Quality Analyst II

Employment Type

: Full-Time

Industry

: Information Technology



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Quality Analyst II



**job details:**



+ location:North Billerica, MA

+ salary:$42,000 - $58,000 per year

+ date posted:Thursday, September 19, 2019

+ experience:Experienced

+ job type:Permanent

+ reference:S_800956

+ questions:...@randstadusa.com978-###-####



**job description**



Quality Analyst II



Perform testing on incoming materials, finished products and stability studies in QC Laboratory. Work in both lab and warehouse areas. May be trained as fork truck operator.



Responsibilities:

Perform routine QC testing in accordance with SOPs and cGMP guidelines. Some supervision required.

Perform verification of data to ensure accuracy. Perform approval upon discretion of supervisor.

Assist with audit readiness of laboratory area and calibration and maintenance of laboratory equipment.

Utilize a range of electronic systems such as LIMS and document/equipment management software.

Author SOP changes; participate in change controls, CAPAs and other quality systems.

Resolve routine problems by utilizing appropriate resources. Assist in investigations.

May assist on special projects as needed. Help with continuous improvement.



Working hours: 8:00 AM - 5:00 PM



Skills:

Train on and maintain knowledge of current regulatory requirements and relevant internal procedures.

Work independently and as a team player with quality and attention to detail. Good communication skills both oral and written. Effectively and efficiently participate in assigned tasks in a quality manner.

Actively promote safety rules and awareness. Report and take initiative to correct safety & environmental hazards. Work with potentially hazardous chemical, radiological and/or biological materials on a daily basis. Demonstrate good safety practices at all times including the appropriate use of protective equipment.



Education:

Bachelors



Experience:

Experienced



Qualifications:

Testing also includes visual inspections, dimensional verifications and analytical testing.

Additional materials tested include components, printed materials and chemicals.

Group is additionally responsible for raw materials, chemical sampling, the release of materials, retaining inventory, and stability setup and pulls.

Typically requires 1-3 years of previous experience in the pharmaceutical industry, related GMP environment, or equivalent. Previous experience preferred.

Requires a BA/BS degree in a related scientific discipline (e.g. chemistry, biology) or equivalent combination of education and experience.

Some non-routine travel may be required.

Flexibility with scheduling requirements-may include shifts, overtime, weekends and holiday coverage, including during adverse weather conditions.

Must be able to lift 50 lbs.



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Randstad is a world leader in matching great people with great companies. Our experienced agents will listen carefully to your employment needs and then work diligently to match your skills and qualifications to the right job and company. Whether you're looking for temporary, temporary-to-permanent or permanent opportunities, no one works harder for you than Randstad. EEO Employer: Race, Religion, Color, National Origin, Citizenship, Sex, Sexual Orientation, Gender Identity, Age, Disability, Ancestry, Veteran Status, Genetic Information, Service in the Uniformed Services or any other classification protected by law.
Associated topics: automation, performance test, process, prevention, quality assurance, quality assurance analyst, software quality, software quality engineer, software quality assurance engineer, test engineer

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