Latest Pharma Job at Thermo Fisher Scientific | Pharmacy Professionals Apply
Looking for a Pharma Job in quality and regulatory operations? Thermo Fisher Scientific is hiring a Quality Specialist II in Bangalore. This opportunity is ideal for pharmacy professionals seeking experience in post-market surveillance, quality documentation, regulatory compliance, and quality management systems while building a successful Thermo Fisher Career.
- Job Title: Quality Specialist II
- Job ID: R-01355650
- Job Location: Bangalore, Karnataka, India
About the Company
Thermo Fisher Scientific is a global leader in scientific research, healthcare solutions, laboratory technologies, and life sciences services. The company supports customers worldwide by delivering innovative products and services that improve healthcare, scientific discovery, and patient outcomes. For professionals seeking a rewarding Pharma Job, Thermo Fisher Scientific offers opportunities to work on impactful projects that support quality, compliance, and healthcare innovation.
Professionals pursuing a Thermo Fisher Career gain exposure to global quality systems, regulatory frameworks, and advanced healthcare technologies while building expertise through a challenging and growth-oriented Pharma Job environment.
Job Description
This Pharma Job focuses on supporting Post-Market Surveillance (PMS) activities within Thermo Fisher Scientific’s Center of Excellence. The role involves maintaining and updating PMS reports, ensuring regulatory compliance, managing document lifecycle activities, and supporting global business units with audit-ready quality documentation.
The Quality Specialist II will contribute to ongoing product lifecycle surveillance activities while ensuring consistency, traceability, and compliance with applicable quality and regulatory requirements
Key Responsibilities
- Update PMS reports, including PMSR, PSUR, PMPF, and Literature Reviews.
- Maintain version control and documentation traceability.
- Compile and integrate business unit data into standardized templates.
- Ensure documentation accuracy, compliance, and audit readiness.
- Identify inconsistencies and escalate potential safety concerns.
- Collaborate with global teams to gather inputs and incorporate feedback.
- Support annual and periodic updates of PMS documentation.
- Contribute to process standardization and continuous improvement initiatives.
Eligibility Criteria
- Education: Bachelor’s Degree in Pharmacy
- Experience: 1–3 years of experience in quality, regulatory, medical device, or IVD environments.
Required Skills
- Strong technical writing and documentation skills.
- Knowledge of quality systems and regulatory compliance.
- Data interpretation and analytical abilities.
- Familiarity with IVDR and MDR regulations preferred.
- Attention to detail and document control expertise.
- Proficiency in Microsoft Office applications.
- Strong communication and cross-functional collaboration skills.
This Pharma Job at Thermo Fisher Scientific offers an excellent opportunity for professionals interested in quality systems, regulatory compliance, and post-market surveillance activities. The role provides valuable exposure to global quality processes, documentation management, and regulatory standards. Candidates seeking long-term growth through a Thermo Fisher Career can benefit from working in a highly respected and innovation-focused organization.
