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Site Quality Head Jobs

Site Quality Head Jobs
By Johnson & Johnson At ,
Must have excellent organizational, management, and people development skills.
Develops and manages budget, organizational structure and business requirements to accommodate business needs and assure meeting JSC metrics.
ESSENTIAL JOB DUTIES AND RESPONSIBILITIES:
The incumbent must have 9 years QA/QC experience in the pharmaceutical industry.
Strong knowledge in regulatory compliance, Quality Systems, pharmaceutical industry, pharmaceutical methods and procedures
Must use interpersonal and teamwork skills to build interdependent partnerships.
Site Quality Technician (M/F/D)
By Nordex SE At ,
Experience in quality management and quality control processes; Wind Turbine Assembly experience preferred
Generates and presents periodic reports to the Nordex supplier management team.
Performs Quality Lead responsibilities in the Quality Lead’s absence.
Minimum of 3 years of mechanical/construction supervisory experience; Wind Farm mechanical construction experience preferred
WTG on-site assembly experience preferred
Analytical skills – must be able to reach conclusions and make recommendations based on collected data
Site Quality Lead, Travel/Remote (M/F/D)
By Nordex SE At ,
Experience in quality management/quality control processes
Strong computer skills including knowledge of MS office applications (i.e.: Word, Excel, PowerPoint)
DEPARTMENT: Project Management (Site Management / Erection / I
Serves as a key member of the Wind Farm Site leadership team, and the on-site representative of the Quality Manager.
Prepares reports for the Site Manager and the Quality Manager summarizing the status of all quality issues and activities on site.
Monitors the project plan and rotation schedule to anticipate manning requirements and provide timely recommendations on staffing.
Site Quality Lead Jobs
By Johnson & Johnson At , El Paso
Might be designated as Management Representative and/or Head of Quality Make for the Site by the Operating Company.
Responsible for communicating business related issues or opportunities to next management level
15 or more years of related experience and/or training; or equivalent combination of education and experience
Analyzes, evaluates, and presents information concerning factors such as business situations, production capabilities, manufacturing problems and quality systems indicators.
Develops initial and subsequent modifications of product assurance programs to delineate areas of responsibility, personnel requirements, and operational procedures within program.
Organizes, plans, leads and manages quality related projects in alignment with company goals Facilitates the development and training of immediate staff.
Site Quality Manager Jobs
By Meta At , Remote $143,000 - $199,000 a year
BS in Construction Management or Engineering or equivalent work experience.
Experience in personnel management, and staffing and scheduling.
Experience in contractor, consultant and vendor management.
Provide training of personnel to ensure awareness of quality procedures and specific responsibilities in the QA/QC process.
7+ years’ experience in quality control & quality assurance (QA/QC) programs for data centers or mission critical construction projects.
Experience with Design-Build and Design-Bid-Build construction programs.
Head Of Quality/Quality Manager
By Michigan Spring and Stamping, a KERN-LIEBERS Company At Muskegon, MI, United States
Five to eight years direct experience in quality control management, preferably in a spring environment.
Acts as the Management Representative for Michigan Spring and Stamping’s registered quality systems.
Proven experience as a quality manager
Excellent math abilities and working knowledge of data analysis/statistical methods
Understands customer needs and requirements to develop effective quality control processes
Conducts and/or manages studies to determine cause, effect and corrective measures required to remedy deviations impairing desirable standards of quality.
General Manager / Site Head
By Morgan Prestwich - Life Sciences Executive Search At New Jersey, United States
Develop clear accountabilities and handoffs between the process development, MS&T and technical operations organizations.
BS in a scientific or related field with 10+ years progressive leadership experience in a biotechnology or pharmaceutical company
CDMO industry experience would be highly desirable.
Experience with global supply chains for biologics and/or advanced therapies
Deliver strategic leadership and vision to ensure successful scale up of client-specific manufacturing programs.
Promote scientific rigor and ensure industry-leading manufacturing operations.
Site Head Of Quality
By Life Science People At Pleasanton, CA, United States
Certifications in quality management (e.g., Six Sigma, Lean) are highly desirable.
Establish and maintain a robust quality management system, including documentation control, change control, and deviation management.
Strong knowledge of regulatory requirements, such as FDA regulations, GMP guidelines, and ICH guidelines.
Proven track record of implementing and managing a quality management system in accordance with industry standards.
Collaborate with cross-functional teams to ensure quality requirements are met throughout the product lifecycle, from development to manufacturing and distribution.
Minimum of 10 years of progressive experience in quality assurance and quality control in the biotech or pharmaceutical industry.
Site Head Of Ehs And Facilities
By MilliporeSigma At Jaffrey, NH, United States
Knowledgeable in Process Safety Management (PSM) requirements.
Experienced with ISO 14001, 9001, 45001 management systems.
Demonstrated risk management skills and business continuity planning.
Knowledgeable of Occupational Health requirements.
Five plus years progressive leadership experience focused in EHS or manufacturing operations
Knowledgeable of US EPA, OSHA, DOT and NH DES regulations.
Quality Site Head – Internal Manufacturing
By CRISPR Therapeutics At Framingham, MA, United States
Responsible for end-to-end Quality within the site, including FUSE qualification/validation, materials management, batch record reviews, change control, and deviations
Collaborate with internal partners to enable compliant and successful manufacturing (e.g. technology transfers, validation, testing, and lifecycle management)
Direct experience hosting Health Authority inspections
Prior experience in the manufacture of cell and gene therapy products
Provide strategic direction and operational leadership for the site Quality function at CRISPR’s internal manufacturing facility
Chair the site Quality Review Board and establish quality metrics to demonstrate adherence to GMP regulations and CRISPR procedures
Us Site Head(Bd Vp)
By Nanjing Taorui Business Management Consulting Co., Ltd At San Diego County, CA, United States
2.Responsible for the operation management of the US subsidiary to realize the
provide accurate market basis for the company's management decision-making.
2. More than 5 years of sales/BD experience in Biotech & Pharmaceutical companies,
BD VP, US Subsidiary Head
1. Led the US sales team to develop customers and achieve business growth targets.
3.Analyze the market conditions of US and provide market analysis reports, and
Us Site Head(Bd Vp)
By Nanjing Taorui Business Management Consulting Co., Ltd At New Jersey, United States
2.Responsible for the operation management of the US subsidiary to realize the
provide accurate market basis for the company's management decision-making.
2. More than 5 years of sales/BD experience in Biotech & Pharmaceutical companies,
BD VP, US Subsidiary Head
1. Led the US sales team to develop customers and achieve business growth targets.
3.Analyze the market conditions of US and provide market analysis reports, and
Us Site Head(Bd Vp)
By Nanjing Taorui Business Management Consulting Co., Ltd At Greater Boston, United States
2.Responsible for the operation management of the US subsidiary to realize the
provide accurate market basis for the company's management decision-making;
2. More than 5 years of sales/BD experience in Biotech & Pharmaceutical companies,
1. Led the US sales team to develop customers and achieve business growth targets;
3.Analyze the market conditions of US and provide market analysis reports, and
4.Lead the team to search for business development clues, complete the
Site Quality Head, East Norriton
By BioSpace At East Norriton, PA, United States
Accountable for timely notification and effective management of internal and Client-related changes
Comprehensive knowledge of global GMP regulatory requirements for cell & gene therapy products
Experience with facility commissioning and qualification
Provides compliance and strategic guidance during the design and qualification of the plant expansions.
Manages effectively the site’s GMP training program. Champions initiatives for continued learning and development.
Develops and manages departmental goals and corresponding budget in alignment with corporate vision and goals
Senior Director, Site Quality Head
By Nationwide Technical & Executive Search, Inc. At Bristol, TN, United States
Knowledge and understanding of pharmaceutical quality management systems and drug manufacturing.
Skilled in project management and ability to problem solve utilizing a collaborative approach to resolutions.
Regulatory knowledge relating to approval and maintenance of drug applications, regulatory submission process and requirements, including post marketing requirements.
Demonstrated proficiencies with auditing, and CAPA (corrective and preventive action) development/management.
Establish and manage Quality policies and procedures for receipt, manufacturing, packaging, testing, documentation, storage, and transporting applicable products.
Minimum of ten years QC/QA technical pharmaceutical leadership experience.
Site Quality Head Jobs
By Curia At Springfield, MO, United States
Minimum 10-12 years’ experience in aseptic production/processing cleaning practices within a regulatory environment, including 5 years in a managerial role
Manage inspection readiness program and activities and provide support during regulatory inspections and customer audits.
Strong verbal and written communication skills
Strong knowledge of business process needs of quality assurance
Ability to enable and empower managers and hold them accountable for results
Supervise, coach and develop Quality staff
Site Quality Control Jobs
By Bergelectric At Panama City, FL, United States
Collaborate with the management team to develop, implement and continuously improve quality-focused standards, procedures, and processes
Manage team to conduct preparatory, initial, and follow-up inspections for all features of work to ensure all project requirements are met
Must have 5+ years of experience / knowledge of electrical construction
Update the Project Manager regarding all quality issues as well as the progress of problem resolutions
Strong knowledge related to NEC code
Experience in Low Voltage systems (Fire Alarm, Tele-Data, Security, Audio/Visual, etc.)
Site Quality Supervisor Jobs
By Kenco At , Oxnard, 93030, Ca $70,000 - $85,000 a year
Investigate customer complaints and non-conformance issues and perform root cause and corrective action investigations to improve the quality management system.
Collect and compile statistical quality data and analyze to identify areas for improvement to the quality management system.
Knowledge and experience with ISO 9001:2015
2-4 years’ experience in a quality assurance role, regulatory affairs experience (FDA, DEA, etc.) desired.
ASQ or other accredited certification as ISO lead auditor preferred
Manages ambiguity by operating effectively, even when the path lacks clarity or certainty.
Senior Director, Site Head Of Quality
By KBI Biopharma At , The Woodlands, Tx $203,000 - $230,000 a year
Responsible for management, leadership and oversight of the Quality Assurance and Quality Control departments.
Responsible for ensuring site compliance with GMP and regulatory requirements.
Must have thorough knowledge of cGMPs and biotechnology-derived product regulations. Also requires a demonstrated track record in the following key areas:
Strong collaboration and team building skills
Experience developing, implementing, and executing strategic plans and objectives for organizations and departments.
Sterile Manufacturing experience at a GMP Sterile Manufacturing Facility
Site Quality Engineer (Qa/Qc)
By Sky Systems, Inc. (SkySys) At Queens, NY, United States

Location: Oniste - Long Island City, NY Duration: Long term (3 years) Job Responsibilities: Defining & implementing quality control related to Electrical, Civil & Electro Mechanical Work in ...