delay if requested. Further information on theUniversity is available on the website. Latest date for receipt of completed application forms to the Human Resources Office is 1.00 pm on Friday 19th September 2025 Applications received after the closing date will not be accepted. Appointments will be subject to Garda vetting. The University operates an online recruitment system. All applications must be made via the eRecruitment system. Interview: Interviews will be held in person in Tralee. The University regrets that it cannot pay expenses for candidates attending interviews for this post(s) or for taking up the position, if appointed. General: The information given in this document is of a general information nature only and should not be taken as contractual. The Human Resources Office, Munster Technology University, Tralee, Co Kerry Telephone: Web Site Email: MTU is an Equal Opportunities Employer
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API External Manufacturing: Technical Services and Manufacturing Scientist Peptide Advisor

Kinsale, Munster Lilly

Posted 16 days ago

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At Lilly, we unite caring with discovery to make life better for people around the world. We are a global healthcare leader headquartered in Indianapolis, Indiana. Our employees around the world work to discover and bring life-changing medicines to those who need them, improve the understanding and management of disease, and give back to our communities through philanthropy and volunteerism. We give our best effort to our work, and we put people first. We're looking for people who are determined to make life better for people around the world.
**Job Description**
Join the energetic and growing Active Pharmaceutical Ingredient - External Manufacturing Organization (API-EM) that delivers a diverse portfolio of medicines essential to our patients around the world. The API EM TS/MS Advisor will provide technical and scientific expertise within a dynamic external manufacturing environment. The Advisor is responsible for ensuring delivery of commercialization efforts including technical transfers, process validations, and process optimization for the peptide portfolio, including Mounjaro ( . This position requires comprehensive knowledge of the pharmaceutical industry, Good Manufacturing Practices (GMP), regulatory requirements, and the essential role scientists play in making medicine and creating real-world solutions.
**Key Objectives/Deliverables:**
+ Provide technical oversight and stewardship for peptide manufacturing processes, including synthetic processing steps and downstream purification.
+ Leads resolution of technical issues including those related to control strategy and manufacturing.
+ Employ excellent communication skills to manage internal and external relationships.
+ Build and maintain relationships with development and central technical organizations to influence process control strategies.
+ Ensure proper characterization of processes and products and ensure effective documentation of the process description, measures, acceptable ranges, and specifications (and the justification of these measures, acceptable ranges, and specifications).
+ Ensure that processes are compliant, capable, in control, and maintained in a validated or qualified state.
+ Optimize and execute site control strategies.
+ Successfully deliver on strategic initiatives.
+ Authors and provides guidance on Regulatory Submissions, IRs, and changes.
+ Influence and implement the network technical agenda and drive continuous improvement.
+ Maintaining peptide processes in a state of compliance with US and global regulations
+ Understanding the scientific principles required for manufacturing intermediates and drug substances, including the interaction of chemistry and equipment.
+ Understand the chemistry and stability of biomolecules.
+ Operate with 'Team Lilly' in mind - including coaching and mentoring of peers and other scientists.
**Basic Requirements:**
+ Ph.D. in scientific disciplines of Biochemistry, Chemistry, Chemical Engineering, Pharmacology, or related fields, or equivalent industry experience (8 years +).
+ Demonstrated experience and proficiency with pharmaceutical manufacturing and working knowledge of regulatory expectations.
**Additional Information**
+ Occasional travel required 5 - 15%.
**LOCATION:**
+ Indianapolis, IN or Kinsale, Ireland
Lilly is dedicated to helping individuals with disabilities to actively engage in the workforce, ensuring equal opportunities when vying for positions. If you require accommodation to submit a resume for a position at Lilly, please complete the accommodation request form ( ) for further assistance. Please note this is for individuals to request an accommodation as part of the application process and any other correspondence will not receive a response.
Lilly is proud to be an EEO Employer and does not discriminate on the basis of age, race, color, religion, gender identity, sex, gender expression, sexual orientation, genetic information, ancestry, national origin, protected veteran status, disability, or any other legally protected status.
Our employee resource groups (ERGs) offer strong support networks for their members and are open to all employees. Our current groups include: Africa, Middle East, Central Asia Network, Black Employees at Lilly, Chinese Culture Network, Japanese International Leadership Network (JILN), Lilly India Network, Organization of Latinx at Lilly (OLA), PRIDE (LGBTQ+ Allies), Veterans Leadership Network (VLN), Women's Initiative for Leading at Lilly (WILL), enAble (for people with disabilities). Learn more about all of our groups.
Actual compensation will depend on a candidate's education, experience, skills, and geographic location. The anticipated wage for this position is
$123,750 - $198,000
Full-time equivalent employees also will be eligible for a company bonus (depending, in part, on company and individual performance). In addition, Lilly offers a comprehensive benefit program to eligible employees, including eligibility to participate in a company-sponsored 401(k); pension; vacation benefits; eligibility for medical, dental, vision and prescription drug benefits; flexible benefits (e.g., healthcare and/or dependent day care flexible spending accounts); life insurance and death benefits; certain time off and leave of absence benefits; and well-being benefits (e.g., employee assistance program, fitness benefits, and employee clubs and activities).Lilly reserves the right to amend, modify, or terminate its compensation and benefit programs in its sole discretion and Lilly's compensation practices and guidelines will apply regarding the details of any promotion or transfer of Lilly employees.
#WeAreLilly
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Sr. Scientist Technical Services/Manufacturing Science API-EM

Kinsale, Munster Lilly

Posted 16 days ago

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Job Description

At Lilly, we unite caring with discovery to make life better for people around the world. We are a global healthcare leader headquartered in Indianapolis, Indiana. Our employees around the world work to discover and bring life-changing medicines to those who need them, improve the understanding and management of disease, and give back to our communities through philanthropy and volunteerism. We give our best effort to our work, and we put people first. We're looking for people who are determined to make life better for people around the world. **Organization Overview:** Join the energetic and growing Active Pharmaceutical Ingredient - External Manufacturing Organization (API-EM) that delivers a diverse portfolio of medicines essential to our patients around the world. The API-EM TS/MS (Technical Services / Manufacturing Science) Sr. Scientist will provide technical and scientific expertise within a dynamic external manufacturing environment. The Sr. Scientist is responsible for providing technical support to achieve the reliable and compliant manufacture of API drug substance at external contract manufacturing groups to predetermined global quality standards. This person interacts daily with a wide variety of people, primarily external partners team members and site management. The candidate will be responsible for process monitoring, response to issues, and improvements where necessary. A strong understanding of manufacturing principles and Lilly systems is required to ensure those same standards are applied to the external contract manufacturers. This is a Large Molecule (mAb and ADC) position. The position requires knowledge of cGMPs, applicable global regulatory manufacturing guidance, and the corporate/industry standards. The position requires working cross-functionally within the site and other functions to deliver on technical objectives. **Responsibilities:** + Provide technical oversight for monoclonal antibody and antibody drug conjugate manufacturing processes. + Leads resolution of technical issues including those related to control strategy and manufacturing. + Employ excellent communication skills to manage internal and external relationships. + Build and maintain relationships with development and central technical organizations. + Ensure proper characterization of processes and products and ensure effective documentation of the process description, measures, acceptable ranges, and specifications (and the justification of these measures, acceptable ranges, and specifications). + Ensure that processes are compliant, capable, in control, and maintained in a validated or qualified state. + Understand, justify and document the state of validation with data that evaluate the capability of the manufacturing process to meet its stated purpose. + Influence and implement the network technical agenda and drive continuous improvement. + Maintaining mAb and ADC processes in a state of compliance with US and global regulations + Understanding the scientific principles required for manufacturing intermediates and drug substances, including the interaction of chemistry and equipment. + Operate with 'Team Lilly' in mind - including coaching and mentoring of peers and other scientists. **Basic Requirements:** + Bachelors in scientific disciplines of Biotech, Chemistry, Biochemistry, Biology, Pharmacy, or Engineering (Biotech/Biochemistry strongly preferred) + 3+ years of demonstrated hands on working experience and proficiency with pharmaceutical manufacturing and working knowledge of regulatory expectations. **Additional Preferences:** + Strong understanding of regulatory requirements and their application in a manufacturing environment + Proficient in data management practices across manufacturing operations + Demonstrates adaptability, a collaborative mindset, and a positive attitude toward change + Proven ability to effectively communicate and influence across diverse technical and business teams + Skilled in managing and delivering complex, cross-functional initiatives + Demonstrated project management expertise with a track record of coordinating and executing multifaceted projects **Additional Information:** + Some travel (<25%) is required + Some off-shift work (night/weekend) may be required to support 24/7 operations. Lilly is dedicated to helping individuals with disabilities to actively engage in the workforce, ensuring equal opportunities when vying for positions. If you require accommodation to submit a resume for a position at Lilly, please complete the accommodation request form ( ) for further assistance. Please note this is for individuals to request an accommodation as part of the application process and any other correspondence will not receive a response. Lilly is proud to be an EEO Employer and does not discriminate on the basis of age, race, color, religion, gender identity, sex, gender expression, sexual orientation, genetic information, ancestry, national origin, protected veteran status, disability, or any other legally protected status. Our employee resource groups (ERGs) offer strong support networks for their members and are open to all employees. Our current groups include: Africa, Middle East, Central Asia Network, Black Employees at Lilly, Chinese Culture Network, Japanese International Leadership Network (JILN), Lilly India Network, Organization of Latinx at Lilly (OLA), PRIDE (LGBTQ+ Allies), Veterans Leadership Network (VLN), Women's Initiative for Leading at Lilly (WILL), enAble (for people with disabilities). Learn more about all of our groups. Actual compensation will depend on a candidate's education, experience, skills, and geographic location. The anticipated wage for this position is $64,500 - $167,200 Full-time equivalent employees also will be eligible for a company bonus (depending, in part, on company and individual performance). In addition, Lilly offers a comprehensive benefit program to eligible employees, including eligibility to participate in a company-sponsored 401(k); pension; vacation benefits; eligibility for medical, dental, vision and prescription drug benefits; flexible benefits (e.g., healthcare and/or dependent day care flexible spending accounts); life insurance and death benefits; certain time off and leave of absence benefits; and well-being benefits (e.g., employee assistance program, fitness benefits, and employee clubs and activities).Lilly reserves the right to amend, modify, or terminate its compensation and benefit programs in its sole discretion and Lilly's compensation practices and guidelines will apply regarding the details of any promotion or transfer of Lilly employees. #WeAreLilly
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