QA Specialist III Night Shift (2-2-3)

Work Schedule

Environmental Conditions

Job Description

Thermo Fisher Scientific Inc. is the world leader in serving science with annual revenue exceeding $40 billion. Our Mission is to enable our customers to make the world healthier cleaner and safer. Whether our customers are accelerating life sciences research solving complex analytical challenges improving patient diagnostics and therapies or growing efficiency in their laboratories we are here to support them. Our global organization of more than 100000 colleagues delivers an outstanding combination of innovative technologies purchasing convenience and pharmaceutical services through our industry-leading brands including Thermo Scientific Applied Biosystems Invitrogen Fisher Scientific Unity Lab Services and Patheon. For more information please visit .

GROUP/DIVISION SUMMARY

The Drug Product Division - North America (DPD-NA) is one of the five divisions that make up the Pharma Services Group. We are made up of approximately 4400 colleagues across six sites who specialize in taking sterile injectable and oral solid dose drug products from development to commercialization.

POSITION SUMMARY

In this position youll drive quality execution across the sterile operations including manufacturing filling packaging and inspection and associated non batch specific activities in for both commercial and product development services products. Additionally this position will provide quality guidance and expertise for implementation of practical process improvements and continuous improvement initiatives. Typical hours are 6p - 6a on a 2-2-3 rotation.

Key Responsibilities:

Perform daily quality assessments of facility personnel and documentation both classified and non-classified areas to uncover errors or deficiencies assure quality and compliance per site procedures and cGMPs.

Daily interaction with employees to assist with troubleshooting documentation corrections/notes and guidance with aseptic technique

Champions quality culture by aiding personnel in understanding application of policies and controls

Participates in RAPID event response and provides quality guidance for deviation events

Advances deviation events to the appropriate area and quality management

Performs quality review and approval of procedures training documents and forms of moderate to high complexity

Performs quality review and approval of deviation and change control of moderate to high complexity

Participates as the quality assurance representative in Root Cause Analysis to support deviation investigations of moderate to high complexity

Performs quality batch record review

Aids in identification of continuous improvement opportunities; Participates in practical process improvement initiatives

Qualifications:

A minimum of 4 years of experience with previous experience in Quality Assurance or Quality control or Operations/Manufacturing

Previous experience in pharmaceutical industry; preferably aseptic or steriles processes strongly preferred experience in other regulated environments may be considered (i.e. ISO 9001)

Ability to capture data analyze & troubleshooting process issues equipment problems along with production leadership

Ability to troubleshoot process and equipment issues

Hard-working demonstrated ownership & responsibility.

Ability to lead support & empower a team/peers

Technical Writing experience

Professional certifications (ex: CQA) and training (Six Sigma) are a plus

Primary responsibilities require consistent production floor presence which necessitate physical fitness for prolonged standing walking and repetitive bending and aseptic and non-aseptic gowning.

Education:

Bachelors degree preferably in technology engineering or microbiology related field required.

Equivalent combinations of education training and relevant work experience may be considered

Physical Requirements:

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 1035-pound pounds. Arm hand and finger dexterity including ability to grasp and type for prolonged periods of time. Visual acuity to use a keyboard computer monitor operate equipment and read materials for prolonged periods of time. Ability to sit reach with hands and arms talk and hear for prolonged periods of time. Safety glasses safety shoes lab coat nitrile or similar gloves safety apron organic respirator occasionally.

BENEFITS

We offer competitive remuneration annual incentive plan bonus healthcare and a range of employee benefits. Thermo Fisher Scientific offers employment with an innovative forward-thinking organization and outstanding career and development prospects. We offer an exciting company culture that stands for integrity intensity involvement and innovation. Apply today!

Thermo Fisher Scientific is an EEO/Affirmative Action Employer and does not discriminate on the basis of race color religion sex sexual orientation gender identity national origin protected veteran status disability or any other legally protected status.

Accessibility/disability access

Job Seekers with a Disability: Thermo Fisher Scientific offers accessibility service for job seekers requiring accommodations in the job application process. For example this may include individuals requiring assistance because of hearing vision mobility or cognitive impairments. If you are a job seeker with a disability or assisting a person with a disability and require accessibility assistance or an accommodation to apply for one of our jobs please submit a request by telephone at 1-*. Please include your contact information and specific details about your required accommodation to support you during the job application process.