Top 4 Senior inspector Jobs in Greenville, Nc

Sr. QA Technician: Records Specialist (8hr days, Monday-Friday)
Thermo Fisher Scientific —Greenville, NC
- 8 hour shift
- Ability to walk for extended periods
- Mid-level
- Office
7d
Sr QA Technician: Batch Records Release (8hr days, Mon-Fri)
Thermo Fisher Scientific —Greenville, NC
- 8 hour shift
- Ability to walk for extended periods
- Basic math
- Mid-level
Sr QA Technician (8hr days, Monday-Friday)
Thermo Fisher Scientific —Greenville, NC
- 8 hour shift
- Ability to walk for extended periods
- Laboratory experience
- Mid-level
7d

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Sr. QA Technician: Records Specialist (8hr days, Monday-Friday)

Thermo Fisher Scientific -
Greenville, NC

Apply Now

Job Details

Full-time
7 days ago

Qualifications

GMP
High school diploma or GED
Manufacturing facility experience
Quality assurance experience within pharmaceutical industry
Pharmaceutical manufacturing facility experience

Full Job Description

Work Schedule

First Shift (Days)

Environmental Conditions

Office

Job Description

Job Description

Location/Division Specific Information

As part of the Drug Product Division (DPD), the Greenville, North Carolina site is a multi-purpose pharmaceutical development, manufacturing, and packaging campus. The operation specializes in taking both sterile injectable and oral solid dose drug products from development phase through to commercialization.

How Will You Make an Impact

The Sr. Quality Technician, Provides direct quality support to ensure compliance with regulations that govern pharmaceuticals. Ensures the site operates in compliance with regulatory standards that ensures product quality, avoids stoppages and reinforces customer satisfaction. Day shift hours are Monday-Friday, 8am-5pm.

A Day in the Life

Follow all job-related safety and other training requirements.
Performs document reviews and makes determinations as to whether work performed meets current procedures and regulatory expectations.
Communicates and coordinates with other departments as required to resolve issues and compliance concerns detected during review.
Conducts risk assessments and take appropriate actions during quality oversight activities (e.g. during review/approval) to ensure adequate controls in relation to the level of product quality, safety and business risks.
Advances deviation events to the appropriate area and quality management.
Performs processes and projects of moderate complexity, ensuring adherence to current regulations with little dependence on others.
Provides leadership and team participation as assigned for assignments related to quality initiatives and compliance improvements, product transfers, facility expansions, etc.
Advances deviation events to the appropriate area and quality management

Education

High School Diploma or equivalent required
Associates degree or higher in Science or Technology is preferred

Experience

Required: Minimum of 2 years of work experience in QA or QC or related field
Required: Experience in a cGMP environment
Equivalent combinations of education, training, and relevant work experience may be considered.

Knowledge, Skills, Abilities

Outstanding attention to detail and organizational skills.
Self-starter, mature, independent and reliable
Ability to work in a fast-paced environment under pressure and able to multi-task.
Effective time management and prioritization skills.
Requires discretion and independent judgment.
Highly effective verbal and written communication skills.
Ability to work on a team and help lead that team to be successful and productive.

Physical Requirements/Work Environment

Use Personal Protective Equipment (PPE) and understand chemical hygiene.
Infrequently lift and manipulate up to 50 pounds max unassisted.
Stand and move about including reaching, bending, stooping, grasping.
Use hand tools and equipment including forceful gripping, grasping, pushing and pulling.
Position requires ordinary ambulatory skills and physical coordination sufficient to move about office locations; ability to stand, walk, stoop, kneel, crouch periodically for prolonged periods of time; manipulation (lift, carry, move) of light to medium weights of 10-35 pounds.

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senior inspector jobs in greenville, nc

Sr. QA Technician: Records Specialist (8hr days, Monday-Friday)

Sr QA Technician: Batch Records Release (8hr days, Mon-Fri)

Sr QA Technician (8hr days, Monday-Friday)

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