Monomer Purification Operator Job Description Sample
Lead Water Purification Plant Operator
This position requires a demonstrated ability to perform advanced functions related to the operator and maintenance of equipment at all water treatment facilities. This position functions as a Lead Operator and also as Chief Plant operator when required, performing complex analysis of the Water Treatment Plant operations and having direct charge of the operation of a water treatment facility or Water Production Facilities. Positions at this level provide instruction and assistance to lower level Water Treatment Plant Operators. This position is normally filled by advancement from the Water Treatment Operator II. Position requires three to five years of experience in a Surface Water Treatment Plant Operator and must possess a minimum of a Class 'C' Surface Water Treatment Plant Operator Certificate issued by the Texas Commission on Environmental Quality at the time of accepting position.
Essential Job Duties:
Incumbents may not perform all of the list duties and/or may be required to perform additional or different duties from those set forth below to address business needs and changing business practices.
Operates the water treatment plant including related subsystems and instrumentation.
Monitors the treatment process from the control board/computer screen; monitors various treatment processes including coagulant feed, rapid mix, flocculation, sedimentation, filtration and disinfection; monitors the addition of chemicals added for taste and odor control.
Monitors water quality by performing laboratory tests at various stages in the treatment process including tests for chlorine residual, ph, turbidity, hardness, alkalinity, odors and other tests as necessary to maintain water quality; calibrates laboratory equipment; maintains laboratory records.
Determines chemical dosage and makes adjustments to plant processes as necessary including for ferric Sulfate/Aluminum Sulfate, chlorine, ammonia, potassium permanganate, caustic soda, powdered activated carbon, and other chemicals.
Reads gauges and meter; interprets data to maintain the proper treatment process, proper distribution operation, security, and alarm status; make flow adjustments.
Operates pumps and valves utilizing a SCADA system; monitors systems for alarms, make adjustments, and provides appropriate response; notifies Plant Management or appropriate staff as necessary to respond to problems.
Operates mechanical equipment including pumps and motors, chemical feed pumps and systems, air compressors, and manual, electrical, and pneumatically operated valves; operates hard and power tools; operates a light truck.
Operates chlorination equipment related to the chlorine performs maintenance on chlorine system including chemical piping system; participates in calibration of chemical feed equipment.
Orders chemicals, Inventories and takes delivery of bulk chlorine.
Maintains operational logs and records.
Makes visual inspections; monitors facilities and roads to insure adequate security.
Performs preventative and predictive maintenance on treatment plant equipment; assists Maintenance personnel in making major and/or specialized repairs to equipment; coordinates work of contractors and of other departments.
Operates the City's water production system including elevated and ground storage and pump stations; ensures adequate availability and pressure to all service connections.
Provides appropriate response to emergencies and spills including those involving hazardous materials; wears respirators including self contained breathing apparatus as required.
Responds to inquiries from the vendors, suppliers, and public; answers questions from customers pertaining to water quality, low pressure, and leak reports.
Supervises and Trains operators.
Performs related duties as assigned or required
Physical and Environmental Conditions:
The conditions herein are representative of those that must be met by an employee to successfully perform the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential job functions.
Environment: Water treatment plant. Exposure to noise of plant machinery and other equipment; mechanical and electrical hazards of operating equipment; fumes and odors of chemicals and gases; toxic substances such as chemicals, cleaners, solvents, and gases; all types of weather and temperature conditions. Work and/or walk for long periods of time on various types of surfaces including slippery or uneven surfaces and rough terrain. Subject to 24-hour emergency callbacks and requires working varying hours, overtime, weekends, and holidays. Work environment is informal, team-oriented, having both routine and variable tasks with variable pace and pressure. Work is performed in both indoors and in plant area and outdoors in field and collateral facilities.
Physical: Primary functions require sufficient physical ability to work in a plant and field setting and operate assigned equipment. CONTINUOUS walking, balancing, bending, stooping, kneeling, crouching, lifting of objects weighing up to 10lbs from below waist level to above shoulder level and transporting for distances up to 100 yards, fine finger dexterity to operate tools and controls, firm grasp to lift and carry objects; FREQUENT sitting, standing, reaching, twisting at waist, upward and downward flexion of neck, side to side turning of neck, lifting of objects weighing 11-25lbs from below waist level to above shoulder level and transporting up to 100 yards; OCCASIONAL climbing, pushing/pulling, lifting of objects weighing from 26-50lbs from below waist level to above shoulder level and transporting for distances up to 10 yards; INFREQUENT crawling, lifting objects weighting from 51-100lbs below waist level; with assistance, and transporting for distances up to 10 feet with assistance. Must be able to climb 150+ foot ladder and work effectively at the height.
Other: Safety regulations prohibit Operators from wearing contact lenses when working with certain chemicals or from wearing beards or other facial har that prevents a proper respirator fit. Must pass annual respirator physical and fit testing.
The following generally describes the knowledge and ability required to enter the job and/or be learned within a short period of time in order to successfully perform the assigned duties.
Operations, services, and activities of a water treatment system.
Principles, practices, materials, chemicals, and operating procedures related to operation and maintenance of a water treatment plant.
Operating principles of plant equipment including valves, pumps, and motors.
Methods and techniques of reading and interpreting gauges, recording devices, and related monitoring systems.
Tools and equipment used in the operation and maintenance of water treatment plant facilities.
Maintenance and repair principles and practices including preventatvie maintenance procedures.
Emergency maintenance and repair procedures related to water treatment facilities.
Methods and techniques of conducting laboratory tests and procedures related to water treatment analysis.
Mathematical calculations used in the water treatment operations.
Hydraulic and distribution principles.
Pertinent federal, state, and local laws, codes, and regulations.
Operational and safety regulations pertaining to water treatment plant operations.
Occupational hazards and standard safety precautions.
Principles and procedures used in the proper handling of chemiclas.
Principles and practices of customer service.
Office procedures, methods, and equipment including computers and applicable software applications.
Principles and practices of record keeping
Principles of training.
Operate, monitor, and maintain a variety of water treatment plant equipment, facilities and systems.
Perform complex inspections and preventive maintenance of treatment plant facilities and equipment.
Read and interpret gauges, meters and other instrument readings and take effective course of action.
Diagnose complex operational problems and perform effective maintenance on equipment.
Respond to changing demands on water flow, water quality, and equipment requirements.
Monitor and adjust plant processes.
Compile and record complex data and material.
Work well with others in a team environment.
Complete work within an assigned time frame.
Perform math calculations related to water works.
Operate assigned equipment and tools in a safe and effective manner.
Operate office equipment including computers and applicable software applications.
Work independently in the absence of supervision.
Demonstrate an awareness and appreciation of the cultural diversity of the community.
Communicate clearly and concisely, both orally and in writing.
Establish and maintain effective working relationships with those contacted in the course of work.
Education and Experience: High School Diploma or GED required supplemented by TCEQ training courses in the Surface and Ground Water related fields also management training is highly desirable.
Experience: Three to Five years of experience in a Surface Water Treatment Plant Operator.
License or Certificate: Possession of a Class 'C' Surface Water Treatment Plant Operator Certificate issued by the Texas Commission on Environmental Quality Required. Must be able to obtain and acquire a valid class 'B' Water works license issued by the Texas Commission on Environmental Quality within (2) years of accepting position. Possession of a valid Texas Class C Texas driver's license is required.
Monomer First Line Supervisor
PLEASE USE A WEB BROWSER OTHER THAN INTERNET EXPLORER IF YOU ENCOUNTER ISSUES (CHROME, FIREFOX, SAFARI, ETC.)
As we create a colorful, capable and cleaner world through chemistry, we invite you to join our team to harness the power of chemistry to shape markets, redefine industries and improve lives for billions of people around the world.
At Chemours, our purpose is to help create a colorful, capable and cleaner world through the power of chemistry!
The Chemours Washington Works facility located in Washington, WV has a First Line Supervisor position available. This is a highly visible, key role within the Company and the Operations function. This position will report to the Monomer Area Superintendent of Production
The responsibilities of the position include, but are not limited to, the following:
Accountable for personal safety and process safety of shift teams.
Accountable for positive environmental performance of the shift team.
Ensure shift teams meet uptime, quality, and cost goals.
Accountable for the Organizational Health of the shift teams.
Assign tasks to the shift teams
Manage work flow for the shift teams
Monitor the quality of work of the shift teams.
Formally coach shift personnel to enhance personal and team growth.
Communcate to/with area management
Communicate to/with the Monomer supply chain.
Interface with Maintenance, Manufacturing Technical, Supply Chain, and Reliability Engineering personnel.
In order to be qualified for this role, you must possess the following:
Minimum of 4-years' experience working in PSM High Hazard Operations
Experience as a detail supervisor or other supervisory position
SAP PM experience
SAP Operations Experience
The following skill sets are preferred by the business unit:
Six Sigma Greenbelt
Demonstrated continuous improvement experience (problem solving, DuPont Production System ITF membership, etc.)
Previous leadership experience or detail supervision experience
Operating experience with Highly Toxic Materials (HCL, HF, PFIB, HFP, etc.)
Chemours is an equal opportunity employer.
Chemours is an E-Verify employer.
Candidates must be able to perform all duties listed with or without accommodation
If the spirit of customer centricity, refreshing simplicity, collective entrepreneurship, safety obsession and unshakable integrity we are the home of some of the world's greatest brands and greatest employees! Learn how you could be a catalyst for change at Chemours.
At Chemours, you will find sustainability in our vision, our business and your future. If you want to work on the leading edge of your field and have a desire to make a difference, join Chemours and discover what it means when we say "We Are Living Chemistry".
Scientist, HTP Expression Purification (41)
Scientist - HTP Expression Purification
We are seeking a skilled molecular biologist and protein chemist at a Scientist level to join the high-throughput expression and purification group. The candidate will be expected to work on a variety of projects to purify antibodies from multiple species and heterologous expression systems using automated platforms.
General molecular biology involving isolation, manipulation, and characterization of DNA, RNA and proteins.
Design of mammalian cell expression vectors for recombinant proteins.
Mammalian cell culture and transfection using viral and lipid transfection systems.
Purify antibodies using variety of systems (protein A/G/L and ion exchange).
Analyze antibodies using automated protein characterization methods (SDS-PAGE/CE-SDS, SEC-MALLS, endotoxin, etc.).
Clone, express, and purify antibodies using automated systems at small to medium-scale.
Perform experiments with strong attention to detail and documentation.
Excellent written and oral skills are necessary.
Accomplish goals under project team time lines.
PhD in Biochemistry, Structural Biology, or related field with 0-5 years of industrial experience.
Demonstrated experience in design and construction of cell expression plasmid constructs, site-directed mutagenesis, and recombinant protein vector design.
Experience in expression of antibodies from small to medium scale is required.
Experience using automation and programming jobs on automation workstations is highly desirable.
Excellent time management, record keeping and organizational skills.
Demonstrated ability to work in a multidisciplinary team.
Senior Scientist II, Protein Purification
The Global Protein Sciences (GPS) Group is seeking a highly motivated Senior Scientist to join its Protein Purification Group at AbbVie Bioresearch Center in Worcester, MA. As a member of the group, the candidate will be responsible for working in cross functional teams with other scientists in various therapeutic areas as well as the Biologics generation group in Worcester to advance the pipeline. The successful candidate will have experience in protein engineering and purification of immunogens and therapeutics with a good understanding of technologies for generating proprietary biotherapeutics.
Key Responsibilities Include:
Design alternate therapeutic formats (Multi-specifics, Non-Ig Scaffolds etc.), fusion proteins, immunogens from concept using computational tools (Rosetta/pymol/others) and execute through experimental production and characterization
Enable progression of targets through the pipeline with appropriate reagents that elucidate a mechanistic understanding of target biology
Design, express, purify and characterize soluble and membrane protein targets with enhanced expression and stability enabling functional studies and antibody discovery
Purify integral membrane proteins/complexes for querying target biology, therapeutic development and structural studies.
Introduce and lead innovative science enabling publication and external presentations
BS, MS or PhD with a strong foundation in biochemistry, protein purification, structural biology, and at least 12-14+ (BS), 10-12+ (MS) or 4-6+ (PhD) years of post-graduate experience in protein design and purification
Significant research experience as demonstrated by a track record of publications and scientific accomplishments
Experience with commercially available automated purification systems
Experience with expression and purification from various host expression systems such as mammalian (HEK/CHO), insect/baculovirus and E.Coli.
Experience in display technologies (phage, yeast) is a plus
Demonstrated ability to work with multidisciplinary biologics groups in a fast paced discovery team setting
Participation in project teams and effective communication with team members throughout the organization.
Highly developed leadership skills and ability to engage collaborators across the organization
Equal Opportunity Employer Minorities/Women/Veterans/Disabled
Purification Leader, Technical Dev And Manufacturing Science
The individual will be part of a strategic and dynamic Technical Development and Manufacturing Sciences group that is highly focused on the rapid development of new therapeutic treatments and supporting life cycle strategies of commercial products. We look for highly energetic individuals who have deep technical knowledge in one of the biotech manufacturing process development areas: cell culture, purification, analytical development, formulation, fill finish, and device development, and are also excellent cross-functional team leaders to lead CMC teams and/or other technology development teams to achieve departmental and corporate goals.
The current position will primarily be responsible for leading purification process development efforts for all Bioverativ pipeline products, and support downstream manufacturing activities. Responsibilities include:
Provide guidance to contract development organizations (CDOs) on downstream process development of BIVV pipeline products
Lead resolution for major MFG deviations at CMOs
As downstream SME, Ensure proper process validation activities are executed
Draft relevant sections of CMC filings
Respond to agency questions on downstream processes
The individual will be experienced with process development from early clinical stage through commercialization. Knowledge in biologics purification process development, virus and impurity clearance, risk assessment, process validation and cGMP requirements is essential.
The ideal candidate should also possess the ability to solve complex problems and communicate succinctly. Additionally the candidate should have the ability to successfully interface with multidisciplinary teams, engage and collaborate with external partners in process development and manufacturing.
QUALIFICATIONS AND EDUCATION:
Ph.D. in Chemical Engineering/Biochemistry/Chemistry or related field with 8+ years' experience or MS with 14+ years of experience in process development, analytical chemistry, biochemistry and spectroscopy. Candidates must have extensive hands-on experimental experience as well as theoretical understanding of chromatography and filtration method development used in bio-pharmaceutical manufacturing.
Bioverativ, a Sanofi company, is aglobal biotechnology company dedicated to transforming the lives of people withhemophilia and other rare blood disorders through world-class research,development and commercialization of innovative therapies. Launched in 2017 asan independent company spun out of Biogen's hemophilia business, we build upona strong heritage of scientific innovation and are committed to activelyworking with the rare blood disorders community.
The company's mission is tocreate progress for patients where they need it most and its hemophiliatherapies when launched represented the first major advancements in hemophiliatreatment in more than two decades. For more information, visit www.bioverativ.com or follow @bioverativ on Twitter.
We are an equal opportunityemployer. We evaluate qualified applicants without regard to race, color,religion, sex, sexual orientation, gender identity, national origin,disability, veteran status, or any other protected characteristic. VEVRAAFederal Contractor
WeRequest Priority Protected Veteran and Disabled Referrals for all ourlocations.
Bioverativ is an E-Verify Employer in the UnitedStates
Process Development Engineer Purification Development
Known for its scientific and operational excellence, Regeneron is a leading science-based biopharmaceutical company that discovers, invents, develops, manufactures, and commercializes medicines for the treatment of serious medical conditions. Regeneron commercializes medicines for eye diseases, high LDL-cholesterol, atopic dermatitis and a rare inflammatory condition and has product candidates in development in other areas of high unmet medical need, including rheumatoid arthritis, asthma, pain, cancer and infectious diseases.
We are seeking a process development engineer who enjoys working on projects collaboratively and is also capable of recognizing when someone needs to take the lead, and is equally comfortable doing so. This role is a hands-on junior management position within the Purification Development group within Preclinical Manufacturing and Process Development (PMPD). This engineer will be involved in the full scope of the department's work supporting our robust pipeline from preclinical evaluation all the way through commercial licensure and life cycle management of the processes providing important medications to our patients with unmet medical needs.
This position includes leading and performing Quality by Design (QbD) driven, state of the art downstream process development, based on Regeneron's suite of proprietary technologies. This engineer will be relied upon to support technology transfer of these processes to our GMP manufacturing facilities around the world. This position will also have a highly visible role within the department while driving the group's technical development priorities forward.
This individual would be entrusted with the career development of junior engineers and would be given the resources, time and training to effectively mentor and develop them. The ideal candidate would not only be an effective leader of their own subgroup, but be willing to be a non-positional leader within their larger group.
Development of Innovative Polishing chromatography separations, within a cross functional team of other SME's to deliver a final process that has been prospectively developed using the principals of QbD to ensure robust, uninterrupted supply of safe medicines for our patients.
Utilizes subject matter expertise in field of chromatography to design, lead, and react to experiments/projects independently.
Experienced leader that knows when and how to delegates tasks, inspires individuals whether direct reports or project team members, and demonstrates strong leadership and poise in approach to their work and the management of their group.
Analyzes data and interprets experimental results within context of "project" goals and makes recommendations to management. Use of statistics, such as ANOVA, nonlinear least square regression, and well-designed DoE's, etc. to characterize design space and generate statistical models of process performance, variation and failure rate.
Communication with all levels in the organization, demonstrating meticulous organization and high attention to detail. Conduct research and development in area of subject matter expertise with minimal guidance. Makes Science-based recommendations by novel incorporation of learning from internal and external (literature) sources.
Potential additional responsibilities include participation in viral clearance studies for clinical and commercial drug candidates and process transfer to Regeneron's manufacturing facilities. The position may require travel (5-10%) and occasional work on weekends.
The ideal candidate will have a degree in Chemical Engineering or Biochemical Engineering.
PhD. 0-2 years of experience, M.S.c with 5-7 years' experience, or B.Sc. with 8-10 years of experience.
Relevant experience with:
Akta Explorer/Avant, Akta Pilot, BioProcess Skid, Depth Filtration, Tangential Flow Filters, Normal Flow Filters, Chromatographic Columns, HPLC, UPLC, Diafiltration Skid , Laminar Flow Hood, Chemical Fume Hood, Empower, Unicorn, JMP, LlMS, Tech Transfer Experience to GMP Manufacturing. Small Scale Purification Model Development.
Level will be commensurate with experience
This is an opportunity to join our select team that is already leading the way in the Pharmaceutical/Biotech industry. Apply today and learn more about Regeneron's unwavering commitment to combining good science & good business.
To all agencies: Please, no phone calls or emails to any employee of Regeneron about this opening.
All resumes submitted by search firms/employment agencies to any employee at Regeneron via-email, the internet or in any form and/or method will be deemed the sole property of Regeneron, unless such search firms/employment agencies were engaged by Regeneron for this position and a valid agreement with Regeneron is in place. In the event a candidate who was submitted outside of the Regeneron agency engagement process is hired, no fee or payment of any kind will be paid.
Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, sexual orientation, gender identity, disability status, protected veteran status, or any other characteristic protected by law.
Technical Lead/Associate Director, Purification Process Development
Technical Lead/Associate Director, Purification Process Development
If interested and qualified, please include Requisition # 2018-343 in the subject line when emailing resume to: firstname.lastname@example.org.
For more information on CRISPR Therapeutics, please click here.
As a member of the Technical Operations team, this individual will lead the purification process development activities for company's product development programs. The position requires enthusiasm, passion, attention to detail and a desire to create new medicines for patients.
Provide leadership and subject matter expertise for all purification process development activities across different modalities, including Cas9, guide RNA, and adeno-associated viral vectors
Collaborate closely with internal and external functional areas to develop robust, scalable purification process
Contribute to technology transfer to external CMO and provide manufacturing oversight as needed
Prepare, review, revise technical documents
Support regulatory filing
in Biology or related scientific discipline with at least 5 years of experience in biotech/pharmaceutical industry
Sound scientific understanding of current purification technologies for protein, small RNA, and viral vectors
Demonstrated ability to develop purification processes; hands-on experience in different modes of chromatography
Experience in technology transfer, process and analytical development
Experience in process development for adeno-associated vectors.
Experience in writing regulatory documents and submissions
Experience in working with and managing outside vendors
Collaborative – One Team.
Undaunted – Fearless. Can-do attitude.
Results Orientation – Delivering progress toward our mission. Sense of urgency in solving problems.
Entrepreneurial Spirit – Proactive. Ownership mindset.
If interested and qualified, please include Requisition # 2018-343 in the subject line when emailing resume to: email@example.com.
For more information on CRISPR Therapeutics, please click here.
Director, Protein Purification
The Director, Protein Purification will report to the VP of Process Sciences, and will lead the development of robust, cost-effective, and well-characterized 2nd generation processes for purification of monoclonal antibodies and cell culture derived recombinant proteins for commercial and pipeline drug development. The ideal candidate should be in expert in protein biochemistry and bioprocess techniques as it relates to protein purification process development.
The successful candidate will:
Establish, lead and manage a team of scientists / technical staff focused on downstream process development / protein purification activities.
Establish state-of-the-art scale small-scale downstream models and capabilities
Work collaboratively with upstream, analytical, project management, and manufacturing groups to develop an increased depth of knowledge for the drug substance process for a given product and identify improvement opportunities
Establish and maintain familiarity with contemporary industrial standards, practices and technology focused on purification process development
Establish and maintain awareness of current process and product control strategies, critical parameter identification and assessment and in-process control strategies as applied to upstream operations
Establish and implement platform approaches for activities and technologies applicable to downstream operations
Support change control processes when needed with downscale model data and subject matter expertise
Support commercialization of molecules with a focus on the transition from late-stage-development to launch as well as post-approval lifecycle management.
Graduate degree (minimum M.S. degree, PhD preferred) in chemistry, biochemical/chemical engineering, biochemistry, or other relevant science or engineering field is preferred.
Minimum of 8+ years' previous experience in downstream process development setting, including hand-on experience with protein process purification via chromatography and filtration-based methods.
Experience with protein purification of (monoclonal) antibodies/biologics, required.
Experience in conjugating cytotoxins/ADCs is a plus.
Management experience, including a demonstrated ability to effectively manage staff and multiple tasks utilizing organization.
Experienced in supporting launch and commercial manufacturing.
Proven track record in building high-performing teams and leadership of department or functional group activities related to a development project.
Ability to learn and act on dynamic information at a rapid pace.
We are looking for a driven individual to join our enzyme manufacturing team as a Purification Scientist in Madison, Wisconsin. In this role you will be responsible for manufacturing the enzyme reagents used in the Illumina sequencers. You will work closely with other purification scientist within an industry setting to produce highly purified enzyme reagents.
Purify of a variety of molecular biology enzymes and nucleic acid binding proteins to aid in our growing product lines.
Work as part of a scientific team and participate in team meetings and initiatives.
Identify and implement continues improvement ideas within Production process.
Complete in-process assays, including SDS-PAGE gels as well as standard protein characterization assays and contamination assays.
Execute inventory control of reagents, chemicals, and supplies using proper labeling and computerized systems.
Maintain general lab organization (6S) of lab supplies, equipment and reagents.
Other duties that may be determined by management.
3+ years of experience in protein purification or related biochemistry areas.
Hands-on experience in purification at various industrial scales using both non-automated methods and automated FPLC systems (e.g. the AKTA platform), as well as homogenization, batch purification, precipitation, dialysis, and tangential flow filtration.
Experience with buffer preparation including pH and conductivity measurements.
High level of technical proficiency, initiative, independent thought, and collaborative ability.
Excellent laboratory, organizational, and analytical skills.
Experience writing SOPs and Work Instructions.
Additional experiences that are desired, but not mandatory:
Purification experience within an industry setting
CGMP Experience and Good Documentation practices (GDP)
Experience working in an Operational Excellence Culture
Computerized Inventory Control ERP systems (e.g. SAP)
Computerized Compliance systems (e.g. EtQ Reliance)
- B.S. in biochemical engineering, biochemistry, protein biochemistry or related field
Illumina believes that everyone has the ability to make an impact, and we are proud to be an equal opportunity employer committed to providing employment opportunity regardless of sex, race, creed, color, gender, religion, marital status, domestic partner status, age, national origin or ancestry, physical or mental disability, medical condition, sexual orientation, pregnancy, military or veteran status, citizenship status, and genetic information. If you have a disability or special need that requires accommodation, please contact us at firstname.lastname@example.org. To learn more, visit: https://www.dol.gov/ofccp/regs/compliance/posters/pdf/eeopost.pdf
Sr. Purification Scientist
Job Description: Job ID: BIO000569
Pall Corporation is a global leader in high-tech filtration, separation, and purification, serving the diverse needs of customers across the broad spectrum of life sciences and industry.
Pall Life Sciences provides cutting-edge products and services to meet the demanding needs of customers discovering, developing and producing biotech drugs, vaccines, cell therapies and classic pharmaceuticals. Pall offers advanced medical technologies, which are often a patient's last line of defense from dangerous pathogens. Pall's food and beverage products provide critical protection from contaminants during various manufacturing steps.
Pall Industrial serves a diverse range of customers in the microelectronics, aerospace, fuels, petrochemical, chemical, automotive, and power generation industries. Pall is a key supplier to the innovative and demanding semiconductor and consumer electronics industries, and provides filtration products used in critical applications on commercial and military aerospace vehicles.
Pall products are key to the reliability of industrial equipment. Pall's engineered solutions help municipal and industrial customers address mounting water quality, scarcity and demand issues, and help energy companies maximize production and develop commercially successful next generation fuels.
Headquartered in Port Washington, New York, Pall has offices and plants throughout the world.
To learn more about Pall, please visit www.pall.com/green.
The position has the responsibility for development of purification processes for virus production. The individual will be focusing on purification activities in the laboratory, developing processes from material produced in bench-top bioreactors through a rigorous scientific / engineering approach. The candidate ideally has experience in bioprocessing, and more specifically, with bioreactor viral vector production processes This individual must be competent in the analysis and interpretation of data, and will ideally have experience with plate-based, and/or qPCR assays.
Planning and execution of experiments for Pall downstream process development services including, depth filtration, chromatography, TFF testing along with some of the analytics
Prepare project summaries, by combining all data from a specific project from multiple individuals.
Help with administrative functions for this project – preparation of report drafts, budget tracking, draft proposals
Plan and execute experiments for DSP, analyze data
Do some of the required analytic assays, possibly including gels, ELISA, qPCR
Analyze project results and summarize for discussion with team. Make recommendations for further optimization
Help with administrative functions for this project – organize meets, help prepare reporting docs for MIT, etc.
Skills and Knowledge:
Experience with purification of viral particles (gene therapy and/or vaccine fields)
A good understanding of protein purification mechanisms and basic protein analysis tool (gels, ELISA)
Prior experience compiling information into technical reports
Ability to solve moderately complex issues independently
Strong computer, scientific, and organizational skills
Multi-tasker with good organizational skills
Ability to communicate effectively
Strong team oriented work style
Self-starter w/ ability to execute technical tasks and projects with minimal supervision
Computer literate (Word, Excel, Powerpoint)
Adequately record, analyze and document analytical data
Reproducibly follow established procedures and critically analyze data using statistical tools.
Work effectively with cross-functional groups.
Hands-on and productive in the laboratory.
Bachelors in biological science / chemical engineering or related discipine
6+ years of experience in protein purification or MS in biology / chem engineering & 4+ years of experience in protein purification
Pall Corporation is an Equal Opportunity Employer who encourages diversity in the workplace. All qualified applicants will receive consideration for employment without regard to gender, race, color, national origin, ancestry, citizenship, religion, age, physical or mental disability, medical condition, sexual orientation, gender identity or gender expression, military or protected veteran status or marital status.
Danaher Corporation Overview
Danaher is a global science & technology innovator committed to helping our customers solve complex challenges and improve quality of life worldwide. Our world class brands are leaders in some of the most demanding and attractive industries, including life sciences, medical diagnostics, dental, environmental and applied solutions.
Our globally diverse team of 67,000 associates is united by a common culture and operating system, the Danaher Business System, which serves as our competitive advantage. We generated $18.3B in revenue last year. We are ranked #162 on the Fortune 500 and our stock has outperformed the S&P 500 by more than 1,200% over 20 years.
At Danaher, you can build a career in a way no other company can duplicate. Our brands allow us to offer dynamic careers across multiple industries.
We're innovative, fast-paced, results-oriented, and we win. We need talented people to keep winning. Here you'll learn how DBS is used to shape strategy, focus execution, align our people, and create value for customers and shareholders. Come join our winning team.
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