Job details
Salary $13 - $28 an hour job type full-time contract number of hires for this role 1
Qualifications
Bachelor`s (preferred)
Full job description
Position is remote/onsite as needed
Job description:
Responsibilities:
Work independently to assist in investigation of process deviations, data trending, change controls and other documentationPerform manual or automated process performance data extraction, reporting and analysis.
Coordinate the execution of process validation protocols, including scheduling, communication, coordination of sample delivery and data collection.
Coordinate activities between manufacturing technology, manufacturing operating groups, supply chain, and qa/qc to meet project timelines.
Achieve high customer satisfaction through effective communication of both technical and non-technical topics with all levels of the organization both verbally and in writing.
Education:
Bs degree in science or engineering related to biopharmaceutical process technology
Experience:
Minimum of 1-2 years biopharmaceutical or equivalent industry experience.
Excellent verbal & written communications skills.
Interpersonal / facilitation skills necessary to interface with and influence all levels of the organization.
Broad knowledge of biopharmaceutical facility design and manufacturing operations is highly desirable.
Electronic database systems and statistical analytical packages is highly desirable
Job types: full-time, contract
Pay: $13.00 - $28.00 per hour
Schedule:
8 hour shift
Monday to friday
Ability to commute/relocate:
Ayer, ma: reliably commute or planning to relocate before starting work (preferred)
Education:
Bachelor`s (preferred)
Experience:
Quality deviations: 2 years (preferred)
Quality investigation: 2 years (preferred)
Process validation protocols: 2 years (preferred)
Change controls: 2 years (preferred)
Work location:
One location
Work location: one location
