PharmEng Technology

Quality Assurance Consultant

PharmEng Technology  •  Helsinki, FI (Onsite)  •  8 days ago
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Job Description

The Quality Assurance Consultant is responsible for the implementation, maintenance, and oversight of the Quality Management System (QMS) in local affiliates. This role ensures compliance with regulatory requirements, quality standards, and company policies. The Quality Assurance Consultant will manage quality risk, complaints, change controls, deviations, CAPA, authority inspections, self-inspections, GxP surveillance, product quality reviews, training, local product release, and oversight of GDP requirements for local warehousing and distribution.

Key Responsibilities:

  • QMS implementation, maintenance, and oversight in local affiliates.
  • Maintenance of the local Quality Manual and Site Master File.
  • Quality risk management in local affiliate, including risk identification, analysis, communication, control, and escalation as required.
  • Complaint management, acting as the Local Complaint Coordinator for reporting, local assessment, and local investigation.
  • Change control management, QA assessment, site change control, QA review for change implementation and closure.
  • Deviation management for internal, external, and transport deviations.
  • CAPA management from deviations, internal audits, external audits, and self-inspections.
  • Management of authority inspections and self-inspections.
  • Local GxP surveillance and assessment.
  • Product quality review (PQR).
  • Training management, including maintenance of training matrix, training of local staff, annual GxP refresher training, and handling of training assignments in the LMS.
  • Local product release (local QP), shipment review of transport performance, goods receipt check, and deviation handling.
  • Oversight of GDP requirements for local warehousing and distribution.
  • Shipping lane qualification and local transport performance of secondary distribution.
  • Secondary distribution transport performance review.
  • Return management, including QA evaluation against return criteria and collaboration with distributors.
  • Product recall management, including local recall execution, communication with customers, communication with HA, recall reconciliation, and local product destruction.
  • GxP suppliers management, including supplier identification, qualification, approval, annual compliance status evaluation, quality audit planning, conduct quality audits, and CAPA approval and closure.
  • Local repackaging and relabeling, including change management, protocol, execution, QA review, and release.

Qualifications:

  • Bachelor's degree in Quality Management, Life Sciences, or a related field.
  • Minimum of 5 years of experience in Quality Assurance within the pharmaceutical or healthcare industry.
  • Strong knowledge of GxP regulations and quality standards.
  • Excellent analytical, problem-solving, and communication skills.
  • Ability to work independently and collaboratively in a team environment.
  • Proficiency in using Quality Management Systems and Learning Management Systems (LMS).

Key Competencies:

  • Attention to detail and accuracy.
  • Strong organizational and time management skills.
  • Effective leadership and team management abilities.
  • Proactive and results-oriented mindset.
PharmEng Technology

About PharmEng Technology

PharmEng Technology, now part of Efor Group, leader in Compliance Engineering, is a leading provider of technical services and solutions to the pharmaceutical, biotechnology, and healthcare industries. With over 25 years of experience, we specialize in Commissioning, Qualification, and Validation (CQV) services for facilities, utilities, equipment, and processes.

As part of Efor’s global network of 3,000 experts across 12 countries, we are better equipped than ever to deliver innovative and comprehensive solutions tailored to the unique needs of clients worldwide. This integration strengthens our ability to combine global expertise with local proximity, positioning PharmEng as a strategic partner for the industry’s most prominent players.

Our team of highly skilled professionals brings a wealth of industry expertise and knowledge to every project, ensuring that our clients receive the highest quality services and solutions. We pride ourselves on our ability to provide flexible, innovative, and cost-effective solutions that meet our clients' unique challenges.

At PharmEng Technology by Efor, we are committed to delivering excellence in everything we do. We work closely with our clients to understand their goals and objectives, developing customized solutions that deliver measurable results. Our focus on quality, safety, and compliance ensures that our clients can trust us to meet their most critical needs.

Specialties: PharmEng Technology specializes in the planning, design, construction, and validation of Health Care, Laboratory, API Pharmaceutical, and Biotechnology facilities and equipment, including computer systems. We provide professional services that meet both regulatory and business demands, following current Good Manufacturing Practices (cGMP), Good Engineering Practices (GEP), and Good Laboratory Practices (GLP).

Industry
Chemicals & Materials
Company Size
201-500 employees
Headquarters
Toronto, CA
Year Founded
Unknown
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