The Quality Control Technical Transfer Analyst 3 will act as a team member of the Quality Control department to support production by contributing to the completion of the technical transfer activitIes. Also participate in quality testing for customer in-process, final product testing and stability studies when needed.
Applies job skills and company's policies and procedures to complete a variety of tasks of increased scope. Works on assignments that are semi-routine in nature where ability to recognize deviation from accepted practice is required. Works on problems of moderate scope in which analysis of situation or data requires a review of identifiable factors.
location: Portsmouth, New Hampshire
job type: Contract
salary: $28.05 - 33.00 per hour
work hours: 9 to 5
education: Associate
responsibilities:
- Applies job skills and company's policies and procedures to complete a variety of tasks.
- Running test samples for In-Process, Lot Release, and Stability studies.
- Running test samples for (but not limited to) investigations, transfers, and validations.
- Reviewing assays.
- Training others.
- Writing Quality Records (Deviations, CAPA, Change Control) and Test Methods.
- Handling projects such as method transfers, new instruments, and method qualifications.
- Applying Data Integrity principles in all aspects of work, in compliance with Lonza DI policies, guidelines, and procedures.
- Working on assignments that are semi-routine in nature where the ability to recognize deviation from accepted practice is required.
- Working on problems of moderate scope in which analysis of a situation or data requires a review of identifiable factors.
- Exercising judgment within defined procedures and practices to determine appropriate action.
- Performing other duties as assigned.
qualifications:
Technical Skills:
- Use of Microsoft Suites (Word, Excel, PowerPoint).
- Use of Laboratory computer systems.
- Potential previous use of GMP Quality Systems such as TrackWise, LIMS.
- Strong ability to interpret data both alone and with guidance.
- Prioritization and problem-solving.
- Brainstorming.
- Ability to comprehend and follow instructions.
- Strong ability to speak publicly.
- Strong ability to communicate in both written and verbal format.
- Ability to relate to others in a team setting.
- Self-motivated team player.
- Ability to direct, control, and plan tasks/projects.
- Completes assignments on-time and accurately.
- Displays commitment to quality and performs job functions to the best of his/her ability.
- Maintains a positive attitude in a team environment.
- Demonstrates timeliness in completing assigned tasks.
- Works entire assigned shift, including arriving on time.
- Associate's Degree in Microbiology, Biochemistry, or Related Science Fields.
skills: GMP (Good Manufacturing Practice), Laboratory Information Management System (LIMS), Corrective and Preventive Actions (CAPA)
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.
