Chemist Instrumentation Job Description Sample
Performs sample preparation, Gas Chromatography (GC) and/or High Pressure Liquid Chromatography (HPLC) and dissolution on raw material, finished product and in-process samples. Responsible for recording results in appropriate format and evaluating data to client or compendial specifications. Performs duties according to LSS Global direction and in compliance with cGMP and GLP regulations and SGS Integrity programs.
Operates and maintains laboratory equipment and instrumentation required for cGMP analysis of samples.
Prepares chemical solutions following standard operating procedures and appropriate testing methods.
Operates and maintains Gas Chromatograph and/or High Pressure Liquid Chromatograph.
Keeps an inventory of laboratory chemicals and disposable equipment necessary for the daily functioning of the laboratory.
Performs wet chemistry and raw material analysis as requested.
Perform testing in accordance with specified methods.
Document activities in accordance with cGMP.
Maintains orderly work area.
Bachelor s degree in Chemistry or a related science degree and one year related analytical experience. Or
A minimum of 5 years of technical experience and knowledge in analytical laboratory operations and services.
General knowledge of chemistry and knowledge of various analytical techniques and methodologies.
Communication skills including grammar and composition.
Ability to work well with others & independently.
Proven time management skills and a strong attention to detail.
Knowledge of another language besides English (French or Spanish) is an asset.
This job is performed in an indoor temperature controlled environment.
Extended hours may be required from time to time.
To perform this job successfully, an individual must be able to perform each essential duty satisfactorily with or without reasonable accommodations. The requirements listed above are representative of the knowledge, skill, and/or ability required.
This job description should not be construed as an exhaustive statement of duties, responsibilities or requirements, but a general description of the job. Nothing contained herein restricts the company s rights to assign or reassign duties and responsibilities to this job at any time.
SGS is an EOE AA M/F/Vet/Disability employer.
Qualified applicants will receive consideration for employment without regard to their race, color, religion, national origin, sex, protected veteran status or disability.
If you are applying for a position within the United States and you have difficulty completing the on-line employment application because of a disability, please call 201-###-#### for assistance and leave a message. You will be called back shortly. Please note, this phone number is not for general employment information, but is only for individuals who are experiencing difficulty applying for a position due to a disability.
Associated topics: biochemistry, ceramic, chemistry, formulation, glass, latex, material, material science, polyurethane, rubber
Quality Control - Chemist (Bulk)
Chemist (Bulk) Job Number: 223654 Category: Production Description:
A Quality Control Chemist job in Myerstown, PA is currently available through Belcan. In this role, you will be responsible for Quality Control testing of over the counter pharmaceuticals manufactured in Myerstown. This is a fast-paced, energetic team that works together across two shifts to meet aggressive throughput times to support a lean manufacturing operation.
To be considered for this role you have a B.S. degree in Chemistry/Biology or Pharmacy or a related four year science degree required. Chemistry degree is preferred. This is a long term 2nd shift position with the start time flexibility between 2:00pm
4:00pm to 10:30pm- 12:30pm depending on the selected start time for this job. JOB DUTIES: • Perform the analysis on in-process, finished products, stability products following prescribed procedures to provide the information base leading to raw product disposition. • Assist in troubleshooting and problem solving. • Perform standard qualitative and quantitative analysis on: in-process products, and finished pharmaceutical preparations employing accepted gravimetric and spectrophotometer procedures, in accordance with approved testing procedures of the organization, the National Formulary (NF) and the United States Pharmacopoeia (USP). • Utilize standard "bench" chemistry technique as well as sophisticated electronic instrumentation, including spectrophotometer, viscometer, etc. • Maintain records of all analysis information of assigned products on data sheets for permanent file and proper entry of information on laboratory forms. • Evaluate all data obtained from analysis; if discrepancy or deviation occurs, consult with Supervisor and recommend additional testing if necessary. • Perform routine analytical testing of raw materials purchased from prospective suppliers to determine that the materials meet compendia and/or company standards. • Adhere to the pertinent aspects of Corporate and plant safety programs and adhering to GMP’s, ISO standards or other regulations. • Assist in investigating non-compliance investigations. • Assist with troubleshooting analytical methodology and instrumentation malfunctions. • Perform special assignments as directed by supervisor. • Assist in validation of manufacturing and production lines and equipment pertinent to chemistry (e.g. equipment and room cleaning validation) if requested.
QUALIFICATIONS: • Bachelor’s degree in Chemistry, Biology, Pharmacy, or related 4 year science degree required. Chemistry degree is preferred. • At least 1 year of lab experience preferred (outside of bachelor’s degree), preferably in pharmaceutical or nutritional industry. • Knowledge, practical application, and understanding of analytical chemistry is required. • Demonstrated capability for communicating ideas, concepts, and work results effectively to colleagues and supervision. • Demonstrated ability to be self-motivated as well as to work collaboratively in a team-based environment is required. • Must demonstrate initiative and a willingness to learn. • Good working knowledge of advanced laboratory instrumentation and personal computer skills are required. • Competencies required: analytical problem solving, alertness, work within established policies and procedures, commitment to task, decisiveness, effective written and interpretive communication skills, and organization and planning skills. • Experience in wet analytical methods and instrumentation techniques preferred; HPLC, UV, GC, IR, and AA preferred. • A working knowledge of statistics, data processing and good manufacturing practices is desirable. • A thorough understanding of National Formulary (NF); United States Pharmacopoeia (USP); and European Pharmacopoeia (EP) testing procedures, as well as, US Pharmaceutical Industry Good Manufacturing Practices (GMP’s), quality control methods and procedures preferred. Location: Myerstown , PA Minimum Experience (yrs): One Required Education:
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Senior Analytical Chemist
Senior Analytical Chemist Tracking Code 2016-19 Job Description
GENEROUS RELOCATION ASSISTANCE!! + #1 small molecule API Contract Manufacturing Organization (CMO) in the USA
Double digit sales growth each of the last 5 years
Recent $50 million expansion of our large-scale API facility
Winner of 30 CMO Leadership Awards in 2017 + #6 ranked state for best place to live by US News and World Report
Leading Western supplier of generic APIs including ADHD and other controlled substances The Senior Analytical Chemist will provide technical support and leadership to multiple project teams. The Senior Analytical Chemist will evaluate and interpret analytical results, develop, validate and transfer analytical methods for APIs, API intermediates and raw materials. Strict compliance with cGMP guidelines is required to perform most job tasks. Job Responsibilities
With minimal supervision, safely and effectively develop, establish, and validate analytical testing methodologies used to control raw materials, production intermediates, and final products.
Investigate and solve analytical technical issues within Analytical Development, Chemical Development, Process Support Group and Quality Control.
Perform analytical chemistry assays based on new and existing methodologies
Operate analytical instrumentation such as HPLC, GC, GC/MS, FTIR, Titrator, Particle Size Analyzer
Write technical reports to document analytical methods
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 necessary.
Qualify reference materials. Job Qualifications
Advanced Chemistry degree desired, with a PhD preferred
Minimum BS degree in Chemistry or closely related field required, with 3+ years of experience in manufacturing support laboratory
Experience with dissolution and chemosensory testing highly desired
Familiarity with compliance requirements within cGMP, safety and regulatory environments
Operational knowledge of analytical instrumentation like HPLC, GC, GC-MS, FTIR, UV-VIS equipment, and data stations required
Demonstrated computer literacy, including word processing, spreadsheets, structural drawings, and databases preferably in a Windows environment
The ability to solve extremely complex problems where analysis of situations or data requires an evaluation of intangible variables
Ability to work in a highly independent and self-directed work environment. 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. COMPANY INFORMATION 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 LinkedIn Twitter Thank you for your interest in Cambrex Charles City! Agencies should not forward resumes to Cambrex through this source. Please visit www.cambrex.com to become a preferred vendor and submit a Request for Proposal (RFP) online for consideration. Cambrex will not be responsible for any fees arising from the use of resumes through this source. Equal Opportunity Employer M/F/D/V. Job Location Charles City, Iowa, United States Position Type Full-Time/Regular
Water and soil sample analysis, preferably using Aglient ICPMS, Thermo ICP and CETAC or Brooks Rand Mercury instrumentation
Routine instrument maintenance and troubleshooting
Peer review of raw data generated from other department analysts
Compilation of final CLP-like data packages
Method development and implementation of new technologies
Preparation and recordkeeping of standards and reagents
Providing assistance to metals preparation group as needed
Other duties as assigned Required Knowledge, Skills & Abilities:
Proven track record of successful instrument operation
Strong technical understanding of analytical chemistry
Strong commitment to quality and integrity
Diligent work ethic and the ability to work independently
Strong organizational skills with the ability to multitask
- Excellent verbal and written communication skills
Bachelor’s degree in Chemistry or a related Science degree, plus a minimum of 5 years of experience in environmental metals analysis. Physical Demands:
The ability to stand for intervals of up to 8 hours while working;
Able to speak and hear clearly while communicating with co-workers and managers;
Dexterity in hands and fingers to operate equipment and handle glassware;
Must have average vision and able to see to read reports and operate equipment;
Hearing and speech to communicate in person and over th We would like to thank everyone for their interest in ALS but only candidates selected for an interview will be contacted. "ALS is proud to be an equal opportunity employer committed to achieving and maintaining a workforce which reflects and affirms the diversity of our society" ALS is a VEVRAA Federal Contractor. EOE AA Minority, Female, Veteran, Individuals with Disabilities Click Here to view the EEO is the Law poster Click Here to view the FMLA Law poster Click Here to view the EPPA Law Poster Click Here to view the Pay Transparency Provision Click Here to view company E-Verify Participation Poster ID: 2017-4873 External Company URL: alsglobal.com
CGS - Power Plant Chemist
CGS - Power Plant Chemist Apply now » Apply now
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Please wait... Date: Jan 2, 2018 Location:
St Johns, AZ, US Company: SRP SRP is one of the largest public power and water utilities in the U.S. providing electricity to approximately one million customers in the greater metropolitan Phoenix area. Since its founding in 1903, SRP has fostered a culture of stewardship and customer service consistently ranking as an industry leader in customer service according to J.D.
SRP continues to adapt to its changing business environment by seeking innovative ways to reimagine utility service and the provision of critical resources essential to the life and economy of Arizona. Job Brief Provide planning, engineering and scientific services to SRP in a technologically sound, timely and cost effective manner to enable SRP to realize its goals and objectives for providing low cost/high value water and energy services. Any one position may not include all duties nor do the example of duties include all tasks, which may be found in the position of this class.
Responsible for implementation and management of chemistry program for a Coal- fired Power Plant. Makes recommendations to plant personnel to ensure proper equipment operation with appropriate chemical treatment. Maintains on-line chemistry monitoring instrumentation for boilers and boiler make-up equipment.
Ensures instrumentation down-time is a minimum. Manages bulk chemical inventory, including physically climbing chemical storage silos for level determination. Monitors potable water and wastewater treatment systems to ensure compliance with state regulations.
Maintains state certifications for water and wastewater treatment plant operator. Performs analysis of carbon traps for power plant mercury emissions monitoring program. Provides 24 hour on-call coverage on a rotating day basis for chemical emergencies, including unit start-ups and shut-downs of main generating units. Job Responsibilities
Performs engineering and scientific studies.
Performs as a project leader.
Evaluates study methodologies.
Prepares recommendation material for management consideration.
Prepares and/or conducts written and oral reports and presentations.
Prepares engineering and scientific analysis and forecasts.
Designs and/or codes computer programs.
Evaluates corporate operating environment and related engineering, scientific, political, economic, sociological and demographic issues.
Integrates engineering and scientific facts with political, economic and social aspects of issues.
Other duties as assigned.
Employee must work safely and efficiently in the performance of their job duties. Must maintain effective working relationships with other employees, customers and the public.
Must have the ability to understand and carry out oral and written instructions, and have the ability to accurately and legibly complete applicable paper work. May be required to work a reasonable amount of overtime. Education Completion of a Bachelor's Degree from an accredited institution that prepares the employee for the assignment.
Experience Promotion to Level 2 requires a minimum of two years experience at Level 1; demonstrated capability to perform advanced and more difficult work as determined by the supervisor. Promotion to Senior Level requires a minimum of three years experience at Level 2; is fully competent in all aspects of functional area of assignment and as such would be recognized as a specialist in area of assignment and may have periodic or occasional lead responsibilities. Additional Information Industrial water treatment experience preferred.
PRIMARY JOB DUTIES: PERFORMS SAMPLE COLLECTION AND ANALYSIS FOR PLANT WATER AND SCRUBBER SLURRY SYSTEMS. MAINTAINS DATA SPREADSHEETS IN MICROSOFT EXCEL AND PROVIDES REPORTS TO ENGINEERING AND MANAGEMENTS AS NECESSARY.
MAKES RECOMMENDATIONS TO PLANT PERSONNEL TO ENSURE PROPER EQUIPMENT OPERATION WITH APPROPRIATE CHEMICAL TREATMENT. MAINTAINS ON-LINE CHEMISTRY MONITORING INSTRUMENTATION FOR BOILERS AND BOILER MAKE-UP EQUIPMENT. ENSURES INSTRUMENTATION DOWN-TIME IS A MINIMUM.
MANAGES BULK CHEMICAL INVENTORY, INCLUDING PHYSICALLY CLIMBING LIME AND SODA ASH SILOS FOR LEVEL DETERMINATION. MONITORS POTABLE WATER AND WASTEWATER TREATMENT SYSTEMS TO ENSURE COMPLIANCE WITH STATE REGULATIONS. MAINTAINS STATE CERTIFICATIONS IN THESE AREAS.
PERFORMS ANALYSIS OF CARBON TRAPS FOR CGS MERCURY PROGRAM IN SUPPORT OF THE ENVIRONMENTAL GROUP. PROVIDES 24 HOUR ON-CALL COVERAGE ON A ROTATING DAY BASIS FOR CHEMICAL EMERGENCIES, INCLUDING UNIT START-UPS AND SHUT-DOWNS OF MAIN GENERATING UNITS. ALSO PROVIDES BACKUP COVERAGE TO THE ACTING ON-CALL CHEMIST WHEN 24 HOUR COVERAGE IS NECESSARY.
Occasional travel for specialized training and utility business meetings occasional contact with utility engineers and scientists from other companies and outside agencies. Ability to work effectively using services of various organizational groups within SRP. Effective interpersonal skills to communicate study work and results to high level management.
Ability to use complex computer software tools. Ability to discreetly prepare and use proprietary and sensitive information. State professional engineering registration if the individual does not hold an ABET accredited Bachelor's degree in engineering or a Master's degree in engineering.
Requisition Details Requisition ID: 7757 EOE - SRP encourages a diverse workforce All candidates must be legally authorized to work in the United States. Currently, SRP does not sponsor H1B visas. Why Work at SRP SRP's success is rooted in our employees' happiness, health and safety.
That's why we offer a comprehensive benefits package to meet the needs of our employees and enhance their well-being. In addition to competitive pay and performance incentives, eligible employees can take advantage of the following benefits: • 401(k) plan with employer matching • Retirement pension • Paid vacation • Parental leave • Holiday pay • Sick leave • Medical, vision, dental and life insurance • Wellness programs • Pre-tax benefits • Short and long-term disability plans • Tuition assistance
Quality Control Chemist (Bulk)
US-PA-Myerstown Job Number: 17209157 CTG is seeking a Quality Control Chemist (Bulk) tow work at their clients site in Myerstown, PA 17067. This is a 12 month contract position that has the potential to extend longer. Pay rate: $24/hr - W-2 basis, no C2C or 1099's.
This is a 2nd shift position. Starting time is flexible between 2 and 4pm The bulk testing team is responsible for Quality Control testing of over the counter pharmaceutical in process and finished packaged goods manufactured in Myerstown. The stability testing team is responsible for ensuring over the counter drug products within the stability program are tested according to the stability schedule and meet shelf life specifications.
This is a fast-paced, energetic team that works together across two shifts to meet aggressive throughput times to support a lean manufacturing operation. The testing for both teams is very similar and allows for the opportunity to support both teams depending on the workload and schedule. POSITION SUMMARY Perform the analysis on in-process, finished products, stability products following prescribed procedures to provide the information base leading to raw product disposition.
Assist in troubleshooting and problem solving as directed. POSITION DUTIES & RESPONSIBILITIES • Perform standard qualitative and quantitative analysis on: in-process products, and finished pharmaceutical preparations employing accepted gravimetric and spectrophotometer procedures, in accordance with approved testing procedures of the client, the National Formulary (NF) and the United States Pharmacopoeia (USP). • Utilize standard "bench" chemistry technique as well as sophisticated electronic instrumentation, including spectrophotometer, viscometer, etc. • Maintain records of all analysis information of assigned products on data sheets for permanent file and proper entry of information on laboratory forms. • Evaluate all data obtained from analysis; if discrepancy or deviation occurs, consult with Supervisor and recommend additional testing if necessary. • Perform routine analytical testing of raw materials purchased from prospective suppliers to determine that the materials meet compendia and/or company standards. • Adhere to the pertinent aspects of Corporate and plant safety programs and adhering to GMP’s, ISO standards or other regulations. • Assist in investigating non-compliance investigations. • Assist with troubleshooting analytical methodology and instrumentation malfunctions. • Perform special assignments as directed by supervisor. • Assist in validation of manufacturing and production lines and equipment pertinent to chemistry (e.g. equipment and room cleaning validation) if requested.
In this position, the incumbent will be expected to draw upon previous analytical experience, as well as continuously learn Quality Control systems and effectively engage in relationships with peers in the laboratories, Manufacturing/Production, and personnel in other departments as needed.
Once the incumbent is assigned specific materials on which to perform the quality control tests, or provide development or troubleshooting, the incumbent will have considerable impact on results from his/her work. Product can be rejected and manufacturing procedures can be altered significantly either in schedule changes or in process itself. Education Requirement(s): • Bachelor’s degree in Chemistry, Biology, Pharmacy, or related 4 year science degree required.
Chemistry degree is preferred. Skill & Competency
• Knowledge, practical application, and understanding of analytical chemistry is required to perform the functions of this position. • Demonstrated capability for communicating ideas, concepts, and work results effectively to colleagues and supervision. • Demonstrated ability to be self-motivated as well as to work collaboratively in a team-based environment is required. • Must demonstrate initiative and a willingness to learn. • Good working knowledge of advanced laboratory instrumentation and personal computer skills are required. • Competencies required: analytical problem solving, alertness, work within established policies and procedures, commitment to task, decisiveness, effective written and interpretive communication skills, and organization and planning skills. • Experience in wet analytical methods and instrumentation techniques preferred; HPLC, UV, GC, IR, and AA preferred. Preferences: • At least 1 year of lab experience preferred (outside of bachelor’s degree), preferably in pharmaceutical or nutritional industry. • A working knowledge of statistics, data processing and good manufacturing practices is desirable. • A thorough understanding of National Formulary (NF); United States Pharmacopoeia (USP); and European Pharmacopoeia (EP) testing procedures, as well as, US Pharmaceutical Industry Good Manufacturing Practices (GMP’s), quality control methods and procedures preferred.
This position is compensated at $24.00 per hour on a W2 hourly basis (no C2C or 1099's). apply below or send your resume to MJ Slaughter at firstname.lastname@example.org. Please reference job 17209157/B-12080 in the subject line. CTG’s Benefits Plan allows you to select insurance coverage that best suits your lifestyle, and take part in our savings programs and educational plans.
We offer Flexible Spending Accounts, a 401(k) Retirement Plan, and an Employee Stock Purchase plan. Our educational plan comprises access to more than 2,000 web-based technical, professional and business development courses.
CTG is the most reliable IT services provider, built on 50 years of meeting our commitments to make technology work for clients and deliver real business value.
CTG provides industry-specific IT strategy, services, and solutions that address the business needs and staffing challenges of clients in high-growth industries, including major technology companies, large corporations, and government entities located in North America and Western Europe. CTG's greatest asset is its people, and as such we are committed to providing employees programs and processes to support their performance, hone their skills, and advance in their careers. This commitment is reflected by CTG being named a Best Places to Work Company by Modern Healthcare (since 2013) in North America, and a Best Places to Work Company in the United Kingdom (2013), Belgium (since 2007), and Luxembourg (since 2011). CTG will consider for employment all qualified applicants including those with criminal histories in a manner consistent with the requirements of all applicable local, state, and federal laws.
CTG is an Equal Opportunity/Affirmative Action Employer and strong advocate of workforce diversity. Minority/Female/Sexual Orientation/Gender Identity/Disability/Veteran. Job: Chemistry
Company Overview Teledyne is an Equal Opportunity/Affirmative Action employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, religious creed, gender, sexual orientation, gender identity, gender expression, transgender, pregnancy, marital status, national origin, ancestry, citizenship status, age, disability, protected Veteran Status, genetics or any other characteristic protected by applicable federal, state, or local law. If you need assistance or an accommodation while seeking employment, please email or call (805)373-4545. Determinations on requests for reasonable accommodation will be made on a case-by-case basis. Please note that only those inquiries concerning a request for reasonable accommodation will receive a response.
Position Summary and Responsibilities
Installs CETAC chemical sample introduction equipment at customer sites. Provides technical and applications support to customers and product managers. Develops chemical analysis methods and conducts sample analysis to support product development, sales and marketing.Apply knowledge of instrumentation and chemical principles for analysis of customer samples. Responsible for customer support with regards to products and the proper operation and maintenance of laboratory equipment.
Analyze customer and in-house samples in support of marketing and sales.
Provide technical and applications support (phone and e-mail) to current and prospective customers.
Perform instrument demonstrations for prospective customers.
Provide technical and applications support (phone and e-mail) to the sales group.
Provide in-house training for the sales group and worldwide dealers.
Operate and maintain the demo units for the liquids product line.
Maintain samples, standards, and chemical reagent inventory consistent with applicable safety precautions.
Operate and maintain the ICP-OES and ICP-MS instruments and any other relevant equipment.
Prepare customer application reports.
As needed, assist the Quality Control (QC) Department with any product testing.
Assist the R&D group and the liquids product manager in any testing of new products.
Attend trade shows where products are exhibited.
Attend manufacturer training courses for any new ICP-OES or ICP-MS Instrument acquired.
As needed, install equipment at the customer site.
Give product presentations at seminars, conferences, and tradeshows.
Other duties as required.
Knowledge and Skill
Good working knowledge of Microsoft Word, Excel, and PowerPoint
Atomic spectroscopy (AA, ICP-OES, ICP-MS)
Good organizational skills
Sound judgment and interpersonal skills
- At least 3 years experience in Laboratory instrumentation
- B.S. degree in Chemistry or related field
- Up to 50% travel Requisition Post Information : Posted Date* 1/8/2018
Company NameTeledyne CETAC Technologies
Shift1st Shift - DayCitizenship/Visa RequirementNo Restrictions
Instrumentation & Controls Technician I - Instrumentation And Controls Technician I - Swing Shift
Instrumentation & Controls Technician I - Instrumentation and Controls Technician I - Swing Shift Hiring department Fac Operations & Maint Monthly salary $3,426+ depending on qualifications Hours per week 40.00 Variable Posting number 17-10-03-01-5360 Job Status Open FLSA status Non-exempt Earliest Start Date Immediately Position Duration Funding expected to continue Position open to all applicants Location Austin (main campus) Number of vacancies 1 General Notes ADDITIONAL 256 DOLLARS A MONTH FOR SHIFT DIFFERENTIAL. 40 hours a week, swing shift position, hours are 2:30 PM - 11:00 PM with possible later start time. Some overtime, weekends and holidays possible.
Hiring decision contingent upon applicant clearing a security background check. Applications will be reviewed online by the hiring department. Required Application Materials
A Resume is required in order to apply
A List of 3 References is required in order to apply. Additional Information Purpose Provide journey level skilled work associated with pneumatic and electronic instrumentation and control systems to ensure efficient and effective control of building operational processes.
Essential Functions Responds to heating and cooling trouble calls, interfaces with customers, troubleshoots electronic and pneumatic controls systems and components to maintain HVAC comfort control in university buildings. Performs preventive maintenance and calibrates electronic and pneumatic controls and sensors to prevent failures and to keep the building HVAC equipment operating at optimum performance for maximum energy conservation. Renovates and upgrades control systems to provide efficient operation of HVAC equipment and improve building comfort.
Assists others as requested to help troubleshoot HVAC and other equipment to limit the equipment downtime and to resolve concerns related to the campus HVAC equipment. Interprets and works from drawings, specifications, and sketches, for assigned projects to ensure university standards are maintained. Commissions control systems for new and renovation construction projects to ensure final control installation meets standards and functional requirements.
Performs work independently from written or verbal instructions and in accordance with established safety procedures to complete tasks in a timely manner. Researches and recommends repair components and test equipment to assist in procuring components. Creates material lists and acquires materials for efficient work.
Keeps accurate records of materials used and maintains daily time reports to efficiently complete work and document details of the functions performed. Keeps accurate and up-to-date documentation of all systems. Assists other shops and team members in the accomplishment of shop goals related to key performance indicators.
Assists outside entities. Responds to urgent issues across campus and at PRC. Provides timely and courteous customer service, keeps supervisors up-to-date on daily work order status to ensure clear, concise, and necessary communication channels are maintained and customer expectations are met.
Gathers building HVAC and mechanical field data to facilitate analysis and improvement of HVAC performance. Participates in the On-Call Program. Driving University owned vehicles to job sites will be required.
Licenses: Class "C" Operator's Driver's License. Applicant selected must provide a current three year Driving Record from the current state of residence. If not currently a Texas resident, must obtain a Texas Driver's License within 30 days after entering Texas as a new resident.
Marginal/Incidental functions Other related functions as assigned. Maintain acceptable driver rating as established in University Policy 157, Section 5.4. Required qualifications High school or GED.
Three years of journey-level experience with the installation, repair, maintenance and operation of pneumatic and DDC instrumentation and control systems. Equivalent combination of relevant education and experience may be substituted as appropriate. Demonstrate excellent communication skills.
Demonstrated ability to follow written and verbal instructions. Current Class "C" Operator Driver License required. Prior to date of hire, applicant selected must provide a Motor Vehicle Report (MVR) showing a driving history going back 36 months.
This includes all states resided in for the past 36 months. MVR will be evaluated to determine eligibility to drive a University-owned vehicle. If not currently a Texas resident, must obtain a Texas Driver License within 30 days after entering Texas as a new resident.
Preferred Qualifications Associates degree in a technical field. More than three years of journey level experience with the installation, repair, maintenance and operation of pneumatic and DDC instrumentation and control systems. International Society of Automation Certified Controls Systems Technician (ISA CCST) Level 1 certification.
Experience at the University of Texas or in a university setting. Demonstrated ability to adhere to safety rules and regulations. Demonstrated ability to handle responses.
Demonstrated ability to give a verbal sequence to a response. Demonstrated ability to work well within a team environment. Successful completion of the Leader Development Program.
Working conditions Uniforms and/or personal protection equipment (furnished) May work in all weather conditions May work in extreme temperatures May work around chemical fumes May work around standard office conditions May work around biohazards May work around chemicals May work around electrical and mechanical hazards Repetitive use of a keyboard at a workstation Use of manual dexterity Climbing of stairs Climbing of ladders Lifting and moving Conditions found in mechanical/electrical rooms. May work in elevated spaces/confined areas. Work from ladders/scaffolds.
Ability to lift and move up to 50 lbs. May require tuberculosis screening and occasional use of a respirator. A criminal history background check will be required for finalist(s) under consideration for this position.
The retirement plan for this position is Teacher Retirement System of Texas (TRS), subject to the position being at least 20 hours per week and at least 135 days in length. The University of Texas at Austin, as an equal opportunity/affirmative action employer, complies with all applicable federal and state laws regarding nondiscrimination and affirmative action. The University is committed to a policy of equal opportunity for all persons and does not discriminate on the basis of race, color, national origin, age, marital status, sex, sexual orientation, gender identity, gender expression, disability, religion, or veteran status in employment, educational programs and activities, and admissions.
If hired, you will be required to complete the federal Employment Eligibility Verification form, I-9. You will be required to present acceptable, original documents to prove your identity and authorization to work in the United States. Information from the documents will be submitted to the federal E-Verify system for verification.
Documents must be presented no later than the third day of employment. Failure to do so will result in dismissal. UT Austin is a Tobacco-free Campus
QC Chemist II, 2Nd Shift - Shirley, NY
Luitpold Pharmaceuticals, Inc. Luitpold Pharmaceuticals, Inc., a Daiichi Sankyo Group Company, is dedicated to the development and marketing of innovative, quality drugs and medical devices for healthcare professionals, clinics, and hospitals across the United States and Canada. We specialize in sterile injectables, bone regeneration materials for dental procedures, as well as innovative products for veterinary medicine use. The QC Chemist II is an integral part of the QC Chemistry laboratory, to ensure that all testing is performed efficiently and effectively while simultaneously following governmental pharmaceutical regulations, safety standards, and environmental policies. This position is for the 2nd shift, 4pm-12:30am. Essential Duties and Responsibilities
Perform testing of all raw materials, in-process products, and all finished products
Perform testing of stability samples, as required
Perform all wet chemistry procedures including titrations, extractions, and pH measurements
Perform process validation testing of new products as required.
Operate all instrumentation including the following:
Karl Fischer Titrator Qualifications and Requirements
Bachelors of Science in Chemistry, or a related field
Two (2) years minimum pharmaceutical laboratory experience
Knowledge of MS Word, Excel, and Outlook
Detail oriented, analytical, strong time management skills, and strong communication skills. Physical Environment and Physical Requirements
While performing duties of the job, incumbent is occasionally required to stand; walk; sit; use hands to finger, handle or feel objects, tools or controls; reach with hands and arms; balance; talk and hear.
Must have 20/20 vision, corrected if necessary.
Must successfully pass Color Blindness Screening (D15) Job Title: QC Chemist II, 2nd shift - Shirley, NY Employment Type: Full Time Classification: B Date Posted: 10/03/2017 Requisition ID: 1798
QC Chemist III (Sun - Wed 6:30 Am - 5:00 Pm)
QC Chemist III (Sun
Wed 6:30 am
Login Email Me Similar JobsEmail Me This Job JOB SUMMARY- This position will have responsibility for supporting all activities in the Quality Control Laboratory with special emphasis on method development and validation. This also include performing instrument validations, cleaning validations, and method qualifications as necessary.The person in this position has knowledge of commonly-used concepts, practices, and procedures within the field of his/her responsibilities. Also, must be familiar with cGMPs as they relate to analytical test methodologies and practices. The person must also have increased knowledge and experience developing and validating methods, especially chromatographic methods, in a fast paced pharmaceutical environment. JOB DUTIES-
Independently or operating in a lead capacity, develop and validate analytical methods in support of manufacturing projects assuring project timelines are met
Serve as a liaison for assigned projects between LSNE, clients, and analytical testing vendors to support activities including analytical methods transfer, qualification, validation and implementation
Perform routine and complex analytical testing of samples supporting incoming raw materials, in-process production, finished product, and validation samples. Troubleshoot assay and instrumentation issues as necessary
Technical lead for deviation investigation, out-of-specification or aberrant results and process changes Determination and/or execution of corrective and preventative actions
Author, review and/or approve of GMP documentation including test methods, protocols, reports and raw data
Perform analytical equipment validation, and ensure routine calibration and preventive maintenance is performed at the required intervals
Logging and tracking of samples and chemicals. Order chemicals and laboratory supplies as needed
Documents/reviews laboratory work using laboratory notebooks/worksheets. Documentation is detailed, timely and in compliance with cGMP requirements
Other duties, as needed EDUCATION, PROFESSIONAL SKILLS, & EXPERIENCE-
Bachelors of Science (minimum) Advanced Degree preferred in Analytical Chemistry, Chemistry, Pharmaceutical Sciences or a closely related area of study + 10-15 years relevant Analytical Chemistry experience, preferably in Analytical Development & Quality Control, in a pharmaceutical manufacturing company
Proficiency with performing analytical testing using the following types of equipment: HPLC, GC, MS, ICP, SEM-EDS, FTIR, UV/VIS, Karl Fisher, Particle Size Analyzer, Densitometer, Osmometer is required.
Background in Analytical Method Development and Validation
Knowledge of cGMP, ICH, USP, and global compendial regulations and guidances, particularly as related to analytical method development and validation
Excellent organizational skills and ability to present technical data
Excellent interpersonal skills and the ability to communicate well orally and in writing
Ability to multi-task in a dynamic environment with changing priorities
Ability to work independently on scientific projects
Must have strong attention to detail, strong problem-solving skills, as well as the ability to work in a cross-functional team environment
Proficient in MS Office And lab based data management systems
Scientific technical writing ability including authoring and revising SOPs or technical reports
Experience troubleshooting of assay and equipment issues PHYSICAL REQUIREMENTS -
Required to stand; walk; sit; use hands to finger, handle or feel objects, tools or controls; reach with hands and arms; balance; talk and hear
Ability to sit or stand for prolong periods of time
Must be able to walk and drive between locations
Physically able to wear laboratory protective gowning and equipment, including but not limited to gowning, goggles, face shields, respirators, and protective gloves
Must maintain a clean-shaven appearance each working shift to wear tight-fitting respirators properly
Must be able to occasionally lift and/or move up to 50 pounds
Comfortable with working/handling of hazardous materials COMMUNICATIONS & CONTACTS -
Works closely with quality assurance and quality control staff in performing varied work procedures and activities. Interacts with Operations staff. MANAGERIAL & SUPERVISORY RESPONSIBILITIES -Not Applicable The above statements are intended to describe the general nature and level of work being performed by people assigned to this classification. They are not intended to be construed as an exhaustive list of all responsibilities, duties and skills required of personnel so classified. LSNE offers a competitive compensation and benefits package and a very generous paid time off benefit
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