Associate I, Quality
Quality control analyst job in Byhalia, MS
This is where your work makes a difference.
At Baxter, we believe every person-regardless of who they are or where they are from-deserves a chance to live a healthy life. It was our founding belief in 1931 and continues to be our guiding principle. We are redefining healthcare delivery to make a greater impact today, tomorrow, and beyond.
Our Baxter colleagues are united by our Mission to Save and Sustain Lives. Together, our community is driven by a culture of courage, trust, and collaboration. Every individual is empowered to take ownership and make a meaningful impact. We strive for efficient and effective operations, and we hold each other accountable for delivering exceptional results.
Here, you will find more than just a job-you will find purpose and pride.
Job Description
Your role at Baxter
The Quality Associate I is responsible for providing Quality support to the Global Logistics Center. Inspects products, initiates and updates procedures, reviews temperature monitoring data, and ensures compliance with GMP/QSRs requirements, according to corporate and local Standard Operating Procedures, and all applicable FDA and state regulations.
What we offer from day 1
Paid Time Off and Paid Holidays
Medical, Dental, Disability and Life Insurance coverage
Vision and Voluntary Benefits
Paid Parental Leave
Retirement Savings Plan
Employee Stock Purchase Program
Flexible Health Care Spending Accounts
Educational Assistance Plan
What you'll be doing
Perform physical inspection of products and comparison/assessment to all related documentation within the warehouse as needed (certificate or analysis, packing list, bill of lading, Temptale management, etc.)
Initiate procedure revisions as needed to support continuous improvement. Ensure that procedures are current and that facility employees perform tasks according to procedures through direct observation.
Activate, distribute and file procedures related to both local and corporate changes.
Manage official forms distributed throughout the facility.
Support assigned activities to ensure compliance with the Baxter COI program.
Collaborate with the Training Administrator to ensure training requirements are met prior to activation of all procedures.
Manage the state licensure program to ensure no licenses expire.
Support Temperature Monitoring of the MGLC Warehouse which includes operating the Rees system, reporting all temperatures on a spreadsheet for daily management review and uploading data from the backup digital data loggers throughout the facility. Investigate and resolve any Rees system alarms and document monthly MKT requirements.
Manage the document retention program.
Support assigned responsibilities for document tracking and overall facility documentation control.
Prepare monthly Quality Management & Data Review Presentations.
Perform Internal Assessments for continuous improvement of MGLC Quality Systems.
Assist other members of the Quality Department and facility management team to ensure timely closure of any audit observations.
Serve as a back-up for processing local hold requests using the Warehouse Management System (WMS) and JD Edwards (JDE) systems as needed.
Serve as a back-up for processing corporate FCA hold requests using Cardinal Health's FCA Tracking System, Baxter's Warehouse Management System (WMS) and Baxter's JD Edwards (JDE) system. Conduct audits of FCA hold product.
Serve as a back-up for processing product dispositions linked to local and corporate holds and report through the appropriate people and systems to ensure timely response/closure.
Perform manual product releases after verification of release by manufacturing plant in Batch Release System (BRS) as necessary.
Support all lean implementation initiatives in the Quality Department and throughout the facility, including periodic 6S audits and closure of any assigned action items.
Work in collaboration with other members of the Quality Department to prepare for internal and external auditors.
Support the Quality Department by completing other duties, projects and/or tasks that may be assigned as needed.
What you'll bring
Bachelor's degree or Associate degree required.
Minimum one year of relevant experience.
Experience with a medical device/pharma or other similarly regulated industry preferred.
Strong interpersonal skills and great attention to detail are necessary
Must be able to handle multiple projects concurrently.
Knowledge of FDA Regulations, Application of Good Manufacturing Practices.
Must be a strong team player with good problem solving and good verbal and written communication skills.
We understand compensation is an important factor as you consider the next step in your career. At Baxter, we are committed to equitable pay for all employees, and we strive to be more transparent with our pay practices. The estimated base salary for this position is $64,000.00 - $88,000.00 USD annually. The estimated range is meant to reflect an anticipated salary range for the position. We may pay more or less than of the anticipated range based upon market data and other factors, all of which are subject to change. Individual pay is based on upon location, skills and expertise, experience, and other relevant factors.
Join our dedicated team at Baxter Healthcare Corporation and be part of our mission to improve healthcare outcomes for patients worldwide. Apply today and take the next step in your career!
Applicants must be authorized to work for any employer in the U.S. We are un-able to sponsor or take over sponsorship of an employment visa at this time
US Benefits at Baxter (except for Puerto Rico)
This is where your well-being matters. Baxter offers comprehensive compensation and benefits packages for eligible roles. Our health and well-being benefits include medical and dental coverage that start on day one, as well as insurance coverage for basic life, accident, short-term and long-term disability, and business travel accident insurance. Financial and retirement benefits include the Employee Stock Purchase Plan (ESPP), with the ability to purchase company stock at a discount, and the 401(k) Retirement Savings Plan (RSP), with options for employee contributions and company matching. We also offer Flexible Spending Accounts, educational assistance programs, and time-off benefits such as paid holidays, paid time off ranging from 20 to 35 days based on length of service, family and medical leaves of absence, and paid parental leave. Additional benefits include commuting benefits, the Employee Discount Program, the Employee Assistance Program (EAP), and childcare benefits. Join us and enjoy the competitive compensation and benefits we offer to our employees. For additional information regarding Baxter US Benefits, please speak with your recruiter or visit our Benefits site: Benefits | Baxter
Equal Employment Opportunity
Baxter is an equal opportunity employer. Baxter evaluates qualified applicants without regard to race, color, religion, gender, national origin, age, sexual orientation, gender identity or expression, protected veteran status, disability/handicap status or any other legally protected characteristic.
Know Your Rights: Workplace Discrimination is Illegal
Reasonable Accommodations
Baxter is committed to working with and providing reasonable accommodations to individuals with disabilities globally. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application or interview process, please click on the link here and let us know the nature of your request along with your contact information.
Recruitment Fraud Notice
Baxter has discovered incidents of employment scams, where fraudulent parties pose as Baxter employees, recruiters, or other agents, and engage with online job seekers in an attempt to steal personal and/or financial information. To learn how you can protect yourself, review our Recruitment Fraud Notice.
Auto-ApplyQA Operator 2nd Shift
Quality control analyst job in Hazlehurst, MS
PRIMARY FUNCTION:
Primarily responsible for verification of production processes, packaging, food safety and monitoring of operational sanitation. Responsible for proper documentation, inventory control, and release of hold product. Assist production Team Members, Team Leaders, and Supervisors in assuring that safe and quality products are produced according to specification. Performs all work in compliance with company policies, NCC Animal Welfare Guidelines and local, state and federal policies, laws and regulation
RESPONSIBILITIES AND TASKS:
Under minimal supervision, communicate with Production & QA Team Members, Team Leaders, and Supervisors to assure proper handling of all products and timely correction of deficiencies
Monitor lines and paperwork throughout the day to assure specification compliance for each product
Verify and help enforce GMP's
Verify labels, lot codes, bags, boxes, and pallets are correctly adhered, printed, sealed, and stacked
Verify receiving of incoming raw materials and ingredients, informs Shipping/Receiving Team Leader and QA Team Leader or QA Coach if any product does not meet specifications
Assist Production with day to day quality problems to reach workable solutions
Assure microbiological swabs and samplings are performed at correct times and correct positions
Assist in making sure all quality and food safety policies and procedures are being followed
Work in compliance with all company policies, NCC Animal Welfare Guidelines and local, state and federal policies, laws and regulations
All other duties as assigned
EDUCATION AND CERTIFICATIONS:
High School Diploma or equivalent
EXPERIENCE AND SKILLS:
Minimum 1 year experience in quality assurance or 6 months Wayne Farms employee
Intermediate math (add, subtract, multiply and divide) and computer skills
Detail oriented
Must have the ability to effectively communicate in English, both verbal and written, with internal and external customers in a timely and professional manner; ability to communicate in multiple languages preferred
Sound work ethic, honesty and moral character
SAFETY REQUIREMENTS:
Follow departmental and company safety policies and programs
Must wear Personal Protective Equipment (PPE) at all times in areas where required.
PHYSICAL REQUIREMENTS:
Stand up to 8 hours.
Lift up to 60 lbs.
Exposure to wet and dusty environment.
Frequently reaching, bending, stooping, kneeling and crawling.
Work around raw, live animal odors
Ability to work nights, weekends, holidays and extended shift hours
We are an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, disability status, protected veteran status, or any other characteristic protected by law.
Auto-ApplyLaboratory Analyst 1
Quality control analyst job in Starkville, MS
This position performs laboratory analyses utilizing standard methodologies and procedures. It typically performs laboratory tasks, including instrument-based analyses. This classification works under direction from senior staff.
Salary Grade: 13
Please see Staff Compensation Structure or Skilled Crafts and Service Maintenance Compensation Schedule for salary ranges. For salary grade UC, these positions are "Unclassified" and salary ranges are determined by the hiring department.
Department Profile:
Mississippi State Chemical Laboratory (MSCL) is a state-appropriated regulatory agency for the State of Mississippi as well as a fee-for-service laboratory located on the campus of Mississippi State University. Our mission is to provide analytical data to ensure the quality, accurate labeling and safety of all fertilizers, animal feeds, human foods pesticides, and petroleum products sold in the State of Mississippi.
Essential Duties and Responsibilities:
1. Perform duties with focus on customer service, such as: sample custody, laboratory
preparatory work of samples, chain-of-custody protocols, use of the LIMS for sample
tracking and data entry.
2. Ensures that all assigned analyses are performed within required holding times and
laboratory established turnaround times.
3. Performs assigned analyses according to established QA/QC requirements, including
all documentation and verifies that analytical level quality control criteria are met as
required for compliance with appropriate regulations promulgated by federal agencies,
state agencies, and other regulatory bodies.
4. Participates in proficiency tests (PTs) including conceptual knowledge to demonstrate
analytical competency.
5. Calculates results generated in the process of laboratory analyses, evaluates against
QA/QC standards, and reports final data.
6. Performs duties in advanced-level analytical techniques that could include: GC,
GC/MS, LC, HPLC, ICP, ICP/MS, microbiological and/or other analyses as
appropriate in areas of Chemical Regulatory, Industrial and Agricultural Services,
Research, or Petroleum Products.
7. May maintain lab supply inventories and purchasing records.
8. May assist in preparatory work for more advanced procedures.
9. As a team member, participates in implementation of updated and new protocols and
procedures.
10. Acquires new knowledge in the field by reading, attending seminars and workshops;
participates in continuing education.
11. Performs related duties as assigned.
Supervisory Responsibility
Does not have supervisory responsibility.
The above essential duties are representative of major duties of positions in this position. Specific duties and
responsibilities may vary based upon departmental needs. Other duties may be assigned to the above consistent
with the knowledge, skills and abilities required for the job. Not all of the duties may be assigned to a position.
Minimum Qualifications:
A professional employee with a bachelor's degree and demonstrated competence can begin
work at the Lab Analyst I level. To start at the Lab Analyst II level, one must have a
bachelor's degree, a minimum of 3 years of relevant experience, and the equivalent of a
master's degree. For the Lab Analyst III level, a bachelor's degree, a minimum of 6 years of
relevant experience, and the equivalent of a master's degree are required.
Alternatively, a professional employee with a master's degree and a minimum of 1 year of
relevant experience, along with demonstrated competency, can begin work at the Lab Analyst
II level. To start at the Lab Analyst III level, one must have a master's degree and a minimum
of 3 years of experience.
Indicated education is required; no substitutions allowed.
Preferred Qualifications:
1. Bachelor's degree in chemistry or in a related field.
2. Demonstrate competence in the principles, methods, and techniques of analytical chemistry.
3. Field and laboratory work experience beyond the minimum required.
Knowledge, Skills, and Abilities:
• Thorough knowledge of good laboratory practices (GLP), methodologies, and safety.
• Thorough knowledge of concepts and principles of chemistry, biology, mathematics, microbiology and/or other related scientific fields.
• Thorough knowledge of relevant regulations and quality control standards.
• Ability to uphold principles of laboratory ethics as applied to the production of valid analytical data.
• Possess problem-solving skills.
• Ability to pay attention to detail and precision in conducting experiments and reviewing results.
• Ability to adapt and learn to apply new techniques and technologies.
• Ability to work both independently and as part of a team.
• Ability to pass all proficiency tests and competencies.
• Skilled in using laboratory equipment and computer software to conduct sample and data analysis.
Working Conditions and Physical Effort
Work in this class series is typically performed in a laboratory environment. It may require lifting up to 50 pounds; collecting samples in all weather conditions; wearing protective gear; being exposed to hazardous materials; working a flexible schedule including afternoons, evenings, designated holidays, and/or weekends.
Instructions for Applying:
Link to apply: ***********************************
Link to apply: ***********************************
All applicants must apply online and attach a cover letter, current resume or curriculum vitae, and the complete contact information for at least three professional references. Search, screening, and selection process will begin as soon as the required posting period is completed.
Restricted Clause:
Position is contingent upon continued availability of funding.
Equal Employment Opportunity Statement:
MSU is an equal opportunity employer, and all qualified applicants will receive consideration for employment without regard to race, color, ethnicity, sex, religion, national origin, disability, age, sexual orientation, genetic information, pregnancy, gender identity, status as a U.S. veteran, and/or any other status protected by applicable law. We always welcome nominations and applications from women, members of any minority group, and others who share our passion for building a diverse community that reflects the diversity in our student population.
What do I do if I need an accommodation?
In compliance with the ADA Amendments Act (ADA), if you have a disability and would like to request an accommodation in order to apply for a position with Mississippi State University, please contact the Department of Human Resources Management at tel: ************** or *******************.
If you have any questions regarding this policy, contact the Department of Human Resources Management at ************** or *******************. Upon request, sections of this job listing are available in large print, and readers are available to assist the visually impaired.
Quality Control Laboratory Chemist
Quality control analyst job in Gulfport, MS
An experienced Quality Control Laboratory Chemist is needed to support testing activities in a regulated laboratory environment. The role involves conducting chemical analyses on raw materials, in-process samples, finished goods, and stability samples to ensure product quality and compliance with industry standards.
Key Responsibilities
Conduct chemical testing on raw materials, in-process products, finished products, and stability samples.
Operate, maintain, and calibrate analytical instrumentation (e.g., HPLC, GC, UV/VIS, FTIR).
Prepare reagents and samples in alignment with established procedures.
Accurately document and report results according to regulatory and quality system requirements.
Support method development, validation, and transfer activities.
Troubleshoot and investigate testing or equipment-related issues.
Collaborate with cross-functional teams and provide mentorship to junior staff when needed.
Required Qualifications
3 to 5 years of hands-on chemistry experience in a regulated QC or manufacturing laboratory.
Proficiency with chromatography techniques, particularly HPLC and GC.
Familiarity with additional analytical tools (e.g., UV/VIS, FTIR, AA, IC, ICP-MS, dissolution testing).
Experience with laboratory software (e.g., Empower, Microsoft Office).
Solid understanding of cGMP principles and quality systems (e.g., change control, deviations, CAPAs).
Strong attention to detail, communication skills, and ability to manage multiple tasks in a fast-paced setting.
Additional Information
Degree preferred, but equivalent industry experience will be considered in place of formal education.
Must be able to lift 50 lbs regularly and work on their feet for extended periods.
Quality Control Technician
Quality control analyst job in Flowood, MS
Temp To Full-Time
Job Title: Quality Control Technician
Job Type: Full-Time
Job Summary: As a Quality Control Technician, you will be responsible for ensuring that products meet the highest quality standards across various manufacturing environments. You will conduct inspections, testing, and audits to maintain compliance with ISO 9001 regulations and contribute to our clients' commitment to quality and customer satisfaction.
Key Responsibilities:
Perform regular inspections and tests of raw materials, in-process products, and finished goods to ensure adherence to specifications.
Maintain accurate documentation related to quality control processes, including inspection reports and non-conformance records.
Assist in the development and implementation of quality assurance policies and procedures in alignment with ISO 9001 standards.
Collaborate with production and engineering teams to identify quality issues and develop corrective action plans.
Conduct internal audits to assess compliance with ISO 9001 standards and report findings to management.
Analyze data to identify trends and areas for improvement within the quality management system.
Provide training and support to staff on quality control processes and ISO 9001 requirements.
Participate in root cause analysis and problem-solving activities to enhance product quality.
Qualifications:
Associate's degree in a related field or equivalent experience.
2+ years of experience in quality control or assurance, preferably in a manufacturing environment.
Strong understanding of ISO 9001 standards and quality management principles.
Proficient in using quality measurement tools and techniques (e.g., calipers, gauges, statistical process control).
Excellent attention to detail and analytical skills.
Strong communication and teamwork abilities.
Ability to work independently and manage multiple tasks effectively.
What We Offer:
Competitive salary and benefits package after completing a probationary period.
Opportunities for professional growth and development.
A collaborative and supportive work environment.
How to Apply: Please call TempStaff at 601-353-3777 and reference job number 249212.
Or, submit at application by visiting www.tempstaff.net/hrcenter
Quality Control Technician A
Quality control analyst job in Pascagoula, MS
Job Title: Quality Control Technician A General Function: The Quality Control Technician A is responsible for performing in-process and final inspections to ensure compliance with drawings, specifications, and all applicable requirements. This role operates under the general supervision of a Quality Control Manager, Supervisor, or other designated manager.
Typical Duties:
The following statements describe the general nature and level of work performed and should not be considered an exhaustive list of responsibilities:
* Inspect and/or test parts, assemblies, welds, and other manufactured products to ensure compliance with quality standards.
* Document inspection results and test findings accurately.
* Accept or reject materials and assemblies that do not conform to design specifications or approved deviations.
* Inspect purchased parts and specialty items from suppliers, setting up disposition procedures for non-conforming materials.
* Collaborate with engineering to explore alternative methods and consult with production supervision regarding product issues or faulty workmanship.
* Maintain detailed records and files related to quality control inspections and product evaluations.
Required Knowledge, Skills & Abilities:
* Strong understanding of detail and assembly drawings used in manufacturing processes.
* Knowledge of relevant codes, standards, and regulations applicable to the assigned manufacturing area.
* Proficiency in using tools, gauges, measuring devices, and test equipment required for the inspection process.
* Ability to maintain accurate inspection records and documentation.
* Strong communication skills with the ability to interface effectively with plant supervisors, managers, and customer quality assurance personnel.
Experience & Training:
* High school diploma supplemented by coursework in drafting, applied mathematics, or industrial technology, with considerable to extensive experience in manufacturing processes.
* Or, an equivalent combination of education and training that provides the required knowledge, skills, and abilities.
* A minimum of 5 years "Shipbuilding" experience.
Bollinger is an equal opportunity employer and is committed to providing employment opportunities to minorities, females, veterans and disabled individuals, and without regard to sexual orientation and gender identity.
Lab Analyst I - Volatiles
Quality control analyst job in Scott, LA
We are SGS - the world's leading testing, inspection and certification company. We are recognized as the global benchmark for sustainability, quality and integrity. Our 99,600 employees operate a network of 2,600 offices and laboratories, working together to enable a better, safer and more interconnected world.
Our Scott, LA laboratory is looking for a Laboratory Analyst to join their Volatiles (VOA) team! The Lab Analyst will prepare and analyze samples with accuracy and precision in accordance to SGS' analytical SOPs. Work independently and as part of a team to meet daily production targets and ensure hold times and turnaround times are met. Understand and apply basic analytical chemistry principles. Always follow safe laboratory practices and maintain a safe working environment.
Job Functions
* After appropriate training independently prepare and analyze samples according to SGS' analytical SOPs using instrumentation specific to the department and analytical methodologies
* Performs routine operation, maintenance, calibration of laboratory instruments/equipment
* May assist with validation and MDL studies.
* Assists with investigation, and preparation of responses to client inquiries and CARs.
* Inputs and maintains technical information as needed to support the laboratory functions/operations.
* Maintains Laboratory Notebook where applicable.
* Adheres to internal standards, policies and procedures.
* Performs other duties as assigned.
Qualifications
* Associate Degree in a Chemistry or similar scientific discipline (Required)
* 0-2 years of experience in Analytical Chemistry Laboratories OR 3 years of relevant experience (i.e. Sample Prep) (Required)
* Bachelor's Degree in a Chemistry or similar scientific discipline (Preferred)
* 1-2 years of years' relevant experience in Analytical Chemistry Laboratories (Preferred)
* Ability to lift, carry, push and/or pull upwards of 25 lbs on a frequent basis (Required)
Additional Information
SGS is an Equal Opportunity Employer, and as such we recruit, hire, train, and promote persons in all job classifications without regard to race, color, religion, sex, national origin, disability, age, marital status, sexual orientation, gender identity or expression, genetics, status as a protected veteran, or any other characteristics protected by law.
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, skills, and/or abilities 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.
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 ************ for assistance and leave a message. You will receive a call back. 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.
Laboratory Analyst
Quality control analyst job in New Orleans, LA
Eurofins Scientific is an international life sciences company, providing a unique range of analytical testing services to clients across multiple industries, to make life and our environment safer, healthier and more sustainable. From the food you eat, to the water you drink, to the medicines you rely on, Eurofins laboratories work with the biggest companies in the world to ensure the products they supply are safe, their ingredients are authentic and labelling is accurate.
The Eurofins network of companies is the global leader in food, environment, pharmaceutical and cosmetic product testing and in agroscience Contract Research Organisation services. It is one of the market leaders in certain testing and laboratory services for genomics, discovery pharmacology, forensics, advanced material sciences and in the support of clinical studies, as well as having an emerging global presence in Contract Development and Manufacturing Organisations. It also has a rapidly developing presence in highly specialised and molecular clinical diagnostic testing and in-vitro diagnostic products.
In over 30 years, Eurofins has grown from one laboratory in Nantes, France to 58,000 staff across a decentralised and entrepreneurial network of 900 laboratories in over 54 countries. Eurofins companies offer a portfolio of over 200,000 analytical methods to evaluate the safety, identity, composition, authenticity, origin, traceability and purity of biological substances and products.
In 2021, Eurofins generated total revenues of EUR 6.72 billion, and has been among the best performing stocks in Europe over the past 20 years.
Job Description
Shift: (Full-Time) Monday- Friday: 8am- 4:30pm with additional hours as needed.
The Chemical Laboratory Analyst receives sufficient authority from, and is accountable to the respective Department Manager or appointed designate, for the successful completion of assigned duties and responsibilities and has the authority to take action necessary to carry out the duties and responsibilities of this position.
The Chemical Laboratory Analyst has authority to identify the occurrence of departures from the quality system or from the procedures for carrying out sample testing, so long as such action does not deviate from established company guidelines, is consistent with sound business or technical judgment, and follows the practices of the laboratory.
OVERALL OBJECTIVES AND RESPONSIBILITIES
Main Assignment
Responsible for all operational activities relative to processing of chemical analytical methods on incoming samples, in compliance with all applicable quality systems.
Care and maintenance of equipment associated with this testing.
Specific Assignments
Perform test methods in accordance with Standard Operating Procedure and applicable Quality Control Procedures
Clean workplace and equipment in accordance with Standard Operating Procedures and general housekeeping requirements.
Maintain and monitor ongoing individual performance of analytical methods with control charts. Notify Department Manager when a batch does not meet batch Quality Control criteria.
Provide feedback to the Department Manager for suggested improvement of analytical methods.
Monitor and meet TAT requirements for sample workflow, and keep the Department Manager informed when capacity constraints are anticipated that may delay TAT.
Record supplies taken from stockroom in logbook, and note any supplies that may need ordering and/or rush delivery.
Maintain assigned equipment and instrumentation according to Standard Operating Procedures. Perform any and all Operational Qualifications prior to analysis according to Standard Operating Procedures.
Qualifications
Bachelor's degree in chemistry, biology or microbiology, or a high school diploma with the equivalent of 5 years chemical laboratory experience, and basic skills in laboratory techniques.
Willing to work overtime, weekends and holidays
Authorization to work in the United States indefinitely without restriction or sponsorship
Additional Information
Shift: (Full-Time) Monday- Friday: 8am- 4:30pm with additional hours as needed. Candidates currently living in a commutable distance to New Orleans, LA, are encouraged to apply.
Excellent full time benefits including comprehensive medical coverage, dental, and vision options
Life and disability insurance
401(k) with company match
Paid vacation and holidays
Eurofins Scientific is an international life sciences company, providing a unique range of analytical testing services to clients across multiple industries, to make life and our environment safer, healthier and more sustainable. From the food you eat, to the water you drink, to the medicines you rely on, Eurofins laboratories work with the biggest companies in the world to ensure the products they supply are safe, their ingredients are authentic and labelling is accurate.
The Eurofins network of companies is the global leader in food, environment, pharmaceutical and cosmetic product testing and in agroscience Contract Research Organisation services. It is one of the market leaders in certain testing and laboratory services for genomics, discovery pharmacology, forensics, advanced material sciences and in the support of clinical studies, as well as having an emerging global presence in Contract Development and Manufacturing Organisations. It also has a rapidly developing presence in highly specialised and molecular clinical diagnostic testing and in-vitro diagnostic products.
In over 30 years, Eurofins has grown from one laboratory in Nantes, France to 58,000 staff across a decentralised and entrepreneurial network of 900 laboratories in over 54 countries. Eurofins companies offer a portfolio of over 200,000 analytical methods to evaluate the safety, identity, composition, authenticity, origin, traceability and purity of biological substances and products.
In 2021, Eurofins generated total revenues of EUR 6.72 billion, and has been among the best performing stocks in Europe over the past 20 years.
Eurofins USA Food Testing is a Disabled and Veteran Equal Employment Opportunity employer.
Laboratory Analyst
Quality control analyst job in New Orleans, LA
Eurofins Scientific is an international life sciences company, providing a unique range of analytical testing services to clients across multiple industries, to make life and our environment safer, healthier and more sustainable. From the food you eat, to the water you drink, to the medicines you rely on, Eurofins laboratories work with the biggest companies in the world to ensure the products they supply are safe, their ingredients are authentic and labelling is accurate.
The Eurofins network of companies is the global leader in food, environment, pharmaceutical and cosmetic product testing and in agroscience Contract Research Organisation services. It is one of the market leaders in certain testing and laboratory services for genomics, discovery pharmacology, forensics, advanced material sciences and in the support of clinical studies, as well as having an emerging global presence in Contract Development and Manufacturing Organisations. It also has a rapidly developing presence in highly specialised and molecular clinical diagnostic testing and in-vitro diagnostic products.
In over 30 years, Eurofins has grown from one laboratory in Nantes, France to 58,000 staff across a decentralised and entrepreneurial network of 900 laboratories in over 54 countries. Eurofins companies offer a portfolio of over 200,000 analytical methods to evaluate the safety, identity, composition, authenticity, origin, traceability and purity of biological substances and products.
In 2021, Eurofins generated total revenues of EUR 6.72 billion, and has been among the best performing stocks in Europe over the past 20 years.
Job Description
Shift: (Full-Time) Monday- Friday: 8am- 4:30pm with additional hours as needed.
The Chemical Laboratory Analyst receives sufficient authority from, and is accountable to the respective Department Manager or appointed designate, for the successful completion of assigned duties and responsibilities and has the authority to take action necessary to carry out the duties and responsibilities of this position.
The Chemical Laboratory Analyst has authority to identify the occurrence of departures from the quality system or from the procedures for carrying out sample testing, so long as such action does not deviate from established company guidelines, is consistent with sound business or technical judgment, and follows the practices of the laboratory.
OVERALL OBJECTIVES AND RESPONSIBILITIES
Main Assignment
Responsible for all operational activities relative to processing of chemical analytical methods on incoming samples, in compliance with all applicable quality systems.
Care and maintenance of equipment associated with this testing.
Specific Assignments
Perform test methods in accordance with Standard Operating Procedure and applicable Quality Control Procedures
Clean workplace and equipment in accordance with Standard Operating Procedures and general housekeeping requirements.
Maintain and monitor ongoing individual performance of analytical methods with control charts. Notify Department Manager when a batch does not meet batch Quality Control criteria.
Provide feedback to the Department Manager for suggested improvement of analytical methods.
Monitor and meet TAT requirements for sample workflow, and keep the Department Manager informed when capacity constraints are anticipated that may delay TAT.
Record supplies taken from stockroom in logbook, and note any supplies that may need ordering and/or rush delivery.
Maintain assigned equipment and instrumentation according to Standard Operating Procedures. Perform any and all Operational Qualifications prior to analysis according to Standard Operating Procedures.
Qualifications
Bachelor's degree in chemistry, biology or microbiology, or a high school diploma with the equivalent of 5 years chemical laboratory experience, and basic skills in laboratory techniques.
Willing to work overtime, weekends and holidays
Authorization to work in the United States indefinitely without restriction or sponsorship
Additional Information
Shift:
(Full-Time) Monday- Friday: 8am- 4:30pm with additional hours as needed. Candidates currently living in a commutable distance to New Orleans, LA, are encouraged to apply.
Excellent full time benefits including comprehensive medical coverage, dental, and vision options
Life and disability insurance
401(k) with company match
Paid vacation and holidays
Eurofins Scientific is an international life sciences company, providing a unique range of analytical testing services to clients across multiple industries, to make life and our environment safer, healthier and more sustainable. From the food you eat, to the water you drink, to the medicines you rely on, Eurofins laboratories work with the biggest companies in the world to ensure the products they supply are safe, their ingredients are authentic and labelling is accurate.
The Eurofins network of companies is the global leader in food, environment, pharmaceutical and cosmetic product testing and in agroscience Contract Research Organisation services. It is one of the market leaders in certain testing and laboratory services for genomics, discovery pharmacology, forensics, advanced material sciences and in the support of clinical studies, as well as having an emerging global presence in Contract Development and Manufacturing Organisations. It also has a rapidly developing presence in highly specialised and molecular clinical diagnostic testing and in-vitro diagnostic products.
In over 30 years, Eurofins has grown from one laboratory in Nantes, France to 58,000 staff across a decentralised and entrepreneurial network of 900 laboratories in over 54 countries. Eurofins companies offer a portfolio of over 200,000 analytical methods to evaluate the safety, identity, composition, authenticity, origin, traceability and purity of biological substances and products.
In 2021, Eurofins generated total revenues of EUR 6.72 billion, and has been among the best performing stocks in Europe over the past 20 years.
Eurofins USA Food Testing is a Disabled and Veteran Equal Employment Opportunity employer.
Quality Control Chemist
Quality control analyst job in Gulfport, MS
Job Description
Job Title: Quality Control Laboratory Chemist
Department: Quality Control Reports To: Quality Control Manager Employment Type: Full-Time | On-Site Compensation: Median $23-$25/hour (commensurate with experience)
About the Role
Our client is seeking an experienced Quality Control Laboratory Chemist to join their Quality Control team. In this role, you will play a critical part in ensuring the quality and compliance of human and veterinary drug products by conducting a wide range of chemical analyses in a GMP-regulated laboratory environment. This position requires a strong background in chromatography and a proven track record of working within cGMP standards.
Please note that you must have experience beyond a university based laboratory setting to be considered for this position.
Key Responsibilities
Perform chemical analyses on raw materials, in-process products, finished products, and stability samples.
Operate, maintain, and calibrate analytical instruments (HPLC, GC, etc.).
Prepare reagents and samples in compliance with SOPs and regulatory requirements.
Accurately document and report test results according to GMP guidelines.
Contribute to method development, validation, and transfer activities.
Troubleshoot and investigate testing or equipment-related issues.
Collaborate with QC team members and cross-functional departments.
Mentor and support junior chemists when needed.
Qualifications & Requirements
3-5 years of direct hands-on experience in a GMP-regulated QC or manufacturing laboratory.
Strong background in chromatography (HPLC, GC, UV/VIS, FTIR).
Experience with analytical tools such as AA, IC, ICP-MS, and dissolution testing.
Proficiency with Empower, Microsoft Office, and laboratory data systems.
Solid understanding of cGMP, quality systems, and regulatory compliance (change control, deviations, CAPAs).
Excellent attention to detail, communication, and organizational skills.
Ability to multitask and prioritize in a fast-paced environment.
Note: Applicants with only academic or research lab experience will not be considered. A degree is not required. Relevant industry skills and experience are what matter most.
Physical Requirements
Must be able to lift 50 lbs. or more daily.
Ability to stand, walk, or sit for 8+ hours per day.
Senior Quality Control Microbiologist
Quality control analyst job in Gulfport, MS
Job Description
Required Skills/Abilities:
• Proficiency in microbiological techniques such as aseptic testing, microbial monitoring,
gram staining, and plating.
• Knowledge and control of analytical equipment including calibration and maintenance.
• Ability to understand and perform all required tasks by adhering to company Standard
Operating Procedures and all current Good Manufacturing Practices.
• Understanding of quality systems including change control, deviations and CAPAs.
• Ability to handle multiple tasks concurrently and complete tasks in a timely manner.
• Strong written and verbal language skills to effectively read and write SOP's and related
lab reports and communicates with personnel at all levels in the organization.
• Excellent teamwork skills, organizational skills, and strong attention to detail.
Education and Experience
• B.S. in Biology or equivalent experience.
• 5+ years' experience in Microbiology.
• 2 + years Pharmaceutical Manufacturing Laboratory experience.
• Knowledge of computer software, including relevant applications such as Microsoft Office.
• Expert knowledge and understanding of quality control, SOPs, cGMPs, OSHA, and FDA
policies and regulations.
Physical Requirements:
• Ability to lift 50lbs. or more daily.
• Ability to walk, stand, or sit 8 or more hours a day.
• Ability to walk, stand, or sit 8 or more hours a day.
Quality Control Lab Technician I
Quality control analyst job in Hattiesburg, MS
Resinall Corp currently has an opening for a QC Lab Technician I. This is an entry level shift position in the Resinall Hattiesburg Laboratory that serves all the analytical aspects of in-process, finished products, raw materials, and other required samples. The Laboratory Technician tests samples, evaluates data for accuracy, and reports results. The Technician will focus on becoming proficient in basic testing requirements. This will consist of the use of Rheometers, Gas Chromatographs, as well as viscosity and solubility measurements.
Position Qualifications:
* Two (2) year associate's degree or work experience assessed as equivalent by the Laboratory Supervisor
* Successful completion of training requirements as outlined by the laboratory training program
* Training or work experience in a laboratory environment preferred
* Good math and computer skills
* Good communication skills with managers and employees required
* Must have successfully completed and passed a Functional Job Capacity Evaluation (FCE)
* Ability to work rotating shifts, including weekends
Responsibilities Include the Following:
* Practice good laboratory safety habits and participate in all safety training as required
* Maintain a clean, organized, and safe laboratory environment at all times
* Maintain and follow ISO 9001 standard practices and procedures
* Identify and report deviations from the laboratory's quality management system, SQC program, or from procedures for performing lab activities
* Report to laboratory management on the performance of the laboratory's quality management system and any need for improvement
* Ensure the effectiveness of laboratory activities
* Maintain required inventory levels of all supplies for continuous laboratory operation
* Maintenance and disposal of retained samples
* Proper handling and cleanliness of all equipment
* Perform equipment calibrations as dictated by procedures or standard lab practice
* Available for callout when scheduled
Additional Training and Qualifications (post hire):
* Technician is hired as a Quality Laboratory Technician I
* Complete and pass periodic competency (Frequency will be up to the management team.)
* Attend monthly safety meetings with laboratory
* Failure to complete the required training and qualifications could result in a 30-day probation, leading into grounds for disciplinary action as determined by management.
Must be able to pass a pre-employment drug screen, background check, physical, and MVR.
__________________________________________________________________________________________
Why Ergon Inc.?
At Ergon, we are a relationship-driven, family-owned company that values each employee's growth and contributions. Headquartered in Flowood, Mississippi, we take pride in maintaining a close-knit, small-company atmosphere while offering exceptional career opportunities. Our comprehensive benefits package includes:
* Competitive pay
* 401(k) matching & profit sharing
* Health, Dental, Vision, and Life Insurance
* Short- and Long-Term Disability Plans
* Additional voluntary benefits
* Paid holidays, vacation, and sick leave
* Tuition assistance
At Ergon Inc., we live by our core values:
* Empowered Service: Together, we're committed to delivering unparalleled service. We do what's right, provide solutions and foster stronger relationships with our teams and customers. Employee safety is our top priority and the first consideration in all aspects of our service. That's empowered service.
* Selfless Leadership: We lead with compassion and put those around us before ourselves. We don't say we're the experts, we demonstrate it through technical expertise, category innovation and care for what we do. We call this selfless leadership.
* Purposeful Growth: We believe employee growth and company growth go hand in hand. We build our legacy together to ensure future success through purposeful growth. The company has always reinvested tremendously back into the business, but not just growing for the sake of growing, but growing in a careful and strategic way.
* Respectful Relationships: And together, we foster a culture of respect, acceptance and diversity of ideas and of people. Our differences make us stronger. And we're united by our shared values, always forging respectful relationships.
Come and join the Ergon team!
We are an EEO/AAP employer.
Job Role: QC Lab Technician I
Location: Hattiesburg, MS
Employment offer contingent upon pre-employment drug test, background check, and MVR.
QC Inspector - AEX
Quality control analyst job in Alexandria, LA
TITLE : QC Inspector - AEX
REPORTS TO: Manager, QC.
The QC Inspector is responsible for performing inspection functions in accordance with Global X's Continuous Airworthiness Maintenance Program (CAMP) and FAA regulations. This role ensures that parts, materials, maintenance, and workmanship meet Global X standards, while monitoring performance measures through audits of internal and vendor organizations.
ESSENTIAL FUNCTIONS AND RESPONSIBILITIES:
Perform Line Maintenance, Remain Overnight (RON), and Receiving Inspections (RI).
Monitor maintenance, workmanship, and materials for compliance with Global X procedures and FAA standards.
Perform RII in-process inspections and ensure proper documentation.
Audit completed aircraft records (logbooks, work cards, non-routines, engineering documents, etc.) generated by C-Check, RON, and Line Maintenance.
Provide oversight during Heavy or Special Maintenance visits.
Perform Borescope inspections within qualified method and level.
Ensure accuracy and completeness of all work documents and records.
Initiate discrepancies in maintenance logbooks and non-routine forms.
Provide “buy-back” of RII and non-RII maintenance actions.
Approve return-to-service of maintenance, preventive maintenance, and alterations.
Issue Airworthiness Releases (AWR).
Reject unsatisfactory work or non-conforming parts per procedures.
Prepare and issue audit reports identifying hazards/risks, corrective actions, and track resolution progress.
Conduct inspections and audits of contractors/vendors (e.g., repair/overhaul services, contract maintenance, deicing, fueling, and parts distributors).
Follow all safety rules to maintain a safe working environment.
Perform other duties as assigned by the DOM/DQC.
SKILLS AND QUALIFICATIONS:
Knowledge of the TRAX system.
Valid FAA A&P license, held for at least 5 years.
Previous verifiable inspection experience (OJT, training records, certificates, etc.), including RII Authorization.
Preferred: prior experience with NDT methods such as Liquid Penetrant, Eddy Current, and Borescope inspections.
Strong analytical, problem-solving, and communication skills.
Previous experience with aircraft parts and materials handling.
Work Location and Schedule
This position is based in Alexandria, LA. The standard schedule follows a four-days-on, three-days-off rotation with 10-hour shifts. Work hours and shift assignments may vary, and the schedule is subject to change based on operational needs. Flexibility is required to support the demands of a dynamic aviation maintenance environment.
PHYSICAL DEMANDS:
The QC Inspector role is performed in a safety-sensitive aviation environment that includes both office settings and aircraft maintenance areas, such as hangars, line stations, and ramp operations. The position requires frequent exposure to varying weather conditions, noise levels, and physical activities associated with aircraft inspections. QC Inspectors must be able to stand, walk, bend, climb, and climb into confined spaces as needed to access aircraft structures and components. The role also involves extended periods of reviewing technical documents and records. Strict adherence to safety protocols and regulatory requirements is essential to maintain a safe and compliant work environment.
OTHER DUTIES:
Please note this job description is not designed to cover or contain a comprehensive listing of activities, duties or responsibilities that are required of the employee for this job. Duties, responsibilities, and activities may change at any time.
Global Crossing Airlines provides equal employment opportunities to all team members and applicants for employment and prohibits discrimination and harassment of any type without regard to race, color, religion, age, sex, national origin, disability status, genetics, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state, or local laws. This policy applies to all terms and conditions of employment, including recruiting hiring, placement, promotion, termination, layoff, recall, transfer, leaves of absence, compensation and training.
Auto-ApplyAircraft Quality Control Inspector
Quality control analyst job in Hammond, LA
The Aircraft Quality Control Inspector is responsible for ensuring that assigned aircraft are maintained within required specifications of 14 CFR Parts 43, 91 and 125 and other FAA and DOD regulations, OEM instructions and CBP directives as required and are airworthy before operation.
Principal Accountabilities:
+ Inspect the work of Aircraft Mechanics performing maintenance repairs and modifies aircraft structures, aircraft engines, electrical, avionics and aircraft sub-systems.
+ Apply technical knowledge and expertise in determining proper equipment installation and operation.
+ Apply comprehensive technical expertise to assist the maintenance department to solve complex problems by interpreting technical documentation such as blueprints or manufactures' manuals.
+ Make entries in aircraft logs and records and is responsible for providing guidance and technical expertise to lower-level technicians throughout all aircraft modifications and/or maintenance efforts.
+ Perform the receiving, in-process, final quality, flight safety inspections and functional operational tests during organizational, intermediate and depot level maintenance, modification and repair of military tactical aircraft systems or associated components.
+ Approve or reject work accomplished by field team members to ensure compliance with customer specifications, standards, and technical data.
+ Review and approve locally developed procedures and solutions to complex repair situations.
+ Perform analysis of defects and interprets quality control rejection and failure trends.
+ Monitor safety, training, and certification requirements.
+ Using checklists, perform daily work site Safety Inspections and Foreign Object Damage Inspections.
+ Monitor tool control programs, inspects and maintains records to ensure that measuring and test equipment meets calibration requirements.
+ Maintain Quality, Safety, Training and Certification Records.
+ Coordinate with the Customer Quality Assurance Representative concerning quality matters, mandatory inspection points and final acceptance inspection of contract end items or services.
+ Inspect forms and records related to aircraft maintenance.
+ The inspector monitors' the maintenance departments program, such as but not limited to, engine oil consumption, logs and records processes, hydraulic contamination, NDI, electrical static discharge, employee certification programs, confined space entry, tool control, foreign object damage, material control receiving inspections, weight and balance, fall protection and safety programs.
+ The inspector assists in the development and maintenance of ground and flight operation standard operating procedures, quality plan and safety plans. Assists maintenance in briefing and debriefing functional check flights.
+ Possess knowledge of basic computer skills sufficient to use Government computer system to access various technical references for airframe repairs and Government training requirements.
+ Document maintenance as per Quality Assurance (QA) and established regulatory requirements.
+ Comply with work order timekeeping system procedures.
+ Maintain high state of cleanliness and utilize a clean-as-you-go process when executing maintenance duties.
+ Perform weekly Foreign Object Damage (FOD) walk-downs.
+ Maintain situational awareness, stay cognitive-focused, and mitigate risks.
+ Comply with processes and procedures as per DHS/DOD documents and publications.
+ Immediately report missing, lost, found, or unattended tools to the supervisor. Maintain and control tools IAW tool control policy and instructions. Inventory and inspect tools on a regular basis to identify when to replace worn or broken tools and report the need for replacement tools to the supervisor.
+ Clean work area as necessary, assuring all hazardous materials are properly stored; Handle hazardous materials, expired materials and wastes in accordance with applicable laws and regulatory requirements.
+ Comply with safety rules and procedures and perform work in a manner that enhances the safety of the work area. Promptly report accidents, injuries, safety, violations, and/or unsafe practices or procedures to supervisor.
+ Perform weekly break room and smoking area cleaning duties.
+ Perform other duties as assigned.
Minimum Requirements:
+ Must be able to obtain and maintain a CBP Background Investigation Suitability clearance. Note: US Citizenship is required to obtain the clearance.
+ High School Diploma or equivalent is required.
+ Five (5) years of experience in aircraft maintenance.
+ Valid Airframe and Power Plant (A&P) License required.
+ Valid FAA Inspection Authorization (IA) required.
+ Ability to obtain a government flight line driver's license.
+ Possess a valid United States driver's license.
+ Possess the experience and ability to provide technical support to structural/mechanical engineers and customers alike, must possess excellent organizational skills in prioritizing workload to meet aircraft delivery schedule.
+ Ability to read and interpret data is required.
+ Ability to read, write, speak and understand English.
Physical Requirements/Working Environment:
+ Capable of performing tasks that frequently require lifting, reaching, bending, walking, pulling, sitting, standing, crouching, stooping, kneeling, and stretching for prolonged periods of time.
+ Must be capable of performing tasks in cramped, awkward, and strained positions and/or climbing up and down ladders, work platforms, scaffolding, and aircraft structures.
+ Must be capable of carrying items up to 40 pounds or, for heavier objects, must seek assistance of other workers or weightlifting devices.
+ Must be capable of wearing cumbersome personal protective equipment for HAZMAT operations.
+ May be required to work night shifts.
+ May work in Aircraft maintenance hangar or outside.
+ Some domestic travel may be required
Amentum is proud to be an Equal Opportunity Employer. Our hiring practices provide equal opportunity for employment without regard to race, sex, sexual orientation, pregnancy (including pregnancy, childbirth, breastfeeding, or medical conditions related to pregnancy, childbirth, or breastfeeding), age, ancestry, United States military or veteran status, color, religion, creed, marital or domestic partner status, medical condition, genetic information, national origin, citizenship status, low-income status, or mental or physical disability so long as the essential functions of the job can be performed with or without reasonable accommodation, or any other protected category under federal, state, or local law. Learn more about your rights under Federal laws and supplemental language at Labor Laws Posters (********************************* SkbztPuAwwxfs) .
QC Inspector
Quality control analyst job in Baton Rouge, LA
More information about this job The Site QC Coordinator will ensure continuous production of systems is consistent with established standards. Will coordinate all QA/QC activities with the site QC Manager and coordinate all quality related correspondence with the customers' representatives. Must learn and understand all safety hazards related to the work and learn to safely and effectively use or operate work related tools and equipment. Will be required to work in a plant operations or construction jobsite setting.
Responsibilities
* The following are intended as general illustrations of the work in this job class and are not all-inclusive for this position.
* Monitor all quality related activities on the project
* Coordinate with management for quality improvements
* Complete site quality control instructions and action remedial responses
* Verify that contractor quality requirements are specified to vendors and confirms contractor documentation submittals
* Ensure that safety is adhered to at site
* Ensure all technical documents relative to site quality control are current in status
* Put test packages together for client
* Assist other craft workers as needed
Qualifications
Physical
* Must be able to lift up to 25 lbs., but may occasionally lift up to 50 lbs.
* Hearing and comprehension is necessary for giving and receiving directions
* Will need to perform sedentary to heavy work
* Will operate office equipment of all types
* Will operate inspection hand gages of all types
* Climb and maintain balance on steel/wood framework, stairs, ladders and scaffolds
* Required to use hands to grasp, lift, handle, carry or feel objects on a frequent basis
* Position may require prolonged bending/twisting, walking, reaching overhead, squatting, sitting or standing and lifting
* Must be able to manipulate and traverse uneven terrain, ladders, and multi-floor buildings with no elevator
* Must be able to walk on uneven surfaces, muddy conditions, loose rock, loose/soft sand, etc.
* Will be exposed to adverse weather conditions (Heat, Cold, Rain, Etc.)
* Vision requirements include close vision, distance vision, and ability to adjust focus
* Ability to drive cars/trucks as needed
Mental
* Must have the ability to communicate effectively with management/ supervision
* Talking and reading & writing comprehension is necessary for giving and receiving directions to perform work and/or safety policy
* Ability to use math/complete calculations
* Work at various tempos, and concentrate amid distractions
* Decision making skills necessary
* Detail-oriented; must be able to remember, examine, and observe details
Auto-ApplyFacilities Gas Chemical Technician
Quality control analyst job in Louisiana
Company TSMC Arizona Corporation Career Area Manufacturing (fabs) Posted Jul 08, 2025 We are seeking experienced Gas and Chemical Technicians to join our growing Facilities team onsite. As the world's leading dedicated foundry, TSMC has over 55,000 employees across Asia, Europe and North America. We are at the center of today's technology industry, producing 24% of the world semiconductor excluding memory output value. Our semiconductors are the digital engines inside nearly 11,000 electronic products created by over 500 companies, from coffee machines and smart phones to airliners and cloud data centers. Become part of a unique team of technology enthusiasts joined in a common purpose - to unleash innovations that lead to sustainable economic growth and a smarter, better world. Nowhere is that opportunity greater than in the semiconductor industry. Our employees' success is our most prized achievement, and we are proud so many of them have made TSMC the place to build their life-long careers. As a part of the Facilities team, you'll be part of something special, unleashing innovations that lead to sustainable economic growth and a smarter, better world.
Responsibilities:
The Gas/Chemical Technician is responsible for operating, maintaining, and troubleshooting Chemical/Gas/Slurry distribution systems and equipment.
* Must accurately and reliably follow standard operating procedures for troubleshooting chemical and gas distribution systems, perform laboratory testing, and complete chemical and gas container change outs.
* Read and measure plant operating parameters to determine process changes required to maintain operations within specifications.
* Maintains a clean, orderly, and safe workplace
* Performs rounds and readings of gas/chemical distribution equipment
* Performs Gas/Chemical container change outs to ensure constant flow to factory tools
* Operates and controls gas/chemical distribution systems. Ensures equipment is operating within controls/specifications
* Makes recipe adjustments to ensure correct gas/chemical concentrations are blended for factory tools
* Sets up and adjusts indicating and controlling devices, for example gas/chemical analyzers, temperature indicators and pressure/flow controlling devices, or gauging instruments to facilitate simultaneous analysis and control of process conditions
* Observes gauges, signals, and recording instruments, turns valves, and moves controls to regulate temperatures, pressures, and flow of steam
* Performs preventive maintenance procedures at specified intervals to keep process equipment clean, and performing at optimum levels
* Performs diagnostic and troubleshooting practices to determine root cause and corrective actions needed to maintain systems operation within specifications
* Performs emergency and corrective maintenance actions to repair damaged equipment or correct out of specification conditions
* Draws samples of product at specified stages of operation and performs pH, gas/chemical analyses, or other standard tests to determine if material concentration or quality is within factory specifications
* Maintains log of gauge readings, shift throughput, and equipment malfunctions
* Patrols area to inspect equipment for leaks and hazards and to record tank levels and gauge readings
* Ensures processing conditions and process output are within regulatory limits. Responsible for correcting conditions and alerting management of discrepancies
* Ensure all requirements as specified by the manufacturer of equipment systems are met, and equipment operations, repairs, modifications, and maintenance meet environmental protection requirements
* Additional duties based on business needs, including ERT
Knowledge and Personal skills:
The Gas/Chemical Technician must have knowledge of industry standards, codes and regulations, and the ability to apply to maintenance operation of site Gas/Chemical distribution systems.
* Follow all safety policies and procedures at all times
* Fundamental understanding of chemical and gas semiconductor distribution systems. Pumping, filtration and automation.
* Ability to read, interpret, and understand engineering drawings and specifications.
* Ability to work cooperatively with other technicians, supervisors, engineers, and managers
* Team building, Analytical and problem solving skills
* Sound decision making skills
* Effective written, verbal, presentation, and listening communications skills
* Computer skills including the ability to operate Corporate email, spreadsheets, word processing, engineering drawing databases at a highly proficient level
* Capable of working independently and exhibit effective time management skills
* Willingness and ability to work overtime when needed for business purposes, or to be called-in to work in the event of emergency or business needs
* Contributes recommendations and suggestion for work method improvements, safety, materials, and tools
* The Gas/Chemical Technician must have an appropriate focus on personal, process, and work force safety
* Attributes should include honesty, trustworthiness, respect for others, flexibility, and sound workplace ethics
* Duties will include any and all other directions of supervision that can safely be performed by the incumbent.
Experience, Education, and Training:
* High School graduation or GED is required
* Technical College or Trade Program is preferred
* Experience with laboratory or analytical equipment is preferred
* Previous knowledge in operation of industrial and/or commercial processing equipment
* Five years' experience with process piping systems, working in an industrial setting are highly preferred
* Competency in basic mathematic skills including fractions, addition, subtraction, division
Physical Requirements:
* May spend extended hours working inside and outside in all weather conditions, and in awkward body positions which can cause physical discomfort and strain.
* Required to regularly lift up to 50 lbs and to adjust heavy objects.
* The position will come in contact with sharp, hot, and cold equipment, and parts.
* Must be medically qualified to wear a personal respirator.
* Sensory demands include exposure to the smells associated with industrial chemical operations, exposure to the sounds associated with powered tools and industrial equipment.
* Must have the ability to safely climb ladders, and work at elevation from ladders, scaffolding, lifts, roofs, or platforms, and the ability to work in confined spaces.
Work Location: Phoenix AZ 85083
Work Type: Onsite
Training: Onsite
*
*
2nd shift Quality Technician - Control Wiring Test
Quality control analyst job in Crystal Springs, MS
Job ID:
R0109339
Company Name:
HITACHI ENERGY USA INC
Profession (Job Category):
Quality Management
Job Schedule:
Full time
Remote:
No
Job Description:
The opportunity
Step into a role where precision meets purpose! At Hitachi Energy's Crystal Springs location, we're seeking a Quality Assurance Technician who thrives on accuracy and innovation. You'll play a key role in ensuring our products meet the highest standards of quality and safety before they reach customers worldwide. This is your chance to join a global leader in energy solutions, work with cutting-edge technology, and contribute to a sustainable future. If you're detail-oriented, proactive, and passionate about continuous improvement, we want you on our team!
How you'll make an impact
Inspect raw materials and finished products to ensure compliance with quality and safety standards.
Develop and maintain inspection reports and quality plans.
Perform wiring functional tests on control cabinets.
Calibrate and verify test equipment functionality.
Identify and report quality anomalies to engineering teams.
Represent the Quality department on the production line to ensure compliance with operating procedures.
Support process improvements in quality control practices.
Draft reports and compile data with strong visual accuracy.
Responsible to ensure compliance with applicable external and internal regulations, procedures, and guidelines.
Your background
Associate degree in electrical/electronic technology or industrial electrical testing.
Proven experience in a production environment as a Quality Technician, Inspector, or similar role.
Knowledge of ISO 9000 concepts and quality control techniques.
Ability to read and interpret 2D technical drawings; strong analytical skills.
Proficiency in Microsoft Office and SAP ERP (or equivalent).
Experience with control wiring connection and testing preferred.
More about us
At Hitachi Energy, we live our values of safety, integrity, and innovation every day.
We offer global opportunities for growth, learning, and career development.
Join a diverse and inclusive team committed to shaping the future of energy.
Equal Employment Opportunity
(EEO)-Females/Minorities/Protected Veterans/Individuals with Disabilities
Protected veterans and qualified individuals with a disability may request a reasonable accommodation if you are unable or limited in your ability to use or access the Hitachi Energy career site as a result of your disability. You may request reasonable accommodations by completing a general inquiry form on our website. Please include your contact information and specific details about your required accommodation to support you during the job application process.This is solely for job seekers with disabilities requiring accessibility assistance or an accommodation in the job application process. Messages left for other purposes will not receive a response.
Auto-ApplyQuality Control
Quality control analyst job in Monroe, LA
Primary Duties and Responsibilities: * Perform testing and measurement of products to ensure compliance with Orchid Monroe, LLC and customer requirements. * Conduct in-house calibration of instruments, maintain calibration schedules, and accurately document results in the calibration system and on instruments.
* Inspect and test incoming raw materials and components, including dimensional, chemical, and soft-magnetic properties.
* Perform internal product audits and ensure audit findings are addressed appropriately.
* Operate and maintain specialized testing equipment such as fluoroscopy machines, Epstein testers, and humidity chambers.
* Conduct customer-specific testing (e.g., phosphate thickness via XRF) in accordance with customer specifications.
* Properly document, contain, and control all non-conforming products, ensuring timely resolution.
* Maintain quality documentation and records in compliance with ISO/IATF requirements.
* Support PPAP submissions, engineering changes, and the validation of gauges and Control Plans/QRRs.
* Provide quality support to manufacturing operations, assisting in root cause analysis, problem-solving, and corrective/preventive actions.
* Participate in continuous improvement activities to enhance processes, reduce waste, and improve product reliability.
* Ensure the laboratory environment and equipment meet operational and cleanliness standards.
* Analyze and interpret test data, including statistical calculations (cpk, ppk, standard deviations, trends, etc.), and communicate results in clear, concise reports or presentations.
* Enforce compliance with safety regulations and promote a culture of workplace safety.
* Execute quality checks per Control Plans/QRRs and document objective evidence.
* Stop production if processes produce nonconforming product or waste.
* Validate gauges, initiate recalls when calibration issues are found, and ensure corrective actions.
* Control and quarantine nonconforming product, escalating to supervision and Quality Assurance as necessary.
* Maintain current knowledge of quality documentation, requesting updates or revisions when appropriate.
* Perform other related duties as assigned by supervision.
Qualifications:
* Education & Experience:
* Associate's Degree in Quality, Engineering Technology, or related field; or equivalent work experience.
* Minimum of five (5) years of quality assurance experience in a manufacturing environment, preferably in metrology.
* ASQ Certified Quality Technician (CQT) strongly preferred.
* Technical Skills:
* Proficient in operating manual and DCC/CMM systems and vision measuring systems.
* Strong ability to interpret engineering drawings, with emphasis on GD&T and 3D datum structures.
* Advanced data analysis skills using Microsoft Excel or equivalent tools (e.g., cpk, ppk, SPC analysis).
* Solid math skills applicable to measurement, SPC, GD&T, and MSA.
* Knowledge of ISO 9001:2015 and IATF 16949:2016 standards.
* Communication Skills:
* Ability to read, write, and interpret technical content in English.
* Strong verbal and written communication skills for cross-functional collaboration.
* Other Requirements:
* Physical ability to work safely in a manufacturing and lab environment (standing, kneeling, lifting product, vision acuity for inspection, etc.).
* Work distribution: Lab (40%), Manufacturing Floor (20%), Desk/Computer (40%).
Diversity & Inclusion Statement
UPG Electrical is an equal opportunity employer committed to a diverse and inclusive workforce.
Inter Organization Transfer (IOT) - Principal Cost Control Analyst - P3 - (Onsite)
Quality control analyst job in Forest, MS
**Country:** United States of America ** Onsite **U.S. Citizen, U.S. Person, or Immigration Status Requirements:** U.S. citizenship is required, as only U.S. citizens are authorized to access certain necessary systems.
**Security Clearance:**
None/Not Required
At Raytheon, the foundation of everything we do is rooted in our values and a higher calling - to help our nation and allies defend freedoms and deter aggression. We bring the strength of more than 100 years of experience and renowned engineering expertise to meet the needs of today's mission and stay ahead of tomorrow's threat. Our team solves tough, meaningful problems that create a safer, more secure world.
Operations Supply Chain (OSC) within Raytheon supporting Land & Air Defense System (LADS) Strategic Business Unit has an immediate opening for a Principal Specialist, Program Controls Financial Analyst to join our team supporting inter organization contracts.
As a member of the OSC Finance team, the successful candidate will be able to train a group of financial analysts responsible for the daily business and financial activities for programs within the Inter organization transfer (IOT) function. You will be responsible for cost/schedule control and analysis, Earned Value Management Systems (EVMS), Forecasting, Estimate-at-Completion (EAC), Latest Revised Estimates (LRE), variance analysis, data reviewing and reporting, partnering with the Program Manager and CAMs, and providing financial leadership in the successful execution of various production contracts. You will drive the operations finance process, monitor program health and compliance, and partner with other functional team members to improve program financial metrics. In addition, this position is responsible for actively identifying risks that affect cost and/or schedule and providing proactive analysis of all financial aspects of the responsible programs. Performance of additional ad-hoc analysis will be required as well as support of 5 Year and AOP forecasting.
The ideal candidate would be able to work in a challenging fast paced team environment, have a strong earned value analysis skillset, be a success-minded team member who possesses strong self-initiative and multi-tasking skills, be able to provide analytical support while under critical deadlines and be involved in process improvement initiatives. Additionally, the ability to effectively communicate analysis and results with RMD East IOT customer is important to this role.
**What You Will Do**
+ You will be responsible for supporting the financial performance and execution of programs in the LADS IOT portfolio. This role requires a business partner approach to independent work effort under the direction of finance management.
+ You will be responsible for implementing, reporting, and maintaining financial data within SAP APEX and other standard company tools. You should be able to problem-solve given sufficient input and create methods to analyze data and identify potential issues.
+ Implementation and maintenance of Earned Value Management ensuring compliance and accurate reporting.
+ Establish and maintain program logs (MR, UB, BCRs, etc.)
+ Develop and support Bi-Annual Estimate-at-Completion (EAC) and Monthly Latest Revised Estimate (LRE)
+ Prepare and lead program financial forecasts, monitor actual costs, and explain variances to plans and forecasts.
+ Financial point of contact for Program Management and be able to provide financial guidance to Program Operations Managers and non-finance organizations including Engineering, Supply Chain, and Operations.
**Qualifications You Must Have**
+ **Typically requires:** A University Degree or equivalent experience and minimum 5 years prior relevant experience, _or_ An Advanced Degree in a related field and minimum 3 years experience
+ Experience in using SAP Business Systems APEX EV & PRISM EV.
+ Program Controls experience with data analysis, reporting and/or process improvement.
+ Experience with Accounting/Financial information systems and Earned Value (EV) tools.
+ Experience with Microsoft Excel (i.e., pivot tables, advanced formulas), Word and/or PowerPoint.
**Qualifications We Prefer**
+ Previous experience using SAP, APEX, APEX EV, Business Warehouse, and Program Management Excellence (PMX) preferred.
+ Demonstrated analytical and problem-solving skills.
+ Ability to work in a highly collaborative team setting.
+ Must be detail oriented .
+ Self-starter and takes ownership of assignments .
+ Willing and able to learn new systems/tools and processes.
+ Excellent oral and written communication skills, including demonstrated ability to communicate clearly and concisely across functional teams and with immediate management.
**What We Offer**
+ Our values drive our actions, behaviors, and performance with a vision for a safer, more connected world. At RTX we value: Trust, Respect, Accountability, Collaboration, and Innovation.
**Learn More & Apply Now!**
+ Please consider the following role type definition as you apply for this role. Onsite: Employees who are working in Onsite roles will work primarily onsite. This includes all production and maintenance employees, as they are essential to the development of our products.
**_As part of our commitment to maintaining a secure hiring process, candidates may be asked to attend select steps of the interview process in-person at one of our office locations, regardless of whether the role is designated as on-site, hybrid or remote._**
The salary range for this role is 82,000 USD - 164,000 USD. The salary range provided is a good faith estimate representative of all experience levels.
RTX considers several factors when extending an offer, including but not limited to, the role, function and associated responsibilities, a candidate's work experience, location, education/training, and key skills.
Hired applicants may be eligible for benefits, including but not limited to, medical, dental, vision, life insurance, short-term disability, long-term disability, 401(k) match, flexible spending accounts, flexible work schedules, employee assistance program, Employee Scholar Program, parental leave, paid time off, and holidays. Specific benefits are dependent upon the specific business unit as well as whether or not the position is covered by a collective-bargaining agreement.
Hired applicants may be eligible for annual short-term and/or long-term incentive compensation programs depending on the level of the position and whether or not it is covered by a collective-bargaining agreement. Payments under these annual programs are not guaranteed and are dependent upon a variety of factors including, but not limited to, individual performance, business unit performance, and/or the company's performance.
This role is a U.S.-based role. If the successful candidate resides in a U.S. territory, the appropriate pay structure and benefits will apply.
RTX anticipates the application window closing approximately 40 days from the date the notice was posted. However, factors such as candidate flow and business necessity may require RTX to shorten or extend the application window.
_RTX is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, age, disability or veteran status, or any other applicable state or federal protected class. RTX provides affirmative action in employment for qualified Individuals with a Disability and Protected Veterans in compliance with Section 503 of the Rehabilitation Act and the Vietnam Era Veterans' Readjustment Assistance Act._
**Privacy Policy and Terms:**
Click on this link (******************************************************** to read the Policy and Terms
Raytheon Technologies is An Equal Opportunity/Affirmative Action Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or veteran status, age or any other federally protected class.
Laboratory Analyst III
Quality control analyst job in Starkville, MS
The Mississippi State Chemical Laboratory (MSCL) is searching for an advanced laboratory analytical level analyst that performs highly technical and advanced scientific and/or instrumental analysis procedures in a specialized area, utilizing both standard and non-routine methodologies and procedures. This analyst will conduct analyses that rely on advanced instrumentation and complex computer software and develop and implement complex analytical techniques. This position is distinguished from the Laboratory Analyst II by the independent and self-directed nature of the work and by its required advanced knowledge in areas of inorganic chemistry, organic chemistry, or microbiology.
Salary Grade: 13
Please see Staff Compensation Structure or Skilled Crafts and Service Maintenance Compensation Schedule for salary ranges. For salary grade UC, these positions are "Unclassified" and salary ranges are determined by the hiring department.
Department Profile:
The Mississippi State Chemical Laboratory (MSCL) is a state-appropriated regulatory agency for the State of Mississippi as well as a fee-for-service laboratory located on the campus of Mississippi State University. MSCL is dedicated to ensuring the quality and safety of fertilizers, pesticides, animal feeds, petroleum products, and manufactured and retail food. It provides fast, defensible, and reliable analytical data to:
1. The State's regulatory agencies, including MDAC Bureau of Plant Industry.
2. The State's federations and councils, such as the MS Farm Bureau and Delta Council.
3. The State's industries, including Poultry, Catfish, and Manufacturing.
4. The State's citizens.
The MSCL adheres to the highest professional standards and provides quality analytical services in a timely manner.
Essential Duties and Responsibilities:
1. Performs advanced scientific and/or instrumental analyses exercising independent judgment in data interpretation and evaluation of compliance with regulatory requirements as promulgated by federal agencies, state agencies, and other regulatory bodies. Advanced-level analytical techniques could include: GC, GC/MS, LC, HPLC, ICP, ICP/MS, microscopic, microbiological and/or other analyses as appropriate.
2. Provides technical expertise for all aspects of environmental analyses in a specialized area; where applicable, researches special environmental/analytical problems and writes reports of findings; participates in interdepartmental meetings on a range of specialized technical and/or scientific subjects as needed.
3. Develops, implements, and maintains appropriate QA/QC controls and procedures. Integrates technical knowledge of regulatory requirements and applicable standards into all laboratory practices and procedures in a specialized area. Manages special projects and assignments related to assigned specialized area.
4. Participates in proficiency studies to demonstrate analytical competency, to examine and investigate problematic areas, and to research and develop improved preparatory and/or analytical techniques.
5. Gathers, evaluates, and interprets analytical and environmental data to determine regulatory compliance, ambient conditions, and process control trending.
6. Troubleshoots and maintains sophisticated analytical instrumentation, performing day-to-day routine care and more complex periodic maintenance, as well as reporting, investigating, correcting, and documenting serious instrumental malfunctions and problems.
7. May review analytical data produced by other analysts and specialists, following established standards and requirements; evaluates data for integrity and validity of the results.
8. Trains and/or leads analytical personnel engaged in preparatory and analytical work in designated specialization; serves as a reference and provides technical assistance to project managers and other personnel.
9. Contributes to development and implementation of short and long-range laboratory plans and objectives; participates in inter-departmental meetings on organizational, technical, and/or scientific subjects when assigned.
10. Researches and acquires new knowledge in the field by reading, attending seminars and workshops.
11. Performs related duties as assigned.
Minimum Qualifications:
A professional employee must possess a bachelor's degree in chemistry (biochemistry, analytical, inorganic, and organic), toxicology, microbiology, or related field OR completion of a bachelor's degree program at an accredited college or university with a minimum equivalent of 34 semester hours in toxicology, chemistry, microbiology, or related field and a minimum of 6 years of analytical testing experience.
Special Requirements:
Requires a degree in chemistry, environmental science, biology, microbiology, or a related field, and three to five years of progressively responsible instrumental and/or scientific chemical analysis experience, or equivalent
Preferred Qualifications:
1. Master's degree in chemistry or in a related field,
2. Demonstrate competence in the principles, methods, and techniques of analytical chemistry.
3. Field and laboratory work experience beyond the minimum required.
Substitution allowed:
A master's degree in chemistry, microbiology, or related field and a minimum of 3 years of relevant experience and demonstrated competence may be substituted to begin at the Laboratory Analyst III position.
A professional employee with a doctoral degree in chemistry, microbiology, or related field with 1 year of relevant experience and demonstrated competence can begin work at the Laboratory Analyst III level.
Knowledge, Skills, and Abilities:
Knowledge of:
• Principles of scientific analysis and established laboratory methodology.
• Inorganic chemistry, organic chemistry, environmental sciences, biology, mathematics, microbiology and/or other related scientific fields.
• Laboratory and chemical principles, terminology, material, equipment, procedures, and techniques.
• Quality control and quality assurance techniques.
• Regulatory requirements related to laboratory analysis.
• Principles of laboratory ethics as applied to the production of valid analytical data.
Ability to:
• Independently learn and develop new complex laboratory procedures.
• Perform complex laboratory analyses and produce high quality data.
• Work safely with hazardous substances.
• Perform QA/QC activities objectively and without outside influence.
• Establish and maintain effective working relationships with coworkers and managers, including representative outside groups and agencies.
• Research environmental and analytical problems.
Skilled in:
• Using complex analytical techniques including GC, GC/MS, LC, HPLC, ICP, ICP/MS, Microscopic, Microbiological and/or other analyses as appropriate.
• Advanced data processing and reporting using spreadsheets, databases, and specialized software.
• Interpreting analytical data and evaluating results.
• Troubleshooting analytical problems.
• Utilizing laboratory equipment and computers to conduct sample and data analyses.
• Oral and written communication and communicating technical concepts.
• Diagnosing and correcting problems with laboratory equipment and/or procedures.
• Providing direction to staff engaged in specialization, including assigning, and reviewing work.
• Demonstrating techniques and providing training to others.
Knowledge of:
• Principles of scientific analysis and established laboratory methodology.
• Inorganic chemistry, organic chemistry, environmental sciences, biology, mathematics, microbiology and/or other related scientific fields.
• Laboratory and chemical principles, terminology, material, equipment, procedures, and techniques.
• Quality control and quality assurance techniques.
• Regulatory requirements related to laboratory analysis.
• Principles of laboratory ethics as applied to the production of valid analytical data.
Ability to:
• Independently learn and develop new complex laboratory procedures.
• Perform complex laboratory analyses and produce high quality data.
• Work safely with hazardous substances.
• Perform QA/QC activities objectively and without outside influence.
• Establish and maintain effective working relationships with coworkers and managers, including representative outside groups and agencies.
• Research environmental and analytical problems.
Skilled in:
• Using complex analytical techniques including GC, GC/MS, LC, HPLC, ICP, ICP/MS, Microscopic, Microbiological and/or other analyses as appropriate.
• Advanced data processing and reporting using spreadsheets, databases, and specialized software.
• Interpreting analytical data and evaluating results.
• Troubleshooting analytical problems.
• Utilizing laboratory equipment and computers to conduct sample and data analyses.
• Oral and written communication and communicating technical concepts.
• Diagnosing and correcting problems with laboratory equipment and/or procedures.
• Providing direction to staff engaged in specialization, including assigning, and reviewing work.
• Demonstrating techniques and providing training to others.
Working Conditions and Physical Effort
• Fine Motor Skills: Laboratory analysts need good fine motor skills to handle delicate equipment, pipettes, and small samples with precision. This includes tasks such as pipetting, micro-dispensing, and manipulating small objects.
• Visual Acuity: Good vision is essential for observing samples, reading measurements, and other tasks. Corrective eyewear may be necessary.
• Color Vision: Some laboratory work may involve the ability to distinguish colors, especially in fields like histology or chemistry where color changes indicate reactions or results.
• Manual Dexterity: Laboratory analysts must have the ability to perform tasks that require steady hands and coordination, including operating laboratory instruments, adjusting settings, and conducting intricate procedures.
• Standing or Sitting: Depending on the laboratory and the specific job tasks, laboratory analysts may need to stand for extended periods while working at laboratory benches or sit at computer workstations for data analysis and reporting.
• Lifting and Carrying: There may be a need to lift and carry laboratory supplies, equipment, or samples, which can vary in weight. The specific weight requirements will depend on the laboratory setting.
• Bending and Stooping: Laboratory analysts may need to access samples, equipment, or lower shelves, which may require bending or stooping.
• Wearing Personal Protective Equipment (PPE): PPE is mandatory. This can include wearing gloves, lab coats, safety goggles, and, in some cases, respirators. Comfortably wearing and using PPE is essential.
• Repetitive Movements: Laboratory work often involves repetitive movements, such as pipetting, which can put strain on wrists and hands. Proper ergonomics and the use of ergonomic equipment can help reduce the risk of repetitive strain injuries.
• Adequate Mobility: Laboratory analysts should have the ability to move around the laboratory space, reach equipment, and navigate safely in a potentially crowded environment.
At this time, MSU is unable to offer H-1B visa sponsorship for this role. This applies until further notice.
Instructions for Applying:
Link to apply: ***********************************
All applicants must apply online and attach a cover letter, current resume or curriculum vitae, and the complete contact information for at least three professional references.
Restricted Clause:
Position is contingent upon continued availability of funding.
Equal Employment Opportunity Statement:
Mississippi State University is an equal opportunity institution. Discrimination is prohibited in university employment, programs or activities based on race, color, ethnicity, sex, pregnancy, religion, national origin, disability, age, sexual orientation, genetic information, status as a U.S. veteran, or any other status to the extent protected by applicable law. Questions about equal opportunity programs or compliance should be directed to the Office of Civil Rights Compliance, 231 Famous Maroon Band Street, P.O. 6044, Mississippi State, MS 39762, **************.
What do I do if I need an accommodation?
In compliance with the ADA Amendments Act (ADA), if you have a disability and would like to request an accommodation in order to apply for a position with Mississippi State University, please contact the Department of Human Resources Management at tel: ************** or *******************.
If you have any questions regarding this policy, contact the Department of Human Resources Management at ************** or *******************. Upon request, sections of this job listing are available in large print, and readers are available to assist the visually impaired.