Binding Cutter Synthetic Cloth Job Description Sample
Operator I - Cloth Inspector - Production
Responsible for operation of the Intra cloth inspection machine to include quality, safety and mechanical requirements. Operates light-duty bench- or floor-type machine tools and automation equipment. May set up machining machines and make adjustments, and perform maintenance on machines. Checks work using prescribed gauges, jigs and fixtures to measure close tolerances. Some machines may be numerically controlled. May monitor and verify quality in accordance with statistical process or other control procedures.
Must observe all safety precautions and regulations at all times in all areas where duties are performed. Will be responsible for reporting all safety hazards and potential unsafe working conditions. Must attend all monthly scheduled Safety Meetings.
Responsible for producing a quality product.
Run and inspect cloth according to specified inspection standards and as to construction for shipping rolls.
Arrange cloth rolls from hold table for Intra machine.
Attach ends of cloth together with cloth already in the Intra by using seaming tape and automatic seam to complete a shipping roll of various lengths.
Cut out all defects that do not meet inspection standards. (Ex. Oil spots, thin places and place where leno is out on the selvage, etc.)
Keep records as to what loom number roll was run on in each shipping roll, the number of seams, and the total yardage in the shipping roll. This information goes with each shipping roll that is doffed from each batcher on a ticket from the Intra machine.
Immediately report poor quality loom rolls to the lead person or the Weaving Production Supervisor so quality issues can be immediately addressed.
Report any unusual noises or circumstances that the Intra machine might make or cause while working.
Keep good housekeeping around his/her machine or area of responsibility.
Record total production run during assigned shift with a break down of yardage run by style and number of hours worked.
Total amount of waste by category at end of shift and record this information along with total production.
Wipe off main motor and fluid holding tank. Remove all strings from rollers and Intra frame. Clean and remove strings and tape from air guider. Sweep up around seaming area.
Unload and stack tubes.
Pull cloth from back of machine to rethread when needed.
Get loom rolls off floor and arrange on table by style.
Assist in putting bales back on machine at style change.
Help Team Leader carry waste to Waste House when needed. Sort waste and place in bins.
Change set screws in collars as needed.
Follow all safety rules, plant rules, department rules and implement total quality at all times.
Participate in Plant Corrective Action Team Program.
Participate in Plant Safety Program.
Report all unsafe conditions in a timely manner.
High School Diploma/ GED; one to three months' related experience and/or training.
Ability to read and interpret documents such as safety rules, operating and maintenance instructions and procedure manuals.
Ability to write simple correspondence.
Ability to effectively present information in one-on-one and small group situations to customers, clients, and other associates of the organization.
Ability to apply common sense understanding to carry out detailed written or oral instructions.
Ability to deal with problems involving a few concrete variables in standardized situations.
Hazards / Safe Guards
Safety glasses as required and OSHA approved hearing protection.
Required to wear a safety glove and safety knife when cutting open packages.
Must also wear safety goggles and a dust mask if within 50 feet of a blow down operation.
Must wear safety shoes in areas where required.
What is expected of you and others at this level
Applies basic skills and techniques to complete routine tasks within assigned area
Maintains appropriate licenses, training and certifications
Works on basic and routine assignments
Works within clearly defined Standard Operating Procedures and/or scientific methods
Adheres to all quality guidelines
Works under close supervision. All work is reviewed for accuracy
Any deviations from the norm are approved by the supervisor before proceeding
Senior Binding Underwriter, Maxum~Alpharetta, GA
Analyze applications submitted (submissions) by E&S wholesale brokers to build a book of primary and excess property business by utilizing underwriting guidelines and rating rules while leveraging relationships to achieve growth and profitability objectives.
Review submissions to determine acceptability of risk in accordance with underwriting guidelines and Binding/Property risk appetite.
Prioritize and manage inventory of new business opportunities, renewal business, and in-force policy endorsement and service requests.
Understand pricing components and rating methodology to price business based on risk characteristics, financial review and competitive analysis.
Demonstrate technical underwriting skills through strategic account review and detailed file pricing and risk documentation.
Review Broker and Manuscript forms as for compliance with company standards.
Keeps current on state/territory issues, regulations and trends.
Communicate underwriting decisions and risk appetite to the brokerage community.
Manage assigned producer relationships to achieve gross written premium, profitability, rate, retention, product mix and new business production goals.
Develop and maintain producer relationships through targeted travel to build broker intelligence and drive performance to meet and exceed results.
Follow broker specific production plans, monitors performance, and suggests adjustments to plan to ensure profitable growth.
Participate in projects supporting profitable appetite expansion for the division.
3 years (T8) 5 years (T7) of commercial lines underwriting experience in the insurance industry.
5 years of E&S Binding, underwriting experience.
Proficient in risk selection and pricing to achieve an underwriting profit.
Proven exceptional marketing skill and dynamic relationship building ability.
Existing wholesale broker relationships preferred.
Ability to thoroughly analyze financial statements for acceptability standards.
Ability to review and understand risk engineering reports.
Outstanding oral and written communication skills.
Strong analytical and problem solving skills.
Knowledge of rates, rules, and forms for assigned product line.
Competent in use of technology as a tool to improve underwriting efficiency
Ability to function in a highly collaborative, team environment.
Four year college degree preferred.
Behaviors at the Hartford
Deliver Outcomes – Demonstrate a bias for speed and execution that serves our shareholders and customers.
Operate as a Team Player – Work together to drive solutions for the good of The Hartford.
Build Strong Partnerships – Demonstrate integrity and build trust with others.
Strive for Excellence – Motivate yourself and others to achieve high standards and continuously improve.
Equal Opportunity Employer/Females/Minorities/Veterans/Disability/Sexual Orientation/Gender Identity or Expression
Synthetic Medicinal Chemist/Cheminformatics
GlaxoSmithKline is committed to developing medicines for global health challenges including respiratory, immuno-inflammation, oncology and infectious diseases. We know that finding cures means not just finding new drugs, but finding new ways to discover drugs.
One of our endeavors at GSK's NCE Discovery site in Cambridge, MA, is developing screening technologies based on affinity selection – a discovery paradigm to screen unprecedented chemical diversity at a fraction of the time and cost of traditional methods. Our industry-leading platform based around DNA encoded small molecules (Encoded Library Technologies) is poised to achieve new levels of productivity following advances in selection methods, chemoinformatics, and high throughput chemistry. We are looking for experienced medicinal chemists to integrate the output of ELT selections into a strategy for pipeline progression.
Experience with analyzing and interpreting large data sets is essential. The successful candidate will interface with business partners on therapeutic area target teams to conceive, articulate, and execute on the strategy.
Why You?Basic qualifications:
PhD in organic or medicinal chemistry with 5+ years or MS with 10 years of medicinal chemistry experience in the pharmaceutical industry
Expert in synthetic organic chemistry methods and analytical tools
Experienced in use of cheminformatics and other computational tools for drug design a must.
Highly independent in lab work, data analysis, and interpreting / presenting results
Track record of success as demonstrated by publications, patents, or presentations
Expertise in medicinal chemistry with track record in small molecule Hit to Lead and Lead Optimization processes.
Desire to lead initiatives in platform building
Demonstrated ability to learn and influence outside of core area of expertise
Excellent skill set and use of computational tools
Outgoing personality with track record of working in a matrix setting
Ability to multitask and experienced in collaborating across disciplines
Excellent oral and written communications
Passion for contributing to new ways of working and pushing beyond boundaries
For further information see the following references:
Clark et al. Design, Synthesis and Selection of DNA-Encoded Small-Molecule Libraries. Nat. Chem. Biol. 2009, 5, 647-654.
Arico-Muendel. From haystack to needle: finding value with DNA encoded library technology at GSK.
MedChemComm 2016, 7, 1898-1909. DOI:10.1039/c6md00341A
Machutta & Kollmann et al. Prioritizing multiple therapeutic targets in parallel using automated DNA-encoded library screening.
Commun. 2017, 8, 16081. DOI:10.1038/ncomms16081
You may apply for this position online by selecting the Apply now button.
If you require an accommodation or other assistance to apply for a job at GSK, please contact the GSK HR Service Centre at 1-877-694-7547 (US Toll Free) or +1 801 567 5155 (outside US).GSK is an Equal Opportunity/Affirmative Action Employer. All qualified applicants will receive equal consideration for employment without regard to race, color, national origin, religion, sex, pregnancy, marital status, sexual orientation, gender identity/expression, age, disability, genetic information, military service, covered/protected veteran status or any other federal, state or local protected class.
Important notice to Employment businesses/ Agencies
GSK does not accept referrals from employment businesses and/or employment agencies in respect of the vacancies posted on this site. All employment businesses/agencies are required to contact GSK's commercial and general procurement/human resources department to obtain prior written authorization before referring any candidates to GSK.
The obtaining of prior written authorization is a condition precedent to any agreement (verbal or written) between the employment business/ agency and GSK. In the absence of such written authorization being obtained any actions undertaken by the employment business/agency shall be deemed to have been performed without the consent or contractual agreement of GSK. GSK shall therefore not be liable for any fees arising from such actions or any fees arising from any referrals by employment businesses/agencies in respect of the vacancies posted on this site.
Please note that if you are a US Licensed Healthcare Professional or Healthcare Professional as defined by the laws of the state issuing your license, GSK may be required to capture and report expenses GSK incurs, on your behalf, in the event you are afforded an interview for employment. This capture of applicable transfers of value is necessary to ensure GSK's compliance to all federal and state US Transparency requirements. For more information, please visit GSK's Transparency Reporting For the Record site.
Scientist, Medicinal Chemistry Position Summary: Seeking A Highly Motivated And Productive Synthetic Organic Chemist To Synthesize Target Molecules For Exciting Early Drug Discovery Projects. Primary Duties And Responsibilities: Design, Plan And Execute Mu
Seeking a highly motivated and productive synthetic Organic Chemist to synthesize target molecules for exciting early drug discovery projects.
Primary Duties and Responsibilities:
Design, plan and execute multi-step organic synthesis and purification of high quality target molecules for biological screening.
Participate in brainstorming and contribute new proposals and ideas.
Interact with colleagues in biology, pharmacology, and DMPK groups.
Analyze SAR according to biological, pharmacological and toxicological findings.
Prioritize the chemistry efforts to ensure timeline adherence and project alignment to meet group and company goals.
Work cross-functionally with counterparts in process chemistry and CMC groups.
Assist in the preparation of patents, publications, and project planning.
Collaboration & Teamwork: Relates to employees and management in a cooperative manner that helps others to achieve their best.
Productivity/Planning: Meets deadlines, demonstrates effective use of time.
The ability to convey both written and verbal information effectively and efficiently.
Willingness to Acknowledge Areas for Growth: Understands need for growth and is receptive to constructive feedback.
Education, prior work experience, and specialized skills and knowledge:
- Ph.D. in synthetic organic chemistry completed in 2017 or will complete in 2018
- Sound knowledge of organic chemistry principles
Cable Technician - Late Binding (Aws Govcloud Region)
At Amazon we are working to be the most customer-centric company on earth. To get there we need exceptionally bright, talented, and driven people who are willing to work hard and have fun. If you would like to help us build Amazon Web Services, this could be your opportunity to help us make history.
The Data Center Operations organization is looking for a Late Binding Cabling Infrastructure Technician with strong leadership skills and a progressive career history in structured cabling.
The ideal candidate will possess a technology background that enables them to understand the complexities of the sophisticated network architecture of Amazon data centers. To be a qualified candidate for this role you must have a background of structured cabling and experience operating in large-scale data centers.
You must possess: technical aptitude and the ability to communicate advanced technical information with a variety individuals of varying technical knowledge, good situational awareness, the capability to contribute to strong inter and intra-team development, strong analytical skills, demonstrated problem solving ability, and the ability to operate solo or as part of a team with varying degrees of supervision. This position requires the ability to successfully operate in high-pressure, time-sensitive situations while handling multiple critical priorities simultaneously. Successful candidates must be able to demonstrate effective examples of situations where personal initiative and judgment were used to benefit team objectives.
Professional traits that are not unique to this position, but necessary for success at Amazon:
Think outside of box, nothing is off the table when it comes to new design and solutions
Challenge the status-quo, achieve what's impossible with a passion to deliver results.
Relentlessly high standards - never satisfied with the status quo
Strong customer focus, and dedicated to meeting the expectations and requirements of internal and external customers; gets first-hand customer information and uses it for improvements in products and services; acts with customers in mind; establishes and maintains effective relationships with customers and gains their trust and respect.
Strong results orientation
Exhibits excellent judgment
Able to dive deep and is never out of touch with the details of the business or the technology
Strive for innovation and simplification
Have passion and convictions and the innate ability to inspire passion in others
Effective May 15, 2017, logical access to the AWS GovCloud region will be restricted to Amazon employees who are U.S. Citizens. (GovCloud may NOT be accessed from outside of the United States)
Amazon is an Equal Opportunity-Affirmative Action Employer – Minority / Female / Disability / Veteran / Gender Identity / Sexual Orientation.
Postdoctoral Research Fellow - Synthetic Chemistry
We are seeking a highly skilled and well self-motivated Postdoctoral Research Fellow with a passion for synthetic chemistry and personal drive to publish in world class journals. The initial research will center around the elucidation of new reactions and reagents for regio-selective late stage fluorination as well as novel synthetic chemistry and the development of innovative chemical systems such as flow chemistry, to enable an access to novel fluorinated biologically active molecules. It is expected that there will be significant opportunity to publish and, once the initial work plan is completed, there will be significant research opportunities which it is expected will be inspired by the Postdoctoral Research Fellow.
Hold a Ph.D. (or in the process of obtaining a Ph.D.) in Chemistry with graduation date 2017-2018.
The ideal candidate will have experience in one or more of these areas: methodology development, target oriented synthesis, basic analytical chemistry and NMR spectroscopy.
While considered a plus, no previous fluorine chemistry experience is required.
Current US work authorization.
Preferred Additional Skills:
Exceptional written and verbal communication skills.
Excellent decision making and organization skills.
Committed to the values of integrity, accountability, transparency, scientific rigor and drive.
Ability to travel domestically and internationally.
Senior Scientist, Vaccine Sciences - Elisa, Function Or Ligand Binding Assay, Validation, Optimization
Senior Scientist, Vaccine Sciences - ELISA, Ligand Binding Assay, Validation, Optimization
PPD is a leading global contract research organization. At PPD we are passionate, deliberate, and driven by our purpose - to improve health.
PPD Laboratories offer the most comprehensive set of laboratory services available in the industry. Our services are designed to accelerate pharmaceutical development for small molecules, biologics, and vaccines, allowing our clients to make faster decisions about their compounds.
As a Senior Scientist, you are committed to excellence and high quality results in your complex laboratory analysis of key pharmaceutical products. Beyond the bench, you work as a project leader with a strong sense of urgency aligned to our customers, and you are committed to delivering results.
Grow your career within the scientific ladder, pursue project management, or develop into a leader. These are just a few career pathways available once you chose to Be with PPD.
Join PPD in our relentless pursuit of excellence - apply now!
Performs complex laboratory analysis of pharmaceutical products and proficiently uses analytical instrumentation, calculates and analyzes data and records data in adherence with PPD SOP's and the industry.
Routinely acts as the project leader on multiple projects, interacts with clients, reviews and evaluates data, writes reports and protocols.
Responsible for the scientific conduct of the project and communication of regulatory issues with senior level team members.
Education and Experience:
Bachelor's degree in lab sciences field such as biology, chemistry or related
Previous experience that provides the knowledge, skills, and abilities to perform the job (comparable to 4 years') or equivalent combination of education, training, & experience. OR Masters degree and previous experience that provides the knowledge, skills, and abilities to perform the job (comparable 2 year) OR PhD
Knowledge, Skills and Abilities:
Solid experience with ELISA, immunoassays
Experience with Ligand Binding Assays a plus
Knowledge of Validation, Optimization preferred
Experience with vaccine testing, immunology or similar
Experience in a GLP environment
Full understanding of laboratory requirements, PPD & client SOPs, ICH guidelines, USP requirements and FDA guidance
Ability to utilize Microsoft Excel and Word to perform tasks
Proficiency on technical operating systems
Proven problem solving and troubleshooting abilities
Effective oral and written communication skills
Proven ability in technical writing skills
Time management and project management skills
Ability to work in a collaborative work environment with a team
Proven problem solving and troubleshooting abilities
Ability to train junior staff
Work is performed in a laboratory and/or a clinical environment with exposure to electrical office equipment.
Occasional drives to site locations, occasional domestic travel.
Exposure to biological fluids with potential exposure to infectious organisms.
Rare exposure to skin and lung irritants, radiation, toxic materials and hazardous waste.
Personal protective equipment required such as protective eyewear, garments and gloves.
Exposure to fluctuating and/or extreme temperatures on rare occasions.
Ability to work in an upright and /or stationary position for 6-8 hours per day.
Repetitive hand movement of both hands with the ability to make fast, simple, repeated movements of the fingers, hands, and wrists to operate lab equipment.
Occasional mobility needed.
Occasional crouching, stooping, with frequent bending and twisting of upper body and neck.
Light to moderate lifting and carrying (or otherwise moves) objects including luggage and laptop computer with a maximum lift of 15-20 lbs.
Ability to access and use a variety of computer software developed both in-house and off-the-shelf.
Ability to communicate information and ideas so others will understand; with the ability to listen to and understand information and ideas presented through spoken words and sentences.
Frequently interacts with others to obtain or relate information to diverse groups.
Works independently with little guidance or reliance on oral or written instructions and plans work schedules to meet goals. Requires multiple periods of intense concentration.
Performs a wide range of variable tasks as dictated by variable demands and changing conditions with little predictability as to the occurrence. Ability to perform under stress. Ability to multi-task.
Regular and consistent attendance.
Pharmaceutical Product Development, LLC is firmly committed to Equal Employment Opportunity (EEO) and prohibits employment discrimination for employees and applicants based on age, race, color, pregnancy, gender, gender identity, sexual orientation, national origin, religion, marital status, citizenship, disability or protected veteran or other status protected by federal, state, and/or local law.
Bioanalytical Scientist Chemist Biochemist Biologist lab laboratory bio analytical assay assays ligand binding protein large molecule molecular ELISA enzyme linked immunosorbent assay immuno immunology immunoassay validate validation develop developer development testing sample analysis PI clinical sample preclinical vaccine vaccination bacteria bacteriology virus virology pathogen
Post-Doctoral Fellow (Genomic Medicine And Synthetic Biology)
J. Craig Venter Institute (JCVI) is seeking a Post-Doctoral Fellow to join our team in the Genomic Medicine and Synthetic Biology groups at our Rockville, MD location.
The Fellow will work on an DoD-funded innovative Bacteriophage engineering project. Responsibilities will include the use of novel synthetic biology tools to assemble whole bacteriophage genomes as well as initial testing of the resulting viruses. The Fellow is also expected to help develop new scientific projects by assisting with the preparation of proposals and to publish the results of their work in peer-reviewed journals.
?JCVI offers an excellent working environment and a competitive benefit package. For more information and to apply to this position, please visit our website at www.jcvi.org Equal Opportunity Employer AA M/F/Vet/Disability.Qualifications
Qualified candidates will possess a Ph.D. in biological sciences or other disciplines with significant training and experience in molecular biology, microbiology and/or virology.
Spiral Binding Operator- NJA
Are you our next Mimiac?
1.A smart, enthusiastic and overly zealous person who loves working at Mimeo.
Spiral Binding Operator- NJA
HOURS: Tuesday- Friday : 6:00 am - 4:30 pm
As the Bindery Associate, you will be responsible for performing bindery functions by either manual or mechanical means ensuring superior quality of multiple printed documents.
Responsible for completing all finishing services.
Could involve binding, cutting, folding, gathering, stapling, stitching, trimming, and other finishing functions.
Thorough communication with management.
Thorough communication with other areas as needed.
Ensure adherence to all documented processes and procedures.
Other duties as assigned.
Experience and Qualifications:
High School Diploma or GED equivalent required.
6 months experience in a printing environment preferred.
Thorough knowledge of all binding processes and equipment.
Must be able to work under deadlines and pressure to meet goals.
Good communication and comprehension skills – including written and verbal.
Must be dependable; have the ability to work overtime with little or no notice.
Team-oriented and flexible; goal-oriented; capable of multi-tasking.
Ability to stand and walk frequently.
Ability to bend, stoop, reach and lift up to 50lbs occasionally.
Who we are:
Mimeo is the innovator of online, on-demand document printing and distribution. Our mission, to power the world's print, describes our commitment to providing the worlds' best workflow for managing documents from anywhere to everywhere. We measure ourselves against our ability to deliver speed, quality and value at levels which not only define the industry but exceed those offered by the nearest competitor.
Mimeo.com offers a fun and exciting culture as well as one of the most generous benefits packages in the area, including low cost medical, life insurance, STD/LTD, PTO and 401k.
Part-Time Synthetic Biology Researcher
Requisition ID 108798BR Date updated 01/18/2018
The Information and Knowledge Technologies department at Raytheon BBN Technologies is looking to hire part-time synthetic biology researchers (20 to 24 hours a week) in the Cambridge, Massachusetts or Columbia, Maryland
office. Candidates should have a strong computational background (both software and data analysis), experience in the field of synthetic biology, and the ability to work in a self-directed manner as part of a team. We are primarily interested in hiring at the postdoc / new PI level, but are open to considering strong candidates at any level.
Strong programming skills, particularly in Java and Matlab (or close equivalents)
Creative problem solving and experimental design
Excellent oral and written communication skills
Experience with synthetic biology
Strong mathematical background, and/or
Software engineering experience, and/or
Knowledge representation background
- BS (in Computer Science or related field) with 6+ years, or MS (in Computer Science) with 4+ years, or PhD (in Computer Science) with 0-3 years 108798
Business Unit Profile
Raytheon Space and Airborne Systems (SAS) builds radars and other sensors for aircraft, spacecraft and ships. The business also provides communications and electronic warfare solutions and performs research in areas ranging from linguistics to quantum computing. SAS is headquartered in McKinney, Texas USA. As a global business, our leaders must have the ability to understand, embrace and operate in a multicultural world -- in the marketplace and the workplace. We strive to hire people who reflect our communities and embrace diversity and inclusion to advance our culture, develop our employees, and grow our business.
Raytheon is headquartered in Waltham, Massachusetts. Follow us on Twitter.
None / Not Required
Information and Knowledge Systems
Type Of Job
MA - Cambridge
MD - Columbia
Raytheon is an Equal Opportunity/Affirmative Action employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, creed, sex, sexual orientation, gender identity, national origin, disability, or protected Veteran status.
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