We are seeking a highly experienced and proactive Software Testing Manager to oversee our Quality Assurance team.

The Testing Manager will be responsible for developing, implementing, and maintaining quality assurance protocols to ensure our products and services meet the highest standards and fulfill customer expectations.

Experience the freedom of remote work from anywhere in Georgia, whether from the comfort of your home, our modern offices in Tbilisi and Batumi or a coworking space in Kutaisi.

Responsibilities

• Develop and enforce quality assurance policies, leading the QA team to set and achieve defined targets, ensuring all products and services meet established standards and customer expectations

• Conduct comprehensive audits and assess existing processes for potential improvements, aiming to improve product quality and process optimization

• Focus on people management and growth by mentoring team members, fostering a collaborative environment, and encouraging continuous professional development to build a high-performing team

Requirements

• Minimum of 5 years of experience in quality assurance, including at least 2 years in a managerial role, demonstrating a proven track record in effective team management and successful project execution

• Strong knowledge of quality assurance methodologies and tools, coupled with excellent analytical and problem-solving skills to identify issues and develop viable solutions

• Demonstrated leadership skills, with effective communication and interpersonal abilities, essential for managing, motivating, and leading a team while ensuring productive interactions with various stakeholders

We offer

• We connect like-minded people

  • Delivering innovative solutions to industry leaders, making a global impact

  • Enjoyable working environment, whether it is the vibrant office or the comfort of your own home

  • Opportunity to work abroad for up to two months per year

  • Relocation opportunities within our offices in 55+ countries

  • Corporate and social events

• We invest in your growth

  • Leadership development, career advising, soft skills and well-being programs

  • Certifications, including GCP, Azure and AWS

  • Unlimited access to LinkedIn Learning and Get Abstract

  • Free English classes with certified teachers

• We cover it all

  • Participation in the Employee Stock Purchase Plan

  • Monetary bonuses for engaging in the referral program

  • Comprehensive medical & family care package

  • Five trust days per year (sick leave without a medical certificate)

  • Benefits package (sports activities, a variety of stores and services)

Full job description

Key Responsibilities:

• Develop and maintain QA processes, inspection plans, and testing standards to ensure product reliability and compliance.

• Oversee quality operations in manufacturing environments within life sciences or regulated industries.

• Lead root cause investigations and implement effective CAPA to prevent recurrence.

• Assess supplier quality performance and drive improvement initiatives with vendors.

• Review and approve engineering changes to align with internal quality and regulatory expectations.

• Support internal and external audits, ensuring timely resolution of quality issues.

• Manage product complaints, returns, and trend reporting to leadership.

• Utilize digital systems and data tools (e.g., MES, PLM, analytics platforms) to monitor quality metrics and ensure data integrity.

Qualifications:

• Bachelor’s degree in Engineering, Life Sciences, or related discipline.

• Minimum 5 years of quality experience in regulated manufacturing (medical device, pharma, or similar).

• Familiarity with key regulatory frameworks (FDA, ISO 13485, risk management standards).

• Certifications in Six Sigma, Quality Engineering, or Auditing are highly preferred.

Job Type: Contract

Pay: $50.00 - $60.00 per hour

Expected hours: 40 per week

Benefits:

• Health insurance

Application Question(s):

• No C2C - Only w2

Experience:

• Medica Devices: 5 years (Required)

• MES: 3 years (Required)

• PLM: 3 years (Required)

• Quality Assurance: 5 years (Required)

• Green Belt, Black Belt, or CQE certification : 1 year (Preferred)

• FDA 21 CFR 820/803/806, ISO 13485, and ISO 14971: 3 years (Required)