QA Jobs at Precision Medicine Group
Are you searching for rewarding QA Jobs in the life sciences industry? Precision Medicine Group is offering an exciting opportunity for professionals passionate about quality systems, supplier management, and regulatory compliance. This role is ideal for candidates seeking Life Science Jobs in a globally recognized organization where quality, innovation, and scientific excellence drive success. If you have experience in quality assurance within a regulated environment, this could be your next career breakthrough.
About Precision Medicine Group
Precision Medicine Group is a leading global organization providing clinical research, laboratory services, commercialization, and data solutions to the life sciences industry. The company partners with pharmaceutical, biotechnology, and healthcare organizations to accelerate the development of innovative therapies. Through various Precision Medicine Group Jobs, professionals gain opportunities to work in quality, research, regulatory affairs, and clinical development while contributing to advancements in healthcare and precision medicine.
Job Details:
- Job Title: Quality Assurance Specialist I
- Company: Precision Medicine Group
- Location: Bengaluru, Karnataka, India
- Employment Type: Full-Time
Position Summary
The Quality Assurance Specialist I (Supplier Management Support) is responsible for supporting the maintenance and continuous improvement of the organization’s Supplier Management Program. The role involves supplier qualification, audit coordination, supplier documentation management, quality agreement administration, supplier corrective action tracking, and communication of supplier-related quality metrics to key stakeholders.
The position also provides backup support to team members when required and may assist with broader quality assurance activities, including non-conformance management, complaints, and change control processes.
Key Responsibilities
Supplier Management and Quality Assurance
- Support the implementation and maintenance of an effective Supplier Management Program.
- Assist in supplier qualification and onboarding activities.
- Manage, organize, and maintain supplier-related quality documentation.
- Coordinate and schedule supplier audits in collaboration with internal stakeholders.
- Maintain the Approved Supplier List (ASL) and ensure supplier records remain current and accurate.
- Prepare, review, and manage Quality Agreements with suppliers.
- Monitor and manage Supplier Corrective Action Requests (SCARs) to ensure timely closure and compliance.
- Communicate supplier notifications and quality-related updates to relevant stakeholders.
- Compile, analyze, and report monthly supplier management Key Performance Indicators (KPIs).
Additional Quality Support
- Support quality assurance activities related to:
- Non-conforming events
- Customer or supplier complaints
- Change control processes
- Contribute to quality system compliance and continuous improvement initiatives.
Qualifications
Minimum Requirements
- Bachelor’s degree or an equivalent combination of education and relevant experience.
- Minimum 2 years of Quality Assurance experience within a life sciences or regulated industry environment.
Required Skills and Competencies
- Strong organizational and administrative capabilities with the ability to manage multiple priorities and meet deadlines.
- Proficiency in Microsoft Office applications, including:
- Microsoft Word
- Microsoft Excel
- Microsoft PowerPoint
- Ability to work independently in a minimally supervised environment.
- Exceptional attention to detail and commitment to accuracy.
- Strong written, verbal, and interpersonal communication skills.
- Ability to effectively collaborate with cross-functional teams and stakeholders.
- Fluency in reading, writing, speaking, and understanding English.
- Flexibility to work extended hours when required to meet business needs.
Preferred Qualifications
- Experience working within a Quality Assurance department in a life sciences or other regulated environment.
- Prior exposure to supplier management processes, supplier qualification activities, and supplier quality systems.
- Familiarity with quality management systems, audits, corrective actions, and compliance requirements within regulated industries.
