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Baker Tilly is a full-service accounting and advisory firm that offers industry specialised services in assurance, tax and advisory. With a focus on serving entrepreneurs, family-owned business, not-for-profits to public-listed companies, we help our clients plan for the future.
The Governance and Risk Team in Baker Tilly is a dynamic and fast expanding team within the Advisory Practice which prides itself in delivering high standards of professional services to clients. The services that we offer include:
· Internal audit outsourcing/ co-sourcing
· Enterprise risk management
· Forensic/ investigative reviews
· Business processes, strategy and management consulting
· ESG & sustainability consulting
We are the trusted advisor to many public listed companies in Singapore, Hong Kong and beyond. These clients span from family owned enterprises, multinationals, small and medium enterprises to not for profit organizations. They belong to varied industries and operate in many jurisdictions across the world. We consider the circumstances that are unique to every client and tailor our recommendations in a way that seeks to exceed the expectations of the client.
We are an equal opportunity employer, committed to diversity and inclusion, offering a work environment free from discrimination and harassment. Our dedication to employees, offering opportunities for challenges and growth, celebrating team and individual achievements, creates boundless opportunities for our employees to shine. A highly collaborative culture defines who we are and we strive to maintain a culture that facilitates sharing, candour, growth and encouraging our employees to become the best version of themselves.
Job Purpose
The IT Advisory Director/Senior Manager is responsible for managing and providing IT advisory services to a portfolio of international and local clients.
Responsibilities
Requirements
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Your new company
Continued market success has created a new opportunity for a Manager or Associate Director with an engineering or scientific background to join a Top 4 Accountancy Firm in Birmingham. This Firm offers global integrated professional services in an approach that combines intellectual leadership, industrial expertise, insight, consulting and problem-solving to help and support their clients. The UK Government provides tax incentives to businesses performing R&D and this is an opportunity to join a market leader in helping clients secure these incentives. This Firm can offer coaching and support for returners to refresh knowledge and skills to help transition back into the workplace.
Your new role
As the Associate Director/Manager within this Firm's R&D team, you will be client facing and lead the technical aspects of R&D claims, interviews and prepare documentation to support R&D claims. You will be working with senior technical and finance staff.
Key Duties:
What you'll need to succeed
The successful R&D professional will have a degree in Engineering or Science with post-grad experience of working in an engineering, manufacturing or scientific role. Experienced in leading project teams to both internal and external customers. Strong communication skills and be happy working within multidisciplinary teams.
What you'll get in return
You will have the opportunity to apply your technical knowledge across a wide range of areas and to help companies identify the R&D claims for these incentives. This R&D can involve activities starting from basic research, through to early stage new product & process development, industrial scale trials and ongoing process improvement activity across all areas of engineering and manufacturing. This Firm offers flexible working arrangements, an excellent salary package and benefits, along with outstanding career prospects.
What you need to do now
If you're interested in this role, click 'apply now' to forward an up-to-date copy of your CV, or call us now.
If this job isn't quite right for you but you are looking for a new position, please contact us for a confidential discussion on your career.
Hays Specialist Recruitment Limited acts as an employment agency for permanent recruitment and employment business for the supply of temporary workers. By applying for this job you accept the T&C's, Privacy Policy and Disclaimers which can be found at hays.co.uk
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As a Conference and Event Manager, you will help to curate impactful event experiences for audiences. This will help to support CLC’s targeted engagements with key stakeholders.
Through our research, partnerships, capability development and other work, CLC continually acquires and develops knowledge on how urban planning and governance can make cities more liveable and sustainable. Conference and event management at CLC focuses on the planning and organisation of the flagship World Cities Summit (WCS) and the Mayors Forum (MF), and other related CLC outreach activities. It is a creative and practical planning and organisational role that involves curating contents and programme, and actualising them into immersive events and platforms that deliver value to audience and stakeholders.
The World Cities Summit (WCS) seeks to equip and inspire a global community of city leaders and allied professionals dedicated to making our cities more liveable and sustainable. The ability of WCS to convene and engage this community of foreign government and city leaders, International Organisations, sponsors and other partners is critical to its success, impact and value.
Working with CLC Marcoms team and the appointed Event Organiser, the Conference and Event manager will support the organising of the CLC in-person and virtual events; especially the biennial WCS, and, in alternate years, the overseas MF. The role involves researching and proposing suitable themes, topics, formats, speakers and writers. Staff will work with global urban leaders and experts, as well professional editors, designers, video producers and event organisers to deliver world class, high impact content. The Conference and Event manager will support the WCS organising committee to deliver an engaging experience through quality content and programming.
CLC seeks candidates who will push beyond boundaries to deliver high value, impactful work to very senior local and global audience of Ministers, Mayors, CEOs and experts.
Requirements:
1. Relevant leadership experience in conference and event organisation, with an interest in urban issues.
2. Prior experience in a related sector such as architecture, planning, smart cities, urban governance, geography, economics and real estate would be advantageous.
3. Good communication skills and ability to engage with senior officials or business leaders.
4. Resourceful, self-motivated, team player and keen learner. Attention to detail and ability to handle multiple tasks and deadlines.
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Who are we?
Equinix is the world’s digital infrastructure company®, operating over 250 data centers across the globe. Digital leaders harness Equinix's trusted platform to bring together and interconnect foundational infrastructure at software speed. Equinix enables organizations to access all the right places, partners and possibilities to scale with agility, speed the launch of digital services, deliver world-class experiences and multiply their value, while supporting their sustainability goals.
A career at Equinix means you will collaborate on work that impacts the world and be surrounded by endless opportunities to learn new skills and grow in varied directions. We embrace diversity in thought and contribution and are committed to providing an equitable work environment that is foundational to our core values as a company and is vital to our success.
Job Summary
The Director, Partner Program directs a worldwide channel and partnership program strategy that expands global growth of the business by bringing in new strategic enterprise logos and partnerships. Drives growth by bringing an aggressive, solution-oriented, disciplined program approach and process to the Channel Organization.
Responsibilities
This director position is a global position responsible for overseeing the compliance and governance aspects of the channel partner program around the world, ensuring that the program aligns with the company’s strategic objectives, policies, and regulations and that partners comply with program policies
Duties of this role include developing and implementing compliance and governance frameworks, standards, and procedures for the channel program while aligning with local business guidelines and teams
Working cross functionally to communicate and enforce program policies inside of Equinix and with partner representatives
Monitoring and reporting on the performance and compliance of channel partners
Monitoring and enforcement of Equinix’s execution of the program
Articulating business requirements to business process and technical teams to support systems development for measuring and tracking key program elements
Conducting audits and assessments of channel partners
Providing training and education to channel partners and internal stakeholders on compliance and governance issues
Managing risks and resolving issues related to the channel program
Qualifications
Bachelor’s degree or higher in business, law, finance, or a related field
10+ years in channel program management, compliance, governance, or risk management
Knowledge of relevant laws and regulations affecting the channel program
Strong analytical, communication, leadership, and problem-solving skills
Proficiency in using various tools and systems for compliance and governance purposes
Exceptional oral and written communication and presentation skills required
Strong problem-solving and negotiation skills
Ability to conceptualize and sell ideas internally
Excellent time-management and multi-tasking abilities
Innovation and the ability to gain consensus is necessary
Ability to travel if needed and comply with the company’s travel policies
Equinix is an Equal Employment Opportunity and, in the U.S., an Affirmative Action employer. All qualified applicants will receive consideration for employment without regard to unlawful consideration of race, color, religion, creed, national or ethnic origin, ancestry, place of birth, citizenship, sex, pregnancy / childbirth or related medical conditions, sexual orientation, gender identity or expression, marital or domestic partnership status, age, veteran or military status, physical or mental disability, medical condition, genetic information, political / organizational affiliation, status as a victim or family member of a victim of crime or abuse, or any other status protected by applicable law.
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* Strong passion in Culinary and F&B industry
* Career growth from Mid to Senior Management level
* Stability and well-established organization
Job Responsibilities:
Job Requirements:
Interested applicant, to email resume linna.chua@recruithaus.com.sg or contct 62251232
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Director, Logistics Safety and Compliance
Home Office - Richmond, VA
About this job
CarMax is seeking a Director of Logistics Safety and Compliance to join the Logistics Team located at the Home Office in Richmond Virginia. As a safety-minded professional, the Director of Logistics Safety and Compliance is responsible for leading a broad range of programs and initiatives including safety, compliance, and training to ensure the prevention of injury and illness as well as continuous improvement and development of the Logistics Safety Program.
This role is designed to build, develop and implement safety and compliance programs to instill an unmatched safety culture and ensure regulatory compliance. This person is also accountable for influencing and persuading across various levels of the organization, including partners in Legal, Environment, Health and Safety and Executive Leadership. This role will lead a team accountable for content and subject-matter expertise for best-in-class training programs.
Vision, Strategic Leadership and Collaboration
Develops and implements strategic initiatives for the Central Support of Fleet Safety and Compliance.
Responsible for ensuring the broader CarMax organization, our nationwide fleet of 1300+ drivers and 600+ trucks, and our fleet partners are in regulatory compliance with DOT, FMCSA, and all regulatory agencies.
Develop and reinforce a safety culture that prevents accidents, incidents and injuries.
Provide oversight and strategic direction of a team responsible for developing safety and compliance-related training program content for all Logistics roles.
In partnership with Procurement, select and manage vendor partners to develop and execute a best in class safety, compliance and training program.
Manages multiple initiatives impacting the Logistics organization ranging from medium to enterprise wide in scope.
Team Development
Leverage existing and emerging technologies that will streamline processes and increase efficiency for the Logistics organization, thereby allowing associates to engage in more critical thinking activities and decision support
Promote a culture of high performance and continuous improvement that values learning and a commitment to quality.
Mentor and develop associates using a supporting and collaborative approach assigning accountabilities, setting objectives, establishing priorities and monitoring and evaluating results.
Engage with leadership and team members to develop opportunities for mentoring, cross-training, and development of team members with an eye toward building bench for succession within Logistics and the broader business.
What you will do: Essential Responsibilities
Safety Program Development:
Oversee the development, implementation, and management of comprehensive fleet safety programs to minimize accidents and injuries.
Establish safety policies and procedures, ensuring alignment with industry standards and regulations.
Regulatory Compliance:
Stay abreast of and ensure compliance with federal, state, and local regulations governing fleet operations.
Monitor changes in regulations and update policies and procedures accordingly.
Work closely with legal and regulatory affairs teams to address compliance issues.
Risk Management:
Identify potential risks within the fleet operations and implement strategies to mitigate them.
Ensure the team is appropriately investigating accidents and incidents, conducting root cause analyses and implementing corrective actions. Provide guidance and direction for critical or escalated cases as needed.
Manage relationships with insurance providers and participate in claims management.
Safety Performance Metrics:
Establish and monitor key performance indicators (KPIs) related to fleet safety.
Analyze data to identify trends and areas for improvement in safety performance.
Implement strategies to continuously improve safety metrics.
Driver Training and Certification:
Oversee driver training content to ensure compliance with safety regulations and industry best practices.
Implement certification programs for drivers, ensuring they meet necessary qualifications and standards.
Technology Integration:
Evaluate and capture requirements for technology solutions that enhance fleet safety and compliance.
Utilize telematics and other tools such as Electronic Data Logs, Driver App, In-Cab and Side-View cameras to monitor driver behavior and vehicle performance.
Audit and Inspection Management:
Oversee a team of Field Auditors and ensure regular audits and inspections of fleet operations are conducted to ensure compliance with safety standards.
Collaborate with internal and external auditors to address findings and implement corrective actions.
Budget Management:
Develop and manage the budget for the fleet safety and compliance department.
Optimize resource allocation to achieve safety and compliance goals efficiently.
Qualifications and Requirements
The requirements listed below are representative of the knowledge, skill, and/or ability required. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.
Master’s degree in an equivalent field preferred. Bachelor’s degree required.
7+ years Fleet Safety and Compliance experience
In depth knowledge of FMCSA and DOT 49 CFR and state regulations governing drivers and fleet requirements.
Ability to understand latest industry trends and their potential impact for CarMax.
Team management experience, strongly preferred.
Training design and delivery experience, preferred.
Retail management experience, preferred.
CarMax field experience, preferred.
About CarMax
CarMax disrupted the auto industry by delivering the honest, transparent and high-integrity experience customers want and deserve. This innovative thinking around the way cars are bought and sold has helped us become the nation’s largest retailer of used cars, with over 200 locations nationwide.
Our amazing team of more than 25,000 associates work together to deliver iconic customer experiences. Along the way, we help every associate grow their career and achieve their best, at work and in their community. We are recognized for our commitment to training and diversity and are one of the FORTUNE 100 Best Companies to Work For®.
Our Commitment to Diversity and Inclusion:
CarMax is committed to bringing together people from different backgrounds and perspectives, providing employees with a safe, welcoming, and inclusive work environment.
CarMax is an equal opportunity employer, and all qualified candidates will receive consideration for employment without regard to age, race, color, religion, sex, sexual orientation, gender identity, genetic information, national origin, protected veteran status, disability status, or any other characteristic protected by law.
Upon an applicant's request, CarMax will consider reasonable accommodation to complete the CarMax Job Application.
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Job Description
L’organisation du Service d’approvisionnement clinique mondial (GCS) est responsable de la gestion de la chaîne d’approvisionnement clinique intégrée de bout en bout pour l’ensemble du portefeuille d’essais cliniques de la division Recherche et développement. GCS est responsable de la planification, de l’approvisionnement, de l’étiquetage, de l’emballage et de la livraison des fournitures cliniques aux sites cliniques du monde entier. L'organisation GCS Planning est l'interface clé entre les équipes de développement clinique et les branches opérationnelles/exécutives au sein de l'entreprise.
Le Chef de projet des fournitures cliniques du programme (Program CSPM) sert de principal point de contact GCS au niveau du programme, représentant l'organisation de planification GCS auprès des clients internes et externes à GCS et sert de porte-parole principal de GCS dans les domaines cliniques et liés au développement. Travaillant de manière indépendante, le programme CSPM conçoit des plans stratégiques et opérationnels pour toutes les activités d'approvisionnement clinique associées aux études cliniques dans les composés/programmes qui leur sont attribués. Le titulaire du poste doit avoir une compréhension des concepts de développement de médicaments, de recherche clinique et/ou de chaîne d'approvisionnement clinique, ainsi que des compétences interpersonnelles avec une capacité démontrée à négocier avec les principaux groupes de parties prenantes et à générer/influencer les résultats dans un environnement dynamique.
Les principales activités comprennent, sans s’y limiter :
Activités générales :
Interagir avec diverses organisations en tant que représentant principal du programme de planification de GCS, comme Sciences cliniques et gestion des études (SCGÉ); Réglementation, CMC, Sciences pharmaceutiques, Développement de formulation et Qualité du développement mondial, au besoin, pour régler des questions liées à l’approvisionnement en médicaments.
Travailler directement dans le système SAP pour établir une prévision consolidée et visible pour tous les besoins des produits à l’étude (produits pharmaceutiques en vrac et produits finis cliniques).
Être responsable de l’utilisation des outils clés dans la planification et la gestion des fournitures cliniques pour les programmes qui lui sont attribués. Cela peut comprendre des plans sur Microsoft Project, des entrées sur Journaux des mesures, problèmes et risques, des outils prévisionnels (SAP), etc.
Appuyer la collecte de données sur la chaîne d’approvisionnement clinique afin de décrire la santé de l’entreprise et de déterminer les points à améliorer sur le plan opérationnel.
Être responsable du lancement des activités de planification des produits pharmaceutiques non commercialisés par notre compagnie pour les nouveaux protocoles.
Assumer un rôle de soutien ou de direction pour l’escalade des problèmes d’approvisionnement clinique vers le leadership de GCS (en tant que responsable des questions ou à l’appui d’autres GPSC qui soutiennent les programmes attribués).
Encadrer les nouveaux membres de l’équipe et soutenir le perfectionnement du personnel, au besoin.
Participer en tant que responsable principal des processus opérationnels ou expert dans un domaine d’expertise particulier.
Promouvoir et diriger les initiatives d’amélioration des processus d’affaires, au besoin.
Expérience et compétences requises :
Baccalauréat en sciences, en affaires ou dans une discipline connexe requis; maîtrise/maîtrise en administration des affaires, un atout.
Au moins huit années d’expérience en gestion de projets.
Au moins trois années d’expérience dans la planification, l’établissement de calendrier, la coordination et le traitement d’activités d’approvisionnement clinique, ou l’équivalent.
Compréhension des systèmes MRP et des principes de planification de la demande.
Compétences en matière d’organisation, de gestion du temps et de résolution de problèmes.
Axé sur les résultats et capacité éprouvée à mener à bien des projets de collaboration et à développer une expertise en la matière. Compétences exceptionnelles en communication écrite et verbale et en relations, grande intégrité personnelle, crédibilité et énergie.
Capacité à prioriser les tâches et les initiatives de manière appropriée pour atténuer les risques liés à l’approvisionnement.
Maîtrise avancée de Microsoft Excel, PowerPoint et Word.
Expérience de la gestion du changement et de la conduite d’initiatives d’amélioration des processus.
Expérience et compétences souhaitées :
Capacité démontrée à négocier, à résoudre des conflits, à participer à la prise de décisions, à établir des partenariats et à exercer une influence dans l’ensemble des domaines fonctionnels et des organisations.
Excellente connaissance de la gestion de projets et de la gestion des relations avec les clients cliniques.
Connaissance des processus et des procédures de développement, de production, de distribution, d’expédition, de destruction et de rapprochement des médicaments.
Connaissance de la gestion des commandes, des opérations de la chaîne d’approvisionnement et du contrôle documentaire.
Expérience de la supervision d’équipes
Déplacements à prévoir : moins de 10 %
Conformément à la Stratégie de milieu de travail hybride de notre entreprise, ce poste sera exécuté au moyen d’une combinaison de travail à distance et de travail en personne (siège social de Kirkland) en fonction de la nature du travail à effectuer.
Nous sommes fiers d'être une entreprise qui embrasse la valeur de rassembler des personnes diversifiées, talentueuses et engagées. La façon la plus rapide d’innover est de rassembler des gens de diverses opinions dans un environnement inclusif. Nous encourageons nos collègues à remettre en question avec respect les problèmes de réflexion et d’approche de l’un et de l’autre. Nous sommes un employeur souscrivant au principe de l’égalité d’accès à l’emploi et nous sommes déterminés à favoriser un milieu de travail inclusif et diversifié.
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Current Contingent Workers apply HERE
Secondary Language(s) Job Description:
The Global Clinical Supply (GCS) organization is accountable for managing the 'end-to-end' integrated clinical supply chain across the Research & Development Division portfolio of clinical trials. GCS is accountable for the planning, sourcing, labeling, packaging and delivery of clinical supplies to clinical sites globally. The GCS Planning organization is the key interface between clinical development teams and the operational/executional arms within the business.
The Program Clinical Supplies Project Manager (Program CSPM) serves as the primary program-level GCS point of contact representing the GCS Planning organization to customers both internal and external to GCS and serves as the lead GCS spokesperson at clinical and development related meetings. Working independently, the Program CSPM designs strategic and operational plans for all clinical supply activities associated with the clinical studies in their assigned compound(s)/ program(s). The incumbent is expected to have an understanding of the concepts of drug development, clinical research, and/or clinical supply chain, as well as, interpersonal skills with a demonstrated ability to negotiate with key stakeholder groups and drive/influence results in a dynamic environment.
Primary activities include, but are not limited to:
General Activities:
Interacts closely with key partner organizations (as a lead GCS Planning program representative) such as clinical development, regulatory, quality and other supply chain areas to negotiate timelines, strategies and other related topics for all clinical supplies across all assigned program(s).
Responsible and accountable for establishing the timelines for bulk manufacturing needs and release of drug product across assigned program(s).
Works directly in the SAP system to establish a consolidated, visible forecast for all products used within the assigned program(s) (i.e. Bulk Drug Product).
Oversees all bulk drug supply management and ensures proper allocation of drug product as needed across studies within assigned program(s).
Responsible for identifying significant supply risks associated with clinical bulk activities in addition to serving in a lead role for clinical supply issue escalation within their program(s) (and subsequent manage thereof) to GCS Leadership.
Responsible for the clinical supply budget for respective program(s) and for supporting all protocol and program cost estimates requested by Product Development Teams.
Responsible for authoring clinical supply documentation in support of labeling and packaging activities as well as supply chain documentation to support critical CMC activities.
Support the collection of clinical supply chain metrics and/or participate in critical non-pipeline activities as a subject matter expert in a particular area of expertise.
Mentors new team members and supports staff development, as needed
Required Experience and Skills:
Bachelor’s degree in a scientific, business, or related discipline required, MS/MBA preferred.
At least 6 years of experience in project management.
At least 3 years of experience in planning, scheduling, coordination and processing of supply chain activities, or the equivalent.
Understanding of the concepts of material requirements planning (MRP) systems and demand planning principles
Strong organizational, time management and problem solving skills
Exceptional written and verbal communication and relationship skills along with high personal integrity, credibility, and energy.
Ability to prioritize tasks and initiatives appropriately to mitigate supply risks.
Advanced proficiency in Microsoft Excel, PowerPoint, and Word.
Experience with change management and leading process improvement initiatives.
Preferred Experience and Skills:
Demonstrates ability to negotiate, resolve conflicts and engage in decision making as well as partner and influence across functional areas and organizations
Strong knowledge of the principles of project management and clinical customer relationship management.
Strong knowledge of drug development, production, distribution, shipping, destruction, and reconciliation processes and procedures.
Knowledge of order management, supply chain operations and document control.
Experience leading teams
Familiarity with data analytics/visualization software.
Travel required: less than 10%
In line with our Company’s Hybrid Workplace Strategy, this position will be performed through a combination of remote work and in-person (Kirkland Head Office) based on the nature of work to be done.
We are proud to be a company that embraces the value of bringing diverse, talented, and committed people together. The fastest way to breakthrough innovation is when diverse ideas come together in an inclusive environment. We encourage our colleagues to respectfully challenge one another’s thinking and approach problems collectively. We are an equal opportunity employer, committed to fostering an inclusive and diverse workplace.
Search Firm Representatives Please Read Carefully
Merck & Co., Inc., Rahway, NJ, USA, also known as Merck Sharp & Dohme LLC, Rahway, NJ, USA, does not accept unsolicited assistance from search firms for employment opportunities. All CVs / resumes submitted by search firms to any employee at our company without a valid written search agreement in place for this position will be deemed the sole property of our company. No fee will be paid in the event a candidate is hired by our company as a result of an agency referral where no pre-existing agreement is in place. Where agency agreements are in place, introductions are position specific. Please, no phone calls or emails.
Employee Status:
RegularRelocation:
No relocationVISA Sponsorship:
NoTravel Requirements:
10%Flexible Work Arrangements:
HybridShift:
1st - DayValid Driving License:
YesHazardous Material(s):
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