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“At CommBank we are proud to support flexibility, let’s discuss what this means for you”
Please note – We are seeking Expressions of Interest within these teams for present and future vacancies. Successful candidates will be contacted for a further conversation around suitability.
Impact and Role Contribution:
As a Manager, Controls Assurance, you will join our high performing Chief Controls Office teams and assist in supporting the business to identify, assess and manage the risk inherent in providing a range of operations services to the CBA group.
You will also partner with key stakeholders to deliver insights, utilising analytical skills and complex data. You will need the adaptability to work in a fast-paced environment and the ability to build relationships and work collaboratively with the extended leadership team across Line 2 and Group Audit.
In any given week you will:
We're interested in hearing from people who have:
Your qualifications:
What’s next?
Our team is looking to connect with Risk professionals who are interested in being part of a high performing, customer-focused and passionate culture to build a simpler, better bank. We welcome you to express your interest and learn more about Risk opportunities. We will be in contact with suitable candidates.
We're aware of some accessibility issues on this site, particularly for screen reader users. We want to make finding your dream job as easy as possible, so if you require additional support please contact HR Direct on 1800 989 696
We support our people with the flexibility to balance where work is done with at least half their time each month connecting in office. We also have many other flexible working options available including changing start and finish times, part-time arrangements and job share to name a few. Talk to us about how these arrangements might work in the role you are interested in.
If you're already part of the Commonwealth Bank Group (including Bankwest, x15ventures), you'll need to apply through Sidekick to submit a valid application. We’re keen to support you with the next step in your career.
We're aware of some accessibility issues on this site, particularly for screen reader users. We want to make finding your dream job as easy as possible, so if you require additional support please contact HR Direct on 1800 989 696.
Official account of Jobstore.
Job Title
Control Systems LeadJob Description Summary
Job Description
C&W Services is the industry leader in Integrated Maintenance Solutions providing service to more than 600 companies worldwide and is a sister company of Cushman & Wakefield.
C&W Services offers:
About the Role:
As a Control Systems Lead, you will lead service technicians on the team with maintaining, troubleshooting, and modifying Material Handling (MHE) controls systems equipment to ensure operational performance. You will support the Operations Maintenance team by designing solutions for difficult problems and managing projects. You will help train, and mentor service technicians and contract technicians.
Responsibilities include, but are not limited to:
Basic Qualifications:
Preferred Qualifications:
PHYSICAL DEMANDS:
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.
In compliance with the Americans with Disabilities Act Amendments Act (ADAAA), if you have a disability and would like to request an accommodation in order to apply for a position at Cushman & Wakefield, please call the ADA line at 1-888-365-5406 or email HRServices@cushwake.com. Please refer to the job title and job location when you contact us.
Official account of Jobstore.
Job Title
Control Systems TechnicianJob Description Summary
Job Description
C&W Services is the industry leader in Integrated Maintenance Solutions providing service to more than 600 companies worldwide and is a sister company of Cushman & Wakefield.
C&W Services offers:
About the Role:
As a Control Systems Technician, you will focus on equipment troubleshooting and maintaining material handling equipment (MHE) such as conveyors, sortation systems, scanners, cameras, print and apply labeling systems, scales, HMI systems, and control cabinets. In addition to developing your skills, you will mentor junior technicians to grow in their roles.
Responsibilities include, but are not limited to:
Basic Qualifications:
Preferred Qualifications:
PHYSICAL DEMANDS:
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.
In compliance with the Americans with Disabilities Act Amendments Act (ADAAA), if you have a disability and would like to request an accommodation in order to apply for a position at Cushman & Wakefield, please call the ADA line at 1-888-365-5406 or email HRServices@cushwake.com. Please refer to the job title and job location when you contact us.
Official account of Jobstore.
ERM is seeking a Consultant, Environmental Air Quality Compliance to join our team in Walnut Creek, San Francisco, or Sacramento California (location flexible).
The successful candidate will work on a variety of interesting technical projects and programs for clients in the Technology, Media and Telecom (TMT), Manufacturing, Power and other sectors throughout California and nationally. This role will involve supporting ERM’s commercial initiatives including multi-disciplinary environmental permitting and compliance assessments that require working knowledge of state and Federal requirements.
This role will engage ERM's international team of experts in sharing and developing best practices across the industry and ongoing learning opportunities. This is an excellent career opportunity to work with a global consulting firm in assisting a diverse set of clients with challenging business needs.
RESPONSIBILITIES:
Participate as a team member on a range of projects; specific areas of focus will be air quality but may include multi-disciplinary environmental compliance plans including air permits and compliance assurance programs for a variety of industrial clients.
Interact with local regulators and clients to steward permit application review and issuance.
Prepare emission inventory reports; quantify air pollutant emissions impacts; and prepare permit applications and permit modifications.
Assess regulatory compliance, perform regulatory applicability evaluations and implement environmental compliance management systems and processes.
Individual will also help prepare Material Business Plans (HMBPs), Storm Water Pollution Prevention Plans (SWPPP), Emergency Planning Community Right-to-Know Act (EPCRA) reporting, Wastewater Permitting and Compliance reports, Spill Prevention Control Countermeasure (SPCC), and others.
Interact with local regulators and clients to steward permit application review and issuance.
Fieldwork may include data collection, conducting air compliance assessments, and field work for other media including storm water sampling, media inspections, hazardous waste audits, compilation of waste and chemical inventories, on-site environmental compliance support, and other field-based assignments to support compliance-based documents and plans.
Collaborate, interact and maintain successful relationships with clients, ERM employees, and subcontractors.
To develop successful relationships, the candidate must have strong communication skills. These relationships will not only be in California but also nationwide and globally.
Shows potential for serving as a project manager and involvement in business development.
Promote a culture of safety, collaboration and excellence.
REQUIREMENTS:
BS in engineering (chemical, environmental, civil engineering) or related discipline; MS degree preferred.
3+ years of air quality and environmental permitting and compliance experience
Direct consulting or industry experience in the environmental field with working regulatory knowledge of local air districts SCAQMD and other local air districts, state, federal programs, Title V and RECLAIM facilities.
Strong pollution controls and equipment systems knowledge/experience is a plus.
Field experience with conducting air compliance monitoring, and assessment and permitting evaluation.
Other field work experience such as, stormwater inspections, and technical experience with writing and updating of stormwater plans/SWPPPs), managing and updating HMBPs HMBP preparation, preparing wastewater permit applications is a plus.
PREFERRED EXPERIENCE AND QUALIFICATIONS:
Previous experience working with local, state, and federal agencies such as Los Angeles County Sanitation District (LACSD), South Coast Air Quality Management District (SCAQMD), San Joaquin Valley Air Pollution Control District (SJVAPCD), Bay Area Air Quality Management District (BAAQMD) and other air quality agencies in California.
Other agencies experience such as Los Angeles County Sanitation District (LACSD), Regional Water Quality Control Board (RWQCB) and Environmental Protection Agency (EPA) is a plus.
Demonstrated ability to manage multiple assignments while maintaining clear communication with clients and colleagues.
Ability to multi-task, maintain flexibility, travel, and work independently with minimal supervision.
Ability to read, understand, and apply environmental regulations and agency guidance documents.
Strong analytical and computational skills to solve technical problems and implement effective solutions.
Effective management of multiple projects, and building client relationships that result in repeat business.
Excellent written and verbal communication skills – including technical writing experience.
Strong self-management skills including time management and organization.
Strong MS Office computer skills, with an advanced understanding of PowerPoint and Excel required.
Ability to thrive in a fast-paced consulting environment, handling multiple project assignments, meeting strict deadlines, and traveling to clients as needed.
Apply a collaborative approach and enjoy teaming with colleagues around the world.
Positive and enthusiastic attitude; motivated to deliver outstanding client service and grow the business.
For the Consultant, Environmental Air Quality Compliance position, we anticipate the annual base pay of $80,000 – $91,000. An employee’s pay position within this range will be based on several factors including, but not limited to, relevant education, qualifications, certifications, experience, skills, geographic location, performance, shift, travel requirements, sales or revenue-based metrics, and business or organizational needs. We also may have instances where employee’s fall outside of the range based on the factors noted above. This job is also eligible for bonus pay.
We offer comprehensive package of benefits including paid time off, medical/dental/vision insurance, 401(k), and any other benefits to eligible employees.
You can apply for this role through https://www.erm.com/careers/apply/ or through the internal careers portal if you are a current employee.
Note: No amount of pay is considered to be wages or compensation until such amount is earned, vested, and determinable. The amount and availability of any bonus, commission, or any other form of compensation that are allocable to a particular employee remains in the Company's sole discretion unless and until paid and may be modified at the Company’s sole discretion, consistent with the law.
Who We Are:
As the largest global pure play sustainability consultancy, we partner with the world’s leading organizations, creating innovative solutions to sustainability challenges and unlocking commercial opportunities that meet the needs of today while preserving opportunity for future generations.
At ERM we know that creating a diverse, equitable and inclusive work environment is an essential part of making our company a great place to build a career. We also see our diversity as a strength that helps us create better solutions for our clients. Our diverse team of world-class experts supports clients across the breadth of their organizations to operationalize sustainability, underpinned by our deep technical expertise in addressing their environmental, health, safety, risk and social issues. We call this capability our “boots to boardroom” approach for its comprehensive service model that allows ERM to develop strategic and technical solutions that advance objectives on the ground or at the executive level.
Please submit your resume and brief cover letter. Based on review of these responses, shortlisted candidates will be invited for interviews.
ERM does not accept recruiting agency resumes. Please do not forward resumes to our jobs alias, ERM employees or any other company location. ERM is not responsible for any fees related to unsolicited resumes.
ERM is proud to be an Equal Employment Opportunity employer. We do not discriminate based upon race, religion, color, national origin, gender, sexual orientation, gender identity, age, status as a protected veteran, status as an individual with a disability, or other applicable legally protected characteristics.
Thank you for your interest in ERM!
Official account of Jobstore.
The Opportunity
This position works out of our Austin, TX location in the Diabetes Care division. We’re focused on helping people with diabetes manage their health with life-changing products that provide accurate data to drive better-informed decisions. We’re revolutionizing the way people monitor their glucose levels with our new sensing technology.
As the Senior Quality Engineer, you will be responsible for conducting quality-related activities to deliver consistent; high quality documents; services; products and processes.
MAIN PURPOSE OF ROLE
This position is responsible for developing and maintaining quality engineering methodologies and providing quality engineering support within new product development, manufacturing, or system/services support.
MAIN RESPONSIBILITIES
• Reviews pre-defined deliverables/activities as identified in the Validation Process and/or Product Quality Process/project plan or equivalent project plan.
• Apply sound, systematic problem-solving methodologies in identifying, prioritizing, communicating, and resolving quality issues
• Identifies areas for process improvement and provides supporting information for change, including reasons and justifications.
• Participates in the development or modification of validation packages and deliverables, including, assessments (including risk assessments, e.g., FMEAs), plans, requirements, and protocols.
• Works independently with objectives given by the Quality Manager.
• Can plan and coordinate own work according to higher level project schedules.
• Review documentation for accuracy, clarity, consistency, completeness and compliance to internal and external requirements for multiple projects, including but not limited to specifications/requirements documents, valida tion protocols & reports, trace matrices, validation events, change control packages, etc.
• Report unexpected events, issues or software bugs which occur during validation to project team and management.
• Assist team members and cross functional colleagues in meeting their goals by providing coaching and mentoring as needed.
• Drive to meet validation schedule as aligned with project(s) goals.
• Ensure that appropriate procedures, controls, and recovery plans are incorporated into equipment/systems.
• Lead the investigation, resolution and prevention of product and process nonconformances, CAPA investigations, or other quality system records
• Participate in or lead teams in supporting quality disciplines, decisions, and practices (e.g., represent the Quality function as a Core Team Member)
• Lead in the completion and maintenance of risk analysis
• Work with cross functional teams to ensure quality and compliance requirements are considered during activities (e.g., work with microbiology to ensure appropriate environmental monitoring and that microbiology require ments are considered in product and process development activities)
• Support projects and Divisional initiatives as identified by management
• Performs other related duties and responsibilities, on occasion, as assigned.
QUALIFICATIONS
Education Level Major/Field of Study Or Education Level
Bachelor's Degree (± 16 years) Engineering or Technical Field ☒ an equivalent combination of education and work experience
Experience/Background Experience
Experience Details
Minimum 5 years experience in medical device/pharmaceutical manufacturing
Demonstrated supervisory experience preferred.
Validation experience and demonstrated use of Quality tools/methodologies.
Detailed knowledge of FDA, GMP, ISO 13485, and ISO 14971.
Solid communication (written and oral) and interpersonal skills.
Strong project management and leadership skills, including the demonstrated ability to lead multidepartmental project teams and resolve quality-related issues in a timely and effective manner
Advanced computer skills, including statistical/data analysis and report writing skills.
Prior medical device experience preferred.
Experience implementing various product and process improvement methodologies (e.g., Six Sigma and Lean Manufacturing).
Experience working in a broader enterprise/cross-division business unit model preferred.
Ability to work in a highly matrixed and geographically diverse business environment.
Ability to work within a team and as an individual contributor in a fast-paced, changing environment.
Ability to leverage and/or engage others to accomplish projects.
Strong verbal and written communications with ability to effectively communicate at multiple levels in the organization.
Multitasks, prioritizes and meets deadlines in timely manner.
Strong organizational and follow-up skills, as well as attention to detail.
Ability to maintain regular and predictable attendance.
Licenses and Certifications
License/Certification ASQ CQE or other certifications preferred
* Participants who complete a short wellness assessment qualify for FREE coverage in our HIP PPO medical plan. Free coverage applies in the next calendar year.
Learn more about our health and wellness benefits, which provide the security to help you and your family live full lives: www.abbottbenefits.com
Follow your career aspirations to Abbott for diverse opportunities with a company that can help you build your future and live your best life. Abbott is an Equal Opportunity Employer, committed to employee diversity.
Connect with us at www.abbott.com, on Facebook at www.facebook.com/Abbott and on Twitter @AbbottNews and @AbbottGlobal.
related industry.
The base pay for this position is
$71,300.00 – $142,700.00In specific locations, the pay range may vary from the range posted.
Abbott is an Equal Opportunity Employer of Minorities/Women/Individuals with Disabilities/Protected Veterans.
EEO is the Law link - English: http://webstorage.abbott.com/common/External/EEO_English.pdf
EEO is the Law link - Espanol: http://webstorage.abbott.com/common/External/EEO_Spanish.pdf
Official account of Jobstore.
ERM seeks an experienced Managing Consultant Air Quality to provide technical expertise, project and team management, and business development support for our Air Quality Service Area in Walnut Creek, San Francisco, or Sacramento in California. This is an excellent opportunity for a senior professional to manage and contribute technically to challenging air quality compliance assurance, permitting, climate change, and related compliance projects for oil & gas, chemical, energy, technology, and industrial clients in California, throughout the US, and potentially international locations. The successful candidate will also network with ERM's national air quality technical team to share best practices and consulting opportunities, as you build a rewarding career path with a global environmental leader.
ERM’s Air Quality & Climate Change technical community pursues and wins highly innovative engagements for the most interesting clients, providing the full breadth of air quality and climate change services. With annual global sales in excess of $50 million, ERM’s Air Quality & Climate Change service area is one of the largest among its peers in our industry and is steadily growing at a double-digit pace. In North America alone, ERM has more than 300 dedicated air quality and climate change professionals assisting clients with projects as diverse as developing responses to emerging Low Carbon Fuel Standards, to leading complex capital projects through the many hurdles associated with the NSR permitting program.
RESPONSIBILITIES:
REQUIREMENTS:
For the Managing Consultant Air Quality position, we anticipate the annual base pay of $84,007 to $108,150. An employee’s pay position within this range will be based on several factors including, but not limited to, relevant education, qualifications, certifications, experience, skills, geographic location, performance, shift, travel requirements, sales or revenue-based metrics, and business or organizational needs. We also may have instances where employee’s fall outside of the range based on the factors noted above. This job may be eligible for bonus pay (casual and fixed term/flex force employees are NOT bonus eligible).
We offer a comprehensive package of benefits including paid time off, medical, dental, vision, 401(k), life & disability insurance to benefits eligible* employees.
*Benefits Eligibility is limited to Regular employees regularly scheduled to work 20 or more hours per week. Fixed-Term employees (including flex force) who are regularly scheduled to work 20 hours a week or more are eligible for a limited benefits package. Casual employees are NOT benefits eligible. See your recruiter for more details.
You can apply for this role through https://www.erm.com/careers/apply/ or through the internal careers portal if you are a current employee.
Note: No amount of pay is considered to be wages or compensation until such amount is earned, determinable, and payable. The amount and availability of any bonus, commission, or any other form of compensation that are allocable to a particular employee remains in the Company's sole discretion unless and until paid and may be modified at the Company’s sole discretion, consistent with the law.
Who We Are:
As the largest global pure play sustainability consultancy, we partner with the world’s leading organizations, creating innovative solutions to sustainability challenges and unlocking commercial opportunities that meet the needs of today while preserving opportunity for future generations.
At ERM we know that creating a diverse, equitable and inclusive work environment is an essential part of making our company a great place to build a career. We also see our diversity as a strength that helps us create better solutions for our clients. Our diverse team of world-class experts supports clients across the breadth of their organizations to operationalize sustainability, underpinned by our deep technical expertise in addressing their environmental, health, safety, risk and social issues. We call this capability our “boots to boardroom” approach for its comprehensive service model that allows ERM to develop strategic and technical solutions that advance objectives on the ground or at the executive level.
Please submit your resume and brief cover letter.
ERM does not accept recruiting agency resumes. Please do not forward resumes to our jobs alias, ERM employees or any other company location. ERM is not responsible for any fees related to unsolicited resumes.
ERM is proud to be an Equal Employment Opportunity employer. We do not discriminate based upon race, religion, color, national origin, gender, sexual orientation, gender identity, age, status as a protected veteran, status as an individual with a disability, or other applicable legally protected characteristics.
Thank you for your interest in ERM!
Official account of Jobstore.
Major duties include, but are not limited to:
Official account of Jobstore.
Official account of Jobstore.
At Citi, we get to connect millions of people across hundreds of cities and countries every day. And we've been doing it for more than 200 years. We do this through our unparalleled global network. We provide a broad range of financial services and products to our clients – whether they be consumers, corporations, governments, or institutions – to help them meet their biggest opportunities and face the world's toughest challenges.
We’re currently looking for a high caliber professional to join our team as Risk & Control and TSA/PMO Activities Manager based in Ho Chi Minh City Vietnam.
In this role, you’re expected to:
As a successful candidate, you’d ideally have the following skills and exposure:
This job description provides a high-level review of the types of work performed. Other job-related duties may be assigned as required.
Working at Citi is far more than just a job. A career with us means joining a family of more than 230,000 dedicated people from around the globe. At Citi, you’ll have the opportunity to grow your career, give back to your community and make a real impact.
Take the next step in your career, apply for this role at Citi today
https://jobs.citi.com/dei
-------------------------------------------------
Job Family Group:
Project and Program Management-------------------------------------------------
Job Family:
Program Management------------------------------------------------------
Time Type:
Full time------------------------------------------------------
Citi is an equal opportunity and affirmative action employer.
Qualified applicants will receive consideration without regard to their race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or status as a protected veteran.
Citigroup Inc. and its subsidiaries ("Citi”) invite all qualified interested applicants to apply for career opportunities. If you are a person with a disability and need a reasonable accommodation to use our search tools and/or apply for a career opportunity review Accessibility at Citi.
View the "EEO is the Law" poster. View the EEO is the Law Supplement.
View the EEO Policy Statement.
View the Pay Transparency Posting
Official account of Jobstore.
About Abbott
Abbott is a global healthcare leader, creating breakthrough science to improve people’s health. We’re always looking towards the future, anticipating changes in medical science and technology.
Working at Abbott
At Abbott, you can do work that matters, grow, and learn, care for yourself and family, be your true self and live a full life. You’ll also have access to:
The Opportunity
This position works out of our Austin, TX location in the Diabetes Care division. We’re focused on helping people with diabetes manage their health with life-changing products that provide accurate data to drive better-informed decisions. We’re revolutionizing the way people monitor their glucose levels with our new sensing technology.
As the Senior Specialist Quality Assurance you will be responsible for conducting quality-related activities to deliver consistent; high quality documents; services; products and processes.
What You’ll Work On
Provides solutions to a wide range of difficult problems.
Ensures that solutions are compliant, innovative, thorough, practical and consistent with organizational objectives.
May Leads quality projects with cross-functional or broader scope.
Defines project goals and milestones.
Responsible for timely project completion.
Interacts effectively with employees, manager, and cross-functional peers.
May represent own team while on cross-functional project teams with other functional leaders.
Communicates confidently and effectively with management, peers, and key stakeholders.
Implements tactical solutions related to assignment.
Able to contribute functional skills and expertise broadly.
Directly influences project direction and scope. Scope includes one or more QA functions, with general knowledge of other
related disciplines.
Provides guidance and trains others. May provide oversight to one or more QA professionals
and/or contractors.
• Quality System Compliance:
Demonstrates good, general understanding of the standards and regulatory bodies that regulate our industry.
Ensures compliance to site level policies and procedures and demonstrates a solid understanding of Division and Corporate policies and procedures by promptly addressing noncompliance issues within Division and Corporation as appropriate.
Ensures adherence and maintains the effectiveness of the Quality System, including the Subsystems and Key processes that govern the area by promptly addressing non-compliance issues.
• Risk Management:
Ensures evaluation of product safety and efficacy and elevation of risk-based issues.
Creates and reviews risk management documentation to reduce or eliminate risk.
Makes independent decisions within defined parameters while assuring that these decisions are compliant with site level policies and procedures and are aligned with the appropriate quality system. Authors risk control packages and demonstrates the ability to analyze, evaluate, and control risk decisions by utilizing common practices throughout the quality.
•Design Control / Documentation & Change Control:
Formulates thorough reason and justification for change.
Identifies critical parameters associated with change.
May represent the site as an SME or Process Community member.
• Quality Engineering:
Applies solid understanding of quality system elements from product inception through launch.
While recognizing project interdependencies and with minimal oversight, leads complex quality discussions across various
departments including, as needed, external suppliers.
• Validation:
May act as Subject Matter Expert (SME) for minimum of at least one respective Validation Subsystem.
Required Qualifications
Bachelors Degree In Life Science, Engineering, or closely related discipline or an equivalent combination of education and work experience
Minimum 5 years In Quality or related field experience; Less experience may be appropriate with advanced degree.
Preferred Qualifications
Preferred experience in the Healthcare industry.
Has a history of completing successful projects and driving positive compliance outcomes.
* Participants who complete a short wellness assessment qualify for FREE coverage in our HIP PPO medical plan. Free coverage applies in the next calendar year.
Learn more about our health and wellness benefits, which provide the security to help you and your family live full lives: www.abbottbenefits.com
Follow your career aspirations to Abbott for diverse opportunities with a company that can help you build your future and live your best life. Abbott is an Equal Opportunity Employer, committed to employee diversity.
Connect with us at www.abbott.com, on Facebook at www.facebook.com/Abbott and on Twitter @AbbottNews and @AbbottGlobal.
The base pay for this position is
$80,700.00 – $161,300.00In specific locations, the pay range may vary from the range posted.
Abbott is an Equal Opportunity Employer of Minorities/Women/Individuals with Disabilities/Protected Veterans.
EEO is the Law link - English: http://webstorage.abbott.com/common/External/EEO_English.pdf
EEO is the Law link - Espanol: http://webstorage.abbott.com/common/External/EEO_Spanish.pdf
Official account of Jobstore.
ERM is seeking a Consultant, Environmental Air Quality Compliance to join our team in Walnut Creek, San Francisco, or Sacramento California (location flexible).
The successful candidate will work on a variety of interesting technical projects and programs for clients in the Technology, Media and Telecom (TMT), Manufacturing, Power and other sectors throughout California and nationally. This role will involve supporting ERM’s commercial initiatives including multi-disciplinary environmental permitting and compliance assessments that require working knowledge of state and Federal requirements.
This role will engage ERM's international team of experts in sharing and developing best practices across the industry and ongoing learning opportunities. This is an excellent career opportunity to work with a global consulting firm in assisting a diverse set of clients with challenging business needs.
RESPONSIBILITIES:
Participate as a team member on a range of projects; specific areas of focus will be air quality but may include multi-disciplinary environmental compliance plans including air permits and compliance assurance programs for a variety of industrial clients.
Interact with local regulators and clients to steward permit application review and issuance.
Prepare emission inventory reports; quantify air pollutant emissions impacts; and prepare permit applications and permit modifications.
Assess regulatory compliance, perform regulatory applicability evaluations and implement environmental compliance management systems and processes.
Individual will also help prepare Material Business Plans (HMBPs), Storm Water Pollution Prevention Plans (SWPPP), Emergency Planning Community Right-to-Know Act (EPCRA) reporting, Wastewater Permitting and Compliance reports, Spill Prevention Control Countermeasure (SPCC), and others.
Interact with local regulators and clients to steward permit application review and issuance.
Fieldwork may include data collection, conducting air compliance assessments, and field work for other media including storm water sampling, media inspections, hazardous waste audits, compilation of waste and chemical inventories, on-site environmental compliance support, and other field-based assignments to support compliance-based documents and plans.
Collaborate, interact and maintain successful relationships with clients, ERM employees, and subcontractors.
To develop successful relationships, the candidate must have strong communication skills. These relationships will not only be in California but also nationwide and globally.
Shows potential for serving as a project manager and involvement in business development.
Promote a culture of safety, collaboration and excellence.
REQUIREMENTS:
BS in engineering (chemical, environmental, civil engineering) or related discipline; MS degree preferred.
Minimum 2-3 years of air quality and environmental permitting and compliance experience
Direct consulting or industry experience in the environmental field with working regulatory knowledge of local air districts SCAQMD and other local air districts, state, federal programs, Title V and RECLAIM facilities.
Strong pollution controls and equipment systems knowledge/experience is a plus.
Field experience with conducting air compliance monitoring, and assessment and permitting evaluation.
Other field work experience such as, stormwater inspections, and technical experience with writing and updating of stormwater plans/SWPPPs), managing and updating HMBPs HMBP preparation, preparing wastewater permit applications is a plus.
PREFERRED EXPERIENCE AND QUALIFICATIONS:
Previous experience working with local, state, and federal agencies such as Los Angeles County Sanitation District (LACSD), South Coast Air Quality Management District (SCAQMD), San Joaquin Valley Air Pollution Control District (SJVAPCD), Bay Area Air Quality Management District (BAAQMD) and other air quality agencies in California.
Other agencies experience such as Los Angeles County Sanitation District (LACSD), Regional Water Quality Control Board (RWQCB) and Environmental Protection Agency (EPA) is a plus.
Demonstrated ability to manage multiple assignments while maintaining clear communication with clients and colleagues.
Ability to multi-task, maintain flexibility, travel, and work independently with minimal supervision.
Ability to read, understand, and apply environmental regulations and agency guidance documents.
Strong analytical and computational skills to solve technical problems and implement effective solutions.
Effective management of multiple projects, and building client relationships that result in repeat business.
Excellent written and verbal communication skills – including technical writing experience.
Strong self-management skills including time management and organization.
Strong MS Office computer skills, with an advanced understanding of PowerPoint and Excel required.
Ability to thrive in a fast-paced consulting environment, handling multiple project assignments, meeting strict deadlines, and traveling to clients as needed.
Apply a collaborative approach and enjoy teaming with colleagues around the world.
Positive and enthusiastic attitude; motivated to deliver outstanding client service and grow the business.
For the Environmental Air Quality Compliance Consultant position, we anticipate the annual base pay of $63,211 – $82,166. An employee’s pay position within this range will be based on several factors including, but not limited to, relevant education, qualifications, certifications, experience, skills, geographic location, performance, shift, travel requirements, sales or revenue-based metrics, and business or organizational needs. We also may have instances where employee’s fall outside of the range based on the factors noted above. This job is also eligible for bonus pay.
We offer comprehensive package of benefits including paid time off, medical/dental/vision insurance, 401(k), and any other benefits to eligible employees.
You can apply for this role through https://www.erm.com/careers/apply/ or through the internal careers portal if you are a current employee.
Note: No amount of pay is considered to be wages or compensation until such amount is earned, vested, and determinable. The amount and availability of any bonus, commission, or any other form of compensation that are allocable to a particular employee remains in the Company's sole discretion unless and until paid and may be modified at the Company’s sole discretion, consistent with the law.
Who We Are:
As the largest global pure play sustainability consultancy, we partner with the world’s leading organizations, creating innovative solutions to sustainability challenges and unlocking commercial opportunities that meet the needs of today while preserving opportunity for future generations.
At ERM we know that creating a diverse, equitable and inclusive work environment is an essential part of making our company a great place to build a career. We also see our diversity as a strength that helps us create better solutions for our clients. Our diverse team of world-class experts supports clients across the breadth of their organizations to operationalize sustainability, underpinned by our deep technical expertise in addressing their environmental, health, safety, risk and social issues. We call this capability our “boots to boardroom” approach for its comprehensive service model that allows ERM to develop strategic and technical solutions that advance objectives on the ground or at the executive level.
Please submit your resume and brief cover letter. Based on review of these responses, shortlisted candidates will be invited for interviews.
ERM does not accept recruiting agency resumes. Please do not forward resumes to our jobs alias, ERM employees or any other company location. ERM is not responsible for any fees related to unsolicited resumes.
ERM is proud to be an Equal Employment Opportunity employer. We do not discriminate based upon race, religion, color, national origin, gender, sexual orientation, gender identity, age, status as a protected veteran, status as an individual with a disability, or other applicable legally protected characteristics.
Thank you for your interest in ERM!
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À propos d’Abbott
Abbott est un chef de file mondial de l’industrie des soins de santé qui crée des solutions scientifiques révolutionnaires visant à améliorer la santé des gens. L’entreprise est résolument tournée vers l’avenir, à l’affût des changements qui pourraient survenir dans le domaine des sciences et des technologies médicales.
Être à l’emploi d’Abbott
En étant à l’emploi d’Abbott, vous pourrez faire un travail qui compte, vous perfectionner et apprendre, prendre soin de vous et des membres de votre famille, rester fidèle à ce que vous êtes et vivre pleinement. Vous pourrez :
• profiter de possibilités d’avancement professionnel au sein d’une entreprise internationale qui vous permettra de bâtir la carrière dont vous rêvez;
• travailler pour une entreprise reconnue dans des douzaines de pays partout dans le monde comme étant un excellent milieu de travail et figurant parmi les entreprises les plus admirées dans le monde dans le classement Fortune;
• travailler pour une grande entreprise reconnue comme étant l’une des meilleures où travailler, notamment pour ce qui a trait à la diversité du personnel, à la conciliation travail-famille ainsi qu’à la place des femmes dans les postes de cadres et les postes scientifiques.
L’occasion à saisir
Nous cherchons à pourvoir un emploi à Victoriaville, au Québec, au sein de la division des produits pharmaceutiques établis (DPE). Dans cette division, nous nous engageons à apporter les avantages de nos médicaments de confiance à un plus grand nombre de personnes dans les pays à la croissance la plus rapide du monde. Notre vaste portefeuille de médicaments génériques de marque, différenciés et de haute qualité, couvre de nombreux domaines thérapeutiques, notamment la gastro-entérologie, la santé des femmes, les troubles cardiométaboliques, la gestion de la douleur et du système nerveux central, et les troubles respiratoires.
Relevant de la Directrice qualité, le spécialiste de la qualité sera responsable de fournir une expertise en AQ pour la fabrication de lactulose et la chaîne d’approvisionnement associée.
Ce que vous ferez
• Développer et diriger des programmes d’assurance qualité pertinents sur le site assurant ainsi la continuité de l’approvisionnement et de l’exécution réussie de la qualification des fournisseurs en fonction des besoins de l’entreprise;
• Diriger les enquêtes sur les problèmes de performance du produit, en fournissant des solutions soutenant le site, par exemple, des questions de carence;
• Soutenir l’exécution des projets d’amélioration et de conformité des produits et des processus pour toutes les modifications réglementaires et/ou de fabrications proposées;
• Intégrer l’expertise technique et les connaissances de l’équipe d’AQ opérationnelle à Victoriaville sur la fabrication, l’analyse et la libération de lactulose;
• Favoriser l’amélioration continue, l’innovation et la simplification alignées sur la stratégie d’Abbott et de DPÉ;
• Soutenir l’amélioration continue du ou des produits avec une portée interfonctionnelle;
• Gérer la prise de décisions appropriées basées sur le risque;
• Maintenir le programme de qualification des fournisseurs;
• Aider le directeur de l’AQ à bien exécuter le programme d’audit interne et externe (FDA);
• Exécuter et/ou participer à des audits de qualité internes et externes;
• Appuyer les événements d’exception et CAPA, du point de vue technique de l’AQ, en veillant à ce que l’impact des incidents soit évalué de manière appropriée et documentée;
• Établir les changements de processus qui ont un impact sur la qualité ou la réglementation, tout en assurant une communication en temps opportun et la mise en œuvre des changements conformément aux exigences réglementaires;
• Soutenir le PQR (Examen de la qualité des produits) et les examens de surveillance (système d’eau, lutte antiparasitaire, surveillance environnementale, programmes de stabilité, système d’air comprimé, programme de nettoyage);
• Remplacer le superviseur AQ - SQ et supporter le Spécialiste Assurance Qualité en cas d’absence.
Compétences requises
• Baccalauréat ou niveau d’études équivalent dans une discipline scientifique pertinente ou une autre expérience technique / scientifique ou de l’industrie avec une exposition suffisante aux industries pharmaceutiques ou connexes;
• Compréhension complète des exigences de fabrication d’ingrédients pharmaceutiques actifs (IPA) et de BPF;
• Expérience des industries pharmaceutiques ou des industries contrôlées par les normes GMP (BPF);
• Détenir les connaissances des systèmes de qualité internationaux et locaux et des lois et normes de conformité;
• Connaissance des outils de la Suite Microsoft Office (Excel, Word, PowerPoint, etc.,);
• Être familiarisé avec l’utilisation de systèmes informatisés;
• Posséder d’excellentes compétences en communications orales et écrites en français et en anglais;
• Avoir le sens de l’organisation, de l’autonomie et du leadership.
Réalisez vos aspirations professionnelles en saisissant diverses occasions de carrière chez Abbott, une entreprise qui peut vous aider à bâtir votre futur et vivre au meilleur de vos possibilités. Abbott est un employeur souscrivant au principe de l’égalité d’accès à l’emploi et ayant à cœur de favoriser la diversité au sein de sa main-d’œuvre.
Visitez notre site www.abbott.com ou suivez-nous sur Facebook, à www.facebook.com/Abbott, et Twitter @AbbottNews et @AbbottGlobal.
About Abbott
Abbott is a global healthcare leader, creating breakthrough science to improve people’s health. We’re always looking towards the future, anticipating changes in medical science and technology.
Working at Abbott
At Abbott, you can do work that matters, grow, and learn, care for yourself and family, be your true self and live a full life. You will have access to:
• Career development with an international company where you can grow the career you dream of.
• A company recognized as a great place to work in dozens of countries around the world and named one of the most admired companies in the world by Fortune.
• A company that is recognized as one of the best big companies to work for as well as a best place to work for diversity, working mothers, female executives, and scientists.
The Opportunity
This position works out of our Victoriaville, QC location in the Established Pharmaceuticals division (EPD). In this division, we are committed to bringing the benefits of our trusted medicines to more people in the world’s fastest-growing countries. Our broad portfolio of high-quality and differentiated branded generic medicines reaches across multiple therapeutic areas including gastroenterology, women's health, cardiometabolic, pain management/central nervous system, and respiratory.
Reporting to the Director of Quality Assurance, the Quality Specialist is responsible for supporting the PQR (Product Quality Review) and monitoring reviews (water system, pest control, environmental monitoring, stability programs, compressed air system, cleaning program).
What You’ll Do
• Develop and lead site relevant QA programs assuring continuity of supplies and successful execution of supplier qualification based on business needs;
• Provide QA expertise for the Lactulose and associated manufacturing supply chain;
• Drive investigation of product performance issues, providing solutions supporting the site, e.g. deficiency questions;
• Support execution of product/process improvements and compliance projects for all proposed manufacturing or regulatory changes;
• Embeds the technical expertise and knowledge in the operational QA team in Victoriaville on manufacturing, tests and release of Lactulose;
• Promotes continuous improvement, innovation, simplification aligned with Abbott and EPD strategy;
• Support the continuous improvement of the product(s) with cross-functional scope;
• Embeds and drives appropriate risk-based decision making;
• Maintain the Supplier Qualification Program;
• Assist the QA Director to complete the internal and external audit program;
• Execute and / or participate in internal and external quality audits;
• Support exception events and CAPA, from a technical QA perspective ensuring events are appropriately assessed for impact and documented;
• Support process changes which have a quality or regulatory impact, ensuring timely communication and implementation of changes in line with regulatory requirements;
• Support the PQR (Product Quality Review) and monitoring reviews (water system, pest control, environmental monitoring, stability programs, compressed air system, cleaning program);
• Support and replace Quality Specialists when absent.
Required Qualifications
• Bachelor’s degree or equivalent level of education at a relevant scientific discipline or other technical/scientific, or industry experience with sufficient exposure to pharmaceutical or related industries;
• Comprehensive understanding of an Active Pharmaceutical Ingredient (API) Manufacturing and GMP’s requirements;
• Experienced of the Pharmaceutical industries or GMP controlled industries;
• Knowledge of international and local quality system and compliance legislations and standards;
• Knowledge of Microsoft tools (Excel, Word, PowerPoint, etc.);
• Facility to use computerized systems;
• Excellent oral and written communication skills in French and English;
• Sense of organization, autonomy, and leadership.
Follow your career aspirations to Abbott for diverse opportunities with a company that can help you build your future and live your best life. Abbott is an Equal Opportunity Employer, committed to employee diversity.
Connect with us at www.abbott.com, on Facebook at www.facebook.com/Abbott and on Twitter @AbbottNews and @AbbottGlobal.
The base pay for this position is
N/AIn specific locations, the pay range may vary from the range posted.
Official account of Jobstore.
About Abbott
At Abbott, we believe people with diabetes should have the freedom to enjoy active lives. That’s why we’re focused on helping people with diabetes manage their health more effectively and comfortably, with lifechanging products that provide accurate data to drive better-informed decisions. We’re revolutionizing the
way people monitor their glucose levels with our new sensing technology.
Working at Abbott
At Abbott, you can do work that matters, grow, and learn, care for yourself and family, be your true self and live a full life. You’ll also have access to:
· Career development with an international company where you can grow the career you dream of.
· Free medical coverage for employees* via the Health Investment Plan (HIP) PPO
· An excellent retirement savings plan with high employer contribution
· Tuition reimbursement, the Freedom 2 Save student debt program and FreeU education benefit - an affordable and convenient path to getting a bachelor’s degree.
· A company recognized as a great place to work in dozens of countries around the world and named one of the most admired companies in the world by Fortune.
· A company that is recognized as one of the best big companies to work for as well as a best place to work for diversity, working mothers, female executives, and scientists.
The Opportunity
The Sr. Specialist, QA is responsible for ensuring the TPM meets quality standards and expectations. This role will join a team which supports a high-volume, fully automated TPM manufacturing operation.
What You'll Work On
Required Qualifications
Participants who complete a short wellness assessment qualify for FREE coverage in our HIP PPO medical plan. Free coverage applies in the next calendar year.
Learn more about our health and wellness benefits, which provide the security to help you and your family live full lives: www.abbottbenefits.com
Follow your career aspirations to Abbott for diverse opportunities with a company that can help you build your future and live your best life. Abbott is an Equal Opportunity Employer, committed to employee diversity.
Connect with us at www.abbott.com, on Facebook at www.facebook.com/Abbott and on Twitter @AbbottNews and @AbbottGlobal
The base pay for this position is
$71,300.00 – $142,700.00In specific locations, the pay range may vary from the range posted.
Abbott is an Equal Opportunity Employer of Minorities/Women/Individuals with Disabilities/Protected Veterans.
EEO is the Law link - English: http://webstorage.abbott.com/common/External/EEO_English.pdf
EEO is the Law link - Espanol: http://webstorage.abbott.com/common/External/EEO_Spanish.pdf
Official account of Jobstore.
The roles and responsibilities of a quality assurance varies across different industries. The duties include regulate, arrange and concur on quality procedures, standards and specifications, assess requirements and ensure everything is complied.
The type of jobs related to quality assurance encompass analyst, associate, maintenance technician, audio & video equipment technician, manager of quality assurance, quality assurance assistant manager, quality engineer, quality assurance technician, maintenance manager, safety technician, HVAC technician, consultant, coordinator, director, quality inspector, field service engineer, specialist and supervisor.
The role of quality control is to examine products and materials for defects or deviations from specifications. Responsibilities include monitor operations to ensure that they meet production standards, recommend adjustments to the assembly process, test products being produced, discuss inspection results and report inspection.
The role of quality assurance is to ensure a product or service meets the established standards of quality including reliability, usability and performance required for distribution. Responsibilities include devise sampling procedures, review the implementation of inspection system, document internal audits, investigate customer complaints, compile statistical quality data and analyse data to identify areas of improvement in the quality system.
The role of quality assurance/quality control(QAQC) engineer is to work with quality assurance supervisors, analysing manufacturing processes for improvement using various methods of testing and inspection. Responsibilities include implementing methods for process control, promote quality standards, assist in process certification and review suppliers purchase orders while establishing supplier quality requirements.
The role of QC inspector is to monitor the quality of incoming and outgoing products for a company. Responsibilities include reading blueprints to understand the requirements of products/services, measure product dimensions, recommend improvements to the production process to ensure quality control, document inspection outcomes by completing detailed reports, advise production team about quality control concerns to improve product excellence and supervise the production process.
