Qualification Specialist Job at Vodafone (Budapest)

Medical Billing – Qualification Specialist

Location

United States , Plymouth Meeting

Salary:

Not provided

Beacon Hill

Expiration Date

Until further notice

Requirements

High school diploma or equivalent
Proven experience with insurance verification, prior authorizations, or reauthorizations in a medical or healthcare setting
Strong knowledge of Medicare, Medicaid, private insurance, and managed care plans
Working knowledge of medical terminology, CPT codes, and ICD-10 coding
Experience using EHR/EMR systems, insurance portals, and billing software
Excellent attention to detail, organization, and written and verbal communication skills
Strong customer service skills with the ability to communicate effectively with patients, providers, and insurance representatives

Audit and Supplier Qualification Specialist

The role is to implement and execute tasks relating to GMP auditing and supplier...

Location

Ireland , Stamullen, Co. Meath

Salary:

Not provided

PCI Pharma Services

Expiration Date

Until further notice

Requirements

Bachelor’s or associate degree or Diploma / Certificate in Pharmaceutical and/or life science (e.g. quality assurance, or similar). May substitute experience in lieu of educational requirements
3-5 years previous supplier management and auditing experience is preferred with particular emphasis on hosting and conducting audits
Good working knowledge of cGMP and associated regulations (Eudralex Volume 4
ISO 13485)
Experience in a similar role / working in Quality Assurance, Quality Systems, Compliance
To have demonstrable experience within Quality Systems
Capability to follow clear goals, communicate clearly and ensure progress to completion meeting predefined targets
Ability to manage multiple tasks and set priorities
Good interpersonal skills
Good Written communication skills

Job Responsibility

Support, participate and host both Client and Regulatory audits
Management of audit responses and ensure closure of actions within agreed timeframes
On-going interaction with clients in relation to audits to ensure expectations and timelines are communicated in a proactive and timely manner
Management and co-ordinate all aspects on site Supplier Management Programme, including supplier audits, preparation of QTA’s and supplier qualification
Ensure on-going compliance with customer, regulatory and internal requirements
Ensure safe work practices are being followed at all times, report any near misses immediately to the EHS Department
Raise Deviations, Corrective Action Requests, and Non-Conformance reports as required in a timely manner and ensure that issues are communicated to the auditing Manager/designee
Generation of SOP/Forms/JA's/WI's on MasterControl
Ensure safe work practices are being followed at all times, report any defects immediately to the Safety Officer and attend Health & Safety meetings
Interact and communicate daily with staff and support departments

Fulltime

Autoclave Performance Qualification Specialist

We are seeking a skilled Autoclave Performance Qualification Specialist to join ...

Location

United States , Juncos

Salary:

Not provided

Cencora

Expiration Date

Until further notice

Requirements

Bachelor's degree in Engineering, Life Sciences, or a related field (Master's preferred)
3+ years of experience in pharmaceutical or biotech validation, with a focus on autoclave or sterilization equipment
Proficiency in validation software (e.g., Kaye Validator, Ellab), statistical tools (e.g., Minitab), and regulatory standards
Strong analytical skills, attention to detail, and ability to work in a fast-paced, regulated environment
Excellent communication and teamwork abilities

Job Responsibility

Design, execute, and document performance qualification protocols for autoclave systems, including cycle development, validation, and re-qualification
Perform risk assessments, data analysis, and statistical evaluations to verify autoclave efficacy (e.g., heat distribution, penetration, and lethality)
Collaborate with cross-functional teams (Engineering, Validation, and Operations) to resolve equipment issues and implement improvements
Maintain detailed records, generate reports, and ensure compliance with regulatory requirements (e.g., 21 CFR Part 11, Annex 1)
Train staff on autoclave operations and participate in audits and inspections
Stay updated on industry best practices and emerging technologies in sterilization validation

What we offer

medical
dental
vision care
comprehensive suite of benefits that focus on the physical, emotional, financial, and social aspects of wellness
support for working families (backup dependent care, adoption assistance, infertility coverage, family building support)
behavioral health solutions
paid parental leave
paid caregiver leave
training programs
professional development resources

Fulltime

Commissioning and Qualification Specialist

We are looking for a skilled Commissioning and Qualification Specialist to join ...

Location

Belgium

Salary:

Not provided

Amaris Consulting

Expiration Date

Until further notice

Requirements

Bachelor’s degree in Engineering, Life Sciences, or a related field
Minimum of 4 years of experience in the pharmaceutical sector, specifically in commissioning and qualification of HVAC systems and clean rooms
Strong knowledge of regulatory requirements (FDA, EMA, etc.) and industry standards (GMP, ISO)
Excellent problem-solving skills and attention to detail
Strong communication and interpersonal skills, with the ability to work collaboratively in a team environment

Job Responsibility

Lead the commissioning and qualification processes for HVAC systems and clean rooms in compliance with industry regulations and company standards
Develop and execute validation protocols, including IQ, OQ, and PQ documentation
Collaborate with engineering, operations, and quality assurance teams to ensure seamless project execution
Conduct risk assessments and provide recommendations for improvements in systems and processes
Maintain accurate records and documentation of all commissioning and qualification activities
Stay updated on industry trends, regulations, and best practices related to commissioning and qualification

What we offer

Competitive salary and performance-based incentives
Comprehensive benefits package, including health insurance, retirement plans, and paid time off
Opportunities for professional development and career advancement
A collaborative and innovative work environment

Commissioning & Qualification Specialist

Airswift is looking for a Commissioning & Qualification Specialist to work with ...

Location

United States , Birmingham

Salary:

Not provided

Airswift Sweden

Expiration Date

Until further notice

Requirements

Bachelor’s degree preferably in Engineering or Science discipline
3 to 5 experience in validation / qualification of aseptic pharmaceutical processes and / or equipment
Strong understanding of Regulatory Guidance Framework FDA/EU, Industry Best Practices and GMPs
Comprehensive knowledge of pharmaceutical manufacturing equipment and processes

Job Responsibility

Develop URS, SIC and SRA for new and existing aseptic facilities and equipment
Develop and execute Commissioning (COM) and Installation qualification (IQ) protocols
Perform operational qualification (OQ) and performance qualification (PQ) activities
Ensure all documentation is compliant with regulatory requirements and internal quality standards
Conduct risk assessments and implement mitigation strategies for aseptic processes
Proficient in the use of word processing, spreadsheet and presentation software programs
Proficient in use if Kaye Validator AVS and Val Probe Systems
Knowledge on following equipment qualifications: Homogenizers, Pump Skids, SIP & CIP Skids, Temperature control units, Tanks, Requalification of CTU’s
Develop and implement validation plans for computerized systems
Conduct risk assessments to identify potential issues related to system functionality and data integrity

Lead Qualification Specialist

The Lead Qualification Specialist is responsible for researching, screening, and...

Location

Salary:

Not provided

My Amazon Guy

Expiration Date

Until further notice

Requirements

Minimum of 1–2 years of experience in lead qualification, sales operations, or data research (experience with Amazon sellers or eCommerce preferred)
Strong understanding of sales funnels and lead qualification processes
Proficient in CRM systems, preferably HubSpot (experience managing lead data, lifecycle stages, and reports)
Exceptional research and data validation skills, with high attention to detail and accuracy
Strong organizational and time management skills to handle multiple lead requests and prioritize effectively
Excellent written and verbal communication skills for collaborating with BDRs, CCSS, and Account Executives
Ability to analyze and interpret customer data to identify potential qualified leads
Tech-savvy with working knowledge of Google Workspace, Excel/Sheets, and online research tools
Proactive, resourceful, and results-oriented, able to meet or exceed key performance targets
Comfortable working in a fast-paced, remote environment with minimal supervision

Job Responsibility

Qualify leads for BDRs and make sure they have complete information that BDRs need such as Amazon products and email addresses
Manage a list of qualified leads and assign them to BDRs
Process requests of BDR, CCSS & AEs about qualifying their leads or finding additional information they need
Screen and qualify potential sales leads that fit an ideal customer’s profile with the intent of purchasing My Amazon Guy’s services
Collect business information of Amazon sellers such as Amazon seller links, email addresses, and phone numbers and document in Hubspot
Provide accuracy of customer data to provide quality leads to the Business Development Team
Lead Generation and other relevant market research
Be readily available to take on other side projects
Use the lead qualification criteria to ensure accuracy and consistency with client data
Keep in file both qualified and unqualified leads in the sales cycle for current and future references

What we offer

Permanent work-from-home setup
Unlimited FREE access to MAG School courses and SOP Library
Opportunities for professional development and career advancement

Fulltime

Qualification & Validation Specialist

Location

Italy , Milano

Salary:

Not provided

S.T.B. ValiTech S.r.l.

Expiration Date

Until further notice

Requirements

Degree in Engineering or Biotechnology
At least three years of previous experience in the role
Knowledge of industrial processes
Familiarity with computer systems
Proficiency in English
Willingness to travel to client sites and undertake business trips if necessary

Job Responsibility

Conduct validation activities for processes, machinery, equipment, computer systems, and instruments that have a qualitative impact on services, primarily in the chemical-pharmaceutical sector
Ensure quality standards and compliance with company policies and international regulations
Prepare technical and qualification documentation to provide support
Perform Risk Analysis

What we offer

A stimulating growth path with leading clients in the pharmaceutical sector

Specialist - Material Qualification Engineer

Location

India , Chennai

Salary:

Not provided

Nordex Group

Expiration Date

Until further notice

Requirements

University degree in Mechanical/Material Engineering or similar
4-8 years experience within composite material industry, blade manufacturing is required, preferred in process or material department
Hands-on mentality
Willingness to work in shopfloor projects
Ready to work in shifts when required
Strong communication skills on engineering level as well as in blue collar level
Fluency in English is preferred

Job Responsibility

Plan and coordinate new material industrialization trials within the blade plants
Supervise initial material trials, industrialization trials up to serial implementation
Feedback and status reporting within interdisciplinary qualification team
Involvement into technical discussions with the material supplier, engineering and quality departments to improve quality and performance
Ensuring lessons learnt are implemented in documentation and execution, eliminating recurring quality issues during industrialization

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Qualification Specialist

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