QC/ Junior QA Job at Join.To.IT (Kyiv)

Critical Deviation Investigations Manager

The Critical Deviation Investigations Manager is responsible for leading, managi...

Location

Belgium , Bruxeles

Salary:

Not provided

Amaris Consulting

Expiration Date

Until further notice

Requirements

Bachelor’s degree in Pharmaceutical Sciences, Chemistry, Biology, Biochemistry, Chemical Engineering, or a related field
Master’s or PhD preferred
Minimum 5–7 years of experience in pharmaceutical in deviation investigations and CAPA management
Proven experience in managing critical deviations in a regulated environment (GMP, FDA/EMA compliant)
In-depth understanding of GMP regulations, ICH guidelines, and regulatory inspection expectations
Experience with electronic quality systems (EQS) such as MasterControl, SAP QM, TrackWise, or similar
Strong analytical, problem-solving, and decision-making skills
Excellent written and verbal communication skills
ability to present findings clearly to technical and non-technical audiences
Leadership and mentoring experience with QA teams or cross-functional groups

Job Responsibility

Lead end-to-end investigations of critical deviations across manufacturing, packaging, laboratory testing, storage, and distribution processes
Conduct or oversee root cause analysis (RCA) using validated methodologies (e.g., 5 Whys, Fishbone, Fault Tree Analysis, FMEA) to ensure scientifically sound conclusions
Ensure all investigations are completed within defined timelines and in full compliance with GMP (Good Manufacturing Practice), GDP (Good Distribution Practice), ICH Q10, FDA 21 CFR Part 211, and EU GMP Annex 1 & 15
Author and review detailed Investigation Reports, Deviation Logs, CAPA Plans, and Final Closure Reports with clear evidence and traceability
Collaborate with cross-functional teams including Manufacturing, R&D, Packaging, QA, QC, Regulatory Affairs, and Supply Chain to gather data and implement solutions
Manage and mentor junior QA personnel involved in deviation investigations
Monitor and analyze deviation trends to identify systemic risks and recommend proactive quality improvements
Ensure CAPAs are effectively implemented, monitored, and verified for closure
assess effectiveness through follow-up audits and data review
Support internal and external audits and inspections by providing clear, documented evidence of investigation processes and outcomes

What we offer

Rapid growth: Amaris has doubled its workforce in Belgium in two years, providing numerous growth opportunities for employees
Prestigious projects: Candidates will work with renowned clients in the pharmaceutical, biotechnology, and European institutions sectors on impactful missions
International environment: An agile and dynamic structure promotes intrapreneurship and meritocracy, with international exposure at the heart of Europe

Fulltime

Structural Project Manager

Our Michigan division is hiring a Structural Project Manager to work on complex ...

Location

United States , East Lansing

Salary:

Not provided

RimePro Inc

Expiration Date

Until further notice

Requirements

Licensed Professional Engineer (PE) in Michigan (required)
10+ years of structural engineering experience with a focus on bridge design, rehabilitation, and inspection
Strong familiarity with MDOT standards, including Bridge Design Guide (BDG), AASHTO LRFD, MDOT load rating requirements, and CADD standards
Proven experience delivering MDOT bridge projects from concept through construction
Ability to perform and review complex structural calculations and load ratings
Proficiency in relevant engineering software (e.g., MDOT MiBridge, LEAP Bridge, MDX & MicroStation)
Demonstrated experience managing project scope, schedule, and budget for multiple concurrent projects
Strong leadership skills with the ability to mentor and supervise engineers, designers, and technicians
Experience leading multi-disciplinary coordination with roadway, hydraulics, geotechnical, and environmental teams
Ability to oversee QC/QA processes to ensure deliverables meet MDOT and industry standards

Job Responsibility

Lead and manage structural engineering projects involving MDOT bridge design, rehabilitation, and inspection, from planning through completion
Serve as the primary client contact for MDOT and other stakeholders, ensuring compliance with MDOT Bridge Design Guide (BDG), AASHTO LRFD, and project-specific requirements
Oversee preparation of bridge design plans, specifications, and cost estimates in accordance with MDOT standards
Coordinate with multidisciplinary teams, including roadway, geotechnical, and hydraulics, to ensure integrated project delivery
Manage project schedules, budgets, and deliverables to meet contractual and quality requirements
Conduct quality control (QC) and quality assurance (QA) reviews on structural calculations, drawings, and reports
Supervise and mentor junior engineers, designers, and technicians, providing technical guidance and career development support
Facilitate project progress meetings with clients, contractors, and internal teams
Review and approve shop drawings, RFIs, and construction submittals for structural compliance
Perform site visits for construction observation, bridge inspection, and condition assessment

What we offer

Insurance
Retirement plans
Wellness programs
Tuition reimbursement for job-related courses
Ongoing professional development through resources like Red Vector, LinkedIn Learning, technical team meetings, knowledge-sharing training sessions
Personalized training and career development plans
Funding for training, committee work, professional organization memberships, and licenses/certifications
Flexible work schedules and hours, including work-from-home options (dependent on the role)
Generous Paid Time Benefits (PTB)
Ten days of paid parental leave for birth, adoption, or foster placement

Fulltime

Senior QA Engineer

VarSome.com is the world’s leading website for professional human genetics. VarS...

Location

Poland

Salary:

Not provided

Saphetor

Expiration Date

Until further notice

Requirements

BSc and/or MSc Degree in Computer Science, Engineering, or other STEM degrees
At least 4 + years of experience in Quality Assurance, focusing on test automation, including designing, implementing, and maintaining test frameworks and test cases
Familiarity with test management/documentation tools (e.g., TestRail, QC)
Working knowledge of API testing tools (e.g., Postman, SoapUI)
Hands-on experience with Selenium WebDriver and test frameworks such as Pytest
Programming experience with Python
Strong analytical skills, attention to detail, and ability to work independently as well as in a team
Fluency in English (written and spoken)
Be a flexible team player and have the ability to manage a project
Highly motivated and detail-oriented individual

Job Responsibility

Conduct automation and manual testing, while documenting test methodologies
Gain in-depth knowledge of our clinical platform, which enables fast and accurate variant detection, annotation, and interpretation of NGS data for whole genomes, exomes, and gene panels to give the highest quality to our customers
Participate in the full product development life-cycle: defining test requirements at the start of a project, tracking and managing test issues, ensuring that the software meets its acceptance criteria, signing off on releases for quality purposes and reviewing test documentation
Continue to develop our automation suite and embed this within our development process
Write concise documentation and revise older test cases to achieve greater testing coverage
Develop new testing frameworks where necessary
Mentor junior QA engineers and promote best testing practices across the team

What we offer

A position in a fascinating healthcare growth domain, at the cutting edge of technology
A competitive compensation package
Remote work with occasional meetings
Endless learning opportunities while transferring new technologies from academics to clinical practice all over the world

Fulltime

Senior QA Engineer

VarSome.com is the world’s leading website for professional human genetics. VarS...

Location

Romania

Salary:

Not provided

Saphetor

Expiration Date

Until further notice

Requirements

BSc and/or MSc Degree in Computer Science, Engineering, or other STEM degrees
At least 4 + years of experience in Quality Assurance, focusing on test automation, including designing, implementing, and maintaining test frameworks and test cases
Familiarity with test management/documentation tools (e.g., TestRail, QC)
Working knowledge of API testing tools (e.g., Postman, SoapUI)
Hands-on experience with Selenium WebDriver and test frameworks such as Pytest
Programming experience with Python
Strong analytical skills, attention to detail, and ability to work independently as well as in a team
Fluency in English (written and spoken)
Be a flexible team player and have the ability to manage a project
Highly motivated and detail-oriented individual

Job Responsibility

Conduct automation and manual testing, while documenting test methodologies
Gain in-depth knowledge of our clinical platform, which enables fast and accurate variant detection, annotation, and interpretation of NGS data for whole genomes, exomes, and gene panels to give the highest quality to our customers
Participate in the full product development life-cycle: defining test requirements at the start of a project, tracking and managing test issues, ensuring that the software meets its acceptance criteria, signing off on releases for quality purposes and reviewing test documentation
Continue to develop our automation suite and embed this within our development process
Write concise documentation and revise older test cases to achieve greater testing coverage
Develop new testing frameworks where necessary
Mentor junior QA engineers and promote best testing practices across the team

What we offer

A position in a fascinating healthcare growth domain, at the cutting edge of technology
A competitive compensation package
Remote work with occasional meetings
Endless learning opportunities while transferring new technologies from academics to clinical practice all over the world

Fulltime

Senior QA Engineer

VarSome.com is the world’s leading website for professional human genetics. With...

Location

Greece , Athens

Salary:

Not provided

Saphetor

Expiration Date

Until further notice

Requirements

BSc and/or MSc Degree in Computer Science, Engineering, or other STEM degrees
At least 4 + years of experience in Quality Assurance, focusing on test automation, including designing, implementing, and maintaining test frameworks and test cases
Familiarity with test management/documentation tools (e.g., TestRail, QC)
Working knowledge of API testing tools (e.g., Postman, SoapUI)
Hands-on experience with Selenium WebDriver and test frameworks such as Pytest
Programming experience with Python
Strong analytical skills, attention to detail, and ability to work independently as well as in a team
Fluency in English (written and spoken)
Be a flexible team player and have the ability to manage a project
Highly motivated and detail-oriented individual

Job Responsibility

Conduct automation and manual testing, while documenting test methodologies
Gain in-depth knowledge of our clinical platform, which enables fast and accurate variant detection, annotation, and interpretation of NGS data for whole genomes, exomes, and gene panels to give the highest quality to our customers
Participate in the full product development life-cycle: defining test requirements at the start of a project, tracking and managing test issues, ensuring that the software meets its acceptance criteria, signing off on releases for quality purposes and reviewing test documentation
Continue to develop our automation suite and embed this within our development process
Write concise documentation and revise older test cases to achieve greater testing coverage
Develop new testing frameworks where necessary
Mentor junior QA engineers and promote best testing practices across the team

What we offer

A competitive compensation package combined with additional benefits
Endless learning opportunities, while transferring new technologies from academics to clinical practice all over the world

Fulltime

Senior Account Manager

The Senior Account Manager manages and leads day to day relationships with key/t...

Location

United States , Syracuse; Rochester

Salary:

75000.00 - 120000.00 USD / Year

Pinckney Hugo Group

Expiration Date

Until further notice

Requirements

5+ years of agency experience in an account management role
Experience working with CPG (Consumer Packaged Goods) clients
Bachelor’s degree in advertising, marketing, business or related degree required
Strong understanding of advertising and marketing disciplines, advertising and sales promotion programs, media advertising, direct mail, trade shows, public relations, point-of-purchase and online advertising strategies
Computer proficiency including word processing, data entry, spreadsheets and generating reports using standard software applications
Ability to communicate effectively, both orally and in writing
Ability to read, write, analyze and interpret general business periodicals and professional journals
Ability to write reports and business correspondence
Ability to effectively present information and respond to questions from groups of managers, clients, customers and the general public
Ability to analyze and solve problems

Job Responsibility

Acts as voice of client on day-to-day work
Understands and shares client business & marketing objectives
Drives work forwarding providing thoughtful input & briefs
Contributes to client's organic growth
Responsible for the client budget, managing costs & profitability, deliverables and resources
Owns budget tracking, billing and after-action reports
Provide marketing leadership on client business and internally. Knows the why and stays curious.
Manages & delivers projects by developing project plans & scopes, estimates along with understanding resourcing assignments and ensures they are adhered
Ensures QA & QC is integrated into project plans and is executed to provide high quality outputs
Responsible for ensuring business requirements are understood, documented and met.

What we offer

Hybrid work – split your week between working in our office or at home
Generous PTO policy, including flex time
Paid parental leave
Medical, vision, dental benefits
Resources for savings and investments such as our 401(k) plan with company match
Company-sponsored events and swag
Dog friendly work environment
Opportunities to learn, develop, network, and connect

Fulltime

Client Experience Manager

Responsible for providing expertise to both external and internal clients for al...

Location

Germany , Cologne

Salary:

Not provided

Sotheby's

Expiration Date

Until further notice

Requirements

Minimum of 5 years of appropriate experience
Excellent Client Service Skills
High level of initiative with effective time management skills
Strong management and leadership with the ability to motivate teams and work with senior levels of management
Good communication and interpersonal skills
Excellent organizational skills
Decisive, flexible, versatile and innovative
Agility of mind, ability to plan, prioritize and multitask
Logical, structured, organized and disciplined
Able to work with complexity and ambiguity

Job Responsibility

Manage, motivate and lead the Client Experience Team in Cologne
Switzerland and Milan
Rapid resolution to enquiries and issues with a preparedness to respond and answer client communication in support of the team
Provide mentorship and professional development for the junior members of the CX Team
Ensure the daily monitoring of SLAs to ensure we are meeting our CX Objectives (through Freshdesk / 8x8)
Manage overall resources to balance workload / business needs with staffing and promote consistency within group
Work alongside the Head of Client Experience to ensure consistency of communication and service delivery to clients
Ensure resources are allocated appropriately to provide optimum coverage and support to CX activity
Organization of training so team members remain competent in the delivery of their duties
Be prepared to dynamical support CX teams across EMEA and globally to ensure that we are effectively responding and managing activity as well as proactively forecasting potential windows of increased activity

Senior QC Analyst

At Target Healthcare Group, we are pioneers in the pharmaceutical industry, comm...

Location

Salary:

Not provided

360 Resourcing Solutions

Expiration Date

Until further notice

Requirements

Bachelor’s or Master’s degree in Chemistry, Biochemistry, Pharmaceutical Sciences, or a related field
Minimum 5–8 years of QC laboratory experience in the pharmaceutical or biopharmaceutical industry
Strong working knowledge of analytical techniques such as HPLC, GC, UV-Vis, FTIR, TOC and dissolution
Proven experience in method validation, instrument troubleshooting, and data integrity compliance
Excellent understanding of cGMP, GLP, and regulatory requirements
Strong attention to detail and analytical thinking
Proficiency in laboratory software including Chromeleon
Strong communication, leadership, and mentoring skills
Ability to work independently and manage multiple priorities under tight timelines

Job Responsibility

Perform qualitative and quantitative chemical and microbiological analyses of raw materials, in-process samples, finished products, and stability samples using validated methods (e.g., HPLC, GC, UV, FTIR, Dissolution)
Review and verify analytical data, ensuring accuracy, completeness, and compliance with cGMP and SOPs
Lead out-of-specification (OOS), out-of-trend (OOT), and deviation investigations, including root cause analysis and CAPA development
Support release testing and timely completion of batch records to ensure uninterrupted product supply
Participate in method validation, method transfer, and equipment qualification activities
Develop and optimise analytical methods as required to support new product development or process changes
Troubleshoot complex analytical and instrumentation issues independently and provide guidance to peers
Ensure all activities comply with cGMP and ICH, and other applicable regulatory guidelines
Prepare, review, and maintain laboratory documentation including test records, logbooks, and SOPs
Support internal and external audits and respond to audit findings

What we offer

Active Social and charity committee
Cycle to Work Scheme
Electric Vehicle Scheme
Eye Care Vouchers

QC/ Junior QA

Join.To.IT

Location:
Ukraine , Kyiv

Category:
IT - Software Development

Contract Type:
Not provided

Salary:

Job Description:

Job Responsibility:

Requirements:

Additional Information:

Job Posted:
March 18, 2026

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