CHEMIST
Chemist job in Washington, DC
The PALACE Acquire Program offers you a permanent position upon completion of your formal training plan. As a Palace Acquire Intern you will experience both personal and professional growth while dealing effectively and ethically with change, complexity, and problem solving. The program offers a 3-year formal training plan with yearly salary increases. Promotions and salary increases are based upon your successful performance and supervisory approval.
Summary
The PALACE Acquire Program offers you a permanent position upon completion of your formal training plan. As a Palace Acquire Intern you will experience both personal and professional growth while dealing effectively and ethically with change, complexity, and problem solving. The program offers a 3-year formal training plan with yearly salary increases. Promotions and salary increases are based upon your successful performance and supervisory approval.
Overview
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Accepting applications
Open & closing dates
09/29/2025 to 09/28/2026
Salary $55,486 to - $99,314 per year
Salary will vary by location.
Pay scale & grade GS 7 - 9
Locations
Few vacancies in the following locations:
Gunter AFB, AL
Maxwell AFB, AL
Davis Monthan AFB, AZ
Edwards AFB, CA
Show morefewer locations (38)
Los Angeles, CA
Travis AFB, CA
Vandenberg AFB, CA
Buckley AFB, CO
Cheyenne Mountain AFB, CO
Peterson AFB, CO
Schriever AFB, CO
Joint Base Anacostia-Bolling, DC
Cape Canaveral, FL
Eglin AFB, FL
Hurlburt Field, FL
MacDill AFB, FL
Tyndall AFB, FL
Robins AFB, GA
Barksdale AFB, LA
Hanscom AFB, MA
Aberdeen Proving Ground, MD
Andrews AFB, MD
Offutt AFB, NE
Holloman AFB, NM
Kirtland AFB, NM
Nellis AFB, NV
Rome, NY
Heath, OH
Wright-Patterson AFB, OH
Tinker AFB, OK
Dyess AFB, TX
Fort Sam Houston, TX
Goodfellow AFB, TX
Lackland AFB, TX
Randolph AFB, TX
Hill AFB, UT
Dahlgren, VA
Langley AFB, VA
Pentagon, Arlington, VA
Fairchild AFB, WA
Joint Base Lewis-McChord, WA
Warren AFB, WY
Remote job No Telework eligible No Travel Required Occasional travel - You may be expected to travel for this position. Relocation expenses reimbursed No Appointment type Internships Work schedule Full-time Service Competitive
Promotion potential
12
Job family (Series)
* 1320 Chemistry
Supervisory status No Security clearance Secret Drug test No Position sensitivity and risk Noncritical-Sensitive (NCS)/Moderate Risk
Trust determination process
* Suitability/Fitness
Financial disclosure No Bargaining unit status No
Announcement number K-26-DHA-12806437 Control number 846730500
This job is open to
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The public
U.S. Citizens, Nationals or those who owe allegiance to the U.S.
Students
Current students enrolled in an accredited high school, college or graduate institution.
Recent graduates
Individuals who have graduated from an accredited educational institute or certificate program within the last 2 years or 6 years for Veterans.
Clarification from the agency
This public notice is to gather applications that may or may not result in a referral or selection.
Duties
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GS-07
* Performs developmental assignments in the application of professional principles, techniques, methods, and procedures relating to the investigation, analysis, and interpretation of the composition, molecular structure, and properties of substances.
* Performs recurring assignments. Independently performs recurring assignments of limited, but gradually increasing, difficulty and complexity as directed by the supervisor or team lead.
* Participates in special initiatives, studies, and projects. Works with other specialists to plan, perform research, and conduct special initiatives, studies, and projects.
* Prepares written correspondence and other documentation. Drafts or prepares a variety of documents to include responses to routine inquiries, reports, letters, and other related material.
GS-09
* Performs developmental assignments in the application of professional principles, techniques, methods, and procedures relating to the investigation, analysis, and interpretation of the composition, molecular structure, and properties of substances, the transformations which they undergo, and the amounts of matter and energy included in these transformations.
* Performs recurring assignments. Incumbent determines the practices and procedures to use in accomplishing conventional tasks, and
interprets and adapts guidelines in order to resolve procedural or factual issues
* Carries out special projects and participates in special initiatives and studies. Works with other specialists in planning and conducting studies.
* Prepares written correspondence and other documentation. Drafts or prepares a variety of documents to include
newsletter items, responses to routine inquiries, reports, letters, and other related documents.
Requirements
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Conditions of employment
* Some position under this announcement may require either a secret, top secret, or special sensitive clearance.
* This public notice is to gather applications that may or may not result in a referral or selection.
* Please read this Public Notice in its entirety prior to submitting your application for consideration.
* U.S. Citizenship is required
* Males must be registered for Selective Service, see ***********
* PCS expenses if authorized will be paid IAW JTR and Air Force Regulations
* Recruitment incentives may be authorized
* A security clearance may be required
* Mobility - you may be required to relocate during or after completion of your training
* You will be required to serve a one year probationary period
* Successful completion of all training and regulatory requirements as identified in the applicable training plan
* Must meet suitability for Federal employment
* Disclosure of Political Appointments
* Grade Point Average - 2.95 or higher out of a possible 4.0
* Total salary varies depending on location of position
* Position may be subject to random drug testing
Qualifications
BASIC REQUIREMENTS:
Degree: physical sciences, life sciences, or engineering that included 30 semester hours in chemistry, supplemented by course work in mathematics through differential and integral calculus, and at least 6 semester hours of physics.
You may qualify if you meet one of the following:
1. GS-7: You must have completed or will complete a 4-year course of study leading to a bachelor's from an accredited institution AND must have documented Superior Academic Achievement (SAA) at the undergraduate level in the following:
a) Grade Point Average 2.95 or higher out of a possible 4.0 as recorded on your official transcript or as computed based on 4 years of education or as computed based on courses completed during the final 2 years of curriculum; OR 3.45 or higher out of a possible 4.0 based on the average of the required courses completed in your major field or the required courses in your major field completed during the final 2 years of your curriculum.
2. GS-9: You must have completed 2 years of progressively higher-level graduate education leading to a master's degree or equivalent graduate degree:
a) Grade Point Average - 2.95 or higher out of a possible 4.0 as recorded on your official transcript or as computed based on 4 years of education or as computed based on courses completed during the final 2 years of curriculum; OR 3.45 or higher out of a possible 4.0 based on the average of the required courses completed in your major field or the required courses in your major field completed during the final 2 years of your curriculum. If more than 10 percent of total undergraduate credit hours are non-graded, i.e. pass/fail, CLEP, CCAF, DANTES, military credit, etc. you cannot qualify based on GPA.
KNOWLEDGE, SKILLS AND ABILITIES (KSAs): Your qualifications will be evaluated on the basis of your level of knowledge, skills, abilities and/or competencies in the following areas:
* Professional knowledge of the concepts, theories, principles, and standard practices of Chemistry, methods, and techniques of the occupation sufficient to perform assignments.
* Skill in applying the principles, concepts, and practices of the occupation to perform assignments.
* Knowledge of the occupation to perform studies and prepare reports, documentation, and correspondence to communicate factual and procedural information clearly.
* Ability to communicate information clearly, both orally and in writing, as well as work in a professional manner with peers and management.
* Ability to plan/organize work, consult effectively with coworkers and apply analytical investigative techniques to accomplish work in the subject-matter field.
PART-TIME OR UNPAID EXPERIENCE: Credit will be given for appropriate unpaid and or part-time work. You must clearly identify the duties and responsibilities in each position held and the total number of hours per week.
VOLUNTEER WORK EXPERIENCE: Refers to paid and unpaid experience, including volunteer work done through National Service Programs (i.e., Peace Corps, AmeriCorps) and other organizations (e.g., professional; philanthropic; religious; spiritual; community; student and social). Volunteer work helps build critical competencies, knowledge and skills that can provide valuable training and experience that translates directly to paid employment. You will receive credit for all qualifying experience, including volunteer experience.
Education
This position has an education requirement. You MUST provide transcripts to support your educational claims. Education must be accredited by an accrediting institution recognized by the U.S. Department of Education. **************************************************
Please submit copies of all transcripts to include transferred hours-
Official copies are not required at time of application. If selected, you will be required to provide official copies of all transcripts. *NOTE*
Degree Audits are not accepted.
If you qualify based on undergraduate education and you have not graduated prior to applying to this position, you may be offered a position contingent upon your final grade point average or class ranking.
IF USING EDUCATION TO QUALIFY: You MUST provide transcripts to support your educational claims. Education must be accredited by an accrediting institution recognized by the U.S. Department of Education.
PLEASE SUBMIT COPIES OF ALL TRANSCRIPTS TO INCLUDE TRANSFERRED HOURS - OFFICIAL COPIES ARE NOT REQUIRED AT TIME OF APPLICATION. IF SELECTED, YOU WILL BE REQUIRED TO PROVIDE OFFICIAL COPIES OF ALL TRANSCRIPTS. *NOTE* Degree Audits are not accepted.
FOREIGN EDUCATION: Education completed in foreign colleges or universities may be used to meet the requirements. You must show proof the education credentials have been deemed to be at least equivalent to that gained in conventional U.S. education program. It is your responsibility to provide such evidence when applying.
Additional information
For DHA Positions:These positions are being filled under Direct-Hire Authority for the Department of Defense for Post-Secondary Students and Recent Graduates. The Secretary of the Air Force has delegated authority by the Office of the Secretary of Defense to directly appoint qualified post-secondary students and recent graduates directly into competitive service positions; these positions may be professional or administrative occupations and are located Air Force-Wide. Positions may be filled as permanent or term with a full-time or part-time work schedule. Pay will vary by geographic location.
* The term "Current post-secondary student" means a person who is currently enrolled in, and in good academic standing at a full-time program at an institution of higher education; and is making satisfactory progress toward receipt of a baccalaureate or graduate degree; and has completed at least one year of the program.
* The term "recent graduate" means a person who was awarded a degree by an institution of higher education not more than two years before the date of the appointment of such person, except in the case of a person who has completed a period of obligated service in a uniform service of more than four years.
Selective Service: Males born after 12-31-59 must be registered or exempt from Selective Service. For additional information, click here.
Direct Deposit: All federal employees are required to have direct deposit.
Disabled veteran leave is available to a Federal employee hired on/after 5 Nov 2016, who is a veteran with a service-connected disability rating of 30% or more. For more information, click here.
If you have questions regarding this announcement and have hearing or speech difficulties click here.
Tax Law Impact for PCS: On 22-Dec-2017, Public Law 115-97 - the "Tax Cuts and Jobs Act of 2017" suspended qualified moving expense deductions along with the exclusion for employer reimbursements and payments of moving expenses effective 01-Jan-2018 for tax years 2018 through 2025. When you perform a Civilian Permanent Change of Station (PCS) with the government, the Internal Revenue Service (IRS) considers the majority of your entitlements to be taxable. Visit GSA Bulletin FTR 20-04 here for additional information.
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Candidates should be committed to improving the efficiency of the Federal government, passionate about the ideals of our American republic, and committed to upholding the rule of law and the United States Constitution.
Benefits
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A career with the U.S. government provides employees with a comprehensive benefits package. As a federal employee, you and your family will have access to a range of benefits that are designed to make your federal career very rewarding. Opens in a new window Learn more about federal benefits.
Review our benefits
Eligibility for benefits depends on the type of position you hold and whether your position is full-time, part-time or intermittent. Contact the hiring agency for more information on the specific benefits offered.
How you will be evaluated
You will be evaluated for this job based on how well you meet the qualifications above.
For DHA Positions:
These positions are being filled under Direct-Hire Authority for the DoD for Post-Secondary Students and Recent Graduates. The Secretary of the Air Force has delegated authority by the Office of the Secretary of Defense to directly appoint qualified students and recent graduates directly into competitive service positions; positions may be professional or administrative occupations and located Air Force-Wide. Positions may be filled as permanent/term with a full-time/part-time work schedule. Pay will vary by geographic location.
* The term "Current post-secondary student" means a person who is currently enrolled and in good academic standing at a full-time program at an institution of higher education; and is progressing toward a baccalaureate or graduate degree; and has completed at least 1 year of the program.
* The term "recent graduate" means a person awarded a degree by an institution of higher education not more than 2 years before the date of the appointment of such person, except in the case of a person who has completed a period of obligated service in a uniform service of more than 4 years.
Your latest resume will be used to determine your qualifications.
Your application package (resume, supporting documents, and responses to the questionnaire) will be used to determine your eligibility, qualifications, and quality ranking for this position. Please follow all instructions carefully. Errors or omissions may affect your rating or consideration for employment.
Your responses to the questionnaire may be compared to the documents you submit. The documents you submit must support your responses to the online questionnaire. If your application contradicts or does not support your questionnaire responses, you will receive a rating of "not qualified" or "insufficient information" and you will not receive further consideration for this job.
Applicants who disqualify themselves will not be evaluated further.
Benefits
Help
A career with the U.S. government provides employees with a comprehensive benefits package. As a federal employee, you and your family will have access to a range of benefits that are designed to make your federal career very rewarding. Opens in a new window Learn more about federal benefits.
Review our benefits
Eligibility for benefits depends on the type of position you hold and whether your position is full-time, part-time or intermittent. Contact the hiring agency for more information on the specific benefits offered.
Required documents
Required Documents
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The following documents are required and must be provided with your application for this Public Notice. Applicants who do not submit required documentation to determine eligibility and qualifications will be eliminated from consideration. Other documents may be required based on the eligibility/eligibilities you are claiming. Click here to view the AF Civilian Employment Eligibility Guide and the required documents you must submit to substantiate the eligibilities you are claiming.
* Online Application - Questionnaire
* Resume: Your resume may NOT exceed two pages, and the font size should not be smaller than 10 pts. You will not be considered for this vacancy if your resume is illegible/unreadable. Additional information on resume requirements can be located under "
Scientist II or III - Analytical Chemist Metrology Specialist
Chemist job in Washington, DC
We are looking to fill a **Scientist II or III - Metrology Specialist** position working as a full-time employee of Parexel FSP on long-term assignment onsite at one of our clients located in **Rahway, NJ.** This position offers full benefits, sick time, 401K, paid holidays, and paid time off. **This position does not offer sponsorship.**
**Metrology specialist is responsible for the oversight of regulated and non-regulated laboratory equipment** . This role will oversee the lifecycle of the lab instrumentation covering acquisition and installation, performance or coordination of routine maintenance, computer system validation, and regulated systems retirement
**Qualifications -** B.S./M.S. in Chemistry, Biochemistry, Engineering, or a related discipline
+ **Scientist II** - B.S. with 1-2 years of relevant experience or M.S. with 0-1 years of relevant experience
+ **Scientist III** - B.S. with 3-5 years of relevant experience or M.S. with 1-2 years of relevant experience
**Responsibilities**
+ Prepare, review, and approve instrument/equipment documentation such as master equipment lists, qualification documentation, and calibration documentation
+ Coordinate service activities across a variety of vendors and service engineers while building and maintaining strong working relationships
+ Gain a working knowledge of laboratory equipment to facilitate with troubleshooting and/or perform maintenance or calibration activities
+ Participate in computer system validation activities associated with new or upgraded equipment or software packages
+ Support the purchase, installation, and equipment qualification of new laboratory equipment
+ Collaborate with metrology staff across multiple testing labs and sites for process improvement, cross-training and cross-site support
+ Originate and progress Notice of Event (NOE) and Change Management (CM) records
+ Perform and document investigations and assist in developing/implementing CAPA plans
+ Represent the laboratory on all aspects of laboratory equipment during audits
+ Ensure compliance with all regulatory requirements (cGMP) and internal policies and procedures
**Required Skills and Experience**
+ Experience working within a regulated (GMP) laboratory
+ **Experience maintaining or operating laboratory equipment including HPLCs, GCs, UVs, dissolution systems, or other specialized computerized systems**
+ Familiarity with standalone computer system validation requirements
+ Highly organized, and capable of multi-tasking to manage a variety of laboratory equipment or system related schedules, documents, and maintenance tasks
+ Capable of working independently under moderate supervision
+ Strong verbal and written communication skills
+ Strong interpersonal skills. Comfortable interacting with a variety of on-site and off-site collaborators
**Desired Skills and Experience**
+ Experience with maintenance of analytical instrumentation such as HPLC, UPLC, GC, UV, IR, Karl Fischer, and dissolution with ability to troubleshoot them.
+ Experience with computerized standalone systems GMP validation requirements
+ Familiarity with authoring relevant instrument standard operating procedures (SOPs)
**About Parexel**
Parexel FSP includes the CMC Operations group. We provide pharmaceutical and biopharmaceutical companies with qualified and talented technical professionals to support the development and delivery of new therapies.
For results-driven and caring individuals who want to make a meaningful difference in the world, Parexel is trusted by life sciences companies to meet their long-term staffing needs for scientists and engineers and related professionals in discovery and development of novel therapies, keeping patients at the center of everything we do, and where an inclusive community helps you be your best, transforming any career into a life-changing achievement.
**Come join us!**
\#LI-DK1
EEO Disclaimer
Parexel is an equal opportunity employer. Qualified applicants will receive consideration for employment without regard to legally protected status, which in the US includes race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or protected veteran status.
Supervisory Chemist
Chemist job in Washington, DC
General Job Information This position is located in the Department of Forensic Sciences (DFS), Public Health Laboratory (PHL) Division. The mission of the DFS is to provide high-quality, timely, accurate, and reliable forensic science services using best practices and best available technology, focusing on unbiased science and transparency to enhance public safety and health.
The incumbent serves as a Supervisory Clinical Chemist who supports the chemical terrorism (CT) initiative under Centers for Disease Control and Prevention (CDC) cooperative agreement and performs as the CT Coordinator for the District.
Duties and Responsibilities
Performs specific analytical tests utilizing protocols transferred from the Centers for Disease Control and other general methods where there are established protocols and practices available. Under minimal supervision, modifies existing methodologies for new testing compounds, matrixes or testing instrumentation. Acts as lead technical specialist in two of three analytical platforms (GC-MS, LC-MS/MS, high resolution mass spectrometry or ICP MS), provides training and acts as a subject matter expert (SME) for the method and instrumentation. Performs technical review of data collected from unit staff; Independently leads projects including but not limited to: method development, research projects, and training programs. Leads validation of new methods and protocols; maintains journals, logs and other records pertinent to method validation. Reviews scientific literature to determine the chemical and biological characteristics of samples to be analyzed to facilitate sample preparation and analysis. Leads in interpretation and evaluation of test results to determine validity and scientific significance.
Performs periodic maintenance and calibration of instruments and related equipment within the chemistry laboratory. Performs preventive maintenance and quality control on instruments as outlined in the manufacturer's instructions and Standard Operating Procedures. Leads in the training of lower-level personnel and students in the theoretical and practical aspects of chemistry and quality assurance. Prepares reports and maintains records of work performed on patient specimens and samples; maintains reagent lot numbers for quality control and files such records in an appropriate manner. Provides the full range of supervisory services, as required to manage and direct the work efforts of subordinate staff and activities of assigned operations. Develop quantitative and qualitative measures for evaluating the work performance of staff. Supervises and assigns duties and responsibilities; formulates overall plans for resources; approves and disapproves leave requests; recommends job selections, promotions, incentive recognition and corrective or adverse actions; establishes work standards; and identifies developmental and training needs.
Qualifications and Education
Degree: physical sciences, life sciences, or engineering that included 30 semester hours in chemistry, supplemented by course work in mathematics through differential and integral calculus, and at least 6 semester hours of physics.
Or
Combination of education and experience -- course work equivalent to a major as shown in A above, including at least 30 semester hours in chemistry, supplemented by mathematics through differential and integral calculus, and at least 6 semester hours of physics, plus appropriate experience or additional education.
Licenses and Certifications
None
Working Conditions/Environment
The work is performed in an office setting and laboratory setting. The office setting is when preparing documentation and the laboratory setting is during the testing and analysis phase. The incumbent may be exposed to hazardous materials, toxic substances, and blood borne pathogens and is required to follow safe laboratory practices and wear protective clothing gear such as laboratory coats, fume hoods, safety goggles, radiation badges, aprons, gloves, and shields, etc. and to adopt sterile techniques.
The nature of the DFS mission necessarily involves the potential risks associated with biological or chemical hazards, including morgue functions. Although contact with these functions is intended to be minimal, the risks are nevertheless possible; training to recognize, address, and mitigate these risks is required as is dealing with potentially personally difficult topics, such as crime, death, and disease.
Other Significant Factors
Tour of Duty: Monday - Friday, 8:30am to 5:00pm
Pay Plan, Series and Grade: MS-1320-13
Promotion Potential: No known promotion potential
Type of Appointment: Management Supervisory Service (MSS). Positions in the Management Supervisory Service (MSS) serve at the pleasure of the appointing authority and may be terminated at any time with or without cause.
Collective Bargaining Unit: This position is not covered under a collective bargaining agreement.
Position Suitability: This position has been deemed Safety Sensitive under the guidelines of the DC Personnel Manual and is subject to mandatory pre-employment and periodic criminal background checks and traffic records checks (as applicable). This position is also subject to mandatory pre-employment and random drug and alcohol testing. In this position, you may be disqualified from employment based on the presence of marijuana in test results, even if you possess a medical card authorizing the use of medical marijuana.
Position Designation: This position has been designated as Essential and acceptance of this offer confirms you agree to adhere to the policies in sections 1271 and 1274 of DPM Chapter 12, regarding essential/emergency employees. As an emergency employee, you will be required to either report to work, stay at work, or telework (if directed to do so) during a declared emergency or during a period of non-emergency where your duties have been deemed as critical District government functions/operations. You may be required to perform other duties outside of your position description during a period of a declared emergency (such as manual labor, shelter services, etc.).
Residency Preference: Applicants claiming "Residency Preference" will be required to maintain residency in the District of Columbia for a minimum of seven (7) years. Failure to do so may result in forfeiture of employment.
EEO Statement: The District of Columbia Government is an Equal Opportunity Employer. All qualified candidates will receive consideration without regard to race, color, religion, national origin, sex, age, marital status, personal appearance, sexual orientation, family responsibilities, matriculation, physical handicap, or political affiliation.
Analytical Chemist
Chemist job in Washington, DC
JRAD has an immediate opening for an Analytical Chemist in Washington DC.
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Analyzes environmental and/or air samples for Chemical contamination
Operates and maintains laboratory equipment (e.g., Gas and Liquid Chromatography, Mass Spectrometers, and performs basic maintenance and checks on common laboratory systems
Uses Laboratory Information Management System (LIMS) software for managing analytical data
Participates in laboratory proficiency testing activities and maintains QAQC records to include performance charts, control limits, and detection and reporting limits for analytical methods governing use of laboratory instrumentation
Maintains operator manuals and procedures, providing training to new staff in the operation and use of Lab equipment and LIMS
Meticulously adheres to laboratory procedures, data management practices and safety protocols in accordance with Laboratory Quality Assurance Plans and safety policies/regulations
Supports formal audits of laboratory quality control systems and practices, the inspection of safety practices and the review of Job Hazard Analyses
Maintains inventory of lab supplies
Required Skills and Education:
Bachelor's Degree in Chemistry, Biochemistry, or similar, from an accredited college or university
More than 3 year of experience with quantitative analysis of chemical compounds, and 2 years' experience with screening environmental samples for toxic industrial compounds (TICs)
Must have demonstrated analytical laboratory skills as evidenced by participation in a Proficiency Test such as a Precision and Accuracy performance test or equivalent
Must have experience with quality management standards (e.g., ISO 17025 or similar), sample preparation methods, techniques, regulations, protocols, safety measures, and the operation and maintenance of chemical laboratory instrumentation
Working knowledge of Microsoft Office products including Excel, Project, Word, Access and Power Point
Excellent written and oral communication skills
Multiple experience level positions available for Journeyman to Senior level Chemists
Minimum of 10 years of experience with a Bachelors Degree, or 6 years of experience with a Masters Degree
Security Clearance
Ability to obtain and maintain a secret security clearance
When you work for JRAD you will never be just a number. We put people before profits!
JRAD is committed to the health and well-being of its employees. We offer more paid time off than the average company upon hire, and the following benefits are available to all full-time employees:
Health Insurance
Dental Insurance
Vision Insurance
Life & Accidental Death and Dismemberment Insurance
Section 125 Flexible Spending Accounts for unreimbursed Medical & Dependent Day Care
Disability Insurance
401K Plan
Tuition Reimbursement
JRAD is an equal opportunity employer as to all protected groups, including protected veterans and individuals with disabilities.
Please note this job description in no way states or implies that these are the only duties to be performed by this employee. The employee will be required to follow any other instructions and to perform any other duties requested by the supervisor.
The JRAD salary range for this position is a general guideline only and not a guarantee of compensation or salary. There are many factors considered when determining the compensation provided in an offer. These factors include, but are not limited to position responsibilities, education, experience, knowledge, skills, and contract terms and conditions.
Analytical Chemist II /Bio-Chemist (Pharmaceutical Manufacturing)
Chemist job in Chantilly, VA
Granules Pharmaceuticals Inc., (GPI) is a subsidiary of Granules India LTD. Over the past 34 years, we have worked towards strengthening our core and we are currently the 10th fastest growing generic pharma company in the US!
With our sites in Chantilly and Manassas, Virginia, we have R&D through manufacturing and packaging of our medicines including pulsatile drug release in tablet and capsule dosage form, orally disintegrating modified release tablets (XR, MR, ER), modified release suspension and controlled substances capabilities in an abuse deterrent technology platform.
We are dedicated to excellence in manufacturing, quality, and commercialization of generic drugs to give customers reliable and affordable options.
**Multiple positions available in QC and R&D**
Job Summary:
The role of QC Biochemist/Analytical Chemist II is responsible for supporting the operations and manufacturing process by performing routine and non-routine analytical testing raw materials, in-process, finished formulations, stability samples, method development and/or transfers, and cleaning validations. Follows standard procedures to complete tasks, some of which may vary in scope, sequence, complexity, and timing. Responsible for the safe and efficient execution of job duties.
JOB DUTIES & RESPONSIBILITIES:
Conduct routine analytical/microbiological testing of raw materials, packaging materials, finished product release and stability using approved methods and various instrumentation while adhering to cGMP and established policies.
Conduct analytical USP method verifications, validations, and method transfer activities for raw materials and finished dosage forms.
Perform the Calibration, Qualification, Preventive maintenance and routine trouble shooting of analytical instruments like UPLC, HPLC, GC, UV spectrophotometer, Dissolution apparatus, KF Auto titrator, FT-IRS spectrophotometer, Polarimeter and Refractometer.
Compile laboratory test data and perform appropriate analyses that include physical (solubility, viscosity),chemical (titration) and analytical (FTIR, HPLC, ICP-MS, UV-Vis, KF, IC) testing etc.
Complete documentation needed to support testing procedures including test forms and logbooks.
Interpret test results, compare them to established specifications and control limits, and ensure appropriateness of data for release. Treats data with a high level of integrity and ethics.
Participate in out-of-specification and failure investigations. Support all aspects of laboratory investigations.
Prepare, review and approve analytical data, technical reports and analytical methods.
Coordinate Microbiological, preservative efficacy/ antimicrobial effectiveness testing requirement as per USP/USP-NF for Active pharmaceutical ingredients, Inactive and Finished products and stability samples for regulatory filings.
Physical Requirements/Working Environment:
Physical & mental requirements e.g. lift 40 pounds, walk across plant/warehouse, business travel (% of time), driving as part of work responsibilities, etc.
Commitment to long hours of work when necessary to achieve goals.
Respirator, lab coat and safety glasses required. Ability to work with potent substances using a glove-box.
Job Type
: Full-time
This Job Is Ideal for Someone Who Is:
Dependable -- more reliable than spontaneous
People-oriented -- enjoys interacting with people and working on group projects
Adaptable/flexible -- enjoys doing work that requires frequent shifts in direction
Detail-oriented -- would rather focus on the details of work than the bigger picture
Achievement-oriented -- enjoys taking on challenges, even if they might fail
Autonomous/Independent -- enjoys working with little direction
Innovative -- prefers working in unconventional ways or on tasks that require creativity
High stress tolerance -- thrives in a high-pressure environment
Requirements
Preferred Knowledge & Skills:
Strong knowledge of the major analytical techniques: HPLC/UPLC, GC, dissolution, etc. FT-IR, FDA/ICH regulations.
Solid knowledge of FDA/ICH regulations.
Required Experience & Education:
BS or MS in Chemistry, Pharmacy, Biochemistry, Biology or Biotechnology or related field.
Minimum 2 - 5 years of experience in using analytical instrument techniques including HPLC/GC/FT-IR, UV-Vis, Dissolution Apparatus, Ovens/Auto Titrators/KF Titrator/Particle size analyzers/ Ion-Chromatography.
Analytical Chemist II /Bio-Chemist (Pharmaceutical Manufacturing)
Chemist job in Chantilly, VA
Job DescriptionDescription:
Granules Pharmaceuticals Inc., (GPI) is a subsidiary of Granules India LTD. Over the past 34 years, we have worked towards strengthening our core and we are currently the 10th fastest growing generic pharma company in the US!
With our sites in Chantilly and Manassas, Virginia, we have R&D through manufacturing and packaging of our medicines including pulsatile drug release in tablet and capsule dosage form, orally disintegrating modified release tablets (XR, MR, ER), modified release suspension and controlled substances capabilities in an abuse deterrent technology platform.
We are dedicated to excellence in manufacturing, quality, and commercialization of generic drugs to give customers reliable and affordable options.
**Multiple positions available in QC and R&D**
Job Summary:
The role of QC Biochemist/Analytical Chemist II is responsible for supporting the operations and manufacturing process by performing routine and non-routine analytical testing raw materials, in-process, finished formulations, stability samples, method development and/or transfers, and cleaning validations. Follows standard procedures to complete tasks, some of which may vary in scope, sequence, complexity, and timing. Responsible for the safe and efficient execution of job duties.
JOB DUTIES & RESPONSIBILITIES:
Conduct routine analytical/microbiological testing of raw materials, packaging materials, finished product release and stability using approved methods and various instrumentation while adhering to cGMP and established policies.
Conduct analytical USP method verifications, validations, and method transfer activities for raw materials and finished dosage forms.
Perform the Calibration, Qualification, Preventive maintenance and routine trouble shooting of analytical instruments like UPLC, HPLC, GC, UV spectrophotometer, Dissolution apparatus, KF Auto titrator, FT-IRS spectrophotometer, Polarimeter and Refractometer.
Compile laboratory test data and perform appropriate analyses that include physical (solubility, viscosity),chemical (titration) and analytical (FTIR, HPLC, ICP-MS, UV-Vis, KF, IC) testing etc.
Complete documentation needed to support testing procedures including test forms and logbooks.
Interpret test results, compare them to established specifications and control limits, and ensure appropriateness of data for release. Treats data with a high level of integrity and ethics.
Participate in out-of-specification and failure investigations. Support all aspects of laboratory investigations.
Prepare, review and approve analytical data, technical reports and analytical methods.
Coordinate Microbiological, preservative efficacy/ antimicrobial effectiveness testing requirement as per USP/USP-NF for Active pharmaceutical ingredients, Inactive and Finished products and stability samples for regulatory filings.
Physical Requirements/Working Environment:
Physical & mental requirements e.g. lift 40 pounds, walk across plant/warehouse, business travel (% of time), driving as part of work responsibilities, etc.
Commitment to long hours of work when necessary to achieve goals.
Respirator, lab coat and safety glasses required. Ability to work with potent substances using a glove-box.
Job Type
: Full-time
This Job Is Ideal for Someone Who Is:
Dependable -- more reliable than spontaneous
People-oriented -- enjoys interacting with people and working on group projects
Adaptable/flexible -- enjoys doing work that requires frequent shifts in direction
Detail-oriented -- would rather focus on the details of work than the bigger picture
Achievement-oriented -- enjoys taking on challenges, even if they might fail
Autonomous/Independent -- enjoys working with little direction
Innovative -- prefers working in unconventional ways or on tasks that require creativity
High stress tolerance -- thrives in a high-pressure environment
Requirements:
Preferred Knowledge & Skills:
Strong knowledge of the major analytical techniques: HPLC/UPLC, GC, dissolution, etc. FT-IR, FDA/ICH regulations.
Solid knowledge of FDA/ICH regulations.
Required Experience & Education:
BS or MS in Chemistry, Pharmacy, Biochemistry, Biology or Biotechnology or related field.
Minimum 2 - 5 years of experience in using analytical instrument techniques including HPLC/GC/FT-IR, UV-Vis, Dissolution Apparatus, Ovens/Auto Titrators/KF Titrator/Particle size analyzers/ Ion-Chromatography.
Associate Scientist II/Scientist I (Biologics Expression and Purification)
Chemist job in Rockville, MD
MacroGenics is a leader in the discovery and development of innovative medicines that utilize our next generation antibody-based technologies. Our team of 350+ dedicated individuals is advancing a pipeline of product candidates to treat patients with cancer. Our products and platforms have attracted multiple partnerships with leading pharmaceutical and biotechnology companies around the globe.
The Company considers its employees to be its most valuable asset and we are committed to providing opportunities for individuals to learn and grow as a means to further their professional development. MacroGenics' corporate culture promotes an atmosphere of innovation, open communication and teamwork where employees can see firsthand how they contribute to the success of the organization.
Summary of Position
As a member of the Protein Science team, this individual will set up transfections to express proteins in mammalian cells followed by their purification and characterization to support the Biologics discovery pipeline.
Job duties
* Culture of mammalian cells in suspension following aseptic techniques and cell-line specific protocols.
* Transient transfection of cell lines or expansion of stable cell pools, from 3 ml - 10 L scale, to express proteins of interest. Monitor and optimize culture conditions to maximize protein quality and expression.
* Protein purification from milligram to gram scale using semi-automated FPLC systems.
* Analytical characterization of purified proteins to support research projects for drug discovery.
* Collect, analyze, and summarize experimental data in electronic lab notebook for archiving and sharing.
* Maintain lab and lab equipment in optimal functioning condition. Report any problems to supervisor.
Qualifications:
Education/Experience
Associate Scientist II
* Bachelor's degree in Biology or Biochemistry or a related field of study with a minimum of 2 years of bench-related experience
Scientist I
* Bachelor's degree in Biology or Biochemistry or a related field of study with a minimum of 3 years of bench-related experience
or
Master's degree in Biology or Biochemistry or a related field of study. Laboratory experience gained through undergraduate coursework, graduate research, or an internship is required. A minimum of 1 year of bench-related experience, strongly preferred.
Knowledge, Skills and Abilities
* Experience with mammalian cell culture, transfections, maintaining cell lines, etc. with meticulous sterile technique and lab practices.
* Experience with recombinant protein purification and analytical characterization (CE or SDS-PAGE, SEC).
* Experience with experimental design and execution with minimal supervision.
* Experience with standard lab software for data analysis (MS Excel, Prism, etc.). Good organizational skills and ability to multi-task.
* Good verbal and written communication skills. Demonstrated ability to work in a collaborative environment with other team members.
* Willingness to work on occasional weekends.
Preferred Experience
* Experience with antibody purification using automated FPLC system.
* Experience with quantitative assays (BLI Octet, ELISA, etc.).
Supervisory Responsibilities: None
Additional Information
The annual rate of pay for the Associate Scientist II position ranges from $67,200 - $102,500. The annual rate of pay for the Scientist I position ranges from $84,400 - $128,800. For non-exempt roles, and according to applicable regulations, there may be the possibility for overtime pay. This role is eligible for the Company's discretionary bonus and discretionary equity incentives. Eligible employees may participate in the Company's benefits programs, including medical / dental / vision / prescription coverage, employee wellness resources, 401(k) plan with employer match, access to an Employee Stock Purchase Plan, (ESPP), paid time off & paid parental leave benefits, and disability benefits.
The annual pay rate range is described in good faith, and the Company believes is the range of possible compensation for this role at the time of this posting depending on the candidate's experience, qualifications, geographic location, and other factors permitted by law. The Company may ultimately pay more or less than the posted range, and this range may be modified in the future. No amount is considered to be wages or compensation until such amount is earned, vested, and determinable under the terms and conditions of the applicable policies and plans. The amount and availability of any bonus, commission, benefits, or any other form of compensation and benefits that are allocable to a particular employee remains in the Company's sole discretion unless and until paid and may be modified at the Company's sole discretion, consistent with the law.
Statement
MacroGenics is proud to be an equal opportunity employer. Employment selection and related decisions are made without regard to race, color, national origin, sex, gender identity, sexual orientation, religion, age, disability, protected veteran status, or any other characteristic protected by federal, state or local law. We are committed to working with and providing reasonable accommodation to individuals with disabilities. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the employment process, please email ******************** or call ************** and/or 711 for TTD/TTY service.
Equal Opportunity Employer/Veterans/Disabled
We do not accept non-solicited resumes or candidate submittals from search/recruiting agencies.
Associate Scientist I
Chemist job in Sterling, VA
Come join our family! Microbac Laboratories is an essential business offering competitive pay and benefits including medical, dental, vision, life insurance, disability, generous paid time off including vacation, holidays and flex-time, a wellness program, referral bonus, tuition reimbursement and more!
Whether you are just starting your career in science or looking to further it, Microbac will put you on the path of an exciting career with room to grow. Quality, safety, giving back to our communities, diversity and inclusion, customer success and employee wellbeing are part of our core culture. We are looking for motivated individuals to join our family as an Associate Scientist I .
ABOUT MICROBAC
Microbac Laboratories, Inc. is a premier commercial laboratory testing firm that partners with clients worldwide, offering laboratory solutions to the life science, food and nutrition, and environmental industries and serves our clients with the utmost expertise and respect for their market requirements, constraints, and challenges. We embody a company-wide commitment to exceptional customer experience, which has been refined over nearly 50 years of trusted, analytical and measurement experience.
Through our network of laboratories, offices, and field services, we have the flexibility to meet the unique requirements for each client, project, and scope.
As a privately held third-party testing company, Microbac operates with a commitment to safety, quality, and compliance. Our diverse work portfolio includes broad accreditation offerings and tested insights across the environmental, food and nutrition and life science markets.
JOB SUMMARY
The Associate Scientist I, working in an accredited commercial laboratory, is responsible for assisting with the conduct of microbiological assays and associated activities to determine antimicrobial efficacy of household and commercial cleaning products.
ESSENTIAL FUNCTIONS:
Following established SOP's and adhering to state, federal and other accrediting body requirements, collect information about the antimicrobial properties of substances/samples to support the analytical testing needs of our clients for such purposes as quantitative or qualitative analysis, and product development
Perform laboratory housekeeping duties to include autoclaving and glassware processing
Prepare necessary standards, solutions, reagents, media, etc., required for sample analyses
Perform equipment and instrumentation set up
Operate basic and specialized laboratory instrumentation
Prepare and analyze samples
Accurately record observations and data and interpret results
Assists in the development and validation of new analytical methods
Assists in the development of new laboratory procedures
Assist department supervisors and managers with staff training
Sign off on final certificates of analysis
Contribute to writing, editing, and reviewing SOP's
Monitor and address sample backlog issues
Perform peer review of data to ensure accuracy
Maintain accurate, up to date logs, notebooks, and equipment records
Perform necessary laboratory administrative functions such as filing paperwork, photocopying, reviewing of data, and entering data into computerized LIMS
Comply with and promote Personnel, Safety, and Quality Program
MINIMUM REQUIREMENTS:
Bachelor's degree from a four-year accredited institution in a related field of applied science
Prior analytical testing experience
Above average knowledge of principles, terminology, practices, techniques, and instrumentation commonly used in a laboratory setting
Ability to interpret data and prepare reports
Ability to effectively prioritize work and manage time to meet deadlines and rush orders
Computer literacy
Ability to work with delicate laboratory equipment
Ability to communicate effectively in both written and verbal formats
WORKING CONDITIONS AND PHYSICAL REQUIREMENTS:
The physical demands and working conditions described here are representative of those that must be met by an employee to successfully perform the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.
Physical Requirements:
While performing the duties of this job, the employee is regularly required to use hands to finger, handle, or feel objects, tools; talk or hear. The employee is required to stand, walk, and sit.
The employee must regularly lift and/or move up to 25 pounds. Specific vision abilities required by this job include color vision and depth perception.
Working Conditions:
While performing the duties of this job, the employee will be in a general laboratory and office environment.
The noise level in the work environment is usually moderate.
This job may require travel less than 20%
As a privately held third-party testing company, Microbac operates with a commitment to safety, quality and compliance. Our diverse work portfolio includes broad accreditation offerings and tested insights across the environmental, food and life science markets.
OTHER:
This is not an exhaustive list of all duties an employee may be required to perform. Microbac reserves the right to revise the job description at any time.
Employment is at-will. Microbac, promotes a drug-free, alcohol-free workplace. Applicants considered for hire must pass a drug test before beginning work. Refusal to submit to testing will result in disqualification of further employment consideration.
Microbac is an Equal Opportunity Employer - We are committed to equal employment opportunity regardless of race, color, ancestry, religion, sex, national origin, sexual orientation, age, citizenship, marital status, disability, gender identity or Veteran status. All qualified applicants will receive consideration for employment.
Auto-ApplyAssociate Scientist, Discovery
Chemist job in Rockville, MD
Who We Are
Arcellx is a public, clinical-stage biotechnology company reimagining cell therapy by engineering innovative immunotherapies for patients with cancer and other incurable diseases. We believe that cell therapies are one of the forward pillars of medicine and our mission is to destroy cancer and advance humanity by developing cell therapies that are safer, more effective, and more broadly accessible.
Our team members are made up of talented innovators and dreamers working from our offices in Gaithersburg, Maryland, and Redwood City, California. At Arcellx, we hire exceptional people and create a fun, diverse, supportive, and informal environment that allows everyone to do their best work.
What Matters to Us
Living our core values is essential to maintaining a work environment that is high-performing, inclusive, and collaborative. We look for candidates who demonstrate strong values alignment and bring different backgrounds, viewpoints, and abilities to the team.
Arcellx Core Values
Start with authenticity:
We foster an inclusive environment where each person can bring their authentic self to work.
Think ‘we' before ‘me':
We prioritize collective success, collaborating and supporting one another to achieve our shared goals.
Embrace the challenge:
We deliver exceptional results by working with shared determination and a commitment to doing what's right.
How You'll Make a Difference
As an
Associate Scientist
, you will use molecular biology, protein purification and characterization methods to support Discovery's protein engineering and technology development efforts. Engaging with a cross-functional team in a fast-paced environment, you'll identify and develop Arcellx's lead therapeutic candidates. Our potentially life-saving treatments would not exist without the work of our talented Discovery scientists; this role will have a tremendous impact on our pipeline and ability to deliver novel and effective drugs to patients.
The “Fine Print” - What You'll Do
Work with other scientists to design, generate and characterize recombinant proteins to be used in cancer therapy discovery and development.
Assist with selection and/or screening strategies used in protein discovery workflows employing phage display, yeast display, ELISA, BLI and flow cytometry as needed.
Communicate detailed observations on experiments and assist in the preparation of technical reports, summaries, and protocols.
Skills and Experience We Look For
Bachelor's or master's degree in the life sciences (e.g., biology, genetics, biochemistry, chemistry, chemical engineering, bioengineering).
Minimum of 3 years of experience in a laboratory setting.
Ability to work both independently and collaboratively. Ability to effectively plan, organize, and prioritize work activities.
Must demonstrate proficiency with molecular biology methods
, including primer design, PCR, gel electrophoresis, plasmid DNA preparation, cloning and sequence analysis using SnapGene or similar software.
Preferred skills include those related to recombinant protein expression (e.g. transient transfection), purification (e.g. nickel and Protein A affinity chromatography) and characterization (e.g. ELISA, BLI, SDS-PAGE, protein quantitation and flow cytometry).
Rewards at Arcellx
Our people are our greatest asset, and supporting their well-being is an essential part of delivering on our mission and impacting the lives of patients. Putting this belief into practice means offering strong compensation and benefits.
The base salary range for this position is $75,000 - $95,000 per year. Where a candidate falls within that range is determined by factors such as years of experience. Our compensation package also includes an annual bonus based on company goals and an equity (RSU) grant. We do offer relocation assistance for roles if required.
Our market-leading benefits package includes: 100% coverage for medical, dental and vision for team members and dependents, unlimited vacation, a 3-day weekend every month, fully-paid parental leave for up to 6 months, tuition reimbursement, 401k employer contribution and more.
Join us in our quest to reimagine cell therapy and destroy cancer. For more on our technology, culture, and team, go to ****************
#LI-Onsite
Auto-ApplyAssociate Scientist
Chemist job in Gaithersburg, MD
US Tech Solutions is a global staff augmentation firm providing a wide-range of talent on-demand and total workforce solutions. To know more about US Tech Solutions, please visit our website ************************
We are constantly on the lookout for professionals to fulfill the staffing needs of our clients, sets the correct expectation and thus becomes an accelerator in the mutual growth of the individual and the organization as well.
Keeping the same intent in mind, we would like you to consider the job opening with US Tech Solutions that fits your expertise and skillset.
Job Description
• BioProcess Engineering (BPE) department is responsible for scale up, tech transfer, and facility fit of clinical and commercial processes to manufacturing. BPE is also responsible for producing development drug substance material and data from pilot facilities. Members of Development Scale-up Center (DSC), within BPE, produce materials up to 500L scale for toxicology and process development studies, to confirm process performance and to troubleshoot issues in GMP facility, and work with cross functional team on technology evaluations.
• This position is focused on upstream cell culture and fermentation processes supporting scalability and production of therapeutic proteins in DSC. Position is a hands-on laboratory and production-based role. Responsibilities include but are not limited to media preparations, routine sub-culturing of cells and fermentations. The candidate will assist in adaptation of transferred information for scale-up processes from late stage development to DSC as well as assisting in the production of various tox and development materials, troubleshooting and resolving technical issues with the production processes and/or equipment, identifying root causes for deviations, implementing corrective/preventative actions, assisting in implementing new technologies, and trending/analyzing data.
• The candidate will assist in compiling data and expected to summarize and assist in interpreting results. The candidate will also maintain production and laboratory equipment.
Qualifications
Education:
• Bachelor of Science (BS) or Master of Science (MS) in scientific, engineering or related field.
Experience:
• For the RA, we require a BS with 2 - 5 years or a MS with 0 - 2 years of relevant experience.
• For the AS, we require a BS with a minimum of 5 years or MS with a minimum of 2 years of relevant experience.
Additional Information
Special Skills/ Abilities
• Hands on proficiency in cell culture and/or fermentation and good aseptic techniques. Bioreactor/fermenter operation experience is preferred.
• Good documentation, writing and communication skills in a team based setting are essential.
Laurel Plant - R&D Laboratory Technician
Chemist job in Laurel, MD
Milliken & Company is a global manufacturing leader whose focus on materials science delivers tomorrow's breakthroughs today. From industry-leading molecules to sustainable innovations, Milliken creates products that enhance people's lives and deliver solutions for its customers and communities. Drawing on thousands of patents and a portfolio with applications across the textile, flooring, chemical and healthcare businesses, the company harnesses a shared sense of integrity and excellence to positively impact the world for generations. Discover more about Milliken's curious minds and inspired solutions at Milliken.com and on Facebook, Instagram, LinkedIn and Twitter.
POSITION OVERVIEW
Milliken's Laurel Plant in Gainesville, FL, is seeking a qualified individual to join its manufacturing team as an R&D laboratory technician. The technician performs routine work in the Research and Development Laboratory to safely develop chemical processes and produce products on a small scale.
JOB RESPONSIBILITIES
• Operate and maintain mechanical laboratory equipment, including vacuum pumps, stirrers, and pressurized systems.
• Safely set up and operate lab-scale glassware, distillation columns, and instrumentation for tests, research, process development, or small-scale manufacturing.
• Operate and maintain electronic laboratory equipment, such as temperature controllers, timers, and distillation controllers.
• Develop familiarity with standard analytical procedures used for material characterization, including IR spectrometry, UV spectrometry, gas chromatography, Refractive Index, Specific Gravity, Viscosity, Flash Point, and % Solids.
• Document records completely, accurately, neatly, and legibly.
• Learn basic functions of other departments, such as Quality, Analytical, Shipping, Customer Service, EHS, Production, Maintenance, and Purchasing, to work with respective areas.
QUALIFICATIONS
• High School Diploma or GED, along with some work experience in a lab setting.
• Experience using Microsoft Office suite applications.
• Ability to plan and prioritize daily tasks.
Milliken is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to actual or perceived race, color, creed, religion, sex or gender (including pregnancy, childbirth or related medical condition, including but not limited to lactation), sexual orientation, gender identity or gender expression (including transgender status), ancestry, national origin, citizenship, age physical or mental disability, genetic information, marital status, veteran or military status or any other characteristic protected by applicable law.
Senior Image Annotation/Quality Control Analyst
Chemist job in Herndon, VA
About Us:
BlackSky is a real-time intelligence company. We own and operate the world's most advanced space-based intelligence platform and provide customers satellite imagery, automated analytics and high-frequency monitoring of strategic locations, economic assets and events from around the globe. BlackSky is trusted by the most demanding allied military and intelligence organizations and commercial companies to deliver foresight into critical matters that affect national security and the economy. BlackSky's data enables governments and businesses to see, understand and anticipate change as it happens, giving them the ultimate strategic advantage so they can act quickly. Our global team works with cutting-edge technology to make a difference around the world and prides itself on being people-first, customer-focused and fun.
BlackSky is looking for a talented and creative Senior Image Annotation/Quality Control Analyst to support the development, operation, and capability evolution of Spectra AI, BlackSky's cutting edge AI/ML Platform. As part of the machine learning team, you are instrumental in shaping our computer vision products by managing the quality of data that trains AI/ML models. You will help manage and grow the entire labeling process that trains Spectra AI, overseeing remote data labeling teams and actively assessing the quality of trained models, which create critical timely insights for our customers.
While the locations listed in the job posting are ideal, we would love candidates near either our Herndon, VA or Seattle, WA offices. We may also consider remote candidates in certain states.
Responsibilities:
Lead and manage data labeling teams, providing oversight for labeling campaigns.
Research for AI product development, identifying geographic areas where objects exist, developing object ontologies, building annotation instructions, and identifying imagery for annotation.
Collaborate with machine learning and product teams to define metrics, assess, and report on the quality of machine learning models in development and production using statistical and quality assurance approaches.
Work with the machine learning and product teams to define and measure the performance of machine learning models against SLAs.
Identify customer requirements and liaise with computer vision team to codify specifications for training datasets.
Create processes, tools, and scripts to manage and track data quality and labeling performance.
Take part in the entire project lifecycle from requirements development to deployment.
Innovate and streamline data annotation processes.
Other job-related duties as assigned.
Required Qualifications:
Minimum of five (5) years of hands-on experience as a data quality engineer, imagery analyst, GIS analyst, or quality assurance engineer in the space of satellites, computer vision, or machine learning.
Bachelor's Degree or higher in one of the following fields: computer science, GIS, data science, mathematics, physics, statistics, or another scientific field.
Experience interpreting satellite imagery to identify objects, behaviors, or activities and working with GIS datasets.
Hands on experience with annotation platforms such as LabelBox, SuperAnnotate, AWS Sagemaker, or CVAT.
Experience managing remote annotation workforces such as CloudFactory, Hive, or iMerit.
Collaborates well with others and able to communicate ideas to those with other backgrounds.
Experience with quality assurance practices, model testing & evaluation, and computing metrics & statistics from data.
Attention to detail and ability to define, enforce, and follow rigorous process controls for managing data.
The program this role will support requires Us-born citizenship.
Preferred Qualifications:
Experience with AI advancements in image annotation such as the Segment Anything Model (SAM).
Embeddings and other AI Assistance tools.
Experience writing code and scripts, especially for processing and evaluating large amounts of data.
Proficiency with Python for automation and data manipulation tasks.
Knowledge and experience working in an AWS Cloud environment.
Demonstrated ability to lead and manage small teams.
Ability to obtain and maintain a US security clearance.
Life at BlackSky for full-time US benefits eligible employees includes:
Medical, dental, vision, disability, group term life and AD&D, voluntary life and AD&D insurance
BlackSky pays 100% of employee-only premiums for medical, dental and vision and contributes $100/month for out-of-pocket expenses!
15 days of PTO, 11 Company holidays, four Floating Holidays (pro-rated based on hire date), one day of paid volunteerism leave per year, parental leave and more
401(k) pre-tax and Roth deferral options with employer match
Flexible Spending Accounts
Employee Stock Purchase Program
Employee Assistance and Travel Assistance Programs
Employer matching donations
Professional development
Mac or PC? Your choice!
Awesome swag
The anticipated base salary range for candidates in Seattle, WA is $100,000-115,000 per year. The final compensation package offered to a successful candidate will be dependent on specific background and education. BlackSky is a multi-state employer, and this pay scale may not reflect salary ranges in other states or locations outside of Seattle, WA.
BlackSky is committed to hiring and retaining a diverse workforce. We are proud to be an Equal Opportunity/Affirmative Action Employer All Qualified applicants will receive consideration for employment without regard to race, color, religion, sex, age, national origin, sexual orientation, gender identity, disability, protected veteran status or any other characteristic protected by law.
To conform to U.S. Government space technology export regulations, including the International Traffic in Arms Regulations (ITAR) you must be a U.S. citizen, lawful permanent resident of the U.S., protected individual as defined by 8 U.S.C. 1324b(a)(3), or eligible to obtain the required authorizations from the U.S. Department of State. #LI-Remote
EEO/AAP/ Pay Transparency Statements:
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Auto-ApplyCounter Proliferation Analyst - Chemical SME (TS/SCI)
Chemist job in Reston, VA
Reston, VA, USA
Full-time
Clearance: Top Secret/SCI
As a Counter-Proliferation Analyst (Chemical SME), you will serve as a chemical subject-matter expert and technical authority with a focus on current/near-term events, plans, developments, and trends pertaining to the proliferation of WMD and chemical events; issues impacting chemical security; force protection; and force operability and survivability against a broad spectrum of nuclear, biological, chemical, and other WMD events. As a Chemical Subject Matter Expert, conducts applied research on specific intelligence issues pertaining to the WMD threats to US and allied nations; provides written input to reports and briefings; assists with answering requests for information (RFI); assists in research and analytical entries related to WMD; all for dissemination to Agency leadership and its personnel, Combatant Commands, and the Intelligence Community (IC). You will serve on a unique, multi-discipline team assisting DTRA, CCMDs, and IA and IC partners to fuse operations and intelligence information to enhance Whole of Government efforts against chemical WMDs, threats, and counter-proliferation efforts, and the threat networks that facilitate or employ those threats. You will adhere to DTRA production standards supporting the Government's Request for Support (RFS) and Named Area of Interest (NAI) processes. You will assist in the preparation and the conduct of leader engagements with DTRA and commanders globally, to assist in developing processes that enhance situational understanding of chemical WMD and improvised threats, and the networks that employ or facilitate them to enable DOD, IA, and IC efforts focused on dismantling, disrupting, and defeating those threats.
Responsibilities:
As a Counter-Proliferation Analysts with specialized experience in chemical warfare and defense, you will analyze and produce intelligence products for the Defense Threat Reduction Agency (DTRA) focused on chemical WMDs, and counter-proliferation threats using advanced all source analytic capabilities. You will apply expertise in chemical WMD, Counter-proliferation, and network analysis (Counter Threat Network), social network analysis, and command and control systems. You will serve as an all-source counter-proliferation intelligence analyst with specialized experience in chemical warfare and defense whose primary responsibility will be informing DTRA activities through structured research using multiple sources and analytic tool suites. You will deliver products that increase the client's situational understanding and comprehension of chemical WMD and improvised threats, and associated counter-proliferation networks. You will assist in evaluating paths to chemical WMDs, including state WMD programs and potential proliferation, and support real-world missions in a dynamic client environment.
The Counter-Proliferation Analyst (Chemical SME) will respond to strategic operational and tactical collection needs based on raw intelligence and apply knowledge of related collection techniques and possess working knowledge of tradecraft and tools used in the chemical WMD and counter-proliferation collection environment. You will assist in enabling DOD, IA, and IC communities of action to dismantle, disrupt, and defeat chemical WMD and counter-threat networks. To do this, you will prioritize and categorize requests for support, conduct near- and long-term analyses of device and network-centric problem sets, and fuse multiple intelligence disciplines. You will directly support embedded teammates, answer requests for support from customers and work closely with the senior analysts to develop high-quality products, and work closely with other members of the team to identify valuable information on chemical WMD and counter-proliferation threats, and enemy organizations; identify trends, patterns, and key nodes; and highlight relationships to the targeted enemy networks.
Qualifications
Required Skills:
Current Top Secret/Specialized Compartmented Information Security Clearance.
Bachelor's degree in chemical-related field (chemistry, biochemistry, analytical chemistry, chemical engineering, inorganic chemistry, organic chemistry, physical chemistry)
More than 3 years of experience providing intelligence analysis for DoD and/or an intelligence agency in an analyst role, including multi-intelligence WMD or counter-proliferation production in the past 7 years
More than 2 years of direct experience with DoD and IC All-Source analysis tools, collecting and analyzing information in support of DoD or other government organizations, or direct experience managing analytic production, or the exploitation of multi-intelligence data focused on WMD or counter-proliferation
More than 1 year of experience providing Attack the Network (AtN) analysis focused on WMD, CT, or counter-proliferation/improvised threat networks.
Practical understanding of collection techniques and working knowledge of tradecraft and tools used in the WMD and counter-proliferation collection environment
Practical understanding of network analysis tools such as Analyst Notebook and Palantir.
Practical understanding of geospatial Intel tools such as ArcGIS and Google Earth.
Practical understanding of Intel-related databases such as M3, TAC, NCTC Online, TIDE, ICReach SIGINT database, Cultweave SIGINT database, PROTON SIGINT Database.
Practical understanding of MS Office, Excel, and big-data analytic techniques for structured and unstructured data.
You must also possess the ability to effectively communicate both orally and in writing.
Willing to work rotating shifts if needed - that may include nights and weekends.
Bachelor's degree and more than three years of experience, or an associate degree and five years of experience, or seven years of relevant work experience.
Desired Skills:
Graduate degree in chemical related field (chemistry, biochemistry, analytical chemistry, chemical engineering, inorganic chemistry, organic chemistry, physical chemistry
Previous experience with CBRN/WMD-related intelligence (i.e. chemical security, counter-proliferation, policy, health/medical, arms control, weapons technology, etc.)
Scientific or technical education or background
Experience with the DTRA including its planning processes
Experience with the terminology used in the collection of data for chemicals, biologics, and WMDs and their proliferation
Knowledge of advanced internet-based research, including Boolean logic, advanced research techniques, search engine and database resources, and Internet sources, including social media, social networking tools, and commercial and industry-based databases.
Experience accessing, researching, and exploiting global and regional digital platforms and PAI data.
Expert understanding of collection techniques and working knowledge of tradecraft and tools used in the chemical WMD and counter-proliferation collection environment
Expert understanding of network analysis tools such as Analyst Notebook and Palantir.
Expert understanding of geospatial Intel tools such as ArcGIS and Google Earth.
Expert understanding of Intel-related databases such as M3, TAC, NCTC Online, TIDE, ICReach SIGINT database, Cultweave SIGINT database, PROTON SIGINT Database.
Expert understanding of MS Office, Excel, and big-data analytic techniques for structured and unstructured data.
More than ten years of military experience, and/or a combination of military and IC Agency experience, including recent combat deployments, and be well-versed in all areas of military intelligence, WMD, and Counter-proliferation.
Expert understanding of MS Office, Excel, and big-data analytic techniques for structured and unstructured data
Chemical and Nuclear Surety Analyst
Chemist job in Washington, DC
Chimera Enterprises International is seeking a Chemical and Nuclear Surety Analyst to support the Army Treaty Compliance and Surety Division (DAMO-SSD), Deputy Assistant Secretary of the Army for Environment Safety & Occupational Health (DASA(ESOH)), and U.S. Army Nuclear and Countering Weapons of Mass Destruction Agency (USANCA)
Description
The ideal candidate will have substantial experience in chemical and nuclear surety, as well as familiarity with Department of Defense (DoD) guidelines and regulations. The Chemical and Nuclear Surety Analyst will support DAMO-SSD by ensuring compliance with U.S. laws and DoD directives related to chemical and nuclear surety, providing technical and policy support, participating in related meetings, and maintaining oversight of surety-related activities.
Mission
To ensure the Army's adherence to chemical and nuclear surety requirements by providing expert analysis, strategic guidance, and comprehensive support. This role involves implementing surety programs and policies in alignment with DoD and Army guidelines to ensure the safety, security, and accountability of chemical agents and special nuclear materials (SNM).
Clearance Level Required: SECRET
JOB DESCRIPTION AND RESPONSIBILITIES:
Provide continuous support to DAMO-SSD, including the study and assessment of USG, DoD, Joint, and Army surety guidance issues.
Determine the impact of chemical and nuclear surety and accident and incident response on Army operations, plans, force structure, training, and resources.
Provide operations, program oversight, and staff support to DAMO-SSD to assist in the execution of its responsibilities for developing, implementing, and overseeing compliance with surety guidance measures.
Utilize database management systems to collect, analyze, present, communicate, and file information related to surety guidance and surety I&C planning.
Attend and participate in meetings, conferences, briefings, seminars, training courses, and guidance meetings.
Support and accompany the Department of the Army Inspector General (DAIG) on surety-related inspections.
Monitor available information sources for surety-related matters and provide regular updates and reports.
Prepare synopses, after-action reports (AAR), trip reports, significant activity reports (SIGACT), information memorandums, and information papers as required.
Recommend special studies and research and analysis topics pertaining to surety issues for approval and assignment by the Government.
Review and comment on U.S. government, DoD, and Army documents and publications related to chemical and nuclear surety.
Support the revision of formal Army surety-related guidance documents such as AR 50-5, AR 50-6, AR 190-17, and DA Pam 50-5.
Assist with implementation of chemical and surety-related guidance, including reviewing requests for exceptions and surety status termination.
Knowledge, Skills, and Abilities:
Minimum of two (2) years of experience interacting with Service Staff, Joint Staff, and Office of the Secretary of Defense (OSD) organizations.
Strong knowledge of chemical and nuclear surety operations and compliance measures.
Proficiency in database management and the ability to utilize them for surety analysis.
Excellent analytical skills with the capability to develop and implement compliance measures.
Strong communication and interpersonal skills for effective collaboration with various stakeholders.
Ability to draft, review, and update technical and policy documents related to surety.
Minimum Qualifications:
Education: Bachelor's Degree in engineering, scientific, technical, management, or a related discipline relevant to this PWS.
Experience: 2 to 5 years' experience in managing and overseeing chemical and nuclear surety programs and interacting with high-level DoD personnel.
Clearance: SECRET
Location: Primarily on-site in the National Capital Region (NCR), with occasional travel as required.
Chimera Enterprises International is committed to equal opportunity and affirmative action in hiring and retaining a diverse workforce, including protected veterans and individuals with disabilities.
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Chemical Weapons Convention Analyst (Lead) III
Chemist job in Washington, DC
Mahalo for your interest in this role! Please see the full position description below and click Start Your Application when ready. For more information about DAWSON, please visit dawsonohana.com.
This position is intended to support the Naval Treaty Implementation Program (NTIP) in its role for implementation and compliance of the specific arms control treaties and agreements under NTIP s purview. The work for this position will be located at the Washington Naval Yard, Washington District of Columbia (D.C.)
Job Description
Work with the Government to identify and assign qualified personnel to critical functions in support of the assistance team
Accompany Department of the Navy (DON) personnel to the DON facility designated for inspection
Store, periodically test, maintain, and rapidly deploy inspection support equipment to the Point of Entry at Dulles International Airport and to the DON installation designated for a Challenge Inspection s (CI) or CI exercise
Provide day-to-day support to the NTIP staff in the conduct of routine business
Attend meetings, draft Memoranda for Record, prepare presentations, and reports
Monitor the arms control treaty community for movement toward any type of new or altered framework or arms control agreements
Provide research and analytical support to program and resource management decision making
Assess impacts to the Department of the Navy, as required
Prepare and deliver all technical studies, analysis, research, documentation
Qualifications
Secret Security Clearance
Bachelor s degree from an accredited institution
Seven (7) plus years of experience in arms control, international relations, national security, or a related field
Available to deploy to an affected DON installation as directed
*Position is Contingent Upon Award
DAWSON is an Equal Opportunity/Affirmative Action/VEVRAA federal contractor. All qualified applicants will receive consideration for employment without regard to race, color, religion, gender, national origin, disability status, protected veteran status, or any other characteristic protected by law.
DAWSON offers a best-in-class benefits program including medical, dental, and vision insurance; a 401(k) program with employer match; paid vacation and sick leave; employer-paid basic life and AD&D insurance; an Employee Assistance Program; and a flexible work environment. Additionally, employees can choose from several voluntary benefits including critical illness coverage; accident insurance; identity theft coverage; pet insurance, and more.
DAWSON gives preference to internal candidates. If no internal candidate meets our qualifications, external candidates will be given consideration.
Senior Chemical Weapons Analyst
Chemist job in Fort Belvoir, VA
Founded in 1989, SOSi is among the largest private, founder-owned technology and services integrators in the defense and government services industry. We deliver tailored solutions, tested leadership, and trusted results to enable national security missions worldwide.
Job Description
Overview
SOSi is seeking a Senior Chemical Weapons Analyst to support foreign Weapons of Mass Destruction (WMD) and counterproliferation efforts.
Essential Job Duties
Apply in-depth knowledge and understanding of chemical weapons
Exhibit mastery of qualitative and quantitative analytical methodologies
Pursue developments in academia or other fields that affect trade craft methodology
Demonstrate the ability to define comprehensive, new, or unique research approaches that enable rigorous assessments
Clearly articulate key findings in relation to chemical weapons
Review analytic products for cogent arguments, tradecraft standards, and adequate support for conclusions and routinely test analytic rigor of products.
Define problems, supervise studies and lead surveys to collect and analyze data to provide and/or recommend solutions on chemical weapons
Display the ability to provide strategic advice, technical guidance, and expertise to Defense planners and policymakers (e.g. Undersecretary level or higher) on CW matters.
Qualifications
Minimum Requirements
Master's degree in a chemical related field
8 years of experience conducting analysis with at least a portion of the experience within the last two years relevant to chemical weapons or a total of 12 years in lieu of a degree
Active DoD Top Secret Clearance with SCI and CI Poly.
Understanding of JP 3-40, JP 3-25, and ICD 206
Ability to effectively communicate both orally and in writing.
Demonstrates in-depth knowledge and understanding of the related field activities required
to meet mission requirements.
Willingness to work rotating shifts if needed that may include nights and weekends
Preferred Qualifications
Minimum of 15 years of experience conducting analysis with at least a portion of the experience within the last 5 years that is relevant to chemical weapons
Doctorate degree in chemical related field
Expert understanding of JP 3-40, JP 3-25, and ICD 206
Additional Information
Work Environment
Normal office conditions
On-site
Working at SOSi
All interested individuals will receive consideration and will not be discriminated against for any reason.
Sr Analyst, Real Estate QC Underwriting
Chemist job in McLean, VA
PenFed is hiring a (Hybrid) Sr Analyst, Real Estate QC Underwriting at our Omaha, Nebraksa; San Antonio, Texas; Eugene, Oregon or Tysons, Virginia location. The primary purpose of this job is to perform quality control reviews for first trust conventional, VA, FHA and equity real estate loans. This role will evaluate the integrity and quality of the credit, compliance, and collateral aspects of the mortgage loan origination process through pre-funding and post-funding loan reviews designed to verify the accuracy and integrity of the information and loan documentation used to support the lending decision for conventional, VA, FHA, and Equity Line of Credit loans. It will validate adherence to PenFed's policies and procedures and secondary marketing investor guidelines. This role requires expertise in evaluating property valuations, including all types of appraisals, AVMs and property condition inspections, with knowledge of Interagency guidelines and Appraisal Independence Requirements.
Responsibilities
Reasonable accommodation may be made to enable individuals with disabilities to perform the essential functions. This is not intended to be an all-inclusive list of job duties, and the position will perform other duties as assigned.
+ Conduct reviews of first trust conventional, VA, FHA and equity mortgage loans to ensure that loans were properly underwritten, and that sound judgment was used in the underwriting process. Complete a thorough analysis of loan files to determine member credit worthiness and collateral values were adequate. Review legal and compliance documentation as applicable.
+ Conduct reviews of mortgage loans to evaluate the accuracy and integrity of the information and loan documentation used to support the lending decision.
+ Conduct reviews of mortgage loans to ensure compliance with PenFed's policy and procedures, investor, agency, and secondary market requirements.
+ Analyze and determine accurate defect ratings based on investor's loan eligibility requirements. Evaluate the entire credit package and collateral for residential mortgage loans and ultimately ensure an investment quality loan product.
+ Follow up on previous deficiencies and examine samples of corrected files.
+ Ability to work collaboratively with Mortgage Operations, providing clarification of review results as needed.
+ Understand and interpret all credit underwriting documentation required to be reverified in each loan file and conduct further research as necessary.
+ Perform peer reviews and provide guidance to junior analysts as needed.
+ Assist with process testing as assigned and participate in special projects.
+ Maintain a working knowledge of internal policies, procedure, external regulations, secondary market underwriting guidelines, investor, and private mortgage insurance guidelines.
+ Maintain current knowledge of Fannie Mae, Veterans Administration (VA), Freddie Mac, FHA and external investors.
Qualifications
Equivalent combination of education and experience is considered.
+ Bachelor's degree in business, accounting, finance, or another related field required.
+ Minimum of three (3) years progressive experience in real estate lending with underwriting experience required, preferably in a bank or credit union environment.
+ Advanced knowledge of real estate loans (origination, processing, closing, funding) required. Broad knowledge of consumer real estate lending, including first trust mortgage loans, home equity loans and lines of credit.
+ Knowledge of lending compliance regulations and system definitions.
+ Active or recent VA SAR and/or FHA DE underwriting authority preferred.
+ Proficiency with Encompass is highly desirable.
Supervisory Responsibility
This position will not supervise employees.
Licenses and Certifications
There are no additional certifications required.
Work Environment
While performing the duties of this job, the employee is regularly exposed to an indoor office setting with moderate noise.
*Most roles require working in an office setting with moderate noise and the ability to lift 25 pounds.*
Travel
The ability to travel to various worksites and be on-call may be required.
#LI-Hybrid
About Us
Established in 1935, PenFed today is one of the country's strongest and most stable financial institutions with over 2.9 million members and over $31 billion in assets. We serve members in all 50 states and the District of Columbia, as well as in Guam and Puerto Rico. We are federally insured by NCUA and we are an Equal Housing Lender. We are available to members worldwide, via the web, seven days a week, twenty-four hours a day. We provide our employees with a lucrative benefits package including robust medical, dental and vision plan options, plenty of paid time off, 401k with employer match, on-site fitness facilities at our larger locations, and more. Equal Employment OpportunityPenFed management will maintain and observe personnel policies which will not discriminate or permit harassment or retaliation against a person because of race, color, creed, age, sex, gender, gender identity, gender expression, religion, national origin, ancestry, marital status, military or veteran status or obligation, the presence of a physical and/or mental disability or medical condition, genetic information, sexual orientation, and all statuses protected by applicable state or local law in all recruiting, hiring, training, compensation, overtime, position classifications, work assignments, facilities, promotions, transfers, employee treatment, and in all other terms and conditions of employment. PenFed will also prohibit retaliation against individuals for raising a complaint of discrimination or harassment or participating in an investigation of same. PenFed will also reasonably accommodate qualified individuals with a disability so that they can apply for a job or perform the essential functions of a job unless doing so causes a direct threat to these individuals or others in the workplace and the threat cannot be eliminated by reasonable accommodation or if the accommodation creates an undue hardship to PenFed. Contact human resources (HR) with any questions or requests for accommodation at ************.
Associate Scientist, Bioanalytical Lab & QC Support
Chemist job in Rockville, MD
Job DescriptionWho we are REGENXBIO is an exceptional place to work. You'll have the opportunity to collaborate with some of the best and the brightest people, touch amazing science, and be a part of extraordinary plans. Our core values: Trust, Accountability, Perseverance, and Innovation drive everything we do. We aim to bring these values to life every day with all that we do, and we believe that what we do matters - to patients, to their families, and to their communities.
As a member of our Bioanalytical Sciences team, you will be responsible for performing nonclinical and clinical sample testing (PK, Immunogenicity, PCR, etc.) following developed, qualified, and/or validated bioanalytical methods in support of REGENXBIO projects and programs. You will also be responsible for developing and validating bioanalytical methods for gene therapy products.
You will also be responsible for performing QC review of documentation produced in the Bioanalytical laboratory, including assay runs, summary tables, reports, protocols and collaborate with various departments to ensure compliance with regulatory expectations.What you'll be doing
Conduct assay operations and maintains accurate testing records.
Review technical documents.
Perform QC peer reviews and manages project-related activities.
Troubleshoot analytical method issues and maintains lab inventories.
Support Sample receipt/Accession, buffer preparation and lab maintenance
Performs additional tasks or assist with special projects as assigned or needed.
We set our employees up for success. To be successful in this role and help us achieve our goals, we are looking for someone with the following skills and qualifications:
Bachelor's degree in a relevant scientific field with 2+ years of industry experience, or Master's with 1+ year.
Hands-on experience with immunoassays (ELISA, MSD), cell-based assays, qPCR, and/or LC-MS.
Analytical, problem-solving, and organizational skills with excellent attention to detail.
Collaborative team player with strong written and verbal communication skills.
Proficient in data analysis software (e.g., SoftMax) and Microsoft Office applications.
By joining REGENXBIO, you will have the opportunity to be a part of a growing company and incredible team passionate about developing novel AAV gene therapy products to our patients. In addition, professional development is important to us. By joining our team, you'll have the opportunity to be exposed to challenging projects and development resources to help you grow personally and professionally.
We are proud to offer a comprehensive rewards package which includes a market-competitive base salary, an annual performance-based bonus program, stock grants at all levels, and benefits such as health, dental, and vision insurance, retirement plan with 401(k) match, summer hours, and more! The estimated compensation range for this role is $66,000-$89,000 annually. The actual salary offered to the final candidate depends on a number of factors such as relevant work experience, skills, education, and years of experience.
Lab Analyst - Metals
Chemist job in Lanham, MD
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 98,000 employees operate a network of 2,650 offices and laboratories, working together to enable a better, safer and more interconnected world.
Our
Lanham, MD laboratory
is looking for
a Lab Analyst
to join their
Metals department
! The Lab Analyst I prepares and analyzes samples with accuracy and precision in accordance to SGS' analytical SOPs. The Lab Analyst I works independently and as part of a team to meet daily production targets and ensure hold times and turnaround times are met. The Lab Analyst I understands and applies basic analytical chemistry principles. The Lab Analyst I always follows safe laboratory practices and maintains a safe working environment.
Job Functions
After appropriate training independently prepares and analyzes samples according to SGS' analytical SOPs using instrumentation specific to the department and analytical methodologies.
Maintain sample archival and disposal per SGS' analytical SOPs.
Performs routine operation, maintenance, calibration of laboratory instruments/equipment.
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
Bachelor's Degree in a Chemistry or similar scientific discipline (Required)
Bachelor's Degree in a Chemistry or similar scientific discipline and 1-2 years of years' relevant experience using FLAA or ICP-MS (Preferred)
Advanced English language skills (Required)
Basic reasoning and mathematical skills (Required)
Basic computer skills (Required)
Ability to lift/carry/push and/or pull upwards of 25 lbs on a frequent basis (Required)
The hourly rate for this position is
$
21.50-23.50 per hour
(dependent on experience). This position is eligible for overtime pay.
In addition, your compensation package includes the following benefits:
Participation in the Company's benefit programs coincident or following the first of the month in which you are hired.
Immediate eligibility to participate in the Company's 401K Retirement Plan
Paid vacation
Four (4) floating holidays annually
Seven (7) company observed holidays paid
Sick time accrual
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.
Associate Scientist
Chemist job in Gaithersburg, MD
US Tech Solutions is a global staff augmentation firm providing a wide-range of talent on-demand and total workforce solutions. To know more about US Tech Solutions, please visit our website ************************ We are constantly on the lookout for professionals to fulfill the staffing needs of our clients, sets the correct expectation and thus becomes an accelerator in the mutual growth of the individual and the organization as well.
Keeping the same intent in mind, we would like you to consider the job opening with US Tech Solutions that fits your expertise and skillset.
Job Description
• BioProcess Engineering (BPE) department is responsible for scale up, tech transfer, and facility fit of clinical and commercial processes to manufacturing. BPE is also responsible for producing development drug substance material and data from pilot facilities. Members of Development Scale-up Center (DSC), within BPE, produce materials up to 500L scale for toxicology and process development studies, to confirm process performance and to troubleshoot issues in GMP facility, and work with cross functional team on technology evaluations.
• This position is focused on upstream cell culture and fermentation processes supporting scalability and production of therapeutic proteins in DSC. Position is a hands-on laboratory and production-based role. Responsibilities include but are not limited to media preparations, routine sub-culturing of cells and fermentations. The candidate will assist in adaptation of transferred information for scale-up processes from late stage development to DSC as well as assisting in the production of various tox and development materials, troubleshooting and resolving technical issues with the production processes and/or equipment, identifying root causes for deviations, implementing corrective/preventative actions, assisting in implementing new technologies, and trending/analyzing data.
• The candidate will assist in compiling data and expected to summarize and assist in interpreting results. The candidate will also maintain production and laboratory equipment.
Qualifications
Education:
• Bachelor of Science (BS) or Master of Science (MS) in scientific, engineering or related field.
Experience:
• For the RA, we require a BS with 2 - 5 years or a MS with 0 - 2 years of relevant experience.
• For the AS, we require a BS with a minimum of 5 years or MS with a minimum of 2 years of relevant experience.
Additional Information
Special Skills/ Abilities
• Hands on proficiency in cell culture and/or fermentation and good aseptic techniques. Bioreactor/fermenter operation experience is preferred.
• Good documentation, writing and communication skills in a team based setting are essential.