Overview
On Site
USD 38.39 - 43.39 per hour
Contract - W2
Skills
Onboarding
Training
Swing
Preventive Maintenance
Performance Management
Project Management
Quality Control
Assays
Documentation
Business Process
Laboratory Equipment
Auditing
Inspection
Effective Communication
Partnership
Accountability
Management
Life Sciences
Good Manufacturing Practice
Pharmaceutics
Testing
Analytical Skill
Reasoning
Conflict Resolution
Problem Solving
Supervision
System Integration Testing
Communication
MEAN Stack
Customer Service
Training And Development
SAP BASIS
Job Details
Software Guidance & Assistance, Inc., (SGA), is searching for a Quality Control Technician I for a contract assignment with one of our premier Pharmaceutical clients in Hillsboro, OR.
Available Shifts: Sunday to Wednesday and Wednesday to Saturday, 4x10's* (onboarding and initial training period may require Mon-Fri, 5X8s, shift)
Day: 6:30am to 5:00pm
Swing: 11:30am to 10:00pm
Contract duration: 12 months with possible extension
Responsibilities :
SGA is an Equal Opportunity Employer and does not discriminate on the basis of Race, Color, Sex, Sexual Orientation, Gender Identity, Religion, National Origin, Disability, Veteran Status, Age, Marital Status, Pregnancy, Genetic Information, or Other Legally Protected Status. We are committed to providing access, equal opportunity, and reasonable accommodation for individuals with disabilities in employment, and our services, programs, and activities. Please visit our company to request an accommodation or assistance regarding our policy.
#LI-PA2
Available Shifts: Sunday to Wednesday and Wednesday to Saturday, 4x10's* (onboarding and initial training period may require Mon-Fri, 5X8s, shift)
Day: 6:30am to 5:00pm
Swing: 11:30am to 10:00pm
Contract duration: 12 months with possible extension
Responsibilities :
- Responsibilities include Implementing, modifying, and enforcing Quality Control policies, procedures, specifications and testing methods consistent with cGMP, regulations, appropriate compendium, and firm standards, policies, plans, objectives and procedures.
- Routine sampling, performing, and reviewing a variety of assays in the Quality Control organization in support of In-process, drug product, finished product, raw materials and incoming inspection, and environmental monitoring testing in a cGMP environment.
- Must be able to Interpret data, troubleshoots, assay failures and equipment issues while adhering to strict guidelines on cGMP documentation.
- Supports method validation activities, performance qualifications, method transfers, discrepancy/out-of-specification investigations and collaborates with stakeholders to identify improvement opportunities in technology and business processes.
- Ensure maintenance and calibration of laboratory equipment and systems.
- Support during cGMP audits and Health Authority inspections as needed and follow up on any corrective measures as required.
- Impacts quality of own work and the work of others on the team; works within guidelines and policies.
- Maintain a state of inspection readiness.
- Works autonomously with guidance only on complex new assignments.
- Uses ability as a technical/functional expert to contribute in development of concepts and techniques, and to complete complex assignments in creative and effective ways.
- Perform environmental monitoring and water sampling.
- Has interaction at the Supervisor and Manager levels on matters pertaining to the immediate area of work. Interactions require tact and effective communication skills as they often involve complex and sensitive information.
- Participate in the design and implementation of department and cross-functional initiatives.
- Apply basic theory and technical principles to address moderately complex problems.
- Troubleshoot and initiate the resolution of Quality issues by fostering effective interdepartmental and cross functional partnerships.
- Serve as a technical subject matter expert (SME) in support of department functions.
- Be accountable for behaviors as described in firm's Core, Common, and Critical
- Perform any other tasks as requested by Management to support Quality oversight activities
- B.A. or B.S. degree (preferably in Life Science) and at minimum 3 years' experience in a cGMP pharmaceutical, biopharmaceutical industry
- Hands-on industrial laboratory experience with aseptic sampling and testing techniques.
- Demonstrated ability to apply knowledge of scientific theories, principles, and techniques used in analytical or biological test procedures.
- Routinely exercises sound judgment, reasoning and problem solving.
- Capable of working under moderate supervision and determining own short-term priorities.
- Work in office and laboratory environment. Lift up to 25lbs may be required.
- Ability to sit, stand and move within workspace for extended periods. May be required to sit at a computer terminal for extended periods.
- Strong verbal and written communication skills, ability to organize and present information in a formal and informal group setting.
SGA is an Equal Opportunity Employer and does not discriminate on the basis of Race, Color, Sex, Sexual Orientation, Gender Identity, Religion, National Origin, Disability, Veteran Status, Age, Marital Status, Pregnancy, Genetic Information, or Other Legally Protected Status. We are committed to providing access, equal opportunity, and reasonable accommodation for individuals with disabilities in employment, and our services, programs, and activities. Please visit our company to request an accommodation or assistance regarding our policy.
#LI-PA2
Employers have access to artificial intelligence language tools (“AI”) that help generate and enhance job descriptions and AI may have been used to create this description. The position description has been reviewed for accuracy and Dice believes it to correctly reflect the job opportunity.