Acid Purifier Job Description Sample
Manager Of Phosphoric Acid Technology
With 2016 revenues of approximately $10.9 billion, Jacobs Engineering Group Inc. (Jacobs) is one of the largest publicly traded (NYSE: JEC) and diverse providers of professional technical services in the world. Founded in 1947, the company now has nearly 54,000 employees that help us prosper in diverse industries by holding true to our values and culture. Headquartered in Dallas, Texas, our global network spans more than 230 offices in countries across North America, South America, Europe, the Middle East, Australia, Africa and Asia.
The company's service portfolio consists of a comprehensive range of business solutions related to engineering, architecture, construction, operations and maintenance and scientific and specialty consulting.
Participates in the design of phosphoric acid plants including new and revamped units. Lead responsibility for the technical direction of the technology formulating process technology improvements and developing new design concepts and techniques.Acts as the process lead on phosphoric acid plant projects. Mentors younger, less experienced engineers. International travel is expected.
Develops PFD's and heat and material balances
Develops piping and instrument drawings working closely with the instrumentation department
Prepares equipment data sheet specifications (e.g. reactors, fume scrubbers, concentration units, ball mills, filters, etc.)
Develops operating manuals
Participates in startup and performance testing
Maintains effective communication with project team members and with the customer
Writes and presents technical papers at International Conferences
Participates in the preparation of proposals together with associated man-hour estimates
Initiates, directs and participates in R&D activities
Recognized Bachelor's degree in Chemical Engineering or Master's degree in engineering or technical field from an accredited college or University required
10-15 years of experience in the phosphate industry required
Extensive experience in process engineering of phosphate related chemical plants is required
Experience in debottlenecking and optimization of Phosphoric Acid Plants required
Specific background in design of Phosphoric Acid Plant unit processes preferred
Excellent oral and written communication skills required
Recognized as a subject matter expert
Experience with pilot plants required
English speaking required, French, Spanish and or Arabic preferred
P.E. License preferred
Process Engineer - Nitric Acid
CF Industries is a global leader in transforming natural gas into nitrogen. The chemical processes we use ensure we have the nitrogen we need to support life on earth - from fertilizer that feeds the crops that feed the world to products that remove harmful emissions from industrial activities. Through our nine world-class manufacturing complexes and best-in-class distribution system, we serve agricultural and industrial customers. We invite you to be a part of our nearly 3,000 employees making a difference every day.
Engineering and Engineering Services
CF Industries has many exciting and challenging opportunities at its world class production facility in Yazoo City Mississippi. The Process Engineer will support the operations area by working with engineering, maintenance and the operations team to implement and support projects, turnarounds and other efficiency efforts.
Provide process engineering expertise to initiate and evaluate improvements to site production units.
Provide process engineering support to site engineering staff in development and execution of various projects.
Provide process trouble-shooting assistance to site operations and maintenance staff.
Assist in Process Hazard Analysis studies and Management of Change evaluations.
Lead assigned projects through development and execution.
Perform economic analyses of various improvement projects.
Work with operations team on reliability measurements and improvements.
SUCCESSFUL INCUMBENTS WILL HAVE:
B.S. degree in Engineering required. Chemical Engineering degree preferred
3+ years of process engineering experience in the chemical process industry desired
Hands-on experience in a chemical production unit
Skilled in excel modeling; application of unit operations; development of process flow diagrams; piping and instrument diagrams; process equipment specification and process hazard analysis
Proficient in Microsoft Office IT environment - must have strong presentation skills sufficient to communicate thoughts succinctly to management
Strong written and verbal communication skills required. Both informal and formal project written documentation will be required
The talented members of the CF Industries Yazoo City Nitrogen Complex have a passion for safety, performance and are motivated by the team based work approach.
Our facility is proud to be named one of the Best Places to Work in Mississippi. We are known as a community leader and are proud to sponsor events that support our educational system which builds the foundation for the future of our youth.
CF Industries is an Equal Opportunity/Affirmative Action employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, disability, or protected Veteran status.
Employees in the US can learn more about their rights by viewing the federal "EEO is the Law" poster (PDF) and the Pay Transparency Policy Statement can be found on this link: http://www.dol.gov/ofccp/PayTransparencyNondiscrimination.html.
If you need any assistance seeking a job opportunity at CF Industries, or if you need reasonable accommodation with the application process, please call 847-405-2400 or contact us at firstname.lastname@example.org.
JOIN OUR TALENT NETWORK
Driver - Acid Midland, TX - 1721
Drives assigned equipment to and from customer sites to haul various types of fluids, materials, or equipment. Assigned equipment could include: vacuum truck, fluid hauling, acid truck, winch truck, cement truck, sand or gravel truck.
Major Responsibilities May Include
Drives required equipment safely to and from location
Loads and unloads cargo
Completes the associated paperwork for each job to include pre and post0trip inspections, work tickets, DOT logs
Performs routine maintenance and repair of equipment
Performs other duties as assigned
Qualifications and Skills
Class A CDL with appropriate endorsements where required
Ability to pass a DOT Physical and maintain a current medical card
Understands applicable DDOT rules
6 mos. - 1 yr experience
Ability to lift and position vehicle equipment weighing 75-100 lbs
Ability to sit long periods while driving
Ability to stand long periods while cargo is being loaded and unloaded
Reach your full potential.
Basic offers interesting and challenging opportunities for dynamic individuals who want to be part of the exciting oilfield services industry. We are an equal opportunity employer that recognizes the value and individual contributions of every employee.
Highly competitive salaries
Performance-based financial rewards
Equal Opportunity Employer/Drug Free Environment
MS Or Phd Scientist, Nucleic Acid Therapeutics Delivery
We have a formulation scientist position open in the Nucleic Acid therapeutics unit of NIBR Biologics Center (NBC) at our Cambridge, MA site. We are seeking a highly motivated and experienced candidate having a strong background in the delivery of nucleic acid therapeutics.
The position will be laboratory based, but requires project management and leadership responsibilities within and external to the Nucleic Acid team. Hands-on responsibilities will include the development and characterization of suitable formulations for the therapeutic delivery of mRNA and oligonucleotides, evaluating external (academic and private sector) delivery technologies and tracking a variety of key delivery vehicle attributes such as stability and toxicity.
The successful candidate will have a high degree of independence regarding the planning and execution of experiments but must be able to multi-task and work in a team atmosphere. Strong verbal communication skills, a well-organized working style as well as timely and accurate technical reporting and documentation are essential to the position.
Other duties include:
Evaluate the proposed formulations and provide recommendations to the team and senior management as to which formulations are appropriate to pursue for toxicology and clinical testing.
Track progress against project plans, generate regular status updates, and communicate progress and issues to management.
Maximize automation for formulation processes
Be creative and innovation in problem solving. 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 - Ph.D. in Chemistry, Molecular Biology, Biochemistry, or Analytical Chemistry or a Masters with 3-5 years of relevant experience.
Extensive experience working with nucleic acids (mRNA, antisense, CRISPR/CAS9) and corresponding formulations (lipid nanoparticles, polymer-based…)
Knowledge of formulation development and scale up in support of preclinical and clinical development is beneficial.
Demonstrated ability to troubleshoot instruments and analytical assays
Strong experience with formulation characterization, assessment of quantities and quality
Proven track record of innovative project contributions including peer reviewed publications.
Ability to lead projects, interact and innovate within multidisciplinary team of chemists, biologists and pharmacologists.
Equipment Operator - Oilfield Acid Operator
This job will be located in Union City, Oklahoma.
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.
- Must have a valid driver license and clean driving history. Must have Hazmat Endorsements.
Senior Scientist - Analytical, Nucleic Acid
The candidate will develop analytical assays and design, plan and execute the qualification and transfer of these assays in support of Vaccine development, including materials release and stability for early phase vaccine programs. The focus of this position is for assay development for nucleic acid and nucleic acid lipid delivery platform formulations utilizing standard analytical techniques such as HPLC, CE, UV-Vis, Mass Spectrometry and other applicable techniques.
The individual should be able to identify key Vaccine drug substance and drug product attributes and provide hands on support to develop robust assays for routine use with a focus on nucleic acid vaccines
The individual should be familiar with basic regulatory expectations and the ICH guidelines for method qualification
Contribute to the selection of the methodology and techniques to be used
Independently analyze, interpret, provide conclusions and present experimental data internally
Perform routine sample analysis
Independently design, plan, and execute assay development, qualification and transfer studies to support the release, stability and characterization of vaccine candidates
Collaborate with colleagues within Vaccine Research and Development – Bioprocess, Analytical, and Formulation Development and appropriate partner lines
Author and review laboratory methods and reports
Keep abreast of scientific/ technological development by participating in scientific meetings/ seminars and through regular scientific review
As needed, introduce and utilize new technologies and establish those technologies to characterize the vaccines under development Where applicable, perform job responsibilities in compliance with GLP and all other regulatory agency requirements
PhD in Chemistry, Biochemistry, or related discipline with at least 2 years of academic, pharmaceutical, or biotechnology postdoctoral experience or an MS plus 7 years of related work experience is required.
Experience in analytical assay development for nucleic acid and nucleic acid lipid delivery platform is essential.
A strong background in separation-based analytical techniques and method qualification using ICH guidelines is essential. Experience with applying these methodologies to biomolecules, such as nucleic acid is preferred. Proficiency and ability to utilize techniques such as HPLC, CE, and UV-Vis to develop methods to analyze potential vaccine antigens and other vaccine components.
Proficiency with personal computers including word processing, spreadsheets, PowerPoint and relevant scientific software is desirable. Strong verbal and written communication skills are required.
EEO & Employment Eligibility
Pfizer is committed to equal opportunity in the terms and conditions of employment for all employees and job applicants without regard to race, color, religion, sex, sexual orientation, age, gender identity or gender expression, national origin, disability or veteran status. Pfizer also complies with all applicable national, state and local laws governing nondiscrimination in employment as well as work authorization and employment eligibility verification requirements of the Immigration and Nationality Act and IRCA. Pfizer is an E-Verify employer.
Pfizer reports payments and other transfers of value to health care providers as required by federal and state transparency laws and implementing regulations. These laws and regulations require Pfizer to provide government agencies with information such as a health care provider's name, address and the type of payments or other value received, generally for public disclosure. Subject to further legal review and statutory or regulatory clarification, which Pfizer intends to pursue, reimbursement of recruiting expenses for licensed physicians may constitute a reportable transfer of value under the federal transparency law commonly known as the Sunshine Act. Therefore, if you are a licensed physician who incurs recruiting expenses as a result of interviewing with Pfizer that we pay or reimburse, your name, address and the amount of payments made currently will be reported to the government. If you have questions regarding this matter, please do not hesitate to contact your Talent Acquisition representative.
Other Job Details:
Eligible for Relocation Package
Eligible for Employee Referral Bonus
Pfizer is an equal opportunity employer and complies with all applicable equal employment opportunity legislation in each jurisdiction in which it operates.
Acid Blast Operator
Grit Blast (using manual Grit Blasting machines), clean, and/or chemically remove coating and/or plasma spray form components
Visually inspect parts for signs of acid effectiveness
Maintain supply of materials on hand
Perform preventative maintenance as needed
Complete OJT program, or successfully complete related Vo-tech training (e.g. precision tools, process controls)
Maintain work area in a clean and orderly manner
Ensure all environment, health and safety rules, requirements and procedures are adhered to
Maintain solution levels and mix solutions in tanks as required
Dispose of waste solutions per SOP requirements
Perform other duties as required to support company objectives
(Sr) Research Associate, RNA
Generate and purify in vitro transcribed RNA on both small and large scale
Establish and independently perform protocols that characterize RNA purity, activity, and stability in vitro
Collaborate across teams for appropriate sample preparation and downstream sample analysis
Assist in the analytical development and implementation of biochemical assays to characterize mRNA and gRNA in the context of Cas9 activity
Conduct, troubleshoot, and design experiments that drive decision making, both independently and in collaboration with colleagues to reach desired goals.
Communicate research and development findings with internal and external partners
Familiarity with nucleic acid, particularly RNA, chemistry, structure, and manipulation
Experience performing enzymatic reactions with nucleic acids such as PCR and in vitro transcription
Experience with assays relevant to nucleic acids and proteins, especially gel and capillary electrophoresis
Experience in biochemical assay development
Experience with enzymatic or kinetic based assays
Familiarity with purification techniques such as HPLC, FPLC, and gel electrophoresis
B.S. degree in Chemistry, Biochemistry, or Molecular Biology with at least 2 years of industry experience, or M.S. degree in Chemistry, Biochemistry, or Molecular Biology
Local candidates strongly preferred
Ability to thrive in a team-oriented and collaborative environment
Strong communication skills (both written and oral)
Excellent documentation skills and attention to detail
Exceptional time management
POSITION: Full-Time, Exempt
EEOC Statement: Intellia believes in a diverse environment, and is committed to equal employment opportunity for all its employees and qualified applicants. 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. Intellia will make reasonable accommodations for qualified individuals with known disabilities, in accordance with applicable law.
Scientist – Discovery Biology
Req ID 38768 Title Scientist – Discovery Biology City Greenfield State / Province Indiana Country United States Region North America Company Overview Elanco is a global research-based company that develops and delivers product and services to enhance animal health and production. We value innovation, both in scientific research and daily operations, and strive to cultivate a collaborative work environment for more than 7,000 employees worldwide. Founded in 1954, Elanco is a division of Lilly. Our worldwide headquarters and research facilities are in Greenfield, Indiana Responsibilities The Scientist will use their skills and knowledge in Molecular Biology, Virology, Bacteriology, and Biochemistry to discover and optimize new vaccines, antivirals, and antibiotic alternatives. The incumbent may also participate in biotherapeutic molecule discovery efforts (e.g., monoclonal antibodies) in the Elanco Research Laboratories. This position is laboratory-based and will require routine interaction with senior scientists across multiple discovery and core research laboratories at Elanco. The incumbent scientist will be expected to support multiple projects at any given time.
Functions, Duties, Task:
Manipulate microbial (virus & bacteria) genetic material using contemporary molecular biology techniques.
Perform molecular cloning, PCR, Gibson Assembly, qPCR, and nucleic acid extraction, purification, & sequence analysis.
Express (CHO/293/E. coli), purify (FPLC), and analyze proteins e.g.by SDS-PAGE, SDS-CE, Western, or BLI (Octet)
Bacterial isolation, identification and characterization.
Culturing of mammalian cell lines.
Perform cellular bioassays
38768BR Basic Qualifications
Bachelor degree in molecular biology, virology, bacteriology, microbiology, immunology, or biochemistry or relevant scientific discipline
3 years of experience working on R&D projects in the human or animal health industries.
Qualified candidates must be legally authorized to be employed in the United States. Lilly does not anticipate providing sponsorship for employment visa status (e.g., H-1B or TN status) for this employment position
Effective oral and written communications skills.
High personal ethical and quality standards.
Exceptional problem solving and decision-making skills.
Must be able to work productively in an interdisciplinary team environment
MS degree and ability to demonstrate subject matter expertise in a relevant scientific disciple (as above)
Proven project leadership skills
Knowledge and experience in viral and bacterial reverse genetics and/or strain engineering
Additional Information Lilly is an EEO/Affirmative Action Employer and does not discriminate on the basis of age, race, color, religion, gender, sexual orientation, gender identity, gender expression, national origin, protected veteran status, disability or any other legally protected status.
Senior PCS (Pump / Chiller / Scrubber) Equipment Maintenance Technician
Summary of Role:
PCS Equipment Maintenance Technicians execute preventative and corrective maintenance of semiconductor manufacturing equipment vacuum pumps, abatement units, and chiller and heat exchangers. GLOBALFOUNDRIES manufacturing operations are 24 x 7, as such the PCS technician will be required to work one of four compressed work week (alternating 3 & 4 days) 12-hour shifts.
- Perform visual inspections (quality check)
Upon completion of prescribed training, independently perform basic preventive maintenance activities on various supplier vacuum pumps,
abatement systems, and heat exchangers as per documented procedures and practices.
Read and interpret engineering drawings, schematics, and diagrams.
React to error messages of factory systems and/or equipment.
Recover from equipment interruptions and execute corrective maintenance.
Identify and address potential areas for improvement and optimize PCS system performance, contributing to manufacturing equipment availability, cycle time, utilization and cost.
Complete all required reporting and documentation
Perform all activities in a safe and responsible manner and support all Environmental, Health, Safety &
Security requirements and program as working safely and within prescribed requirements is an expectation of employment.
Actively participate in continuous improvement processes, learning and skills development
Assist in the creation and amendment of operations and maintenance specifications and procedures.
Assist Management in identifying training requirements and safety procedures in assigned specialty areas
Strong interpersonal skills with the proven ability to effectively provide technical on the job training.
Mentor, coach, and train less experienced technicians in your work group.
Ability to work with minimal direction or supervision
Strong customer services focus with the ability to effectively communicate tool status and plans of internal customer's equipment.
Support the site Emergency Response Team and / or safety committee
Perform all activities in a safe and responsible manner and support all Environmental, Health, Safety & Security requirements and programs
- 2 Year Technical/Associates Degree in Science, Math,
Engineering, Semi-Conductor Manufacturing or a related discipline or
Military training/experience in a technical field, or
6 years of previous work experience in a maintenance role
Fluency in English Language – written & verbal
Physical Capacity Demands-
Able to perform shift work on a 12 hours per day (days or nights) shift schedule if required
Able to work in a cleanroom environment per semi-conductor protocol/requirements
Able to wear all required clean room protective clothing and equipment for normal 12 hour per day shift (excluding breaks)
Able to wear appropriate PPE, including SCBA, air purifying respirator, acid apron, gloves, and face/splash shields.
Ability to perform work in a standing position for majority of a12 hour shift (excluding breaks)
Able to lift a minimum of 50 pounds on a periodic basis throughout the shift (preventive maintenance) and/or process issues
Able to perform work in a standing position for majority of a 12 hour shift (excluding breaks)
3-5 years' experience maintaining vacuum and abatement systems
Strong technical skills and knowledge of semiconductor processing and process equipment
Demonstrated knowledge of Semiconductor FAB systems and related equipment
Demonstrated ability to operate computer programs including Microsoft Office, Google Business, and experience with FDC, CMMS, and SPC programs.
Demonstrated ability to follow detailed instructions and procedures to complete tasks and required documentation.
Demonstrated work performance in an environment requiring high level of attention to detail and timeliness.
Demonstrated ability to handle multiple tasks simultaneously and prioritize activities.
Demonstrated knowledge of job hazard analysis and hazardous waste handling
Demonstrated mechanical abilities with experience in maintenance and operation of equipment
Strong team player with ability to work well within a global team
Occasional domestic and/or international travel may be required
Familiarity with Lean processes & activities and Kaizen teams
If you need a reasonable accommodation for any part of the employment process, please contact us by email at email@example.com and let us know the nature of your request and your contact information. Requests for accommodation will be considered on a case-by-case basis. Please note that only inquiries concerning a request for reasonable accommodation will be responded to from this email address.
An offer of employment with GLOBALFOUNDRIES is conditioned upon the successful completion of a background check and drug screen, as applicable and subject to applicable laws and regulations.
GLOBALFOUNDRIES is an Equal Opportunity/Affirmative Action employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, gender, sexual orientation, gender identity, national origin, disability, or protected Veteran status.
Making better hires starts with building better job descriptions
- Browse 100s of templates across 40+ industries
- Customize your template with your company info & job requirements
- Post it to 20+ job boards in seconds – for FREE!