10 Quality Assurance And Engineering jobs in Beijing.

Hiring now: Quality Compliance Lead @ Amgen, Quality Operation Mgr @ Novo Nordi, Quality Mgr @ Iqvia, Mgr Qa Reg Compliance @ Syneos Hea.Explore more at jobswithgpt.com.

🔥 Skills

Regulatory Compliance (4) Quality Assurance (3) Audits (3) GxP (2) Inspection Readiness (2) Clinical Research Associate (2) site qualification (2) regulatory compliance (2) Good Clinical Practice (2) site management (2)

đź“Ť Locations

Beijing (10)
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Amgen

Quality Compliance Lead Beijing
Skills & Focus: Quality Assurance, Clinical Trials, Risk Management, GCP, Audits, Regulatory Compliance, Data Quality, Pharmaceutical, Vendor Management, Quality Oversight
About the Company: Amgen is a leading biotechnology company that develops innovative human therapeutics.
Experience: Minimum 7 years in pharmaceutical industry
Type: Full time

Novo Nordisk

Quality Operation Manager Beijing
Skills & Focus: QA governance, GMP, GSP, RDC QA management, carrier management, post-marketing surveillance, licenced pharmacist, auditor experience, communication skills, problem solving
About the Company: At Novo Nordisk we recognize that it is no longer good enough to aspire to be the best company in the world. We need to aspire to be the best company for the w…
Experience: Above 5 years quality Compliance experience in GMP or GSP area. At least 2 years quality Compliance experience in GSP area.

Iqvia

Quality Manager Beijing
Skills & Focus: clinical quality, inspection readiness, audit response, risk plans, GCP quality, development, clinical trials, regulatory requirements, clinical operations, training
About the Company: IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industrie…
Experience: At least 5 years of increasingly responsible positions in Clinical Operation and/or Clinical Development Quality.
Type: Full time
Benefits: Benefits programs are designed to meet your total well-being needs so you can thrive at work and at home.

Syneos Health

Mgr, QA & Reg Compliance Beijing
Skills & Focus: Quality Assurance, Audits, Regulatory Compliance, GxP, Inspection Readiness, Audit Reports, Training, Data Management, Team Management, Customer Audits
About the Company: Syneos Health® is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success. We translate unique clinical, medic…
Experience: Requires significant experience and expertise in all aspects of GxP quality assurance auditing.
Benefits: Supports a diverse, equitable, and inclusive culture.
Clinical Research Associate I/II Beijing
Skills & Focus: Clinical Research Associate, site qualification, regulatory compliance, Good Clinical Practice, site management, monitoring, data integrity, investigational product, auditor readiness, pharmacovigilance
About the Company: Syneos Health® is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success.
Experience: Bachelor’s degree or RN in a related field or equivalent combination of education, training and experience
Benefits: Career development and progression; supportive and engaged line management; technical and therapeutic area training; pe…

Iqvia

HGR Specialist Beijing
Skills & Focus: clinical research, site identification, regulatory, start-up, maintenance activities, site documentation, contracts, performance metrics, project timelines, feasibility
About the Company: IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industrie…
Experience: 1 - 3 years’ clinical research or other relevant experience;
Type: Full time
Benefits: Benefits programs are designed to meet your total well-being needs so you can thrive at work and at home.

Novo Nordisk

Product Safety Manager Beijing
Skills & Focus: pharmacovigilance, regulatory compliance, safety management, product approval, clinical medicine, medical devices, stakeholder engagement, audit readiness, safety information, local procedures
About the Company: Novo Nordisk is committed to bringing our products to the Chinese market with the fastest speed and top quality, and applying the most scientific way to commun…
Experience: Min 6 years' experience in pharmaceutical industry or related industry like medical devices or healthcare industry; Min 5 years in pharmacovigilance function.

Syneos Health

Mgr, QA & Reg Compliance Beijing
Skills & Focus: Quality Assurance, Regulatory Compliance, Audits, GxP, Clinical Development, Inspection Readiness, Root Cause Analysis, Personnel Management, Technical Expertise, Cultural Sensitivity
About the Company: Syneos Health® is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success. We translate unique clinical, medic…
Experience: significant experience and expertise in all aspects of GxP quality assurance auditing
Clinical Research Associate II Beijing
Skills & Focus: Clinical Research Associate, regulatory, ICH-GCP, site management, Good Clinical Practice, site qualification, monitoring, data integrity, subject safety, clinical data
About the Company: Syneos Health® is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success. We translate unique clinical, medic…
Type: Full-time
Benefits: Career development and progression; supportive and engaged line management; technical and therapeutic area training; pe…

Novo Nordisk

Product Safety Manager Beijing
Skills & Focus: Product Safety, Pharmacovigilance, Regulatory Compliance, Post-marketing Programs, Safety Information, Audit/Inspection Readiness, Local Procedures, Healthcare, Clinical Medicine, Stakeholder Engagement
About the Company: Novo Nordisk A/S is a global healthcare company with a leading position in diabetes care and strong pipeline of new treatment options for people living with ch…
Experience: Min 6 years' experience in pharmaceutical industry or related industry like medical devices or healthcare industry; Min 5 years in pharmacovigilance function