Acid Supervisor Job Description Samples

Results for the star of Acid Supervisor

Development Associate Iii, Nucleic Acid Technology

Position Summary This Development Associate III position will contribute to the optimization of manufacturing processes for Alexion’s biotherapeutic candidates and to the development of nucleic acid analytical/characterization methods. This position will be involved in development efforts ranging from discovery to early-stage clinical manufacture. This role will require collaboration with internal departments and outside partners to support the manufacture of nucleic acid-based therapeutics. Principal Responsibilities

  • Support the development and manufacture of nucleic acid drug candidates from preclinical to early-stage clinical, with emphasis on nucleic acid formulation.

  • Execute analytical method development and testing to support nucleic acid process development and formulation.

  • Facilitate interactions with external partners and CROs in assay development, assay transfer, sample analysis and troubleshooting.

  • Serve as a technical expert on lab instrumentation, software and/or assay procedures.

  • Document study results in technical reports.

  • Support group objectives associated with technology transfers and regulatory filings. Qualifications + 5+ years’ relevant work experience in the biopharmaceutical industry is required.

  • Experience in biophysical, chemical, and/or physicochemical analytical methods for nucleic acid formulations characterization is required.

  • Experience developing assays to support biotherapeutic process development is preferred.

  • Experience working with nucleic acids and in a sterile/RNase-free environment is preferred.

  • Knowledge of nucleic acid delivery technologies, including nanoparticulate and conjugate systems, is preferred.

  • Experience coordinating testing and method development at CROs is preferred.

  • Knowledge of the CMC/regulatory environment as related to nucleic acid therapeutics is preferred.

  • The ability to process, interpret, compile data and generate technical reports is required.

  • A high level of organization and the ability to handle multiple tasks/projects simultaneously are required.

  • Good written and oral communication skills are required.

  • Strong inter-personal skills and a willingness to collaborate with colleagues at the bench and on project teams are required. Education MS in relevant engineering, chemistry, or biological science field with a minimum of 3 years of experience in a pharmaceutical or biotechnology setting, or BS degree in relevant field with a minimum of 5 years of experience in a pharmaceutical or biotechnology setting. *LI-DD1 [[filter5]], [[filter1]] [[filter4]] Alexion is a global biopharmaceutical company focused on developing and delivering life-transforming therapies for patients with devastating and rare disorders. Alexion developed and commercializes Soliris® (eculizumab), the first and only approved complement inhibitor to treat patients with paroxysmal nocturnal hemoglobinuria (PNH) and atypical hemolytic uremic syndrome (aHUS), two life-threatening ultra-rare disorders. As the global leader in complement inhibition, Alexion is strengthening and broadening its portfolio of complement inhibitors, including evaluating potential indications for eculizumab in additional severe and ultra-rare disorders. Alexion’s metabolic franchise includes two highly innovative enzyme replacement therapies for patients with life-threatening and ultra-rare disorders, Strensiq® (asfotase alfa) to treat patients with hypophosphatasia (HPP) and Kanuma™ (sebelipase alfa) to treat patients with lysosomal acid lipase deficiency (LAL-D). In addition, Alexion is advancing the most robust rare disease pipeline in the biotech industry, with highly innovative product candidates in multiple therapeutic areas. As a leading employer in our industry, Alexion is proud to offer a highly competitive package of base and incentive compensation as well as a comprehensive benefits program designed to support the health, wellness and financial security of our employees and their families. Benefits include group medical, vision and dental coverage, group and supplemental life insurance, 401(k) with company match, tuition reimbursement, relocation assistance and much more. To learn more about Alexion, please visit www.alexionpharma.com or download our App for iPhones and Blackberries. Alexion is an Equal Opportunity /Affirmative action employer

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Sales Manager-Food Grade Amino Acids

CheilJedang (CJ) was founded in 1953 specializing in food products. Since then it has grown into a global lifestyle brand with a business portfolio built around the four sectors - Food & Food Service, Bio & Pharma, Entertainment & Media, and Shopping & Logistics. With over 30,000 employees around the world, CJ promotes healthier, happier and convenient living through its many products and services. For more information, please visit www.cjamerica.com This position will lead our US based sales team to drive growth in our portfolio of food grade amino acids and other offerings we may acquire or develop. Success in this position requires leadership, collaboration, and the ability to develop strong relationships with existing and potential customers. Strong analytical and communication skills are also required to lead a successful and diverse team of professional account managers.

  • Hours of work: Some flexibility in hours is allowed, but the employee must be available during core work hours of Monday – Friday, 8:00am-5:00pm. Evening and weekend work may be required as job duties demand.

  • Work location: This position may be home office or Downers Grove office based, depending on business needs.

  • Travel: This position requires up to 50% travel. Frequently travel is outside the local area and overnight.

  • Carries out supervisory responsibilities in accordance with the organization's policies and applicable laws. Responsibilities may include interviewing, hiring and training employees; planning, assigning and directing work; appraising performance; rewarding and disciplining employees; addressing complaints and resolving problems.

  • Builds and maintains relationships with customers, industry influencers and key strategic partners within the food industry.

  • Manage and lead the sales team with account strategies, territory planning and administrative planning to ensure a high level of customer satisfaction is maintained.

  • Assists the sales team with contract negotiations as needed.

  • Assists with the planning of sales exhibits.

  • Attends trade shows as needed.

  • Achieve revenue budget and growth targets through strong tactical implementation.

  • Develop and implement growth plans which increase customer loyalty and retention.

  • Lead the development of key account plans by subordinates.

  • Present and negotiate commercial offers which adhere to marketing strategies.

  • Coordinate across multi-disciplinary teams including but not limited to marketing, supply chain, division leadership and technical service.

  • Provide leadership to the food sales team with a focus on skill development, coaching and creating an environment that fosters teamwork.

  • Develops and implements procedures pertinent to the effective and efficient operation of the sales department.

  • Develops and implements strategic sales plans to meet objectives and goals.

  • Sets performance standards of the sales department to meet company goals.

  • Keeps informed of food industry market trends, competitor activity and developments.

  • Resolve customer complaints or issues while protecting company assets and interests.

  • Create reports as needed.

  • Perform other duties as necessary.

  • Bachelor Degree in a related field; + 8+ years sales experience in food grade amino acids, or in a similar industry such as nutritional/dietary supplements, pharmaceuticals, cosmetics, pet food for companion animals; + 3-5 years experience managing a team with demonstrated success; + Previous experience in a customer facing role + Knowledge of food grade amino acids, or experience in a similar industry such as nutritional/dietary supplements, pharmaceuticals, cosmetics, pet food for companion animals; + Strong analytical and competency using technology to improve results; + Ability to interact at multiple levels in customer organizations, including the ability to develop business relationships at the executive level; + Excellent verbal and written communications skills including the ability to present technical data; + Demonstrated success in a results driven, team environment with the ability to lead by example; + Computer skills, i.e. Microsoft Office Suite; SAP + Must be able to maintain confidentiality; Successful passing of a post offer criminal background check is required. External Company Name: CJ America, Inc.

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Scientist, Nucleic Acids Therapeutics, Nibr Biologics Center (Nbc)

We have a research scientist position open in the Nucleic Acids Sciences unit of NIBR Biologics Center (NBC) at our Cambridge, MA site. We are seeking a highly motivated and experienced candidate with at least 3 years of hands-on experience with cell culture and molecular biology techniques, and a proven track record in the execution, analysis and interpretation of in vitro cellular and molecular biology assays. The candidate will engage in a variety of lab-based investigative, mechanistic nucleic acids research efforts related to the identification and evaluation of novel therapeutic nucleic acid modalities. The successful candidate must be able to multi-task and work in a team atmosphere but will have a high degree of independence regarding the planning and execution of experiments. Strong verbal communication skills, a well-organized working style as well as timely and accurate technical reporting and documentation are essential to the position. EEO Statement The Novartis Group of Companies are Equal Opportunity Employers and take pride in maintaining a diverse environment. We do not discriminate in recruitment, hiring, training, promotion or any other employment practices for reasons of race, color, religion, gender, national origin, age, sexual orientation, marital or veteran status, disability, or any other legally protected status. Minimum requirements - MS degree in biochemistry, molecular or cell biology, or a related field, or a BS degree and at least 2 years of relevant laboratory experience.

  • Develop and optimize cell based assays for transfection of nucleic acid constructs (mRNA, antisense, CRISPR, DNA, AAV...) using lipid and polymer based formulations in multiple cell lines and using molecular biology techniques such as Luminescence/Fluorescence based assays and ELISA, cytotoxicity and cell proliferation assays.

  • Perform formulation optimization for nucleic acid delivery and assist in biophysical characterizations such as particle size analysis, zeta potential and encapsulation using instruments such as Malvern ZetaSizer and gel based imaging.

  • Assist in planning and delivery of nucleic acids formulations for in vivo studies.

  • Demonstrated ability to troubleshoot instruments and analytical assays.

  • Ability to interact and innovate within multidisciplinary team of chemists, biologists and pharmacologists

  • Excellent oral presentation and communication skills.

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Acid Process Engineer


Job Description:

As a member of the Nitrocellulose/Acid team, the successful candidate will be responsible for supporting our manufacturing operations. This person will be responsible for evaluating current processes and configuring manufacturing systems to reduce cost, improve sustainability, and develop best practices within the production process. Excellent communication and organizational skills will be required to provide real-time floor support, guidance, and direction to operations personnel. This individual will work closely with other Process Engineers on key projects and initiatives.
The successful candidate should exhibit sound judgment, initiative and self-motivation, and be able to complete tasks with minimal supervision. Solid communication, teamwork and integration skills will be required to work effectively across functions at multiple levels. The ability to manage time effectively while dealing with a variety of issues in a dynamic environment will be key to the success of this individual.

Manufacturing support will include:
Provide process engineering support to the Acid Manufacturing Department
Develop new and redline existing Piping & Instrumentation Diagrams
Provide technical support to meet schedules in accordance with quality standards, safety requirements, and regulatory standards
Facilitate and/or support improvement projects, maintenance projects, and aid in process troubleshooting
Provide technical assistance and troubleshooting with process control systems
Provide on call Technical support
Author, maintain and update necessary Procedures & assist with training when applicable
Develop cost estimates for new/existing products and projects
Collaborate and function in a team based environment
Develop Process Flow Diagrams and Heat & Material Balances
Interact with customers and suppliers
Lead/support Process Hazard Analysis for new and existing processes
Support Environmental Risk Management Plan

Interact and support modernization projects within the Acid Area
Develop new and redline existing Process Narratives
Develop and implement quality, safety, and process improvements
Minimum Education and Experience:
Bachelor's Degree and 2 years work experience or equivalent experience
Required Skills and Education:
Bachelor s Degree in a technical or engineering discipline
Preferred Skills and Education:
Degree in Chemical Engineering. Manufacturing experience working in chemical a process. Experience with energetics manufacturing.
About BAE Systems Platforms & Services Posting:
BAE Systems is a premier global defense and security company with approximately 90,000 employees delivering a full range of products and services for air, land and naval forces, as well as advanced electronics, security, information technology solutions and customer support and services. With headquarters in Arlington, Virginia, this Platform and Services Group of BAE Systems employs nearly 11,000 professionals at more than 30 locations worldwide. Platform and Services is a global leader in the design, development, production, and service support of armored combat vehicles, major and minor caliber naval guns and missile launchers, canisters, artillery systems, and intelligent munitions. People are the greatest asset in any Company. Equal Opportunity Employer/Females/Minorities/Veterans/Disabled/Sexual Orientation/Gender Identity/Gender Expression

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Development Associate Iii, Nucleic Acid Technology

Position Summary

This Development Associate III position will contribute to the optimization of manufacturing processes for Alexion's biotherapeutic candidates and to the development of nucleic acid analytical/characterization methods. This position will be involved in development efforts ranging from discovery to early-stage clinical manufacture. This role will require collaboration with internal departments and outside partners to support the manufacture of nucleic acid-based therapeutics.

Principal Responsibilities

  • Support the development and manufacture of nucleic acid drug candidates from preclinical to early-stage clinical, with emphasis on nucleic acid formulation.

  • Execute analytical method development and testing to support nucleic acid process development and formulation.

  • Facilitate interactions with external partners and CROs in assay development, assay transfer, sample analysis and troubleshooting.

  • Serve as a technical expert on lab instrumentation, software and/or assay procedures.

  • Document study results in technical reports.

  • Support group objectives associated with technology transfers and regulatory filings.

Qualifications

  • 5+ years' relevant work experience in the biopharmaceutical industry is required.

  • Experience in biophysical, chemical, and/or physicochemical analytical methods for nucleic acid formulations characterization is required.

  • Experience developing assays to support biotherapeutic process development is preferred.

  • Experience working with nucleic acids and in a sterile/RNase-free environment is preferred.

  • Knowledge of nucleic acid delivery technologies, including nanoparticulate and conjugate systems, is preferred.

  • Experience coordinating testing and method development at CROs is preferred.

  • Knowledge of the CMC/regulatory environment as related to nucleic acid therapeutics is preferred.

  • The ability to process, interpret, compile data and generate technical reports is required.

  • A high level of organization and the ability to handle multiple tasks/projects simultaneously are required.

  • Good written and oral communication skills are required.

  • Strong inter-personal skills and a willingness to collaborate with colleagues at the bench and on project teams are required.

Education

MS in relevant engineering, chemistry, or biological science field with a minimum of 3 years of experience in a pharmaceutical or biotechnology setting, or BS degree in relevant field with a minimum of 5 years of experience in a pharmaceutical or biotechnology setting.

  • LI-DD1

New Haven, CT, United States

No Selection

Alexion is a global biopharmaceutical company focused on developing and delivering life-transforming therapies for patients with devastating and rare disorders. Alexion developed and commercializes Soliris® (eculizumab), the first and only approved complement inhibitor to treat patients with paroxysmal nocturnal hemoglobinuria (PNH) and atypical hemolytic uremic syndrome (aHUS), two life-threatening ultra-rare disorders. As the global leader in complement inhibition, Alexion is strengthening and broadening its portfolio of complement inhibitors, including evaluating potential indications for eculizumab in additional severe and ultra-rare disorders. Alexion's metabolic franchise includes two highly innovative enzyme replacement therapies for patients with life-threatening and ultra-rare disorders, Strensiq® (asfotase alfa) to treat patients with hypophosphatasia (HPP) and Kanuma™ (sebelipase alfa) to treat patients with lysosomal acid lipase deficiency (LAL-D). In addition, Alexion is advancing the most robust rare disease pipeline in the biotech industry, with highly innovative product candidates in multiple therapeutic areas.

As a leading employer in our industry, Alexion is proud to offer a highly competitive package of base and incentive compensation as well as a comprehensive benefits program designed to support the health, wellness and financial security of our employees and their families. Benefits include group medical, vision and dental coverage, group and supplemental life insurance, 401(k) with company match, tuition reimbursement, relocation assistance and much more. To learn more about Alexion, please visit www.alexionpharma.com or download our App for iPhones and Blackberries.

Alexion is an Equal Opportunity /Affirmative action employer


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Equipment Operator - Oilfield Acid Operator

JOB LOCATION

This job will be located in Union City, Oklahoma.

SUMMARY

The Equipment Operators primary responsibility will be the rigging up and rigging down of Acid Treating Equipment. The Equipment Operators will also be responsible for operating and transporting all equipment in a safe manner in accordance with the FMCSA.

DUTIES AND RESPONSIBILITES

  • Safe operation and maintenance of assigned equipment
  • Transporting US DOT regulated vehicle on public roads and on location.
  • Safely rig up, operate and maintain Blenders, Pumps, Chem Add and Hydration Units.
  • Safely rig up, operate and maintenance of high pressure iron.
  • Proper DOT logging.
  • Pre-trip inspections and post trip inspections.
  • Usage and care of proper PPE.
  • All other job duties as assigned.

KNOWLEDGE AND SKILL REQUIREMENTS

  • Must possess a CDL.
  • Must possess hazardous material and tanker endorsements.
  • Fracturing / Acid experience is preferred, oilfield experience a plus.
  • High school diploma or equivalent.

PHYSICAL DEMANDS AND WORK ENVIRONMENT

  • Work involves occasional to frequent lifting of 50 pounds.
  • Work area, machinery, and tool operations require the use of safety equipment to include but not limited to; eye safety glasses, hearing protection, steel toe boots, protective clothing and hardhats.
  • Manual dexterity required for operating tools, machinery and computers.
  • Working in extreme weather conditions may be required.
  • Working of irregular hours required.
  • Will involve shift work and overtime.
  • Travel, overnight and multiple stay is a requirement.

MANDATORY QUALIFICATIONS

  • Must have a valid driver license and clean driving history. Must have Hazmat Endorsements.
Job Posted by ApplicantPro

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Acetic Acid Process Engineer

Overview

Celanese Corporation is a global technology leader in the production of specialty materials and chemical products which are used in most major industries and consumer applications. Our products, essential to everyday living, are manufactured in North America, Europe and Asia. Known for operational excellence, sustainability and premier safety performance, Celanese delivers value to customers around the globe with best-in-class technologies. Based in Dallas, Texas, the company employs approximately 7,100 employees worldwide and had 2015 net sales of $5.7 billion, with approximately 67% generated outside of North America. For more information about Celanese Corporation and its global product offerings, visit www.celanese.com.

Responsibilities

'- Provide process engineering support for an acetic acid operating facility- Publish process letters detailing solutions for process engineering studies in support of capital and expense projects and PSM activities- Work closely with Operations to resolve operating issues that arise- Participate in and/or lead process Hazard Analyses (PHA) as scheduled- Participate in Management of Change activities- Work closely with Project Managers to ensure successful Project implementation- Mentor junior engineers

Qualifications

Required Knowledge/Skills/Abilities:

  • Detailed understanding of basic chemical processes (e.g. distillation, heat transfer, hydraulics, reaction kinetics, etc.)
  • Ability to work with multiple disciplines (Operations, Technical, Maintenance, Reliability) - Basic troubleshooting skills

  • Ability to multi-task and work independently

  • Ability to work successfully in a strong team environment

  • Strong problem solving skills and results orientation

  • Ability to prioritize multiple assignments

Desirable Knowledge/Skills/Abilities:

'- Familiarity with APSEN Engineering Suite

  • Familiarity with Microsoft Office Suite

  • Familiarity with PHAST dispersion modelling tools

  • Familiarity with PI data historian

  • In depth knowledge of acetic acid chemistry

Required Yrs Exp:

5 to 10 years

Required Education:

B.S. Chemical Engineering


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UPP Equipment Operator 3 - Acidizing

DESCRIPTION

Job Title

UPP Equipment Operator 3 - Acidizing

Location

Midland, TX, US

Organization Name

Univeral Pressure Pumping

Department Description

Universal Pressure Pumping, Inc. provides pressure pumping and well services to oil and gas exploration and production companies in Texas.

Brief Description

The Equipment Operator 3 is responsible for performing work in rigging up and rigging down of equipment requiring advanced skills and/or training in operating and maintaining equipment for an assigned field job, either cementing, fracturing, acidizing, or other, as needed. The Equipment Operator 3 will pass the Company driving tests and requirements within first 90 days of employment.
The employee will meet and satisfy all the competency requirements of the Equipment Operator 2 level.
This position will work under the direction of the Service Supervisor, with a dotted reporting line to the Field Supervisor/Operations Manager.

Detailed Description

  • Perform work in operating and maintaining assigned equipment in a safe manner

  • Drive equipment to and from the well site and other locations

  • Performs all DOT-required duties (including DOT logs, DVIRs, pre-trip and post-trip inspections, etc.), to remain in compliance with DOT regulations

  • Perform rigging up and rigging down duties as required

  • Act as a mentor to other Equipment Operators

  • Operate and maintain one or more of the following equipment: FRAC pump, SandStorm, Blender, Chem-add, Hydration unit, field bin, Cement pump, bulk truck, etc.

  • Perform Job Safety Analysis (JSA) functions as required

  • Perform the duties as gate guard for all incoming traffic to customer locations

  • Perform clean-up as required before, during, and after the job

  • Perform other related duties as assigned

Job Requirements

This position requires the ability to follow instructions and work well in a team environment.

Minimum Qualifications

  • High school diploma or GED certificate

  • Minimum three (3) years or more of related work experience in the oil field, with at least six months working as Equipment Operator 2

  • Have and maintain a valid Class A CDL, with manual shift experience, a satisfactory driving record for the past 3 years, with no DWI convictions within the past 5 years, and no current DWI charges

  • Must have a Hazmat and Tanker endorsements

  • Able to pass a DOT drug test and DOT medical examination

  • Meet the minimum physical requirements (Work Step Evaluation)

  • Able and willing to work in extreme climate and work conditions

  • Demonstrate the ability to work well with others, and work independently when required

Additional Details

Employee must work with an emphasis on safety for themselves and others, including coworkers and third parties, including wearing all required personal protective equipment (PPE) at all designated times. This position requires the employee to work outdoors for long periods of time in all types of weather conditions typical of the area where the job is located, including dust, humidity, sleet, snow, rain, mud, cold, heat, wind, and other inclement weather. Working conditions for this position may involve exposure to varying outdoor conditions, including environmental chemicals, gases, noise, dampness, fumes, radiation and heights. Employee must be able to work closely with others in the confined area of the job, in a fast-paced team environment, and work independently when required or directed, taking initiative when necessary.

How To Apply

To apply, click the "apply now" button at the lower right hand corner of the screen and follow the directions.

Employing subsidiaries of Patterson-UTI Energy, Inc. (Patterson-UTI) are equal opportunity employers and maintain a drug-free workplace. All qualified applicants will be considered for employment without regard to race, sex, color, religion, national origin, disability, marital status, covered veteran status, genetic information, sexual orientation, gender identity or any other characteristic protected under state, federal, or local law.

Amount of Travel

Work At Home


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Program Supervisor

Supervise ABA Programs While Working Towards BCBA
Autism Spectrum Therapies ("AST") 
autismtherapies.com
, one of the largest and most respected autism services organizations in the county, is looking for an exceptional master's-level ABA professional to join our team as a Program Supervisor.  This position is ideal for an experienced candidate ready to build their supervision skills while working toward becoming a BCBA.Work under the direction of a BCBAAccrue indirect supervision hours towards becoming a BCBAOversee a team of up to 5 Behavior Interventionist and clinical programs

Support parent training and education

Write progress reports and conduct regular team meetingsAST currently employs nearly 100 BCBAs with offices in 7 states and growing.  We offer continual professional development opportunities and the ability to participate in AST sponsored research projects.  This is a great opportunity to join a first-class, growing organization and position yourself for success in the field of ABA. 
Qualifications:
Master's degree

Minimum one year experience working with children with autismBCBA eligible or accruing hours towards certification

Extensive prior experience with applied behavioral analysis

Demonstrated fluency with all aspects of the Behavior Interventionist position

Demonstrated ability to train others

Strong communication and writing skillsBCaBA preferred, not required

Bilingual skills highly preferred, not required

In addition to a competitive salary, AST also offers the following benefits to their employees:Ample paid, non-billable time

Health Insurance (Medical, Dental, & Vision)401(k)Paid time off (PTO)Mileage ReimbursementiPadOn-site CPI trainingAST/Learn It Systems is an Equal Opportunity Employer.  Candidates must be presently eligible to work in the United States.


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Assistant EMS Supervisor

We have an opening for a Full-time Paramedic to work as an Assistant EMS Supervisor at our employer health center located inElmont, NY!

Premise Health is a leading worksite health and patient engagement company dedicated to improving the cost and quality of employee healthcare. We believe healthcare should be about helping people get, stay and be well. That’s our mission and it’s the foundation of everything we do. With more than 40 years of experience, Premise Health manages more than 500 worksite-based health and wellness centers across the country. The company serves more than 200 of the nation’s leading employers, including a significant number of the
Fortune 1000. Summary:
This role is Wednesday through Sunday from 10a-6p.


Essential Functions:

  • Typically oversees the supervision of a team of EMTs within a health center
  • Dual role combines clinical, professional expertise and supervisory responsibilities
  • Fulfills the job expectations of a Paramedic dedicating an agreed upon percentage of time to clinical duties
  • Manages a limited number of employees – responsible for following appropriate processes for talent acquisition, staff development and performance management and provides input to the Director of Site Operations for the final staffing decisions. Responsible for interviewing, training and onboarding new colleagues
  • Manages daily operations, workflow, work schedules, timecard monitoring etc. to ensure efficient and effective health center performance
  • Identifies process improvement opportunities and presents resolutions and recommendations to the Director of Site Operations
  • Makes recommendations regarding staffing model based on objective scheduling & volume analysis – presents to Director of Site Operations for approval
  • Understands and complies with all regulatory, procedural, policy and licensing requirements
  • Completes incident reports as needed and provides assistance to Medical Care and outcomes dept regarding investigations and the resolution of complaints
  • Communicates and coordinates corporate messages and ensures implementation of policies or procedures is followed
  • Coaches and provides feedback to staff on a regular basis
  • Manages internal budget, reviews expenses, purchases supplies, inventories equipment, medication etc.
  • Assists in the identification and use of local per diems to ensure appropriate staffing levels are met
  • Communicates regularly with staff, conducts meetings and shares information regularly
  • Works collaboratively with the Medical Leader at the site to manage internal site issues
  • Other duties as assigned

    If you want to join a team of knowledgeable, compassionate, like-minded healthcare professionals, join Premise Health for an unlimited opportunity with the company that is changing the face and the place of the healthcare industry as we know it.

    We are an equal opportunity employer.

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