Chemist Instrumentation Job Description Sample
The Princeton University Department of Chemistry seeks a full-time lab manager at the professional specialist rank for the femtosecond laser facilities in the Scholes lab along with a range of responsibilities as follows:
Manage femtosecond laser facilities in the Scholes labs, provide mentorship for students, and leadership in scholarly activities.
Manage the chemistry department femtosecond transient absorption facility (50%FTE). This will involve running experiments on samples provided, maintaining the instrument, managing data, analyzing results, and assisting preparing the results for publication.
Assist students and postdocs with experiments and data analysis as well as writing papers. Provide guidance and assistance for undergraduate research students, visiting scientists and collaborators. Execute experiments and communications for collaborative projects.
Assist with scholarly administrative responsibilities for Professor Scholes' graduate teaching, e.g. drafting assignments, exams and grading.
Identify funding opportunities and help with drafting grant proposals, letters of intent, white papers, etc.
There will be freedom to pursue research projects in the lab and the candidate will be expected to publish regularly (at least two papers per year where substantive contributions to the writing have been made).
This full-time position has an initial appointment of one year with the possibility of renewal based on satisfactory performance and funding availability. This position is subject to the University's background check policy.
Applicants must apply online at http://jobs.princeton.edu (requisition No. ________) and include a CV, cover letter, and contact information for 3 references.
Ph.D. in Chemistry or other closely related field;
Demonstrated experience in femtosecond laser experiments and photophysics;
Excellent publication record;
Excellent communications skills
Experience in multidimensional electronic spectroscopy;
Knowledge of femtosecond laser technology;
Expertise in molecular photophysics and/or biophysics, fluorescence, transient absorption
Reg Prof Specialist &Technical
"Princeton University is an Equal Opportunity/Affirmative Action Employer and all qualified applicants will receive consideration for employment without regard to age, race, color, religion, sex, sexual orientation, gender identity or expression, national origin, disability status, protected veteran status, or any other characteristic protected by law. "
QA Chemist (46626)
Coloplast has a new opportunity available in North Mankato, MN for a QA Chemist to join our quality team.
As a QA Chemist, you will be is responsible for performing inspections and tests on raw materials, in-process products, bulk products, finished goods and stability samples to ensure conformance to established specifications.
Areas of Accountability:
Perform in-process inspections and determine any adjustments required. Perform bulk and finished product inspections, testing and analyses. Confirm samples meet established standards and specifications and release items as appropriate.
Develop and validate analytical methods based on USP requirements and local needs and available instrumentation.
Record test data and results using standard laboratory data calculations. Verify notebook entries and calculations for lab staff.
Assure equipment is calibrated prior to use and complete preventative maintenance.
Clean glassware and work stations and properly dispose of solvents and solvent containers.
Purchase necessary reagents, gases, components for instruments and lab supplies.
Assist with the maintenance of retain/shelf sample program and inspections as needed. If needed, enter samples into accelerated and real-time stability programs and manage testing per schedule.
Document analysis results and trending in Annual Product Reviews.
Write product and test method validation and revalidation protocols, perform actions, document results and issue reports.
Assure validation of suppliers' certificates of analysis for chemicals used in the manufacture of drug products per schedule and coordinate testing to confirm reported results.
Generate Out of Specification (OOS) reports and utilize problem solving techniques to determine root cause and corrective actions.
Initiate non-conformity reports as needed and provide investigations and supporting data.
Follow requirements of cGMPs, ISO, USP, Coloplast and other regulatory standards and guidelines.
Follow safe lab practices and observe MSDS precautions.
Any duties necessary to promote efficient functioning of the Quality department or Skin Care Value Stream
Position requires a bachelor's degree in chemistry or related scientific field.
0-5 years of experience working in drug, medical device, biotechnology or food industries.
Experience with laboratory equipment and analytical test methods (e.g. FTIR, GC, HPLC, atomic absorption, IR and UV-VIS spectroscopy, pH meter).
Proficient in use of analytical balances, volumetric glassware and sample preparation (i.e. "wet lab" technique).
Knowledge, Skills, and Abilities:
Knowledge of drug and medical device cGMPs and ISO requirements.
Ability to prioritize and perform tasks in established timeframes and communicate on technical issues.
Ability to follow written and verbal instructions.
Experience with Microsoft Office Excel and Word software.
Ability to stand, perform some repetitive motions, reach above shoulder height, and handle containers (including various size drums and bags up to fifty pounds) for extended periods of time.
Interaction with all departments of GO Mankato and outside suppliers
Interaction with internal and external auditors, including those conducting ISO and FDA audits
The job information contained herein will apply to the candidate successful in being hired for the position. If interested, please apply today!
Pursuing an ambitious growth agenda, Coloplast develops and markets products and services that make life easier for people with very private and personal medical conditions. Employing more than 10,000 people and with products available in more than 100 countries, we are one of the world´s leading medical device companies. We are constantly growing our business and always looking for new ways to move forward – we explore, learn and look for new ways of doing things. Curiosity works here.
Visit us on Coloplast.com. Follow us on LinkedIn. Like us on Facebook.
Research And Development Laboratory Chemist Manager
Postdoctoral Fellowships in Genomic Diagnostics
The Carl R. Woese Institute for Genomic Biology at the University of Illinois at Urbana-Champaign offers a number of fellowships for truly exceptional young scholars who have completed their PhD within the last several years, and who are looking for a stimulating and supportive interdisciplinary environment to carry out independent and collaborative research in the field of anticancer drug discovery.
IGB Fellows will typically spend two or more years conducting research in one of the IGB themes. A personalized mentoring plan will be developed for each Fellow. Annual salary is $50,000, in addition to a $7,500 allowance.
Omics Nanotechnologies for Cancer Precision Medicine
A goal of the ONC-PM Theme is to identify and exploit novel nucleic acid and protein biomarkers of cancer that can be noninvasively and rapidly measured from a single blood fingerstick using new technology platforms, to eventually measure diagnostic biomarkers in cancer patients to identify cancer sub-classes, monitor recurrence, and track therapy, to provide a more personalized approach toward patient care. Working jointly with the IGB and the Micro and Nanotechnology Laboratory (MNTL), we seek an individual who will serve in a research and leadership role to facilitate collaboration between interdisciplinary teams.
The Fellow will develop ultra-sensitive technologies that incorporate nanostructured optical biosensors, high contrast nanoparticle tags (quantum dots and plasmonic nanoparticles), and microscopy-based detection instrumentation. Candidates with a PhD in Bioengineering, Electrical and Computer Engineering, Chemistry, Biochemistry, or related discipline preferred. Experience in the development and characterization of biosensors with an emphasis on optics-based approaches such as fluorescence, surface-enhanced Raman spectroscopy, or label-free detection are desired.
Preference will be given to candidates familiar with instruments used for optical detection, including microscopes, imaging camera technology, and laser excitation sources. A track record of high impact peer-reviewed journal publications and excellent communication skills are required. Applicants should submit a CV, a research summary, and the names of three recommenders who can write letters on their behalf.
This information should be sent to Professor Brian T. Cunningham (Theme Leader), email@example.com in advance of the August 30, 2019 closing date. The University of Illinois is an Affirmative Action/Equal Opportunity Employer. Visit www.igb.illinois.edu for additional information.
Chemist Associate - Chemist
The Chemist position is critical in supporting the compliance and regulatory business of Generation and Distribution and is responsible for performing professional-level chemical analysis of water, wastewater, and/or industrial wastes. Chemists have the ability to perform complex analyses using all of the following instrumentation:
Auto-titrator, Continuous Flow Analyzer, Ion Chromatograph, Total Organic Carbon Analyzer, Inductively Coupled Plasma/Mass Spectrometer, and Inductively Coupled Plasma/Optical Emission Spectrometer. The Chemist also provides support in developing methods and procedures for the analysis of water and/or wastewater samples, maintains several pieces of vital equipment, and diagnoses problems in processes and equipment.
Essential Job Functions:
Perform daily operations for chemical analyses:
1.Assists in the development of environmental, health and safety policies for everyday tasks.
2.Performs routine analytical activities with minimal direction form higher-level employees.
3.Uses scheduling techniques for work management.
4.Coordinates multiple analytical techniques and the work of technicians
Adherence to policies and procedures:
1.Follows policies, practices, standards and rules of the company and those regulations and procedures required by external agencies.
2.Understands and practices safe laboratory procedures.
3.Ensure work quantity and quality by requiring strict adherence to NIOSH methods and standard operating procedures for respirable crystalline silica, total and respirable dust, lead base paint, welding fumes, respirable metals and hexavalent chromium.
4.Ensure work quantity and quality by requiring strict adherence to EPA (and EPA-approved) methods and standard operating procedures for chemical constituents in water, wastewater, waste, solid, oil, and process samples.
5.Ensure work quantity and quality by requiring strict adherence to ASTM (and ASTM-modified) or AEP-developed methods and standard operating procedures for chemical constituents, identification, and characterization of liquid, solid, organic and airborne process samples.
6.Ensure work quantity and quality by requiring strict adherence to NIOSH methods, EPA (and EPA-approved) and ASTM (and ASTM-modified) standard operating procedures as appropriate.
Documents daily operations and activities:
1.Demonstrates ability to prepare and issue routine analytical reports, verbal and written skills for effective communication of analytical data and chemical information.
2.Develops, reviews, or presents routine technical reports clearly, concisely and effectively.
3.Demonstrates ability to extrapolate beyond known facts to reach logical conclusions.
4.Prepare lab reports for submission to customers, and prepares reports on laboratory activities.
5.Provides basic training and guidance to lower level employees. Effectively trains other employees.
Problem solving and decision making within department:
1.Identifies and initiates solutions to routine problems which usually require additional definition or clarification before analysis can begin.
2.Demonstrates ability to identify problems that are beyond the normal routine.
3.Makes decisions, subject to review within established policies and procedures, concerning the validity of analytical test data.
4.Demonstrates proficiency in application and use of economic analysis techniques.
5.Initiates priority changes when analytical objectives are not met.
6.Develops an awareness of the relationships among sample turnaround time, sample load, and internal and external customer requirements; and makes routine decisions in the scheduling of assigned work based on these relationships.
Criminalist - Forensic Chemist
Summary of Job Duties
- This posting is scheduled to close on Monday, September 17, 2018 at 12 noon, however is subject to close at any time without prior notice. Thank you*
Performs analysis of forensic evidence through a variety of methods including wet chemical analysis and/or instrumental analysis, processing suspected drug evidence for latent print impressions using a variety of methods.
At the City of Aurora, we demonstrate our work by modeling the CORE 4 Values of: Integrity, Respect, Professionalism, and Customer Service. We welcome all who share these values to apply.
To be employed by the Aurora Police Department you will need to successfully pass a background check, polygraph test, and fingerprint screening, along with other conditions of employment; drug test and verification of employment. Because of this, there is a longer recruitment process, we thank you in advance for your patience.
Despite the changes in Colorado law, the City of Aurora maintains a drug free workplace. A positive test of marijuana is grounds for disqualification or termination once hired.
PRIMARY DUTIES & RESPONSIBILITIES
Analyze suspected drug evidence for the presence of controlled substances as defined by the Colorado State Statutes and Federal Department of Justice
Analyze blood for the presence of ethanol in DUI cases and other criminal cases as requested
May analyze Fire Debris cases for the presence of accelerants to assist the Aurora Fire Department or Police Department in their investigations
May process various items of evidence for latent prints.
Issue reports regarding analysis of evidence
Maintain secure custody of evidence while in their custody
Assist and advise investigators and prosecuting attorneys regarding cases, results, and expected testimony
Testify as an expert witness in municipal, state, and federal courts as necessary regarding analysis
It may be necessary to assist processing crime scenes for evidence, photograph evidence, and prepare reports relating to duties performed as a Crime Scene Investigator
Perform additional duties as assigned
Education: Bachelor's Degree in chemistry or directly related scientific field
Experience: At least 2 years of experience as a forensic chemist in a law enforcement laboratory or directly related environment. An equivalent combination of education, training and experience that demonstrates required knowledge, skills and abilities may be considered.
Knowledge of wet chemistry techniques and instrumental analysis.
Knowledge of safe handling practices for chemicals in use by the laboratory. Knowledge of investigative methods and techniques and rules of evidence.
Abilities: Ability to communicate effectively both orally and in writing; organize and prioritize work; properly use and maintain scientific equipment; prepare reagents; prepare accurate reports; maintain secure custody of evidence while in their possession; work independent of direct supervision; testify effectively on scientific matters in judicial and quasi-judicial proceedings.
LICENSES OR CERTIFICATES REQUIRED: Colorado Driver's License with a good driving record.
Physical Demands: Regular standing, hand/eye coordination to operate computer, laboratory instruments, and other testing instruments; foot/eye coordination to operate motor vehicle; visual acuity correctable to 20/40 with no color impairment to interpret data; speech communication, hearing, and listening to maintain communications with other employees and citizens. May be required to perform light to moderate physical work requiring ability to lift a maximum of 50 pounds with or without assistance.
Equipment Used: Computer; laboratory instruments to include GC, GC/MS, FTIR, microscopes; and camera.
Work Environment: Works primarily in a laboratory environment.
Some work outdoors at crime scenes may be required. Exposure to chemical and bio-hazard contamination, odors, and noise.
For Veterans points: Please show all of your employment history, including military service and related documentation (DD214) on the application.
The City of Aurora is an equal opportunity employer. We are required by state and federal agencies to keep certain statistical records on applicants. It will not be used in any way to discriminate against you because of your sex, race, age, sexual orientation, creed, national origin, disability or military status, gender identity, unless related to a bona fide occupational qualification as defined by the Colorado Civil Rights Commission and the Equal Opportunity Commission.
If you need assistance in completing this application, please feel free to contact our office at: 303-739-7225 or visit us at 15151 E Alameda Pkwy., Suite 3500, Aurora, CO 80012.
Coding Products (Kalkaska, MI) is a member of the ITW Specialty Films division of Illinois Tool Works Inc. (ITW), a Fortune 200 global multi-industrial manufacturing leader, and is part of the Specialty Products Segment. ITW Specialty Films designs, manufactures and markets specialized coated and/or metalized films for the Transaction Card, Security Documents, Medical IV bags, and Consumer Packaging markets. The division leverages unique core competencies and technologies in films, foils, laminates, holography and transfers to address customer needs globally. The Division has operation in North America and Europe.
As Plant Chemist you will support day-to-day operations in our solvent based coating facility. As part of a dynamic operational team, you will help manage quality, manufacturing processes and customer support projects from concept to commercialization reporting to the Quality Manager. After developing an understanding of our products, you will also be instrumental in helping improve existing products and processes to reduce scrap and reduce cost. The Plant Chemist works internally with personnel at all levels of the organization supporting both internal and external customers.
What you will do . . .
Interact with manufacturing staff to make determinations regarding coating uniformity, print quality, color control, mix ratios and formulation adjustment.
Diagnose performance issues and understand the functions of each chemical component in a formulation.
Management of manufacturing documents. Reviewing and archiving documents.
Review quality control documents and procedures. Perform quality audits and verify current practices against documentation. Update standard operation procedures when necessary.
Maintain and verify function of test equipment.
Customer complaint management with plant personnel.
Quality team member.
Customer technical support with an ability to troubleshoot customer problems onsite. Answer questions from Sales, Customer Service and Vendors.
Assist with new process development, coating and evaluating raw materials and products.
Use, understand and maintain laboratory equipment.
Understand documentation, safety requirements and safe practices for use of chemicals.
Understand the operation of ERP software (Microsoft NAV) and provide technical support to operations (coating, mixing, slitting and customer service) to help resolve ERP operations related issues.
Safety Data Sheet management and understanding.
Perform other duties as required.
What skills, abilities and experience we are looking for. . .
Bachelor's degree in Chemistry or Chemical Engineering with a minimum 5 years of relevant experience preferred.
Ability to build effective partnerships with cross-functional team members at all levels within the organization to achieve quality and operational goals.
Ability to effectively analyze a situation and determine the best path to resolution.
Good communications skills.
Ability to work with chemical and solvents
Ability to use Word, Excel, PowerPoint and Outlook.
Take this opportunity to join a successful and enthusiastic team where you have an opportunity to make a significant impact immediately. You will enjoy a competitive salary and benefits package that includes medical, dental, prescription drug, vision, life insurance, 401K with an immediate company match and additional company contribution, wellness programs, employee discounts, paid vacation and holidays, and a corporate matching gift program for charitable donations!
ITW Specialty Films is an Equal Opportunity / Affirmative Action employer. All qualified applicants will receive consideration for employment without regard to sex, gender identity, sexual orientation, race, color, religion, national origin, disability, protected veteran status, age, or any other characteristic protected by law.
If you are a qualified individual with a disability and are unable or limited in your ability to use or access the online application system due to your disability, please email hrdept@ itwsf.com to request assistance. No other requests will be acknowledged.
AD Chemist III (2019-00)
If you're looking for a dynamic career move, look no further.
Cambrex is an innovative life sciences company with a refreshingly human approach. Driven by passion, our pharmaceutical products, expertise and technologies are accelerating small molecule therapeutics into the market to help businesses grow.
We are tried and trusted across branded and generic API markets
We put all of our energy and experience into being a partner of choice
Our people are the experts customers enjoy working with
Headquartered in East Rutherford, New Jersey, Cambrex supports its customers worldwide with a network of API R&D and cGMP manufacturing facilities across the US and Europe.
As the number one contract manufacturing organization (CMO) for small molecule APIs in the USA and one of the fastest growing CMOs in Europe, we are leading the way in terms of small molecule API development and manufacturing. Not only that, our passionate people love what they do and always go the extra mile for our customers.
Create a better world at Cambrex
Known for our manufacturing excellence, experience and innovative science, we offer a range of career opportunities across our global network of locations. As a team, we share one goal – to improve quality of life for our customers' patients across the world.
Cambrex Charles City, Inc. is a subsidiary of Cambrex and develops and manufactures active pharmaceutical ingredients, fine chemicals and pharmaceutical intermediates for a wide range of applications.
Find out more about life at Cambrex
Watch our video: Meet the Cambrex experts
Safely and effectively collecting analytical data to help develop, establish, and validate analytical testing methodologies used to control raw materials, production intermediates, and final products;
Perform analytical chemistry assays based on new and existing methodologies;
Operate analytical instrumentation such as HPLC, GC, GC/MS, LC/MS, FTIR, Titrator, Particle Size Analyzer;
Maintain laboratory notebooks documenting work;
Maintain compliance with GMP SOPs and DEA regulations;
Transfer documented analytical methods to the QC and Process Support Group departments;
Set up new or existing analytical methods for compound identification, purity and potency testing;
Coordinate off-site testing as necessary;
Conduct testing of analytical samples for the Chemical Development Department as needed; and
Collect analytical data to help qualify reference materials.
Master's or equivalent in a Chemistry or Biochemistry field;
2 years of experience in the job offered or in a R&D role in the pharma industry;
Must be familiar with compliance requirements within cGMP, safety and regulatory environments; have operational knowledge of analytical instrumentation like HPLC, GC, GC/MS; and experience with QC testing.
Cambrex Charles City offers an extraordinary opportunity, a competitive salary, and an exceptional benefits package including medical, dental, vision care and prescription, life, LTD, STD; 401(k) with employer match; tuition reimbursement; and the 'Arthur I. Mendolia Scholarship Program.' Relocation assistance will be offered for this position. Post offer physical and drug screen are required. Interested candidates should submit a resume and cover letter with salary requirements to Human Resources, Cambrex Charles City, Inc.: online: www.cambrex.com.
Thank you for your interest in Cambrex Charles City!
Equal Opportunity Employer M/F/D/V.
QC Chemist II
QC Chemist II – Weekend Shift
The QC Chemist II will support the Quality Control department in a regulated testing environment. This is a 12 hour weekend day shift position working hours from 6:00 AM to 6:30 PM every Friday-Sunday and every other Monday. This position will depend on you to test raw materials, bulk intermediate, finished good and stability samples. This position also includes maintaining, troubleshooting and servicing laboratory equipment.
Test samples for specific quality attributes
Use and maintain HPLC, GC, IC, FTIR and UV/VIS
Perform a variety of wet lab techniques including but not limited to: titrations, pH, ISE
Write and revise SOPs and test methods as needed
Use and follow test methods and SOPs according to GMP
Document test results for batch release using good documentation practices
Document and investigate Out of Specification (OOS) results as required
Prepare reports and review data
WHY WORK WITH ULTRADENT:
Ultradent Products, Inc., is a collaborative and hard-working company with a 40-year history of innovation. Ours is a fun, fast-paced work environment dedicated to providing unique, solution-oriented products to dentists—and their patients—across the globe. Our company was built on a foundation of innovation, integrity, hard work, quality, and care, and we put those values into everything we do.
WHAT YOU'LL NEED TO SUCCEED:
Bachelor of Science in Chemistry or related science
At least three years of laboratory experience in a cGMP, FDA regulated, and/or ISO 13485 environment
Advanced knowledge of laboratory instruments such as HPLC, GC, IC, FTIR and UV/VIS
Method validation, method verification, method transfer experience a plus
WHAT WE'RE LOOKING FOR IN YOU:
Microsoft Office, Empower, ChemStation, Chromeleon, LIMS knowledge
Understanding of regulatory guidance documents relevant to RX and OTC drug manufacture in the US, EU and Canada
Strong technical writing skills to create and revise documents including SOPs and test methods
Excellent organizational skills and time management skills to ensure multiple targets and deadlines are consistently met
Self-motivated and ability to work independently
WHAT BENEFITS AND PERKS YOU'LL GET AT ULTRADENT:
Medical/Dental (eligible the first of the month after 60 days)
Health savings account with employer Contribution
On-site cafeteria (breakfast & lunch)
On-site fitness center
Employee access to discounted Ultradent products
Five days paid time off between Christmas and New Years
Ultradent is an Equal Opportunity and Affirmative Action Employer. All qualified applicants will receive consideration for employment without regards to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status.
VEVRAA Federal Contractor: For more information please contact us at Recruiting@ultradent.com.
The Chemist I of Analytical Quality Control will performing basic testing of raw materials and finished products, maintenance and calibration of analytical instruments in compliance with cGMP. The position will provide assistance to analytical quality control manager to meet project timelines and improve laboratory compliance.
Perform routine testing, both wet chemistry and instrumental analysis, according to SOPs, testing methods, protocols, compendia (USP/EP/JP).
Perform testing of raw materials, APIs, finished products, stability samples and cleaning verification samples.
Experience with HPLC/GC analysis
Document laboratory work according to cGMPs and SOPs.
Troubleshoot, calibrate and maintain instruments as required.
Prepare and label laboratory reagents, reference standards, or solutions according to SOPs.
Perform peer review of analytical documentation.
Follow safety procedures when working in laboratory.
Understand and comply with cGMPs and other regulations.
Maintain the laboratory in an organized and neat manner.
Sampling of controlled materials and managing reference standard inventory.
Coordinating the shipment of samples to contract laboratories and to clients.
Other duties as required by organizational demands.
Ability to work in an office and analytical laboratory setting.
Position may require some extended hours including evenings and weekends.
BS degree required, preferred in science degree.
Familiar with fast paced contract manufacturing environment and be able to work under pressure while maintain high quality.
Experience working with potent, or cytotoxic materials preferred.
Working experience with parenteral drug products preferred.
Analytical Chemist I-Schenectady, NY
DSM – Bright Science. Brighter Living.™
Royal DSM is a purpose-led global science-based company in Nutrition, Health and Sustainable Living. DSM is driving economic prosperity, environmental progress and social advances to create sustainable value for all stakeholders. DSM delivers innovative business solutions for human nutrition, animal nutrition, personal care and aroma, medical devices, green products and applications, and new mobility and connectivity. DSM and its associated companies deliver annual net sales of about €10 billion with approximately 23,000 employees. The company is listed on Euronext Amsterdam. More information can be found at www.dsm.com.
To analyze and / or test under raw materials, intermediates and finished products applying validated or compendia methods. Performs/Applies knowledge and skills to diverse and complex reactions. Release testing of products according to current compendia, regulatory and corporate quality systems and principles.
Autonomous accomplishment of analysis in the laboratory.
Prepares standards, mobile phases, and reagents.
Maintains, calibrates, validates, monitors and troubleshoots laboratory equipment (HPLC, ICP, IR, etc.)
Analyzes raw materials, intermediates, stability samples and finished products for required tests by various analytical and instrumental methods.
Performs calculations, collects and prepares data for evaluation.
Reviews data to ensure accuracy prior to reporting.
Orients and trains new colleagues.
Perform administrative lab tasks, such as updating Specification sheets and SOP's. (LOP's and TM's)
Keeps supervisor informed of work status and suggests follow-up action to resolve atypical results and any problems encountered.
Investigation of OOS/NI and supports Lab Tech II & III in OOS/NI investigations
Maintains good documentation practices.
performs all other duties as assigned by supervisor
Display and promote positive safety behaviors at all times; use proper personal protective equipment, appropriate safety tools, equipment and procedures to ensure that self and others go home safe each day; that area and equipment operate at the highest safety levels; that all people in the area (lab techs, quality personnel, maintenance, visitors, contractors, etc.) comply with the safety directives and keep the area neat and clean.
Ensures incidents are investigated, reported, and risks are assessed in a timely basis.
Acts in such a way that safety awareness & accident prevention are considered in performing all tasks
Bachelor's degree in a relevant Scientific discipline required, Chemistry preferred.
Broad / General knowledge of quality control techniques and methods.
Broad understanding of safety, laboratory hygiene and GMP rules.
5-12 years of experience of analytical lab experience utilizing various instrumentation (HPLC, ICP, IR, etc.)
Experience in the food industry is preferred.
Experience in Microsoft Office (outlook, word, and excel)
Working for DSM means the opportunity to really contribute to improve people's lives and solving the challenges of today's world. Challenging jobs, career opportunities and an inspiring environment allow you to enhance your personal development. DSM recognizes that the on-going success of the company depends on the continued development and engagement of our employees and pursues a fair and competitive remuneration policy, recognizing individual and team competencies and performance.
Procedure & Contact
Interested in this position? Please apply on-line by sending us your resume and cover letter via the career portal (www.dsm.com/careers).
Reference check procedures are part of the DSM Recruitment & Selection Process. You will be
contacted when these references checks are required.
Royal DSM is an equal employment opportunity and affirmative action employer and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, age, protected veteran status, status as a qualified individual with a disability, or any other characteristic protected by law.
Royal DSM and its associated companies deliver annual net sales of about €10 billion with approximately 23,000 employees. The company is listed on Euronext. For more information about DSM see http://www.dsm.com or connect on
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