chemist ii & iii

job summary:
As the world's largest staffing and recruitment agency in the world, we can commit to find 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. We supply prestigious life sciences and biopharma companies with job seekers like you to achieve their business goals. If you're looking for a position where you can serve as an asset to your company while making a difference in others' lives, we have the ideal position for you!

location: Wilson, North Carolina
job type: Contract
salary: $45.54 - 53.57 per hour
work hours: 9 to 5
education: Bachelors

responsibilities:
Job Description

Support operations by providing analytical testing for material and products, including data analysis and reporting

Responsibilities - Chemist II

• Demonstrates an understanding of technical concepts supporting methodology and systems in Material or Product Testing
• Performs troubleshooting and initial investigative work related to OOS, OOE, OOT.
• Leads others consistently in productivity, quality and teamwork metrics. Drives continuous improvement initiatives within Quality control
• Demonstrates independence and proficiency in performing tests for most products supported by work group. Reviews peer work for accuracy and compliance
• Identifies suspect data and works with management to complete investigations
• Identifies technical and compliance issues and works with management on implementing solutions
• Performs other duties as assigned
• Adhere to all applicable procedures, cGMPs, company policies and any other quality or regulator requirements. (For example: OSHA, DEA, FDA, EMEA, ANVISA, HS&E, Etc)

Responsibilities - Chemist III

• Preforms troubleshooting and initial investigative work related to OOS, OOT. Identifies suspect data an works with management to complete an investigations
• Demonstrates a higher level of understanding of technical concepts supporting methodology and systems in Material or Product Testing. Leads consistently in productivity, quality and teamwork and compliance.
• Demonstrates independence and proficiency in performing tests for most products supported by work group. Conducts all testing in compliance with cGMP and SOP's. May participate in activities related to method development, optimization and validation.
• Works with supervisors to plan and complete testing, data evaluation and LIMS reporting
• Identifies suspect data and works with management to complete investigations. Can write KLE, Phase 1 investigations
• Proactively identifies technical and compliance issues and leads initiatives to resolve issues and implement other improvements.
• Maintains proper documentation of laboratory data (which requires adequate proficiency in written and computational skills). Can write protocols, methods and other technical documents.
• Can represent QC in regulatory audits with coaching support
• IF A TEAM LEAD - Will lead in the testing and training of others within workgroup. Communicates to the team any changes in SOPs or policies required for improvement. Takes the leadership role in communicating and implementing ideas from the team for system improvements. Has a basic understanding of project management.
• IF A TEAM LEAD - Communicates with supervisors and tam members regarding prioritization of product testing. Communicates with outside departments regarding team deliverables. Advises supervisors of any problems/conflicts within teams
• IF A TEAM LEAD - Working from Control Center Report, ensures that all testing is completed by time commitments. Assist with the organization of work flow and resources. Provides materials and tools for team on as needed basis.
• IF A TEAM LEAD - Provides final approval of log books. Spends 95% of time on the lab floor performing testing of material and products for support of production and assure quality. Assist in makes decisions regarding the allocation of work and resources.
• Performs other duties as assigned.
• Adheres to all applicable procedures, cGMPs, company policies and any other quality or regulatory requirements. (For example: OSHA, DEA, FDA, EMEA, ANVISA, HS&E, etc.)

qualifications:
Education / Background

• BS/BA in Chemistry or Life Science, preferred
• MUST have Pharmaceutical GMP experience
• Fluent in written and spoken English
• FOR Chemist II 2-4 years of related exp
• FOR Chemist III 5-8 Years of related exp

skills: Chemistry, 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.

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 health, an incentive and recognition program, and 401K contribution (all benefits are based on eligibility).




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.