Thermo Fisher Scientific
Engineer II, QA Floor
Thermo Fisher Scientific, St Louis, Missouri, United States,
Work Schedule
First Shift (Days)
Environmental Conditions
Adherence to all Good Manufacturing Practices (GMP) Safety Standards, Cleanroom: no hair products, jewelry, makeup, nail polish, perfume, exposed piercings, facial hair etc... allowed
Job Description
Job Title: Engineer II, QA Floor
Requisition ID:
About Thermo Fisher Scientific
Thermo Fisher Scientific Inc. is a global leader in serving science, enabling our customers to make the world healthier, cleaner, and safer. With our mission to enable our customers to make the world a better place, we are dedicated to delivering exceptional products and services to support scientific research and discovery.
Location/Division Specific Information
St. Louis MO / Pharma Services Group
The St Louis site is a fast-paced biologic drug substance manufacturing facility. It operates around the clock and employs around 1k people. The facility is focused on cell process development to support clinical and commercial manufacturing. The products produced here treat chronic health conditions, including cancers and other life-threatening diseases.
This is a non-supervisory role, working with the Supervisor of QA Operations. This position will be expected to work a shift schedule that includes weekend work and on-call rotation (Wednesday-Saturday, 6AM-4:30PM).
Discover Impactful Work:
Quality Engineer II is a quality assurance professional with substantial prior experience of working within a Quality, Process Engineering, or Manufacturing organization in a highly regulated industry. This individual specializes in evaluation of production processes and performance in manufacturing and participates in projects to engineer quality improvements of existing production processes as well as the development of new processes to improve quality and efficiency. Other job duties include but are not limited to understanding contamination/cross-contamination, observing aseptic practices, performing daily GEMBAs of manufacturing areas, continuously assessing fit and finish of the facility, and performing compliance inspections within manufacturing areas. This role supports Manufacturing and Process Engineering by providing Quality input as needed, and requesting the initiation of deviations as they are identified. All activities are in support of producing and releasing quality bulk drug substance for clinical and commercial clients.
What will you do? (Responsibilities)
Spend the majority of work hours in manufacturing areas supporting active processing and working closely with Manufacturing and Process Engineering to oversee activities from a quality perspective and provide QA-related input
Collaborate with multi-functional teams to develop, optimize, and improve processes to enhance efficiency, productivity, and quality
Conduct thorough audits and inspections to ensure sustained compliance with industry standards and regulations in preparation for internal quality audits, client audits, and regulatory inspections
Observe aseptic practices and provide immediate coaching to site colleagues to prevent contamination and cross-contamination
Participate in client and regulatory audits as a SME on the Fit and Finish, Changeover, and Change Control procedures and practices
Observe critical process steps assuring alignment with guiding procedures, batch records, and established aseptic practices and be available to manufacturing and PE for support in real time
GEMBA all active areas daily as well as other areas within the core as scheduled, and provide immediate feedback to colleagues and area management to ensure compliance with cGMP’s, site procedures, and regulatory requirements
Perform QA approval of suite and equipment changeover between client processes
Perform autoclave logbook review and facilitate corrections
Perform Fit and Finish inspections per the risk assessment and guiding procedures
Perform monthly aseptic observations of critical activities performed in Biosafety Cabinets
Attend and actively participate in MFG huddles
Lead/attend and actively participate in QA OTF Tier 1 huddles
Act as Quality Management Representative for the company as needed
Take actions to develop one’s own knowledge and skills
Perform all training requirements in a timely manner
Provide training, coaching, and mentorship to new and/or less experienced team members on quality standards and effective strategies
Qualify new team members to perform tasks that require QSME training
Write and review deviations in Trackwise as required
Author, revise, and review procedures in eDMS as required
Write and implement CAPA’s as needed
Conduct/participate in investigation interviews/RAPIDs as required
Individuals in this group must be able to obtain buy-in and cooperation to resolve issues and maintain quality culture and quality standards throughout Operations with no direct authority over the people with whom they interact. Utilization of tact and diplomacy with internal and external customers is essential
Education and Experience
Bachelor's Degree (BA/BS) in Life Sciences (biology, chemistry, biochemistry), Engineering, or another science related field combined with a minimum of three (3) years of relevant experience is required
Experience with cell culture, protein purification, formulations, or facilities/utilities in a GMP pharmaceutical or biopharmaceutical environment is preferred
Cleanroom manufacturing experience is highly preferred along with a comfort level with full ISO 5 and ISO 7 gowning requirements
Non-science degrees will be considered if combined with a minimum of seven (7) years of directly related work experience in biopharmaceutical manufacturing
Knowledge
Understanding ‘why’ and not just the ‘how’ of processes and practices
Knowledge of Quality practices and cGMP regulations and other international health authority guidelines
Experience with investigational writing software system (TrackWise) along with root cause analysis tools used in deviation investigations
Technical writing skills and the ability to write/revise procedures in document management software
Tech transfer experience is a plus
Experience with Lean Manufacturing and Six Sigma methodologies is a plus
Excellent problem-solving and analytical skills
Skills
Analytical, critical thinking, and problem solving skills
Strong interpersonal skills
Strong written and oral communication skills
Strong math skills
Strong attention to detail
Strong Microsoft Office skills (especially Word and Excel)
Strong time management and organization skills
Abilities
Understand and carry out instructions
Effectively multi-task
Work effectively in a dynamic environment
Able to work under pressure
Able to work independently
Proven ability to lead others
Able to coordinate workload for junior team members
Able to understand departmental as well as site priorities
Ability to collaborate with colleagues at all levels of organization
Physical Requirements / Work Environment
Lifting < 50 lbs. Walking, sitting, focus on computer screen for long periods.
Able to gown, wear PPE, and work successfully in a clean room environment.
Benefits
We offer competitive remuneration, annual incentive plan bonus, healthcare, and a range of employee benefits. Thermo Fisher Scientific provides an innovative, forward-thinking environment with outstanding career and development prospects. Our culture stands for integrity, intensity, involvement, and innovation.
Apply today! http://jobs.thermofisher.com
Accessibility/Disability Access
Accessibility services are available for job seekers with disabilities at Thermo Fisher Scientific. If you need assistance or an accommodation to apply for a job, please call 1-855-471-2255 and provide your contact information and accommodation details.
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.
First Shift (Days)
Environmental Conditions
Adherence to all Good Manufacturing Practices (GMP) Safety Standards, Cleanroom: no hair products, jewelry, makeup, nail polish, perfume, exposed piercings, facial hair etc... allowed
Job Description
Job Title: Engineer II, QA Floor
Requisition ID:
About Thermo Fisher Scientific
Thermo Fisher Scientific Inc. is a global leader in serving science, enabling our customers to make the world healthier, cleaner, and safer. With our mission to enable our customers to make the world a better place, we are dedicated to delivering exceptional products and services to support scientific research and discovery.
Location/Division Specific Information
St. Louis MO / Pharma Services Group
The St Louis site is a fast-paced biologic drug substance manufacturing facility. It operates around the clock and employs around 1k people. The facility is focused on cell process development to support clinical and commercial manufacturing. The products produced here treat chronic health conditions, including cancers and other life-threatening diseases.
This is a non-supervisory role, working with the Supervisor of QA Operations. This position will be expected to work a shift schedule that includes weekend work and on-call rotation (Wednesday-Saturday, 6AM-4:30PM).
Discover Impactful Work:
Quality Engineer II is a quality assurance professional with substantial prior experience of working within a Quality, Process Engineering, or Manufacturing organization in a highly regulated industry. This individual specializes in evaluation of production processes and performance in manufacturing and participates in projects to engineer quality improvements of existing production processes as well as the development of new processes to improve quality and efficiency. Other job duties include but are not limited to understanding contamination/cross-contamination, observing aseptic practices, performing daily GEMBAs of manufacturing areas, continuously assessing fit and finish of the facility, and performing compliance inspections within manufacturing areas. This role supports Manufacturing and Process Engineering by providing Quality input as needed, and requesting the initiation of deviations as they are identified. All activities are in support of producing and releasing quality bulk drug substance for clinical and commercial clients.
What will you do? (Responsibilities)
Spend the majority of work hours in manufacturing areas supporting active processing and working closely with Manufacturing and Process Engineering to oversee activities from a quality perspective and provide QA-related input
Collaborate with multi-functional teams to develop, optimize, and improve processes to enhance efficiency, productivity, and quality
Conduct thorough audits and inspections to ensure sustained compliance with industry standards and regulations in preparation for internal quality audits, client audits, and regulatory inspections
Observe aseptic practices and provide immediate coaching to site colleagues to prevent contamination and cross-contamination
Participate in client and regulatory audits as a SME on the Fit and Finish, Changeover, and Change Control procedures and practices
Observe critical process steps assuring alignment with guiding procedures, batch records, and established aseptic practices and be available to manufacturing and PE for support in real time
GEMBA all active areas daily as well as other areas within the core as scheduled, and provide immediate feedback to colleagues and area management to ensure compliance with cGMP’s, site procedures, and regulatory requirements
Perform QA approval of suite and equipment changeover between client processes
Perform autoclave logbook review and facilitate corrections
Perform Fit and Finish inspections per the risk assessment and guiding procedures
Perform monthly aseptic observations of critical activities performed in Biosafety Cabinets
Attend and actively participate in MFG huddles
Lead/attend and actively participate in QA OTF Tier 1 huddles
Act as Quality Management Representative for the company as needed
Take actions to develop one’s own knowledge and skills
Perform all training requirements in a timely manner
Provide training, coaching, and mentorship to new and/or less experienced team members on quality standards and effective strategies
Qualify new team members to perform tasks that require QSME training
Write and review deviations in Trackwise as required
Author, revise, and review procedures in eDMS as required
Write and implement CAPA’s as needed
Conduct/participate in investigation interviews/RAPIDs as required
Individuals in this group must be able to obtain buy-in and cooperation to resolve issues and maintain quality culture and quality standards throughout Operations with no direct authority over the people with whom they interact. Utilization of tact and diplomacy with internal and external customers is essential
Education and Experience
Bachelor's Degree (BA/BS) in Life Sciences (biology, chemistry, biochemistry), Engineering, or another science related field combined with a minimum of three (3) years of relevant experience is required
Experience with cell culture, protein purification, formulations, or facilities/utilities in a GMP pharmaceutical or biopharmaceutical environment is preferred
Cleanroom manufacturing experience is highly preferred along with a comfort level with full ISO 5 and ISO 7 gowning requirements
Non-science degrees will be considered if combined with a minimum of seven (7) years of directly related work experience in biopharmaceutical manufacturing
Knowledge
Understanding ‘why’ and not just the ‘how’ of processes and practices
Knowledge of Quality practices and cGMP regulations and other international health authority guidelines
Experience with investigational writing software system (TrackWise) along with root cause analysis tools used in deviation investigations
Technical writing skills and the ability to write/revise procedures in document management software
Tech transfer experience is a plus
Experience with Lean Manufacturing and Six Sigma methodologies is a plus
Excellent problem-solving and analytical skills
Skills
Analytical, critical thinking, and problem solving skills
Strong interpersonal skills
Strong written and oral communication skills
Strong math skills
Strong attention to detail
Strong Microsoft Office skills (especially Word and Excel)
Strong time management and organization skills
Abilities
Understand and carry out instructions
Effectively multi-task
Work effectively in a dynamic environment
Able to work under pressure
Able to work independently
Proven ability to lead others
Able to coordinate workload for junior team members
Able to understand departmental as well as site priorities
Ability to collaborate with colleagues at all levels of organization
Physical Requirements / Work Environment
Lifting < 50 lbs. Walking, sitting, focus on computer screen for long periods.
Able to gown, wear PPE, and work successfully in a clean room environment.
Benefits
We offer competitive remuneration, annual incentive plan bonus, healthcare, and a range of employee benefits. Thermo Fisher Scientific provides an innovative, forward-thinking environment with outstanding career and development prospects. Our culture stands for integrity, intensity, involvement, and innovation.
Apply today! http://jobs.thermofisher.com
Accessibility/Disability Access
Accessibility services are available for job seekers with disabilities at Thermo Fisher Scientific. If you need assistance or an accommodation to apply for a job, please call 1-855-471-2255 and provide your contact information and accommodation details.
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.