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2 jobs found for underwriter in maryland

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    • rockville, maryland
    • temp to perm
    • $25 - $28.84 per hour
    Randstad is seeking several  Associate Scientists for a major life science organization. This client is the North American life science brand of a major German based biotech/pharma organization – a leading science and technology company. It offers a broad range of innovative products and services to biotech and pharmaceutical drug therapies businesses. Through dedicated collaboration with the scientific and engineering communities, and as one of the top three R&D investors in the life science tools industry, the brand serves as a strategic partner to customers and helps advance the promise of life science.  These are 4-8 month contract to permanent hire opportunities for both Associate Scientist level I and II!We'll be hosting virtual Career Fairs on July 6th, 7th & 13th! We are looking to hire for both 1st & 2nd shift; some roles may require weekend work.salary: $25 - $28.84 per hourshift: First & Secondwork hours: 8 AM - 4 PM or 3 PM- 11PMeducation: BachelorYour Role:Perform assays/ testing for a laboratory within Biologics. This position does not have supervisory responsibilities.PURPOSE OF THE POSITIONThe Associate Scientist will perform safety testing required to manufacture clinical and commercial products. The AS is required to make scientific observations, maintain detailed workbooks/documentation and ensure all documentation fulfills generally accepted professional/industry standards. Additionally, they are required to maintain a thorough understanding of BioReliance services, technical principles and applications.ESSENTIAL JOB FUNCTIONS Conducts assigned testing with minimal supervision within constraints of lab scheduling.Performs testing in accordance with SOPs and regulations (cGMP and GLP).Maintains complete and comprehensive records for study integrity.Makes detailed observations and documents results.Operates and maintains lab equipment as required by SOPs and testing procedures.Performs peer review of assay batch/lab records to ensure Right First Time (RFT)Utilizes applicable computer programs during testing and routine tasks (i.e. Word, Excel, Oracle, LIMS, BRIQS, etc.).Utilizes problem solving/ trouble shooting skills.Communicates deviations/ events, progress and interim results to Study Management.Informs supervisor of deviations or factors that may affect quality and accuracy of data.Maintains a working knowledge of lab procedures and assays.Assists with revisions to SOPs, laboratory records and other documentation as assigned.Complies with company health and safety regulations and procedures.Performs other duties as assigned. BASIC QUALIFICATIONSEducation (minimum requirements): BA/BS in scientific discipline with 0-2 years or relevant experienceOr equivalent relevant experience Experience: Experience with relevant laboratory practices, techniques, equipment, materials and mathematical calculations. Knowledge and Skills: Basic skills in applicable computer programsGood oral and written communication skillsWorks well in a team based environmentPCR (1 year of experience is preferred)qPCRAsceptic Techniques (1 year of experience is preferred)ELISA (1 year of experience is preferred) Qualifications Years of experience: 1 yearExperience level: Entry Level Randstad is a world leader in matching great people with great companies. Our experienced agents will listen carefully to your employment needs and then work diligently to match your skills and qualifications to the right job and company. Whether you're looking for temporary, temporary-to-permanent or permanent opportunities, no one works harder for you than Randstad.Equal Opportunity Employer: Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status. For certain assignments, Covid-19 vaccination and/or testing may be required by Randstad's client or applicable federal mandate, subject to approved medical or religious accommodations. Carefully review the job posting for details on vaccine/testing requirements or ask your Randstad representative for more information.
    Randstad is seeking several  Associate Scientists for a major life science organization. This client is the North American life science brand of a major German based biotech/pharma organization – a leading science and technology company. It offers a broad range of innovative products and services to biotech and pharmaceutical drug therapies businesses. Through dedicated collaboration with the scientific and engineering communities, and as one of the top three R&D investors in the life science tools industry, the brand serves as a strategic partner to customers and helps advance the promise of life science.  These are 4-8 month contract to permanent hire opportunities for both Associate Scientist level I and II!We'll be hosting virtual Career Fairs on July 6th, 7th & 13th! We are looking to hire for both 1st & 2nd shift; some roles may require weekend work.salary: $25 - $28.84 per hourshift: First & Secondwork hours: 8 AM - 4 PM or 3 PM- 11PMeducation: BachelorYour Role:Perform assays/ testing for a laboratory within Biologics. This position does not have supervisory responsibilities.PURPOSE OF THE POSITIONThe Associate Scientist will perform safety testing required to manufacture clinical and commercial products. The AS is required to make scientific observations, maintain detailed workbooks/documentation and ensure all documentation fulfills generally accepted professional/industry standards. Additionally, they are required to maintain a thorough understanding of BioReliance services, technical principles and applications.ESSENTIAL JOB FUNCTIONS Conducts assigned testing with minimal supervision within constraints of lab scheduling.Performs testing in accordance with SOPs and regulations (cGMP and GLP).Maintains complete and comprehensive records for study integrity.Makes detailed observations and documents results.Operates and maintains lab equipment as required by SOPs and testing procedures.Performs peer review of assay batch/lab records to ensure Right First Time (RFT)Utilizes applicable computer programs during testing and routine tasks (i.e. Word, Excel, Oracle, LIMS, BRIQS, etc.).Utilizes problem solving/ trouble shooting skills.Communicates deviations/ events, progress and interim results to Study Management.Informs supervisor of deviations or factors that may affect quality and accuracy of data.Maintains a working knowledge of lab procedures and assays.Assists with revisions to SOPs, laboratory records and other documentation as assigned.Complies with company health and safety regulations and procedures.Performs other duties as assigned. BASIC QUALIFICATIONSEducation (minimum requirements): BA/BS in scientific discipline with 0-2 years or relevant experienceOr equivalent relevant experience Experience: Experience with relevant laboratory practices, techniques, equipment, materials and mathematical calculations. Knowledge and Skills: Basic skills in applicable computer programsGood oral and written communication skillsWorks well in a team based environmentPCR (1 year of experience is preferred)qPCRAsceptic Techniques (1 year of experience is preferred)ELISA (1 year of experience is preferred) Qualifications Years of experience: 1 yearExperience level: Entry Level Randstad is a world leader in matching great people with great companies. Our experienced agents will listen carefully to your employment needs and then work diligently to match your skills and qualifications to the right job and company. Whether you're looking for temporary, temporary-to-permanent or permanent opportunities, no one works harder for you than Randstad.Equal Opportunity Employer: Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status. For certain assignments, Covid-19 vaccination and/or testing may be required by Randstad's client or applicable federal mandate, subject to approved medical or religious accommodations. Carefully review the job posting for details on vaccine/testing requirements or ask your Randstad representative for more information.
    • rockville, maryland
    • contract
    • $30 - $35.25 per hour
    job summary: As the world's largest staffing and recruitment agency in the world, we can commit to finding you the perfect role that gives you the opportunity to learn and grow in the life sciences arena. Utilizing a recruiter for your job search gives you access to a large network of top employers as well as detailed information about hundreds of positions. Focusing on immune diseases like HIV that affect a large percentage of the population, the work our longtime partner conducts is imperative to a better, healthier future. To be recognized as a crucial part to furthering this goal, join this growing team now! This role requires employees to be fully vaccinated against COVID-19 as a condition of employment, subject to a valid medical or religious accommodation.   location: Rockville, Maryland job type: Contract salary: $30.00 - 35.25 per hour work hours: 9 to 5 education: Bachelors   responsibilities: - Provides clerical and administrative support related to documentation processes and systems. - Creates logbooks to be used in production (Lab Notebooks, Logbooks and Documents). - Scans, verifies and archives documentation and records as needed. - Performs general word processing tasks. Checks format and conformance to document templates. - Ensure the correct and timely input of database entries. - Participates in function meetings. - Notifies manager of compliance questions and issues. - Provides additional support and assistance on tasks and projects as directed by management - Assists in the preparation for and participation in regulatory agency inspections, corporate and customer audits. - Performs audit observation follow-up for global quality assurance audits and regulatory inspections as requested. - Participates in applicable root cause analysis teams to review and agree to the CAPA plan, the CAPA performance measures and the assessment dates. - Verify that applicable CAPA has been delivered as committed and that the CAPA remains "in-place" and "in-use". - Assists in creating and administering training on procedures and GMP topics. - Provide metrics to Manager and identify potential trends and gaps.   qualifications: - Minimum of Bachelor of Science in Business, Technical or Scientific Discipline. - Thorough technical and regulatory knowledge of current pharmaceutical manufacturing techniques and the applicable current regulatory and company requirements. - Solid ethics and integrity; confidentiality, impartiality, independent, straight forward, and sensitivity to problems. - Excellent written and oral communication skills. - Must be proficient in MS Office Suite. Veeva and be able to quickly learn new software. - Must have a complete knowledge of current Good Manufacturing Practices, United States Pharmacopeia, current Code of Federal Regulations (21CFR parts 11, 210, and 211) and other DFA, European and global guidance's - Ability to read and interpret documents such as safety rules, operating and maintenance instructions, and procedure manuals. - While performing duties of the job, the employee is frequently required to stand. - Requires physical activity such as standing for long periods of time, walking, bending, and working with hands.   skills: MS-WORD, CAPA, MS-EXCEL, GMP (Good Manufacturing Practice) Equal Opportunity Employer: Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status. For certain assignments, Covid-19 vaccination and/or testing may be required by Randstad's client or applicable federal mandate, subject to approved medical or religious accommodations. Carefully review the job posting for details on vaccine/testing requirements or ask your Randstad representative for more information.
    job summary: As the world's largest staffing and recruitment agency in the world, we can commit to finding you the perfect role that gives you the opportunity to learn and grow in the life sciences arena. Utilizing a recruiter for your job search gives you access to a large network of top employers as well as detailed information about hundreds of positions. Focusing on immune diseases like HIV that affect a large percentage of the population, the work our longtime partner conducts is imperative to a better, healthier future. To be recognized as a crucial part to furthering this goal, join this growing team now! This role requires employees to be fully vaccinated against COVID-19 as a condition of employment, subject to a valid medical or religious accommodation.   location: Rockville, Maryland job type: Contract salary: $30.00 - 35.25 per hour work hours: 9 to 5 education: Bachelors   responsibilities: - Provides clerical and administrative support related to documentation processes and systems. - Creates logbooks to be used in production (Lab Notebooks, Logbooks and Documents). - Scans, verifies and archives documentation and records as needed. - Performs general word processing tasks. Checks format and conformance to document templates. - Ensure the correct and timely input of database entries. - Participates in function meetings. - Notifies manager of compliance questions and issues. - Provides additional support and assistance on tasks and projects as directed by management - Assists in the preparation for and participation in regulatory agency inspections, corporate and customer audits. - Performs audit observation follow-up for global quality assurance audits and regulatory inspections as requested. - Participates in applicable root cause analysis teams to review and agree to the CAPA plan, the CAPA performance measures and the assessment dates. - Verify that applicable CAPA has been delivered as committed and that the CAPA remains "in-place" and "in-use". - Assists in creating and administering training on procedures and GMP topics. - Provide metrics to Manager and identify potential trends and gaps.   qualifications: - Minimum of Bachelor of Science in Business, Technical or Scientific Discipline. - Thorough technical and regulatory knowledge of current pharmaceutical manufacturing techniques and the applicable current regulatory and company requirements. - Solid ethics and integrity; confidentiality, impartiality, independent, straight forward, and sensitivity to problems. - Excellent written and oral communication skills. - Must be proficient in MS Office Suite. Veeva and be able to quickly learn new software. - Must have a complete knowledge of current Good Manufacturing Practices, United States Pharmacopeia, current Code of Federal Regulations (21CFR parts 11, 210, and 211) and other DFA, European and global guidance's - Ability to read and interpret documents such as safety rules, operating and maintenance instructions, and procedure manuals. - While performing duties of the job, the employee is frequently required to stand. - Requires physical activity such as standing for long periods of time, walking, bending, and working with hands.   skills: MS-WORD, CAPA, MS-EXCEL, GMP (Good Manufacturing Practice) Equal Opportunity Employer: Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status. For certain assignments, Covid-19 vaccination and/or testing may be required by Randstad's client or applicable federal mandate, subject to approved medical or religious accommodations. Carefully review the job posting for details on vaccine/testing requirements or ask your Randstad representative for more information.

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