404 Quality Control Manager jobs in Ireland

Company Overview

ODS (O'Dwyer Steel) is a leading structural steel engineering and fabrication business serving industrial, commercial, offsite and modular sectors across Ireland and the UK. We deliver a full service from design and fabrication to finishing and on-site installation, operating under CE marking to EN 1090 and ISO-certified management systems.

Position Overview

The Quality Control Manager owns product and process quality across the fabrication workshops ensuring compliance with EN 1090 and ISO 9001. You will lead inspection and test plans (ITPs), welding coordination support, materials traceability and non-conformance management, and will coach teams to deliver right-first-time outcomes. Working with Engineering/Detailing, Production, Coatings, Procurement and Project Management, you will maintain audit-ready records and a robust Factory Production Control (FPC) system.

ODS operate across three sites all based in Tipperary. The Quality control manager will ensure quality process flows are maintained at all sites – Mild steel fabrication facility, 3D modular assembly facility and our Modular fitout facility.

Key Responsibilities

• FPC & QMS leadership:
   Own the EN 1090 Factory Production Control (EXC up to 3/4 as applicable) and act as ISO 9001 management representative.
• Procedures & ITPs:
   Develop and enforce quality procedures, ITPs and hold points for cutting, fit-up, welding, modular 3d assembly, galvanising/painting, Modular final fitour and final inspection, Modular FAT.
• Welding quality:
   Manage WPS/WPQR libraries and welder qualifications; provide IWS/IWT/IWE-level coordination and visual inspection to ISO standards.
• Dimensional control:
   Ensure jigs/fixtures and surveys achieve tolerances per EN and drawings; oversee first-article and in-process inspections.
• NDT coordination:
   Plan and witness VT/MT/PT/UT; brief third-party NDT providers; review reports and close out actions.
• Materials & traceability:
   Verify EN certs, heat numbers and marking; maintain full traceability through cutting lists, parts and assemblies.
• Coatings & galvanising:
   Manage surface prep, DFT/adhesion checks and holiday testing; verify galvanising quality and vent/drain hole compliance.
• Calibration:
   Maintain the calibration system for gauges, torque tools, weld meters and measuring devices; quarantine non-conforming equipment.
• NCR/CAR & improvement:
   Lead NCR/CAR/8D, root-cause reviews and concessions; drive prevention through standard work and training.
• Supplier quality:
   Audit and approve steel/bolt/coating/galvanising suppliers; set clear QA requirements in POs; manage incoming inspection.
• Documentation & CE:
   Compile MDR/quality dossiers, DoP and EN 1090 documentation; ensure complete, accurate records for audits and client handover.
• Audits & KPIs:
   Run ISO 9001/EN 1090 internal audits; produce KPI dashboards; lead management reviews and improvement plans.
• Manage team of quality techninicians ensuring full qc checks carried out on all fabrications. Quality team checkers will report to the Quality Manager.
• Training & coaching:
   Maintain competence matrix; deliver toolbox talks on defects, inspection techniques and standards.
• Digital QA:
   Align weld maps, revisions and traceability in the EDMS/BIM workflow (e.g., Tekla outputs, barcode/QR); standardise templates/reporting.

Skills and Experience (Required):

• 7+ years' QA/QC experience in structural steel fabrication, including workshop inspection and site quality close-out.
• Deep knowledge of EN 1090-1/-2, ISO 9001 and (ideally) ISO 3834; fluent with welding symbols, tolerances and steelwork standards.
• Coatings knowledge with ICorr/NACE (or willingness to obtain) and practical DFT/adhesion/holiday testing experience.
• Strong root-cause capability (e.g., 8D, 5-Why) and a track record of reducing rework and non-conformances.
• Excellent communication, coaching and stakeholder skills; able to set standards and hold teams/suppliers accountable.
• Proficient with MS Office and comfortable with EDMS/BIM outputs and QA reporting tools.
• Right to work in Ireland; full, clean driving licence; willingness to visit suppliers and sites across Ireland/UK

Desirable

• ISO 9001 Lead Auditor qualification.
• Client-facing experience in regulated sectors (pharma, data centre, utilities) with stringent documentation demands.

What We Offer

• Competitive salary and benefits with professional development support (e.g., auditor, coating or welding certifications).
• Influential role improving quality outcomes across landmark industrial and modular projects.
• Stable, growth-oriented environment with modern facilities and ISO-certified systems.
• Supportive team culture and genuine ownership of the quality function.

1. JOB PURPOSE

Responsible for maintaining quality control processes, analyzing the results, and giving feedback and guidance to the product development and production team. In addition to overseeing stringent quality control measures, the QC Manager will also act as an integral part of the purchasing team, ensuring that purchased materials align with approved supplier lists and quality criteria while maintaining the highest standards of product quality and reliability.

1. DUTIES AND RESPONSIBILITIES

2. Liaises with Director of Operations, Head of Quality and Regulatory Affairs, Production Manager,

Project Managers, Process Scientist and Quality Assurance.

• Responsible for ensuring raw materials, intermediates, and manufactured products meet standard standards of quality, reliability, and performance.
• Ensure proper maintenance of detailed records encompassing quality tests, procedures, and established standards, facilitating a comprehensive repository that guarantees traceability and compliance within the quality control framework.
• Establish procedures and processes for sampling, recording, and reporting of quality data.
• Request quotes from suppliers for product specific materials or services.
• Carry out research to identify ways to reduce waste and maximize resources.
• Ensures that all production materials are purchased from suppliers that are listed on the Approved

Supplier List.

• Ensure manufacturing processes are in compliance with both national and international standards of production.
• Oversee and execute comprehensive quality control protocols to guarantee adherence to established standards and procedures within the organization.
• Provide strategic recommendations to company management aimed at enhancing and optimizing existing quality control processes for heightened efficiency and superior output quality.
• Supervise QC technicians to ensure they perform their duties in line with established quality

procedures.

• oversee and analyze the product development processes to promptly identify and address any

deviations or variances from established quality policies and standards.

• Approve compliant products and reject defective ones.
• Compile and present reports detailing quality control activities and findings to upper management

to provide transparent updates on the organization's adherence to quality standards and initiatives.

• Maintain proper records of quality test, procedures and standards.
• Develops and implements an electronic Quality Management System in compliance with

ISO13485, IVDR 2017/746 and FDA 21CFR820.

• Act as a Functional Manager.

• Other duties as defined by your manager a from time to time.

• QUALIFICATIONS

• A bachelor's degree in a related field; a graduate degree is recommended for advancement.

• 3 years experience within a similar role within a regulated industry
• Good communication skills for effective liaison and teamwork.
• Problem-solving skills, analytical skills, and attention to detail.
• Excellent organisational skills and the ability to work on several tasks or projects concurrently.
• Commercial acumen and an awareness of the business value of work undertaken.
• Presentation skills - for presenting ideas and findings to colleagues and customers.
• The ability to work well independently, with minimum supervision.

• Drive, enthusiasm, and self-motivation.

• WORKING CONDITIONS

• The work environment characteristics described here are representative of those an employee encounters while performing the essential functions of this job.

• Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.

• The noise level in the work environment is usually moderate.

• PHYSICAL REQUIREMENTS

• The physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of this job.

• The employee must occasionally lift and/or move up to 10 pounds. Specific vision abilities required

by this job include close vision, distance vision, peripheral vision, depth perception and ability to adjust focus.

The above job description is not intended to be an all-inclusive list of duties and standards of the position. Incumbents will follow any other instructions, and perform any other related duties, as assigned by their manager.

Job Type: Full-time

Pay: €55,000.00-€60,000.00 per year

Benefits:

• Bike to work scheme
• Company pension
• Employee assistance program
• On-site parking

Work authorisation:

• Ireland (required)

Work Location: In person

This job operates on a 16/5 cycle shift pattern. This job specification outlines the general responsibilities associated with the role of Manager QC Microbiology on the Amgen Manufacturing site. This role will be responsible for managing the QC Microbiology team and owning, facilitating, and undertaking activities pertaining to Microbiology within QC and Manufacturing. The successful candidate will focus on compliance, continuous improvement and implementing a lean culture and Right First Time (RFT) for QC Microbiology duties and testing, including release of commercial and global release testing. The role also represents the QC unit by liaising with internal and external stake holders.

The site is focused on continuous improvement of all work processes and practices and all colleagues are required to be flexible in this regard. This means that they may be asked to carry out additional work functions that are not described in this specification but are associated with their role. This role will be responsible for oversight of some analytical in-process methods and may require shift work depending on company needs.

Key Responsibilities:

• Supervision/Management of QC Microbiology team.
• Ensure the QC Microbiology area is operated in a safe manner.
• Overall responsibility for QC In process, Environmental Monitoring, Release and Stability testing and the associated test and laboratory documentation.
• Develop and maintain quality systems within the QC laboratories to ensure ongoing compliance to cGLP Compliance with Standard Operating Procedures and Registered specifications.
• Provide an effective and efficient QC service to operations by supervising, developing and coaching the QC team.
• Ensure timely completion of Laboratory Investigation Reports and deviations through the Deviation procedures.
• Issue trend reports on investigations, non-conformances and Environmental Monitoring and identify laboratory practices and procedures for further development/improvement.
• Keeps abreast of current Corporate and industry requirements and compliance trends as they pertain to laboratory operations and aseptic manufacturing.
• Approval of SOP's, trend data, investigations, non-conformances, validation protocols, reports, method validation/verifications and equipment qualifications.
• Participate in regulatory agency inspections as required.
• Plan and implement procedures and systems to maximise operating efficiency.
• Manage and contribute to the achievements of department productivity and quality goals.

Primary knowledge, skills, competencies and relevant experience Knowledge:

Broad technical knowledge within Microbiology and expanding knowledge of related disciplinary areas Recognizes and understands the cross-dependencies of the role and understands the impacts on the organization Enhances own knowledge through understanding business trends and objectives Knowledge of industry and business principles Understands the core business process and purpose of the functional area in Amgen's commercialization process Developing own project management techniques

Problem Solving:

Applies analytical skills to evaluate and interpret complex situations/ problems using multiple sources of information Creates new procedures and processes to drive desired results Handles diverse scope of issues that require evaluation of a variety of factors including current business trends

Autonomy:

Managerial/Supervisory experience with a proven record in a Supervisor/ Team Lead role Experience leading cross-functional teams is desirable Work is guided by operational and project objectives Manages multiple assignments and processes Independently determines approach to project May be responsible for specific programs and/or projects Independently develops solutions that are thorough, practical, and consistent with functional objectives

Contribution:

Contributes to work group/team by ensuring quality of tasks/services provided by self and others with a strong focus on RFT and Lean Provides training and guidance to others Extends capabilities by working closely with senior staff/experts within and outside the internal organization

Skills:

Lead with initiatives to identify and drive improvements Communication skills (verbal and written) at all levels Strong Technical writing skills for GMP documentation (e.g. investigations, procedures, change controls) Presentation skills Escalate issues professionally and in a timely basis and know when to escalate Decision Making skills – will be require to make decisions independently Teamwork, Coaching and motivating others Negotiation and Influence skills, Planning and organisation skills Investigation skills Demonstrated ability to interact with regulatory agencies Experience working with interdepartmental and cross functional teams and influencing decisions

Relevant experience:

Bachelor's degree in a Science related field is required. 6+ years of biopharmaceutical QC experience or related quality control or GMP laboratory experience in the pharmaceutical or medical device industry, with 2 – 3 years of specific Microbiology management experience desirable. Experience with regulatory compliance in cGMP manufacturing and testing of pharmaceutical products. Some analytical experience for oversight of analytical in-process methods would be an advantage. Possess key competencies to include planning/organisation, problem solving, communication, teamwork, flexibility, coaching and motivating. Proven experience of leading teams.

Avery Dennison Corporation (NYSE: AVY)
is a global materials science and digital identification solutions company. We are Making Possible products and solutions that help advance the industries we serve, providing branding and information solutions that optimize labor and supply chain efficiency, reduce waste, advance sustainability, circularity and transparency, and better connect brands and consumers. We design and develop labeling and functional materials, radio frequency identification (RFID) inlays and tags, software applications that connect the physical and digital, and offerings that enhance branded packaging and carry or display information that improves the customer experience. Serving industries worldwide — including home and personal care, apparel, general retail, e-commerce, logistics, food and grocery, pharmaceuticals and automotive — we employ approximately 35,000 employees in more than 50 countries. Our reported sales in 2024 were $8.8 billion. Learn more at

Avery Dennison is an equal opportunity employer

Please let us know if we can support you with reasonable accommodations throughout the application process by contacting our team via

We do not accept unsolicited referrals or resumes from any source other than directly from candidates
.

*
We are unable to offer sponsorship or relocation for this role
*

*This role is subject to right-to-work checks as per local employment laws*

Job Description

You will manage the quality function by providing work direction for quality engineers and inspectors and interact regularly with engineering, manufacturing and service functions to establish quality standards for raw material, work in process and finished products.

Primary Responsibilities and Essential Job Functions:

• Formulate a strategy to foster a high performance culture with quality right first time suitable for a world class medical device contract and legal manufacturer.
• Coaching and development of staff who support the quality function during the manufacturing process and driving the culture of quality awareness.
• Drive improvements to the quality system that ensures its suitability, adequacy, and effectiveness.
• Understand and ensure compliance with cGMP, ISO 13485, and FDA 21 CFR Part 820 regulations.
• Work closely with commercial and operations to build value with top 10 key accounts and engage with customer quality representatives directly. Implement strategies and tactics to drive short, medium and long-term innovation and improvement plans in the relentless pursuit of zero defects.
• Provide operational support related to defining accurate problem statements, issue resolution and problem solving, product quality/risk assessment, and product disposition.
• Assist in the investigation of non-conformances as required.
• Support investigation of product complaints and assignment of root cause determinations when required.
• Provide QA support in the review and approval of plant related validation protocols, reports, and change requests. Support Project Management Office in timely pursuit of progression of priority activities.
• Provide facility quality support and representation in new product development, scale up, design transfer, and facility validation activities.
• Represent quality and/or regulatory on core design change and new product development teams to ensure the design control process is followed effectively.
• Participate in the ISO 13485 certification process and regulatory inspection.
• Provide support in customer, supplier, and regulatory audits.
• Develop quality SOPs to ensure compliance.
• Adopt key enablers such as best practice, automation and ICT platforms that drive efficiency and improvements.
• Prepare reports on Key Quality Metrics, for monthly management meetings and management review.

Team management responsibilities:

• Primary Responsibilities and Essential Job Functions:
• Activity planning, co-ordination and deployment.
• -Defining roles, responsibilities and accountability.
• -Production support and monitoring.
• -Root cause analysis and problem solving
• -Cost of quality optimization.
• -Training and succession planning. Skills and training matrix
• -NCMRs, MBR, Deviation requests.
• -cGMP, cGLP, micro testing.
• Highlight any specifics around incoming / GRN, raws, sub-assembly, manufacturing, sterilisation, batch-release etc.

Qualifications

• Bachelor's degree in Engineering or scientific related field.
• A minimum of 4 years of experience in the medical device or pharmaceutical industry with at least 3 years of experience in regulatory compliance and quality systems.
• At least 4 years of experience in managing a team
• Thorough knowledge of ISO 13485 and 21CFR Part 820.
• Certified Quality Engineer (CQE) and/or Certified Quality Auditor (CQA) and/or Certified Manager of Quality/Operational Excellence (CMQ/OE).
• Experience handling multiple responsibilities with minimal direction.
• Strong written and verbal communication skills; strong presentation skills.
• Able to effectively work with various functions and levels within the organization.

Additional Information

What we can offer:

• Workplace Flexibility
• Structured learning and development
• Mentoring program
• Competitive total rewards

Who we are - Our Story:

Every voice. Every day
Eight Values
. One Team

Being open to every voice, every day, brings our value of diversity to life and makes Avery Dennison a vibrant and engaging place to be. We understand diversity and equal opportunities as enrichment for our future-oriented work. Across our diverse, global team, every voice makes us stronger. When we listen to and learn from each other, there is no limit to what we can achieve together. Each of us is unique, and we appreciate bringing together different personalities and talents.

Avery Dennison is an equal-opportunity employer. In the
EMEA region
, we have these
Employee Resource Groups
:

• EmpoWer
• focusing on the engagement, mentoring, and promotion of women
• Mental Health
• striving to provide a safe space for employees to discuss mental health issues in the workplace
• Unite
• supporting the LGBTQI+ and ally community in the EMEA region

To find out more about
all our employee resources groups globally
as well as our
Diversity, Equity & Inclusion
approach, please go to our Diversity and Inclusion pages in the About Us section of our website:

At Avery Dennison, we do what we love, and we love what we do - Just click here, and get to know us better:
Life @ Avery Dennison
(

)

Alliance Medical are delighted to announce we are now hiring a Radiopharmacy Quality Control Manager to lead our QC function. This is a key leadership role, ensuring all Radiopharmaceutical product meet the highest standard of quality, safety, and compliance before reaching patients.

This role offers a full time, 37.5 hours per week, permanent contract.

Closing date: Friday 19th September 2025

Overall Purpose
Ensure that radiopharmaceuticals are routinely tested for the required quality in accordance with the marketing authorisation, manufacturing licence, and the EU-GMP Guidelines. Ensure every batch manufactured by Alliance Medical Ireland is produced and tested before release to market. Responsible for managing a team of QC chemists, and for the continuous analysis of PET tracers with early production and distribution times.

Duties To Include

• Guarantee testing of raw materials, intermediates, finished products, containers, packaging, labelling materials and leaflets per written instructions and GMP.
• Approve test instructions, specifications and sampling plans (EU-GMP Ch. 4 & 6) and keep them current.
• Verify test instructions against dossier/CTA file and ensure compliance.
• Ensure results are documented.
• Sign and date test records to confirm compliant testing.
• Ensure compliant shelf-life labelling.
• Document and investigate all deviations.
• Approve or reject materials and intermediates.
• Decide on, contract and supervise external testing labs.
• Oversee maintenance and qualification of QC premises/equipment.
• Validate and periodically review analytical methods and critical tests.
• Organise personnel training.
• Monitor storage conditions for samples and standards.
• Notify authorities of material changes.
• Carry out trend analyses and QC-specific management duties.
• Responsible for the management of engaged and motivated QC chemists, effectively utilising internal resources and supports including induction, buddy system, performance management, delegation, career development, One-to-ones and training.
• Assist in developing and implementing standard operating procedures and training plans for the team.
• Recommend new processes to enhance operational effectiveness.
• Undertake tasks as directed by the site manager to ensure the project is delivered on time and on budget.
• Set clear objectives and fully train all new staff members and ensure all staff are trained in all aspects and duties required on site to ensure resilience during periods of staff leave.
• Record and maintain training competency checklist for new starters during training until all training is complete.
• Manage staff roster and annual leave/absence requests.
• Organise weekly and monthly staff meetings, compile minutes and agendas.

Duties With Head Of Quality Control & Qualified Persons

• SOP/GMP document control, dossier work, EHS compliance, clean-room monitoring, supplier oversight, validations, audits, complaints & recalls, etc.

Skills/Key Competencies & Qualifications

• Qualified Person (QP) status certified by HPRA or relevant regulatory authority.
• Completed scientific training plus = 1-year practical experience in nuclear medicine or (radio)pharmaceutical chemistry environment.
• Completed scientific/medical university degree.
• Leadership/Management qualification desirable.
• An understanding of and track record of implementing regulatory guidelines.
• Technically competent: high technical skill level.
• Excellent communication and people skills.
• Team leadership skills: to motivate and lead strong teams.

Qualities

• Excellent attention to detail.
• Excellent communication and leadership skills.
• Demonstrates initiative and highly motivated.
• Ability to work in a challenging environment with changing priorities.
• Flexibility and adaptability.
• Proven organisational skills.
• Evidence of teamwork/strong team player.

To be considered for this role you will be redirected to and must complete the application process on our careers page. To start the process, click the Apply button below to Login/Register.

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Would you like to join an international team working to improve the future of healthcare? Do you want to enhance the lives of millions of people? Grifols is a global healthcare company that since 1909 has been working to improve the health and well-being of people around the world. We are leaders in plasma-derived medicines and transfusion medicine and develop, produce and market innovative medicines, solutions and services in more than 110 countries and regions.

At Grifols, we believe that diversity adds value to our business, our teams, and our culture. We are committed to equal employment opportunities that foster an inclusive environment.

We're excited to invite you to lead our Quality Control (QC) Chemistry Laboratory team in our purification and aseptic filling facility at Grifols Worldwide Operations (GWWO). As
QC Chemistry Manager
, you will play a key role in ensuring high-quality laboratory testing of clean utility, raw material, in-process and final container materials, maintaining full compliance with current Good Manufacturing Practices (cGMP) and safety standards.

Key Responsibilities

• Management of the QC Chemistry team to carry out required chemistry, immunochemistry and protein testing as required
• Ensure QC testing of clean utility, raw material, in-process and final container testing is performed as per the production plan
• Manage integrity of Laboratory Data
• Ensure all methods are qualified/validated in line with site procedures and regulatory/compendial requirements
• Ensure all equipment is validated, maintained, calibrated, and requalified in line with site procedures and regulatory/compendial requirements
• Creation, review and update of test methods and SOPs to ensure all aspects of compliance are adhered to
• Drive and oversee process/product/OOS/deviation investigations
• Implementation of Corrective and Preventative Actions
• Maintain, monitor and report QC Chemistry metrics and KPIs
• Ensure training and development of QC Chemistry team members in conjunction with team development and goals via the performance management process
• Represent QC Chemistry in any regulatory, corporate or internal audits
• Ensure regular Quality interaction with other departments within GWWO and Grifols sister sites
• Support site quality activities, including but not limited to: Annual Product Quality Reviews (APQRs), recall activities, change control etc.
• Responsible for any projects impacting QC Chemistry such as Method Transfers, Process Improvement or Harmonisation Projects
• Keep Abreast of the latest developments from regulatory authorities in relation to Quality Compliance activities
• Manage the safety and performance of QC Chemistry in line with safety regulations and site procedures
• Perform additional duties as assigned
• Act as a delegate for activities performed by the QC Senior Manager for QC Chemistry activities

Knowledge & Skills

• Full understanding of relevant cGMP, quality and compliance regulations
• Experience with chromatography instrumentation and methods
• Experience with protein chemistry instrumentation and methods
• Method Transfer and qualification experience
• Understanding of pharmacopoeial requirements and methods
• Excellent communication skills at organisation, team and individual levels
• Demonstrated problem solving skills
• Strong decision making skills
• Strong presentation skills
• Ability to manage multiple projects to plan/budget
• Experience in developing analytical methods is desirable
• Experience with Statistical Process Control (SPC) is desirable
• Experience with Lab Management Systems & SAP is desirable

Qualifications

• BSc or equivalent in chemistry, biochemistry, pharmaceutical science or related field
• Minimum 3 years supervisory/management experience
• 8 years progressive experience as an individual contributor in a fast paced GMP Laboratory environment
• M.Sc. qualification is desirable but not essential

Our Benefits Include

• Highly competitive salary
• Group pension scheme - Contribution rates up to 7%
• Private Medical Insurance for the employee
• Ongoing opportunities for career development in a rapidly expanding work environment
• Succession planning and internal promotions
• Education allowance
• Wellness activities - Social activities eg. Golf, Padel, Summer Events

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.

Location: Grange Castle International Business Park, Grange, Co. Dublin, D22 K2R3
Learn more about Grifols

Within this role you will be responsible for the oversight of Quality Control support operations.

As a Manager within Quality Control a typical day might include, but is not limited to, the following:

• Maintaining oversight of QC equipment lifecycle activities (including procurement, installation, qualification, maintenance, and decommissioning)
• Providing direction to Managers and staff that support the equipment
• Ensuring equipment qualification and maintenance programs are aligned with regulatory agencies requirements, qualified and available for QC laboratory usage
• Interacting with QC partner groups to establish internal requirements for equipment
• Leading QC equipment validation / qualification efforts through partnering and interaction with QA Validation and IT groups
• Managing oversight of the preventive and corrective maintenance monitoring program
• Managing oversight of the QC external laboratories activities and performance monitoring of external testing laboratories
• Supervising the issuance and approval of Quality agreements and SLAs with the contract labs
• Verifying that the site Manufacturing licence and global procedures reflect current contract lab utilization
• Identifying and calling out issues at contract laboratories to QC leadership
• Sourcing, co-ordinating and project management of GMP activities relating to new contract lab introduction
• Travel may be required in support of external contract laboratory testing activities
• Performing personnel management functions including time sheet submissions, scheduling of vacations, personnel development, and performance evaluations
• Responsibility for equipment automation and associated projects

This Role Might Be For You If You

• Possess strong communication and interpersonal skills
• Demonstrate logical troubleshooting and problem-solving skills
• Have a detailed understanding of equipment qualification and maintenance activities and industry compliance norms
• Have the ability to communicate effectively with multiple partners
• Enjoy working in a fast-paced environment
• Demonstrate a collaborative and team-orientated approach

To be considered for this opportunity you should have a BA/BS in chemistry, biology or related field with 8+ years' proven experience preferably in the pharmaceutical or biotechnology industry, and previous supervisory or leadership experience.

Does this sound like you? Apply now to take your first step towards living the Regeneron Way We have an inclusive and diverse culture that provides comprehensive benefits, which often include (depending on location) health and wellness programs, fitness centers, equity awards, annual bonuses, and paid time off for eligible employees at all levels

Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company's business.

For roles in which the hired candidate will be working in the U.S., the salary ranges provided are shown in accordance with U.S. law and apply to U.S.-based positions. For roles which will be based in Japan and/or Canada, the salary ranges are shown in accordance with the applicable local law and currency. If you are outside the U.S, Japan or Canada, please speak with your recruiter about salaries and benefits in your location.

Please note that certain background checks will form part of the recruitment process. Background checks will be conducted in accordance with the law of the country where the position is based, including the type of background checks conducted. The purpose of carrying out such checks is for Regeneron to verify certain information regarding a candidate prior to the commencement of employment such as identity, right to work, educational qualifications etc.