Qc Coordinator Job at Lobellia (Doha)

Qc sample coordinator i

This position will have responsibility for supporting activities in the QC Sampl...

Location

United States , Madison

Salary:

Not provided

PCI Pharma Services

Expiration Date

Until further notice

Requirements

0-3 years relevant business experience
Proficient in MS Office
Must have strong attention to detail
Ability to work in a cross-functional team environment
Professional interpersonal skills
Ability to communicate well orally and in writing
Ability to multi-task in a dynamic environment with changing priorities
Ability to work independently as well as on a team, with limited supervisory oversight
Must be able to walk and drive between local sites
Must be able to physically wear laboratory protective attire and equipment

Job Responsibility

Review all incoming material receipt packets to assess testing needs
Schedule and perform sampling of raw materials across the PCI Madison, WI Sites
Request quotes and purchase orders for testing performed externally
Assist with regular communications with 3rd party labs performing external testing
Complete and submit all applicable sample submission paperwork to the appropriate testing labs
Escalate testing failure or safety concerns to management in a timely fashion
Assist in deviation, out-of-specification or aberrant result investigations, as needed
Assist with the writing and revision of cGMP documents and Raw Material Specifications documents to meet industry standards
Assist with reviewing testing results to ensure accuracy and compliance
Perform routine cleaning of sampling facilities

Fulltime

Qc Sample Coordinator I

This position will have responsibility for supporting activities in the QC Sampl...

Location

United States , Bedford

Salary:

Not provided

PCI Pharma Services

Expiration Date

Until further notice

Requirements

1-3 years relevant business experience
Proficient in MS Office
Must have strong attention to detail as well as ability to work in a cross-functional team environment
Professional interpersonal skills and the ability to communicate well orally and in writing
Ability to multi-task in a dynamic environment with changing priorities

Job Responsibility

Ordering, receipt and management of QC Laboratory supplies, including chemicals, reference standards, and consumable materials in accordance with cGMP and procedural requirements
Inspection, review and receipt of incoming samples for testing. Verification of information against specifications, protocols, and other documentation to ensure compliance.
Maintain sample tracking and chain of custody records in accordance with cGMP and procedural requirements
Complete data entry in validated systems and business tools with a high degree of accuracy.
Request, assemble, and distribute QC testing data packets for support of in-process, lot release, raw material, and stability testing
Assist with coordinating external testing
Request and maintain Quality Control logbooks in accordance with cGMP and procedural requirements
Perform inspections on packaging components

Fulltime

New

Installation Manager

National OnDemand, Inc. is a communications and utilities infrastructure provide...

Location

United States , Columbus

Salary:

Not provided

NATIONAL OnDemand, Inc

Expiration Date

Until further notice

Requirements

High School Diploma or equivalent required
3-5 years of leadership experience
Possession of valid state issued driver’s license required
Must be able to pass a background check and drug screen
Must have a minimum of three years of experience in a related discipline
Proven leadership and teamwork skills fostering an inclusive, supportive environment by motivating and developing staff at all levels
Critical thinking and analytical skills, including the capacity to identify, assess and prioritize competing interests and needs
Proven ability to adjust quickly to shifting priorities, multiple demands, ambiguity, and rapid change
Ability to coordinate and integrate work across multiple disciplines, complete scheduling, and resource planning activities to drive efficient work processes, identify and manage all operational risks, and enhance customer communication and satisfaction
Experience managing multiple locations and leading cross-functional teams

Job Responsibility

Represent the company and attend client’s meetings with Regional Manager and maintain a great relationship with clients
Drive profitability by optimizing profits and controlling expenses
Provides technical support, expertise, leadership, and accountability for field team
Responsible for recruiting, hiring, retention and training needs for field staff
Builds and maintains an effective field operations organization committed to customer and employee satisfaction
Supervise performance of field staff and responds to escalated issues in field
Communicate senior management directives to field staff and ensure compliance (Safety, etc.)
Develops manpower schedules and loading to ensure workload coverage
Site Visits to ensure QC of various projects ensure conformance to client specifications and company requirements
Follows up on customer satisfaction issues and drives resolution

What we offer

paid time off (PTO)
medical
dental
vision
short- and long-term disability
life insurance
Employee Assistance Program (EAP)
401(k)

Fulltime

New

Production Area Leader

We have an exciting opportunity for a Production Area Leader to join our team. T...

Location

United Kingdom , Selby

Salary:

34894.00 GBP / Year

360 Resourcing Solutions

Expiration Date

Until further notice

Requirements

Strong understanding of KPIs, KAIs, and their impact on production performance
Proven ability to motivate and engage teams to improve performance and morale
Solid knowledge of Health & Safety standards and compliance procedures
Experience maintaining quality control (QC) throughout production processes
Strong problem-solving and decision-making skills
Good working knowledge of Microsoft Office and SAP
IOSH Managing Safely (or equivalent) – desirable
Leadership or team leader qualification (ILM or equivalent) – desirable

Job Responsibility

Support Team and Shift Leaders in the day-to-day running of the production line
Coordinate team activities to ensure efficient and safe operations
Manage raw materials from input through to finished product
Drive improvements in production performance, scrap reduction, KPIs, and OEE
Maintain high standards of communication across shifts and teams
Ensure compliance with all Health & Safety and quality procedures
Provide cover for the Team Leader when required
Promote a proactive, flexible, and continuous improvement culture

What we offer

25 days Annual Leave (Plus Bank Holidays)
Profit Related Bonus
Contributory pension scheme
4 x salary Life Assurance
Enhanced Maternity, Paternity & Adoption Leave
Buy & Sell Annual Leave
Service Recognition Rewards
Supported Professional Development

Fulltime

New

Survey Lead

Make your mark as Survey Lead for Boskalis Subsea Services in Aberdeen. You will...

Location

United Kingdom , Aberdeen

Salary:

Not provided

Boskalis

Expiration Date

Until further notice

Requirements

Recognised qualification in surveying, hydrography, geomatics, or a related discipline with academic certification
Demonstrable understanding of survey and ROV systems, their integration, and application in diving and subsea construction
Minimum of 5 years' offshore experience at Senior Surveyor or Party Chief level, including mobilisation and execution of survey scopes
Proven experience in survey-related project engineering or subsea operations
Working knowledge of IMCA and relevant standards, including guidelines for survey competence and offshore operations
Familiarity with frame agreements and coordination with external survey vendors and subcontractors
Demonstrated ability to liaise across multi-disciplinary teams and organisational levels
Excellent verbal and written communication with the ability to present technical information clearly

Job Responsibility

Support the commercial department with tender opportunities, providing clear survey input and solutions
Support Crewing and Competence in maintaining a steady, well-qualified survey workforce via BSS's survey provider
Support projects and clients in defining and delivering survey requirements across offshore and remote operations, identifying opportunities to improve efficiency and delivery
Support equipment preparation to meet project requirements, including collation of pre-mobilisation audits and certification packages
Assume BSS's survey provider's project main point of contact when required
Develop and implement the BSS Remote Operations Centre (ROC) to support survey operations
Define and standardise processes for remote and hybrid survey delivery, including data QC, monitoring, and reporting
Integrate ROC capabilities into project execution in collaboration with internal teams and survey providers

What we offer

Holiday entitlement of 34 days
Contributory pension scheme
Private medical insurance
Death in service benefit
Range of flexible benefits including the opportunity to buy additional holidays each year

Fulltime

New

Milling Production Leader

Reporting to Shift Production Leader, you will oversee daily mill line operation...

Location

Vietnam , My Hanh, Tây Ninh

Salary:

Not provided

PPG Industries

Expiration Date

Until further notice

Requirements

High school or Intermediate's degree in chemical engineering or mechanical engineering is referable
Minimum 3 years' working experience in manufacturing environment and powder coating experience is advantageous
Experienced in utilizing computer tools for reporting and analyzing production data
Production hands-on and people management skills
On the job training skills
Innovative and continuous improvement mindset

Job Responsibility

Supervise all mill line activities to ensure the products are produced according to specifications, work instructions, good manufacturing practices and delivery as scheduled
Ensure and maintain discipline and well behavior of team
Ensure the rules of tidiness are fully and continuously respected and implemented according to 5S standards
Drive milling team to meet production schedule and ready for customer required
Coordinate with the related departments (QC /Technical/Supply Chain/Maintenance) to implement the scheduled preventive maintenance and repair activities
Monitor KPIs performance on milling as OEE/Cycle time/AMU (Absolute Material Utilization) and make shiftly report
Follow safety regulation and risk reduction in all time working
Support Shift Production manager to improve milling process
Participating in CAIR / Quality Failure corrective actions in milling area
Analyze the measurement data and provide improvements via use of statistical analysis

Fulltime

New

Senior QC Specialist (Method Validation & Technical Support)

The Senior QC Specialist (Method Validation & Technical Support) is responsible ...

Location

Singapore , Singapore

Salary:

Not provided

Amaris Consulting

Expiration Date

Until further notice

Requirements

Bachelor's Degree in Chemistry, Biochemistry, Biotechnology, Pharmaceutical Sciences, Life Sciences, or a related discipline
Minimum 5 years of experience in pharmaceutical or biopharmaceutical Quality Control, Analytical Development, or Technical Support functions within a GMP-regulated environment
Hands-on experience in analytical method validation, qualification, verification, transfer, equipment qualification (IQ/OQ/PQ), stability programs, and laboratory investigations (OOS/OOT, deviations, CAPAs, and change controls)
Strong knowledge of GMP requirements, analytical method lifecycle management, root cause analysis, GMP documentation, and global regulatory standards including FDA, USP, EP, ICH, PIC/S, and Data Integrity principles

Job Responsibility

Lead analytical method qualification, validation, verification, transfer, and lifecycle management for chemical and biological testing
Manage qualification of laboratory equipment, analytical instruments, and critical reagents, ensuring compliance throughout their lifecycle
Support introduction of new methods, technologies, materials, and equipment into QC operations
Coordinate and maintain QC stability programs, including data review and trend analysis
Lead investigations of deviations, non-conformances, invalid results, atypical results, and OOS events
perform root cause analysis and drive CAPA implementation
Monitor and implement regulatory and compendial updates to ensure ongoing compliance with GMP, FDA, USP, EP, and ICH requirements
Author, review, and approve GMP documentation including SOPs, protocols, reports, change controls, deviations, and CAPAs
Act as a technical SME, providing guidance, training, and knowledge transfer to QC testing teams
Support internal audits, regulatory inspections, and customer audits as the SME for assigned areas

Fulltime

New

Regulatory Affairs Senior Associate

Join Amgen’s Mission of Serving Patients. At Amgen, if you feel like you’re part...

Location

United States

Salary:

83974.90 - 113613.10 USD / Year

Amgen

Expiration Date

Until further notice

Requirements

Master's degree
or Bachelor's degree and 2 years of regulatory or pharmaceutical experience
or Associate's degree and 6 years of regulatory or pharmaceutical experience
or High school diploma / GED and 8 years of regulatory or pharmaceutical experience

Job Responsibility

Assist US Regulatory Lead (USRL) to support US regulatory activities (e.g. development and submission of Investigational New Drug [IND] applications, Biologic License Applications [BLAs] and New Drug Applications [NDAs]
advisory committee meeting preparations)
Provide and maintain IND/BLA/NDA documentation support (e.g. annual reports, amendments) in collaboration with USRL
Create and maintain product regulatory history documents in the regulatory document management system and appropriately archive all regulatory documents and agency communications
Review US component of the Global Regulatory Strategic Plan (GRSP) and provide input to operational deliverables
perform regulatory research to support the development of content for the GRSP plan as delegated by the Global or US Regulatory Lead
Actively support regulatory compliance and ensure compliance of submissions to the US FDA
Assist the Global or US Regulatory Lead by preparing supportive documentation for regulatory deliverables, including for example regulatory landscapes or research for the regulatory strategy and/or target product label
Coordinate collection of functional documents in support of regulatory applications
Participate on Global Regulatory Teams (GRT) and assist Global Regulatory Leads with GRT meeting management (eg, agendas and meeting minutes)

What we offer

A comprehensive employee benefits package, including a Retirement and Savings Plan with generous company contributions, group medical, dental and vision coverage, life and disability insurance, and flexible spending accounts
A discretionary annual bonus program, or for field sales representatives, a sales-based incentive plan
Stock-based long-term incentives
Award-winning time-off plans
Flexible work models where possible

Fulltime

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Qc Coordinator

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Qc Coordinator

Qc sample coordinator i

Qc Sample Coordinator I

Installation Manager

Production Area Leader

Survey Lead

Milling Production Leader

Senior QC Specialist (Method Validation & Technical Support)

Regulatory Affairs Senior Associate

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