Construct Quality Control Supervisor Ii Jobs

Preferred Qualifications – Education and Experience

Other projects or responsibilities as may be required.

1-3 years of previous experience in a laboratory setting

Familiarity with basic lab equipment and knowledge of lab safety protocols

Excellent organization, communication, and problem solving skills

Experience with some of the following applications: flow cytometry, western blotting, Immunoprecipitation, bioassays, ELISA and IHC/ICC

At least 2 years’ experience working in a laboratory.

A great compensation and benefits and a full relocation package is available for you and your family.

A Bachelor’s or Master’s Degree in a Scientific field.

Please apply if you have:

For more information, please contact Mags Wosik at [email protected] or submit the form below.

N.B. This role is currently open to US residents and Green Card holders.

Minimum of six years’ experience in mortgage lending

Minimum of three years underwriting experience or equivalent with Conventional, FHA and VA loan products preferred

Previous experience with loan closings and regulatory compliance

Experience in ACES, BlitzDocs & Destiny preferred

This position will be eligible for the benefits listed above in accordance with Company policy.

Become a subject matter expert in certain aspects of loan origination, such as regulatory compliance or credit underwriting

High School or General Education Diploma

Read and interpret production travelers and engineering specifications to ensure product conformance at each manufacturing product sequence.

Document part characteristics and measurements on inspection history cards during first article inspections and other inspection sequences.

Record data from inspection history cards on inspection files and maintain accurate and legible inspection records.

Load and/or transport part containers utilizing a forklift, hand truck or manual/motorized pallet jack to assigned locations.

Determine quality (Pass/Fail) of manufactured parts based on dimensional and visual inspection.

Reviews and revises testing and equipment procedures as needed. Performs equipment and procedure qualifications periodically.

Employ sound technical writing skills involving deviation reports, laboratory investigation reports, etc.

Perform or assist with other Quality Unit assigned activities related to MURR facility responsibilities associated with FDA, NRC, and DOT regulations.

Able to independently perform testing on multiple radiopharmaceutical batches manufactured on a weekly basis.

Assists peers with method development and validation activities.

Contribute to the proper maintenance and organization of the laboratory, laboratory equipment, supplies, records, and samples.

Strong leadership and project management skills.

Self-starter with a working knowledge of quality management fundamentals, data analysis, and policy creation.

Strong analytical, organizational, time management, and decision making skills.

Evaluates and provides appropriate solutions for risk issues and presents to Senior and Executive Management.

Associate’s Degree in Business, Finance, or related field of study from an accredited four-year college or university or equivalent experience required.

Continuing education and career certifications

Understanding of scientific principles, ability to communicate with peers and management

Participates in the execution of method/material qualification and analytical improvement projects.

3+ years of relevant experience (B.S. Degree), 6+ years of relevant experience (A.S. degree)

Solid working knowledge of operations/quality systems utilized in QC operations/support teams (e.g. strong test method/scientific base)

Provides timely review of data and documentation generated for or by QC.

Ability to perform color differentiation testing

Support method qualification by creating QC test methods and performance of method qualifications

Review QC data generated from method qualifications, stability studies and GMP testing

Experience in Analytical Development or Quality Control roles supporting GMP testing/manufacturing of cell therapy, gene therapy or gene editing products

Experience or desire to learn HPLC/UPLC methodologies used in a GMP-laboratory.

Plan, coordinate and own preparation/aliquoting of custom critical reagents manufactured internally for use in GMP testing methods

Support logistical aspects of GMP stability programs for drug substances and drug product

Strong project management and planning/organizational skills and the ability to develop and execute realistic action plans

Manage the staffing and training of the quality control department

Develop staff skills and create a rewarding and fulfilling work environment

Act as a knowledgeable and accessible resource for team members

2+ of Quality and/or leadership experience

1+ years of experience leading a team in a warehouse environment

Provides input to quality control reports, requirements, and other information in response to requests for proposals, quotes, and other business opportunities.

Develop and champion an organization of professionals that is able to apply innovation and creativity to technical and managerial challenges.

4+ Experience with laboratory processes and practices, including cGMP compliance regulations required.

Professional experience with HPLC, UPLC, GC, Wet Chemistry, and Chromatography software.

Supervisory or team/project leadership experience required.

Be able to establish priorities, delegate responsibilities, and train, supervise and develop leaders and associates required.

Document findings to provide management with an accurate and detailed picture of the issue

Perform Quality Control Pre-Funding Status Audits as assigned and directed by DHIM Quality Control Management

Knowledge of or experience in mortgage loan processing and underwriting

Maintain a knowledge of all underwriting guidelines

Five to eight years of underwriting experience required

Meet department audit and reporting guidelines

Cooperates in Event Report Management and for all the implementation of relative corrective actions. Systematically records

Manages collaboration of measurement instruments and related certifications.

Must have knowledge of inspection and testing procedures, adjustment methods and certification processes.

Evaluates the qualifications of welders and Non-Destructive Test-NDT technicians with regard to the activities assigned.

Evaluates the qualifications of inspection personnel.

Checks the completeness and conformity to specified applicable requirements, standards and/or directives.

Conduct investigations of OOS, Deviations, Change Control Management, and CAPAs

Prior experience and knowledge in FDA GMPs (21 CFR, 210 and 211)

Manage the Quality Control team’s performance of analytical testing for various samples and incoming, in-process and final products

Good interpersonal skills that support working in a team environment

Strong oral and written communication skills

Strong organizational skills with the ability to multi-task

Three or more years of work experience in Quality Control, Quality Assurance, or Quality Management, required.

Previous people management experience, required.

Knowledge and adherence of Safety, Stewardship, and Quality Management policies.

Compliance of Safety, Stewardship and Quality Management activities.

Manage the selection of lots for seed production.

Practical laboratory supervision experience, strongly preferred.

Computer Skills with working knowledge of MS Office Suite (Outlook, Word, and Excel).

Participate in continuous improvement activities looking to pursue laboratory best practice and offer appropriate feedback when non-value added activities are observed.

Excellent written and verbal communication and interpersonal skills.

Expiry Date: 12 June 2023

Conduct testing of in-process materials, finished product, and stability samples in support of production at the ASPEX client Manufacturing site.

Maintain QC Analytical Laboratory in compliance with regulatory standards and site procedures.

Excellent time-management skills to plan, organize, and prioritize tasks and responsibilities to meet deadlines and adjust to changing priorities

Reports to management on the performance of the quality program, including needs for improvement

Will report to Project Quality Manager and Corporate Quality Manager

Works closely with Divisional/Project Manager(s) with regards to all activities related to qualify for the divisional projects7.

Interact with Client or Client representatives to ensure a Quality Product within code and/or contract requirements

Take necessary steps to resolve Quality Issues as they arise and report those issues as they arise to Project Quality Manager

Plan and organize own work assignments, as well as carry out tasks from management staff

Ability to communicate effectively with audiences that include but are not limited to management, coworkers, clients, vendors, contractors, and visitors

Job related technical knowledge necessary to complete the job

Ability to learn and apply knowledge of applicable local, state/province, and federal/national statutes and guidelines

Provide input to the site manager regarding Quality organization and staffing

Assist site manager with resolution of client complaints that are quality-related

Collect Utility Monitoring Samples (RODI/WFI) routinely and for qualification of systems.

Utilize SDS sheets to properly assess chemical hazards, spill response procedures, and PPE requirements if indicated.

Good attention to detail and ability to utilize problem solving/trouble shooting skills.

Demonstrated written and oral communication skills.

Strong organization and analytical skills.

Experience prolonged standing, some bending, stooping, and stretching.

The following physical abilities are required in order to fulfill the job duties:

You will report to the Manager of Quality Control Raw Materials

Essential: 3 to 5 years of relevant experience

Knowledge: Apply basic principles, theories, and concepts. Limited knowledge of industry standards.

Key Skills: MS Office, LIMS, SAP, Trackwise, EDMS, compliance and strong science understanding.

What Takeda can offer you:

Skill Matrix 설정 및 교육 계획 수립 팀원 역량강화에 대한 지원

CoPQ 현황 관리 및 절감을 위한 개선 활동 주관

CCR, Process PPM 현황 관리 및 절감 개선 활동

고객 감사/내부 공정감사 대응 및 지적 사항에 대한 개선 Follow Up

Quality basic 점검 수립 계획 및 Level up 추진 활동

신규 프로젝트의 양산성 확인을 위한LRC,R-FMEA,R@R, SLP 진행 내용 점검 및 초기 유동 관리에 대한 교육.