controller salaries in raleigh, north carolina

Our client is seeking an individual that is EXPERIENCED with Quickbooks Desktop to join their team as their clientele increases.  This is an onsite role where they are looking for someone to start quickly due to their clientele growth to help with bookkeeping and quarterly reporting.  This is a 40 hour a work week located 100% on site.  If you have the minimum experience of Quickbooks, please apply today to learn more!salary: $42,000 - $52,000 per yearshift: Firstwork hours: 8 AM - 5 PMeducation: No Degree RequiredResponsibilities Perform Bookkeeping and payroll processing for multiple clients Generate quarterly financial reports using Quickbooks Read and interpret income statements and balance sheets Assist with simple tax returns of 1040's that may include schedule C as needed Maintain accurate and timely financial records in accordance with company's policies  SkillsQuickBooks (2 years of experience is required)QualificationsYears of experience: 2 yearsExperience level: ExperiencedRandstad 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.At Randstad, we welcome people of all abilities and want to ensure that our hiring and interview process meets the needs of all applicants. If you require a reasonable accommodation to make your application or interview experience a great one, please contact HRsupport@randstadusa.com.Pay offered to a successful candidate will be based on several factors including the candidate's education, work experience, work location, specific job duties, certifications, etc. In addition, Randstad offers a comprehensive benefits package, including: medical, prescription, dental, vision, AD&D, and life insurance offerings, short-term disability, and a 401K plan (all benefits are based on eligibility).This posting is open for thirty (30) days.

If you are you a meticulous and driven Quality Assurance professional looking to make a significant impact, Randstad is looking for qualified professionals to work onsite with their client in RTP. In this position, you will have an opportunity to work in a well-respected Biotechnology company AND have the support you need with a career coach guiding you towards success :) PLEASE DO NOT APPLY if you live outside the Raleigh-Durham area as this role is 100% onsite.salary: $29.99 - $30 per hourshift: Firstwork hours: 8 AM - 5 PMeducation: BachelorsResponsibilitiesWhat You'll Do: Be a Guardian of Quality: Meticulously review GMP raw data for compliance, ensuring the integrity of our processes and products with your review and approval of batch related documentation (Solution Lot records, Reports, Logbooks and Release of Autoclaved Equipment). Transport batch related documentation across RTP buildings supporting chain of custody and life cycle management. Ensure Compliance Excellence: Support the resolution of technical and compliance issues/gaps. Collaborate and Grow: Partner with key Quality and Manufacturing teams, gaining exposure to diverse aspects of biopharmaceutical production and contributing to the day-to-day implementation of cGMP. Assist in additional responsibilities related to the day-to-day implementation of the Quality Management Systems required to maintain cGMP compliance, ensuring the safety, efficacy and purity of the products. Logistics & Life Cycle Management: Secure transport of critical batch documentation, supporting seamless chain of custody. Opportunity to contribute to projects. Preferred Professional Experience: 2-5 years' experience as a QA associate within a large molecule, drug substance facility Regulatory requirements in the pharmaceutical industry (FDA, EMA) Able to manage multiple tasks in a fast-paced environment Education: Bachelor’s degree in science or other related field of study The essential functions of this role include:working in a smoke free environmentSkillsQuality AssuranceBatch Records (2 years of experience is required)Data Management (2 years of experience is required)cGMP (2 years of experience is preferred)Biotech (2 years of experience is preferred)Biomanufacturing (2 years of experience is preferred)Large Scale Manufacturing (1 year of experience is preferred)Audit - External (1 year of experience is preferred)QualificationsYears of experience: 2 yearsExperience level: ExperiencedRandstad 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.At Randstad, we welcome people of all abilities and want to ensure that our hiring and interview process meets the needs of all applicants. If you require a reasonable accommodation to make your application or interview experience a great one, please contact HRsupport@randstadusa.com.Pay offered to a successful candidate will be based on several factors including the candidate's education, work experience, work location, specific job duties, certifications, etc. In addition, Randstad offers a comprehensive benefits package, including: medical, prescription, dental, vision, AD&D, and life insurance offerings, short-term disability, and a 401K plan (all benefits are based on eligibility).This posting is open for thirty (30) days.

job summary: An Assistant Project Coordinator is needed for a multinational biotechnology company that specializes in the discovery, development, and delivery of therapies for the treatment of neurodegenerative, hematologic, and autoimmune diseases to patients worldwide in the Morrisville, NC area. This role supports MES implementation and operational readiness activities within a large-scale pharmaceutical manufacturing modernization project, requiring technical documentation, coordination, and compliance expertise.   location: Morrisville, North Carolina job type: Contract salary: $61.15 - 79.13 per hour work hours: 8am to 5pm education: Bachelors   responsibilities: Support the operational readiness workstream for MES implementation.Assist Manufacturing Technology Operations (MTO) team with daily project activities.Help with documentation generation and processing in a digital document management system.Attend project meetings and track related actions and decisions.Map batch record traceability and respond to MES design questions.Interact directly with validated MES system and related documentation. Skills: Familiarity with GMP, FDA, and EMA regulatory standards.strong technical writing, communication, and interpersonal skills.Analytical, detail-oriented, and able to manage multiple priorities in a fast-paced setting.Demonstrated success in compliance-driven, regulated environments.Experience working in cross-functional, matrix teams.Proficient with MS Office and digital documentation platforms (e.g., myCIMS, Veeva). Education and Experience: Bachelor's degree in Engineering, Science, or a related technical discipline.5+ years of experience in pharmaceutical/biotech technical operations support.Experience in large molecule drug substance manufacturing.Experience with MES or EBR implementation is preferred. #LI-SJ1   qualifications: Experience level: ExperiencedEducation: Bachelors  skills: Project ManagementComplianceMSOfficeManufacturingOperations 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.At Randstad, we welcome people of all abilities and want to ensure that our hiring and interview process meets the needs of all applicants. If you require a reasonable accommodation to make your application or interview experience a great one, please contact HRsupport@randstadusa.com. Pay offered to a successful candidate will be based on several factors including the candidate's education, work experience, work location, specific job duties, certifications, etc. In addition, Randstad offers a comprehensive benefits package, including: medical, prescription, dental, vision, AD&D, and life insurance offerings, short-term disability, and a 401K plan (all benefits are based on eligibility). This posting is open for thirty (30) days.