101 Quality Control jobs in Ireland
Quality Control Manager
Dublin, Leinster
Amgen
Posted today
Job Viewed
Job Description
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.
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.
This advertiser has chosen not to accept applicants from your region.
0
Quality Control Student
Dublin, Leinster
Takeda Pharmaceuticals
Posted 1 day ago
Job Viewed
Job Description
By clicking the "Apply" button, I understand that my employment application process with Takeda will commence and that the information I provide in my application will be processed in line with Takeda's Privacy Notice and Terms of Use . I further attest that all information I submit in my employment application is true to the best of my knowledge.
**Job Description**
**_JOB PURPOSE:_**
The position will require a basic knowledge of analytical techniques, e.g. IR, UV, HPLC and GC. The position will require knowledge of GMP/GDP requirements and the principles of continuous improvement.
**_RESPONSIBILITIES_** **:**
**Quality Control Laboratory:**
+ Test laboratory samples including raw materials, packaging components, API, validation, stability and purified water.
+ Perform calibration activities and / or checks associated with QC equipment.
+ Ensure that the laboratory is kept clean, tidy and safe at all times and participate in the QC lab 5S program.
+ Participate in QC projects as required.
**General:**
+ Adhere fully to all company safety policies, procedures and regulations and work with others to promote a strong awareness of safety within the plant.
+ Participate fully in any cross functional training initiatives.
+ Drive and promote the corporate values of Takeda-ism within the workplace.
+ Ensure that Accident Reports / Near Miss Forms are completed in a timely manner after an event.
+ Ensure timely completion of all SOP, reading, training and assessment.
+ Other duties as required and as directed by the Manager, Finance or other officer appointed by the Board of Directors.
+ Correct use of personal protective equipment (PPE)/garbing requirements.
**_EDUCATIONAL REQUIREMENTS:_**
+ **Studying towards 3rd Level Honours Degree in Science or other relevant course.**
**_RELEVANT EXPERIENCE/CRITERIA:_**
+ Technical experience in a wide range of analytical techniques e.g. wet chemistry, HPLC and GC analysis, particle size analysis.
+ Good organisational, communication, interpersonal and report writing skills.
+ Good computer skills and knowledge of the Microsoft Office suite of software.
+ Ability to adapt to changing priorities.
Ability to work within a team.
**Locations**
Grange Castle, Ireland
**Worker Type**
Employee
**Worker Sub-Type**
Paid Intern (Fixed Term) (Trainee)
**Time Type**
Full time
**Job Description**
**_JOB PURPOSE:_**
The position will require a basic knowledge of analytical techniques, e.g. IR, UV, HPLC and GC. The position will require knowledge of GMP/GDP requirements and the principles of continuous improvement.
**_RESPONSIBILITIES_** **:**
**Quality Control Laboratory:**
+ Test laboratory samples including raw materials, packaging components, API, validation, stability and purified water.
+ Perform calibration activities and / or checks associated with QC equipment.
+ Ensure that the laboratory is kept clean, tidy and safe at all times and participate in the QC lab 5S program.
+ Participate in QC projects as required.
**General:**
+ Adhere fully to all company safety policies, procedures and regulations and work with others to promote a strong awareness of safety within the plant.
+ Participate fully in any cross functional training initiatives.
+ Drive and promote the corporate values of Takeda-ism within the workplace.
+ Ensure that Accident Reports / Near Miss Forms are completed in a timely manner after an event.
+ Ensure timely completion of all SOP, reading, training and assessment.
+ Other duties as required and as directed by the Manager, Finance or other officer appointed by the Board of Directors.
+ Correct use of personal protective equipment (PPE)/garbing requirements.
**_EDUCATIONAL REQUIREMENTS:_**
+ **Studying towards 3rd Level Honours Degree in Science or other relevant course.**
**_RELEVANT EXPERIENCE/CRITERIA:_**
+ Technical experience in a wide range of analytical techniques e.g. wet chemistry, HPLC and GC analysis, particle size analysis.
+ Good organisational, communication, interpersonal and report writing skills.
+ Good computer skills and knowledge of the Microsoft Office suite of software.
+ Ability to adapt to changing priorities.
Ability to work within a team.
**Locations**
Grange Castle, Ireland
**Worker Type**
Employee
**Worker Sub-Type**
Paid Intern (Fixed Term) (Trainee)
**Time Type**
Full time
This advertiser has chosen not to accept applicants from your region.
1
Quality Control Student
Wicklow, Leinster
Takeda Pharmaceuticals
Posted 3 days ago
Job Viewed
Job Description
By clicking the "Apply" button, I understand that my employment application process with Takeda will commence and that the information I provide in my application will be processed in line with Takeda's Privacy Notice and Terms of Use . I further attest that all information I submit in my employment application is true to the best of my knowledge.
**Job Description**
**JOB DESCRIPTION**
**_JOB TITLE:_** **Quality Control Student**
**_REPORTS TO:_** **Quality Control Team Leader**
JOB PURPOSE:
The student will gain experience working in a laboratory in a pharmaceutical manufacturing company. Reporting to the QC Team Leader the role of QC Student requires dedication to the principle of cGMP, and adherence to Standard Operating Procedures.
RESPONSIBILITIES:
+ To observe GLP/cGMP at all time.
+ Testing of all laboratory samples including Raw Materials, Packaging Components, Product Validation, Stability, Environmental and OH.
+ Performance of laboratory tests as per written procedure or as per pharmacopoeia.
+ Recording of analytical results accurately.
+ Operation, maintenance and calibration of laboratory instruments.
+ To maintain written training records.
+ To ensure that the laboratory is kept clean, tidy and safe at all times.
+ To report any non-conformance, instrument malfunction, accident or other abnormal occurrence to immediate superior.
+ Ordering, receiving and controlling laboratory chemicals, reagents and consumables.
+ Receiving and controlling test samples.
**_GENERAL RESPONSIBILITIES:_**
+ Participate fully in any cross functional training initiatives.
+ Drive and promote the corporate values of Takeda-ism within the workplace.
+ Actively foster, in cooperation with other TIL staff, an ethos and culture of safety awareness where safety is accepted as an integral part of the overall business.
+ Ensure that Accident Reports / Near Miss Forms are completed in a timely manner after an event.
+ Ensure timely completion of all SOP, reading, training and assessment.
+ Other duties as required and directed by the relevant Manager or other Officer appointed by the Board of Directors.
**_EDUCATIONAL REQUIREMENTS:_**
+ Studying towards 3rd Level Degree in Science or other relevant course.
**_RELEVANT EXPERIENCE:_**
+ Experience working in a laboratory environment.
**_SKILLS/COMPETENCIES:_**
+ Have good organisational, communication, interpersonal and report writing skills.
+ Is adaptable to changing priorities.
**Locations**
Bray, Ireland
**Worker Type**
Employee
**Worker Sub-Type**
Paid Intern (Fixed Term) (Trainee)
**Time Type**
Full time
**Job Description**
**JOB DESCRIPTION**
**_JOB TITLE:_** **Quality Control Student**
**_REPORTS TO:_** **Quality Control Team Leader**
JOB PURPOSE:
The student will gain experience working in a laboratory in a pharmaceutical manufacturing company. Reporting to the QC Team Leader the role of QC Student requires dedication to the principle of cGMP, and adherence to Standard Operating Procedures.
RESPONSIBILITIES:
+ To observe GLP/cGMP at all time.
+ Testing of all laboratory samples including Raw Materials, Packaging Components, Product Validation, Stability, Environmental and OH.
+ Performance of laboratory tests as per written procedure or as per pharmacopoeia.
+ Recording of analytical results accurately.
+ Operation, maintenance and calibration of laboratory instruments.
+ To maintain written training records.
+ To ensure that the laboratory is kept clean, tidy and safe at all times.
+ To report any non-conformance, instrument malfunction, accident or other abnormal occurrence to immediate superior.
+ Ordering, receiving and controlling laboratory chemicals, reagents and consumables.
+ Receiving and controlling test samples.
**_GENERAL RESPONSIBILITIES:_**
+ Participate fully in any cross functional training initiatives.
+ Drive and promote the corporate values of Takeda-ism within the workplace.
+ Actively foster, in cooperation with other TIL staff, an ethos and culture of safety awareness where safety is accepted as an integral part of the overall business.
+ Ensure that Accident Reports / Near Miss Forms are completed in a timely manner after an event.
+ Ensure timely completion of all SOP, reading, training and assessment.
+ Other duties as required and directed by the relevant Manager or other Officer appointed by the Board of Directors.
**_EDUCATIONAL REQUIREMENTS:_**
+ Studying towards 3rd Level Degree in Science or other relevant course.
**_RELEVANT EXPERIENCE:_**
+ Experience working in a laboratory environment.
**_SKILLS/COMPETENCIES:_**
+ Have good organisational, communication, interpersonal and report writing skills.
+ Is adaptable to changing priorities.
**Locations**
Bray, Ireland
**Worker Type**
Employee
**Worker Sub-Type**
Paid Intern (Fixed Term) (Trainee)
**Time Type**
Full time
This advertiser has chosen not to accept applicants from your region.
2
Quality Control Analyst
AbbVie
Posted 3 days ago
Job Viewed
Job Description
Company Description
AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas - immunology, oncology, neuroscience, and eye care - and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at Follow @abbvie on X, Facebook, Instagram, YouTube, LinkedIn and Tik Tok ( .
Job Description
We are recruiting Laboratory Analyst (12 months) to join our diverse team in Cork. ( Shift Position)
Are you intrigued? Do you want to learn more?
+ Execute analysis of raw materials, in-process material, and finished product in compliance with schedule.
+ Complete analysis in accordance with SOP and standard methods.
+ Execute analysis of water, cleaning samples etc as required.
+ Execute calibrations and PM of equipment as required to ensure equipment is appropriate for use for analysis.
+ Co-ordinate maintenance schedules with external suppliers to ensure compliance with schedule and in house procedures.
+ Preparation of all solutions, reagents etc. associated with analysis.
+ Execute stock control on laboratory consumables including reagents, solvents to ensure there is adequate supply to execute tasks. Complete purchase orders as required and manage materials on receipt.
+ Participate in the preparation of QC documents including SOPs, specifications, methods.
+ Participate in training and development activities to ensure that new technologies are applied and that skill level is developed.
+ Execute validation studies and transfer studies to ensure equipment, methods and personnel are appropriately qualified.
+ Participation in QC and site projects by representing QC so as to provide an appropriate service to other departments
+ Ensure QC activities are executed in line in in-house procedures and in compliance with requirements of cGMP.
+ Ensure QC activities are executed in line with safety requirements and good laboratory practice.
+ Keep work area clean and tidy.
+ Keep up to date on regulatory development and standards by accessing in house library, accessing current Pharmacopoeias etc.
+ Participation in investigations into failures, out of trends and out of specifications as required.
Qualifications
+ Degree in an analytical science/biochemistry/toxicology is preferred
+ Previous experience in a laboratory environment and direct experience of bioassays and related biological analytical techniques along with HPLC analysis would be an advantage
+ Analytical approach to tasks. Good organisation skills. Technical skills in analysis are important. Microsoft office suite ( excel / word)
Additional Information
AbbVie is an equal opportunity employer and is committed to operating with integrity, driving innovation, transforming lives and serving our community. Equal Opportunity Employer/Veterans/Disabled.
US & Puerto Rico only - to learn more, visit & Puerto Rico applicants seeking a reasonable accommodation, click here to learn more:
AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas - immunology, oncology, neuroscience, and eye care - and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at Follow @abbvie on X, Facebook, Instagram, YouTube, LinkedIn and Tik Tok ( .
Job Description
We are recruiting Laboratory Analyst (12 months) to join our diverse team in Cork. ( Shift Position)
Are you intrigued? Do you want to learn more?
+ Execute analysis of raw materials, in-process material, and finished product in compliance with schedule.
+ Complete analysis in accordance with SOP and standard methods.
+ Execute analysis of water, cleaning samples etc as required.
+ Execute calibrations and PM of equipment as required to ensure equipment is appropriate for use for analysis.
+ Co-ordinate maintenance schedules with external suppliers to ensure compliance with schedule and in house procedures.
+ Preparation of all solutions, reagents etc. associated with analysis.
+ Execute stock control on laboratory consumables including reagents, solvents to ensure there is adequate supply to execute tasks. Complete purchase orders as required and manage materials on receipt.
+ Participate in the preparation of QC documents including SOPs, specifications, methods.
+ Participate in training and development activities to ensure that new technologies are applied and that skill level is developed.
+ Execute validation studies and transfer studies to ensure equipment, methods and personnel are appropriately qualified.
+ Participation in QC and site projects by representing QC so as to provide an appropriate service to other departments
+ Ensure QC activities are executed in line in in-house procedures and in compliance with requirements of cGMP.
+ Ensure QC activities are executed in line with safety requirements and good laboratory practice.
+ Keep work area clean and tidy.
+ Keep up to date on regulatory development and standards by accessing in house library, accessing current Pharmacopoeias etc.
+ Participation in investigations into failures, out of trends and out of specifications as required.
Qualifications
+ Degree in an analytical science/biochemistry/toxicology is preferred
+ Previous experience in a laboratory environment and direct experience of bioassays and related biological analytical techniques along with HPLC analysis would be an advantage
+ Analytical approach to tasks. Good organisation skills. Technical skills in analysis are important. Microsoft office suite ( excel / word)
Additional Information
AbbVie is an equal opportunity employer and is committed to operating with integrity, driving innovation, transforming lives and serving our community. Equal Opportunity Employer/Veterans/Disabled.
US & Puerto Rico only - to learn more, visit & Puerto Rico applicants seeking a reasonable accommodation, click here to learn more:
This advertiser has chosen not to accept applicants from your region.
3
Manager, Quality Control
Sligo, Connacht
AbbVie
Posted 4 days ago
Job Viewed
Job Description
Company Description
AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas - immunology, oncology, neuroscience, and eye care - and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at Follow @abbvie on X, Facebook, Instagram, YouTube, LinkedIn and Tik Tok ( .
Job Description
We are looking for a QC Manager to join our team on our Manorhamilton Road site in Sligo. The QC Lab Manager is integral to managing a team responsible for QC testing, ensuring adherence to product specifications, quality, and safety goals. This role involves overseeing laboratory operations, including analytical testing for API and OSD products, and coordinating with internal teams to meet testing schedules.
Responsibilities:
+ Manage a lab team performing QC testing, ensuring compliance with data integrity policies and regulatory requirements.
+ Conduct and supervise all aspects of API and OSD analytical testing.
+ Ensure timely sampling, inspection, and testing, coordinating with teams for schedules and priorities.
+ Participate in internal and external audits and address audit findings.
+ Prepare technical reports, lead investigations, and implement CAPAs.
+ Provide training and support to lab team to achieve daily and long-term goals.
+ Present technical data to stakeholders to facilitate prompt decision-making.
+ Report to the Senior QC Manager.
Qualifications
+ M.Sc./B.Sc. in Chemistry or a related discipline.
+ Minimum 4 years of experience in people management within a pharmaceutical lab setting.
+ Strong knowledge of QA/QC operations, analytical testing for API and OSD.
+ Excellent presentation and technical report writing skills.
+ Strong communication and interpersonal skills, with a commitment to quality and compliance.
Additional Information
AbbVie is an equal opportunity employer and is committed to operating with integrity, driving innovation, transforming lives and serving our community. Equal Opportunity Employer/Veterans/Disabled.
US & Puerto Rico only - to learn more, visit & Puerto Rico applicants seeking a reasonable accommodation, click here to learn more:
AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas - immunology, oncology, neuroscience, and eye care - and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at Follow @abbvie on X, Facebook, Instagram, YouTube, LinkedIn and Tik Tok ( .
Job Description
We are looking for a QC Manager to join our team on our Manorhamilton Road site in Sligo. The QC Lab Manager is integral to managing a team responsible for QC testing, ensuring adherence to product specifications, quality, and safety goals. This role involves overseeing laboratory operations, including analytical testing for API and OSD products, and coordinating with internal teams to meet testing schedules.
Responsibilities:
+ Manage a lab team performing QC testing, ensuring compliance with data integrity policies and regulatory requirements.
+ Conduct and supervise all aspects of API and OSD analytical testing.
+ Ensure timely sampling, inspection, and testing, coordinating with teams for schedules and priorities.
+ Participate in internal and external audits and address audit findings.
+ Prepare technical reports, lead investigations, and implement CAPAs.
+ Provide training and support to lab team to achieve daily and long-term goals.
+ Present technical data to stakeholders to facilitate prompt decision-making.
+ Report to the Senior QC Manager.
Qualifications
+ M.Sc./B.Sc. in Chemistry or a related discipline.
+ Minimum 4 years of experience in people management within a pharmaceutical lab setting.
+ Strong knowledge of QA/QC operations, analytical testing for API and OSD.
+ Excellent presentation and technical report writing skills.
+ Strong communication and interpersonal skills, with a commitment to quality and compliance.
Additional Information
AbbVie is an equal opportunity employer and is committed to operating with integrity, driving innovation, transforming lives and serving our community. Equal Opportunity Employer/Veterans/Disabled.
US & Puerto Rico only - to learn more, visit & Puerto Rico applicants seeking a reasonable accommodation, click here to learn more:
This advertiser has chosen not to accept applicants from your region.
4
Quality Control Officer
Dublin, Leinster
Excel Recruitment
Posted 1 day ago
Job Viewed
Job Description
Excel Recruitment is seeking a Quality Control Officer for our client who specialises in the fresh produce and food distribution industry. This is an exciting opportunity to join a company with a proud heritage and a strong commitment to quality, innovation, and customer service. Job description Key Responsibilities and Duties Approve incoming materials by confirming specifications, conducting a visual and measurement test, and rejecting and returning unacceptable materials. Approve all finished products by confirming specifications and conducting required tests. Completion of daily records/ traceabilities Ensuring food safety is maintained throughout the process in accordance with BRC and Bord Bia standards. A lot of walking / standing / checking of products in different areas of the packhouse such as Goods-In, Packhouse & Goods-Out Qualifications/Experience Level 7 in food science or similar qualification. Experience in a quality role is desired but not essential. Key Behaviours Excellent attention to detail Excellent communication skills Ability to work on own initiative If you or anyone you know would be interested in this role, please apply with your CV or contact Ciaran #INDUST Skills: quality control officer quality control officer
This advertiser has chosen not to accept applicants from your region.
5
Manager Quality Control
Limerick, Munster
Regeneron Ireland DAC
Posted today
Job Viewed
Job Description
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. 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.
This advertiser has chosen not to accept applicants from your region.
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6
Quality control officer
Dublin, Leinster
Excel Recruitment
Posted today
Job Viewed
Job Description
Excel Recruitment is seeking a Quality Control Officer for our client who specialises in the fresh produce and food distribution industry.
This is an exciting opportunity to join a company with a proud heritage and a strong commitment to quality, innovation, and customer service.
Job description Key Responsibilities and Duties Approve incoming materials by confirming specifications, conducting a visual and measurement test, and rejecting and returning unacceptable materials.
Approve all finished products by confirming specifications and conducting required tests.
Completion of daily records/ traceabilities Ensuring food safety is maintained throughout the process in accordance with BRC and Bord Bia standards.
A lot of walking / standing / checking of products in different areas of the packhouse such as Goods-In, Packhouse & Goods-Out Qualifications/Experience Level 7 in food science or similar qualification.
Experience in a quality role is desired but not essential.
Key Behaviours Excellent attention to detail Excellent communication skills Ability to work on own initiative If you or anyone you know would be interested in this role, please apply with your CV or contact Ciaran #INDUST Skills: quality control officer quality control officer
This is an exciting opportunity to join a company with a proud heritage and a strong commitment to quality, innovation, and customer service.
Job description Key Responsibilities and Duties Approve incoming materials by confirming specifications, conducting a visual and measurement test, and rejecting and returning unacceptable materials.
Approve all finished products by confirming specifications and conducting required tests.
Completion of daily records/ traceabilities Ensuring food safety is maintained throughout the process in accordance with BRC and Bord Bia standards.
A lot of walking / standing / checking of products in different areas of the packhouse such as Goods-In, Packhouse & Goods-Out Qualifications/Experience Level 7 in food science or similar qualification.
Experience in a quality role is desired but not essential.
Key Behaviours Excellent attention to detail Excellent communication skills Ability to work on own initiative If you or anyone you know would be interested in this role, please apply with your CV or contact Ciaran #INDUST Skills: quality control officer quality control officer
This advertiser has chosen not to accept applicants from your region.
7
Manager quality control
Limerick, Munster
Regeneron Ireland DAC
Posted today
Job Viewed
Job Description
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.
#JOBSIEPR 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.
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.
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.
#JOBSIEPR 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.
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.
This advertiser has chosen not to accept applicants from your region.
8
Quality control officer
Dublin, Leinster
Excel Recruitment
Posted today
Job Viewed
Job Description
Excel Recruitment is seeking a Quality Control Officer for our client who specialises in the fresh produce and food distribution industry. This is an exciting opportunity to join a company with a proud heritage and a strong commitment to quality, innovation, and customer service. Job description Key Responsibilities and Duties Approve incoming materials by confirming specifications, conducting a visual and measurement test, and rejecting and returning unacceptable materials. Approve all finished products by confirming specifications and conducting required tests. Completion of daily records/ traceabilities Ensuring food safety is maintained throughout the process in accordance with BRC and Bord Bia standards. A lot of walking / standing / checking of products in different areas of the packhouse such as Goods-In, Packhouse & Goods-Out Qualifications/Experience Level 7 in food science or similar qualification. Experience in a quality role is desired but not essential. Key Behaviours Excellent attention to detail Excellent communication skills Ability to work on own initiative If you or anyone you know would be interested in this role, please apply with your CV or contact Ciaran #INDUST Skills: quality control officer quality control officer
This advertiser has chosen not to accept applicants from your region.
9