Address
Form of work Qualifications
Education Minimum Requirement:•
Bachelor's degree in Science, Chemistry, Biochemistry, Biology, or related science field.
Required Experience and Skills:•
Minimum of one (1) year of experience in Laboratory GMP regulated environment.• Two (2) plus years in a pharmaceutical manufacturing and cGMP environment• GLIMS experience•
Technical communication (written & presentation) skills.A successful candidate will exhibit: -• Understanding of the fundamental business drivers for the company and apply this knowledge in their own work.•
Ability to interpret Company Quality Policies and Guidelines for daily application.• Understanding and active application of regulatory/compliance requirements, including GMP and related regulations, and ability to interpret those regulations for implementation in the workplace.•
A knowledge of theories, processes, and procedures in the Quality Laboratory.• Strong technical writing capabilities.NOTE:This is a 100% onsite role. Candidate should be flexible to come in earlier if needed.Positions available: 2
Responsibilities: •
Perform stability sample pulls using GLIMS and delivery to the laboratory, adhering to GMP processes and procedures.•
Perform receipt of stability samples from production units.• Perform shipment of stability samples to external testing laboratories.•
Perform build and setup of stability studies in GLIMS.• Able to clearly represent individual status/accomplishments.•
Actively promotes an inclusive culture.•
Properly documents, investigates, and identifies proactive measures to ensure right first-time achievements.• Understand and apply Data Integrity concepts.
Job Types: Full-time, Contract
Pay: $25.00 - $27.00 per hour
Expected hours: 40 per week
Schedule:
8 hour shift
Day shift
Monday to Friday
Experience:
pharmaceutical: 2 years (Required)
CGMP: 2 years (Required)
Laboratory: 2 years (Required)
Ability to Relocate:
Wilson, NC 27893: Relocate before starting work (Required)
Work Location: In person
Education Minimum Requirement:•
Bachelor's degree in Science, Chemistry, Biochemistry, Biology, or related science field.
Required Experience and Skills:•
Minimum of one (1) year of experience in Laboratory GMP regulated environment.• Two (2) plus years in a pharmaceutical manufacturing and cGMP environment• GLIMS experience•
Technical communication (written & presentation) skills.A successful candidate will exhibit: -• Understanding of the fundamental business drivers for the company and apply this knowledge in their own work.•
Ability to interpret Company Quality Policies and Guidelines for daily application.• Understanding and active application of regulatory/compliance requirements, including GMP and related regulations, and ability to interpret those regulations for implementation in the workplace.•
A knowledge of theories, processes, and procedures in the Quality Laboratory.• Strong technical writing capabilities.NOTE:This is a 100% onsite role. Candidate should be flexible to come in earlier if needed.Positions available: 2
Responsibilities: •
Perform stability sample pulls using GLIMS and delivery to the laboratory, adhering to GMP processes and procedures.•
Perform receipt of stability samples from production units.• Perform shipment of stability samples to external testing laboratories.•
Perform build and setup of stability studies in GLIMS.• Able to clearly represent individual status/accomplishments.•
Actively promotes an inclusive culture.•
Properly documents, investigates, and identifies proactive measures to ensure right first-time achievements.• Understand and apply Data Integrity concepts.
Job Types: Full-time, Contract
Pay: $25.00 - $27.00 per hour
Expected hours: 40 per week
Schedule:
8 hour shift
Day shift
Monday to Friday
Experience:
pharmaceutical: 2 years (Required)
CGMP: 2 years (Required)
Laboratory: 2 years (Required)
Ability to Relocate:
Wilson, NC 27893: Relocate before starting work (Required)
Work Location: In person
