Job description: reports to the Professional Services Manager of Field Safety Services. Has the ability to issue/write safe work permits, hot… work permits and confined space entry permits. Performs jobsite safety audits. Assists with compliance to client safety…

Expected salary:

Location: Pasadena, TX

Job date: Sat, 21 Oct 2023 22:27:22 GMT

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Job description: Everyone at Olin contributes to our Winning Model. We empower our employees to make a difference at work, home and in their communities. We celebrate and reward our diverse and innovative workforce that defines our future and contributes through leadership, engagement, and productivity.

Join our winning team as an Air Permit Writer in Lake Jackson, Texas. In your role as an Air Permit Writer, you will be responsible for working with assigned plants to ensure all potential air emissions are properly authorized in NSR permits, PBRs and Title V federal operating permits. The incumbent will also assist plants in understanding what is required to demonstrate compliance and facilitate environmental agency investigations for their areas. This is a highly visible and valuable position with significant impact on environmental compliance and growth at the Freeport Olin site. The role is part of a small team of Environmental Air Permit Writers at the site.

Air Permit Writer Essential Job Functions:

• Lead projects through the preparation of permit (NSR, Title V, PSD, PBR, Standard) applications and agency negotiations to ensure optimal permit conditions. This frequently requires working with consultants to negotiate permits details with the TCEQ, EPA, and other environmental agencies.
• Assist plant personnel in the implementation of air permit conditions by providing interpretation guidance and leveraging solutions between plants.
• Serve as lead contact and advise other Olin personnel during inspections/investigations by local, state, or federal agencies.
• Assist plants in preparation of Title V Deviation reports and other regulatory reports, driving site consistency in reasonable inquiry and deviation reporting.
• Evaluate impact of proposed regulations on site plants and facilities and facilitate implementation of new regulations.
• Coordinate Texas EH&S Audit Privilege process and correspondence with agency
• Facilitate compliance issue resolution with appropriate team members.

Air Permit Writer Minimum Requirements:

• Bachelor’s degree* in a technical discipline; Chemical or Environmental Engineering preferred.
• Five years of experience in air permitting and air compliance for chemical, plastic, hydrocarbon and energy facilities required; Previous experience in EH&S preferred.
• Demonstrated ability to establish long-term professional relationships with regulatory agencies.
• Strong written and oral communications skills; strong organizational and prioritization skills; ability to communicate effectively will all levels within the organization.
• Proficient in standard MS Office applications (Word, Excel, PowerPoint)
• Knowledge of the State of Texas and Federal air regulations and their impact on the Chemical Industry is strongly preferred, especially with regards to permits
• Must be able to occasionally visit plants and travel to Austin, TX for regulatory meetings.
• Prior Olin experience in a relevant position strongly preferred.

Grow your career where you are rewarded and valued.

Who We Are
Since 1892, Olin Corporation has steadily grown to become the industry leader in both chemicals manufacturing and ammunition. The three divisions of Olin Corporation, Olin Chlor Alkali Products and Vinyls, Olin Epoxy and Winchester, employ approximately 8,000 global team members in more than 20 countries with customers in nearly 100 countries around the globe.

*Degree must be from a school that is accredited by an accrediting agency recognized by the Secretary of Education of the U.S. Department of Education or equivalent program from an international university.

Olin does not provide any form of sponsorship. We will only employ those who are legally authorized to work in the United States. Individuals with temporary visas such as E, F-1, H-1, H-2, L, B, J or TN or who need sponsorship now or in the future, are not eligible for hire.

Olin is an equal opportunity employer, and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability status, protected veteran status, or any other characteristic protected by law.

Expected salary:

Location: Lake Jackson, TX

Job date: Sat, 11 Nov 2023 00:36:51 GMT

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Job description: TV and Soap Writer – Casual

Location:

London

Department:

The Sun

Salary Details:

Not Specified

Advertising End Date:

Not Specified

Job Description

The Sun is the biggest news brand in the UK, publishing hundreds of stories a day and reaching over 170m unique users digitally every month. Its exclusives set the news agenda and its campaigns have changed the lives of many. In recent years, The Sun has campaigned for victims of domestic abuse, NHS workers and veterans to name only a few.

The Sun has a mass-market audience and aims to appeal to a diverse audience in the UK and beyond.

The role requires a self-motivated, energetic individual who has extensive media experience and is used to operating within a fast-paced news environment. This is an opportunity to work for a famous brand and drive reputation by amplifying positive actions.

Your role: Are you a talented writer/interviewer and passionate about TV? Do you know your Beales from your Barlows? Are you up to date with the biggest TV and streaming series? The team behind the country’s top telly guide, TV Mag, and newspaper supplement TV Soap is looking for a writer to join us, starting in January 2024.

Day to day you will:

• Interview a huge range of TV talent

Write engaging and original features

Direct our readers to the best TV of the week with humorous and knowledgeable previews

Contribute to our vital soap pages in TV Mag and TV Soap

Check schedules from TV channels and staying in touch with PRs to find out when all the big shows start

Attend launches, screenings and visits to the sets of TV shows in production, during working hours and evenings/weekends when required

Come up with fresh ideas to ensure we stay ahead of our rivals

Mindful of IPSO and legal requirements while working speedily and accurately to deadline

What we’re looking for from you:

• Previous experience on a national consumer magazine or supplement. Experience on a TV magazine and knowledge of listings is preferred.

Accurate, fast writing and basic editing skills

Passion for TV and soaps

The ability to work in our London office when needed

A willingness to embrace on-going digital challenges

We are News UK: One of the leading media businesses in the UK and Ireland. Our newsbrands include The Times, The Sunday Times, The Sun, The Sun on Sunday and The TLS. Our national broadcast brands include talkSPORT, Times Radio, TalkTV and Virgin Radio UK, and we have market-leading local radio stations across Ireland. Our world-famous brands provide news, analysis, opinion and entertainment to almost 40 million people each month. Spanning print and pixel, audio and video, events and experiences, our multiplatform brands are home to a plurality of opinion, representing the diverse communities we serve. News UK is wholly owned by News Corp.

Life at News

Driven by passion, guided by principles and acting with purpose. We represent, reflect and reach the nation, telling the stories that matter. We inform our audiences so that they can make decisions based on trusted information.

To do this, we believe our employees must represent different backgrounds, perspectives and experiences. We strive to maximise and encourage every individual’s potential and ensure everyone feels valued. We support this through ourDiversity, Equity and Inclusion Strategy (https://www.news.co.uk/more-than-the-news/diversity-inclusion/) , which focuses on three main priorities – attracting talent from a wider, more representative pool, developing equity programmes to drive better representation in our leadership, and ensuring diversity and inclusivity in our workforce as well as the journalism and content we produce. We also currently have12 employee led networks and groups (https://www.youtube.com/watch?v=IMCi-KiMlL4&t=2s) that support our strategy and connect like minded employees socially.

We want to ensure that everyone we meet has the opportunity to perform to their best when applying for a role. Please let us know, at any stage, whether you require any reasonable adjustments during the recruitment process, and we will do our best to accommodate.

Expected salary:

Location: London

Job date: Sun, 12 Nov 2023 04:17:34 GMT

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Job description: Description

Who We Are

From research and discovery to post-market clinical development, our WWRD engine involves all bench and clinical research and the associated groups that support those endeavors. Our teams work on developing first-in-class and best-in-class therapeutics that provide meaningful advances to patients who live with genetic diseases.

Summary

The Clinical Medical Writer 2 applies intermediate to advanced documentation preparation and document project management skills to assist in the development, drafting, review, editing, and finalization of documents used in conducting clinical studies and reporting clinical study results for regulatory submissions and publications.

Responsibilities

• Drafts and edits documents used in conducting and reporting the results of clinical studies, including protocols, protocol amendments, informed consent forms, and clinical study reports
• Drafts and edits documents used in reporting aggregate safety and efficacy information for a molecule, such as investigator’s brochures and periodic safety reports (PSURs, DSURs, etc.)
• Manages study team participation in the preparation of such documents, including calling/running meetings, developing and managing timelines, and managing the document review and comment adjudication processes
• Provides peer review and editing support for other regulatory documents, such as statistical analysis plans, CRFs, and other study materials
• Adheres to departmental procedures and practices and technical and industry standards during all aspects of work.
• Assists in developing and reviewing standard processes and templates within Clinical Medical Writing
• Works effectively with cross-functional groups within BioMarin
• Other tasks as assigned.

Education & Experience

• Bachelor’s or higher degree required; scientific focus desirable.

• Minimum requirement: University-level medical or technical writing course(s) or equivalent experience in science/technical writing.

• Evidence of medical writing career development desirable, eg, American Medical Writers Association certificate, Editor in Life Sciences certificate, or relevant training through Drug Information Association.

Fulfills one of the following:

• Up to 4 years of as a medical writer in the pharmaceutical industry
• At least 7 years of medical or scientific writing experience as a primary job responsibility

Clinical Studies

• Intermediate to advanced understanding of the drug development process (discovery to market), biostatistical and clinical research concepts, clinical study conduct, and clinical study data collection.
• Basic understanding of scientific concepts integral to nonclinical development, CMC, PK, PD, and antibody detection.
• Intermediate to advanced applied knowledge of:

• documentation required for the conduct of clinical studies
• protocol design (including objectives, efficacy and safety endpoints, and procedures for collecting and reporting AEs and SAEs)
• study results reporting
• Familiarity with documentation in all phases of drug development.

Medical Writing

• Writing high-quality documents that support corporate goals and objectives.
• Experience writing, reviewing, or editing protocols and clinical study reports highly preferred.
• Experience writing, reviewing, or editing INDs and BLA/NDAs preferred.
• Intermediate to advanced applied knowledge of routine document content preparation, including the use of style guides (internal, AMA, CBE, Chicago), medical dictionaries, and guidance documents that prescribe content.
• Ability to interpret basic tabular and graphical clinical data presentations.
• Ability to create basic tables using AMA style (eg, Schedule of Events).
• Intermediate applied knowledge of basic clinical laboratory tests.
• Basic understanding of the concepts of coding dictionaries (MedDRA, WHO Drug).

Computer/office equipment Skills

• Proficient in Microsoft Word (including the use of templates), Excel, Adobe Acrobat, and PowerPoint.
• Experience using document management software (eg, LiveLink, SharePoint, Veeva)
• Experienced with scanners, printers, and copiers.

Regulatory

• Basic knowledge of regulatory requirements and guidances associated with ‘standalone’ regulatory documents (eg, protocols, investigator brochures, and clinical study reports).

Project Management

• Capable of working on multiple tasks and shifting priorities.
• Capable of leading a cross-functional team under strict timelines, including calling/running meetings and managing team review and comment adjudication stages of document preparation.
• Good conflict management skills.
• Motivated and shows initiative.
• Detail oriented.

Communication

• Capable of well organized, concise and clear written and verbal communication.
• Capable of comprehending complex scientific concepts and translating them into clear, concise, appropriately referenced text that meets regulatory requirements.

• Effective at explaining writing principles to a varied audience both in individual and group settings; basic presentation skills.

We are an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion, gender, gender identity, sexual orientation, national origin, disability status, protected veteran status, or any other characteristic protected by law.

Expected salary:

Location: London

Job date: Sun, 05 Nov 2023 01:09:28 GMT

Apply for the job now!

The post Medical Writer 2 – UK, also open in the US appeared first on World News: Entertainment, lifestyle, Health, Technology.

Job description: Description

Who We Are

From research and discovery to post-market clinical development, our WWRD engine involves all bench and clinical research and the associated groups that support those endeavors. Our teams work on developing first-in-class and best-in-class therapeutics that provide meaningful advances to patients who live with genetic diseases.

Summary

The Clinical Medical Writer 2 applies intermediate to advanced documentation preparation and document project management skills to assist in the development, drafting, review, editing, and finalization of documents used in conducting clinical studies and reporting clinical study results for regulatory submissions and publications.

Responsibilities

• Drafts and edits documents used in conducting and reporting the results of clinical studies, including protocols, protocol amendments, informed consent forms, and clinical study reports
• Drafts and edits documents used in reporting aggregate safety and efficacy information for a molecule, such as investigator’s brochures and periodic safety reports (PSURs, DSURs, etc.)
• Manages study team participation in the preparation of such documents, including calling/running meetings, developing and managing timelines, and managing the document review and comment adjudication processes
• Provides peer review and editing support for other regulatory documents, such as statistical analysis plans, CRFs, and other study materials
• Adheres to departmental procedures and practices and technical and industry standards during all aspects of work.
• Assists in developing and reviewing standard processes and templates within Clinical Medical Writing
• Works effectively with cross-functional groups within BioMarin
• Other tasks as assigned.

Education & Experience

• Bachelor’s or higher degree required; scientific focus desirable.

• Minimum requirement: University-level medical or technical writing course(s) or equivalent experience in science/technical writing.

• Evidence of medical writing career development desirable, eg, American Medical Writers Association certificate, Editor in Life Sciences certificate, or relevant training through Drug Information Association.

Fulfills one of the following:

• Up to 4 years of as a medical writer in the pharmaceutical industry
• At least 7 years of medical or scientific writing experience as a primary job responsibility

Clinical Studies

• Intermediate to advanced understanding of the drug development process (discovery to market), biostatistical and clinical research concepts, clinical study conduct, and clinical study data collection.
• Basic understanding of scientific concepts integral to nonclinical development, CMC, PK, PD, and antibody detection.
• Intermediate to advanced applied knowledge of:

• documentation required for the conduct of clinical studies
• protocol design (including objectives, efficacy and safety endpoints, and procedures for collecting and reporting AEs and SAEs)
• study results reporting
• Familiarity with documentation in all phases of drug development.

Medical Writing

• Writing high-quality documents that support corporate goals and objectives.
• Experience writing, reviewing, or editing protocols and clinical study reports highly preferred.
• Experience writing, reviewing, or editing INDs and BLA/NDAs preferred.
• Intermediate to advanced applied knowledge of routine document content preparation, including the use of style guides (internal, AMA, CBE, Chicago), medical dictionaries, and guidance documents that prescribe content.
• Ability to interpret basic tabular and graphical clinical data presentations.
• Ability to create basic tables using AMA style (eg, Schedule of Events).
• Intermediate applied knowledge of basic clinical laboratory tests.
• Basic understanding of the concepts of coding dictionaries (MedDRA, WHO Drug).

Computer/office equipment Skills

• Proficient in Microsoft Word (including the use of templates), Excel, Adobe Acrobat, and PowerPoint.
• Experience using document management software (eg, LiveLink, SharePoint, Veeva)
• Experienced with scanners, printers, and copiers.

Regulatory

• Basic knowledge of regulatory requirements and guidances associated with ‘standalone’ regulatory documents (eg, protocols, investigator brochures, and clinical study reports).

Project Management

• Capable of working on multiple tasks and shifting priorities.
• Capable of leading a cross-functional team under strict timelines, including calling/running meetings and managing team review and comment adjudication stages of document preparation.
• Good conflict management skills.
• Motivated and shows initiative.
• Detail oriented.

Communication

• Capable of well organized, concise and clear written and verbal communication.
• Capable of comprehending complex scientific concepts and translating them into clear, concise, appropriately referenced text that meets regulatory requirements.

• Effective at explaining writing principles to a varied audience both in individual and group settings; basic presentation skills.

We are an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion, gender, gender identity, sexual orientation, national origin, disability status, protected veteran status, or any other characteristic protected by law.

Expected salary:

Location: London

Job date: Sun, 05 Nov 2023 08:17:54 GMT

Apply for the job now!

The post Medical Writer 2 – UK, also open in the US appeared first on World News: Entertainment, lifestyle, Health, Technology.

Job description: DMTC Agency is an all-inclusive, integrated digital marketing agency with offices and teams in Nigeria, Ghana, and Egypt, serving clients across Africa and beyond. We have worked with global brands, household names, healthcare providers, FMCG companies, educational institutions, and service providers.

We are recruiting to fill the position below:

Job Position: Content Writer (Digital)

Job Location: Ikeja, Lagos

Employment Type: Full-time

About Role

• We are searching for a copywriter with a knack for weaving words into wordplays & puns to produce creative and compelling copy for advertisements, scripts, social media material, and websites.
• The ideal candidate is a creative team player, talented wordsmith, and grammar sleuth.
• You will be responsible for developing marketing and communications content that will separate us from the crowd with a keen eye for detail. We’d like to meet with you if you can quickly comprehend project requirements and provide meaningful insight.

Responsibilities

• Writing clear and error-free content for a website that reflects the company’s voice
• Meeting with clients to understand their message, brand voice, and target audience
• Proposing copy concepts in an engaging way for clients and carrying out projects once they are approved
• Create content and maintain effective, cohesive, and engaging brand messaging and content across all platforms including all Social Media Platforms, Websites, Blogs, Emails, newsletters, news, events, landing pages, campaigns, Influencers, PR, digital video scripts other content either with the team assigned or independently.
• Create, maintain and implement an end-to-end digital marketing and editorial calendars
• Identify gaps in current content topics and recommend new content topics across all digital platforms basis client requirements, listening, trends, keyword research, topical, etc on the need basis.
• Interpreting creative direction and technical information and turning them into persuasive copy concepts
• Collaborating with PR and marketing departments to brainstorm and develop a variety of marketing materials
• Working with clients to edit and modify the copy to meet their content expectations
• Client content requirements need to be communicated timely to the content lead at the start of the content calendar as well as on a need basis.
• Assist Content Lead in creating all content
• Put across the content created by Strategy and Content team and Creative team in the content calendar format (PPT) and share with the client for feedback and approval.
• Follow the process like filling out a proper briefing document, kick-off meeting, MOM, and action plan providing support to the media lead and providing the required information, getting all the required details from the client, etc in a timely manner.
• Conduct keyword and SEO research and create content topics and content around it.

Requirements

• 1-3+ years of copywriting experience, preferably at an advertising agency, in-house at a significant brand, or at a publication
• Proofreading skills and knowledge of standard style guidelines are required.
• A strong eye for detail and a love of good design
• To be able to deliver on time, you must be comfortable organizing several projects at the same time.
• Capable of clearly communicating edits to coworkers, even when teams are dispersed across different countries.
• Capable of working both independently and as part of a team.

Method of Application

Interested and qualified candidates should send their CV & Cover Letter to: using the Job Position as the subject of the mail.

Note: We will require you to create and submit up to four writing samples so that we can get a sense of your best work. In your application, feel inclined to include links to your work or portfolio.

Expected salary:

Location: Ikeja, Lagos State

Job date: Sun, 03 Dec 2023 08:37:43 GMT

Apply for the job now!

The post Content Writer (Digital) Job at DMTC Agency appeared first on World News: Entertainment, lifestyle, Health, Technology.

Job description: Initial Posting Date: 11/06/2023

Application Deadline: 11/27/2023

Agency: Department of Environmental Quality

Salary Range: $4,688 – $7,175

Position Type: Employee

Position Title: NPDES Permit Writer (Natural Resource Specialist 3)

Job Description:

The Oregon Department of Environmental Quality strives to build and sustain an inclusive environment that embraces and values diversity. Employees at all levels of the agency work together to foster fairness, equity, inclusion, and belonging. We are an equal opportunity employer and do not discriminate based on race, color, national origin, ethnicity, veteran, gender, sexual orientation, religion, age, or physical or mental disability. Candidates from diverse backgrounds are encouraged to apply. We are most interested in finding the best candidate for the job, and that candidate may not meet every one of our listed preferred qualifications. Lived experience may count towards the preferred qualification. If you are excited about this position, we encourage you to apply. If you are unsure as to whether or not you meet the qualifications of this position, please contact us to discuss your application.

Are you passionate about preserving, enhancing, and protecting Oregon’s environment? If so, please consider a career with the State of Oregon at the . At DEQ, employees have the opportunity to work with a dynamic and supportive team of mission-focused individuals tasked with maintaining, restoring, and enhancing the quality of Oregon’s air, land, and water. Here is a video about DEQ:

The Oregon Department of Environmental Quality has a full-time opportunity available for a NPDES Permit Writer (Natural Resource Specialist 3) in Portland, Oregon.

Please consider joining an innovative team, and work to advance our agency’s mission to protect and improve Oregon’s environmental quality. There are 3 regions (Northwest, Western, and Eastern); this position is in Northwest Region. The Regions provide the following services: compliance inspection of regulated entities; enforcement of permit requirements and administrative rules; issuance of air, water, and solid waste permits; investigation of complaints; issuance of subsurface permits in counties; response to spills or other incidents with environmental impacts; direct contact and liaison with other governmental entities, industries, and the public; and technical assistance to regulated entities and the public.

Click to view a map of all of the DEQ offices.

What you will do!

You will develop National Pollutant Discharge Elimination permits for major or minor wastewater sources in any part of Oregon. You will solve difficult NPDES permit-related problems, such as developing strategies for compliance with water quality standards or discharges to water-quality limited water bodies.

What’s in it for you!

The opportunity to work in a productive and creative environment where no two days are ever the same! We offer a that offers comprehensive medical, dental, and vision plans for the employee and their qualified family members, as well as paid sick leave, vacation leave, personal leave, and 11 paid holidays a year. In addition, we offer membership in the , and you have the opportunity to potentially receive loan forgiveness under the . If you are passionate about Oregon’s environment, apply today!

This is a full-time, AFSCME represented position.

This recruitment may be used to fill future vacancies.

What are we looking for?

Minimum Qualifications: Bachelor’s degree in physical science, environmental science, natural resources, or a closely related field, AND 3 years of experience in a natural resource or environmental field (an equivalent combination of education and experience is acceptable). At least 1 year of experience at a technical or professional level performing activities in a natural resource program such as researching and analyzing data, conducting investigations, applying pertinent laws and regulations, or coordinating and monitoring project activities.

Candidates who are most competitive will also reflect the following:

• Demonstrated understanding of environmental justice and the historical impacts for marginalized and underrepresented communities; ability to take personal responsibility for increasing their knowledge of environmental justice and diversity, equity, inclusion, and belonging.
• Excellent verbal and written communication skills; ability to provide clear, concise, and compelling communication of policy and technical information tailored to the needs of diverse audiences; skill in writing and presenting clear and concise reports that include qualitative and quantitative analyses, recommendations, and conclusions to diverse audiences.
• Experience developing and/or implementing NPDES permits.
• Experience with R programming language.
• Ability to use computer modeling and statistical tools to analyze study results.
• Ability to learn laws, regulations, and permit procedures applicable to the technology and industry under review.
• Excellent project management skills: ability to plan, schedule, and coordinate large, complex projects.

Working Conditions:

DEQ believes in a diverse and inclusive work environment. All employees are expected to contribute to a work environment that collectively values and benefits from respecting its diversity and promotes a culture of inclusiveness.

This position will be based out of DEQ’s Portland Office, however, the successful candidate may be eligible for hybrid work. The logistics of hybrid work will need to be worked out with the Hiring Manager prior to your hire and may be changed at any time given specific job duties and business needs. DEQ will provide necessary hardware (laptop, monitor, keyboard, mouse, and cell phone) for an employee to successfully work from home. At DEQ sites, you will have access to a workspace, however, it may be shared with other employees.

This position requires occasional travel on official State business for public hearings, visits to DEQ regional offices, conferences, trainings, seminars, and meetings, some of which may include evening work, overnight stays, and/or weekend work. Some field work and inspections may include substantial walking, climbing of stairs, kneeling, and stooping.

How to Apply: (complete the application in full)

• External Applicants Click on the “Apply” button and submit your application. Click this

for the External Candidate job aid, and view this for additional information. * Internal Applicants (current State of Oregon employees): Apply through your employee Workday account. View this

for assistance.

Helpful Tips:

• Allow yourself plenty of time to complete and submit the application.
• Workday will timeout after 15 minutes of inactivity.
• This posting closes at 11:59 PM on the close date listed.
• Please save a copy of the job announcement for your reference, as it may not be available for you to view after the job posting closes.
• Be sure to check both your email and Workday account for updates regarding this recruitment.
• Workday performs best in Google Chrome.
• Click here for

and a .

Please Note: In addition to your related work experience and education, DEQ will use the desired attributes and minimum qualifications above, under the “What are we looking for?” section to determine whom to interview. Please make sure your attributes and minimum qualifications are clearly demonstrated in your application material.

Veterans Information:

DEQ provides veterans’ preference points to all eligible veterans. For more information on veterans’ preference, please visit , or call the Oregon Department of Veterans’ Affairs at: 1-800-692-9666. For privacy reasons, please do not attach veterans’ preference documents when initially applying. You will be asked to submit those at a later time.

Pay Equity:

As an employer, the State of Oregon complies with HB 2005, the Pay Equity Bill. We do not discriminate on the basis of protected class in the payment of wages, and we do not screen applicants on the basis of their current or past compensation. Please visit for more information. Please note: the salary listed is the non-PERS qualifying salary range. If the successful candidate is PERS qualifying, the salary range will reflect an additional 6.95% (6% goes to PERS and .95% covers payroll taxes). Please review the page for more details.

Work Authorization:

DEQ does not offer visa sponsorships. On the first day of employment, all hires will be required to complete the US Department of Homeland Security’s Form I-9, confirming authorization to work in the United States. In addition, hires will have three business days from their first day of employment to present documents that establish employment authorization and identity. DEQ is an E-Verify employer and will use E-Verify to confirm that hires are authorized to work in the United States.

Questions/Need Help?

If you have questions about the recruitment or need assistance to participate in the application process, please contact Willa Wilbanks, Human Resources Analyst, at or (503) 347-0029. TTY users: please use the Oregon Telecommunications Relay Service at 1-800-735-2900.

Expected salary: $4688 – 7175 per month

Location: Portland, OR

Job date: Wed, 08 Nov 2023 06:48:27 GMT

Apply for the job now!

The post NPDES Permit Writer (Natural Resource Specialist 3) appeared first on World News: Entertainment, lifestyle, Health, Technology.

Job description: About Careers by Design:

We are an inspired team of Career Professionals (Resume Writers and Transformational Career Coaches) who work independently and as part of a team of like-minded people. We help and support each other, as we help our clients and ourselves to have More Happy Mondays.

Over the years, we’ve helped thousands of people. We just celebrated our 17th birthday and are growing steadily.

About our ideal Resume Writer:

You are a motivated, self-starting writing professional based in Canada. Your work stands out and you continually strive to be a leader in the field. You are aware of current industry trends and seek out personal and professional development to stay at the top of your game.

You have the self management and time management skills to manage your work projects with ease.

Relationships are important to you. You show respect, care and compassion in your interactions with colleagues and clients.

You enjoy the benefits of working from your own home office and are a team player who values opportunities to be part of a team of heart-centered professionals. Attending company events is a priority and a valued part of your professional life.

Helping clients define their Personal Brand and boost their chances of career success excites you. You enjoy helping others feel more confident by bringing out their strengths and articulating their accomplishments in resumes, cover letters and Linked in profiles.

You have experience writing resumes for senior professionals/executives, mid-career & starting out professionals.

If you’re nodding your head in agreement, apply to join our team of like-minded, heart-centred career professionals at Careers by Design. We’re one of the fastest growing career services companies in Canada and we are on a mission to bring more heart to the job search process!

More about the Role:

This position is for a full-time or part-time contractor who is able to maintain a 3 business day turnaround, from time of consultation, on first draft materials sent to clients. Compensation is provided per package completed.

A day in the life of our resume writer:

The writer will be client-facing and involved in all client interaction.

Sales:

The writer will talk with leads who are interested in using our services and be confident and skillful in selling the resume service to those that are a good fit. Please note: these will be very interested people who are already aware of the pricing.

Service Delivery:

The writer will meet with clients who have purchased services via Zoom (from his/her home office) to collect information for the resume and any other materials.

The writer will use the information + client’s existing resume to create documents that will secure interviews. The writer will follow Careers by Design’s guidelines and accomplishments-based resume framework.

The writer will provide all documents to the client within 3 business days. The writer will be available to respond to requests for edits and revisions from the client until the final documents are complete and signed-off by the client.

The writer will maintain record of client work in CRM software.

Main responsibilities:

• Conduct highly professional and motivating intake interviews over Zoom video-conferencing. All client-facing work is done remotely from your own (home) office.
• Conduct phone chats to advise leads of our services and why they should choose us
• Work with our clients to help them better articulate their strengths and talents into finely crafted marketing materials that turn heads and win interviews.
• Use and adhere to our Careers by Design accomplishments-based resume framework and model.
• Provide edits and revisions of documents.
• Maintain quick turn-around times, as per agreed upon deadlines with management.
• Maintain record-keeping of client work in CRM.

Qualifications:

• Excellent written and oral communication skills.
• Strong educational background supporting superior writing skills.
• Exceptionally talented at asking key questions & drawing out accomplishments from an interview setting.
• High attention to detail.
• Knowledge of various industries.
• Understanding of how to write resumes and marketing materials for individuals pursuing a career transition.
• Knowledge of applicant tracking systems and how to write resumes that pass through.
• Adept at customer service.
• Ability to work with clients with empathy and understanding.
• Ability to create resumes and marketing materials with a highly polished design and look.
• Proficiency in Word, InDesign and Adobe Acrobat.
• Ability to work in a virtual team environment with quick access to updates via email.

Experience:

• Have written a minimum of 100 resumes and are committed to a high level of proficiency
• Experience in recruiting, HR or career counselling an asset.

Compensation:

• based on qualifications and experience
• we pay above industry standard

Thank you for your interest in working with us.

Expected salary:

Location: Toronto, ON

Job date: Thu, 31 Aug 2023 07:00:15 GMT

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Job description: By continuing, you will be directed to a site intended only for residents of the United States and Canada. We are called MSD everywhere, except in the United States and Canada where we are known as Merck & Co., Inc., Rahway, NJ, USA.

We are one company, but we operate under two different corporate brand names. We are known as Merck & Co., Inc., Rahway, New Jersey, USA in the United States, Canada & Puerto Rico. We are known as MSD everywhere else.

The link you have selected will take you to a third-party website, owned and operated by AgileOne. Our company does not control, and is not responsible for, the accuracy, content, practices, or standards of the pharmatempjobs.com website and/or AgileOne.

No

Corporate responsibility

Reporting on our commitment to society, people and communities around the world

An initiative to create a world where no woman has to die giving life

About Merck

The global animal health business unit of Merck

Copyright © 2023 Merck & Co., Inc., Rahway, NJ, USA and its affiliates. All rights reserved.

Forward-Looking Statement

Forward-Looking Statement of Merck & Co., Inc., Kenilworth, NJ, USA

This website of Merck & Co., Inc., Kenilworth, NJ, USA (the “company”) includes “forward-looking statements” within the meaning of the safe harbor provisions of the United States Private Securities Litigation Reform Act of 1995. These statements are based upon the current beliefs and expectations of the company’s management and are subject to significant risks and uncertainties. There can be no guarantees with respect to pipeline products that the products will receive the necessary regulatory approvals or that they will prove to be commercially successful. If underlying assumptions prove inaccurate or risks or uncertainties materialize, actual results may differ materially from those set forth in the forward-looking statements.

Risks and uncertainties include, but are not limited to, general industry conditions and competition; general economic factors, including interest rate and currency exchange rate fluctuations; the impact of pharmaceutical industry regulation and healthcare legislation in the United States and internationally; global trends toward healthcare cost containment; technological advances, new products and patents attained by competitors; challenges inherent in new product development, including obtaining regulatory approval; the company’s ability to accurately predict future market conditions; manufacturing difficulties or delays; financial instability of international economies and sovereign risk; dependence on the effectiveness of the company’s patents and other protections for innovative products; and the exposure to litigation, including patent litigation, and/or regulatory actions.

The company undertakes no obligation to publicly update any forward-looking statement, whether as a result of new information, future events or otherwise. Additional factors that could cause results to differ materially from those described in the forward-looking statements can be found in the company’s 2015 Annual Report on Form 10-K and the company’s other filings with the Securities and Exchange Commission (SEC) available at the SEC’s Internet site (www.sec.gov).

No Duty to Update

The information contained in this website was current as of the date presented. The company assumes no duty to update the information to reflect subsequent developments. Consequently, the company will not update the information contained in the website and investors should not rely upon the information as current or accurate after the presentation date.

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Attention

By continuing, you will be directed to a site intended only for residents of the United States and Canada. We are called MSD everywhere, except in the United States and Canada where we are known as Merck & Co., Inc., Rahway, NJ, USA.

Expected salary:

Location: USA

Job date: Sun, 22 Oct 2023 07:29:04 GMT

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Job description: About Lee Valley

Lee Valley is a family-owned Canadian business serving customers all over the world. What began as a small selection of woodworking tools has grown to include gardening tools, hardware, gifts and items for every area of the home. We have 18 stores across Canada and a strong online presence. We have come a long way since the company’s founding in 1978. We pride ourselves on remaining a trusted advisor and the resource of choice to our customers.

When you join the Lee Valley family, you become part of a proud 45-year history of providing high-quality products and gift merchandise to customers worldwide. A position at Lee Valley is more than just a job – we honor the time and dedication that our people give by providing sustained and meaningful employment and we strive to provide an environment where learning and development are encouraged. We follow a simple guiding principle: Treat your customers and colleagues as you would a friend.

Job Description

We are searching for an experienced writer to join our Marketing team. You will use your passion for writing to create engaging copy, collaborate with a design team and be responsible for meeting the requirements of the project briefs while adhering to the Lee Valley brand guidelines for copy, voice and style.

Reporting to the Creative Director, Marketing Communications, you will be part of the Creative Services team. A fast-paced environment, with tight deadlines, schedule target dates and the opportunity to write for a multiple purposes including product description, website needs, SEO, SEM, email campaigns, retail signage, ADOA or any other Marketing purpose.

Key Responsibilities

• Write clear and engaging content for describing woodworking, gardening and home products that aligns to brand voice and guidelines.
• Produce engaging, straightforward content adapted to different advertising channels such as email, websites, digital and print ads, and catalogs. Maintain consistency and brand voice across all channels.
• Implement SEO best practices to ensure content is search engine-optimized for our target audiences.
• Knowledge of writing to meet AODA (Accessibility for Ontarians with Disabilities Act) standards.
• Collaborate with other team members, such as graphic designers, subject matter experts, marketers, and project managers to gather input and feedback for content development that supports the project brief.
• Stay up to date with industry trends and best practices in writing for B2C audiences.
• Present copy concepts and final deliverables to internal team.
• Revise copy based on internal and client feedback.

Requirements

• University degree or 3-year college diploma in English, creative writing, journalism or related humanities field.
• 5-years related writing experience.
• Exceptional writing and research skills with a keen eye for detail.
• A passion for storytelling. You are creative, curious about your subjects, and can write short or long-form copy. Familiarity writing for print and digital marketing campaigns.
• Experience working with Microsoft Office.
• Familiarity with keyword search methods as well as SEO tools.
• Knowledge of AODA requirements.
• Strong verbal and written communication skills.
• Exceptional time-management and organizational skills.
• An analytical mind with a problem-solving attitude.
• Thrive in a fast-paced, collaborative environment with a high-volume workload often requiring short turnaround times.
• A portfolio of copywriting and other marketing samples, targeting B2C.
• A writing exercise may be requested should you be contacted for an interview.

What we offer…

• Competitive compensation program including competitive base salary, a robust health and dental benefits packages well as a matching group retirement plan.
• Paid vacation and sick leave.
• Employee discount
• A family oriented environment that supports growth and development for all employees.

Diversity and Inclusion:

At Lee Valley, we are proud to celebrate and foster a diverse team of professionals. We take pride in nurturing an inclusive culture that empowers our people to be their authentic selves, celebrate their differences and love where they work. Our diverse community combined with our inclusive culture, is what sets us apart in the industry.

We encourage all candidates to apply for job opportunities with Lee Valley regardless of race, national origin, colour, religion, age, gender identity or expression, sexual orientation, marital and family status, or disability.

If you require accommodation during the recruitment and selection process, please do not hesitate to reach out.

Expected salary:

Location: Ottawa, ON

Job date: Wed, 16 Aug 2023 04:38:01 GMT

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